Next Article in Journal
Artificial Neural Network (ANN)-Based Water Quality Index (WQI) for Assessing Spatiotemporal Trends in Surface Water Quality—A Case Study of South African River Basins
Previous Article in Journal
Explicit Scheme for a Hydrological Channel Routing: Mathematical Model and Practical Application
 
 
Correction published on 2 August 2024, see Water 2024, 16(15), 2193.
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Multi-Interacting Natural and Anthropogenic Stressors on Freshwater Ecosystems: Their Current Status and Future Prospects for 21st Century

by
Doru Bănăduc
1,*,
Angela Curtean-Bănăduc
2,
Sophia Barinova
3,
Verónica L. Lozano
4,
Sergey Afanasyev
5,
Tamara Leite
6,
Paulo Branco
6,
Daniel F. Gomez Isaza
7,
Juergen Geist
8,
Aristoteles Tegos
9,10,
Snežana B. Simić
11,
Horea Olosutean
1 and
Kevin Cianfanglione
12,*
1
Faculty of Sciences, Lucian Blaga University of Sibiu, I. Raţiu Street 5-7, 550012 Sibiu, Romania
2
Ecotur Sibiu Association, Grădinilor Street 251, 555301 Cisnădioara, Romania
3
Institute of Evolution, University of Haifa, Mount Carmel, 199 Abba Khoushi Ave., Haifa 3498838, Israel
4
Faculty of Natural Sciences, National University of Salta, CCT Salta-Jujuy CONICET, Av. Bolivia 5150, Salta 4400, Argentina
5
Institute of Hydrobiology National Academy of Sciences of Ukraine, Prospect Geroiv Stalingradu 12, 04210 Kyiv, Ukraine
6
Forest Research Centre (CEF), Associate Laboratory TERRA, School of Agriculture, University of Lisbon, Tapada da Ajuda, 1349-017 Lisboa, Portugal
7
Harry Butler Institute, Murdoch University, Murdoch, WA 6150, Australia
8
Aquatic Systems Biology, TUM School of Life Sciences, Technical University of Munich, Muehlenweg 22, 85354 Freising, Germany
9
Laboratory of Hydrology and Water Resources Development, School of Civil Engineering, National Technical University of Athens, Heroon Polytechneiou 9, 15780 Zographou, Greece
10
Ryan Hanley Ltd. Ireland, 170/173 Ivy Exchange, Granby Pl, Parnell Square W, D01 N938 Dublin, Ireland
11
Department of Biology and Ecology, Faculty of Science, University of Kragujevac, R. Domanovića 12, 34 000 Kragujevac, Serbia
12
ICL, Junia, Université Catholique de Lille, 59000 Lille, France
*
Authors to whom correspondence should be addressed.
Water 2024, 16(11), 1483; https://doi.org/10.3390/w16111483
Submission received: 10 April 2024 / Revised: 4 May 2024 / Accepted: 16 May 2024 / Published: 23 May 2024 / Corrected: 2 August 2024

Abstract

:
The inheritance of historic human-induced disruption and the fierceness of its impact change aquatic ecosystems. This work reviews some of the main stressors on freshwater ecosystems, focusing on their effects, threats, risks, protection, conservation, and management elements. An overview is provided on the water protection linked to freshwater stressors: solar ultraviolet radiation, thermal pollution, nanoparticles, radioactive pollution, salinization, nutrients, sedimentation, drought, extreme floods, fragmentation, pesticides, war and terrorism, algal blooms, invasive aquatic plants, riparian vegetation, and invasive aquatic fish. Altogether, these stressors build an exceptionally composite background of stressors that are continuously changing freshwater ecosystems and diminishing or even destroying their capability to create and maintain ongoing natural healthy products and essential services to humans. Environmental and human civilization sustainability cannot exist without the proper management of freshwater ecosystems all over the planet; this specific management is impossible if the widespread studied stressors are not deeply understood structurally and functionally. Without considering each of these stressors and their synergisms, the Earth’s freshwater is doomed in terms of both quantitative and qualitative aspects.

1. Introduction, Background, and an Analysis of Necessity

The interrelations and synergies among planetary freshwater and a high variety of natural and anthropogenic stressors are logically expected to be very complex. In terms of scientific research approach coverage, a bibliographical analysis of 2083 research papers of the Web of Science Core Collection dealing with freshwater stressors highlights the status and trends in this knowledge advance, and last but not least, it identifies some structural gaps in the science world’s efforts and results in this field of interest (Figure 1).
The temporal trend (Figure 2) of the international scientific community’s studies reveals that modern research have tried to focus on the interactions among different aquatic ecosystem environments, stressors, exposure, biodiversity, interactions, and risks.
The scope of this review is to reveal the importance of the vital freshwater planetary ecosystems’ risks associated with some of the main identified natural and anthropogenic stressors. This work’s objectives were focused on 16 main natural and anthropogenic stressors, which were identified based on publication result gaps and trend analysis (Figure 3, Figure 4, Figure 5, Figure 6, Figure 7, Figure 8, Figure 9, Figure 10, Figure 11, Figure 12, Figure 13, Figure 14, Figure 15, Figure 16, Figure 17, Figure 18, Figure 19, Figure 20, Figure 21, Figure 22, Figure 23, Figure 24, Figure 25, Figure 26, Figure 27, Figure 28, Figure 29, Figure 30, Figure 31 and Figure 32) and their characteristics, interrelations, threats, risks, and management.
For the bibliographical analysis we used scientific materials published on Web of Science Core Collection, using as search terms “freshwater” in combination with each of the seventeen stressors studied in this review paper. The search specified that the terms should be present either in the title or keywords of the analyzed scientific papers. The results were filtered; only articles, reviews, and proceeding papers were selected.
Water is the key to biological entities’ structures, processes, and functions [1,2]. This vital substance for all organisms and ecological systems, fluxes, and circuits is present in large quantities (4.16818183 km3) on Earth. It varies in its richness: 97.24% in marine areas, 2.14% in icecaps and glaciers, 0.61% in groundwater, 0.009% in freshwater lakes, 0.008% in inland seas, 0.005% in soil, 0.001% in atmosphere, and 0.0001% in rivers [3]. This fact gives the illusion of this resource high availability; however, less than 1% of it is suitable for human needs [4]. The heritage of human-induced disruption and the severity of its present impact greatly distress the structure and function of aquatic habitats [5]; specifically, the growing human population is the main cause of the water shortage and its falling quality, and this growth trend continuing [6,7].
Human-induced environmental change is causing a rise in water temperature, declines in dissolved oxygen content, sea level rises, amplified toxicity from pollution, and habitat degradation and loss, among other changes. These impacts will impose strong pressures on aquatic and semi-aquatic habitats, ecosystems, and their associated resources and services and render future water availability uncertain [8,9,10,11,12,13,14].
The proper management of water and related biological and ecological structures and functions, resources, and services can be undertaken at the local, regional, and/or planetary scales. Yet, this may only be accomplished if most threats are approached through an integrated management system to curb human pressures based on state-of-the-art research on freshwater inventory, description, threats, risks, and trends.
In the 20th century, UNESCO began partnerships to cooperate on water-related issues that the Earth is challenged by. The Millennium Development objectives also aim to provide humans with viable access to good-quality water, hygiene, and public health. The Johannesburg Summit proposed that international leaders make safe drinking water and good sanitation available. Have we reached these targets? Are we able to properly manage freshwaters and their associated products and resources? Apart from some local cases, until now, we have failed in this. But do we have the knowledge to adequately manage the many stressors that threaten freshwater ecosystems?
All ecosystems are facing record levels of human-induced stress, pushing them toward global tipping points. Multiple stressors determine these ecosystems’ ecological status at continental and global scales [15,16,17,18,19]. Among them, aquatic ecosystems are affected by a wide range of different stressors [20]. This situation raises difficult challenges for academia and decision-makers, who need a solid knowledge base to manage the environmental change crisis. In this review, we highlight some of the natural and anthropogenic stressors in freshwater ecosystems by providing an overview of their status and future prospects in terms of their description, effects, threats, risks, management elements, and freshwater ecosystem protection elements. Specifically, we reviewed, in this respect, the following freshwater ecosystem stressors: solar ultraviolet radiation (1), thermal pollution (2), nanoparticles (3), radioactive pollution (4), salinization (5), nutrients (6), sedimentation (7), drought (8), floods (9), habitat fragmentation (10), pesticides (11), war and terrorism (12), algal blooms (13), invasive aquatic plants (14), riverine plants (15), and invasive aquatic fishes (16). Our review emphasizes some key stressors that influence the quantitative and qualitative features of freshwater ecosystems.
In the context of the global water management challenges, the main idea of our efforts is to manage present and future challenges facing freshwaters to provide appropriate protection to complex ecosystem structures and functions of freshwaters. The key point of this review is to highlight a sequence of individual and categories of environmental stressors with synergistic negative effects, which must be carefully considered for the assessment, monitoring, and management of freshwater ecosystems.

2. Solar Ultraviolet Radiation (UVR)

There has been a fluctuating interest in the impact of the UVR (solar ultraviolet radiation) stressor on freshwater for researchers in recent years both globally (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources) and in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources), with a significant decrease in interest trends in recent years (Figure 3 and Figure 4). The need for an increase in qualitative and quantitative research efforts is obvious.
Solar radiation influences habitats, organisms, and ecosystems in many different ways depending on its spectral composition [21]. Longer wavelengths (>400 nm) are required for vision in animals and photosynthesis in plants and protists. UV-B radiation (280–320 nm) is harmful to organisms because it damages DNA, biomembranes, and other organelles, whereas UV-A (320–400 nm) can cause damage or stimulate the photo-repair of UV-B damage through photolyases [22].
The UVR effects on organisms depend on diverse levels of exposure, influenced by many factors, including climate change [23]. Climate change is altering the mixing–stratification regimes in the water [24]. These changes are altering key ecosystem services, such as water quality and fishery productivity [25], and impacting biogeochemical cycles, climate-system feedbacks, and biodiversity by inhibiting primary production [26] or rushing the organic matter decomposition through photodegradation, growing the release of greenhouse gases [27]. UVR also alters community structure, distribution and migration patterns, mate choice, foraging, and predator–prey interactions, which ultimately alters trophic interactions and energy transfer efficiency [28]. By contrast, UVR can impact the timing and size of disease outbreaks as it decreases pathogens’ infectivity [29] and parasites’ fitness [30,31] and reduces their habitat suitability [32,33].
Because UVR is a chronic stressor, it is not straightforward to modify or control the stress response. Even though we have a comprehensive understanding of the individual effect of UVR on aquatic ecosystems, we scarcely know how its interaction with other drivers (e.g., temperature, acidification, nutrient inputs, de-oxygenation) could alter the predictions available. The usefulness of data based on single-driver studies in a future scenario of multifaceted planetary change will be limited [34].
The most effective specific strategy to protect life below water from UVR was the implementation of the Montreal Protocol. This implementation, considered the most successful treaty ever, has protected aquatic life by preventing the large increases in UVR that would have occurred due to the Antarctic ozone “hole” (by 20% today, with respect to the 1990s) without the real protection provided by the ozone layer [35].
The impact of UVR on habitats has been greatly increasing eutrophication and browning of water bodies [36,37]. Rising nutrient and organic matter inputs derived from human activities and extreme climate events (i.e., rainfall and wind) are, in many cases, reducing water transparency [38]. Increased water turbidity exerts negative feedback on primary producers because it can limit [39] and inhibit photosynthesis [40]. By contrast, it favors heterotrophic processes, such as respiration, which can trigger anoxia processes that can affect higher trophic levels (e.g., fishes) [41]. These interlinked processes and global-change drivers can not only impair the ecosystems’ functioning but also alter the social perception that we have about ecosystems in a negative way and the provision of several ecosystem services (e.g., food supply, drinking water, recreational activities) [42].
It is critical to quantify the costs of multiple perturbations that freshwater ecosystems are facing. A dialogue between governments, natural area managers, and scientists should be promoted to improve and spread knowledge about how anthropogenic activities and changes in land use affect water quality and other ecosystem services and to build commitment. Thus, funding to perform large-scale and long-term experiments designed to test how communities and ecosystems respond to climatically and anthropogenically driven changes is pivotal for providing knowledge-based decisions that support the practices to be developed in future management and conservation plans.

3. Thermal Pollution

The impact of thermal pollution on freshwater has generated an extremely low level of interest for researchers in recent years, both globally and in Europe (eight studies in the studied period, seven of which are in Europe) (Figure 5). The need for both qualitative and quantitative research on these issues is urgent.
The water temperature in the natural environment varies and depends on the region of the planet and on the source of heat, which can be natural (e.g., volcanoes, hot groundwater) or human-made (e.g., thermal and nuclear power plants). The term thermal pollution is applicable only to the second group of sources. Thermal pollution is one type of physical pollution of the natural environment characterized by a periodic or prolonged input of hot or cold waters to the natural water bodies that cause the degradation of water quality by changes in water temperature associated with human activities [43,44,45].
The water temperature of the water bodies affects not only biological processes but also the growth of aquatic plants and animals [43,46,47,48,49]. Cold water pollution suppresses the development of fauna in freshwater [50]. Conversely, warming increases the rate of photosynthesis due to an increasing number of producers up to a temperature of about 32 °C, with temperatures above this temperature beginning to cause mortality and decomposition by aerobic bacteria [51,52]. Water temperature interacts with other abiotic stressors as a driving force for impact. Its effect on ecological processes is due to the complex combined nature of the interaction of stressors [53]. Thermal pollution is a stress factor for aquatic ecosystems and is also capable of exacerbating the effects of anthropogenic pollution. While chemical pollution factors are classified according to their degree of presence in a natural water body, thermal pollution can be measured in a particularly polluted water body but is not classified among other variables [54]. The reaction of an aquatic ecosystem to thermal pollution is assessed by the change in the state of its biotic part [54]. As a result of thermal pollution of water bodies, the production of organic matter in them begins to prevail over destruction, aerobic processes are replaced by anaerobic ones, the sanitary condition of water bodies deteriorates, and significant changes occur in biota [53]. A drop or increase in water temperature in the receiving water body of about 10 degrees or more is likely a value that leads to intense changes in the biotic part of the ecosystem [43,48].
Since the source of thermal pollution is anthropogenic, the intensity of warm or hot water release can be controlled [55]. However, it is impossible to assess the degrees of damage caused as a result to the aquatic ecosystem by measuring the temperature at the inlet of hot water in the reservoir [56] since the distribution of water temperature and the impact in the receiving reservoir has an uneven character [44,47,57]. In this case, the communities structure [58] turns out to be a particularly sensitive link in the ecosystem, and bioindication [59,60,61] was the most sensitive method for assessing ongoing changes. The innovative methods can lead to positive results in the assessment of the thermal pollution effects on aquatic ecosystems [44,61,62,63,64,65]. It was found that the similarity between thermal pollution and organic pollution impacts [60] can show the parallel in both ecosystem response processes and, therefore, open a new field for thermal influence research [44].
To protect aquatic ecosystems, the United States has an upper temperature limit of 32 °C for surface waters [56] or up to 28 °C according to European Union environmental standards [55]. But, the main thing is to assess the degree of influence of the influx of hot water on the receiving reservoir [66]. The ecosystem can modify its characteristics as the trophic state (e.g. algae or cyanobacteria blooming), the ecosystem’s basic structure [61], invasive organisms’ events, etc. [47].
The monitoring of species content changes in the natural biota of aquatic ecosystems is important for providing forecasts of future changes, which, together with modeling, can be a part of the biodiversity conservation strategy [50,60,62,66].
An analysis of existing approaches to assessing the thermal impact on freshwater ecosystems has shown that more attention is paid to studies of aquatic animals and plants than to microalgae. The system for indicating thermal exposure (cold or hot) has not yet been sufficiently developed. Research is of a more private or experimental nature, while assessments of the impact of temperature anomalies are made on natural open systems. However, assessment methods are developing quite actively.
If we are not able to manage water temperature, the water quality and quantity could be disturbed more than we anticipate, transforming it into an unsafe environment. The water temperature should be kept within the local and regional natural ranges by full real-time monitoring, automatic alerts, and real-time status reporting of the problematic effluents and their strict technological control by insulation, cooling, etc., at the very points of contact with water bodies.

4. Nanoparticles

There has been a steadily increasing number of articles and citations on nanoparticles (NPs) as stressors that impact freshwater in recognition of its importance globally (investigations that include countries with developed and undeveloped scientific networks and financial and human posibilities) but with a sharp decline in recent years—a trend that needs to be reversed for this area of interest in the future—and in Europe (analyses that comprise countries with preeminent developed scientific networks and financial and human resources) (Figure 6 and Figure 7). The need for increasing both qualitative and quantitative research efforts on these issues is evident.
NPs ranging in size from 1 to 100 nanometers [67], have emerged as a relatively new stressor in freshwater aquatic ecosystems. NPs are composed of various materials, including metals, metal oxides, and polymers. Their unique physical and chemical properties make NPs valuable for a wide range of industrial, commercial, and medical applications such as drug delivery, energy production, and electronics. However, their unique properties make them potentially hazardous to the environment.
Once released into the nature, NPs shows high persistence, undergo major transformation, and display high reactivity with other substances around. These characteristics can lead to harmful effects on ecosystems, both by directly impacting and indirectly influencing the complex ecological interactions within multiple-stressor environments.
The presence of NPs in aquatic environments can exert major impacts on organisms, yielding adverse effects. One such result is the induction of reactive oxygen species (ROS) by NPs, leading to oxidative stress within the tissues of organisms. Also, the accumulation of NPs in diverse organs can cause physical stress and tissue damage. NPs can also affect the food chain in aquatic ecosystems by accruing in tissues and being transferred to larger organisms, causing biomagnification. Furthermore, the delicate balance of aquatic microbiota and enzymatic activity can be disrupted by NPs, further exacerbating the negative repercussions on the health of aquatic organisms and water quality [68].
Concerning management elements, the physicochemical characterization (size, surface area, shape, solubility, aggregation, etc.) and the elucidation of biological effects have been proposed [69]. Effective management should involve assessing and monitoring the sources, fate, and transport of NPs in the freshwater ecosystems. Vale et al. [68] highlighted the importance of assessing the dynamic speciation of NPs in the exposure media and identifying specific endpoints for risk assessment studies. In particular, particle size and shape are important factors to consider when assessing the toxicity of NPs in aquatic environments. For example, smaller Ag-NPs present more severe toxicity to aquatic organisms due to their higher particle-related toxicity caused by small particles and higher ion-related toxicity caused by their high dissolution rate and extent [70].
Protection may include implementing green chemistry practices, promoting the use of alternative materials, and developing sustainable manufacturing processes. Strategies to mitigate the effects of NPs on aquatic organisms include the use of nanoremediation techniques and developing early warning systems for NPs contamination.
One rapidly growing field is focused on nanopesticides. When it comes to assessing their aquatic ecotoxicity, it has been suggested that nanopesticides pose a lower environmental risk compared to conventional pesticides due to reduced drift. However, there is still a scarcity of studies that comprehensively evaluate this risk, particularly in comparison to conventional pesticides on an ecosystem scale [71]. Considering the potential environmental contamination resulting from the use of nanopesticides in food production and the potential risks they may pose to aquatic life, there is an urgent need for comprehensive studies on their ecotoxicity prior to their introduction into the market.
In conclusion, we need to urgently and exhaustively monitor environmental contamination and regulate the use and disposal of NPs, prioritizing the reduction of their release into the environment and developing guidelines for their safe handling.

5. Radioactive Pollution

There is fluctuant evolution in the number of articles on radioactive pollution as a stressor with an impact on freshwater, with a significant interest trend in recent years as a recognition of its importance globally (analyses that include states with both developed and undeveloped research networks and financial and human resources), and in Europe (analyses that include states with preponderant advanced scientific networks and financial and human resources), there has been a fluctuant evolution in the number of articles, with a significant interest trend in latest years (Figure 8 and Figure 9). The need for an increase in both quantitative and qualitative research efforts for these issues is clear.
In the last century, the testing and use of nuclear energy resulted in global contamination by artificial radionuclides [72]. Other sources of the technogeneous radionuclides entering freshwaters consist of mining, refining, and hydrometallurgical processing of the uranium ores; production, processing, and storage of nuclear fuel; operation of nuclear power facilities; production and use of radioactive isotopes; radioactive wastes; and nuclear and radiation incidents, accidents, and disasters [73,74,75].
The International Atomic Energy Agency (IAEA) identifies natural or technogeneous radioactive contamination as the occurrence of radioactive compounds where their presence is unintended or undesirable or the process gives rise to their presence [76].
Ecosystem response to radiation depends on species’ sensitivities and the multitude of direct and indirect pathways by which individual organisms can be affected, including the potential for complex interactions across multiple trophic levels [77,78].
The water bodies located near nuclear power plants are the most vulnerable, as they are subjected to thermal discharge, chemical pollution, eutrophication, mechanical stress, and additional irradiation by artificial radionuclides. The liquid discharges of the most widely used WWER-type reactors contain a wide spectrum of radionuclides, mainly the fission products, first of all, 3H, and radioisotopes of biologically essential elements and their chemical analogs 131I, 89, 90Sr, 134, 137Cs, 141, 144Ce, 103, and 106Ru, among others. The other group of radionuclides comprises products of corrosion of the reactor active zone and the first contour of the heat carrier 51Cr, 54Mn, 60Co, etc. [79,80].
The destructive impact of radiation on the nucleic DNA and other molecular components of organelles, which, depending on the impact intensity and duration, can be irreversibly damaged, is accepted as the main threat of radiation [81,82,83].
The radiation dose on the organisms, first by the radionuclides contained in water and bottom sediments, is an important integral criterion of the radioactive pollution effect on the aquatic biota [80,84,85]. At this, the organisms are able to concentrate the radionuclides in organs and tissues, which can result in a notable increase in the dose load owing to internal irradiation [86,87,88]. At the same time, average levels of internal irradiation of aquatic organisms from the radionuclides near nuclear power plants are much lower than irradiation from radionuclides occurring in the environment [79,80].
Despite the relative resistance of aquatic organisms, chronic doses of irradiation can cause damage, mostly mutations, and reduce their vitality, which results in a decrease in the species diversity and changes in the hydrobiocenoses’ structure [78,89,90]. The ecosystems’ response to the stress impact of the radioactive contamination appears in decades, owing to changes in the structural and functional characteristics of populations and communities of the organisms, as certain irradiation doses can stimulate some species or can be ineffective for others, and suppress radiosensitive species [91,92].
The radioactive contamination of freshwater requires optimization of the complex radioecological monitoring systems, which serve as an “end point” of many biologically hazardous long-living radionuclides, as well as an in-depth study of the nuclear energetics impact on the organisms [93,94]. The radioecological monitoring should include regulated collection and analysis of the primary survey data, prompt detection of the radioactive compounds in the aquatic environment, and informational support for assessment and forecast of risk degree for the aquatic ecosystems as well as for decision-making for the radiation and hydro-ecological safety of the nuclear-cycle enterprises [95].
IAEA is authorized to establish and accept safety standards of radiation protection and provide the application of these standards [96].
The irradiation effects on freshwater ecosystems can be mitigated by chemical, physical, and social countermeasures [97,98]. Computerized systems are under development for management support to identify optimal strategies for the rehabilitation of radionuclide-contaminated aquatic ecosystems and the selection of optimal strategies for freshwater ecosystems with different contamination scenarios [98].

6. Salinization

There has been a constant increase in the number of articles on salinization as a stressor that impacts freshwater, with a low decrease in the interest trend in recent years as a recognition of its importance globally (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources), and in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources), there has been a constant increase in the number of articles, with a low decrease in the interest trend in recent years (Figure 10 and Figure 11). The need for qualitative and quantitative research efforts on these issues is clear.
Salinization is the increase in inorganic ions in water bodies [99,100]. Primary salinization results from natural processes such as rainfall, rock weathering, seawater intrusion, and aerosol deposits, and secondary salinization is induced by human activities [101]. Anthropogenic salinization is mainly caused by the runoff from irrigation in agriculture, industrial discharges, mining, and salt use in winter on roads [102,103,104].
The leaching of excess salts increases concentrations of chloride ions and heavy metals in water bodies, which pose a risk to human health and freshwater-related processes [105,106] and can produce temporary yet acute stress on biota [107]. The high salinity levels in rivers create an osmotic pressure on their animals, which can have effects on metabolism, growth, reproduction, and survival [108,109,110,111]. Bacterial, fungal, and macroinvertebrate richness can be reduced with salinity increase, altering organic matter decomposition by microorganisms and detritivores and other ecosystem functions affected by the loss of salinity-sensitive taxa [112,113]. For instance, chlorides negatively impact aquatic organisms but favor the phytoplankton, accelerating eutrophication and increasing algal blooms [114]. Freshwater salt retention also reduces benthic organisms’ diversity, like bivalves sensitive to salinity [115,116]. Acute stress has negative effects on several aquatic species, mostly fish [117,118,119]. Fish have diverse ranges of salt tolerance, depending on species, life stage, salt concentration, temperature, and exposure duration. Exposure to high salinity compromises metabolism and influence osmoregulation, and fish development may be impaired [111,120,121]. Short-term effects of salinization stress on fish include behavior modifications [122,123]. Therefore, if freshwater fish populations are exposed to behavioral disruptors such as salinity, there may be severe ecological implications [124]. In contrast, some research suggests some organisms might be less sensitive or have developed a tolerance for high salinity, like Daphia pulex [125].
The main contributors to the salinization of rivers are humans. There is thus the chance to reduce saline chronic inputs by properly managing land uses and promoting adequate water natural filtering, i.e., riparian forests, and water gathering and treatment, e.g., for the road salts case. Ecosystem-scale experiments, advances in water quality monitoring technology, and models are required to advance and better inform management frameworks for predicting salinization consequences and identifying possible restoration opportunities of freshwater ecosystems [126]. For the chronic input threats, we should add the acute events, like, for example, the well-known case when emergency releases of saline water from chemical plant lagoons led to a complete resetting of all living organisms in the Dniester River for 500 km and triggered the spread of invasive fish species [126].
The management of freshwater secondary salinization must be improved at different scales through mitigation (e.g., source control of main inputs of salt ions, agricultural chemical inputs’ regulation, land-use change limitation, backfilling of mine tailings), remediation (e.g., riparian buffer areas care, solutions to clean-up of surface and groundwater, enhanced wastewater treatment), prevention (e.g., eco-friendly alternatives to roads salts), and monitoring (e.g., assessing salt loads to freshwater ecosystems) [127].
Multiple stressors will likely co-occur in nature in addition to increasing salinity, and sequential stressful events may have additive, synergistic, or antagonistic cumulative effects, intensifying or not, the effects of salinity [128,129,130,131]. Furthermore, these repercussions of human-driven salinization on river systems could additionally be amplified by climate changes [102,104], as temperatures will rise, and evaporation and dilution capacity of freshwater bodies will be affected [132], augmenting residence time and salt concentration in many water bodies, thus endangering many aquatic species and causing biodiversity loss [133,134,135]. Extreme salinity may grant competitive advantages to non-native species and produce a community unbalance that may lead to reduced functional community resilience and the failure of ecological processes.
Secondary salinization is increasing vividly across the globe, and climate changes exacerbate it. Salinity stress threatens biodiversity and changes communities. Understanding the impacts on human health and freshwater taxa is critical to predicting the ecosystem impacts of salinization and informing conservation and management decisions. Coordinated management should take place to prevent future pressure on existing freshwaters.

7. Nutrients

There has been a small number of scientific articles on nutrients as stressors and their impact on freshwater (analyses that include nations with both developed and undeveloped scientific networks and financial and human resources), and in Europe (analyses that include nations with preponderant developed scientific networks and financial and human resources), there has been a small number of scientific articles (Figure 12 and Figure 13). The need for these issues to gain attention in the science world is urgent.
Nutrient pollution has emerged as a major stressor in freshwater ecosystems as a direct consequence of the increasing human population and their activities. Nutrient pollution occurs when nutrients, mainly nitrogen and phosphorus, accumulate in water bodies at excess levels. Nutrients are essential to the maintenance of freshwater ecosystem functioning; however, the accelerated and uncontrolled nature of anthropogenic nutrient pollution has led to nutrient levels reaching historically high levels in freshwaters worldwide [136].
Nutrient pollution is the most pervasive threat impacting freshwater ecosystems worldwide. The overuse of agricultural fertilizers, the combustion of fossil fuels, and increasing urban pressures have led to the mass runoff of nutrients into local waterways [135]. Nutrient pollution is expected to worsen with ongoing human development and is predicted to act synergistically with other global threats to endanger aquatic life [137].
Freshwater ecosystems are completely transformed by long-term excess nutrient inputs. Surface plants and cyanobacteria become over-abundant and dominant over other plant forms, which creates low light conditions for underwater organisms [138]. Low levels of oxygen typically trigger mass fish deaths, which further exacerbate environmental problems [139,140]. Water conditions are also disrupted; hypoxic (low oxygen) episodes become frequent, turbidity levels increase, and high nutrient levels disrupt aquatic life [135,138,141].
Nutrient pollution threatens to endanger aquatic habitats unless targeted management strategies are implemented. Management of nutrient pollution should target the source of the pollution that is limiting the application of nitrogen and phosphorus in agriculture and urban settings through strategies such as fertilization management, conservation tillage, and control of water irrigation [142,143]. Key to source control is the application of strict regulations regarding agricultural practices, though enforcement of regulations remains a challenge [134]. Once in the environment, process controls aim to eliminate nutrients before they leach into the receiving water. For instance, buffer zones (e.g., vegetative buffers) along waterways trap and filter excess nutrients from runoff.
Recent decades have seen technological advancements that can treat industrial and domestic effluent as a protection treatment strategy to curb nutrient pollution in freshwaters [144,145]. Among them are water-saving irrigation, ecological ditches, constructed wetlands, and buffer strips, which have successfully been applied to control agricultural runoff [145]. However, no single technology can manage nutrient pollution at all spatial and temporal scales.
Nutrient pollution presents a strong conservation challenge for aquatic fauna. Under the impact of the high levels of nutrients, an overabundance of algal biomass can destabilize food web dynamics [146], and long-term nutrient disturbance can homogenize freshwater communities across local (α diversity) and regional (β diversity) scales that threaten ecological and evolutionary process [146]. Nutrient pollution can also affect aquatic animals through direct toxic effects [147,148,149,150].
Conservation strategies have focused on determining minimum ecotoxicological endpoints (e.g., lethal concentrations; LC50; [151]), physiological disruptions [148,152], and also sublethal toxicological effects [141] of nutrients on aquatic organisms.
Nutrient pollution presents a growing risk to freshwater ecosystems. Targeted and holistic management strategies and actions, including source control, process control, and end-treatment processes, are required to control nutrient pollution [153].

8. Sediments

There has been a constant increase in the number of global articles and citations on sediments as stressors with an impact on freshwater (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources), and in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources), there has been a constant increase in the number of articles and citations (Figure 14 and Figure 15). The need for these issues to gain attention in the science world is urgent.
Changes in land use are growing erosion, which subsequently introduces excessive amounts of fine sediments in some sectors of aquatic ecosystems [154,155]. In general, both increases and decreases in the transport of suspended sediments can be witnessed as a direct consequence of anthropogenic activities. The building of an extremely high number of dams and barriers along the rivers has had the effect of decreasing the river transport of suspended sediments in numerous systems worldwide, causing the erosion of river delta, coastal lagoons, and coastlines. Global climate change resulting in more extreme weather conditions, such as heavy rainfall, as well as structural stream modifications, such as unwise dam construction in rivers, can exacerbate fine sediment accumulation problems, particularly if they involve changes in flow regimes [156].
The stream bed is a crucial habitat for many riverine organisms as a permanent or temporary habitat. This includes multiple target species of conservation, such as gravel-spawning salmonids and early life stages of endangered freshwater mussels [157]. Increased introductions of fine sediment can result in colmation and reduced oxygen supply to the interstitial zone, which increases mortality in fish eggs of gravel-spawning fishes [158,159], decreases juvenile habitat quality for endangered freshwater mussels [157,160], and can even affect microbial community structure and associated ecosystem services [161]. Fine sediment synergistically interacts with other stressors, such as increased temperature and flow alterations, exacerbating the problems, e.g., related to recruitment in gravel-spawning cold-water fishes [162].
Elements of sediment management in river systems include reducing their introduction, e.g., by buffer strips [154], appropriate management of aquaculture systems connected to hydrographical nets of streams and rivers [163,164], as well as the management of flow regime dynamics [156]. The restoration of stream beds by flushing out fine sediments or introducing gravel has been tested, with lower success in central European streams of intensive agricultural land use compared to forest-dominated Scandinavian streams with forested catchments [165,166].
Since, in the past, a much greater management focus has been placed on freshwater quality, nonstop awareness about the extraordinary importance of the stream bed for stream ecosystem functioning, as well as about the factors that can adversely impact this very important type of habitat, is also fundamental. Several species act as ecosystem engineers and directly interact with fine sediment. For instance, the bioturbation resulting from the burrowing behavior of lampreys, different insect larvae, and mussels can all impact the quality of the stream bed [167,168]. On the other hand, filter-feeding species such as mussels can reduce the amount of suspended fine sediments and turbidity [169]. Protection strategies have to take the interaction of fine sediment with other stressors [162] into account. Protection strategies need to consider complete catchments that govern the process of influencing erosion and sedimentation patterns.
Integrative conservation management of streams and rivers and their biodiversity require the inclusion of stream beds as a fundamental habitat [170]. Maintaining the patchiness and habitat heterogeneity in the end is governed by structurally rich habitats [171] since numerous efforts of restoration, such as the introduction of coarse gravel or the washing out of fine sediments, are very laborious and of limited persistence [171]. In light of the climatic change with warmer temperatures, more severe and prolonged droughts, low-flow conditions, and more extreme weather increasing peak erosion, the conservation and restoration challenges related to functional stream beds will increase.
The too often-overlooked stressor of fine sediment pollution needs to be better considered in the management of rivers and streams habitats quality and biodiversity conservation, especially in light of climatic change, which exacerbates the problem of anoxia in this zone.

9. Extreme Drought

There has been a constant globally increase in the number of articles and citations on drought as a stressor that impacts freshwater, with a decrease in the last few years (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources), and in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources), there has been a constant increase in the number of articles and citations, with a decrease in the last few years in terms of articles but not in terms of the number citations (Figure 16 and Figure 17). The need for these issues to gain attention in the science is urgent.
Meteorological droughts are defined as a period (seasonal, annual, or interannual) of low rainfall relative to the statistical multi-year average for a given location [172,173]. Droughts are a natural characteristic of the hydrological cycle that drives population dynamics and evolutionary processes in freshwater ecosystems [174,175]. Yet, climate warming and human activities are working in tandem to exacerbate drought conditions in freshwaters around the world [175,176,177]. For one, freshwater ecosystems and the life they support are facing the strain of overextraction and catchment degradation due to the competing needs of human development [178,179]. Freshwater faces the compound risk of climate change, where shifts in precipitation and warmer temperatures mean that some regions are forced to contend with less rainfall than historical norms [172].
In freshwaters, droughts develop as below-average rainfall leads to reduced surface runoff and stream inputs and a loss of soil moisture. Periods of drought may cause water bodies to dry up or be reduced to small pools. The receding water column is typically accompanied by a suite of physicochemical changes, including an increase in water conductivity (salinity), decreasing oxygen levels, a buildup of nutrients, and an increased risk of harmful algal blooms [178,179]. The risks of drought are exacerbated by human alterations to freshwater ecosystems, such as water extraction, sedimentation, and the construction of water barriers (dams, weirs) [178]. Drought conditions create a dangerous cocktail of stressors that can result in a reduced abundance and localized extinction of aquatic life, as well as altered ecosystem functioning [179,180,181].
Options for mitigating drought impacts are vast [176,182,183,184] but require a combination of technological and social actions. Technological tools can lessen the impacts of drought on freshwater through improved water conservation, water reuse, and improved water-efficiency devices [184]. Public outreach and strict water conservation policy will be crucial in curtailing extreme drought [182]. For example, policy reforms led to profound changes in public perception of water conservation during Australia’s Millennium Drought [185,186,187]. However, combating the contributions of climate warming to extreme droughts will require intergovernmental actions [185].
Drought protection requires proactive strategies that minimize the impact of man-made alterations to waterways. For example, the restoration of catchments and riverbank zones, maintenance of refuge habitats, and reinstatement of water flow can introduce resilience to freshwaters against increasing drought conditions [178].
Worsening drought conditions pose a significant conservation issue to freshwater ecosystems. Droughts act as a ramp disturbance, meaning that their severity increases with time [188,189]. As such, sensitive species will be lost early in the disturbance, while resistant species could withstand intensifying drought conditions [179,190]. Conservation measures to combat drought will require an understanding of the spatial variation in the severity of drought impacting freshwater habitats [176,190] and the drought sensitivities of regionally important species, coupled with pre-emptive and responsive management actions [180,191], all of which are within the well-known climate change context.
Drought conditions can pose extreme challenges to freshwater. With predictions for longer and more severe droughts, coordinated efforts are required at global, regional, and local levels to ensure the long-term sustainability of freshwater ecosystems.

10. Extreme Floods

There has been a constant globally increase in the number of articles and citations on floods as stressors that impact freshwater (analyses that include states with both developed and undeveloped scientific networks and financial and human resources). By contrast, in Europe (analyses that include states with preponderant developed scientific networks and financial and human resources), it is of low interest, with a small number of articles published annually but a relatively constant increase in the number of citations (Figure 18 and Figure 19). The need for all these complex issues to gain attention in Europe is a necessity.
Extreme fluvial floods are associated with intense natural phenomena resulting in overbank flows in natural river bodies. It is also linked with artificial high flows in strongly modified rivers influenced by the operation of hydropower plants or channelization works to alleviate river water levels. Flooding is the most important environmental parameter in floodplain aquatic environments, and therefore, floodplain wetlands should be considered integrated components of a single dynamic system linked by strong interactions between hydrological and ecological processes [192]. The concept of the flooding pulse was first introduced by Jung et al. [193], defining the flood as a main driving force responsible for the existence, productivity, and interaction of the major biota in river-floodplain systems. Flooding pulses are strongly linked with habitat and organisms’ diversity, nutrient and sedimentation life cycles, etc.
The floodplain habitat expansion during flooding creates important spawning, nursery, and foraging areas for many fish species and a variety of other vertebrates. The alteration of the natural flooding regime may substantially impact aquatic ecosystems since it has been observed that reduced summer floods and increased winter flows cause excessive growths of submerged aquatic macrophytes in some rivers regulated by hydropower stations [194]. The effect of flooding in determining fish access to nurseries and food has been well defined [195,196]. The latter has also been investigated in conjunction with the river regulation for quantifying the value of inundated floodplains for breeding and juvenile habitats [197] and whether the fish will remain trapped in isolated floodplain water bodies or are released back into the river system [198].
Another main way that fluvial flooding is linked with biodiversity is associated with the floodplain alluvium since the duration of floods has been the most vital variable driving riparian dynamics. For example, Poiani et al. [199] predicted that the abundance of mature cottonwood would decrease from 40% to about 20% without flooding within a period of about 120 years and would disappear completely in about 450 years. Other studies present similar outcomes as the flow regulation/stabilization below existing dams reduces floodplain size and substantially impacts the riparian ecosystem by altering the trophic structure and reducing the biodiversity, which is highly adapted to the periodic flooding regime and the associated input of nutrients and sediment [200,201,202,203,204].
Assessing the actual connection between extreme flooding and aquatic health is often a challenging task, as a variety of in situ gauges are required to define interconnected study layers [205,206]. Long-term monitoring gauges for multiple abiotic and biotic parameters, as set out above, should be available to provide wise decisions relating to water/environmental exploitation issues.
To manage the negative effects of extreme flooding in the aquatic systems, there is a strong need to provide multidiscipline approaches based on advanced hydrology, hydrodynamics, and environmental modeling in order to investigate optimal strategies for minimizing the flooding impacts on societies and the environment. Integrated engineering solutions must be considered by thoroughly specifying aquatic environmental impacts and, where possible, by promoting environmental wealth as recently proposed by the natural-based approach [207] and also by integrating ecohydrological views within the new major reservoir infrastructure design [208].
Even though the existing and planned hydropower plants have received criticism for unprecedented negative impacts on the downstream riverine environments [209,210,211,212], the irreplaceable social value of these types of infrastructure [213] in conjunction with modern and holistic environmental modeling approaches [214] can offer benefits to the aquatic, riverine restoration and maintenance.
The well-defined connection degree of flood flows and riverine ecological components in both unregulated and strongly modified river bodies highlights the importance of setting up detailed integrated modeling approaches based on long-term multiparametric gauges for establishing sustainable scientific solutions, as well as developing reliable and environmentally resilient water infrastructure.

11. Habitat Fragmentation

There has been a relatively constant increase in the globally number of articles and citations on habitat fragmentation as a stressor that impacts freshwater, with an obvious decrease in the last 3–4 years (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources). By contrast, in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources), there has been a constant increase in the number of articles and citations (Figure 20 and Figure 21).
Fragmentation can be characterized as the lack of connectedness along the river network. When it is the consequence of human activities, such as the construction of river barriers, it is considered to be one of the most threatening stressors affecting freshwater systems. Fragmentation promotes the isolation of habitat patches or even the separation of a given habitat into smaller isolated habitat patches.
Rivers constitute complex, intricate, and dynamic systems that can be characterized by spatial and temporal fluctuations. These systems have been described as having four classical dimensions: longitudinal—along the river; vertical—between the river channel and the hyporheic zone; lateral—between the river channel and river banks; and temporal—over time [215]. Because habitats relevant for the functioning of the systems and for the life-cycle completion of some species are spatially separated, longitudinal connectivity can be arguably considered the most important. Dams and weirs introduce a breach in the longitudinal connectivity of aquatic systems [216,217,218], which leads to alterations in habitats and flow patterns that can alter environmental cues [219] and affect the biotic communities [220]. These fragmentation effects have been described across various regions, including North America [221,222,223,224], Europe [225,226], Australia [219], Africa [227], and Asia [228,229].
River connectivity is a way of understanding rivers, how these relate and interplay with the spatial components within riverscapes, and how this impacts ecological processes [230]. By the same token, connectivity conservation is a guarantee of ecological processes. To understand to what extent protection should be provided, it is vital to account for classic theories, such as the river continuum concept [231], and for more contemporary hypotheses [232], like the river discontinuum concept [233], network dynamic hypothesis [234], and theory of riverine ecosystem synthesis [235]. The solution to fragmentation along river networks is usually linked with solutions that promote connectivity enhancement at a given barrier when removal is impossible [236]. In this situation, fish passages are probably the most ubiquitous solution that can be used to retrofit existing barriers and serve more than just to fish species, allowing water and sediment movement to be partially restored. Artificial barriers block the communication between spatial elements along river networks. These barriers provide several ecosystem services, such as water storage, agricultural irrigation, energy production, and cultural and scenic values, as well as providing nations with a certain level of energy and water resources security that is currently so appealing [237]. A full understanding is crucial not only for grasping the overall effects of river fragmentation due to different physical barriers on targeted fauna populations but also for devising management strategies to enhance connectivity, aiding in the conservation and management of biodiversity.
Habitat fragmentation is not linearly correlated to the number of barriers present in a system; it is dependent on their features (e.g., height, slope, flow alteration promoted), on the scale of analysis (e.g., river reach, segment, sub-basin, or whole basin), as well as the movement patterns and capability of affected species. River fragmentation by barriers can limit movement and migration along the river, leading to the decline or extinction of numerous native species across Europe [238,239]. Even small obstacles that outnumber bigger barriers may significantly affect flow dynamics, temperature patterns, animal movement, and habitat quality [217,240], potentially altering the composition, structure, and distribution of communities by promoting the loss of genetic diversity, increasing the risk of extinction through demographic, environmental, and genetic uncertainties [216].
The proper management of freshwater systems to maintain a healthy level of connectivity along the network is paramount to fully maintaining ecosystem functioning and allowing the community to be functionally resilient in a time of global changes. The best possible solution to reconnect a system fragmented by the presence of an artificial barrier is to remove it and, by doing so, completely restore longitudinal and lateral connectivity. But, not all barriers can be removed; most, particularly non-obsolete barriers, provide a wide number of ecosystem services and determinants for societal well-being. In such cases, technical as well as nature-based solutions can be applied to existing, non-removable barriers. In these situations, we are enhancing connectivity while maintaining the barrier and its associated ecosystem service provisions. These connectivity enhancements mean that, at least for some species, the connectivity is only partially restored with, at times, severe directional connectivity asymmetries. The maintenance of river connectivity is among the objectives of the Water Framework Directive [241], and the recovery of free-flowing rivers is inscribed in the European Strategy for Biodiversity 2030 [242] as part of the Green Deal’s [243] overall architecture.

12. Pesticides

There has been a constant globally increase in the number of articles and citations on pesticides as stressors that impact freshwater, with a significant decrease in the last years (analyses that include states with both developed and undeveloped scientific networks and financial and human resources), in contrast to Europe (analyses that include states with preponderant developed scientific networks and financial and human resources), where there has a been constant increase in the number of articles and citations, with a significant decrease in the last 4–5 years (Figure 22 and Figure 23).
Pesticides, comprising chemicals or mixtures aimed at pest control, including insects, fungi, and weeds, saw an estimated global usage of 3.5 million tons of different active ingredients in agriculture in 2021 [244]. Despite the existence of over 1680 distinct active ingredients [245], the market boasts more than 100,000 different commercial formulations. These pesticides arrive in aquatic ecosystems through drift, runoff, or direct fumigation, leading to the widespread contamination of freshwater ecosystems worldwide [246,247].
A lot of impacts of pesticides on freshwater ecosystems have been documented. Studies have extended from laboratory experiments to complex mesocosm assessments. The obtained outcomes have revealed an extensive range of effects at the species level, including oxidative stress, alterations in behavior, increased mortality, disruption of endocrine systems, and reproductive impairment. These impacts have been observed across various communities, including algae, cyanobacteria, zooplankton, macrophytes, macroinvertebrates, and vertebrates [248]. Comprehensive investigations at the community and ecosystem levels have unveiled alterations through trophic webs, and some pesticides have exhibited biomagnification phenomena. For instance, glyphosate, the most widely used pesticide [249], has been found to selectively enhance the growth of pico-cyanobacteria in the laboratory, mesocosm, and also in field studies [250,251].
A significant challenge in managing pesticide contamination lies in the fact that they are often detected in mixtures. Even individual commercial formulations consist of various mixtures. Co-formulations have been found to increase toxicity, sometimes surpassing that of the active ingredients alone, as evidenced in studies on algae [252]. Furthermore, the common practice of using combined pesticides exacerbates this complexity. Further studies on the impacts of pesticide mixtures at the ecosystem scale are essential to prevent potential underestimations of risks [253].
Most studies have focused on various forms of bioremediation, yet the ecological ramifications of pesticide contamination can be profoundly significant. Existing evidence regarding glyphosate underscores the imperative to intensify proactive measures against contamination [251,254,255,256]. Mitigating pesticide usage and bolstering safeguards for freshwater bodies stand as paramount challenges of the present.
Strict monitoring and control of pesticide contamination in freshwater bodies are essential for providing early warnings and halting contamination sources. Furthermore, local environmental regulations play a crucial role in formulating protective policies that prevent pollution and promote the transition to more sustainable agricultural practices.
Pesticide contamination stands as one of the most significant stressors on freshwater systems. The presence of highly complex mixtures and various types of impacts have been reported. Avoiding contamination is crucial because persistent ecological impacts continue to be detected despite the environmental persistence of these substances.

13. Terrorism and War

There have been a very small number of articles globally on war and terrorism as stressors that impact freshwater, all of which are outside Europe, despite a present war in our continent. In the new international tense situation, there is an urgent need for this research (Figure 24).
Identification of terrorism and war is important, but until now, there has been no single definition of these terms. For example, contrary to UN resolution 3314, in the Russian Federation, aggression against Ukraine is not called “a war” but a “special military operation” [257]. Terrorism remains undefined beyond a vague sense of “a non-state actor attacking civilian targets to spread fear for some political goal” [258]. Here, we consider that any actions aimed at the destruction of the water management infrastructure, water resource redistribution, or water quality deterioration to achieve political or military goals should be considered water terrorism, which can be considered a multistressor.
The first armed events connected with freshwater resources were mentioned in the Sumerian legend when, over 2500–2400 BC, the Mesopotamian city-states fought over the redistribution of the Tigris and Euphrates Rivers’ flow [259]. Recently, water often serves as the subject of the negative impacts caused by war [260,261]. Such a display of water terrorism is well known. Thus, during the Persian Gulf War, Iraq spilled oil into the sea, which later leaked into the desalinization plants in north Saudi Arabia, and in Zambia, the war destroyed the water pipes supplying about 3 million inhabitants [262].
The main impact on population and aquatic ecosystems is caused by the dams’ destruction. Their explosions were usual over the Second World War (WWII): the Soviet army exploded the dam on the Dnieper River, the British Royal Air Force bombed the dams on German rivers, the German troops destructed dams in Italy, etc. [262,263].
The terroristic war unleashed by Russia against Ukraine brings new facts on the impacts on the aquatic ecosystems [264,265,266,267,268]. There were five main groups of impacts of this war on these ecosystems delineated: the destruction of the hydrotechnical facilities; water bodies’ contamination; destruction and shutdown of the hydropower facilities and disorders of the HPP and NPP cooling ponds regime; navigation issues; and threats to fishery and aquaculture [268,269]. The most drastic display of water terrorism in war was the explosion of the Kakhovka Dam, which had the most catastrophic consequences of our time [270,271,272,273,274].
According to UN prognosis, by the middle of the XXI century, 7 billion persons in 48 states will face a water deficit. Considering climate changes, this increases the risk of wars for water resources [275]. The impact of terroristic actions on freshwater is not reduced to the above-mentioned problems. A complete inventory of the impacts should be carried out on the basis of the waters’ monitoring, which comprises biological, physicochemical, and hydromorphological parameters, and accounts for basin-specific pollutants and compounds to assess the chemical state of the water bodies [276]. The integral assessment of the terroristic actions’ impact on the aquatic ecosystems should be realized by the waters’ monitoring in view of the revelation of the effects on biota and assessment of the actual ecological state of the modified by war aquatic ecosystems. At this, the monitoring programs should be completed by tasks regarding the collection of information to be used for assessment of the losses of the aquatic ecosystems. The precedents of the UN International Court of Justice’s decisions on compensation of environmental losses owing to the hostilities are quite often regarded as just under-received ecological services of the aquatic ecosystems [277].
One of the consequences of the terrible WWII, which affected the aquatic ecosystems as well, consisted of the development of specific international humanitarian legislation, including the Geneva Convention of 1949 and Additional Protocols to it of 1977. Among numerous provisions of these acts, some actually prohibit the use of water and water supply systems as a weapon against the civil population. For example, Article 56 of Protocol I and Article 15 of Protocol II of 1977 of the Geneva Convention prohibit attacks on infrastructure “containing dangerous forces”, including explicitly “dams’ and ‘dykes” if such attacks “may cause the release of dangerous forces and consequent severe losses among the civilian population” [278]. Such a limitation underlies international humanitarian law; however, in our view, the environmental crimes associated with water resources need greater responsibility at the level of international legislation against terrorism.
Last but not least, it is obvious that terrorist activities are triggers for both environmental issues and finally war and associated risks, e.g., the Al-Qaeda pan-Islamist terrorist attack on USA civil targets induced the USA-led coalition—Iraq War—and the Hamas terrorist attacks on Israeli civil targets started the Israel–Hamas-led Palestinian groups War, etc.

14. Algal Blooms

There has been a constant increase in the global number of articles and citations on algal blooms as stressors that impact freshwater (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources), and there has been a constant increase in the number of articles and citations in Europe (analyses that include countries with preponderant developed scientific networks and financial and human resources) (Figure 25 and Figure 26).
In the conditions of global climate change and increasingly intense negative anthropogenic influence, water quality has declined all over the world, and eutrophication of many freshwater ecosystems has been observed more often. Because of the increased concentration of nutrients in the freshwater, there is an overgrowth of algae and cyanobacteria, which are referred to as “Harmful Algal Blooms” (HAB). HAB can be caused by autochthonous, as well as non-native, invasive micro and macro algae and cyanobacteria. In stagnant waters, the bloom of planktonic Cyanobacteria, as well as Dinophyceae, Bacillariophyceae, Euglenophyta, and Chlorophyta, causes a change in the color and smell of the water and the appearance of foam and coatings [279,280]. During the blooming period of green filamentous algae (Cladophora sp., Oedogonium sp., Microspora sp., Pithophora sp.), large mats are formed on the bottom or surface of aquatic ecosystems [281,282]. In river and stream systems all over the world, in recent decades, ‘blooms’ of Bacillariophyceae, primarily the diatom Didimosphaenia geminata, have appeared. This periphyton alga forms large ‘blooms’ in primarily oligotrophic streams and rivers [283,284].
HAB has a negative environmental and socioeconomic impact, and it is a threat to public health [280]. Light and temperature conditions, oxygen, ammonia, and pH concentrations change in the water, which can affect the living conditions of other aquatic or semi-aquatic organisms [284,285]. Different species of cyanobacteria and algae produce different toxins, and they could accumulate in the tissues, cause damage to the tissues and the functioning of certain organ diseases, and cause the death of aquatic organisms, namely fish [286,287].
Due to HAB, there are disruptions in water supply, the use of water for irrigation, as well as for sports and recreational activities [286,288].
General management practices for nuisance algae are divided into two most important categories: nutrient manipulation and direct control techniques [281]. It is also essential to implement effective technologies for the inactivation and removal of toxins [289].
Water quality protection is possible by implementing preventive specific measures: wastewater treatment, proper planning of places where reservoirs are formed, respecting sanitary protection zones, banning or limiting the use of surrounding land for agricultural purposes, creating a buffer zone that will absorb nutrients, implementing anti-erosion measures, maintaining forest zones and macrovegetation, and implementing a good on-site fishing strategy and activities. An important measure is a ban on the transfer of ‘blooming algae’ by fishing tools, fish translocation, gravel, etc. [279].
The appearance of HAB in the future poses significant challenges for preserving ecological balance, biodiversity, and the intended function of aquatic ecosystems.
The occurrence of HAB in aquatic ecosystems is becoming increasingly common, leading to significant environmental and economic consequences. Besides implementing the mentioned protection measures, it is crucial to enhance our ability to predict and prevent the proliferation of “blooming” cyanobacteria and algae by obtaining detailed and relevant information about their ecology and behavior. Furthermore, it is essential to explore the significant biotechnological potential of non-toxic algae biomass [282].

15. Invasive Aquatic Plants

There has been a constant increase in the global number of articles and citations on invasive aquatic plants as stressors that impact freshwater (analyses that include states with both developed and undeveloped scientific networks and financial and human resources), and there has been a constant increase in the number of articles and citations in Europe (analyses that include states with preponderant developed scientific networks and financial and human resources) (Figure 27 and Figure 28).
Aquatic plants are especially vulnerable to any changes in their environment. Invasive plant species pose severe threats to native wildlife. A total of 75% of all European freshwaters are anthropogenically changed [290].
About 42% of endangered or threatened species are affected by invasive species. Invasive species also threaten human health and the economy. Havel et al. [291] reported that the dispersion of microbes over long distances and infection of new hosts might have consequences for human health. Invasive aquatic species (IAS) reproduce very quickly; reduce the habitats of native plant species; have a negative effect on fish, insects, etc.; and lower the biological diversity of aquatic ecosystems. Many alien aquatic plants strongly negatively affect aquatic ecosystems by blocking rivers [292].
Human activity has dramatically increased IAS’s spread rate [293], and global changes accelerate the invasiveness of specific IAS [294].
Biological invasions have become a consequence of globalization [295,296,297]. Pistia stratiotes, an invasive alien species, was introduced to Prilipe, an oxbow in Slovenia. Šajna et al. [298] reported on the successful winter survival of P. stratiotes in a natural thermal stream. Climate change and global warming can accelerate such local populations of invasive species as stepping stones for further dispersal [299]. Šajna et al. [300] recently stated that thermally abnormal waters pose an invasion risk for further deliberation.
Hundreds of non-native organisms are introduced to different parts of the world every year, but not all become invasive. However, for different reasons, most do not survive in the newly invaded environment. Some non-native organisms cannot adapt to the new environment or have a population that is too small to reproduce successfully.
Lind et al. [301] reported that the effects of climate change may lead to an increased abundance and distribution of emergent and floating species and a lowered abundance and distribution of submerged macrophytes, which are most sensitive to global changes. The same authors also claimed that an increase in invasive species would probably occur at high latitudes while not at high altitudes. It makes lakes at higher altitudes in tropical areas hotspots for future conservation measures to protect endemic macrophyte species.
Climate change will cause frequent extreme events of heavy precipitation and drought, impacting hydrological conditions in riverine ecosystems, like flow velocity and evapotranspiration, which will cause drought or runoff due to heavy rainfall [297].
There are several mechanisms with which we can try to stop the spread of IAS, such as lowering the water level, shading, manual and mechanical removal, and measures to reduce the input of nutrients into water bodies, but none of the methods are completely successful.
The spread of IAS is hard to prevent. However, we can limit their spread in various ways. It is important not to remove riparian vegetation, as empty corridors along water bodies are quickly occupied by IAS. It is also important to educate and make people aware of the negative effects of IAS on the aquatic ecosystem.
We will not preserve IAS, but we can take advantage of their positive characteristics. The introduction and large dispersion of miscellaneous non-native species is predominantly detrimental to invaded ecosystems. However, the study provides an example of the positive effects of non-native Eurasian Watermilfoil, Myriophyllum spicatum [299]. Kourantidou et al. [300] also stated in their recent review that IAS has potentially beneficial roles. It was also reported that IAS’s competitive success depends on environmental conditions [302].
We cannot prevent the spreading of IAS to new areas in the world. With increasing globalization and climate change, their occurrence will be even greater. Therefore, it is crucial to make people aware so that they do not intentionally introduce non-native organisms into nature.

16. Riverine Vegetation

There has been a constant increase in the number of articles and citations on riverine vegetation as a stressor that impacts freshwater, with big fluctuations and a significant decrease in interest in the last 3–4 years (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources). There has been a relatively small number of articles published annually and a significant deflection in interest in the last 3–4 years (Figure 29 and Figure 30).
These plant formations and environments are both essential for the hydrogeological balance of water bodies, for ecosystem functionality, and for biodiversity, ensuring protection from hydrogeological catastrophes, environmental connectivity, and ecological dynamics.
In general, freshwater bodies’ bank vegetation is dominated by the presence of azonal vegetation, from the most hydrophilic to the mesic portions. There are also particular cases in which even the most xeric vegetation can contribute to forming communities in riparian environments like, for example, high banks or under other extreme draining conditions.
Riverine environments and related vegetation, in any case, represent important values and provide services, goods, and ecosystem functionality of primary importance, which are essential for the good functioning and for the protection from hydrogeological catastrophes. Naturally, the riverine vegetation follows a gradient from the minor bed to the major riverbed, according to the variations in the topographic conditions and moisture. The characteristics of riverine vegetation also depend on other factors that can lead to further differences, such as the variation of salinity, temperature, precipitations, organic and mineral substances concentration, deposition/erosion, etc. [303,304,305,306]. The anthropogenic-induced effects (fragmentation, deterioration, pollution, urbanization, etc.) generally have modified or eliminated natural habitats’ functions, negatively influencing also the connected ecosystems. This led to an increase in the related risk of natural catastrophes, especially in a scenario of global and local socio-economic and climate changes.
The riverine habitats and vegetation expression have been the most impacted by human activities during history. The banks have been artificialized, canalized, narrowed, rectified, walled up, and reclaimed to obtain greater spaces to be used for agriculture, farming, pastures, fishing, hunting, industrial, and trade goals or for urbanistic purposes (residential, industrial, navigation, portual facilities, etc.). The vegetation in these habitats is often seen as a pest, as something to be eliminated, or in a way that needs strict and strong control. Riverine vegetation is too often seen as dirt that needs to be cleaned up or as a danger that needs to be eliminated. This ends up negatively influencing the stability of the banks of waterways, destroying very important environments and their ecotones, undermining biodiversity, destroying ecological continuity and functionality, increasing land and water management costs, increasing environmental risks, etc. The artificialization of riverine habitats represents a significant degradation of the natural vegetation types, plants aging, fluctuation, regeneration, biological successions, and dead wood cycle, and it influences feeding, nesting, refuge, roost, passage habitats for insects, fishes, reptiles, amphibians, birds, and mammals [307,308].
Many riverine environments that are today widely considered by people as green or natural have instead been greatly altered over time, although they look green, pleasant, or not urbanized [309,310,311]. This happened not only in large lowlands rivers but also in small rivulets and streams up to the mountains [312].
In the hydraulic management of water bodies and forests, it has too often been thought to ensure the greatest quantity of water flows downstream rivers and streams in the shortest possible time. This ended up reducing water body suface, simplifinge their natural complexity, transforming their functioning and changing their forms, altering the processes of erosion/deposition to the point of creating problems such as the beaches’ retreat, siltation of wetlands, or other hydrogeological problems, as well as causing drought and water scarcity. Urbanization has also increased the risks related to flooding. Today, we should rethink this logic and, to the contrary, favor the diversification and the re-naturalization of these areas. We must not only think about the banks or riverbed conditions, but we should pay attention to the whole catchment basin, promoting the vegetation cover (in particular forests), which allows for greater precipitation absorption together with better water redistribution, just as we should encourage or re-establish water storage areas. To ensure the water flow, rather than continuing or promoting the systematic elimination of the woody vegetation on the waterbody banks, with the fallen wood into the rivers, it would be necessary, for example, to rethink the bridge system, avoiding pylons in the rivers, and rethink the management of the banks restoring spaces, forms variability, and functionality of the narrowed/deepened water bodies that are now forced to be artificialized water canals or reservoirs. We should rethink the riverine spaces to leave more green surfaces and more variable forms where vegetation can express itself as freely and as much as possible. Even the water expansion areas must be rethought to be not simple artificial expansion pools but as possible floodable heterogenous wetland habitats as they could have been in the past, before land reclamation and other human interventions. We should rethink artificial water expansion areas as possible natural areas for biodiversity conservation, to be used as wetland vegetation refugia, and to foster ecological connectivity, thinking of spaces where vegetation and ecosystems can develop autonomous dynamics without necessarily being forced or determined by man.
Today, alongside the restoration of those riverine portions, we should also pay attention to artificialized springs and fountains, which remain important historical, architectural, and cultural landmarks. We should rethink those waterpoint areas, considering the ecological function that these waterpoints should perform in the landscape. In that way, we should recreate wetlands, swamps, and mesic forests using the water that flows out of these managed water points, with the possible related potential vegetation communities and related ecosystems. In that way, we can also encourage the communities of animals and plants that live inside those fountains and that are strongly threatened by cleaning or maintenance operations carried out by the users or by the offices in charge, in line with what should also be carried out with different water bodies. We should pay even more specific attention to wet cave environments from tourist management modifications.

17. Fish

There has been a relatively constant increase in the global number of scientific articles and their citations, including in European countries, on invasive fish species as stressors with an impact on freshwater (analyses that include countries with both developed and undeveloped scientific networks and financial and human resources) (Figure 31 and Figure 32).
Fish are aquatic, craniate, and gill-bearing, such as hagfish, lampreys, cartilaginous, and bony fish, and are naturally mostly ectothermic and relatively abundant in most bodies of water in nearly all aquatic environments, exhibiting greater species diversity than any other group of aquatic vertebrates. In spite of the fact that fish are ecological keystones for aquatic environments, ecological indicators, and important resources for humans [312,313,314,315,316,317,318,319,320], some of them can sometimes be undesirable.
Fish can be considered in some circumstances as stressors for their ecosystems and human health.
With a growing world population, over-industrialization, extensive and intensive agriculture development, transport extension and intensity, land-use changes, and wars, aquatic life is susceptible to the harmful effects of agrochemicals, different poisons, heavy metals and non-metals, phytotoxins, microbial toxins, genotoxins, and other contaminants [321,322,323,324]. Fish under environmental pollution induces toxicokinetics, biotransformations, bioaccumulation, or multi-transgenerational effects [325]. Also, the biological uptake and transport vectors for different anthropogenic substances negatively affect both the environment and human health [326,327].
General and specific freshwater ecosystems’ complex point and non-point pollution phenomena that impact the fish, too [300], which became stressors for the environment and human health, can be managed in an integrated way only at the watershed level [328,329,330,331].
Non-native fishes are frequently used to enhance aquaculture and fisheries; some of them will become aggressively invasive, producing adverse ecological effects [332]. Aquatic ecosystems, especially those already disturbed by human activities, appear to be particularly vulnerable to alien and invasive organisms [333]. All these organisms, including fish, can be, in some circumstances, major environmental stressors, impacting native species, habitats, and ecosystems through predation and competition for resources; spreading other organisms and diseases, ultimately disrupting the environment by reducing water quality; contributing to erosion; increasing nutrient levels; etc. [334,335,336].
In this multifaceted context, very complex management actions may be needed to minimize their naturalization, dispersal and impacts. These actions include eradication attempts from specific waters or well-defined spatial areas, population control by suppression (e.g., through removal programs), and containment of existing populations to prevent their further spread. These remedial actions have generally only been undertaken across large spatial areas in developed countries, but the experience suggests fundamental scarce selective removal methods that target the non-native fish species only [337].
A well-balanced ecological status of the ichthyofauna is not possible in disturbed ecosystems and vice versa [338,339].
Consequently, all the needed conservation issues have to be targeted in an integrated manner, not only for the ecologically healthy ichthyofauna but also for their habitats and ecosystems.
The pollution-related larger and more complex circumstance should be necessarily approached in an integrative local, regional, and international crosborders context. In terms of alien and invasive species, almost all fish species are difficult to control once established, but biological control offers some hope in controlling widespread water pest species.

18. Discussion

The issue of environmental stressors on freshwater ecosystems is extremely vast and encompasses a multitude of aspects worldwide.
This work deals with seventeen major stressors from a planetary scale perspective, dealing with their description, induced effects, threats and risks, management, protection, and conservation-related elements.
The present review, even if not exhaustive due to the vastness of the addressed subjected evidence, shows that we are dealing with a wide spectrum of sources that can cause stress on freshwater ecosystems. As could be concluded, agriculture, industry, energy production, transport, and urbanization are the main drivers of the negative effects on freshwater ecosystems, but in changing classic perspectives of the observations, we found that relatively less frequent events, such as, for example, terrorist actions and war, can have effects at least as harmful. Moreover, indirect factors, such as climate changes, can act as vectors amplifying the effects of the aforementioned activities, just as combined actions of these can generate effects of much greater magnitude or can constitute the inflection point of triggering the stress mechanism on the freshwater ecosystems.
Additionally, multiple stressors with cumulative and/or synergistic effects can act on the same freshwater ecosystem with much more significant effects, given the easily formed connection between phenomena from the same spectrum. Thus, for example, the discharge of thermal waters can create conducive conditions for the development of algal blooms, which, in turn, decrease the amount of dissolved oxygen in the water and could favor the spread of invasive fish species, some adapted to conditions with less dissolved oxygen, but more sensible to parasites, etc. In this context, habitat fragmentation can contribute to the confinement in areas with limited extension of algal blooms, not allowing the dispersion of algae over a large area and increasing local-level effects. Thermally polluted waters can favor the spread of invasive aquatic plant species, especially those with higher temperature preferences (such as some species used by aquarists, for example). Military activities can lead to the production of warmer waters, can lead to local increases in radioactivity, and can be responsible for the discharge of nanoparticles into water bodies, in addition to more obvious effects such as intentionally caused floods. Drought periods can lead to the concentration of nutrients in the water, which, in turn, can be the starting point for algal blooms, with the previously discussed effects. Drought can also lead to increased salinity, and floods lead to large quantities of fine sediments being transported into the water, affecting their sharing in the basin and influencing the species that depend on stream beds as their habitat.
The examples of these stressors single and/or interrelated negative effects can infinitely continue as the review highlighted.
Attempting a classification, we can conclude that actions with a stress effect on water bodies can be categorized into three major groups: (1) adding content, (2) disturbing the natural characteristics or normal functions of the water body, and (3) disturbing biological components or processes.
In the first category, we include the addition of waters with different temperatures, altering the local temperature, the discharge of nanoparticles, and chemical and radioactive pollution, all three based on the introduction of unnatural elements into the aquatic circuit. Traditionally, it is assumed that this first category would be the most important.
The second category includes a larger number of stressors: increased salinity, extreme floods and droughts, disturbance of fine sediments, and the increase or concentration of nutrient quantities—factors that, in addition to the way they influence each other, as discussed earlier, have extremely long-lasting, if not permanent, effects on the affected ecosystems, often requiring more complex and costly reparative interventions than those in the first category. Of course, the first category and the second category of stressors can interact and produce cumulative and synergistic effects.
Regarding the last category, it includes algal blooms, invasive or potentially dominant aquatic species, and biocoenotic destructuring, whose effects are among the most serious at the ecosystem level, disturbing the entire structure of the ecosystem and causing effects that are often difficult to reverse. All three categories of stressors can interact and produce cumulative and synergistic effects.
From each stressor perspective, and more than that, from the stressor interactions and the interrelated perspective, it is important to analyze the trajectory of cause—type of influence and effects—and, last but not least, potential solutions specific to each situation.
In relation to the causes, it is important to identify whether we are talking about a direct cause of an impact, or an indirect cause, whether it is solvable through a quick/medium/long period and simple/complex intervention, or whether its effects can no longer be removed by external interventions. Likewise, the type of influence is of similar importance, being necessary to distinguish between direct and indirect, chronic, and acute influences in order to be able to evaluate the impact and propose solutions. In this context, it is necessary to estimate whether the effects of a certain phenomenon are, in principle, quantifiable, given that the reparative intervention on an unquantifiable event is much more difficult.

19. Conclusions

The health of the aquatic ecosystems is a key point where assessments and monitoring of the impact of various stress factors intersect, but these factors themselves, which destabilize biodiversity and ecosystem structure and functions, have been studied to varying degrees. Thus, in the future, it will be productive not only to strengthen the study of individual stressors but also to evaluate their cumulative, additive, and synergistic effects through mathematical modeling and accurate predictions.
The stressors’ influence on freshwater is often combined, and the factors are triggered in a cascade, causing effects on one another, leading to irreversible effects that are costly to counteract in many situations.
To meet the challenges regarding the multi-interacting natural and anthropogenic stressors’ effects on freshwater ecosystems, unified systematic and comprehensive frameworks are needed to identify key questions and for data collection to build ecological conceptual models based on which a proper assessment, monitoring, analysis, and management can be achieved.
Climate change, especially global warming, has an aggravating effect on most of these stressors, making the issue of protecting freshwater bodies even more difficult.
In a context where freshwater resources are of utmost importance to human society, protecting them against a large and complex number of stressors becomes a very difficult endeavor, requiring complex solutions, especially in situations where the effect of some factors is chronic and can only be controlled or maintained at a certain level and not completely or partially eliminated.
As a result, the protection of freshwater ecosystems must be considered in conjunction with the protection of other important ecosystems, whose indirect role in regulating natural processes as fundamental for freshwater, but not only.
Integrated theoretical and applied holistic approaches concepts should be strengthened in a more focused research direction and, last but not least, reliably transferred from a pure scientific niche family of works in an emergent day-by-day tendency of practical in situ freshwater ecosystems sustainable management.

Author Contributions

Conceptualization, D.B., A.C.-B., H.O. and K.C.; data curation, D.B., A.C.-B., H.O. and K.C.; formal analysis, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; funding acquisition, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; investigation, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; methodology, D.B. and A.C.-B.; project administration, D.B. and A.C.-B.; resources, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; supervision, D.B., H.O., A.C.-B. and K.C.; validation, D.B. and A.C.-B.; visualization, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; writing—original draft, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C.; writing—review and editing, D.B., A.C.-B., S.B., V.L.L., S.A., T.L., P.B., D.F.G.I., J.G., A.T., S.B.S., H.O. and K.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was conducted with the support of the Ecotur Sibiu Association. This work was partly supported by the Israeli Ministry of Aliya and Integration. The Ministry of Science, Technological Development and Innovation, Republic of Serbia, 451-03-65/2024-03/200122 to Snežana B. Simić and Universitatea “Lucian Blaga” din Sibiu, LBUS-IRG-2023-09 to Doru Bănăduc. The APC of this paper was funded partly by Ecotur Sibiu Association and Technical University of Munich. This work was supported also by FCT—Fundação para a Ciência e Tecnologia, I.P. by project reference UIDB/00239/2020 of the Forest Research Centre and DOI identifier 10.54499/UIDB/00239/2020. The Open Access was funded by CEF Project UIDB/00239/2020. Paulo Branco is supported by FCT-LA/P/0092/2020.

Data Availability Statement

Publicly available datasets were analyzed in this study. These data can be found in the cited references.

Acknowledgments

The first author thank for the kind support for this review to Marco J. Cabrerizo.

Conflicts of Interest

Aristotelles Tegos was was employed by the company Ryan Hanley Ltd. Ireland, but there is no conflict of interest in this situation. All the other authors declare too that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. Goncharuk, W.; Goncharuk, V.V. Water is everywhere. It holds everything a key to understanding the universe. D. I. Mendeleev’s law is the prototype of the universe constitution. J. Water Chem. Technol. 2019, 41, 341–346. [Google Scholar] [CrossRef]
  2. Maruyama, S.; Ikoma, M.; Genda, H.; Hirose, K.; Yokohama, T.; Santosh, M. The naked planet earth: Most essential pre-requisite for the origin and evolution of life. Geosci. Front. 2013, 4, 141–165. [Google Scholar] [CrossRef]
  3. NOOA National Oceanic and Atmospheric Administration, National Weather Service. Learning Lesson: Water, Water Everywhere. Available online: https://www.weather.gov/jetstream/ll_water (accessed on 11 August 2021).
  4. Longo, S.B.; York, R. Structural Influences on Water Withdrawals: An Exploratory Macro-Comparative Analysis. Hum. Ecol. Rev. 2009, 16, 75–83. Available online: http://www.jstor.org/stable/24707738 (accessed on 27 August 2022).
  5. Antonelli, M.; Laube, P.; Doering, M.; Scherelis, V.; Wu, S.; Hurni, L.; Heitzler, M.; Weber, C. Identifying anthropogenic legacy in freshwater ecosystems. Wiley Interdiscip. Rev. Water 2024, e1729. [Google Scholar] [CrossRef]
  6. Ehrlich, P.R.; Ehrlich, A.H. The Population Bomb Revisited. Electron. J. Sustain. Dev. 2009, 1, 63–71. [Google Scholar]
  7. Boretti, A.; Rosa, L. Reassessing the projections of the World Water Development Report. NPJ Clean Water 2019, 2, 15. [Google Scholar] [CrossRef]
  8. IPCC Science Report: Climate Change Unequivocal, Human Influence at Least 95% Certain. Available online: https://ec.europa.eu/clima/news-your-voice/news/ipcc-science-report-climate-change-unequivocal-human-influence-least-95-certain-2013-09-27_en (accessed on 27 September 2013).
  9. Bănăduc, D.; Marić, S.; Cianfaglione, K.; Afanasyev, S.; Somogy, D.; Nyeste, K.; Antal, L.; Kosco, J.; Marko, C.; Wanzenböck, L.; et al. Stepping Stone Wetlands, Last Sanctuaries for European Mudminow: How Can the Human Impact, Climate Change, and Non-Native Species Drive a Fish to the Edge of Extinction. Sustainability 2022, 14, 13493. [Google Scholar] [CrossRef]
  10. Vorosmarty, C.J.; Green, P.; Salisbury, J.; Lammers, R.B. Globalwater resources: Vulnerability from climate change and population growth. Science 2000, 289, 284–288. [Google Scholar] [CrossRef]
  11. Curtean-Bănăduc, A.; Bănăduc, D. Aspecte privind impactul deversării apelor uzate asupra sistemelor ecologice lotice receptoare. In Apa Resursă Fundamentală a Dezvoltării Durabile. Metode ȿi Tehnici Neconvenţionale de Epurare ȿi Tratare a Apei; Oprean, L., Ed.; Editura Academiei Române: Bucharest, Romania, 2012; Volume 2, pp. 393–416. [Google Scholar]
  12. Bănăduc, D.; Joy, M.; Olosutean, H.; Afanasyev, S.; Curtean-Bănăduc, A. Natural and anthropogenic driving forces as key elements in the Lower Danube Basin-South-Eastern Carpathians-North-Western Black Sea coast area lakes: A broken steping stones for fish in a climatic change scenario? Environ. Sci. Eur. 2020, 32, 73. [Google Scholar] [CrossRef]
  13. Bănăduc, D.; Sas, A.; Cianfaglone, K.; Barinova, S.; Curtean-Bănăduc, A. The role of aquatic refuge habitats for fish, and threats in the context of climate change and human impact, during seasonal hydrological drought in the Saxon Villages area (Transylvania, Romania). Atmosphere 2021, 12, 1209. [Google Scholar] [CrossRef]
  14. Bănăduc, D.; Afanasyev, S.; Akeroyd, J.R.; Năstase, A.; Năvodaru, I.; Tofan, L.; Curtean-Bănăduc, A. The Danube Delta: The Achilles Heel of Danube River-Danube Delta-Black Sea Region Fish Diversity under a Black Sea Impact Scenario Due to Sea Level Rise—A Prospective Review. Fishes 2023, 8, 355. [Google Scholar] [CrossRef]
  15. Scheffer, M.; Carpenter, S.; Foley, J.A.; Folke, C.; Walker, B. Catastrophic Shifts in Ecosystems. Nature 2001, 413, 591–656. [Google Scholar] [CrossRef]
  16. Steffen, K.; Richardson, J.; Rockström, S.E.; Cornell, I.; Fetzer, E.M.; Bennett, R.; Biggs, S.R.; Carpenter, W.; de Vries, C.A.; de Wit, C.; et al. Planetary Boundaries: Guiding Human Development on a Changing Planet. Science 2015, 347, 6223. [Google Scholar] [CrossRef] [PubMed]
  17. Walker, B.; Holling, C.S.; Stephen, R.; Carpenter, A.; Kinzig, P. Resilience, Adaptability and Transformability in Social-Ecological Systems. Ecol. Soc. 2004, 9, 2. [Google Scholar] [CrossRef]
  18. Ferreira, T.; Globevnik, L.; Schinegger, R. Water stressors in Europe: New Threats in the Old World. In Multiple Stressors in River Ecosystems, Status, Impacts and Prospects for the Future; Elsevier: Amsterdam, The Netherlands, 2019; pp. 139–155. [Google Scholar]
  19. Lima, A.C.; Sayanda, D.; Wrona, F.J. A Roadmap for multiple stressors assessment and management in freshwater ecosystems. Environ. Impact Assess. Rev. 2023, 102, 107191. [Google Scholar] [CrossRef]
  20. Reid, A.J.; Carlson, A.K.; Creed, I.F.; Eliason, E.J.; Gell, P.A.; Johnson, P.T.J.; Kidd, K.A.; MacCormack, T.J.; Olden, J.D.; Ormerod, S.J.; et al. Emerging threats and persistent conservation challenges for freshwater biodiversity. Biol. Rev. 2019, 94, 849–873. [Google Scholar] [CrossRef] [PubMed]
  21. Helbling, E.W.; Zagarese, H.E. UV Effects in Aquatic Organisms and Ecosystems; The Royal Society of Chemistry: Cambridge, UK, 2003; pp. 1–575. [Google Scholar]
  22. Barnes, P.W.; Robson, T.M.; Neale, P.J.; Williamson, C.E.; Zepp, R.G.; Madronich, S.; Wilson, S.R.; Andrady, A.L.; Heikkilä, A.M.; Bernhard, G.H.; et al. Environmental effects of stratospheric ozone depletion, UV radiation, and interactions with climate change: UNEP Environmental Effects Assessment Panel, Update 2021. Photochem. Photobiol. Sci. 2022, 21, 275–301. [Google Scholar] [CrossRef]
  23. Barnes, P.W.; Williamson, C.E.; Lucas, R.M.; Robinson, S.A.; Madronich, S.; Paul, N.D.; Bornman, J.F.; Bais, A.F.; Sulzberger, B.; Wilson, S.R.; et al. Ozone depletion, ultraviolet radiation, climate change and prospects for a sustainable future. Nat. Sustain. 2019, 2, 569–579. [Google Scholar] [CrossRef]
  24. Woolway, R.I.; Merchant, C.J. Worldwide alteration of lake mixing regimes in response to climate change. Nat. Geosci. 2019, 12, 271–276. [Google Scholar] [CrossRef]
  25. Williamson, C.E.; Neale, P.J.; Hylander, S.E.; Rose, K.C.; Figueroa, F.L.; Robinson, S.A.; Häder, D.-P.; Wängberg, S.-Å.; Worrest, R.C. The interactive effects of stratospheric ozone depletion, UV radiation, and climate change on aquatic ecosystems. Photochem. Photobiol. Sci. 2019, 18, 717–746. [Google Scholar] [CrossRef]
  26. Neale, P.J.; Thomas, B.C. Inhibition by ultraviolet and photosynthetically available radiation lowers model estimates of depth-integrated picophytoplankton photosynthesis: Global predictions for Prochlorococcus and Synechococcus. Glob. Chang. Biol. 2017, 23, 293–306. [Google Scholar] [CrossRef] [PubMed]
  27. Cory, R.M.; Ward, C.P.; Crump, B.C.; Kling, G.W. Sunlight controls water column processing of carbon in arctic fresh waters. Science 2014, 345, 925–928. [Google Scholar] [CrossRef] [PubMed]
  28. Leech, D.M.; Johnsen, S. Light as an ecological resource. In Encyclopedia of Inland Waters; Mehner, T., Tockner, K., Eds.; Elsevier: Amsterdam, The Netherlands, 2022; Volume 1, pp. 237–256. [Google Scholar]
  29. Overholt, E.P.; Duffy, M.A.; Meeks, M.P.; Leach, T.H.; Williamson, C.E. Light exposure decreases infectivity of the Daphnia parasite Pasteuria ramosa. J. Plankton Res. 2020, 42, 41–44. [Google Scholar] [CrossRef]
  30. Studer, A.; Lamare, M.D.; Poulin, R. Effects of ultraviolet radiation on the transmission process of an intertidal trematode parasite. Parasitology 2012, 139, 537–546. [Google Scholar] [CrossRef]
  31. Shaw, C.L.; Hall, S.R.; Overholt, E.P.; Cáceres, C.E.; Williamson, C.E.; Duffy, M.A. Shedding light on environmentally transmitted parasites: Lighter conditions within lakes restrict epidemic size. Ecology 2020, 101, e03168. [Google Scholar] [CrossRef] [PubMed]
  32. Berry, N.L.; Overholt, E.P.; Fisher, T.J.; Williamson, C.E. Dissolved organic matter protects mosquito larvae from damaging solar UV radiation. PLoS ONE 2020, 15, e0244832. [Google Scholar] [CrossRef]
  33. Lindholm, M.; Wolf, R.; Finstad, A.; Hessen, D.O. Water browning mediates predatory decimation of the Arctic fairy shrimp Branchinecta paludosa. Freshw. Biol. 2016, 61, 340–347. [Google Scholar] [CrossRef]
  34. Häder, D.-P.; Gao, K. Aquatic productivity under multiple stressors. Water 2023, 15, 817. [Google Scholar] [CrossRef]
  35. McKenzie, R.L.; Bernhard, G.H.; Liley, B.; Disterhoft, P.; Rhodes, S.; Bais, A.; Morgenstern, O.; Newman, P.; Oman, L.; Brogniez, C.; et al. Success of montreal protocol demonstrated by comparing High-Quality UV measurements with “world avoided” calculations from two chemistry-climate models. Sci. Rep. 2019, 9, 12332. [Google Scholar] [CrossRef]
  36. Blanchet, C.C.; Arzel, C.; Davranche, A.; Kahilainen, K.K.; Secondi, J.; Taipale, S.; Lindberg, H.; Loehr, J.; Manninen-Johansen, S.; Sundell, J.; et al. Ecology and extent of freshwater browning—What we know and what should be studied next in the context of global change. Sci. Total Environ. 2022, 812, 152420. [Google Scholar] [CrossRef]
  37. Li, Y.; Shang, J.; Zhang, C.; Zhang, W.; Niu, L.; Wang, L.; Zhang, H. The role of freshwater eutrophication in greenhouse gas emissions: A review. Sci. Total Environ. 2021, 768, 144582. [Google Scholar] [CrossRef] [PubMed]
  38. Hintz, N.H.; Schulze, B.; Wacker, A.; Striebel, M. Ecological impacts of photosynthetic light harvesting in changing aquatic environments: A systematic literature map. Ecol. Evol. 2022, 12, e8753. [Google Scholar] [CrossRef]
  39. Senar, O.E.; Creed, I.F.; Strandberg, U.; Arts, M.T. Browning reduces the availability—But not the transfer—Of essential fatty acids in temperate lakes. Freshw. Biol. 2019, 64, 2107–2119. [Google Scholar] [CrossRef]
  40. Helbling, E.W.; Banaszak, A.T.; Villafañe, V.E. Global change feed-back inhibits cyanobacterial photosynthesis. Sci. Rep. 2015, 5, 14514. [Google Scholar] [CrossRef]
  41. Knoll, L.B.; Williamson, C.E.; Pilla, R.M.; Leach, T.H.; Brentrup, J.A.; Fisher, T.J. Browning-related oxygen depletion in an oligotrophic lake. Inland. Waters 2018, 8, 255–263. [Google Scholar] [CrossRef]
  42. Kritzberg, E.S.; Hasselquist, E.M.; Skerlep, M.; Löfgren, S.; Olsson, O.; Stadmark, J.; Valinia, S.; Hansson, L.-A.; Laudon, H. Browning of freshwaters: Consequences to ecosystem services, underlying drivers, and potential mitigation measures. Ambio 2020, 49, 375–390. [Google Scholar] [CrossRef] [PubMed]
  43. Goldberg, V.M.; Gazda, S. Hydrogeological Foundations for the Protection of Groundwater from Pollution; Nedra: Moscow, Russia, 1984; p. 262. Available online: https://fireman.club/inseklodepia/teplovoe-zagryaznenie/ (accessed on 26 February 2023).
  44. Barinova, S. On the Classification of Water Quality from an Ecological Point of View. Int. J. Environ. Sci. Nat. Resour. 2017, 2, 1–8. [Google Scholar] [CrossRef]
  45. Schuelting, L.; Feld, C.; Graf, W. Effects of hydro- and thermopeaking on benthic macroinvertebrate drift. Sci. Total Environ. 2016, 573, 1472–1480. [Google Scholar] [CrossRef]
  46. Jacobs, A.F.G.; Heusinkveld, B.G.; Kraai, A.; Paaijmans, K.P. Diurnal Temperature Fluctuations in an Artificial Small Shallow Water Body. Int. J. Biometeorol. 2008, 52, 271–280. [Google Scholar] [CrossRef]
  47. Protasov, A.; Novoselova, T.; Uzunov, Y.; Barinova, S.; Sylaieva, A. Changes in the Planktonic System of the Nuclear Power Plant Cooling Pond Related to the Invasion of Dreissenidae (Mollusca: Bivalvia). Acta Zool. Bulg. 2021, 73, 275–278. Available online: http://www.acta-zoologica-bulgarica.eu/2021/002433 (accessed on 26 February 2023).
  48. Angilletta, M.J., Jr. Thermal Adaptation: A Theoretical and Empirical Synthesis; Oxford Academic: Oxford, UK, 2009. [Google Scholar] [CrossRef]
  49. Lugg, A.; Copeland, C. Review of cold water pollution in the Murray–Darling Basin and the impacts on fish communities. Ecol. Manag. Restor. 2014, 15, 71–79. [Google Scholar] [CrossRef]
  50. Ling, F.; Foody, G.M.; Du, H.; Ban, X.; Li, X.; Zhang, Y.; Du, Y. Monitoring Thermal Pollution in Rivers Downstream of Dams with Landsat ETM+ Thermal Infrared Images. Remote Sens. 2017, 9, 1175. [Google Scholar] [CrossRef]
  51. Nicolet, P.; Biggs, J.; Fox, G.; Hodson, M.J.; Reynolds, C.; Whitfield, M.; Williams, P. The wetland plant and macroinvertebrate assemblages of temporary ponds in England and Wales. Biol. Conserv. 2004, 120, 261–278. [Google Scholar] [CrossRef]
  52. De Meester, L.; Declerck, S.; Stoks, R.; Louette, G.; Van De Meuter, F.; DeBie, T.; Michels, E.; Brendonck, L. Ponds and pools as model systems in conservation biology, ecology and evolutionary biology. Aquat. Conserv. Mar. Freshw. Ecosyst. 2005, 15, 715–725. [Google Scholar] [CrossRef]
  53. Morgan, E.A.; Brown, A.; Ciotti, B.; Panton, A. Effects of temperature stress on ecological processes. In Stressors in the Marine Environment: Physiological and Ecological Responses; Societal Implications; Solan, M., Whiteley, N., Eds.; Oxford University Press: Oxford, UK, 2016; pp. 213–227. [Google Scholar] [CrossRef]
  54. Raptis, C.E.; Van Vliet MT, H.; Pfister, S. Global thermal pollution of rivers from thermoelectric power plants. Environ. Res. Lett. 2016, 11, 104011. [Google Scholar] [CrossRef]
  55. Directive 2006/44/EC of the European Parliament and of the Council of 6 September 2006 on the Quality of Fresh Waters Needing Protection or Improvement in Order to Support Fish Life (Codified Version) (Text with EEA Relevance). OJL 2006, 264, 20–31. Available online: http://data.europa.eu/eli/dir/2006/44/oj (accessed on 10 February 2024).
  56. Madden, N.; Lewis, A.; Davis, M. Thermal effluent from the power sector: An analysis of once-through cooling system impacts on surface water temperature. Environ. Res. Lett. 2013, 8, 035006. [Google Scholar] [CrossRef]
  57. Novoselova, T.; Barinova, S.; Protasov, A. Long-term dynamics of trophic state indicators in phytoplankton of the cooling reservoir of a nuclear power plant. Transylv. Rev. Syst. Ecol. Res. 2021, 23, 1–14. [Google Scholar] [CrossRef]
  58. Protasov, A.; Barinova, S.; Novoselova, T.; Sylaieva, A. The Aquatic Organisms Diversity, Community Structure, and Environmental Conditions. Diversity 2019, 11, 190. [Google Scholar] [CrossRef]
  59. Protasov, A.A.; Barinova, S.; Novoselova, T.N. Characteristics of the ecological state of the cooling reservoir of nuclear power plant on the basis of bioindicative indices of phytoplankton. Hydrobiol. J. 2017, 53, 3–21. [Google Scholar] [CrossRef]
  60. Barinova, S.; Krupa, E.G.; Protasov, A.A.; Novoselova, T.N. Benthification in the inland water ecosystems of Eurasia, some ecological aspects. MOJ Ecol. Environ. Sci. 2017, 2, 00048. [Google Scholar] [CrossRef]
  61. Dedić, A.; Gerhardt, A.; Kelly, M.G.; Stanić-Koštroman, S.; Šiljeg, M.; Kalamujić Stroil, B.; Kamberović, J.; Mateljak, Z.; Pešić, V.; Vučković, I.; et al. Innovative methods and approaches for WFD: Ideas to fill knowledge gaps in science and policy. Water Solut. 2020, 3, 30–42. [Google Scholar]
  62. Barinova, S. Essential and practical bioindication methods and systems for the water quality assessment. Int. J. Environ. Sci. Nat. Resour. 2017, 2, 555588. [Google Scholar] [CrossRef]
  63. Barinova, S. Ecological Mapping in Application to Aquatic Ecosystems BioIndication: Problems and Methods. Int. J. Environ. Sci. Nat. Resour. 2017, 3, 1–7. [Google Scholar] [CrossRef]
  64. Jeppesen, E.; Brucet, S.; Naselli-Flores, L.; Papastergiadou, E.; Stefanidis, K.; Nõges, T.; Nõges, P.; Attayde, J.L.; Zohary, T.; Coppens, J.; et al. Ecological impacts of global warming and water abstraction on lakes and reservoirs due to changes in water level and related changes in salinity. Hydrobiologia 2015, 750, 201–227. [Google Scholar] [CrossRef]
  65. Burgmer, T.; Hillebrand, H.; Pfenninger, M. Effects of climate-driven temperature changes on the diversity of freshwater macroinvertebrates. Oecologia 2007, 151, 93–103. [Google Scholar] [CrossRef]
  66. Protasov, A.; Tomchenko, O.Ș.; Novoselova, T.; Barinova, S.; Singh, S.K.; Gromova, Y.; Curtean-Bănăduc, A. Remote sensing and in-situ approach for investigation of pelagic communities in the reservoirs of the electrical power complex. Front. Biosci. (Landmark Ed.) 2022, 27, 221. [Google Scholar] [CrossRef] [PubMed]
  67. Khan, I.; Saeed, K.; Khan, I. Nanoparticles: Properties, applications and toxicities. Arab. J. Chem. 2019, 12, 908–931. [Google Scholar] [CrossRef]
  68. Vale, G.; Mehennaoui, K.; Cambier, S.; Libralato, G.; Jomini, S.; Domingos, R.F. Manufactured nanoparticles in the aquatic environment-biochemical responses on freshwater organisms: A critical overview. Aquat. Toxicol. 2016, 170, 162–174. [Google Scholar] [CrossRef]
  69. Oberdörster, G.; Maynard, A.; Donaldson, K.Ș.; Castranova, V.; Fitzpatrick, J.; Ausman, K.; Yang, H. Principles for characterizing the potential human health effects from exposure to nanomaterials: Elements of a screening strategy. Part. Fibre Toxicol. 2005, 2, 1–35. [Google Scholar] [CrossRef]
  70. Zhang, W.; Ke, S.; Sun, C.Ș.; Xu, X.; Chen, J.Ș.Ș.; Yao, L. Fate and toxicity of silver nanoparticles in freshwater from laboratory to realistic environments: A review. Environ. Sci. Pollut. Res. 2019, 26, 7390–7404. [Google Scholar] [CrossRef] [PubMed]
  71. Ale, A.; Andrade, V.S.; Gutierrez, M.F.; Bacchetta, C.; Rossi, A.S.; Santo Orihuela, P.; Desimone, M.F.; Cazenave, J. Nanotechnology-based pesticides: Environmental fate and ecotoxicity. Toxicol. Appl. Pharmacol. 2023, 471, 116560. [Google Scholar] [CrossRef] [PubMed]
  72. Kutlakhmedov, Y.O.; Korogodin, V.I.; Koltover, V.K. Principles of Radioecology; Vyshcha Shkola: Kyiv, Ukraine, 2003; p. 319. [Google Scholar]
  73. Hu, Q.; Weng, J.; Wang, J. Sources of anthropogenic radionuclides in the environment: A review. J. Environ. Radioact. 2010, 101, 426–437. [Google Scholar] [CrossRef] [PubMed]
  74. Kuz’menko, M.I.; Romanenko, V.D. Importance of V. I. Vernadsky’s scientific heritage for development of the freshwater radioecology. Hydrobiol. J. 2013, 49, 3–15. [Google Scholar] [CrossRef]
  75. Gudkov, D.I.; Shevtsova, N.L.; Dzyubenko, E.V.; Pomortseva, N.A.; Kireev, S.I.; Nazarov, A.B. Problems of the long-term radiation exposure of aquatic biota within the Chernobyl accident exclusion zone. In The Lessons of Chernobyl: 25 Years Later; Nova Science Publishers, Inc.: Hauppauge, NY, USA, 2012; pp. 301–315. [Google Scholar]
  76. International Atomic Energy Agency. IAEA Safety Glossary: Terminology Used in Nuclear Safety and Radiation Protection (PDF); IAEA: Vienna, Austria, 2007; ISBN 978-92-0-100707-0. [Google Scholar]
  77. Hevrøy, T.H.; Golz, A.; Xie, L.; Hansen, E.L.; Bradshaw, C. Radiation effects and ecological processes in a freshwater microcosm. J. Environ. Radioact. 2019, 203, 71–83. [Google Scholar] [CrossRef] [PubMed]
  78. Gudkov, D.I.; Shevtsova, N.L.; Pomortseva, N.A.; Dzyubenko, E.V.; Kaglyan, A.E.; Nazarov, A.B. Radiation-induced cytogenetic and hematologic effects on aquatic biota within the Chernobyl exclusion zone. J. Environ. Radioact. 2016, 151, 438–448. [Google Scholar] [CrossRef]
  79. Kessler, G. Nuclear Energetics; Energoatomizdat: Moscow, Russia, 1986; p. 262. [Google Scholar]
  80. Romanenko, V.D.; Kuzmenko, M.I.; Afanasyev, S.O.; Gudkov, D.I.; Lynnyk, P.M.; Protasov, O.O.; Tymchenko, V.M.; Yuryshynets, V.I.; Yakushyn, V.M. Hydroecological Safety of Nuclear Energetics in Ukraine; Visnyk NAN Ukrainy: Kyiv, Ukraine, 2012; pp. 41–51. [Google Scholar]
  81. Averbeck, D.; Rodriguez-Lafrasse, C. Role of Mitochondria in Radiation Responses: Epigenetic, Metabolic, and Signaling Impacts. Int. J. Mol. Sci. 2021, 22, 11047. [Google Scholar] [CrossRef]
  82. Shevtsova, N.L.; Gudkov, D.I. Cytogenetic damages in the common reed Phragmites australis in the water bodies of the Chornobyl exclusion zone. Hydrobiol. J. 2013, 49, 85–98. [Google Scholar] [CrossRef]
  83. Dzyubenko, E.V.; Gudkov, D.I. Cytogenetical and haematological effects of long-term irradiation on freshwater gastropod snails in the Chernobyl accident Exclusion Zone. Radioprotection 2009, 44, 933–936. [Google Scholar] [CrossRef]
  84. Belyaev, V.V.; Volkova, O.M.; Gudkov, D.I.; Prishlyak, S.P.; Skyba, V.V. Radiation dose reconstruction for higher aquatic plants and fish in Glyboke Lake during the early phase of the Chernobyl accident. J. Environ. Radioact. 2023, 263, 107169. [Google Scholar] [CrossRef]
  85. Pradhoshini, K.P.; Priyadharshini, M.; Santhanabharathi, B.; Ahmed, M.S.; Parveen, M.H.S.; War, M.U.D.; Faggio, C. Biological effects of ionizing radiation on aquatic biota—A critical review. Environ. Toxicol. Pharmacol. 2023, 99, 104091. [Google Scholar] [CrossRef] [PubMed]
  86. Kaglyan, O.Y.; Gudkov, D.I.; Kireev, S.I.; Yurchuk, L.P.; Gupalo, Y.A. Fish of the Chernobyl exclusion zone: Modern levels of radionuclide contamination and radiation doses. Hydrobiol. J. 2019, 55, 86–104. [Google Scholar] [CrossRef]
  87. Kaglyan, O.Y.; Gudkov, D.; Belyaev, V.V.; Kireev, S.I.; Yurchuk, L.P.; Drozdov, V.V.; Pomortseva, N.A.; Pryshliak, S.P.; Gupalo, O.O.; Abramiuk, I.I.; et al. Changes in radiation exposure rate of fish of the cooling pond of the Chornobyl NPS and Lake Azbuchyn after water level lowering. Hydrobiol. J. 2023, 59, 96–109. [Google Scholar] [CrossRef]
  88. Belyaev, V.V.; Volkova, O.M.; Gudkov, D.; Pryshliak, S.P.; Skiba, V.V. Reconstruction of the absorbed dose of ionizing radiation in fish of the Glyboke Lake over the early phase of the Chernobyl accident. Hydrobiol. J. 2021, 57, 86–95. [Google Scholar] [CrossRef]
  89. Gudkov, D.I.; Uzhevskaya, S.F.; Nazarov, A.B.; Kolodochka, L.A.; Dyachenko, T.N.; Shevtsova, N.L. Lesion in common reed by gall-producing arthropods in water bodies of the Chernobyl NPP exclusion zone. Hydrobiol. J. 2006, 42, 82–88. [Google Scholar] [CrossRef]
  90. Iavniuk, A.A.; Shevtsova, N.L.; Gudkov, D.I. Disorders of the initial ontogenesis of seed progeny of the common reed (Phragmites australis) from water bodies within the Chernobyl Exclusion Zone. J. Environ. Radioact. 2020, 218, 106256. [Google Scholar] [CrossRef] [PubMed]
  91. Kuzmenko, M.I. Responses of the aquatic organisms to ionizing radiation. Hydrobiol. J. 2018, 54, 3–13. [Google Scholar] [CrossRef]
  92. Pan’kov, V.; Afanas’yev, S.A.; Maksimovich, V.A.; Prityka, T.P. The role of some invertebrates in radionuclide migration through the “bottom sediments—Water column” phase division (interphase). Hydrobiol. J. 2001, 37, 101–108. [Google Scholar] [CrossRef]
  93. Romanenko, V.D.; Gudkov, D.I.; Volkova, Y.N.; Kuzmenko, M.I. Radioecological problems of aquatic ecosystems: 25 years after the accident at the Chernobyl nuclear power station. Hydrobiol. J. 2011, 47, 3–23. [Google Scholar] [CrossRef]
  94. Gudkov, D.I.; Kuzmenko, M.I.; Kireev, S.I.; Nazarov, A.B.; Shevtsova, N.L.; Dzyubenko, E.N.; Kaglyan, A.E. Radioecological problems of aquatic ecosystems of the Chernobyl exclusion zone. Biophysics 2010, 55, 332–339. [Google Scholar] [CrossRef]
  95. Hofman, L.; Monte, P.; Boyer, J.; Brittain, G.; Donchyts, E.; Gallego, D.; Gheorghiu, L.; Håkanson, R.; Heling, A.; Kerekes, G.; et al. Zheleznyak, Computerised Decision Support Systems for the management of freshwater radioecological emergencies: Assessment of the state-of-the-art with respect to the experiences and needs of end-users. J. Environ. Radioact. 2011, 102, 119–127. [Google Scholar] [CrossRef] [PubMed]
  96. Radiation Protection of the Public and the Environment, IAEA Safety Standards Series No. GSG-8, IAEA, Vienna. 2018. 51 Pages. Available online: https://www.iaea.org/publications/11183/radiation-protection-of-the-public-and-the-environment (accessed on 24 February 2024).
  97. Monte, L. A generic model for assessing the effects of countermeasures to reduce the radionuclide contamination levels in abiotic components of fresh water systems and complex catchments. Environ. Model. Softw. 2001, 16, 669–690. [Google Scholar] [CrossRef]
  98. Gallego, E.; Brittain, J.E.; Håkanson, L.; Heling, R.; Hofman, D.; Monte, L. MOIRA: A Computerized Decision Support System for the Management of Radionuclide Contaminated Freshwater Ecosystems. Radioprotection 2004, 98, 83–102. [Google Scholar]
  99. Cañedo-Argüelles, M. A review of recent advances and future challenges in freshwater salinization. Limnetica 2020, 39, 185–211. [Google Scholar] [CrossRef]
  100. Williams, W.D.; Sherwood, J.E. Definition and measurement of salinity in salt lakes. Int. J. Salt Lake Res. 1994, 3, 53–63. [Google Scholar] [CrossRef]
  101. Cañedo-Argüelles, M.; Kefford, B.J.; Piscart, C.; Prat, N.; Schafer, R.B.; Schulz, C.J. Salinisation of rivers: An urgent ecological issue. Environ. Pollut. 2013, 173, 157–167. [Google Scholar] [CrossRef] [PubMed]
  102. Le TD, H.; Kattwinkel, M.; Schutzenmeister, K.; Olson, J.R.; Hawkins, C.P.; Schafer, R.B. Predicting current and future background ion concentrations in German surface water under climate change. Philos. Trans. R. Soc. B 2019, 374, 20180004. [Google Scholar]
  103. Lerotholi, S.; Palmer, C.G.; Rowntree, K. Bioassessment of a river in a semi-arid, agricultural catchment, Eastern Cape. In Proceedings of the 2004 Water Institute of Southern Africa (WISA) Biennial Conference, Cape Town, South Africa, 2–6 May 2004; pp. 338–344. [Google Scholar]
  104. Thorslund, J.; van Vliet, M.T.H. A global dataset of surface water and groundwater salinity measurements from 1980–2019. Sci. Data 2020, 7, 231. [Google Scholar] [CrossRef] [PubMed]
  105. Schuler, M.S.; Relyea, R.A. A Review of the Combined Threats of Road Salts and Heavy Metals to Freshwater Systems. BioScience 2018, 68, 327–335. [Google Scholar] [CrossRef]
  106. Szklarek, S.; Górecka, A.; Wojtal-Frankiewicz, A. The effects of road salt on freshwater ecosystems and solutions for mitigating chloride pollution—A review. Sci. Total Environ. 2022, 805, 150289. [Google Scholar] [CrossRef]
  107. Cañedo-Arguelles, M.; Kefford, B.; Schafer, R. Salt in freshwaters: Causes, effects and prospects—Introduction to the theme issue. Philos. Trans. R. Soc. B 2019, 374, 20180002. [Google Scholar] [CrossRef] [PubMed]
  108. Beermann, A.J.; Elbrecht, V.; Karnatz, S.; Ma, L.; Matthaei, C.D.; Piggott, J.J.; Leese, F. Multiple-stressor effects on stream macroinvertebrate communities: A mesocosm experiment manipulating salinity, fine sediment and flow velocity. Sci. Total Environ. 2018, 610–611, 961–971. [Google Scholar] [CrossRef] [PubMed]
  109. Evans, T.G.; Kültz, D. The cellular stress response in fish exposed to salinity fluctuations. J. Exp. Zool. Part A Ecol. Integr. Physiol. 2020, 333, 421–435. [Google Scholar] [CrossRef] [PubMed]
  110. Hasan, M.M.; Defaveri, J.; Kuure, S.; Dash, S.N.; Lehtonen, S.; Merilä, J.; Mccairns, R.J.S. Kidney morphology and candidate gene expression shows plasticity in sticklebacks adapted to divergent osmotic environments. J. Exp. Biol. 2017, 220, 2175–2186. [Google Scholar] [CrossRef] [PubMed]
  111. Rind, K.; Beyrend, D.; Charmantier, G.; Cucchi, P.; Lignot, J. Effects of different salinities on the osmoregulatory capacity of Mediterranean sticklebacks living in freshwater. J. Zool. 2017, 303, 270–280. [Google Scholar] [CrossRef]
  112. Tyree, M.; Clay, N.; Polaskey, S.; Entrekin, S. Salt in our streams: Even small sodium additions can have negative effects on detritivores. Hydrobiologia 2016, 775, 109–122. [Google Scholar] [CrossRef]
  113. Vander Vorste, R.; Timpano, A.J.; Cappellin, C.; Badgley, B.D.; Zipper, C.E.; Schoenholtz, S.H. Microbial and macroinvertebrate communities, but not leaf decomposition, change along a mining-induced salinity gradient. Freshw. Biol. 2019, 64, 671–684. [Google Scholar] [CrossRef]
  114. Lind, L.; Schuler, M.S.; Hintz, W.D.; Stoler, A.B.; Jones, D.K.; Mattes, B.M.; Relyea, R.A. Salty fertile lakes: How salinization and eutrophication alter the structure of freshwater communities. Ecosphere 2018, 9, e02383. [Google Scholar] [CrossRef]
  115. Porter-Goff, E.R.; Frost, P.C.; Xenopoulos, M.A. Changes in riverine benthic diatom community structure along a chloride gradient. Ecol. Indic. 2013, 32, 97–106. [Google Scholar] [CrossRef]
  116. Todd, A.K.; Kaltenecker, M.G. Warm season chloride concentrations in stream habitats of freshwater mussel species at risk. Environ. Pollut. 2012, 171, 199–206. [Google Scholar] [CrossRef]
  117. Cañedo-Argüelles, M.; Sala, M.; Peixoto, G.; Prat, N.; Faria, M.; Soares AM, V.M.; Barata, C.; Kefford, B. Can salinity trigger cascade effects on streams? A mesocosm approach. Sci. Total Environ. 2015, 540, 3–10. [Google Scholar] [CrossRef]
  118. Haq, S.; Kaushal, S.S.; Duan, S. Episodic salinization and freshwater salinization syndrome mobilize base cations, carbon, and nutrients to streams across urban regions. Biogeochemistry 2018, 141, 463–486. [Google Scholar] [CrossRef]
  119. Koç, C. The environmental effects of salinity load in Great Menderes Basin irrigation schemes. Environ. Monit. Assess. 2008, 146, 479–489. [Google Scholar] [CrossRef]
  120. Griffith, M.B. Toxicological perspective on the osmoregulation and ionoregulation physiology of major ions by freshwater animals: Teleost fish, crustacea, aquatic insects, and Mollusca. Environ. Toxicol. Chem. 2017, 36, 576–600. [Google Scholar] [CrossRef]
  121. Pistole, D.H.; Peles, J.D.; Taylor, K. Influence of metal concentrations, percent salinity, and length of exposure on the metabolic rate of fathead minnows (Pimephales promelas). Comp. Biochem. Physiol.-C Toxicol. Pharmacol. 2008, 148, 48–52. [Google Scholar] [CrossRef]
  122. Leite, T.; Santos, J.M.; Ferreira, M.T.; Canhoto, C.; Branco, P. Does short-term salinization of freshwater alter the behaviour of the Iberian barbel (Luciobarbus bocagei, Steindachner 1864)? Sci. Total Environ. 2019, 651, 648–655. [Google Scholar] [CrossRef]
  123. Leite, T.; Branco, P.; Ferreira, M.T.; Santos, J.M. Activity, boldness and schooling in freshwater fish are affected by river salinization. Sci. Total Environ. 2022, 819, 153046. [Google Scholar] [CrossRef]
  124. Hamilton, T.J.; Krook, J.; Szaszkiewicz, J.; Burggren, W. Shoaling, Boldness, Anxiety-like Behavior and Locomotion in Zebrafish (Danio rerio) are Altered by Acute Benzo[a]Pyrene Exposure. Sci. Total Environ. 2021, 774, 145702. [Google Scholar] [CrossRef]
  125. Hintz, W.D.; Jones, D.K.; Relyea, R.A. Evolved tolerance to freshwater salinization in zooplankton: Life-history trade-offs, cross-tolerance and reducing cascading effects. Philos. Trans. R. Soc. B 2019, 374, 20180012. [Google Scholar] [CrossRef]
  126. Afanasyev, S.O.; Gupalo, O.O.; Lietytska, O.M.; Tymoshenko, N.V.; Roman’, A.M.; Abramiuk, I.I.; Golub, O.O. Alien Fish Species of the Ukrainian Part of the Dniester River Basin: Distribution and Dynamics of Settlement. Hydrobiol. J. 2022, 58, 52–66. [Google Scholar] [CrossRef]
  127. Kaushal, S.S.; Likens, G.E.; Pace, M.L.; Reimer, J.E.; Maas, C.M.; Galella, J.G.; Utz, R.M.; Duan, S.; Kryger, J.R.; Yaculak, A.M.; et al. Freshwater salinization syndrome: From emerging global problem to managing risks. Biogeochemistry 2021, 154, 255–292. [Google Scholar] [CrossRef]
  128. Branco, P.; Santos, J.M.; Amaral, S.; Romão, F.; Pinheiro, A.N.; Ferreira, M.T. Potamodromous fish movements under multiple stressors: Connectivity reduction and oxygen depletion. Sci. Total Environ. 2016, 572, 520–525. [Google Scholar] [CrossRef]
  129. Branco, P.; Santos, J.M.; Amaral, S.; Romão, F.; Pinheiro, A.N.; Ferreira, M.T. Potamodromous Fish Responses to Multiple Stressors: Water Scarcity and Oxygen Depletion. In Proceedings of the 11th ISE 2016, Melbourne, Australia, 8–12 February 2016. [Google Scholar]
  130. Gunderson, A.R.; Armstrong, E.J.; Stillman, J.H. Multiple Stressors in a Changing World: The Need for an Improved Perspective on Physiological Responses to the Dynamic Marine Environment. Annu. Rev. Mar. Sci. 2016, 8, 357–378. [Google Scholar] [CrossRef]
  131. Piggott, J.J.; Townsend, C.R.; Matthaei, C.D. Reconceptualizing synergism and antagonism among multiple stressors. Ecol. Evol. 2015, 5, 1538–1547. [Google Scholar] [CrossRef]
  132. Olson, J.R. Predicting combined effects of land use and climate change on river and stream salinity. Philos. Trans. R. Soc. B 2019, 374, 20180005. [Google Scholar] [CrossRef]
  133. Berger, E.; Fro, O.; Schafer, R.B. Salinity impacts on river ecosystem processes: A critical mini-review. Philos. Trans. R. Soc. B 2018, 374, 20180010. [Google Scholar] [CrossRef]
  134. Kefford, B.J.; Buchwalter, D.; Cañedo-Argüelles, M.; Davis, J.; Duncan, R.P.; Hoffmann, A.; Thompson, R. Salinized rivers: Degraded systems or new habitats for salt-tolerant faunas? Biol. Lett. 2016, 12, 20151072. [Google Scholar] [CrossRef]
  135. Lan TT, P.; Hien TT, T.; Le Cam Tu, T.; Van Khanh, N.; Haga, Y.; Phu, T.M. Salinization intensifies the effects of elevated temperatures on Channa striata, a common tropical freshwater aquaculture fish in the Mekong Delta, Vietnam. Fish. Sci. 2020, 86, 1029–1036. [Google Scholar] [CrossRef]
  136. Lintern, A.; McPhillips, L.; Winfrey, B.; Duncan, J.; Grady, C. Best management practices for diffuse nutrient pollution: Wicked problems across urban and agricultural watersheds. Environ. Sci. Technol. 2020, 54, 9159–9174. [Google Scholar] [CrossRef]
  137. Rodgers, E.M. Adding climate change to the mix: Responses of aquatic ectotherms to the combined effects of eutrophication and warming. Biol. Lett. 2021, 17, 20210442. [Google Scholar] [CrossRef]
  138. Bonsdorff, E. Eutrophication: Early warning signals, ecosystem-level and societal responses, and ways forward. Ambio 2021, 50, 753–758. [Google Scholar] [CrossRef]
  139. McCarthy, B.S.; Zukowski, S.; Whiterod, N.; Vilizzi, L.; Beesley, L.; King, A. Hypoxic blackwater event severely impacts Murray crayfish (Euastacus armatus) populations in the Murray River, Australia. Austral. Ecol. 2014, 39, 491–500. [Google Scholar] [CrossRef]
  140. Jenny, J.-P.; Francus, P.; Normandeau, A.; Lapointe, F.; Perga, M.-E.; Ojala, A.; Schimmelmann, A.; Zolitschka, B. Global spread of hypoxia in freshwater ecosystems during the last three centuries is caused by rising local human pressure. Glob. Chang. Biol. 2016, 22, 1481–1489. [Google Scholar] [CrossRef]
  141. Gomez Isaza, D.F.; Cramp, R.L.; Franklin, C.E. Living in polluted waters: A meta-analysis of the effects of nitrate and interactions with other environmental stressors on freshwater taxa. Environ. Poll. 2020, 261, 114091. [Google Scholar] [CrossRef]
  142. Chilundo, M.; Joel, A.; Wesstrom, I.; Brito, R.; Messing, I. Influence of irrigation and fertilisation management on the seasonal distribution of water and nitrogen in a semi-arid loamy sandy soil. Agric. Water Manag. 2018, 199, 120–137. [Google Scholar] [CrossRef]
  143. Peigné, J.; Ball, B.C.; Roger-Estrade, J.; David, C. Is conservation tillage suitable for organic farming? A review. Soil. Use Manag. 2007, 23, 129–144. [Google Scholar] [CrossRef]
  144. Crini, G.; Lichtfouse, E.; Wilson, L.D.; Morin-Crini, N. Conventional and non-conventional adsorbents for wastewater treatment. Environ. Chem. Lett. 2019, 17, 195–213. [Google Scholar] [CrossRef]
  145. Xia, Y.; Zhang, M.; Tsang, D.C.W.; Geng, N.; Lu, D.; Zhu, L.; Igalavithana, A.D.; Dissanayake, P.D.; Rinkleble, J.; Yang, X.; et al. Recent advances in control technologies for non-point source pollution with nitrogen and phosphorous from agricultural runoff: Current practices and future prospects. Appl. Biol. Chem. 2020, 63, 8. [Google Scholar] [CrossRef]
  146. Tank, J.L.; Dodds, W.K. Nutrient limitation of epilithic and epixylic biofilms in ten North American streams. Freshw. Biol. 2003, 48, 1031–1049. [Google Scholar] [CrossRef]
  147. Donohue, I.; Jackson, A.L.; Pusch, M.T.; Irvine, K. Nutrient enrichment homogenizes lake benthic assemblages at local and regional scales. Ecology 2009, 90, 3470–3477. [Google Scholar] [CrossRef] [PubMed]
  148. Gomez Isaza, D.F.; Cramp, R.L.; Franklin, C.E. Simultaneous exposure to nitrate and low pH reduces the blood oxygen-carrying capacity and functional performance of a freshwater fish. Conserv. Physiol. 2020, 8, coz092. [Google Scholar] [CrossRef] [PubMed]
  149. Gomez Isaza, D.F.; Cramp, R.L.; Franklin, C.E. Thermal plasticity of the cardiorespiratory system provides cross-tolerance protection to fish exposed to elevated nitrate. Comp. Biochem. Physiol. C Toxicol. Phamacol 2021, 240, 108920. [Google Scholar] [CrossRef] [PubMed]
  150. Wang, N.-X.; Hunag, B.; Xu, S.; Wei, Z.-B.; Miao, A.-J.; Ji, R.; Yang, L.-Y. Effects of nitrogen and phosphorus on arsenite accumulation, oxidation, and toxicity in Chlamydomonas reinhardtii. Aquat. Toxicol. 2014, 157, 167–174. [Google Scholar] [CrossRef] [PubMed]
  151. Lou, S.; Wu, B.; Xiong, X.; Wang, J. Short-term toxicity of ammonia, nitrite, and nitrate to early life stages of the rare minnow (Gobiocypris rarus). Environ. Toxicol. Chem. 2016, 35, 1422–1427. [Google Scholar]
  152. Gomez Isaza, D.F.; Cramp, R.L.; Franklin, C.E. Negative impacts of elevated nitrate on physiological performance are not exacerbated by low pH. Aquat. Toxicol. 2018, 200, 217–225. [Google Scholar] [CrossRef] [PubMed]
  153. Royer, M.B.; Brooks, R.P.; Shortle, B.J.; Yetter, S. Shared discovery: A process to coproduce knowledge among scientists, policy makers, and stakeholders for solving nutrient pollution problems. J. Environ. Qual. 2020, 49, 603–612. [Google Scholar] [CrossRef] [PubMed]
  154. Knott, J.; Mueller, M.; Pander, J.; Geist, J. Effectiveness of catchment erosion protection measures and scale-dependent response of stream biota. Hydrobiologia 2019, 830, 77–92. [Google Scholar] [CrossRef]
  155. Bierschenk, A.M.; Mueller, M.; Pander, J.; Geist, J. Impact of catchment land use on fish community composition in the headwater areas of Elbe, Danube and Main. Sci. Total Environ. 2019, 652, 66–74. [Google Scholar] [CrossRef] [PubMed]
  156. Auerswald, K.; Geist, J. Extent and cause of siltation in a headwater stream bed: Catchment and soil erosion is less important than internal stream processes. Land. Degrad. Manag. 2018, 29, 737–748. [Google Scholar] [CrossRef]
  157. Geist, J.; Auerswald, K. Physicochemical stream bed characteristics and recruitment of the freshwater pearl mussel (Margaritifera margaritifera). Freshw. Biol. 2007, 52, 2299–2316. [Google Scholar] [CrossRef]
  158. Sternecker, K.; Cowley, D.; Geist, J. Factors influencing the success of salmonid egg development in river substratum. Ecol. Freshw. Fish. 2013, 22, 322–333. [Google Scholar] [CrossRef]
  159. Nagel, C.; Pander, J.; Mueller, M.; Geist, J. Substrate composition determines emergence success and development of European nase larvae (Chondrostoma nasus L.). Ecol. Freshw. Fish. 2020, 29, 121–131. [Google Scholar] [CrossRef]
  160. Hoess, R.; Geist, J. Spatiotemporal variation of streambed quality and fine sediment deposition in five freshwater pearl mussel streams, in relation to extreme drought, strong rain and snow melt. Limnologica 2020, 85, 125833. [Google Scholar] [CrossRef]
  161. Mueller, M.; Pander, J.; Wild, R.; Lueders, T.; Geist, J. The effects of stream substratum texture on interstitial conditions and bacterial biofilms: Methodological strategies. Limnologica 2013, 43, 106–113. [Google Scholar] [CrossRef]
  162. Wild, R.; Nagel, C.; Geist, J. Climate change effects on hatching success and embryonic development of fish: Assessing multiple stressor responses in a large-scale mesocosm study. Sci. Total Environ. 2023, 893, 164834. [Google Scholar] [CrossRef] [PubMed]
  163. Hoess, R.; Geist, J. Effect of fish pond drainage on turbidity, suspended solids, fine sediment deposition and nutrient concentration in receiving pearl mussel streams. Environ. Pollut. 2021, 274, 116520. [Google Scholar] [CrossRef] [PubMed]
  164. Hoess, R.; Geist, J. Nutrient and fine sediment loading from fish pond drainage to pearl mussel streams—Management implications for highly valuable stream ecosystems. J. Environ. Manag. 2022, 302, 113987. [Google Scholar] [CrossRef] [PubMed]
  165. Pander, J.; Mueller, M.; Geist, J. A comparison of four stream substratum restoration techniques concerning interstitial conditions and downstream effects. River Res. Appl. 2015, 31, 239–255. [Google Scholar] [CrossRef]
  166. Geist, J.; Hoess, R.; Rytterstam, J.; Söderberg, J. Substratum raking can restore interstitial habitat quality in Swedish freshwater pearl mussel streams. Diversity 2023, 15, 869. [Google Scholar] [CrossRef]
  167. Boeker, C.; Geist, J. Effects of invasive and indigenous amphipods on physico-chemical and microbial properties in freshwater substrates. Aquat. Ecol. 2015, 49, 467–480. [Google Scholar] [CrossRef]
  168. Boeker, C.; Geist, J. Lampreys as ecosystem engineers: Burrows of Eudontomyzon sp. and their impact on physical, chemical, and microbial properties in freshwater substrates. Hydrobiologia 2016, 777, 171–181. [Google Scholar] [CrossRef]
  169. Lummer, E.M.; Auerswald, K.; Geist, J. Fine sediment as environmental stressor affecting freshwater mussel behavior and ecosystem services. Sci. Total Environ. 2016, 571, 1340–1348. [Google Scholar] [CrossRef] [PubMed]
  170. Geist, J. Integrative freshwater ecology and biodiversity conservation. Ecol. Indic. 2011, 11, 1507–1516. [Google Scholar] [CrossRef]
  171. Braun, A.; Auerswald, K.; Geist, J. Drivers and spatio-temporal extent of hyporheic patch variation: Implications for sampling. PLoS ONE 2012, 7, e42046. [Google Scholar] [CrossRef]
  172. Wilhite, D.A.; Glantz, M.H. Understanding: The drought phenomenon: The role of definitions. Water Int. 1985, 10, 111–120. [Google Scholar] [CrossRef]
  173. Jentsch, A.; Beierkuhnlein, C. Research frontiers in climate change: Effects of extreme meteorological events on ecosystems. C. R. Geosci. 2008, 340, 621–628. [Google Scholar] [CrossRef]
  174. Dai, A. Increasing drought under global warming in observations and models. Nat. Clim. Chang. 2013, 3, 52–58. [Google Scholar] [CrossRef]
  175. Vörösmarty, C.; McIntyre, P.; Gessner, M.; Dudgeon, D.; Prusevich, A.; Green, P.; Glidden, S.; Bunn, S.E.; Sullivan, C.A.; Reidy Liermann, C.; et al. Global threats to human water security and river biodiversity. Nature 2010, 467, 555–561. [Google Scholar] [CrossRef] [PubMed]
  176. Davis, J.; O’Grady, A.P.; Dale, A.; Arthington, A.H.; Gell, P.A.; Driver, P.D.; Bond, N.; Casanova, M.; Finlayson, M.; Watts, R.J.; et al. When trends intersect: The challenge of protecting freshwater ecosystems under multiple land use and hydrological intensification scenarios. Sci. Total Environ. 2015, 534, 65–78. [Google Scholar] [CrossRef]
  177. Aldous, A.; Fitzsimons, J.; Richter, B.; Bach, L. Droughts, floods and freshwater ecosystems: Evaluating climate change impacts and developing adaptation strategies. Mar. Freshw. Res. 2011, 62, 223–231. [Google Scholar] [CrossRef]
  178. Bond, N.R.; Lake, P.S.; Arthington, A.H. The impacts of drought on freshwater ecosystems: An Australian perspective. Hydrobiologia 2008, 600, 3–16. [Google Scholar] [CrossRef]
  179. Lennox, R.J.; Crook, D.A.; Moyle, P.B.; Struthers, D.P.; Cooke, S.J. Toward a better understanding of freshwater fish responses to an increasingly drought-stricken world. Rev. Fish. Biol. Fish. 2019, 29, 71–92. [Google Scholar] [CrossRef]
  180. Chessman, B.C. Identifying species at risk from climate change: Traits predict the drought vulnerability of freshwater fishes. Biol. Convers. 2013, 160, 40–49. [Google Scholar] [CrossRef]
  181. Atkinson, C.L.; Julian, J.P.; Vaughn, C.C. Species and function lost: Role of drought in structuring stream communities. Biol. Conserv. 2014, 176, 30–38. [Google Scholar] [CrossRef]
  182. Cai, X.; Zeng, R.; Kang, W.H.; Song, J.; Valocchi, A.J. Strategic planning for drought mitigation under climate change. J. Water Resour. Plan. Manag. 2015, 141, 04015004. [Google Scholar] [CrossRef]
  183. Carmona, M.; Costa, M.M.; Andreu, J.; Pulido-Velazquez, M.; Haro-Monteagudo, D.; Lopez-Nicolas, A.; Cremades, R. Assessing the effectiveness of multi-sector partnerships to manage droughts: The case of the Jucar river basin. Earth’s Future 2017, 5, 750–770. [Google Scholar] [CrossRef]
  184. Zeff, H.B.; Herman, J.D.; Reed, P.M.; Characklis, G.W. Cooperative drought adaptation: Integrating infrastructure development, conservation, and water transfers into adaptive policy pathways. Water Resour. Res. 2016, 52, 7327–7346. [Google Scholar] [CrossRef]
  185. AghaKouchak, A.; Mirchi, A.; Madani, K.; Di Baldassarre, G.; Nazemi, A.; Alborzi, A.; Anjileli, H.; Azarderakhsh, M.; Chiang, F.; Hassanzadeh, E.; et al. Anthropogenic drought: Definition, challenges, and opportunities. Rev. Geophys. 2021, 59, e2019RG000683. [Google Scholar] [CrossRef]
  186. Aghakouchak, A.; Feldman, D.; Stewardson, M.J.; Saphores, J.-D.; Grant, S.; Sanders, B. Australia’s drought: Lessons for California. Science 2014, 343, 1430–1431. [Google Scholar] [CrossRef]
  187. Grant, S.B.; Fletcher, T.D.; Feldman, D.; Saphores, J.-D.; Cook, P.L.M.; Stewardson, M.; Low, K.; Burry, K.; Hamilton, A.J. Adapting urban water systems to a changing climate: Lessons from the millennium drought in southeast Australia. Environ. Sci. Technol. 2013, 47, 10727–10734. [Google Scholar] [CrossRef] [PubMed]
  188. Lake, P.S. Disturbance, patchiness, and diversity in streams. J. N. Am. Benthol. Soc. 2000, 19, 573–592. [Google Scholar] [CrossRef]
  189. Humphries, P.; Baldwin, D.S. Drought and aquatic ecosystems: An introduction. Freshw. Biol. 2003, 48, 1141–1146. [Google Scholar] [CrossRef]
  190. Crook, D.A.; Reich, P.; Bond, N.R.; McMaster, D.; Koehn, J.D.; Lake, P.S. Using biological information to support proactive strategies for managing freshwater fish during drought. Mar. Freshw. Res. 2010, 61, 379–387. [Google Scholar] [CrossRef]
  191. Stagge, J.H.; Kohn, I.; Tallaksen, L.M.; Stahl, K. Modeling drought impact occurrence based on meteorological drought indices in Europe. J. Hydrol. 2015, 530, 37–50. [Google Scholar] [CrossRef]
  192. Mihaljević, M.; Špoljarić, D.; Stević, F.; Cvijanović, V.; Kutuzović, B.H. The influence of extreme floods from the River Danube in 2006 on phytoplankton communities in a floodplain lake: Shift to a clear state. Limnol.-Ecol. Manag. Inland Waters 2010, 40, 260–268. [Google Scholar] [CrossRef]
  193. Junk, W.J.; Bayley, P.B.; Sparks, R.E. The flood pulse concept in river-floodplain systems. Can. Spec. Publ. Fish. Aquat. Sci. 1989, 106, 110–127. [Google Scholar]
  194. Bunn, S.E.; Arthington, A.H. Basic principles and ecological consequences of altered flow regimes for aquatic biodiversity. Environ. Manag. 2002, 30, 492–507. [Google Scholar] [CrossRef]
  195. Bayley, P.B. The flood pulse advantage and the restoration of river-floodplain systems. Regul. Rivers Res. Manag. 1991, 6, 75–86. [Google Scholar] [CrossRef]
  196. Heiler, G.; Hein, T.; Schiemer, F.; Bornette, G. Hydrological connectivity and flood pulses as the central aspects for the integrity of a river-floodplain system. Regul. Rivers Res. Manag. 1995, 11, 351–361. [Google Scholar] [CrossRef]
  197. Geddes, M.C.; Puckridge, J.T. Survival and growth of larval and juvenile native fish: The importance of the floodplain. In Proceedings of the Workshop on Native Fish Management; Murray-Darling Basin Commission: Canberra, Australia, 1989; pp. 101–115. [Google Scholar]
  198. McConnell, R.; Lowe-McConnell, R.H. Ecological Studies in Tropical Fish Communities; Cambridge University Press: Cambridge, UK, 1987. [Google Scholar]
  199. Poiani, K.A.; Richter, B.D.; Anderson, M.G.; Richter, H.E. Biodiversity conservation at multiple scales: Functional sites, landscapes, and networks. BioScience 2000, 50, 133–146. [Google Scholar] [CrossRef]
  200. Rood, S.B.; Heinze-Milne, S. Abrupt downstream forest decline following river damming in southern Alberta. Can. J. Bot. 1989, 67, 1744–1749. [Google Scholar] [CrossRef]
  201. Ward, J.V.; Stanford, J.A. Ecological connectivity in alluvial river ecosystems and its disruption by flow regulation. Regul. Rivers Res. Manag. 1995, 11, 105–119. [Google Scholar] [CrossRef]
  202. Molles, M.C., Jr.; Crawford, C.S.; Ellis, L.M.; Valett, H.M.; Dahm, C.N. Managed flooding for riparian ecosystem restoration: Managed flooding reorganizes riparian forest ecosystems along the middle Rio Grande in New Mexico. BioScience 1998, 48, 749–756. [Google Scholar] [CrossRef]
  203. Snyder, E.B.; Arango, C.P.; Eitemiller, D.J.; Stanford, J.A.; Uebelacker, M.L. Floodplain hydrologic connectivity and fisheries restoration in the Yakima River, USA. Int. Ver. Theor. Angew. Limnol. Verhandlungen 2002, 28, 1653–1657. [Google Scholar]
  204. Graf, W.L. Downstream hydrologic and geomorphic effects of large dams on American rivers. Geomorphology 2006, 79, 336–360. [Google Scholar] [CrossRef]
  205. Dimitriadis, P.; Tegos, A.; Oikonomou, A.; Pagana, V.; Koukouvinos, A.; Mamassis, N.; Efstratiadis, A. Comparative evaluation of 1D and quasi-2D hydraulic models based on benchmark and real-world applications for uncertainty assessment in flood mapping. J. Hydrol. 2016, 534, 478–492. [Google Scholar] [CrossRef]
  206. Tegos, A.; Ziogas, A.; Bellos, V. Modern Developments in Flood Modelling. Hydrology 2023, 10, 112. [Google Scholar] [CrossRef]
  207. Pricope, N.G.; Shivers, G. Wetland Vulnerability Metrics as a Rapid Indicator in Identifying Nature-Based Solutions to Mitigate Coastal Flooding. Hydrology 2022, 9, 218. [Google Scholar] [CrossRef]
  208. Koskinas, A.; Tegos, A. StEMORS: A Stochastic Eco-Hydrological Model for Optimal Reservoir Sizing. Open Water J. 2020, 6, 1. [Google Scholar]
  209. Hart, D.D.; Johnson, T.E.; Bushaw-Newton, K.L.; Horwitz, R.J.; Bednarek, A.T.; Charles, D.F.; Kreeger, D.A.; Velinsky, D.J. Dam removal: Challenges and opportunities for ecological research and river restoration: We develop a risk assessment framework for understanding how potential responses to dam removal vary with dam and watershed characteristics, which can lead to more effective use of this restoration method. BioScience 2002, 52, 669–682. [Google Scholar]
  210. Koutsoyiannis, D. Scale of water resources development and sustainability: Small is beautiful, large is great. Hydrol. Sci. J. 2011, 56, 553–575. [Google Scholar] [CrossRef]
  211. Costea, G.; Push, M.T.; Bănăduc, D.; Cosmoiu, D.; Curtean-Bănăduc, A. A review of hydropower plants in Romania: Distribution, current knowledge, and their effects on fish in headwater streams. Renew. Sustain. Energy Rev. 2021, 54, 111003. [Google Scholar] [CrossRef]
  212. Curtean-Bănăduc, A.; Pauli, S.; Bănăduc, D.; Didenko, A.; Sender, J.; Marić, S.; Del Monte, P.; Khoshnood, Z.; Zakeyuddin, S. Environmental aspects of implementation of micro hydro power plants—A short review. Transylv. Rev. Syst. Ecol. Res. 2015, 17, 179–198. [Google Scholar] [CrossRef]
  213. Efstratiadis, A.; Tegos, A.; Varveris, A.; Koutsoyiannis, D. Assessment of environmental flows under limited data availability: Case study of the Acheloos River, Greece. Hydrol. Sci. J. 2014, 59, 731–750. [Google Scholar] [CrossRef]
  214. Tegos, A.; Schlüter, W.; Gibbons, N.; Katselis, Y.; Efstratiadis, A. Assessment of environmental flows from complexity to parsimony—Lessons from Lesotho. Water 2018, 10, 1293. [Google Scholar] [CrossRef]
  215. Ward, J.V. The four-dimensional nature of the lotic ecosystem. J. N. Am. Benthol. Soc. 1989, 8, 2–8. [Google Scholar] [CrossRef]
  216. Branco, P.; Segurado, P.; Santos, J.M.; Ferreira, M.T. Prioritizing barrier removal to improve functional connectivity of rivers. J. Appl. Ecol. 2014, 51, 1197–1206. [Google Scholar] [CrossRef]
  217. Amaral, S.D.; Branco, P.; da Silva, A.T.; Katopodis, C.; Viseu, T.; Ferreira, M.T.; Pinheiro, A.N.; Santos, J.M. Upstream passage of potamodromous cyprinids over small weirs: The influence of key-hydraulic parameters. J. Ecohydraulics 2016, 1, 79–89. [Google Scholar] [CrossRef]
  218. Duarte, G.; Segurado, P.; Haidvogl, G.; Pont, D.; Ferreira, M.T.; Branco, P. Damn those damn dams: Fluvial longitudinal connectivity impairment for European diadromous fish throughout the 20th century. Sci. Total Environ. 2021, 761, 143293. [Google Scholar] [CrossRef] [PubMed]
  219. Mallen-Cooper, M.; Harris, J. Fishways in mainland south-eastern Australia. In Proceedings of the International Symposium on Fishways’90, Gifu, Japan, 8–10 October 1990; pp. 221–230. [Google Scholar]
  220. Larinier, M. Environmental issues, dams and fish migration. In Dams, Fish and Fisheries, Opportunities, Challenges and Conflict Resolution; Marmulla, G., Ed.; FAO Fisheries Technical Paper 419; FAO: Rome, Italy, 2001; pp. 45–89. [Google Scholar]
  221. Quiros, R. Structures Assisting the Migrations of Nonsalmonid Fish: Latin America; FAO-COPESCAL Tech Pap 5; UN FAO: Rome, Italy, 1989. [Google Scholar]
  222. Baum, E.T. Evolution of the Atlantic salmon restoration program in Maine. In A Hard Look at Some Tough Issues; Calabi, S., Stout, A., Eds.; New England Salmon Association Publisher: Newburyport, MA, USA, 1994; pp. 36–41. [Google Scholar]
  223. Meyers, T.F. The program to restore Atlantic salmon to the Conneticut River. In A Hard Look at Some Tough Issues; Calabi, S., Stout, A., Eds.; New England Salmon Association Publisher: Newburyport, MA, USA, 1994; pp. 11–21. [Google Scholar]
  224. Stolte, L.W. Atlantic salmon restoration in the Merrimack River basin. In A Hard Look at Some Tough Issues; Calabi, S., Stout, A., Eds.; New England Salmon Association: Newburyport, MA, USA, 1994; pp. 22–35. [Google Scholar]
  225. Porcher, J.P.; Travade, F. Les dipositifs de franchissement: Bases biologiques, limiteset rappels réglementaires. Bull. Fr. Peche Piscic. 1992, 326–327, 5–15. [Google Scholar] [CrossRef]
  226. Costa, M.J.; Duarte, G.; Segurado, P.; Branco, P. Major threats to European freshwater fish species. Sci. Total Environ. 2021, 797, 149105. [Google Scholar] [CrossRef] [PubMed]
  227. Gourène, G.; Teugels, G.G.; Hugueny, B.; Thys Van Den Audenaerde, D.F. Evaluation dela diversité ichtyologique d’un basin oust-africain après la construction d’un barrage. Cybium 1999, 23, 147–216. [Google Scholar]
  228. Zhong, Y.; Power, G. Environmental impacts of hydroelectric projects on fishresources in China. Regul. Rivers Res. Manag. 1996, 12, 81–98. [Google Scholar] [CrossRef]
  229. Morita, K.; Yamamoto, S. Effects of habitat fragmentation by damming on thepersistence of stream-dwelling charr populations. Conserv. Biol. 2002, 16, 1318–1323. [Google Scholar] [CrossRef]
  230. Torgersen, C.; Le Pichon, C.; Fullerton, A.; Dugdale, S.; Duda, J.; Giovannini, F.; Tales, E.; Belliard, J.; Branco, P.; Bergeron, N.E.; et al. Riverscape approaches in practice: Perspectives and applications. Biol. Rev. 2022, 97, 481–504. [Google Scholar] [CrossRef] [PubMed]
  231. Vannote, R.L.; Minshall, G.; Cummins, K.W.; Sedell, J.R.; Cushing, C.E. The river continuum concept. Can. J. Fish. Aquat. Sci. 1980, 37, 130–137. [Google Scholar] [CrossRef]
  232. Fullerton, A.H.; Burnett, K.M.; Steel, E.A.; Flicroft, R.L.; Pess, G.R.; Feist, B.E.; Torgersen, C.E.; Miller DJand Sanderson, B.L. Hydrological connectivity for riverine fish: Measurement challenges and research opportunities. Freshw. Biol. 2010, 55, 2215–2237. [Google Scholar] [CrossRef]
  233. Poole, G.C. Fluvial landscape ecology: Addressing uniqueness within the river discontinuum. Freshw. Biol. 2002, 47, 641–660. [Google Scholar] [CrossRef]
  234. Benda, L.; Poff, N.L.; Miller, D.; Dunne, T.; Reeves, G.; Pess, G.; Pollock, M. The network dynamics hypothesis: How channel networks structure riverine habitats. BioScience 2004, 54, 413–427. [Google Scholar] [CrossRef]
  235. Thorp, J.H.; Thoms, M.C.; Delong, M.D. The riverine ecosystem synthesis: Biocomplexityin river networks across space and time. River Res. Appl. 2006, 22, 123–147. [Google Scholar] [CrossRef]
  236. Branco, P.; Santos, J.M.; Katopodis, C.; Pinheiro, A.; Ferreira, M.T. Pool-type fishways: Two different morpho-ecological cyprinid species facing plunging and streaming flows. PLoS ONE 2013, 8, e65089. [Google Scholar] [CrossRef] [PubMed]
  237. European Commission. REPowerEU: Joint European Action for More Affordable, Secure and Sustainable Energy; European Commission: Luxembourg, 2022. [Google Scholar]
  238. Northcote, T.G. Migratory behaviour of fish and its significance to movement trough riverine fish passage facilities. In Fish Migration and Fish Bypasses; Jungwirth, M., Schmutz, S., Weiss, S., Eds.; Fishing News Books; Blackwell Science Ltd.: Oxford, UK; London, UK; Berlin/Heidelberg, Germany, 1998; pp. 3–18. [Google Scholar]
  239. Mader, H.; Maier, C. A method for prioritizing the reestablishment of river continuity in Austrian rivers. Hydrobiologia 2008, 609, 277–288. [Google Scholar] [CrossRef]
  240. Branco, P.; Amaral, S.D.; Ferreira, M.T.; Santos, J.M. Do small barriers affect the movement of freshwater fish by increasing residency? Sci. Total Environ. 2017, 581, 486–494. [Google Scholar] [CrossRef] [PubMed]
  241. European Commission. Directive 2000/60/EC of the European Parliament and of the Council of 23 October 2000 establishing a framework for the community action in the field of water policy. Off. J. Eur. Comm.-Legis 2000, 327, 1–72. [Google Scholar]
  242. European Commission. Communication from the Commission to the European Parliament, the Council, the European Economic and Social Committee and the Committee of the Regions. Eu Biodiversity Strategy for 2030; Document 52020DC0380; European Commission: Luxembourg, 2020. [Google Scholar]
  243. European Commission. Communication from the Commission to the European Parliament, the European Council, the Council, the European Economic and Social Committee and the Committee of the Regions the European Green Deal; Document 52019DC0640; European Commission: Luxembourg, 2019. [Google Scholar]
  244. FAOSTAT. Food and Agriculture Organization of the United Nations. Rome. 2024. Available online: http://faostat.fao.org (accessed on 9 February 2024).
  245. PPDB, Pesticide Properties DataBase. 2021. Available online: https://sitem.herts.ac.uk/aeru/ppdb/ (accessed on 9 February 2024).
  246. de Araújo, E.P.; Caldas, E.D.; Oliveira-Filho, E.C. Pesticides in surface freshwater: A critical review. Environ. Monit. Assess. 2022, 194, 452. [Google Scholar] [CrossRef] [PubMed]
  247. Singh, S.; Rawat, M.; Malyan, S.K.; Singh, R.; Tyagi, V.K.; Singh, K.; Kashyap, S.; Kumar, S.; Sharma, M.; Panday, B.K.; et al. Global distribution of pesticides in freshwater resources and their remediation approaches. Environ. Res. 2023, 225, 115605. [Google Scholar] [CrossRef] [PubMed]
  248. Schäfer, R.B.; van den Brink, P.J.; Liess, M. Impacts of pesticides on freshwater ecosystems. Ecol. Impacts Toxic Chem. 2011, 2011, 111–137. [Google Scholar]
  249. Benbrook, C.M. Trends in glyphosate herbicide use in the United States and globally. Environ. Sci. Eur. 2016, 28, 1–15. [Google Scholar] [CrossRef] [PubMed]
  250. Pizarro, H.; Vera, M.S.; Vinocur, A.; Pérez, G.; Ferraro, M.; Menendez Helman, R.J.; Dos Santos Afonso, M. Glyphosate input modifies microbial community structure in clear and turbid freshwater systems. Environ. Sci. Pollut. Res. 2016, 23, 5143–5153. [Google Scholar] [CrossRef]
  251. Berman, M.C.; Llames, M.E.; Minotti, P.; Fermani, P.; Quiroga, M.V.; Ferraro, M.A.; Metz, S.; Zagarese, H.E. Field evidence supports former experimental claims on the stimulatory effect of glyphosate on picocyanobacteria communities. Sci. Total Environ. 2020, 701, 134601. [Google Scholar] [CrossRef]
  252. Lipok, J.; Studnik, H.; Gruyaert, S. The toxicity of Roundup® 360 SL formulation and its main constituents: Glyphosate and isopropylamine towards non-target water photoautotrophs. Ecotoxicol. Environ. Saf. 2010, 73, 1681–1688. [Google Scholar] [CrossRef] [PubMed]
  253. Weisner, O.; Frische, T.; Liebmann, L.; Reemtsma, T.; Roß-Nickoll, M.; Schäfer, R.B.; Schäffer, A.; Scholz-Starke, B.; Vormeier, P.; Knillmann, S.; et al. Risk from pesticide mixtures—The gap between risk assessment and reality. Sci. Total Environ. 2021, 796, 149017. [Google Scholar] [CrossRef] [PubMed]
  254. Vera, M.S.; Di Fiori, E.; Lagomarsino, L.; Sinistro, R.; Escaray, R.; Iummato, M.M.; Juárez, A.; Ríos de Molina, M.D.; Tell, G.; Pizarro, H. Direct and indirect effects of the glyphosate formulation Glifosato Atanor® on freshwater microbial communities. Ecotoxicology 2012, 21, 1805–1816. [Google Scholar] [CrossRef] [PubMed]
  255. Vera, M.S.; Lagomarsino, L.; Sylvester, M.; Pérez, G.L.; Rodríguez, P.; Mugni, H.; Sinistro, R.; Ferraro, M.; Bonetto, C.; Zagarese, H.; et al. New evidences of Roundup® (glyphosate formulation) impact on the periphyton community and the water quality of freshwater ecosystems. Ecotoxicology 2010, 19, 710–721. [Google Scholar] [CrossRef] [PubMed]
  256. Klátyik, S.; Simon, G.; Oláh, M.; Takács, E.; Mesnage, R.; Antoniou, M.N.; Zaller, J.G.; Székács, A. Aquatic ecotoxicity of glyphosate, its formulations, and co-formulants: Evidence from 2010 to 2023. Environ. Sci. Eur. 2024, 36, 1–62. [Google Scholar] [CrossRef]
  257. Gorobets, K. Russian ‘Special Military Operation’ and the Language of Empire. Opinio Juris. Available online: http://opiniojuris.org/2022/05/24/russian-special-military-operation-and-the-language-of-empire/ (accessed on 2 August 2023).
  258. Pipes, D.; Blumenfeld, T. Terrorism Defies Definition. The Washington Times, 24 October 2014. [Google Scholar]
  259. Gleick, P.H. Water, war, and peace in the Middle East- conflict over water rights. Environment 1994, 36, 7–42. [Google Scholar]
  260. Cooley, J.K. The War over Water. Foreign Policy 1984, 54, 3–26. [Google Scholar] [CrossRef]
  261. Gleick, P. Reducing the Risk of Conflict Over Fresh Water Resources in the Middle East. In Water and Peace in the Middle East; Isaac, J., Shuval, H., Eds.; Elsevier: Amsterdam, The Netherlands, 1994; pp. 41–55. Available online: https://www.worldwater.org/conflict/list/ (accessed on 9 February 2024).
  262. Water: A Military Weapon and Target during Armed Conflict. International Year of FreshWater 2003. Available online: http://mandalaprojects.com/ice/ice-cases/sumerianwater.htm (accessed on 28 July 2023).
  263. Gleick, P.H.; Cooley, H.; Morikawa, M.; Morrison, J.; Cohen, M.J. The World’s Water 2008–2009: The Biennial Report on Freshwater Resources; Island Press: Washington, DC, USA, 2009; Volume 6. [Google Scholar]
  264. The Environmental Impact of the Conflict in Ukraine A Preliminary Review. United Nations Environment Programme, Job Number: EO/2466/NA 2022. p. 45. Available online: https://wedocs.unep.org/bitstream/handle/20.500.11822/40746/environmental_impact_Ukraine_conflict.pdf?sequence=3&isAllowed=y (accessed on 11 March 2024).
  265. Shumilova, O.; Tockner, K.; Sukhodolov, A.; Khilchevskyi, V.; De Meester, L.; Stepanenko, S.; Trokhymenko, G.; Hernández-Agüero, J.-A.; Gleick, P. Impact of the Russia–Ukraine armed conflict on water resources and water infrastructure. Nat. Sustain. 2023, 6, 578–586. [Google Scholar] [CrossRef]
  266. Zheleznyak, M.; Donchyts, G.; Maderich, V.; Dronova, I.; Tkalich, P.; Trybushnyi, D.; Faybishenko, B.; Dvorzhak, A. Ecological footprint of Russia’s Ukraine invasion. Science 2022, 377, 1273. [Google Scholar] [CrossRef]
  267. Shevchuk, S.A.; Vyshnevskyi, V.I.; Bilous, O.P. The use of remote sensing data for investigation of environmental consequences of Russia-Ukraine war. J. Landsc. Ecol. 2022, 15, 36–53. [Google Scholar] [CrossRef]
  268. Bănăduc, D.; Simić, V.; Cianfaglione, K.; Barinova, S.; Afanasyev, S.; Öktener, A.; McCall, G.; Simić, S.; Curtean-Bănăduc, A. Freshwater as a sustainable resource and generator of secondary resources in the 21st century: Stressors, threats, risks, management and protection strategies, and conservation approaches. Int. J. Environ. Res. Public Health 2022, 19, 16570. [Google Scholar] [CrossRef] [PubMed]
  269. Afanasyev, S. Impact of War on Hydroecosystems of Ukraine: Conclusion of the First Year of the Full-Scale Invasion of Russia (a Review). Hydrobiol. J. 2023, 59, 3–16. [Google Scholar] [CrossRef]
  270. Vyshnevskyi, V.; Shevchuk, S.; Komorin, Y.; Oleynik, Y.; Gleick, P. The destruction of the Kakhovka dam and its consequences. Water Int. 2023, 48, 631–647. [Google Scholar] [CrossRef]
  271. Protasov, A.; Afanasyev, S. Principal types of Dreissena communities in periphyton. Hydrobiol. J. 1990, 26, 15–23. [Google Scholar]
  272. Protasov, A.; Afanasyev, S. Structure of Periphytic Communities in Cooling Pond of Nuclear Power Plant. Internat. Rev. Gesamt. Hydrobiol. Hydrogr. 1986, 71, 335–347. [Google Scholar] [CrossRef]
  273. Afanas’ev, S.A. Biogenic interference with the water supply to thermal and atomic power stations. Hydrobiol. J. 1998, 34, 27–33. [Google Scholar]
  274. Roman, A.M.; Afanasyev, S.A.; Tkachenko, P.V. New finding of sea zander sander marinus (Pisces, Percidae) in the Dnieper-Bug liman and brief notes on morphology of sympatric species of the genus. Hydrobiol. J. 2018, 54, 40–49. [Google Scholar] [CrossRef]
  275. Yeganeh, Y.; Bakhshandeh, E. Iran’s Model of Water Diplomacy to Promote Cooperation and Prevent Conflict Over Transboundary Rivers in Southwest Asia. World Aff. 2022, 185, 331–358. [Google Scholar] [CrossRef]
  276. Afanasyev, S.O. Problems and progress of investigations of hydroecosystems’ ecological state in view of implementation of EU environmental directives in Ukraine. Hydrobiol. J. 2019, 55, 3–17. [Google Scholar] [CrossRef]
  277. Available online: http://epl.org.ua/wp-content/uploads/2022/04/KR-N-MS-OON.pdf (accessed on 1 August 2023).
  278. Dannenbaum, T. What International Humanitarian Law Says about the Nova Kakhovka Dam. The Lawfare Institute, 9 June 2023. Available online: https://www.lawfareblog.com/what-international-humanitarian-lawsays-about-nova-kakhovka-dam (accessed on 1 August 2023).
  279. Anderson, D.M. Approaches to monitoring, control and management of harmful algal blooms (HABs). Ocean Coast. Manag. 2009, 52, 342. [Google Scholar] [CrossRef]
  280. Watson, S.B.; Whitton, B.A.; Higgins, S.N.; Paerl, H.W.; Brooks, B.W.; Wehr, J.D. Harmful Algal Blooms. In Freshwater Algae of North America: Ecology and Classification, 2nd ed.; Wehr, J.D., Sheath, R.G., Kociolek, J.P., Eds.; Academic Press: Cambridge, MA, USA, 2015; pp. 873–920. [Google Scholar]
  281. Lembi, A.C. Control of nuisance algae. In Freshwater Algae of North America: Ecology and Classification, 2nd ed.; Wehr, J.D., Sheath, R.G., Kociolek, J.P., Eds.; Academic Press: Cambridge, MA, USA, 2015; pp. 805–834. [Google Scholar]
  282. Michalak, I.; Messyasz, B. Concise review of Cladophora spp.: Macroalgae of commercial interest. J. Appl. Phycol. 2021, 33, 133–166. [Google Scholar] [CrossRef]
  283. Sundareshwar, P.V.; Upadhayay, S.; Abessa, M.; Honomichl, S.; Berdanier, B.; Spaulding, S.A.; Sandvik, C.; Trennepoh, A. Didymosphenia geminata: Algal blooms in oligotrophic streams and rivers. Geophys. Res. Lett. 2011, 38. [Google Scholar] [CrossRef]
  284. Clancy, N.G. Do Didymosphenia Geminata Blooms Affect Fishes in the Kootenai River Basin? Doctoral Dissertation, Utah State University, Logan, UT, USA, 2020. Available online: https://digitalcommons.usu.edu/etd/7727 (accessed on 9 February 2024).
  285. Paerl, H.W.; Paul, V. Climate change: Links to global expansion of harmful cyanobacteria. Water Res. 2011, 46, 1349–1363. [Google Scholar] [CrossRef]
  286. Svirčev, Z.; Drobac, D.; Tokodi, N.; Đenić, D.; Simeunović, J.; Hiskia, A.; Kaloudis, T.; Mijović, B.; Šušak, S.; Protić, M.; et al. Lessons from the Užice Case: How to Complement Analytical Data. In Handbook of Cyanobacterial Monitoring and Cyanotoxin Analysis; Meriluoto, J., Spoof, L., Codd, G.A., Eds.; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2017; pp. 298–308. [Google Scholar]
  287. Drobac, D.; Tokodi, N.; Lujić, J.; Marinović, Z.; Subakov-Simić, G.; Dulić, T.; Važić, T.; Nybom, S.; Meriluoto, J.; Codd, G.A.; et al. Cyanobacteria and cyanotoxins in fishponds and their effects on fish tissue. Harmful Algae 2016, 55, 66–76. [Google Scholar] [CrossRef] [PubMed]
  288. Simić, S.B.; Ðorđević, N.B.; Milošević, D. The relationship between the dominance of cyanobacteria species and environmental variables in different seasons and after extreme precipitation. Fundam. Appl. Limnol./Arch. Hydrobiol. 2017, 190, 1–11. [Google Scholar] [CrossRef]
  289. Zhan, M.; Liu, P.; Liu, X.; Hong, Y.; Xie, X. Inactivation and Removal Technologies for Algal-Bloom Control: Advances and Challenges. Curr. Pollut. Rep. 2021, 7, 392–406. [Google Scholar] [CrossRef]
  290. IPBES. 2019. Available online: https://ipbes.net/sites/default/files/inline/files/ipbes_global_assessment_report_summary_for_policymakers.pdf (accessed on 13 November 2021).
  291. Wu, H.; Ding, J. Global Change Sharpens the Double-Edged Sword Effect of Aquatic Alien Plants in China and Beyond. Front. Plant Sci. 2019, 10, 787. [Google Scholar] [CrossRef]
  292. Havel, J.E.; Kovalenko, K.E.; Thomaz, S.M.; Amalfitano, S.; Kats, L.B. Aquatic invasive species: Challenges for the future. Hydrobiologia 2015, 750, 147–170. [Google Scholar] [CrossRef]
  293. Kolar, C.S.; Lodge, D.M. Freshwater nonindigenous species: Interactions with other global changes. In Invasive Species in a Changing World; IMooney, H.A., Hobbs, R.J., Eds.; Island Press: Washington, DC, USA, 2000; pp. 3–30. [Google Scholar]
  294. Lind, L.; Eckstein, R.L.; Relyea, R.A. Direct and indirect effects of climate change on distribution and community composition of macrophytes in lentic systems. Biol. Rev. 2022, 97, 1677–1690. [Google Scholar] [CrossRef]
  295. Mazej Grudnik, Z.; Germ, M. Spatial pattern of native species Myriophyllum spicatum and invasive alien species Elodea nuttallii after introduction of the latter one into the Drava River (Slovenia). Biologia 2013, 68, 202–209. [Google Scholar] [CrossRef]
  296. Meyerson, L.A.; Mooney, H.A. Invasive alien species in an era of globalization. Front. Ecol. Environ. 2007, 5, 199–208. [Google Scholar] [CrossRef]
  297. Reitsema, R.E.; Meire, P.; Schoelynck, J. The Future of Freshwater Macrophytes in a Changing World: Dissolved Organic Carbon Quantity and Quality and Its Interactions with Macrophytes. Front. Plant Sci. 2018, 9, 629. [Google Scholar] [CrossRef] [PubMed]
  298. Šajna, N.; Haler, M.; Škornik, M.; Kaligarič, M. Survival and expansion of Pistia stratiotes L. in a thermal stream in Slovenia. Aquat. Bot. 2007, 87, 75–79. [Google Scholar] [CrossRef]
  299. Jaklič, M.; Koren, Š.; Jogan, N. Alien water lettuce (Pistia stratiotes L.) outcompeted native macrophytes and altered the ecological conditions of a Sava oxbow lake (SE Slovenia). Acta Bot. Croat. 2020, 79. [Google Scholar] [CrossRef]
  300. Šajna, N.; Urek, T.; Kuša, P.; Šipek, M. The Importance of Thermally Abnormal Waters for Bioinvasions—A Case Study of Pistia stratiotes. Diversity 2023, 15, 421. [Google Scholar] [CrossRef]
  301. Alford, S.B.; Rozas, L.P. Effects of Non-native Eurasian Watermilfoil, Myriophyllum spicatum, on Nekton Habitat Quality in a Louisiana Oligohaline Estuary. Estuaries Coasts 2019, 42, 613–628. [Google Scholar] [CrossRef]
  302. Kourantidou, M.; Haubrock, P.J.; Cuthbert, R.N.; Bodey, T.W.; Lenzner, B.; Gozlan, R.E.; Nuñez, M.A.; Salles, J.M.; Diagne, C.; Courchamp, F. Invasive alien species as simultaneous benefits and burdens: Trends, stakeholder perceptions and management. Biol. Invasions 2022, 24, 1905–1926. [Google Scholar] [CrossRef]
  303. Pedrotti, F. Plant and Vegetation Mapping; Springer: Berlin/Heidelberg, Germany, 2013; p. 294. [Google Scholar] [CrossRef]
  304. Loidi, J. Syntaxonomic ranks, biogeography and typological inflation. Veg. Classif. Surv. 2023, 4, 1285–1290. [Google Scholar] [CrossRef]
  305. Preislerová, Z.; Marcenò, C.; Loidi, J.; Bonari, G.; Borovyk, D.; Gavilán, R.G.; Golub, V.; Terzi, M.; Theurillat, J.P.; Argagnon, O.; et al. Structural, ecological and biogeographical attributes of European vegetation alliances. Appl. Veg. Sci. 2024, 27, e12766. [Google Scholar] [CrossRef]
  306. Curtean-Bănăduc, A.; Bănăduc, D. The riverine ligneous vegetation importance elements, on some submountain Carpathian lotic systems (macroinvertebrates and fish). Acta Ichtiologica Romanica 2008, III, 53–58. [Google Scholar]
  307. Curtean-Bănăduc, A.; Schneider-Binder, E.; Bănăduc, D. The importance of the riverine ligneous vegetation for the Danube Basin lotic ecosystems. In L’importanza degli Alberi e del Bosco, Cultura, Scienza e Coscienza del Territorio; Cianfaglione, K., Ed.; Temi Edit.: Trento, Italia, 2014; pp. 187–210. [Google Scholar]
  308. Cianfaglione, K. Plant Landscape and Models of French Atlantic Estuarine Systems. Extended Summary of the Doctoral Thesis. Transylv. Rev. Syst. Ecol. Res. 2021, 23, 15–36. [Google Scholar] [CrossRef]
  309. Verger, F. Marais et Estuaires du Littoral Français; Belin: Paris, France, 2005; p. 335. [Google Scholar]
  310. Di Pietro, F.; Mehdi, L.; Chaudron, C.; Moyon, F. Le lit endigué de la Loire moyenne: De l’image de fleuve sauvage à la reconnaissance de son caractère anthropisé. Norois 2017, 242, 7–23. [Google Scholar] [CrossRef]
  311. Le Dez, M.; Sawtschuk, J.; Bioret, F. Les prairies de l’estuaire de la Loire: Étude de la dynamique de la végétation de 1982 à 2014. Revue trimestrielle sur l’image géographique et les formes du territoire 2017, 119, 1–18. [Google Scholar] [CrossRef]
  312. Cianfaglione, K.; Pedrotti, F. Italy in the Danube Geography: Territory, Landscape, Environment, Vegetation, Fauna, Culture, Human Management and Outlooks for the Future. In Human Impact on Danube Watershed Biodiversity in the XXI Century. Geobotany Studies; Bănăduc, D., Curtean-Bănăduc, A., Pedrotti, F., Cianfaglione, K., Akeroyd, J., Eds.; Springer: Cham, Switzerland, 2020. [Google Scholar] [CrossRef]
  313. Antipa, G. Fauna Ichtiologică a României, IX; Institutul de Arte Grafice “Carol Gobl”: Bucuresci, Romania, 1909; p. 294. [Google Scholar]
  314. Bănărescu, P.M. Fauna Republicii Populare Române 13. Pisces—Psteichthyes: (Pești Ganoizi și Osoși); Editura Academiei Republicii Populare Române: Bucuresti, Romania, 1964; p. 969. [Google Scholar]
  315. Koščo, J.; Heltai, M.; Harka, A.; Sallai, Z.; Szewczyk, M.; Nowak, M.; Mikolajczyk, P.; Brankovic, S.; Kurtyak, F.; Halacka, K.; et al. Bănăduc Doru, Draft Carpathian Red List of fish and Lamprey species. In Carpathian Red List of Forest Habitats and Species, Carpathian List of Invasive Alien Species; Edition Banská Bystrica; Koščo, J., Ed.; State Nature Conservancy of the Slovak Republic: Banská Bystrica, Slovakia, 2014; 234p, ISBN 978-80-89310-81-4. [Google Scholar]
  316. Moyle Peter, B.; Joseph, J. Fishes, an Introduction to Ichthyology, 5th ed.; Benkamin Cummings: San Francisco, CA, USA, 2003; ISBN 978-0-13-100847-2. [Google Scholar]
  317. Bănăduc, D. Fish associations—Habitats quakity relation in the Târnave rivers (Transylvania, Romania) ecological assessment. Transylv. Rev. Syst. Ecol. Res. 2005, 2, 123–136. [Google Scholar]
  318. Nelson Joseph, S. Fishes of the World; John and Wiley & Sons: Hoboken, NJ, USA, 2016; ISBN 978-1-118-34233-6. [Google Scholar]
  319. Afanasyev, S.; Hupalo, O.; Tymoshenko, N.; Lietytska, O.; Roman, A.; Manturova, O.; Bănăduc, D. Morphological and trophic features of the invasive Babka gymnotrachelus (Gobiidae) in the plain and mountainous ecosystems of the Dniester Basin, spatiotemporal expansion and possible threats to native fishes. Fishes 2023, 8, 427. [Google Scholar] [CrossRef]
  320. Shahraki, M.Z.; Keivany, Y.; Dorche, E.E.; Blocksom, K.; Bruder, A.; Flotemersch, J.; Bănăduc, D. Distribution and expansion of alien fish species in the Karun River basin, Iran. Fishes 2023, 8, 538. [Google Scholar] [CrossRef] [PubMed]
  321. Bănăduc, D.; Bakhshalizadeh, S.; Curtean-Bănăduc, A. Natura 2000 a Panacea? Natura 2000 Site Oltul Mijlociu-Cibin-Hârtibaciu (ROSCI132)—A local extinction of a native fish species and a new alien fish arrival case study. Transylv. Rev. Syst. Ecol. Res. 2023, 25, 81–100. [Google Scholar]
  322. Zubcov, N.; Zubcov, E.; Schlenk, D. The dynamics of metals in fish from Nistru and Prut rivers (Moldova). Transylv. Rev. Syst. Ecol. Res. 2008, 6, 51–58. [Google Scholar]
  323. Bhat, I.A.; Bhat, R.A.H.; Yousuf, D.J. Fish Toxicology; Narendra Publishing House: Delhi, India, 2021. [Google Scholar]
  324. Öktener, A.; Bănăduc, D. Ecological Interdependence of Pollution, Fish Parasites, and Fish in Freshwater Ecosystems of Turkey. Water 2023, 15, 1385. [Google Scholar] [CrossRef]
  325. Willet, K.L. Toxicology of Fishes, 2nd ed.; CRC Press: Boca Raton, FL, USA, 2024; pp. 1–465. [Google Scholar]
  326. Curtean-Bănăduc, A.; Burcea, A.; Mihuț, C.; Bănăduc, D. The Benthic Trophic Corner Stone Compartment in POPs Transfer from Abiotic Environment to Higher Trophic Levele—Trichoptera and Ephemeroptera Pre-Alert Indicator Role. Water 2021, 13, 1778. [Google Scholar] [CrossRef]
  327. Curtean-Bănăduc, A.; Olosutean, H.; Bănăduc, D. Influence of Environmental Variables on the Structure and Diversity of Ephemeropteran Communities: A Case Study of the Timiș River, Romania. Acta Zool. Bul. 2016, 68, 215–224. [Google Scholar]
  328. Dórea, J.G. Persistent, bioaccumulative and toxic substances in fish: Human health considerations. Sci. Total Environ. 2008, 400, 93–114. [Google Scholar] [CrossRef] [PubMed]
  329. Curtean-Bănăduc, A.; Mihuț, C.; Burcea, A.; McCall, G.S.; Matei, C.; Bănăduc, D. Screening for Microplastic Uptake in an Urbanized Freshwater Ecosystem: Chondrostoma nasus (Linnaeus, 1758) Case Study. Water 2023, 15, 1578. [Google Scholar] [CrossRef]
  330. Ormerod, S.J. Current issues with fish and fisheries: Editor overview and introduction. J. Appl. Ecol. 2003, 40, 204–213. [Google Scholar] [CrossRef]
  331. Santhi, C.; Arnold, J.G.; Williams, J.R.; Hauck, L.M.; Dugas, W.A. Application of a watershed model to evaluate management effects on point and nonpoint source pollution. Trans. ASAE 2001, 44, 1559–1570. [Google Scholar] [CrossRef]
  332. Yuan, L.; Sinshaw, T.; Forshay, K.J. Review of watershed-scale water quality and nonpoint source pollution models. Geosciences 2020, 10, 25. [Google Scholar] [CrossRef]
  333. Akdogan, Z.; Guven, B. Multi-criteria decision analysis in assessing watershed scale pollution risk: A review of combined approaches and applications. Environ. Rev. 2023, 31, 669–689. [Google Scholar] [CrossRef]
  334. Britton, J.R.; Gozlan, R.E.; Coop, G.H. Managing non-native fish in the environment. Fish Fish. 2011, 12, 256–274. [Google Scholar] [CrossRef]
  335. Lodge, D.M.; Stein, R.A.; Brown, K.M.; Covich, A.P.; Bronmark, C.; Garvey, J.E.; Klosiewski, S.P. Predicting impact of freshwater exotic species on native biodiversity: Challenges in spatial scaling. Aust. J. Ecol. 1998, 23, 53–67. [Google Scholar] [CrossRef]
  336. Stram, W.; Rietbergen, S. Alien invasions from our own planet. IUCN Eur. Programme Newsl. 2001, 27, 3. [Google Scholar]
  337. Anastasiu, P.; Preda, C.; Bănăduc, D.; Cogălniceanu, D. Alien species of European Union concern in Romania. Transylv. Rev. Syst. Ecol. Res. 2017, 19, 93–106. [Google Scholar]
  338. Mark, C. Andersen, Heather Adams, Bruce Hope, Mark Powell, Risk Assessment for Invasive Species. Risk Anal. 2004, 24, 787–793. [Google Scholar]
  339. Radenković, M.; Milošković, A.; Stojković Piperac, M.; Veličković, T.; Curtean-Bănăduc, A.; Bănăduc, D.; Simić, V. Feeding patterns of fish in relation to the trophic status of reservoirs: A case study of Rutilus rutilus (Linnaeus, 1758) in five fishing waters in Serbia. Fishes 2024, 9, 21. [Google Scholar] [CrossRef]
Figure 1. The four interrelated main clusters of freshwater and their stressors and co-occurrence of key terms—network visualization based on 2083 scientific papers published in Web of Science Core Collection. Blue: Articles related to the climate change impact on continental aquatic ecosystems. Green: Articles that analyze methodologies used for water bodies’ quality and microplastic impact. Red: Articles that analyze the impact of chemical pollution. Yellow: Articles that analyze the impact of stressors on aquatic biodiversity.
Figure 1. The four interrelated main clusters of freshwater and their stressors and co-occurrence of key terms—network visualization based on 2083 scientific papers published in Web of Science Core Collection. Blue: Articles related to the climate change impact on continental aquatic ecosystems. Green: Articles that analyze methodologies used for water bodies’ quality and microplastic impact. Red: Articles that analyze the impact of chemical pollution. Yellow: Articles that analyze the impact of stressors on aquatic biodiversity.
Water 16 01483 g001
Figure 2. Co-occurrence of targeted key issues—temporal overlay visualization.
Figure 2. Co-occurrence of targeted key issues—temporal overlay visualization.
Water 16 01483 g002
Figure 3. Distribution of articles (56) and citations based on the year of publication (1995–2024)—ultraviolet radiation (worldwide).
Figure 3. Distribution of articles (56) and citations based on the year of publication (1995–2024)—ultraviolet radiation (worldwide).
Water 16 01483 g003
Figure 4. Distribution of articles (18) and citations based on the year of publication (1995–2024)—ultraviolet radiation (Europe).
Figure 4. Distribution of articles (18) and citations based on the year of publication (1995–2024)—ultraviolet radiation (Europe).
Water 16 01483 g004
Figure 5. Distribution of articles (8) and citations based on the year of publication (2002–2024)—thermal pollution (globally).
Figure 5. Distribution of articles (8) and citations based on the year of publication (2002–2024)—thermal pollution (globally).
Water 16 01483 g005
Figure 6. Distribution of articles (351) and citations based on the year of publication (2008–2024)—nanoparticles (worldwide).
Figure 6. Distribution of articles (351) and citations based on the year of publication (2008–2024)—nanoparticles (worldwide).
Water 16 01483 g006
Figure 7. Distribution of articles (148) and citations based on the year of publication (2008–2024)—nanoparticles (Europe).
Figure 7. Distribution of articles (148) and citations based on the year of publication (2008–2024)—nanoparticles (Europe).
Water 16 01483 g007
Figure 8. Distribution of articles (34) and citations based on the year of publication (1976–2024)—radioactive pollution (worldwide).
Figure 8. Distribution of articles (34) and citations based on the year of publication (1976–2024)—radioactive pollution (worldwide).
Water 16 01483 g008
Figure 9. Distribution of articles (19) and citations based on the year of publication (1996–2024)—radioactive pollution (Europe).
Figure 9. Distribution of articles (19) and citations based on the year of publication (1996–2024)—radioactive pollution (Europe).
Water 16 01483 g009
Figure 10. Distribution of articles (1175) and citations based on the year of publication (1975–2024)—salinization (worldwide).
Figure 10. Distribution of articles (1175) and citations based on the year of publication (1975–2024)—salinization (worldwide).
Water 16 01483 g010
Figure 11. Distribution of articles (374) and citations based on the year of publication (1976–2024)—salinization (Europe).
Figure 11. Distribution of articles (374) and citations based on the year of publication (1976–2024)—salinization (Europe).
Water 16 01483 g011
Figure 12. Distribution of articles (16) and citations based on the year of publication (2009–2024)—nutrients (worldwide).
Figure 12. Distribution of articles (16) and citations based on the year of publication (2009–2024)—nutrients (worldwide).
Water 16 01483 g012
Figure 13. Distribution of articles (8) and citations based on the year of publication (2019–2024)—nutrients (Europe).
Figure 13. Distribution of articles (8) and citations based on the year of publication (2019–2024)—nutrients (Europe).
Water 16 01483 g013
Figure 14. Distribution of articles (987) and citations based on the year of publication (1976–2024)—sediments (global).
Figure 14. Distribution of articles (987) and citations based on the year of publication (1976–2024)—sediments (global).
Water 16 01483 g014
Figure 15. Distribution of articles (491) and citations based on the year of publication (1976–2024)—sediments (Europe).
Figure 15. Distribution of articles (491) and citations based on the year of publication (1976–2024)—sediments (Europe).
Water 16 01483 g015
Figure 16. Distribution of articles (185) and citations based on the year of publication (1996–2024)—drought (global).
Figure 16. Distribution of articles (185) and citations based on the year of publication (1996–2024)—drought (global).
Water 16 01483 g016
Figure 17. Distribution of articles (43) and citations based on the year of publication (1996–2024)—drought (Europe).
Figure 17. Distribution of articles (43) and citations based on the year of publication (1996–2024)—drought (Europe).
Water 16 01483 g017
Figure 18. Distribution of articles (134) and citations based on the year of publication (1975–2024)—floods (worldwide).
Figure 18. Distribution of articles (134) and citations based on the year of publication (1975–2024)—floods (worldwide).
Water 16 01483 g018
Figure 19. Distribution of articles (39) and citations based on the year of publication (1996–2024)—floods (Europe).
Figure 19. Distribution of articles (39) and citations based on the year of publication (1996–2024)—floods (Europe).
Water 16 01483 g019
Figure 20. Distribution of articles (61) and citations based on the year of publication (2000–2024)—habitat fragmentation (worldwide).
Figure 20. Distribution of articles (61) and citations based on the year of publication (2000–2024)—habitat fragmentation (worldwide).
Water 16 01483 g020
Figure 21. Distribution of articles (25) and citations based on the year of publication (1997–2024)—habitat fragmentation (Europe).
Figure 21. Distribution of articles (25) and citations based on the year of publication (1997–2024)—habitat fragmentation (Europe).
Water 16 01483 g021
Figure 22. Distribution of articles (257) and citations based on the year of publication (1976–2024)—pesticides (worldwide).
Figure 22. Distribution of articles (257) and citations based on the year of publication (1976–2024)—pesticides (worldwide).
Water 16 01483 g022
Figure 23. Distribution of articles (117) and citations based on the year of publication (1977–2024)—pesticides (Europe).
Figure 23. Distribution of articles (117) and citations based on the year of publication (1977–2024)—pesticides (Europe).
Water 16 01483 g023
Figure 24. Distribution of articles (4) and citations based on the year of publication (2016–2024)—war and terrorism (worldwide).
Figure 24. Distribution of articles (4) and citations based on the year of publication (2016–2024)—war and terrorism (worldwide).
Water 16 01483 g024
Figure 25. Distribution of articles (192) and citations based on the year of publication (1976–2024)—algal blooms (worldwide).
Figure 25. Distribution of articles (192) and citations based on the year of publication (1976–2024)—algal blooms (worldwide).
Water 16 01483 g025
Figure 26. Distribution of articles (35) and citations based on the year of publication (1976–2024)—algal blooms (Europe).
Figure 26. Distribution of articles (35) and citations based on the year of publication (1976–2024)—algal blooms (Europe).
Water 16 01483 g026
Figure 27. Distribution of articles (164) and citations based on the year of publication (2000–2024)—invasive aquatic plants (worldwide).
Figure 27. Distribution of articles (164) and citations based on the year of publication (2000–2024)—invasive aquatic plants (worldwide).
Water 16 01483 g027
Figure 28. Distribution of articles (59) and citations based on the year of publication (2004–2024)—invasive aquatic plants (Europe).
Figure 28. Distribution of articles (59) and citations based on the year of publication (2004–2024)—invasive aquatic plants (Europe).
Water 16 01483 g028
Figure 29. Distribution of articles (42) and citations based on the year of publication (1981–2024)—riverine vegetation (worldwide).
Figure 29. Distribution of articles (42) and citations based on the year of publication (1981–2024)—riverine vegetation (worldwide).
Water 16 01483 g029
Figure 30. Distribution of articles (19) and citations based on the year of publication (2024–2024)—riverine vegetation (Europe).
Figure 30. Distribution of articles (19) and citations based on the year of publication (2024–2024)—riverine vegetation (Europe).
Water 16 01483 g030
Figure 31. Distribution of articles (179) and citations based on the year of publication (1997–2024)—invasive fish (worldwide).
Figure 31. Distribution of articles (179) and citations based on the year of publication (1997–2024)—invasive fish (worldwide).
Water 16 01483 g031
Figure 32. Distribution of articles (85) and citations based on the year of publication (1997–2024)—invasive fish (Europe).
Figure 32. Distribution of articles (85) and citations based on the year of publication (1997–2024)—invasive fish (Europe).
Water 16 01483 g032
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Bănăduc, D.; Curtean-Bănăduc, A.; Barinova, S.; Lozano, V.L.; Afanasyev, S.; Leite, T.; Branco, P.; Gomez Isaza, D.F.; Geist, J.; Tegos, A.; et al. Multi-Interacting Natural and Anthropogenic Stressors on Freshwater Ecosystems: Their Current Status and Future Prospects for 21st Century. Water 2024, 16, 1483. https://doi.org/10.3390/w16111483

AMA Style

Bănăduc D, Curtean-Bănăduc A, Barinova S, Lozano VL, Afanasyev S, Leite T, Branco P, Gomez Isaza DF, Geist J, Tegos A, et al. Multi-Interacting Natural and Anthropogenic Stressors on Freshwater Ecosystems: Their Current Status and Future Prospects for 21st Century. Water. 2024; 16(11):1483. https://doi.org/10.3390/w16111483

Chicago/Turabian Style

Bănăduc, Doru, Angela Curtean-Bănăduc, Sophia Barinova, Verónica L. Lozano, Sergey Afanasyev, Tamara Leite, Paulo Branco, Daniel F. Gomez Isaza, Juergen Geist, Aristoteles Tegos, and et al. 2024. "Multi-Interacting Natural and Anthropogenic Stressors on Freshwater Ecosystems: Their Current Status and Future Prospects for 21st Century" Water 16, no. 11: 1483. https://doi.org/10.3390/w16111483

APA Style

Bănăduc, D., Curtean-Bănăduc, A., Barinova, S., Lozano, V. L., Afanasyev, S., Leite, T., Branco, P., Gomez Isaza, D. F., Geist, J., Tegos, A., Simić, S. B., Olosutean, H., & Cianfanglione, K. (2024). Multi-Interacting Natural and Anthropogenic Stressors on Freshwater Ecosystems: Their Current Status and Future Prospects for 21st Century. Water, 16(11), 1483. https://doi.org/10.3390/w16111483

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop