Next Article in Journal
Monitoring and Genotyping of Wild Grapevine (Vitis vinifera L. subsp. sylvestris) in Slovenia
Next Article in Special Issue
Linking Seed Traits and Germination Responses in Caribbean Seasonally Dry Tropical Forest Species
Previous Article in Journal
Overexpression of Larch SCL6 Inhibits Transitions from Vegetative Meristem to Inflorescence and Flower Meristem in Arabidopsis thaliana (L.) Heynh.
Previous Article in Special Issue
The Evolution of Agrarian Landscapes in the Tropical Andes
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Sustainable Development versus Extractivist Deforestation in Tropical, Subtropical, and Boreal Forest Ecosystems: Repercussions and Controversies about the Mother Tree and the Mycorrhizal Network Hypothesis

by
Tomas Gabriel Bas
1,*,
Mario Luis Sáez
2 and
Nicolas Sáez
1
1
Escuela de Ciencias Empresariales, Universidad Católica del Norte, Coquimbo 1780000, Chile
2
Facultad de Humanidades, La Serena University, Coquimbo 1700000, Chile
*
Author to whom correspondence should be addressed.
Plants 2024, 13(9), 1231; https://doi.org/10.3390/plants13091231
Submission received: 6 February 2024 / Revised: 23 April 2024 / Accepted: 28 April 2024 / Published: 29 April 2024
(This article belongs to the Special Issue New Perspectives on New World Tropical Forests)

Abstract

:
This research reviews the phenomenon of extractive deforestation as a possible trigger for cascade reactions that could affect part of the forest ecosystem and its biodiversity (surface, aerial, and underground) in tropical, subtropical, and boreal forests. The controversy and disparities in criteria generated in the international scientific community around the hypothesis of a possible link between “mother trees” and mycorrhizal networks in coopetition for nutrients, nitrogen, and carbon are analyzed. The objective is to promote awareness to generate more scientific knowledge about the eventual impacts of forest extraction. Public policies are emphasized as crucial mediators for balanced sustainable development. Currently, the effects of extractive deforestation on forest ecosystems are poorly understood, which requires caution and forest protection. Continued research to increase our knowledge in molecular biology is advocated to understand the adaptation of biological organisms to the new conditions of the ecosystem both in the face of extractive deforestation and reforestation. The environmental impacts of extractive deforestation, such as the loss of biodiversity, soil degradation, altered water cycles, and the contribution of climate change, remain largely unknown. Long-term and high-quality research is essential to ensure forest sustainability and the preservation of biodiversity for future generations.

1. Introduction

Tropical, subtropical, and boreal forests are critical components of the different ecosystems of the Earth, supporting an astonishing variety of species and facilitating the transition to an essential ecological balance [1,2]. Forests sequester approximately 30% of Earth’s carbon [3]. It is often considered a net carbon sink to neutralize atmospheric CO2 along with phytoplankton in the oceans [4]. However, tropical, subtropical, and boreal forests face numerous problems, mainly related to the extractive culture generated in many cases by mining, oil, real estate, and forestry industry consortiums that usually cause massive and often indiscriminate deforestation [5]. Natural resources are an essential pillar for the development and survival of humanity, as they provide the raw materials and energy necessary for its development, so the key is to find a balance between the exploitation of natural resources and socio-economic growth accompanied by sustainable development [6]. The instability caused by deforestation could have a global impact on the weakening of forest biodiversity and the surrounding environment that comprises aerial, surface, and underground ecosystems [7]. Below the ground, there is a geological stratum that extends from the surface of the earth to the water counter of the first free aquifer, known as the ‘vadose zone’, and has key functions within the biosphere [8]. It would serve as a hydrological reservoir, facilitating the supply of water to plants and the atmosphere, simplifying the exchange of nutrients, and facilitating the survival of the ecosystem [9,10].
Suzanne Simard’s research explores a hypothesis that attempts to explain the possible negative effects of intensive deforestation by extracting what they call “mother trees”, referring to groups of older trees that play a protective role over the rest of the trees in their environment [11]. According to her hypothesis, the roots of these trees would be able to collaborate in the exchange of nutrients by forming an intricate communicational network with mycorrhizal fungi sharing some nutrients, particularly carbon and nitrogen [12,13,14,15,16,17,18,19]. Therefore, according to Simard, the roots of older trees would constitute a network with the fungal community located on their roots that would allow plants to exchange some essential nutrients for their survival and growth, and, in turn, the fungi would help the host plants maximize the transfer of some fundamental nutrients [11,17,18,20,21,22,23,24,25]. Their research suggests that the removal of these “mother trees” could break this protective balance between roots and mycorrhizal fungi, affecting the rest of the forest ecosystem, particularly the younger trees. However, the results of this research are not unanimous in the international scientific community and opinions are divided. Some researchers do not adhere to this hypothesis, arguing that such a dependence between fungi and tree roots as suggested by Simard [26] has not been fully demonstrated. Other research argues that mycorrhizal fungi are not extensions of roots but rather organisms that might establish different strategies than host trees. There may even be eco-physiological differences between the different types of mycorrhizae, which may indicate strategies and functions that are unique to them [27].
It is important to note that mycorrhizal fungi are divided into two categories: ectomycorrhizae and endomycorrhizae, which include arbuscular mycorrhizae. These fungi establish symbiotic relationships with more than 80% of terrestrial plant roots, providing them with nutrients synthesized from the soil with which they form interaction networks between two or more plants linked by a fungal symbiont, which are called common mycorrhizal networks or even the “wood-wide-web” [28,29,30,31,32]. These networks may even facilitate interactions between plants, including the transmission of aphid-induced diseases and signals and the activation of chemical defenses in neighboring plants [33]. More recently, molecular research on the identification and gene functions of arbuscular mycorrhizal fungi is being carried out, which will improve our understanding of soil/plant interaction mechanisms in different forests [33,34,35].
In this amalgam of interconnections, competencies, and interrelationships of the forest ecosystem, we propose the notion of ‘coopetition’, originating from the world of management but adaptable to the ‘web of forests’. Coopetition as a theoretical concept originates from inter-institutional cooperation, both bilateral and multilateral [36,37]. In this dynamic, the same authors define coopetition as simultaneous cooperation and competition between two or more competitors. Coopetition belongs to the highest-cost interorganizational relationships, and this results from the contradiction of logic that coopetition is based on trust and conflict at the same time [38]. If we transfer this to nature, the concept of coopetition applied to the forest refers to the fact that trees are capable of competing and cooperating at the same time within an ecosystem for certain resources. The ecosystem could be defined as any element or variable that is associated with another in a system and dependent, and consequently, the relationship between the components preserves the overall survival of the ecosystem [39,40,41]. Based on this logic, it can be said that, in general, an ecosystem is dynamic, which means that the ecosystem constantly incorporates new elements or variables with continuous feedback, allowing for increasing the predominant biodiversity in a given space [42].
Another concept directly related to interrelationships in forests is resilience and its different variants. This research refers to how anthropogenic changes can affect forest disturbance patterns, potentially reducing their capacity to provide ecosystem services [43,44]. This alteration can also influence the distribution and adaptation of forest-dependent species due to abrupt habitat changes [45]. Combined disturbances can change forest trajectories, and an increased frequency of disturbances can weaken forest resilience [46,47]. In close relation to resilience, some studies estimate that tropical forest ecosystems, for example, are capable of actively configuring their environmental parameters, through feedback mechanisms that operate on various spatial scales [48,49]. The same author values these mechanisms as crucial to understanding what is known as hysteresis, which is a form of stability forged from dependence on a previous historical state; hence, its proximity to resilience and a certain capacity that some ecosystems could have to resist change despite the loss of their trees due to extractive deforestation, managing in some cases to recover and likely even adapt to potential climate changes [47]. It is interesting to see how, through resilience, some forests can adapt to disturbances, whether anthropogenic or even natural and in many cases conserve their essential structures and functions [16]. However, it is important to note that some studies show that while tropical forests could recover in the medium term from potential extractive deforestation, in the long term, they would also lose their resilience [48].
It is imperative to note that healthy forests contribute to climate regulation, carbon sequestration, and the water cycle, among other aspects of the ecosystem, making them vital to the well-being of the planet [2,18]. As the human influence on the Earth expands, native forests suffer a highly significant impact, which is reflected in their gradual decline [50,51,52]. Preserving and restoring the integrity of different types of native forests is essential to strategically address the biodiversity crisis, try to curb climate change, and promote medium and long-term sustainability [53]. The preservation of forest integrity must be fundamental to global and local environmental strategies, complementing current efforts against deforestation and, in contrast, in favor of reforestation [54]. Conservation efforts should consider the complex relationships within forests themselves, emphasizing the importance of ecosystems and their impact when forests are completely cleared or when fires (intentional or otherwise) destroy life in their path [55,56].
In many developing countries, public policies aimed at protecting natural resources are generally poor, the institutional framework does not function adequately, and governance is often dominated by high levels of corruption [57,58]. In such an environment, it is very complex to generate regulations that limit the overexploitation of forests generated by the extractive practices of large companies, many of them foreign, which take advantage of the laxity of institutions and governance, circumventing existing regulations. This generates unprecedented overexploitation of native forests (tropical, subtropical, and boreal) and the loss of tree cover and, therefore, the death in some cases of all the biodiversity generated by woodland [59,60,61]. This phenomenon of overexploitation is defined as extractivism, and its conceptual framework covers a wide spectrum of research domains related to the impact on natural capital [62,63,64]. This practice encompasses an intricate interaction of activities framed by power asymmetries and, in many cases, institutional weakness. Corruption is a strong element and often plays a leading role in decisions made concerning the exploitation of natural resources with socio-economic and socioecological impacts. In many of these cases, the beneficiaries tend to be few, to the detriment of populations with fewer resources that inhabit the exploited areas [65,66]. The increase in the monetary values of raw materials during the transition of the last millennium generated an increase in the extractivist phenomenon in Latin America (rich in minerals, oil, aquatic resources, forests, and agriculture), fundamentally affecting the tropical and subtropical woodland of this geographic forest region [49,67]. This voracity occurred regardless of the economic ideology adopted by the respective national administrations, be it ‘neoliberal’, ‘post-neoliberal’, or ‘neosocialist’ [68]. In this context, the term extractivism is elucidated as the extraction and excessive and abusive use of any natural resource, regardless of the strategies and actions used [69]. Therefore, it is essential to implement public policies that limit this extreme practice and prevent it from being a generic term used exclusively for mining, gas, and oil [70]. This would prevent the looting and irreparable damage caused by extractivism to native tropical, subtropical, and boreal forests, which simultaneously affects all the biological organisms and the minerals that depend on them.
In light of the documentary exploration analyzed, the following research questions arise.
-
Is it possible to address the controversies surrounding the ‘mother tree’ hypothesis, along with the lack of conclusive research results from its detractors, and reach a consensus on sustainable forest development?
-
Could genetic engineering techniques provide a deeper understanding of the intricate relationships between ‘mother trees’, mycorrhizal fungi, and younger trees within forest ecosystems?
-
How can we address the controversies surrounding cascading phenomena and the resilience of forest ecosystems while evaluating the effectiveness of public policies to mitigate extractive deforestation and promote sustainable forest management practices?
In this context, two objectives are visualized.
-
Stimulate greater commitment within the international scientific community to investigate the potential impacts of extractive deforestation based on the lack of knowledge of many of the reactions triggered by altering the ecosystem and its biodiversity.
-
Examine the phenomena of coopetition, cascade, and resilience within forest ecosystems, to encourage the generation of public policies that mitigate the potential effects of extractive deforestation and promote sustainable forest management practices.
For the analysis of objectives, a methodology was implemented with a qualitative bibliographic documentary approach [71]. This approach involves a single search phase. The main effort involves a systematic literature review, conducted with meticulous care to compile a comprehensive collection of research that can effectively address the research question and stated objective. The review analyzed Suzanne Simard’s major research topics, including the influence of mother trees on intercommunication, coopetition, the symbiotic function of mycorrhizal fungi, and the resulting impacts on natural capital and surrounding biodiversity. Similarly, a bibliographic search was conducted for the years preceding Simard’s study period to better understand the antecedents that led to the theory of mother trees and the interaction of mycorrhizae (ecto- and endomycorrhizae). Additionally, a bibliographic search was completed for mycorrhizal strains by forest geographic region, as well as the latest studies in molecular research, genetic engineering, and biotechnology that included them. The study examined deforestation, with a particular focus on extractive practices that cause significant forest degradation and loss of biodiversity. Finally, a third aspect concerns the analysis of the significance of public policies, which are often inadequate in developing countries due to poor institutional quality. These countries are home to boreal, tropical, and subtropical forests, and suffer from inefficient governance, often contaminated by corruption that allows corporations to exploit forests and other resources in an inefficient way.
To enhance the search’s effectiveness, we selected appropriate documentary sources, bibliographic databases, and search engines based on the field or subject area. These included Science Direct, Agricola, Compendex, Derwent, Statistics Canada, Scopus, Web of Science Core Collections, Google Scholar, Innovation Index, and GeoIndex. To expand the exploration of search systems, we selected several research tools based on Gusenbauer and Haddaway’s [72] widely used and interdisciplinary approach. The following academic databases were searched: AMiner, ACM, arXiv, BASE (Bielefeld Academic Search Engine), CiteSeerX, DBLP (Digital Bibliography & Library Project), DOAJ (Directory of Open Access Journals), IEEE Xplore Digital Library, JSTOR, Microsoft Academic, Semantic Scholar, SpringerLink, Wiley Online Library, WorldCat, and WorldWideScience.
Syntax analysis was performed to determine the logical structure of high-level concepts in a query. Concepts are automatically extracted and assigned to entities for entity expansion. Data post-processing operations, such as search and derivation filters, are then applied to these entities [73,74]. The selections were combined to avoid any potential data duplication. The literature search was conducted based on the selection criteria, utilizing Boolean relationships between keywords through logical operators such as AND and OR. The approach for the automatic formulation of queries, specific to Boolean queries, is similar to the processes used by information specialists, but without the use of specialized software. The search was structured methodically, taking into account the level of sensitivity (retrieval rate) and specificity (precision rate). The research approach was determined by defining the research question and objective, which allowed focused information retrieval [75]. The framework consists of five steps: query logic composition (1), entity extraction (2), entity expansion (3), keyword mapping (4), and post-processing (5) [73]. According to some authors, a concise representation of the required information, either as a single word or a short phrase (e.g., ‘exploitative extractivist practices’), is necessary for the literature search strategy [75]. To broaden the scope of the investigation, certain concepts were split. For example, the term ‘extractivist practices’ was split into ‘extractivist’ and ‘practices’ based on semantic cues such as Word/cloud and Word/frequency’ [76]. Each word or phrase within a concept or semantic key serves as a synonym or closely related term. Relevant connections are crossed as necessary to obtain totals and frequencies. Boolean operators and parentheses were used to achieve the desired result, along with precise expressions and appropriate field codes. The text has been edited to ensure grammatical correctness and adherence to the desired characteristics.
A systematic literature review was conducted using Natural Language Processing (NLP) through ‘Vectara,’ a free application for data analysis.
The exploration covered the time period from 2015 to 2023 and involved defining and searching for keywords in the aforementioned databases. The time period of 2015–2023 was chosen to cover recent research on the topic, with preceding years added to include earlier studies that contributed to the development of Suzanne Simard’s hypothesis. The frequency of defined keywords in the titles and abstracts of the raw selection was calculated, with a minimum of three occurrences per abstract required. The compound keywords used were as follows: “Mother trees”, also known as “Guardians of ecosystem resilience”, are a key component in the “Suzanne Simard hypothesis” of symbiotic relationships between fungi and plants. These relationships involve the exchange of carbohydrates and water and are crucial for the underground networks of biodiversity and mycorrhizae, including arbuscular mycorrhizae, endomycorrhizae, and ectomycorrhizae. Deforestation, extraction, and biodiversity loss have a significant impact on these networks. It is important to understand and protect these relationships for the health of our ecosystems. The following topics are covered in this text: Mycorrhizae and genetic engineering, biotechnology and mycorrhizae, molecular research on mycorrhizae, rhizome and nitrogen collection, coopetition in the forest, dynamic ecosystem and biodiversity, forest resilience, resilience and disturbance, healthy forests, and overexploitation and resource depletion. The text provided appears to be a list of keywords or phrases related to forest biological diversity, including different types of forests, natural capital, deforestation, and nutrient exchange. The language used is generally clear and objective, but there are a few instances where the meaning could be made more precise through the use of subject-specific vocabulary. The text is grammatically correct and follows a logical structure, but it is not clear what the purpose of the list is or how the different keywords are related to each other. Therefore, no changes have been made to the text, but it would be helpful to have more context or information on how this list will be used or what it is intended to convey. The text discusses various topics related to extractivism, including the alteration of cascading nutrient exchange, vadose zone and water sequences, the modification of water cycles, cascading ecological effects, the importance of public policies, the regulation of the extractivist framework, institutions and governance, extractivism versus sustainability, regulation of extractivist phenomena, and corruption. During the initial phase, a comprehensive repository of 1472 documents was compiled, including research articles from journals indexed in Clarivate and Scopus, reviews, books, book chapters, and conference proceedings. It is important to note that this sample of 1472 documents is representative of the information analyzed but does not encompass all existing documents in the databases consulted.
-
A meticulous manual selection process was used to refine the collected resources, eliminating duplicates and irrelevant entries. Only one instance of identical documents found in different databases was retained. This process resulted in a final collection of 370 documents.
-
Selection based on title and keywords: The retained documents were subjected to a new phase of scrutiny. Their titles and keywords were subjected to a meticulous evaluation guided by an inclusive question: “Does the research contribute to reflect on the close relationship between the forest ecosystem based on Suzanne Simard’s hypothesis, mother trees, mycorrhizae, coopetition, and the unsustainable impact of the extractivist phenomenon on forests, the inability of public policies, institutionalism, and governance to safeguard the fragile balance of biodiversity?”
-
Evaluation through summaries: In this phase, the summaries of the remaining papers were reviewed against the same evaluative question as in the previous step.
-
Reading the full text and determining relevance: the full texts of the selected papers were diligently obtained and thoroughly studied. The evaluation question of the third step was reviewed to assess the alignment with the research objectives.
  • During the comprehensive content analysis of the full text, we identified two fundamental areas influenced by the central research thrusts: the positive impact of mother trees on the larger interconnected forest ecosystem and the negative consequences of extractivism caused by indiscriminate deforestation. Keywords included “Deforestation”; “Extractivist practice”; “Biodiversity”; “Resilience”; “Suzanne Simard”; “Mother trees”; “Mycorrhizal networks”; “Mycorrhizal molecular research”; “Sustainable development”; “Importance of public policies”; “Institutions”; “Governance”; “Regulation of extractivism phenomena”; and “Corruption”. The formulation of queries for systematic literature review searches can be automated without the need for computer specialists or specialized software, as demonstrated by the use of Vectara. This method can lead to efficient searches and provide an overview of the types of studies recovered [72,73].
  • Table 1 shows the frequency of each keyword reflected in the different databases used, with a total of 1472 occurrences.
  • A high frequency indicates that the topic is widely discussed or emphasized in the literature. This indicates that a particular topic is of interest, concern, or research within the field. For instance, if the phrase “Impact of deforestation, extraction, and biodiversity” appears frequently, it implies that these issues are central concerns in the analyzed documents.
  • A moderate count suggests that the topic is relevant, but not as dominant within the literature. It may be more specialized or focused on specific aspects of the broader field.
  • A low frequency indicates that the topic is not a major focus within the literature. A low count may indicate that the topic is niche, emerging, or is not extensively covered in the literature. It could also suggest areas where further research is needed or topics that are less prioritized within the current scope of discussions.

2. Theoretical Framework

This research seeks to reflect and raise awareness about the potential impact that extractive deforestation could have on biodiversity and the interaction of tropical, subtropical, and boreal forest ecosystems and about more sustainable development. The rationale revolves around the conceptual and empirical controversy on the hypothesis proposed by Suzanne Simard’s research on mother trees and their possible influence on both the forest environment and mycorrhizal networks. The analysis is not limited only to the hypothesis developed by Simard but also contains some research contributions that oppose this hypothesis, thus allowing research with different points of view. However, the contribution of this study is broader as a whole, strengthening socioeconomic needs and interests, complementing the actions and responsibility to generate public policies and institutions that support the preservation of the tree resource and the rich and unique natural capital in the biodiversity of each geographic forest region considered for future generations. This is fundamental due to the lack of conclusive data for both positions.

2.1. Tropical, Subtropical, and Boreal Forests and Importance for Biodiversity

Native tropical, subtropical, and boreal forests are all critical to the ecological balance of the planet as they have unique and specific characteristics in terms of biodiversity, ecology, and carbon sequestration [1,77,78,79,80,81]. These differences underscore the complexity of forest ecosystems based on some attributes such as diversity, abundance, transition, resistance, and adaptation [82,83,84,85,86].
Tropical forests are located in an area where they average high temperatures and abundant annual rainfall, soil with very poor nutrient availability, and very high levels of biodiversity and growing seasons that generally extend throughout the year [87]. The tropical forest ecosystem plays a vital role in regulating the global climate and is essential in the water and carbon cycle [88,89]. These forests are geographically close to the equator in regions such as the Amazon rainforest in South America and the Congo rainforest in Africa, which belong to some of the most biodiverse ecosystems on Earth and host more than half of all living species on the planet [90,91,92,93,94]. Some of the plants that grow there could have potential medicinal properties, including some that have not yet been discovered [95,96,97].
However, subtropical forests are located at lower latitudes than tropical forests and serve as transition zones between tropical and temperate climates [98]. These forests exhibit a more marked seasonality compared to the previous ones, with very well-defined wet and dry seasons [99,100,101]. Subtropical forests’ biodiversity is rich and varied, although not as extensive as tropical forests, and they are ecosystems that host a mixture of tropical and temperate species, giving them unique diversity [58,102]. These forests are crucial for buffering the impacts of climate change and improving the stability of ecosystem productivity over time [103,104].
The dominant ectomycorrhizal fungi in most subtropical forests generally have a low host specificity, although there is an exception to this pattern, which is the symbiosis with the genus Alnus [105]. It has been shown that the composition of some communities of these ectomycorrhizal fungi associated with trees of the Alnus rhombifolia species, in subtropical forests, are capable of generating defense against soils with high levels of heavy metals that are highly toxic to trees and their biodiversity [105,106,107]. This symbiotic effect can be attributed to alterations in soil conditions due to leaf litter and root exudates, which in turn play a crucial role in soil protection and carbon storage [108]. Subtropical forests, especially in southern and eastern China, are recognized for their wide diversity of root-associated plants and fungi, which contribute significantly to global ecosystem services such as carbon cycling and primary production [109,110].
Finally, we find boreal forests, also known as taiga forests, which stand out for their resistance and ability to adapt to challenging and extreme environments with a combination of long and very cold winters, with very short growing summers [111,112,113]. The boundary of the circumpolar biome at the interface of boreal forest (taiga) and tundra is a very important ecological transition zone for the planet [114]. They are characterized by a large extension of conifers, preferably of needle-like and broad-leaved deciduous types, capable of supporting cold climates and growing in short seasons. Evergreen coniferous boreal forests have a remarkable ability to acclimate to extremely cold temperatures, which is crucial for their survival in polar regions [115]. However, the same authors suggest that this forest type (mostly composed of conifers) is highly vulnerable to climate change, but further research is needed to understand and somehow mitigate these risks [112,116,117]. These forests are found in the northern regions of North America, Europe, and Asia [118]. The same authors state that biodiversity in boreal forests is less varied compared to the tropics and subtropics, but these forests are crucial for species specifically adapted to extremely cold climates with the presence of unique large mammals and numerous species of birds, fish, and insects. The loss of boreal forests can lead to habitat fragmentation, the displacement of native species, and the disruption of ecological relationships adapted to extreme climates [119]. Taiga is essential for global carbon storage and, at the same time, acts as an important climate regulator [120].
The loss of large tracts of native forests could have dramatic consequences for their immediate environment, altering the intricate and complex ecological interactions on which the living things that inhabit them depend and possibly even impact the carbon cycle [121,122]. The loss of native forests has significant negative consequences for the planet, especially in terms of population and biodiversity changes [123]. This loss can provoke positive and negative responses since changes at the local scale are intensified by up to 48% after forest loss. Additionally, the risk of species being listed as threatened or experiencing population declines increases substantially with deforestation, especially in the wilderness [121,122,124,125]. Selective tree retention practices would be important to promote biodiversity and reshaping boreal forest landscapes [126,127]. Tropical forests have significant implications for human well-being and the achievement of Sustainable Development Goals [128]. This is due to the interconnection of forest fauna and tree species with other plants, animals, and fungi, as well as their role in ecosystem functions and services [129]. The combined effect of biotic and abiotic stressors, exacerbated by climate change, further contributes to forest loss and a decline in biodiversity [130]. The loss of large species, especially vulnerable to extinction, may result in fewer interlinked food webs and reduced ecosystem functionality [92,121,122]. Table 2 shows the summary of the geographical distribution of the main countries with tropical, subtropical, and boreal forests. In addition, we can observe a summary of the different aspects related to climate, vegetation, diversity, impacts on biodiversity, carbon storage, and finally, the importance of the ecosystem of the three geographical forest regions analyzed.

2.2. Forest Degradation versus Extractive Deforestation and Impact on Biodiversity

In the context of global forest dynamics, it is imperative to differentiate the contrasting mechanisms related to two fundamental concepts, namely deforestation and forest degradation [131]. However, it should be noted that there is no scientific consensus on these two notions. There are many overlapping definitions, which complicates the picture when making comparisons between various studies and between countries, regions, and different types of forests [132,133,134]. However, forest loss is characterized by a combination of deforestation and forest degradation. Deforestation, according to our definition, is the permanent transformation over time of forest land, generally intending to give it other uses (agriculture, livestock, urban development, logging, mining, and oil), directly impacting the loss of biodiversity, erosion, and producing climatic changes. That is, deforestation refers to the abrupt change from trees-covered land to tree-free lands without any probability of future growth [135,136]. This characteristic refers to the complete conversion of forests to alternative land uses, leading to the complete loss of forest and ground cover [137].
However, forest degradation is broadly understood as the disturbance caused by human or natural actions in a forest landscape that results in a reduction in the forest’s ability to provide goods and services [138]. Therefore, forest degradation refers to the temporary reduction in tree density in a given area, that is, the thinning of vegetation cover and the depletion of carbon content without altering land use, foreseeing a forest regrowth process in a peremptory time [136]. That is, forest degradation encapsulates the accelerated deterioration of the quality and ecological vitality of existing forest ecosystems, often due to factors such as unsustainable logging, pollution, insect attacks, arson, accidental fires, or changes in the global climate [138]. Forest degradation involves more subtle erosion, but also impacts the inherent health and functionality of forests over time through potential resilience [10,60,139,140,141,142]. From these elements, it is inferred that the environmental impacts of deforestation are more severe and permanent than the degradation produced by the substantial loss of forests in tropical, subtropical, and boreal geographic regions [143]. In this context, Figure 1 highlights some facts related to the loss of forests around the world related to deforestation versus forest degradation. In this case, we can observe the geographical region of tropical forests consisting of countries in Latin America, Southeast Asia, and Africa. Temperate/boreal regions include North America (the United States and Canada), Russia, China, South Asia, Northern Europe, and Southern Oceania. Finally, the subtropical forest region includes southern China, Japan, the southwestern United States, Oceania, southern Chile, and Argentina. Figure 1 also illustrates the loss of forests due to massive deforestation caused by human intervention (extractivism). At the global level, 27% of the 21 million hectares (Mha) of forest lost annually correspond to permanent deforestation, that is, to an irreversible change in land use [136]. This is key because deforested soils can hardly be recovered (due to the elimination of layers of fertile soil composed of networks of ectomycete fungi, rhizomes, and minerals, among other things) [144], while forests that have been degraded have higher chances of recovery in the medium and long term with a greater probability of resilience [145,146]. However, the tropical forest is the one that suffers the greatest combined deforestation and degradation on the planet, while at the same time, it is the richest in biodiversity and ecological complexity, with its loss negatively impacting not only the forest but also the global climate [136].
Continuing with Figure 1, the greatest pressure on these forests (the deforestation rate is observed in dark gray in the left column) is generated by human intervention since agriculture is the main factor responsible for its deforestation, with around 3.4 Mha of annual loss in Latin America alone, 1.6 Mha of loss in Southeast Asia, and finally, a loss of 0.1 Mha in Africa. Forest losses due to degradation in these same tropical forests are not minor, reaching 34% of the total loss. Regarding boreal/temperate forests, the greatest degradation is caused by forest fires and timber plantations (monocultures) to replace the native forest and its diversity for commercial purposes, which is equivalent to a significant 66% of total forest degradation, but that, nevertheless, barely reaches a loss of 5% of the global total due to deforestation [136,147]. Finally, in the subtropical forest region, the richness of tree species that coexist within it is extremely diverse, marked by the different seasons, so the variability in terms of niches and competitive capacities is evident. There is less precision about the volumes of degradation and deforestation in these forests. The largest number of studies related to them belong to research carried out in China and some in Latin America (Paraguay, Argentina, Chile, and Bolivia) [148]. As for Latin America, large areas of its forests have suffered a large amount of systematic deforestation, mainly due to the abusive use of agriculture (mainly pastures for livestock and soybean cultivation) and logging [149]. However, some temperate and subtropical forests have begun to have positive indices by increasing their forest cover, especially in central and southern China, where there is a good correlation between public policies for the implementation of ecological restoration projects and the rapid economic development of this country [150]. On the other hand, forest losses due to fires (accused and natural) in different geographic forest regions drastically change these relationships. Boreal forests have the highest proportion of fire losses, reaching 73%. They are followed by subtropical forests that lose between 19 and 22%, then temperate forests with losses between 17 and 21%, and finally, tropical forests that reach between 6 and 9% [151].

2.3. The Importance of Natural Capital versus Extractivism-Leading to Deforestation

Natural capital is gaining importance and visibility in measuring the economic performance and socio-cultural prosperity of different emerging economies [152]. Natural capital can be defined as the stock of natural resources that includes both land and ecosystems [57]. It occupies a more intrinsic rung of capital compared to anthropogenic constructs such as human capital, social capital, manufactured capital, and financial capital [153]. This distinction comes from its role in providing fundamental requirements for human existence, including biodiversity, livelihoods, and access to clean fresh water and air, as well as indispensable and crucial resources for the functioning of society [154].
From this perspective, extractive industries and natural capital play critical roles. However, it should be noted that extractive industries have historically been focused on three large conglomerates: oil, gas, and mining [155]. An important reflection on this definition leaves a large gap in the literature when it comes to deforestation, as it is largely absent in this trilogy, ignoring the enormous impact it has on the environment [154]. Deforestation as an extractivist phenomenon affects all niches related to natural capital and cascades to all biodiversity [156]. It is important to note that deforestation in general occurs for different reasons. The three most important purposes are related to the exploitation of mining, gas, and oil exploitation; the generation of land for agriculture and livestock; and finally, the construction sector [157,158,159,160,161,162].
Extractivism involves destructive practices that subjugate and deplete natural resources, degrade soil, accelerate species extinction, cause the decline of biological diversity, and destroy forests [66]. All cases are intrinsically related to the pursuit of anthropogenic capital accumulation and the constant drive toward exponential economic growth throughout the world [163]. In parallel, the increase in socioeconomic disparities at the global level in numerous geographic regions is another characteristic that usually drives the phenomenon of extractivism [164,165]. However, extractivism, if measured in the very short term from a socio-economic perspective, could generate a sensation of sometimes alleviating poverty, inequality, and unemployment in emerging countries because it generates financial resources quickly, but without being sustainable over time. However, if measured in the medium and long term, the environmental, social, cultural, and economic impact is generally negative due to the footprint it leaves on the intervened forest ecosystems [166]. At the same time, there is a lack of reciprocity in this practice, as it does not seek to protect these resources and, therefore, opposes sustainability [167]. The effects of extractivism, such as resource depletion, environmental degradation, and socioeconomic inequalities, are often associated with excessive capital accumulation and economic growth of some strong economic groups to the detriment of local communities [168]. These aspects form a systemic context known as disorganized development. Smart [166] analyzed extractivism from a conceptual theoretical perspective toward organizational development aligned with an ethical–political approach of ‘transformative global studies’. One could argue that there has been a shift towards an intensification of extractivism on a global scale [66]. Forest loss alters habitats and niches that support a diverse range of flora and fauna. Above-ground biodiversity, which includes plants, animals, and insects, depends on the forest canopy for shelter, sustenance, and breeding grounds. Deforestation in any of the geographical regions addressed (tropical, subtropical, or boreal) fragments this intricate vertical structure, displacing species and altering trophic interactions and the collective resilience of forest ecosystems [169,170].

2.4. Resilience in Tropical, Subtropical, and Boreal Forest Ecosystems

Resilience in forest ecosystems related to tropical, subtropical, and boreal forests is closely related to another concept known as hysteresis, which refers to the dependence of the current state of an ecosystem on its history and is a complementary indicator of forest resilience [171]. The definition of resilience is complex due to the varied interpretations that the literature makes depending on the discipline that addresses it [16,172]. This ambiguity is due in part to the extensive use of the term in different contexts. Scholars disagree on whether resilience is a system property, a process, or a management outcome [169,171,173,174,175]. However, three main concepts of resilience emerge in the literature: engineering resilience, ecological resilience, and socioecological resilience [57,176]. Nikinmaa [169] elaborates on the three models, where engineering resilience refers to the system response associated with rebuilding following a disturbance or catastrophe, quantified as the time it takes for variables to return to pre-equilibrium of the disturbance. Ecological resilience measures the persistence of the system and its ability to absorb change while preserving different relationships. Finally, socioecological resilience considers that natural and social systems are interconnected and focuses on general adaptive capacity. Furthermore, there is what is known as ‘The Alliance for Resilience’ [177], which characterizes resilience as the ability of a socio-ecological system to withstand disturbances, maintaining its structure and functions. This emphasizes self-organization, learning, and adaptation. Understanding resilience helps navigate the changing environmental and social dynamics for sustainable management of diverse ecosystems [169]. Resilience can be classified as resilient (i.e., no change after impact) or recovery (i.e., returning to the pre-impact state, but considering the development of management options that maintain both ecosystem services and human well-being) [178], which makes it somewhat similar to hysteresis.

2.5. The ‘Mother Tree’ Is the Center of the Resilience of the Ecosystem

Suzanne Simard’s research indirectly points to the importance of natural capital by noting that the interconnectedness of underground forests fosters mutualistic relationships that improve species diversity and resilience [11]. However, it is important to note that the research developed by Simard is the result of an evolution in the scientific understanding that preceded her on the different forest ecosystems [179,180]. In forestry, there is still a tendency to focus on models of stand dynamics driven by competition between trees and plants for limited resources such as light, water, and nutrients [181]. However, this perspective is beginning to change with the deepening of research in plant ecology and, particularly, in mycology [182]. One of the first advances was the recognition of the importance of the role of mycorrhizae and the symbiotic associations between fungi and plant roots with implications on the health and growth of trees in the forest [183,184,185]. This idea was initially explored by scientists such as Franciszek Kamienski and Albert Bernard Frank in the late 19th and early 20th centuries, who studied plant–fungus associations [186]. Later, researchers such as John L. Harper in the 1960s and 1970s provided a theoretical framework for understanding plant population dynamics, including competition and cooperation [187]. These studies began to suggest that plants not only competed with each other but could also cooperate in more complex ways [188]. Subsequently, forest ecology began to integrate these concepts, broadening the understanding of how mycorrhizae influenced plant–plant and plant–environment interactions and began to dig deeper from the further input of molecular biology [189]. Bonfante [190] provides a different perspective on mycorrhizal research, highlighting how past discoveries and hypotheses have formed the basis for the current understanding of plant–fungus interactions, and how these interactions would be fundamental to the health and sustainability of tropical, subtropical, and boreal forests as a whole. According to some authors, mycorrhizal networks would not only help plants absorb nutrients but could also facilitate the transfer of resources between different plants [191,192,193,194]. It could be speculated that these concepts, which are shared by some researchers, would be close to the line of research that Simard applied in some forests on the integration of these concepts based on plant–mycorrhizal interactions [17,21,22,25,195,196,197,198,199,200,201,202,203,204,205,206]. These investigations show a complex subway communication network. In this line, Simard estimates that mother trees would play a crucial role in maintaining the health and stability of the forest ecosystem by transferring nutrients and some signals to other younger and possibly more vulnerable trees in the environment. This mycorrhizal network, which Beiler et al. [207] described as the ‘Wood Wide Web’, would function as an interconnected and even cooperative system, challenging the traditional notion of fierce competition as the sole driver of forest dynamics [11,16].
The concept of “mother trees” understood from the perspective of older trees, with long-range roots and protective functions, emerges as a phenomenon of analysis in forest ecology, although controversial [11,26,205,208]. These trees (always according to Simard’s hypothesis) would be fundamental entities for maintaining forest health, biodiversity, and ecological stability. The mother trees, often characterized by their advanced age, larger size, and extensive root systems, would play a crucial role in shaping the intricate web of interactions that sustain forest ecosystems. The essence of mother trees would be their multifaceted relationships with neighboring trees [209]. Simard and other researchers suggest that through complex networks of root connections, these older trees could function as “nurturing” centers, extending resources and protection to their younger counterparts as a cooperative alternative [210,211]. This process would be mediated by certain mechanisms, including the transfer of essential nutrients, carbon compounds, and even defense-related molecules [11,18,212]. Through this symbiotic exchange of resources, it would not only sustain the growth of individual trees but also strengthen the collective resilience of the forest ecosystem as a whole [169]. One of the fundamental contributions of mother trees to ecosystem resilience, still according to Simard’s research, would be their role in transmitting resources in times of stress. Because these mother trees would apparently possess a large number of resources accumulated over decades of growth, they would be in a position to mitigate the impacts of various stressors, such as drought, disease, or nutrient shortages at any given time, both for themselves and for more vulnerable trees in the environment [213]. If so, this role could become especially crucial in the face of environmental fluctuations or disturbances, where the availability of resources could be limited for younger trees. Carreón-Ortiz and Valdez [214] support the importance of mother trees as reservoirs of resources that contribute to the survival and adaptive capacity of the forest community in the face of adverse conditions. Following these lines of research from a resilience perspective, it could be pointed out that the so-called mother trees, with their complex interaction with mycorrhizae, would play an important cooperative role since they could contribute to the maintenance of biodiversity and nutrient, carbon, and water cycles, essential for the health of ecosystems [11]. In tropical forests, resilience is revealed as the ability of these ecosystems to adapt and recover from events such as deforestation or abrupt and seasonal changes in the rainfall regime [215,216]. Meanwhile, in subtropical forests, resilience is crucial to the rapid adaptation of trees to seasonal variations in rainfall and temperatures and to the progressive changes evident in climate [217,218]. On the other hand, in boreal forests, resilience is observed in their ability to regenerate after natural disturbances, which are, most of the time, generated by forest fires and insects in a highly adverse climate [111,219]. Despite extreme climatic conditions in boreal forests and nutrient-poor soils, the symbiotic relationships between mature trees and mycorrhizae ensure the survival and regeneration of the ecosystem [208]. This resilience is a clear example of resilience and its ability to face and adapt to constant disturbances over different periods.
According to Simard’s research, mother trees would be dominant individuals in the forest, able to share their energy sources with other trees with less access to sunlight, water, and other nutrients. Simard estimates that many seedlings when they first germinate in the understory are colonized by a network of mycorrhizae and begin to receive not only nutrients from the soil but also carbohydrates from these established trees as a nurse effect, where they would be protected from herbivores, organic matter, and even defense signals [208,220].

2.6. The Underground Kingdom of Mycorrhizal Networks Responsible for Forest Biodiversity

Mycorrhizae constitute a crucial component of one of the most extensive and vital biological interactions between different kingdoms, connecting more than 340,000 species of terrestrial plants with around 50,000 taxa of soil fungi [221]. This intricate subterranean kingdom of mycorrhizal plants lies beneath the forest floor, where trees and fungi establish symbiotic relationships that facilitate the exchange of nutrients and vital information [208]. Suzanne Simard’s research has revealed the impact of deforestation on the tangled functioning of these networks, underscoring their role in enabling resource exchange mechanisms between trees and fostering mutual support [222]. Deforestation caused by extractive practices affects not only trees and plants but also mycorrhizal networks and a set of complex connections (a network of interactions between plants and microorganisms) that impact critical ecological processes [223,224]. The loss of forest areas (tropical, subtropical, and boreal) could lead to the breakdown of these intricate connections, which, in turn, would affect critical ecological processes such as nutrient cycling, soil structure and stability, and the complex network of symbiotic interactions between plants and microorganisms [11,208]. Consequently, this alteration could have an impact on ecosystems, influencing the health of plants, biodiversity, and the general functioning of the environment. Mycorrhizal networks represent a fundamental link of interaction between plants and fungi, forming the backbone of intricate ecological systems [225]. Simard’s research emphasizes the interconnection of these networks with the health and resilience of forests and their wider impact on terrestrial ecosystems [208].
Recognizing the importance of mycorrhizal fungi/plant interactions is essential for the informed management and conservation of native forest landscapes and the myriad benefits they confer to both the environment and society. Therefore, it is important to address some specific varieties of mycorrhizal fungi and their main physiological needs depending on whether they are present in tropical, subtropical, or boreal forests and their adaptation to the plants and trees with which they interact and function in each ecological environment [226,227].
In tropical forests, arbuscular mycorrhizae are common and include genera such as Glomus, Acaulospora, and Scutellospora [228,229]. Regarding their physiological needs, these fungi adapt to conditions of high humidity and very warm temperatures [230]. They need soils in which they can exchange nutrients with a wide variety of plants [231]. In addition, they are crucial to facilitate the absorption of phosphorus and other nutrients in soils that are often very poor in organic matter [232].
Subtropical forests are characterized by a mixture of ectomycorrhiza and endomycorrhizas. Ectomycorrhizas include genera such as Pisolithus and Laccaria, while arbuscular endomycorrhizas are also present [233,234]. Ectomycorrhizae in these forests adapt to more variable conditions, including dry and wet seasons [235]. Therefore, these fungi are important for the absorption of nutrients in soils with alternate periods of drought and humidity [236]. Endomycorrhizas play an important role in the assimilation of nutrients, especially in plants that do not form ectomycorrhizas [237].
Finally, in boreal forests, the predominant fungal varieties are ectomycorrhizas, with genera such as Russula, Amanita, and Suillus [238]. These fungi form associations mainly with coniferous trees such as pines and firs [219]. The ectomycorrhizas in these forests are adapted to acid soils and cold climates. They require the ability to survive and function efficiently under low-temperature conditions, often frozen by permafrost, and in soils with low biological activity precisely due to cold [239]. However, these fungi achieve their goal by helping trees access nutrients in an environment where the decomposition of organic material is slow and the availability of nutrients is limited in time [240].

Molecular Studies on Mycorrhizal Fungi in Forests

In the field of forest ecology, molecular research on arbuscular mycorrhizal fungi has gained crucial importance through the use of biotechnology and genetic engineering [241]. These studies have provided a deeper understanding of the symbiotic interactions between trees and fungi, which is essential to better understanding the dynamics of forest ecosystems. Miyauchi et al. [242] have been pioneers in the field of mycorrhizal fungal genomics, providing significant information on the early evolution of the symbiotic traits of these organisms. Through large-scale sequencing, the same authors have brought to light key elements of how these symbiotic interactions have developed and how they work. On the other hand, Shi et al. [243] have examined variations in fungal communities along disturbance gradients in forests, showing how changes in the environment, both natural and anthropogenic, affect mycorrhizal networks and, consequently, the health of the forest ecosystem. This research highlights the sensitivity of mycorrhizae to disturbances and their vital role in ecosystem stability. From a molecular perspective, the interactive roles of different types of fungi in tropical, subtropical, and boreal forest ecosystems have been confirmed by genetic markers [244]. These advances have allowed us to observe in more detail the factors that influence the distribution of mycorrhizal and soil fungi, explore how these organisms interact with their environment, and provide valuable information for the proper management of forest needs [245]. Research on mycorrhizal interactions in orchids, ectomycorrhizal fungi, and ericoids has provided valuable insight into the molecular mechanisms of these symbioses. Studies have identified specific genes and pathways involved in these interactions, such as those related to nitrogen uptake and symbiotic marker genes [246]. Other genomic studies have identified key genes involved in the uptake and symbiosis development, shedding light on the complex dynamics of mycorrhizal associations [247].
In the context of climate change, some studies show how mycorrhizal symbiosis can improve the adaptation of trees to different types of abiotic stress, which is vital for the resilience of forests, mainly temperate and boreal, in the face of environmental changes. [207]. Advances in the functional roles of fungal endophytes in the microbiomes of forest trees have provided a comprehensive view of the interaction between trees and their fungal symbionts that impact forest health [248]. This study highlights the importance of endophytes in the regulation of ecosystem functions and the promotion of forest health. On the other hand, a direct connection has been established between forest tree growth and the composition and function of mycorrhizal fungi [194]. Shi et al. [249] analyzed the impact of deforestation on the soils of fungal diversity and community composition in a tropical rainforest. They found that the richness of saprotrophic soil fungi, including phosphorus-solubilizing fungi such as Penicillium spp., decreased as forest disturbance increased, while facultative pathogenic fungi became more abundant. This change suggests a transition from phosphorus limitation in undisturbed forests to carbon limitation in deforested areas, highlighting a potential obstacle to plant succession after deforestation. The study highlights the sensitivity of soil fungi to forest disturbances, indicating their potential as indicators of soil health and the interaction between above-ground and below-ground ecosystems. In the network of symbiotic interactions between plants and microorganisms, the former act as hosts for a wide range of microorganisms from their environment or inherited from parental sources [250]. This mutual commitment extends to specific bacteria that play a critical role in the support of plant health and growth [251]. Among these bacteria, certain strains offer the unique ability to fix nitrogen, a critical process for enriching the soil with this essential nutrient, which is then taken up by higher plants [248]. Furthermore, these microorganisms influence the regulation of plant hormones, which further contributes to the balance of plant physiology [250].
However, the symbiotic harmony of these processes may be threatened by deforestation generated by extractive practices. The ramifying consequences of forest clearance extend beyond the visible landscape and reverberate through these subway pathways, potentially altering nutrient dynamics and compromising the very basis of forest vitality [252,253]. Soil fertility would be compromised as the nutrient exchange network is dismantled [254]. The finely tuned balance of the nitrogen cycle would be out of balance, resulting in the breakdown of essential biogeochemical processes that underpin ecosystem functionality [39,255]. In essence, the interaction of plants, microorganisms, and their sophisticated connections highlights the important harmony within forest ecosystems, but again, the phenomenon of coopetition comes into play in the whole organization of forest biodiversity [40]. All these studies provide a stronger scientific basis for the importance of mycorrhizal fungi in forest ecosystems and may provide some clues at the same time to Suzanne Simard’s hypothesis on the dependence of arboreal communication on mycorrhizal fungi. Molecular research in this field not only broadens our understanding of forest ecology but also opens new avenues for the conservation and sustainable management of forest ecosystems and the deepening of resilience and the impact of potential ecological cascading effects.

2.7. Cascading Ecological Effects

The ramifications of the effects of deforestation extend far beyond the confines of the forest itself, regardless of whether it is tropical, subtropical, or boreal. They encompass, as we have seen, a complex series of ‘cascading’ ecological effects that impact interconnected ecosystems and, ultimately, forest biodiversity [256]. A profound transformation in land use triggers a chain of repercussions that extends across several environmental compartments, with significant implications for both terrestrial and aquatic domains [257]. One of the main ecological cascades derived from deforestation involves alterations in the dynamics of nutrient cycling [258]. Through different investigations, it has been established that intensive deforestation would have cascading ecological effects, affecting tree growth, carbon assimilation, and concentrations of nonstructural carbohydrates [224,259,260,261,262]. As forests are cleared, the intricate cycle of nutrient exchange that characterizes these ecosystems is disrupted [263]. Organic matter, often rich in nutrients, present in the form of leaf litter, fallen branches, and decaying vegetation, mainly in subtropical forests, plays a fundamental role in soil nutrition and provides essential elements for plant growth [264]. With deforestation, this cycle is broken and the flow of nutrients from vegetation to soil and waterways is affected [265]. This, in turn, decreases soil fertility and causes a reduction in primary productivity, ultimately influencing the composition and structure of the surrounding ecosystems, an element very often seen in tropical forests [266]. Furthermore, deforestation exerts a perceptible impact on hydrological processes [267]. Intact forest cover intercepts rain, slowing its descent to the forest floor. This allows the soil to gradually absorb water and subsequently release it, maintaining a constant flow in local surface and underground waterways. Deforestation disrupts this intricate mechanism, accelerating the flow of rainwater into the soil [268]. Consequently, the ability of the soil to absorb water is compromised, resulting in reduced water retention and increased surface runoff [269]. This leads to increased soil erosion, as sediment-laden runoff washes away the land and is deposited in adjacent water bodies [265]. The alteration of hydrological cycles extends its influence downstream, affecting adjacent waterways and the communities that depend on them [270]. Irregular water flow patterns, altered sediment transport, and changes in water quality can have profound effects on aquatic ecosystems, from the alteration of fish habitats to the degradation of water sources that human populations depend on [271].
The notion of ‘cascading’ ecological effects emphasizes the deep interconnectedness of ecosystems and the intricate interaction of ecological processes. The impacts of deforestation are great, but the effects of reforestation could also be harmful due to the compaction of their soils due to the passage of the heavy machinery used [272,273]. However, it should be noted that not all forest intervention strategies for restoration purposes can be categorized as good or bad, as they depend on numerous variables. In some cases, natural restoration may be the most efficient in recovering much of the ecological services lost through the degradation of some tropical forests, while in others, this may not be the case [223,274,275]. Shimamoto et al. [274] conducted a global meta-analysis of ecological indicators of ecological services provided in restored areas, degraded areas, and reference ecosystems of tropical forests where restoration strategies recovered ecological services to varying degrees, and they reported that in practically all cases, there were positive effects. Some research has reported on the complex relationship between forest extractivism and its relationship with mycorrhizal fungi, suggesting that some stressors, such as deforestation, can cause the loss of the mycorrhizal community, which in turn can lead to tree decline in the form of a vicious cascading cycle [260,261]. In some cases, a virulent attack was evident in some plant species in which disturbance of the forest was observed to alter the composition of the community of ectomycorrhizal fungi and arbuscular mycorrhizae with a lower richness and diversity than in areas that had not suffered disturbance [262].
Beyond the mere loss of forest cover, they resonate through intricate nutrient cycles and hydrological dynamics, affecting not only the immediate environment but also extending its consequences downstream and in the vadose zone [8,276]. Recognizing and understanding these cascading effects is essential to designing effective public intervention strategies for conservation and land-use management that fully consider the long-term consequences of extractive human activities on natural systems.

2.8. Importance of Public Policies, Institutions, and Governance in the Regulation of Extractivism for a More Sustainable Development

Developing countries are often characterized by a confluence of factors that hinder the protection of natural resources and the sustainable management of ecosystems in the form of natural capital [153,277,278]. In these countries, an important challenge is forest management of the overexploitation as a result of extractive practices by large foreign corporations that, in many cases, act with total irresponsibility in the face of regulatory gaps that limit their predatory actions [154]. Institutions and governance, coupled with poor policies and corruption phenomena, create an environment conducive to the vilification of existing regulations, which generally leads to unprecedented ecological degradation [57]. Figure 2 shows the influence that the actions of different ‘external’ agents have on natural ecosystems. Each vertex of the triangle influences and dynamically impacts the whole with its action or inaction, particularly the vertices referring to public policies and extractivist practices.

2.8.1. Poor Public Policies, Governance, and Institutional Frameworks

Public policies play a critical role in shaping the regulatory landscape for the extraction of natural resources [279]. However, many developing countries struggle with inadequately formulated policies that do not adequately address environmental concerns and local social interests [280,281,282]. These policies often lack clarity, enforceability, and provisions to curb overexploitation. Furthermore, institutional frameworks designed to supervise these policies are often poorly equipped, with limited resources, technical expertise, and enforcement capabilities [246]. Corruption within governance compounds the problem by undermining regulatory efforts [282]. When regulations can be circumvented through bribery or other illicit means, many large extractive corporations exploit this vulnerability, aggravating forest degradation [283].

2.8.2. Exploitative Extractivist Practices by Multinational Corporations and Biodiversity Loss

Large multinational corporations often take advantage of weak governance systems and institutional inefficiencies to carry out extractivist practices with minimal regard for ecological sustainability [284]. These practices include indiscriminate logging, open-pit mining, agriculture, and urbanization, leading to massive deforestation and loss of biodiversity [285]. The lack of effective enforcement mechanisms allows these companies to operate beyond the limits of sustainable development [286]. The consequences of overexploitation are dire and lead to the degradation of native forests and the loss of tree cover [287]. The intricate biodiversity that thrives in these ecosystems is in danger, as habitats are destroyed and animal species lose their refuges and plants their substrates [288] without losing sight of the importance of the resilience of socioecological systems [31].

3. Discussion

Geographic regions belonging to tropical, subtropical, and boreal forests constitute some of the ecosystems that most significantly impact the quality of the biosphere of our planet [50,78,289]. Therefore, the different disturbances generated by extractive deforestation carried out in these forests would reveal a complex confluence of factors that go beyond the purely ecological and involve socioeconomic and political agents that demand adequate sustainable management of forest practices [211,290]. In this line, the discussion addresses two essential elements. The first is the importance given to the different coopetition networks that exist between mother trees, their environment, and mycorrhizal fungi. In this context, different conceptual positions in research have contributed to the debate in the scientific community and have not yet been settled [11,16,18,20,21,22,23,24,25,26,27,66,121,122,123,126,127,163,191,192,193,194,195,208,209,212,213,214,220,237]. Some authors estimate that the conservation of these mycorrhizal networks could have a direct impact on the preservation of the health and resilience of forests of the geographic regions addressed [11,26,187,193,291], while others estimate that they are organisms that would act differently depending on the needs and stresses to which they are subjected in the ecosystem [26,27,220]. The second element of the discussion refers to the possible environmental consequences of extractive practices related to deforestation in relation to other less sustainable industries such as agriculture and particularly oil or mining [70,155,211,290]. A specific case of mining extractivism can be observed in the tropical forest geographical region in the Amazon with dire consequences for the surrounding forest ecosystem, affecting its fragile soils, in addition to transporting potential heavy metals to the vadose zone due to water runoff [292,293,294]. In the absence of conclusive scientific evidence, this review invites us to reflect on how the adaptation of best anthropogenic practices can be aligned with natural processes, ensuring more sustainable development, both for forested geographic regions and for humanity in general. All this is from the lessons obtained from hysteresis and resilience to improve our interpretation of the changing dynamics of these intervened ecosystems [171,295,296,297].
Simard’s research has attracted both supporters and detractors among scientists. Still, it is the context-dependency of the results and their extrapolation beyond the systems investigated that drives the controversy. Research that is more aligned with Simard’s hypothesis suggests that some functions of the roots of the mother trees generate a mutual dependence on the mycorrhizal community, which would provide an advantageous resource to evaluate the complexity of forest ecosystems when they are intervened, for example, anthropogenically [191,192,193,194,298]. Other scientists consider this quasi-thoughtful position controversial and therefore a resisted hypothesis since they estimate that mycorrhizal fungal communities could respond almost autonomously to the environment in which they are found, beyond the complex ecosystem of mother trees in which they may be found, and therefore question the mother tree hypothesis, suggesting that evidence of significant transfer of carbon through mycorrhizal networks is lacking [27]. Similarly, other researchers opposing Simard’s hypothesis suggest the possible involvement of a “common symbiosis path” in the establishment and maintenance of ectomycorrhizal associations [224,299]. Other research analyzes the complex relationship between tree decay and mycorrhizal fungi from different perspectives.
In this quest to align this dichotomy of research currents, efforts are being made to identify the role of mycorrhizae in carbon and nitrogen sequestration and their interrelationship with tree roots and other organisms at the molecular level through genetic engineering techniques that should shed more light on this complex discussion [34,35,241,246,247]. Other researchers seek more moderation, as is the case of Marin and Bueno [300], who highlight the need for a more balanced approach to the investigation of mycorrhizae and their interactions. Meanwhile, other research estimates that the formation of mycorrhizal networks next to the roots of some plants not only affects the distribution of scarce nutrients, mainly nitrogen among interconnected plants, but is also vital for the growth of these while building a pathway for carbon assimilated by these plants [301,302,303]. From these mechanisms, we can appreciate the importance that coopetition would assume within the forest ecosystem, which suggests that competition and cooperation between trees of the same and different species can co-exist beneficially, facilitating a dynamic balance that would maintain diversity and ecosystem resilience [304,305]. In this sense, biodiversity is crucial for forest health, as many species would make unique contributions to ecosystem functioning and resilience and also compete with each other, confirming the phenomenon of coopetition. This is essential to understanding the functionality and interaction of these ecosystems based on the simultaneous occurrence of cooperation and competition among trees within the biosphere. While trees compete for sunlight, water, and nutrients, they also cooperate by exchanging essential resources through different subway root systems [306]. This coopetition approach could inspire new intervention, conservation, and sustainable forest management strategies that mimic and take advantage of these natural interactions and, at the same time, can serve as a tourist attraction with important socioeconomic benefits.
However, one of the critical points to highlight in this discussion is to reflect on the detrimental impact of deforestation driven by extractive practices that could transversally alter the delicate balance of forest ecosystems [150,307]. While the exploitation and use of natural resources are essential for human development and economic growth, the uncontrolled exploitation of these resources often leads to rapid environmental degradation, loss of biodiversity, and ultimately, socioeconomic disparities [2]. This is because often a forest sector is overexploited thinking that immediate economic benefits are achieved for local communities, but the consequences are usually disastrous in the long term since forests, soils, and water are extinct, generating more poverty and desertification [308,309]. The concept of extractivism, which is associated with the concept of extractive industries, is based on the accumulation of financial capital and rapid economic growth at any cost, leading to practices that disrupt the intricate relationships within forests and ultimately compromise their resilience and integrity in the medium and long term [66]. Deforestation disrupts the symbiotic relationship between trees and mycorrhizal fungi, crucial for nutrient exchange and plant growth, leading to a decline in forest biodiversity and productivity [310]. Then, it is evident that extractive deforestation should have devastating effects on biodiversity and ecosystem services provided by forests [311]. It is urgent that political institutions address this problem based on the importance of tropical, subtropical, and boreal forests and their complex ecological networks. To this end, the integration of scientific findings on mycorrhizal networks, together with stronger public policies and informed and sustainable forest management, is essential to preserve these vital forest ecosystems for the planet [11,35,184]. However, it is essential to go even deeper to better understand the interactions between plants, soil, and mycorrhizae, and for this, advances at the biotechnological level (molecular and genetic) can provide new approaches to understanding and improving forest health of forests and their ability to withstand environmental and anthropogenic pressures [241,242,243,244,245,312,313]. These new lines of molecular research could reveal innovative strategies for the restoration of damaged forests and the sustainable development of forests [241,242,243,244,245,246,247]. Increasing the capacity to resist stress in the forest ecosystem, adapting to changes in the environment, and recovering from potential disturbances of human or environmental origin are key to the success of a healthy forest that thrives over time [314]. The impacts of deforestation are not only limited to the visible landscape [315]. The interruption of underground networks, such as roots, that facilitate the exchange of nutrients and support interactions between plants and microorganisms has far-reaching consequences, in many cases, greater than what happens on the surface [316,317,318]. This alteration compromises soil fertility, biogeochemical processes, and essential ecological functions, affecting the vitality of the entire ecosystem and its biodiversity [319].
The loss of mother trees usually occurs because, being the most voluminous, they become the most coveted, mainly by the timber industry. The big problem is that when these specimens are removed, not only is species diversity reduced but there is also the risk of fundamentally interrupting the flow that could exist between mycorrhizal networks essential for the exchange of nutrients and signals between young trees of the same and different species and can drastically affect the rest of the forest ecosystem as a whole [211,223,292]. In some cases, an increase in arbuscular mycorrhizae as a consequence of anthropogenic intervention would have the potential to induce the acceleration of nutrients, with critical consequences for forest productivity, carbon availability, and nutrient retention [310]. The dissemination of Simard’s hypothesis on mother trees and mycorrhizal networks (although not yet categorically proven) still offers a preventive and precautionary approach to the sustainable development of natural capital through more responsible forest management [292]. Simard suggests that by protecting and conserving the hub of mature trees (mother trees) and their symbiotic mycorrhizal networks, the resilience and recovery capacity of forests improve when there is deforestation or forest degradation of younger trees [11,320,321]. This perspective highlights the need for a holistic approach to forest management, which recognizes the importance of complex biological interactions and coopetition within diverse forest ecosystems [174,184,322,323,324]. This brings us to the notion of ‘cascading’ ecological effects [325]. A broader perspective, from a hierarchical meta-analysis, reveals the complex interactions between global change factors and ecosystem function [326], with the synthesis of carbon cycling experiments underscoring the need for site-specific considerations in Earth system models [327]. These studies collectively underscore the multifaceted nature of deforestation and the importance of considering its ecological and economic impacts. Deforestation, whether in boreal, tropical, or subtropical forests, appears to trigger a chain reaction or a cascade of domino-style repercussions that could extend beyond the limits of the logged forests, likely affecting hydrological processes, nutrient cycles, and even aquatic ecosystems, negatively impacting even the vadose zone [224,260,261,295,328,329].
Regarding the effects generated by the ‘cascade’ chain, mention must also be made of the aspects related to the socioeconomic and public policies that impact the protection or not of a forest ecosystem. Busch et al. [330] provide evidence of the economic and environmental drivers of deforestation, highlighting the greatest exponent in agriculture. Similarly, Desbureaux and Damania [331] highlight the impact of agriculture as the main link within the cascading effects that accelerate the deforestation processes in many forests around the world. Therefore, it is important to generate the necessary conditions for sustainable forest development in the medium and long term, through coherent public policies, responsible institutions, and governance committed to society and natural capital [54,80,81,82,83,84,85,86,87,88,89,90,91,92,93,332,333,334,335,336,337,338], especially if one considers the lack of conclusive scientific unanimity regarding the functions of mycorrhizae and the relevance of the roots of the mother trees.
Forest overexploitation has been especially promoted in developing countries, due to inadequate public policies, and is fueled in some cases by acts of corruption in their care, affecting the capacity of these ecosystems to act as carbon sinks and jeopardizing global efforts to mitigate climate change [339,340,341]. This means that strengthening public policies, institutions, and governance is crucial to more effectively protect forests in all geographic regions addressed until agreements are reached on the functions of the different components of the forest ecosystem [342,343]. This includes developing strategies that limit extractive exploitation and promote sustainable practices, as well as improving the monitoring and enforcement of existing global environmental regulations [311,344,345].
It is important to note that forests in different geographic regions have different capacities and requirements, but all are transcendentally important. Disturbances affect different ecosystems differently. Some plants and organisms accept disturbed environments well, while others tolerate them poorly, as is the case with mycorrhizal fungi [346]; however, tree decline might affect forest dynamics through plant–soil biota feedback [347]. Tropical forests, located in the equatorial regions of the planet, are a source of exceptional biodiversity [348]. They represent a vibrant mosaic of life and harbor more than half of the terrestrial species, although they cover only a small percentage of the total land area [92]. These forests play a crucial role in the regulation of the global climate and as sinks for enormous amounts of carbon [349]. The interconnectedness between species in these forests, as proposed by Simard’s hypothesis, means that the health of a single parent tree could significantly influence the surrounding forest community by seemingly creating a network of support and nourishment that could likely collaborate in ecosystem health [350,351]. On the other hand, subtropical forests, located at lower latitudes, act as transition zones between tropical and temperate regions [352]. These forests include a variety of ecosystem types, from humid forests to savannas and chaparral [353,354]. Although they do not have as much biodiversity as tropical forests, they are equally crucial to the conservation of numerous species and protection against soil erosion and carbon sequestration [58,92,355]. The importance of older and larger trees in these forests is fundamental, along with the centers of mycorrhizal networks, for the good condition and resilience of subtropical ecosystems [356]. Finally, vast boreal forests represent one of the largest biomes in the world, characterized by their cold climate and predominantly coniferous tree species that are very important in the generation of oxygen on the planet [118,357,358]. Boreal forests are vital for biodiversity, especially as a habitat for species adapted to cold climates and as an important carbon storage [359]. In these forests, Simard’s hypothesis could acquire a particular dimension since the extreme conditions of their climate and poor soils would mean that the interconnection and mutual support between trees through mycorrhizal networks could play an important role in the survival and prosperity of the ecosystem there [360,361].

4. Conclusions

This research shows the complex interaction of ecological, scientific, socioeconomic, and political factors that shape the notion of the phenomenon of extractivism and its potential consequences in the geographical forest regions analyzed.
There are fundamental aspects that emerge about the research questions and the objectives raised in this research. The controversial hypothesis about mother trees put forward by Suzanne Simard with her detractors and supporters stands out. Although Simard’s research has sparked lively debates within the international scientific community, it serves as a wake-up call to the pressing need to generate more knowledge that will allow for a greater understanding related to divergences in the functions of mycorrhizae and trees that make up forest ecosystems. The different scientific currents are far from reaching unanimous agreements on the functionality of mycorrhizal communities and the roots of mother trees, but also on the specific functionality of mycorrhizals and the way they capture carbon and nitrogen. Today, the knowledge gaps about the different postulates in these topics are very wide and there is no evidence that is conclusive or that solves the riddle about the potential impacts related to forest extractivism. However, there are efforts to be more optimistic about closing these gaps. Scientific research is increasingly focusing on the application of advanced genetic engineering techniques in mycorrhizae and the adoption of multidisciplinary research approaches that consider the multifaceted nature of forest ecosystems from a more resilient perspective. In this line, it is crucial to recognize that complexity is provided by the biological requirements and needs of each geographic forest region analyzed.
The concept of coopetition, in which trees compete for vital resources while cooperating across different underground, surface, and aerial networks, challenges conventional notions of competition-driven ecosystems. The coopetition is a generator of knowledge and learning that can allow us to generate more efficient holistic forest management strategies in the medium and long term. However, the threats posed by extractive practices pose a serious threat to forest biodiversity, soil fertility, and the resilience of the ecosystems involved, ultimately endangering the well-being of terrestrial and aquatic ecosystems. This leads us to suggest the urgent implementation of coherent public policies and responsible governance mechanisms to protect forests on a global scale. It is imperative to strengthen public institutions to address critical economic and environmental factors related to both deforestation and reforestation and to promote sustainable practices that protect forest ecosystems for future generations.
In essence, this research underscores the urgent need for a paradigm shift in our approach to forest conservation and management, regardless of the controversies surrounding both Simard’s hypothesis and the other research listed in this research. The aim is to foster a deeper interest and understanding of the intricate relationships within forest ecosystems and to foster the adoption of evidence-based practices. The ultimate objective is to reflect on the problem of forest extractivism and its still unknown consequences on different ecosystems and their biodiversity. In particular, in the absence of greater scientific knowledge, forests are often destroyed and altered irreversibly without quantifying irreparable damage in the future. Prudence should be the rule until more conclusive research results on the function and mode of operation of mycorrhizae and tree roots are available before further progress into the unknown. Even today, despite scientific advances at the molecular level and differences in the positions of researchers, we do not know the potential consequences of an anthropogenic intervention.

5. Future Directions

This theoretical framework becomes an invaluable tool for guiding future research and conservation policies, ensuring the preservation and sustainability of these forest ecosystems crucial to the health of our planet. This may include more detailed studies on symbiotic interactions, forest responses to deforestation by fire or pests, and the development of more sustainable management strategies. Building on the foundation established in this research, a deeper look into the complex interaction between deforestation caused by intentional, accidental, or natural fires and the intricate ecological dynamics within forest ecosystems is crucial. The same happens with the impact caused by the use of heavy machinery used in deforestation, but also frequently used in reforestation, compacting the delicate substrate and killing mycorrhizal networks. This avenue of research is of immense importance as it adds a layer of complexity to the already multifaceted challenges posed by indiscriminate deforestation and extractivism.
We must also investigate the synergistic effects of fire-induced deforestation compared to extractive activities because understanding how intentional or accidental fires differ or are not different from extractivism would provide valuable information on the cumulative effects of these different processes. Researchers could explore how fire alters nutrient cycling and mycorrhizal networks and influences the resilience of mother trees in deforested areas, combined with the benefits it brings to certain biodiversity. Additionally, studying how these combined stressors impact the survival and recovery of forest ecosystems would be essential to guiding effective public policy strategies for forest conservation and restoration. In other words, how do we generate a public policy that addresses extractive practices, ecological training, and forest protection? Furthermore, research could focus on the mechanisms through which natural fires shape forest dynamics in the context of extractive activities. Investigating how natural fire regimes impact the ecological dynamics of biodiversity in the face of extractivism-induced deforestation could reveal valuable insights into the complex feedback loops that influence post-fire recovery and ecosystem resilience. This would involve studying the role of fire-adapted species, the regenerative capacity of mother trees, and the subsequent establishment of mycorrhizal networks in fire-prone landscapes. Incorporating the influence of fire also raises questions and requires a comprehensive assessment of long-term effects on underground biodiversity, such as soil microbial communities and nutrient availability. Examining how fire shapes the functional traits of surviving trees and their connections to mother trees would provide a holistic understanding of ecosystem responses. This could involve implementing controlled burns, sustainable logging practices, and restoration efforts that encourage the recovery of mycorrhizal networks and the nutritional role of parent trees. Along the same line, the contributions of genetic engineering, biotechnology, and molecular research on mycorrhizal networks and the relationships with pre- and post-fire forests would help to understand their dynamics and the extent of the effect of fire in areas deeper underground to be able to act more promptly in the event of an incident of this type.

Author Contributions

Conceptualization, T.G.B., M.L.S. and N.S.; methodology, T.G.B.; validation, T.G.B.; formal analysis, T.G.B.; research, T.G.B.; resources, T.G.B.; data curation, T.G.B.; writing: preparation of the original draft, T.G.B.; writing: review and editing, T.G.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

No new data were created.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  1. Dar, J.A.; Subashree, K.; Bhat, N.A.; Sundarapandian, S.; Xu, M.; Saikia, P.; Khan, M.L. Role of Major Forest Biomes in Climate Change Mitigation: An Eco-biological Perspective. In Socio-Economic and Eco-Biological Dimensions in Resource Use and Conservation: Strategies for Sustainability; Springer International Publishing: Berlin, Germany, 2020; pp. 483–526. [Google Scholar]
  2. Watson, J.E.; Evans, T.; Venter, O.; Williams, B.; Tulloch, A.; Stewart, C.; Lindenmayer, D. The Exceptional Value of Intact Forest Ecosystems. Nat. Ecol. Evol. 2018, 2, 599–610. [Google Scholar] [CrossRef] [PubMed]
  3. Birdsey, R.; Pan, Y. Trends in management of the world’s forests and impacts on carbon stocks. For. Ecol. Manag. 2015, 355, 83–90. [Google Scholar] [CrossRef]
  4. Wang, J.; Sun, J.; Xia, J.; He, N.; Li, M.; Niu, S. Soil and Vegetation Carbon Turnover Times from Tropical to Boreal Forests. Funct. Ecol. 2018, 32, 71–82. [Google Scholar] [CrossRef]
  5. Chagnon, C.W.; Hagolani-Albov, S.E.; Hokkanen, S. Extractivism at Your Fingertips. In Our Extractive Age; Routledge: London, UK, 2021; pp. 176–188. [Google Scholar]
  6. Warnecke-Berger, H.; Burchardt, H.J.; Ouaissa, R. Natural Resources, Raw Materials, and Extractivism: The Dark Side of Sustainability. Extr. Policy Brief. 2022, 1, 1–8. [Google Scholar]
  7. Zhang, J.; Zhang, J. Soil Environmental Deterioration and Ecological Rehabilitation. In Study of Ecological Engineering of Human Settlements; Springer: Singapore, 2020; pp. 41–82. [Google Scholar]
  8. Wiekenkamp, I.; Huisman, J.A.; Bogena, H.R.; Vereecken, H. Effects of Deforestation on Water Flow in the Vadose Zone. Water 2019, 12, 35. [Google Scholar] [CrossRef]
  9. Arora, B.; Dwivedi, D.; Faybishenko, B.; Jana, R.B.; Wainwright, H.M. Understanding and Predicting Vadose Zone Processes. Rev. Mineral. Geochem. 2019, 85, 303–328. [Google Scholar] [CrossRef]
  10. Kyere-Boateng, R.; Marek, M.V. Analysis of the Social-Ecological Causes of Deforestation and Forest Degradation in Ghana: Application of the DPSIR Framework. Forests 2021, 12, 409. [Google Scholar] [CrossRef]
  11. Simard, S.W.; Roach, W.J.; Beauregard, J.; Burkart, J.; Cook, D.; Law, D.; Murphy-Steed, A.; Schacter, T.; Zickmantel, A.; Armstrong, G.; et al. Partial Retention of Legacy Trees Protect Mycorrhizal Inoculum Potential, Biodiversity, and Soil Resources While Promoting Natural Regeneration of Interior Douglas-Fir. Front. For. Glob. Change 2021, 3, 620436. [Google Scholar] [CrossRef]
  12. McCutcheon, J.P.; Lekberg, Y. Symbiosis: Fungi as Shrewd Trade Negotiators. Curr. Biol. 2019, 29, R570–R572. [Google Scholar] [CrossRef]
  13. Simard, S.; Perry, D.; Jones, M.; Myrold, D.D.; Durall, D.M.; Molina, R. Net transfer of carbon between ectomycorrhizal tree species in the field. Nature 1997, 388, 579–582. [Google Scholar] [CrossRef]
  14. Rhodes, S. Current Commentary the whispering world of plants: ‘The Wood Wide Web’. Sci. Progress 2017, 100, 331–337. [Google Scholar] [CrossRef]
  15. Wipf, D.; Krajinski, F.; van Tuinen, D.; Recorbet, G.; Courty, P.E. Trading on the arbuscular mycorrhiza mar-ket: From arbuscules to common mycorrhizal networks. New Phytol. 2019, 223, 1127–1142. [Google Scholar] [CrossRef] [PubMed]
  16. Ibarra, J.T.; Cockle, K.; Altamirano, T.; Van der Hoek, Y.; Simard, S.W.; Bonacic, C.; Martin, K. Nurturing resilient forest biodiversity: Nest webs as complex adaptive systems. Ecol. Soc. 2020, 25, 27. [Google Scholar] [CrossRef]
  17. Song, Y.; Simard, S.; Carroll, A.; Mohn, W.W.; Zeng, R.S. Defoliation of interior Douglas-fir elicits carbon transfer and stress signalling to ponderosa pine neighbors through ectomycorrhizal networks. Sci. Rep. 2015, 5, 8495. [Google Scholar] [CrossRef]
  18. Mildrexler, D.J.; Berner, L.T.; Law, B.E.; Birdsey, R.A.; Moomaw, W.R. Large Trees Dominate Carbon Storage in Forests East of the Cascade Crest in the United States Pacific Northwest. Front. For. Glob. Change 2020, 3, 594274. [Google Scholar] [CrossRef]
  19. Jansa, J.; Forczek, S.T.; Rozmoš, M.; Püschel, D.; Bukovská, P.; Hršelová, H. Arbuscular mycor-rhiza and soil organic nitrogen: Network of players and interactions. Chem. Bio-Log. Technol. Agric. 2019, 6, 10. [Google Scholar] [CrossRef]
  20. Korani, W.; Mouhoub, M.; Spiteri, R.J. Mother Tree Optimization. In Proceedings of the 2019 IEEE International Conference on Systems, Man and Cybernetics (SMC), Bari, Italy, 6–9 October 2019; IEEE: Piscataway, NJ, USA, 2019; pp. 2206–2213. [Google Scholar]
  21. Van Der Heijden, M.G.; De Bruin, S.; Luckerhoff, L.; Van Logtestijn, R.S.; Schlaeppi, K. A widespread plant-fungal-bacterial symbiosis promotes plant biodiversity, plant nutrition and seedling recruitment. ISME J. 2015, 10, 389–399. [Google Scholar] [CrossRef]
  22. Modi, D.; Simard, S.; Bérubé, J.; Lavkulich, L.; Hamelin, R.; Grayston, S.J. Long-Term Effects of Stump Removal and Tree Species Composition on the Diversity and Structure of Soil Fungal Communities. FEMS Microbiol. Ecol. 2020, 96, fiaa061. [Google Scholar] [CrossRef] [PubMed]
  23. Almario, J.; Fabiańska, I.; Saridis, G.; Bucher, M. Unearthing the plant-microbe quid pro quo in root associations with beneficial fungi. New Phytol. 2022, 234, 1967–1976. [Google Scholar] [CrossRef]
  24. Hawkins, B.; Jones, M.; Kranabetter, J. Ectomycorrhizae and tree seedling nitrogen nutrition in forest restoration. New For. 2015, 46, 747–771. [Google Scholar] [CrossRef]
  25. Griggs, K. Finding the Mother Tree: Discovering the Wisdom of the Forest. Nat. Areas J. 2022, 42, 161–162. [Google Scholar] [CrossRef]
  26. Henriksson, N.; Marshall, J.; Högberg, M.N.; Högberg, P.; Polle, A.; Franklin, O.; Näsholm, T. Re-examining the Evidence for the Mother Tree Hypothesis–Resource Sharing Among Trees via Ectomycorrhizal Networks. New Phytol. 2023, 239, 19–28. [Google Scholar] [CrossRef]
  27. Deng, M.; Hu, S.; Guo, L.; Jiang, L.; Huang, Y.; Schmid, B.; Liu, C.; Chang, P.; Li, S.; Liu, X.; et al. Tree mycorrhizal association types control biodiversity-productivity relationship in a subtropical forest. Sci. Adv. 2023, 9, eadd4468. [Google Scholar] [CrossRef]
  28. Simard, S.W.; Beiler, K.J.; Bingham, M.A.; Deslippe, J.R.; Philip, L.J.; Teste, F.P. Mycorrhizal networks: Mechanisms, ecology and modelling. Fungal Biol. Rev. 2012, 26, 39–60. [Google Scholar] [CrossRef]
  29. Deslippe, J.R.; Hart-mann, M.; Grayston, S.J.; Simard, S.W.; Mohn, W.W. Stable isotope probing impli-cates a species of Cortinarius in carbon transfer through ectomycorrhizal fungal myce-lial networks in Arctic tundra. New Phytol. 2016, 210, 383–390. [Google Scholar] [CrossRef]
  30. Figueiredo, A.; Boy, J.; Guggenberger, G. Common mycorrhizae network: A review of the theories and mechanisms behind underground interactions. Front. Fungal Biol. 2021, 2, 735299. [Google Scholar] [CrossRef]
  31. Castro-Delgado, A.L.; Elizondo-Mesén, S.; Valladares-Cruz, Y.; Rivera-Méndez, W. Wood Wide Web: Communication through the Mycorrhizal Network. Rev. Tecnol. Marcha 2020, 334, 114–125. [Google Scholar]
  32. Basiru, S.; Mhand, A.; Hijri, M. Disentangling arbuscular mycorrhizal fungi and bacteria at the soil-root interface. Mycorrhiza 2023, 33, 119–137. [Google Scholar] [CrossRef]
  33. Cao, B.F.; Jiang, H.X.; Liu, L.; Lu, Y.G.; Wang, M.S. Research progress on mechanism of arbuscular common mycorrhizal networks in plant-plant interactions. J. Appl. Ecol. 2021, 32, 3385–3396. [Google Scholar] [CrossRef]
  34. Wang, Y.; Zou, Y.N.; Shu, B.; Wu, Q.S. Deciphering Molecular Mechanisms Regarding Enhanced Drought Tolerance in Plants by Arbuscular Mycorrhizal Fungi. Sci. Hortic. 2023, 308, 111591. [Google Scholar] [CrossRef]
  35. Tedersoo, L.; Bahram, M. Mycorrhizal Types Differ in Ecophysiology and Alter Plant Nutrition and Soil Processes. Biol. Rev. 2019, 94, 1857–1880. [Google Scholar] [CrossRef] [PubMed]
  36. Limaho, H.S.; Sugiarto; Pramono, R.; Christiawan, R. The Need for Global Green Marketing for the Palm Oil Industry in Indonesia. Sustainability 2022, 14, 8621. [Google Scholar] [CrossRef]
  37. Kaempf, D. Coopetition in the Context of the Sustainability Goals: A Systematic Overview. Reg. Bus. Stud. 2022, 14, 47–61. [Google Scholar] [CrossRef]
  38. Cygler, J.; Sroka, W.; Solesvik, M.; Dębkowska, K. Benefits and Drawbacks of Coopetition: The Roles of Scope and Durability in Coopetitive Relationships. Sustainability 2018, 10, 2688. [Google Scholar] [CrossRef]
  39. Palit, K.; Rath, S.; Chatterjee, S.; Das, S. Microbial Diversity and Ecological Interactions of Microorganisms in the Mangrove Ecosystem: Threats, Vulnerability, and Adaptations. Environ. Sci. Pollut. Res. 2022, 29, 32467–32512. [Google Scholar] [CrossRef] [PubMed]
  40. Landi, P.; Minoarivelo, H.O.; Brännström, Å.; Hui, C.; Dieckmann, U. Complexity and Stability of Ecological Networks: A Review of the Theory. Popul. Ecol. 2018, 60, 319–345. [Google Scholar] [CrossRef]
  41. Powell, J.R.; Rillig, M.C. Biodiversity of Arbuscular Mycorrhizal Fungi and Ecosystem Function. New Phytol. 2018, 220, 1059–1075. [Google Scholar] [CrossRef]
  42. Saeidi, R. Quantitative and Qualitative Study to Identify the Latent Interactive Pattern Between Ecosystems. Int. J. Mech. Eng. 2022, 7, 1095–1103. [Google Scholar]
  43. Sommerfeld, A.; Senf, C.; Buma, B.; D’Amato, A.W.; Després, T.; Díaz-Hormazábal, I.; Seidl, R. Patterns and Drivers of Recent Disturbances Across the Temperate Forest Biome. Nat. Commun. 2018, 9, 4355. [Google Scholar] [CrossRef]
  44. Seidl, R.; Albrich, K.; Erb, K.; Formayer, H.; Leidinger, D.; Leitinger, G.; Rammer, W. What Drives the Future Supply of Regulating Ecosystem Services in a Mountain Forest Landscape? For. Ecol. Manag. 2019, 445, 37–47. [Google Scholar] [CrossRef]
  45. Senf, C.; Seidl, R. Mapping the Forest Disturbance Regimes of Europe. Nat. Sustain. 2021, 4, 63–70. [Google Scholar] [CrossRef]
  46. Davis, T.S.; Meddens, A.J.; Stevens-Rumann, C.S.; Jansen, V.S.; Sibold, J.S.; Battaglia, M.A. Monitoring Resistance and Resilience Using Carbon Trajectories: Analysis of Forest Management–Disturbance Interactions. Ecol. Appl. 2022, 32, e2704. [Google Scholar] [CrossRef] [PubMed]
  47. Seidl, R.; Turner, M.G. Post-disturbance Reorganization of Forest Ecosystems in a Changing World. Proc. Natl. Acad. Sci. USA 2022, 119, e2202190119. [Google Scholar] [CrossRef] [PubMed]
  48. Staal, A.; Fetzer, I.; Wang-Erlandsson, L.; Bosmans, J.H.; Dekker, S.C.; van Nes, E.H.; Tuinenburg, O.A. Hysteresis of Tropical Forests in the 21st Century. Nat. Commun. 2020, 11, 4978. [Google Scholar] [CrossRef] [PubMed]
  49. Albrich, K.; Rammer, W.; Seidl, R. Climate Change Causes Critical Transitions and Irreversible Alterations of Mountain Forests. Glob. Change Biol. 2020, 26, 4013–4027. [Google Scholar] [CrossRef] [PubMed]
  50. Prăvălie, R. Major Perturbations in the Earth’s Forest Ecosystems. Possible Implications for Global Warming. Earth-Sci. Rev. 2018, 185, 544–571. [Google Scholar] [CrossRef]
  51. Liu, J.; Coomes, D.A.; Gibson, L.; Hu, G.; Liu, J.; Luo, Y.; Yu, M. Forest Fragmentation in China and Its Effect on Biodiversity. Biol. Rev. 2019, 94, 1636–1657. [Google Scholar] [CrossRef] [PubMed]
  52. Turvey, S.T.; Crees, J.J. Extinction in the Anthropocene. Curr. Biol. 2019, 29, R982–R986. [Google Scholar] [CrossRef] [PubMed]
  53. Ayram, C.A.C.; Etter, A.; Díaz-Timoté, J.; Buriticá, S.R.; Ramírez, W.; Corzo, G. Spatiotemporal Evaluation of the Human Footprint in Colombia: Four Decades of Anthropic Impact in Highly Biodiverse Ecosystems. Ecol. Indic. 2020, 117, 106630. [Google Scholar] [CrossRef]
  54. Chazdon, R.L. Second Growth: The Promise of Tropical Forest Regeneration in an Age of Deforestation; University of Chicago Press: Chicago, IL, USA, 2019. [Google Scholar]
  55. McLauchlan, K.K.; Higuera, P.E.; Miesel, J.; Rogers, B.M.; Schweitzer, J.; Shuman, J.K.; Watts, A.C. Fire as a Fundamental Ecological Process: Research Advances and Frontiers. J. Ecol. 2020, 108, 2047–2069. [Google Scholar] [CrossRef]
  56. Cumming, G.S.; Allen, C.R. Protected Areas as Social-Ecological Systems: Perspectives from Resilience and Social-Ecological Systems Theory. Ecol. Appl. 2017, 27, 1709–1717. [Google Scholar] [CrossRef] [PubMed]
  57. Bas, T.G.; Gagnon, J.; Gagnon, P.; Contreras, A. Analysis of Agro Alternatives to Boost Cameroon’s Socio-Environmental Resilience, Sustainable Development, and Conservation of Native Forests. Sustainability 2022, 14, 8507. [Google Scholar] [CrossRef]
  58. Adams, D.; Adams, K.; Ullah, S.; Ullah, F. Globalisation, Governance, Accountability and the Natural Resource ‘Curse’: Implications for Socio-Economic Growth of Oil-Rich Developing Countries. Resour. Policy 2019, 61, 128–140. [Google Scholar] [CrossRef]
  59. Brancalion, P.H.; De Almeida, D.R.; Vidal, E.; Molin, P.G.; Sontag, V.E.; Souza, S.E.; Schulze, M.D. Fake Legal Logging in the Brazilian Amazon. Sci. Adv. 2018, 4, eaat1192. [Google Scholar] [CrossRef] [PubMed]
  60. Duguma, L.A.; Atela, J.; Minang, P.A.; Ayana, A.N.; Gizachew, B.; Nzyoka, J.M.; Bernard, F. Deforestation and Forest Degradation as an Environmental Behavior: Unpacking Realities Shaping Community Actions. Land 2019, 8, 26. [Google Scholar] [CrossRef]
  61. Kahler, J.S.; Rivera, J.W.; Steele, Z.T. Advancing Applied Research in Conservation Criminology through the Evaluation of Corruption Prevention, Enhancing Compliance, and Reducing Recidivism. Front. Conserv. Sci. 2021, 2, 698755. [Google Scholar] [CrossRef]
  62. Ehrnström-Fuentes, M. Confronting Extractivism–The Role of Local Struggles in the (Un) Making of Place. Crit. Perspect. Int. Bus. 2022, 18, 50–73. [Google Scholar] [CrossRef]
  63. Wynn, G. Forests, Frontiers, and Extractivism. Environ. Hist. 2023, 28, 640–655. [Google Scholar] [CrossRef]
  64. Andrade, D. Neoliberal Extractivism: Brazil in the Twenty-First Century. J. Peasant. Stud. 2022, 49, 793–816. [Google Scholar] [CrossRef]
  65. Grégoire, E.R.; Hatcher, P. Global Extractivism and Inequality. In The Routledge Handbook of Global Development; Routledge: London, UK, 2022; pp. 341–350. [Google Scholar]
  66. Chagnon, C.W.; Durante, F.; Gills, B.K. From Extractivism to Global Extractivism: The Evolution of an Organizing Concept. J. Peasant. Stud. 2022, 49, 760–792. [Google Scholar] [CrossRef]
  67. Walker, R.T.; Simmons, C.; Arima, E.; Galvan-Miyoshi, Y.; Antunes, A.; Waylen, M.; Irigaray, M. Avoiding Amazonian Catastrophes: Prospects for Conservation in the 21st Century. One Earth 2019, 1, 202–215. [Google Scholar] [CrossRef]
  68. Orihuela, J.C.; Cavero, C.P.; Contreras, C. Extractivism of the Poor: Natural Resource Commodification and Its Discontents. Extr. Ind. Soc. 2022, 9, 100986. [Google Scholar] [CrossRef]
  69. Nygren, A.; Kröger, M.; Gills, B. Global Extractivisms and Transformative Alternatives. J. Peasant. Stud. 2022, 49, 734–759. [Google Scholar] [CrossRef]
  70. Gudynas, E. Extractivisms: Tendencies and Consequences. In Reframing Latin American Development; Routledge: London, UK, 2018; pp. 61–76. [Google Scholar]
  71. Barros, M.V.; Salvador, R.; do Prado, G.F.; de Francisco, A.C.; Piekarski, C.M. Circular Economy as a Driver to Sustainable Businesses. Clean. Environ. Syst. 2021, 2, 100006. [Google Scholar] [CrossRef]
  72. Gusenbauer, M.; Haddaway, N.R. Which Academic Search Systems Are Suitable for Systematic Reviews or Meta-Analyses? Evaluating Retrieval Qualities of Google Scholar, PubMed, and 26 Other Resources. Res. Synth. Methods 2020, 11, 181–217. [Google Scholar] [CrossRef]
  73. Scells, H.; Zuccon, G.; Koopman, B.; Clark, J. Automatic Boolean Query Formulation for Systematic Review Literature Search. In Proceedings of the Web Conference 2020, Taipei, Taiwan, 20–24 April 2020; pp. 1071–1081. [Google Scholar]
  74. Scells, H.; Zuccon, G.; Koopman, B. A Comparison of Automatic Boolean Query Formulation for Systematic Reviews. Inf. Retr. J. 2021, 24, 3–28. [Google Scholar] [CrossRef]
  75. Bas, T.G.; Fariña, R.; Gallardo, F.; Vilches, M. Economic–Financial Assessment of Seawater Desalination Plants in Northern Chile to Reduce Hydric Scarcity and a Proposal for the Environmental and Sustainable Use of Brine Waste by Cultivating the Microalga Dunaliella salina to Produce β-Carotene. Processes 2023, 11, 1668. [Google Scholar] [CrossRef]
  76. Lashkari, F.; Ensan, F.; Bagheri, E.; Ghorbani, A.A. Efficient Indexing for Semantic Search. Expert. Syst. Appl. 2017, 73, 92–114. [Google Scholar] [CrossRef]
  77. Ali, A. Forest Stand Structure and Functioning: Current Knowledge and Future Challenges. Ecol. Indic. 2019, 98, 665–677. [Google Scholar] [CrossRef]
  78. Ameray, A.; Bergeron, Y.; Valeria, O.; Montoro Girona, M.; Cavard, X. Forest Carbon Management: A Review of Silvicultural Practices and Management Strategies Across Boreal, Temperate and Tropical Forests. Curr. For. Rep. 2021, 7, 245–266. [Google Scholar] [CrossRef]
  79. Derrien, D.; Barré, P.; Basile-Doelsch, I.; Cécillon, L.; Chabbi, A.; Crème, A.; Fontaine, S.; Henneron, L.; Janot, N.; Lashermes, G.; et al. Current controversies on mechanisms controlling soil carbon storage: Implications for interactions with practitioners and policy-makers: A review. Agron. Sustain. Dev. 2023, 43, 21. [Google Scholar] [CrossRef]
  80. Abbas, S.; Wong, M.S.; Wu, J.; Shahzad, N.; Muhammad Irteza, S. Approaches of Satellite Remote Sensing for the Assessment of Above-ground Biomass Across Tropical Forests: Pan-tropical to National Scales. Remote Sens. 2020, 12, 3351. [Google Scholar] [CrossRef]
  81. Liu, X.; Trogisch, S.; He, J.S.; Niklaus, P.A.; Bruelheide, H.; Tang, Z.; Ma, K. Tree Species Richness Increases Ecosystem Carbon Storage in Subtropical Forests. Proc. R. Soc. B 2018, 285, 20181240. [Google Scholar] [CrossRef] [PubMed]
  82. Webster, C.R.; Dickinson, Y.L.; Burton, J.I.; Frelich, L.E.; Jenkins, M.A.; Kern, C.C.; Willis, J.L. Promoting and Maintaining Diversity in Contemporary Hardwood Forests: Confronting Contemporary Drivers of Change and the Loss of Ecological Memory. For. Ecol. Manag. 2018, 421, 98–108. [Google Scholar] [CrossRef]
  83. Halofsky, J.S.; Donato, D.C.; Franklin, J.F.; Halofsky, J.E.; Peterson, D.L.; Harvey, B.J. The Nature of the Beast: Examining Climate Adaptation Options in Forests with Stand-Replacing Fire Regimes. Ecosphere 2018, 9, e02140. [Google Scholar] [CrossRef]
  84. Mina, M.; Messier, C.; Duveneck, M.; Fortin, M.J.; Aquilué, N. Network Analysis Can Guide Resilience-Based Management in Forest Landscapes Under Global Change. Ecol. Appl. 2021, 31, e2221. [Google Scholar] [CrossRef] [PubMed]
  85. Ibáñez, I.; Acharya, K.; Juno, E.; Karounos, C.; Lee, B.R.; McCollum, C.; Tourville, J. Forest Resilience Under Global Environmental Change: Do We Have the Information We Need? A Systematic Review. PLoS ONE 2019, 14, e0222207. [Google Scholar] [CrossRef] [PubMed]
  86. Isabel, N.; Holliday, J.A.; Aitken, S.N. Forest Genomics: Advancing Climate Adaptation, Forest Health, Productivity, and Conservation. Evol. Appl. 2020, 13, 3–10. [Google Scholar] [CrossRef]
  87. Fujii, K.; Shibata, M.; Kitajima, K.; Ichie, T.; Kitayama, K.; Turner, B.L. Plant–Soil Interactions Maintain Biodiversity and Functions of Tropical Forest Ecosystems. Ecol. Res. 2018, 33, 149–160. [Google Scholar] [CrossRef]
  88. Meakem, V.; Tepley, A.J.; Gonzalez-Akre, E.B.; Herrmann, V.; Muller-Landau, H.C.; Wright, S.J.; Anderson-Teixeira, K.J. Role of Tree Size in Moist Tropical Forest Carbon Cycling and Water Deficit Responses. New Phytol. 2018, 219, 947–958. [Google Scholar] [CrossRef]
  89. Ribeiro, K.; Pacheco, F.S.; Ferreira, J.W.; de Sousa-Neto, E.R.; Hastie, A.; Krieger Filho, G.C.; Ometto, J.P. Tropical Peatlands and Their Contribution to the Global Carbon Cycle and Climate Change. Glob. Change Biol. 2021, 27, 489–505. [Google Scholar] [CrossRef]
  90. Arora, N.K. Biodiversity Conservation for Sustainable Future. Environ. Sustain. 2018, 1, 109–111. [Google Scholar] [CrossRef]
  91. Rajpar, M.N. Tropical Forests Are an Ideal Habitat for Wide Array of Wildlife Species. In Tropical Forests—New Edition; IntechOpen: London, UK, 2018; p. 37. [Google Scholar]
  92. Borma, L.S.; Costa, M.H.; da Rocha, H.R.; Arieira, J.; Nascimento, N.C.C.; Jaramillo-Giraldo, C.; Nobre, C.A. Beyond Carbon: The Contributions of South American Tropical Humid and Subhumid Forests to Ecosystem Services. Rev. Geophys. 2022, 60, e2021RG000766. [Google Scholar] [CrossRef]
  93. Réjou-Méchain, M.; Mortier, F.; Bastin, J.F.; Cornu, G.; Barbier, N.; Bayol, N.; Gourlet-Fleury, S. Unveiling African Rainforest Composition and Vulnerability to Global Change. Nature 2021, 593, 90–94. [Google Scholar] [CrossRef]
  94. Seo, S.N.; Seo, S.N. Giving Forests: A Tale of Amazon Rainforests and Congo River Forests. In Climate Change and Economics: Engaging with Future Generations with Action Plans; Palgrave Macmillan: Cham, Switzerland, 2021; pp. 43–61. [Google Scholar]
  95. Lindberg, K.; Martvall, A.; Lima, M.G.B.; Franca, C.S. Herbal Medicine Promotion for a Restorative Bioeconomy in Tropical Forests: A Reality Check on the Brazilian Amazon. For. Policy Econ. 2023, 155, 103058. [Google Scholar] [CrossRef]
  96. Neudert, R.; Ganzhorn, J.U.; Waetzold, F. Global Benefits and Local Costs–The Dilemma of Tropical Forest Conservation: A Review of the Situation in Madagascar. Environ. Conserv. 2017, 44, 82–96. [Google Scholar] [CrossRef]
  97. Delbanco, A.S.; Burgess, N.D.; Cuni-Sanchez, A. Medicinal Plant Trade in Northern Kenya: Economic Importance, Uses, and Origin. Econ. Bot. 2017, 71, 13–31. [Google Scholar] [CrossRef]
  98. Ashton, P.; Zhu, H. The Tropical-Subtropical Evergreen Forest Transition in East Asia: An Exploration. Plant Divers. 2020, 42, 255–280. [Google Scholar] [CrossRef]
  99. Loidi, J.; Navarro-Sánchez, G.; Vynokurov, D. Climatic Definitions of the World’s Terrestrial Biomes. Veg. Classif. Surv. 2022, 3, 231–271. [Google Scholar] [CrossRef]
  100. Sommer, B.; Beger, M.; Harrison, P.L.; Babcock, R.C.; Pandolfi, J.M. Differential Response to Abiotic Stress Controls Species Distributions at Biogeographic Transition Zones. Ecography 2018, 41, 478–490. [Google Scholar] [CrossRef]
  101. Ge, J.; Xie, Z. Geographical and Climatic Gradients of Evergreen Versus Deciduous Broad-Leaved Tree Species in Subtropical China: Implications for the Definition of the Mixed Forest. Ecol. Evol. 2017, 7, 3636–3644. [Google Scholar] [CrossRef] [PubMed]
  102. Usinowicz, J.; Chang-Yang, C.H.; Chen, Y.Y.; Clark, J.S.; Fletcher, C.; Garwood, N.C.; Wright, S.J. Temporal Coexistence Mechanisms Contribute to the Latitudinal Gradient in Forest Diversity. Nature 2017, 550, 105–108. [Google Scholar] [PubMed]
  103. Schnabel, F.; Liu, X.; Kunz, M.; Barry, K.E.; Bongers, F.J.; Bruelheide, H.; Wirth, C. Species Richness Stabilizes Productivity via Asynchrony and Drought-Tolerance Diversity in a Large-Scale Tree Biodiversity Experiment. Sci. Adv. 2021, 7, eabk1643. [Google Scholar] [CrossRef] [PubMed]
  104. De Lombaerde, E.; Vangansbeke, P.; Lenoir, J.; Van Meerbeek, K.; Lembrechts, J.; Rodríguez-Sánchez, F.; De Frenne, P. Maintaining Forest Cover to Enhance Temperature Buffering Under Future Climate Change. Sci. Total Environ. 2022, 810, 151338. [Google Scholar] [CrossRef] [PubMed]
  105. Kennedy, P.G.; Walker, J.K.; Bogar, L.M. Interspecific Mycorrhizal Networks and Non-Networking Hosts: Exploring the Ecology of the Host Genus Alnus. In Mycorrhizal Networks; Springer: Dordrecht, The Netherlands, 2015; pp. 227–254. [Google Scholar]
  106. Kahle, H. Response of Roots of Trees to Heavy Metals. Environ. Exp. Bot. 1993, 33, 99–119. [Google Scholar] [CrossRef]
  107. Chen, H.; Renault, S.; Markham, J. The Effect of Frankia and Multiple Ectomycorrhizal Fungi Species on Alnus Growing in Low Fertility Soil. Symbiosis 2020, 80, 207–215. [Google Scholar] [CrossRef]
  108. Grover, M.; Maheswari, M.; Desai, S.; Gopinath, K.A.; Venkateswarlu, B. Elevated CO2: Plant Associated Microorganisms and Carbon Sequestration. Appl. Soil Ecol. 2015, 95, 73–85. [Google Scholar] [CrossRef]
  109. Ouyang, S.; Xiang, W.; Gou, M.; Chen, L.; Lei, P.; Xiao, W.; Forrester, D.I. Stability in Subtropical Forests: The Role of Tree Species Diversity, Stand Structure, Environmental and Socio-Economic Conditions. Glob. Ecol. Biogeogr. 2021, 30, 500–513. [Google Scholar] [CrossRef]
  110. Li, X.C.; Qian, X.; Gao, C.; Seitz, S.; Scholten, T.; Wang, Y.L.; Guo, L.D. Plant Identity Strongly Structures the Root-Associated Fungal Community in a Diverse Subtropical Forest. Basic. Appl. Ecol. 2021, 55, 98–109. [Google Scholar] [CrossRef]
  111. Triviño, M.; Potterf, M.; Tijerín, J.; Ruiz-Benito, P.; Burgas, D.; Eyvindson, K.; Duflot, R. Enhancing Resilience of Boreal Forests Through Management Under Global Change: A Review. Curr. Landsc. Ecol. Rep. 2023, 8, 103–118. [Google Scholar] [CrossRef]
  112. Thiffault, E. Boreal Forests and Soils. In Developments in Soil Science; Elsevier: Amsterdam, The Netherlands, 2019; Volume 36, pp. 59–82. [Google Scholar]
  113. Hessburg, P.F.; Miller, C.L.; Parks, S.A.; Povak, N.A.; Taylor, A.H.; Higuera, P.E.; Salter, R.B. Climate, Environment, and Disturbance History Govern Resilience of Western North American Forests. Front. Ecol. Evol. 2019, 7, 239. [Google Scholar] [CrossRef]
  114. Montesano, P.M.; Neigh, C.S.; Macander, M.; Feng, M.; Noojipady, P. The Bioclimatic Extent and Pattern of the Cold Edge of the Boreal Forest: The Circumpolar Taiga-Tundra Ecotone. Environ. Res. Lett. 2020, 15, 105019. [Google Scholar] [CrossRef]
  115. Chang, C.Y.; Bräutigam, K.; Hüner, N.P.A.; Ensminger, I. Champions of winter survival: Cold acclimation and molecular regulation of cold hardiness in evergreen conifers. New Phytol. 2020, 229, 675–691. [Google Scholar] [CrossRef]
  116. Olnest, J.; Kielland, K. Asynchronous Recruitment Dynamics of Snowshoe Hares and White Spruce in a Boreal Forest. For. Ecol. Manag. 2017, 384, 83–91. [Google Scholar] [CrossRef]
  117. Pukkala, T. Effect of species composition on ecosystem services in European boreal forest. J. For. Res. 2017, 29, 261–272. [Google Scholar] [CrossRef]
  118. Kayes, I.; Mallik, A. Boreal Forests: Distributions, Biodiversity, and Management. In Life on Land; Springer: Cham, Switzerland, 2020; pp. 1–12. [Google Scholar]
  119. Sullivan, T.P.; Sullivan, D.S. Influence of Nitrogen Fertilization on Abundance and Diversity of Plants and Animals in Temperate and Boreal Forests. Environ. Rev. 2018, 26, 26–42. [Google Scholar]
  120. Kolomyts, E.G. Predictive Modelling of Boreal Forest Resources in Regulation of the Carbon Cycle and Mitigation of the Global Warming. Int. J. Glob. Warm. 2022, 27, 333–364. [Google Scholar] [CrossRef]
  121. Watson, J.; Shanahan, D.F.; Di Marco, M.; Allan, J.; Laurance, W.F.; Sanderson, E.W.; Mackey, B.; Venter, O. Catastrophic Declines in Wilderness Areas Undermine Global Environment Targets. Curr. Biol. 2016, 26, 2929–2934. [Google Scholar] [CrossRef]
  122. Betts, M.G.; Wolf, C.; Ripple, W.J.; Phalan, B.; Millers, K.A.; Duarte, A.; Butchart, S.H.M.; Levi, T. Global forest loss disproportionately erodes biodiversity in intact landscapes. Nature 2017, 547, 441–444. [Google Scholar] [CrossRef] [PubMed]
  123. Daskalova, G.; Myers-Smith, I.; Bjorkman, A.; Blowes, S.; Supp, S.R.; Magurran, A.E.; Dornelas, M. Landscape-scale forest loss as a catalyst of population and biodiversity change. Science 2020, 368, 1341–1347. [Google Scholar] [CrossRef]
  124. Leal, A.; Benchimol, M.; Costa, H.; Faria, C.; Cazetta, E. Impacts of landscape-scale forest loss and a dry event on the demographic structure of the endangered palm Euterpe edulis Mart. in the Atlantic Forest. Front. For. Glob. Change 2022, 5, 909901. [Google Scholar] [CrossRef]
  125. Lawrence, D.; Coe, M.; Walker, W.; Verchot, L.; Vandecar, K. The Unseen Effects of Deforestation: Biophysical Effects on Climate. Front. For. Glob. Change 2022, 5, 75611. [Google Scholar] [CrossRef]
  126. Lämås, T.; Sandström, E.; Jonzén, J.; Olsson, H.; Gustafsson, L. Tree retention practices in boreal forests: What kind of future landscapes are we creating? Scand. J. For. Res. 2015, 30, 526–537. [Google Scholar] [CrossRef]
  127. Tremblay, J.A.; Savard, J.-P.; Ibarzabal, J. Structural retention requirements for a key ecosystem engineer in conifer-dominated stands of a boreal managed landscape in eastern Canada. For. Ecol. Manag. 2015, 357, 220–227. [Google Scholar] [CrossRef]
  128. Torsten, K.; Tilker, A. How the loss of forest fauna undermines the achievement of the SDGs. Ambio 2021, 51, 103–113. [Google Scholar]
  129. Rivers, M.; Newton, A.C.; Oldfield, S. Scientists’ warning to humanity on tree extinctions. Plants People Planet 2022, 5, 466–482. [Google Scholar] [CrossRef]
  130. Teshome, D.T.; Zharare, G.E.; Naidoo, S. The Threat of the Combined Effect of Biotic and Abiotic Stress Factors in Forestry Under a Changing Climate. Front. Plant Sci. 2020, 11, 601009. [Google Scholar] [CrossRef] [PubMed]
  131. Zeb, A.; Hamann, A.; Armstrong, G.W.; Acuna-Castellanos, D. Identifying Local Actors of Deforestation and Forest Degradation in the Kalasha Valleys of Pakistan. For. Policy Econ. 2019, 104, 56–64. [Google Scholar] [CrossRef]
  132. Hargita, Y.; Giessen, L.; Günter, S. Similarities and Differences Between International REDD+ and Transnational Deforestation-Free Supply Chain Initiatives—A Review. Sustainability 2020, 12, 896. [Google Scholar] [CrossRef]
  133. Fischer, R.; Giessen, L.; Günter, S. Governance Effects on Deforestation in the Tropics: A Review of the Evidence. Environ. Sci. Policy 2020, 105, 84–101. [Google Scholar] [CrossRef]
  134. Aleixandre-Benavent, R.; Aleixandre-Tudó, J.L.; Castelló-Cogollos, L.; Aleixandre, J.L. Trends in Global Research in Deforestation. A Bibliometric Analysis. Land Use Policy 2018, 72, 293–302. [Google Scholar] [CrossRef]
  135. Zambrano-Monserrate, M.A.; Carvajal-Lara, C.; Urgilés-Sanchez, R.; Ruano, M.A. Deforestation as an Indicator of Environmental Degradation: Analysis of Five European Countries. Ecol. Indic. 2018, 90, 1–8. [Google Scholar] [CrossRef]
  136. Curtis, P.G.; Slay, C.M.; Harris, N.L.; Tyukavina, A.; Hansen, M.C. Classifying Drivers of Global Forest Loss. Science 2018, 361, 1108–1111. [Google Scholar] [CrossRef]
  137. Brown, K.; Pearce, D.W. (Eds.) The Causes of Tropical Deforestation: The Economic and Statistical Analysis of Factors Giving Rise to the Loss of the Tropical Forests; Taylor & Francis: Abingdon, UK, 2023. [Google Scholar]
  138. Gao, Y.; Skutsch, M.; Paneque-Gálvez, J.; Ghilardi, A. Remote Sensing of Forest Degradation: A Review. Environ. Res. Lett. 2020, 15, 103001. [Google Scholar] [CrossRef]
  139. Houghton, R.A.; Nassikas, A.A. Negative Emissions from Stopping Deforestation and Forest Degradation, Globally. Glob. Change Biol. 2018, 24, 350–359. [Google Scholar] [CrossRef] [PubMed]
  140. Caballero Espejo, J.; Messinger, M.; Román-Dañobeytia, F.; Ascorra, C.; Fernandez, L.E.; Silman, M. Deforestation and Forest Degradation Due to Gold Mining in the Peruvian Amazon: A 34-Year Perspective. Remote Sens. 2018, 10, 1903. [Google Scholar] [CrossRef]
  141. Thorn, S.; Seibold, S.; Leverkus, A.B. The Living Dead: Acknowledging Life After Tree Death to Stop Forest Degradation. Front. Ecol. Environ. 2020, 18, 505–512. [Google Scholar] [CrossRef]
  142. Sukhbaatar, G.; Purevragchaa, B.; Ganbaatar, B.; Tseveen, B. Deforestation and Degradation of Forests in the Khustai Nuruu Mountains of Northern Mongolia. Sib. J. For. Sci. 2021, 62, 53–63. [Google Scholar]
  143. Ritchie, H. “Not All Forest Loss Is Equal: What Is the Difference Between Deforestation and Forest Degradation?”. 2021. Available online: https://ourworldindata.org/deforestation (accessed on 4 August 2023).
  144. Billings, S.A.; Hirmas, D.; Sullivan, P.L.; Lehmeier, C.A.; Bagchi, S.; Min, K.; Brecheisen, Z.; Hauser, E.; Stair, R.; Flournoy, R.; et al. Loss of Deep Roots Limits Biogenic Agents of Soil Development That Are Only Partially Restored by Decades of Forest Regeneration. Elem. Sci. Anth 2018, 6, 34. [Google Scholar] [CrossRef]
  145. Galatowitsch, S.; Bohnen, J. Predicting Restoration Outcomes Based on Organizational and Ecological Factors. Restor. Ecol. 2020, 28, 1201–1212. [Google Scholar] [CrossRef]
  146. Flores, B.M.; Staal, A.; Jakovac, C.C.; Hirota, M.; Holmgren, M.; Oliveira, R.S. Soil Erosion as a Resilience Drain in Disturbed Tropical Forests. Plant Soil. 2020, 450, 11–25. [Google Scholar] [CrossRef]
  147. Lin, H.; Chen, Y.; Song, Q.; Fu, P.; Cleverly, J.; Magliulo, V.; Fan, Z. Quantifying Deforestation and Forest Degradation with Thermal Response. Sci. Total Environ. 2017, 607, 1286–1292. [Google Scholar] [CrossRef] [PubMed]
  148. Huang, Y.; Chen, Y.; Castro-Izaguirre, N.; Baruffol, M.; Brezzi, M.; Lang, A.; Schmid, B. Impacts of Species Richness on Productivity in a Large-Scale Subtropical Forest Experiment. Science 2018, 362, 80–83. [Google Scholar] [CrossRef] [PubMed]
  149. Baumann, M.; Israel, C.; Piquer-Rodríguez, M.; Gavier-Pizarro, G.; Volante, J.N.; Kuemmerle, T. Deforestation and Cattle Expansion in the Paraguayan Chaco 1987–2012. Reg. Environ. Change 2017, 17, 1179–1191. [Google Scholar] [CrossRef]
  150. Ma, J.; Li, J.; Wu, W. Global Forest Fragmentation Change from 2000 to 2020. Nat. Commun. 2023, 14, 3752. [Google Scholar] [CrossRef] [PubMed]
  151. Tyukavina, A.; Potapov, P.; Hansen, M.C.; Pickens, A.H.; Stehman, S.V.; Turubanova, S.; Parker, D.; Zalles, V.; Lima, A.; Kommareddy, I.; et al. Global Trends of Forest Loss Due to Fire From 2001 to 2019. Front. Remote Sens. 2022, 3, 825190. [Google Scholar] [CrossRef]
  152. Willis, K.J.; Petrokofsky, G. The Natural Capital of City Trees. Science 2017, 356, 374–376. [Google Scholar] [CrossRef]
  153. Hein, L.; Bagstad, K.J.; Obst, C.; Edens, B.; Schenau, S.; Castillo, J.; Barton, D.N.; Bass, S. Progress in Natural Capital Accounting for Ecosystems. Science 2020, 367, 514–515. [Google Scholar] [CrossRef] [PubMed]
  154. Kinda, H.; Thiombiano, N. The Effects of Extractive Industries Rent on Deforestation in Developing Countries. Resour. Policy 2021, 73, 102203. [Google Scholar] [CrossRef]
  155. Schrecker, T.; Birn, A.E.; Aguilera, M. How Extractive Industries Affect Health: Political Economy Underpinnings and Pathways. Health Place 2018, 52, 135–147. [Google Scholar] [CrossRef]
  156. Grantham, H.S.; Tibaldeschi, P.; Izquierdo, P.; Mo, K.; Patterson, D.J.; Rainey, H.; Segan, D.B.; Hole, D.G.; Brooks, T.M.; Butchart, S.H.M.; et al. The Emerging Threat of Extractives Sector to Intact Forest Landscapes. Front. For. Glob. Change 2021, 4, 692338. [Google Scholar] [CrossRef]
  157. Hund, K.; Schure, J.; Van der Goes, A. Extractive Industries in Forest Landscapes: Options for Synergy with REDD+ and Development of Standards in the Democratic Republic of Congo. Resour. Policy 2017, 54, 97–108. [Google Scholar] [CrossRef]
  158. Pendrill, F.; Persson, U.M.; Godar, J.; Kastner, T. Deforestation Displaced: Trade in Forest-Risk Commodities and the Prospects for a Global Forest Transition. Environ. Res. Lett. 2019, 14, 055003. [Google Scholar] [CrossRef]
  159. Weisse, M.; Goldman, E.D. We Lost a Football Pitch of Primary Rainforest Every 6 Seconds in 2019. Available online: https://www.wri.org/insights/we-lost-football-pitch-primary-rainforest-every-6-seconds-2019 (accessed on 4 August 2023).
  160. Hirons, M. How the Sustainable Development Goals Risk Undermining Efforts to Address Environmental and Social Issues in the Small-Scale Mining Sector. Environ. Sci. Policy 2020, 114, 321–328. [Google Scholar] [CrossRef]
  161. González-González, A.; Clerici, N.; Quesada, B. Growing Mining Contribution to Colombian Deforestation. Environ. Res. Lett. 2021, 16, 064046. [Google Scholar] [CrossRef]
  162. Giljum, S.; Maus, V.; Kuschnig, N.; Luckeneder, S.; Tost, M.; Sonter, L.J.; Bebbington, A.J. A Pantropical Assessment of Deforestation Caused by Industrial Mining. Proc. Natl. Acad. Sci. USA 2022, 119, e2118273119. [Google Scholar] [CrossRef] [PubMed]
  163. Bruna, N. A Climate-Smart World and the Rise of Green Extractivism. J. Peasant Stud. 2022, 49, 839–864. [Google Scholar] [CrossRef]
  164. Ye, J.; van der Ploeg, J.D.; Schneider, S.; Shanin, T. The Incursions of Extractivism: Moving from Dispersed Places to Global Capitalism. J. Peasant Stud. 2020, 47, 155–183. [Google Scholar] [CrossRef]
  165. Burchardt, H.J.; Dietz, K.; Warnecke-Berger, H. Dependency, Rent, and the Failure of Neo-Extractivism. In Dependent Capitalisms in Contemporary Latin America and Europe; Palgrave Macmillan: Cham, Switzerland, 2021; pp. 207–229. [Google Scholar]
  166. Smart, S. The Political Economy of Latin American Conflicts Over Mining Extractivism. Extr. Ind. Soc. 2020, 7, 767–779. [Google Scholar] [CrossRef]
  167. MacKenzie, C.A. Risk, Reciprocity and Retribution: Choosing to Extract Resources from a Protected Area. Ecol. Econ. 2018, 143, 314–323. [Google Scholar] [CrossRef]
  168. Raftopoulos, M.; Morley, J. Ecocide in the Amazon: The Contested Politics of Environmental Rights in Brazil. Int. J. Hum. Rights 2020, 24, 1616–1641. [Google Scholar] [CrossRef]
  169. Nikinmaa, L.; Lindner, M.; Cantarello, E.; Jump, A.S.; Seidl, R.; Winkel, G.; Muys, B. Reviewing the Use of Resilience Concepts in Forest Sciences. Curr. For. Rep. 2020, 6, 61–80. [Google Scholar] [CrossRef] [PubMed]
  170. Sage, R.F. Global Change Biology: A Primer. Glob. Change Biol. 2020, 26, 3–30. [Google Scholar] [CrossRef] [PubMed]
  171. Falk, D.A.; van Mantgem, P.J.; Keeley, J.E.; Gregg, R.M.; Guiterman, C.H.; Tepley, A.J.; Marshall, L.A. Mechanisms of Forest Resilience. For. Ecol. Manag. 2022, 512, 120129. [Google Scholar] [CrossRef]
  172. Biesbroek, R.; Dupuis, J.; Wellstead, A. Explaining Through Causal Mechanisms: Resilience and Governance of Social–Ecological Systems. Curr. Opin. Environ. Sustain. 2017, 28, 64–70. [Google Scholar] [CrossRef]
  173. Ungar, M. Systemic Resilience. Ecol. Soc. 2018, 23, 34. [Google Scholar] [CrossRef]
  174. Mori, A.S.; Lertzman, K.P.; Gustafsson, L. Biodiversity and Ecosystem Services in Forest Ecosystems: A Research Agenda for Applied Forest Ecology. J. Appl. Ecol. 2017, 54, 12–27. [Google Scholar] [CrossRef]
  175. Grafton, R.Q.; Doyen, L.; Béné, C.; Borgomeo, E.; Brooks, K.; Chu, L.; Wyrwoll, P.R. Realizing Resilience for Decision-Making. Nat. Sustain. 2019, 2, 907–913. [Google Scholar] [CrossRef]
  176. Hayes, S.; Desha, C.; Burke, M.; Gibbs, M.; Chester, M. Leveraging Socio-Ecological Resilience Theory to Build Climate Resilience in Transport Infrastructure. Transp. Rev. 2019, 39, 677–699. [Google Scholar] [CrossRef]
  177. Holling, C.S. Resilience and Stability of Ecological Systems. Annu. Rev. Ecol. Syst. 1973, 4, 1–23. [Google Scholar] [CrossRef]
  178. Ayala-Orozco, B.; Gavito, M.E.; Mora, F.; Siddique, I.; Balvanera, P.; Jaramillo, V.J.; Martínez-Meyer, E. Resilience of Soil Properties to Land-Use Change in a Tropical Dry Forest Ecosystem. Land Degrad. Dev. 2018, 29, 315–325. [Google Scholar] [CrossRef]
  179. Clemmensen, K.; Bahr, A.; Ovaskainen, O.; Dahlberg, A.; Ekblad, A.; Wallander, H.; Stenlid, J.; Finlay, R.D.; Wardle, D.; Lindahl, B.D. Roots and associated fungi drive longterm carbon sequestration in boreal forest. Science 2013, 339, 1615–1618. [Google Scholar] [CrossRef] [PubMed]
  180. Lau, J.A.; Lennon, J.T. Rapid responses of soil microorganisms improve plant fitness in novel environments. Proc. Natl. Acad. Sci. USA 2012, 109, 14058–14062. [Google Scholar] [CrossRef] [PubMed]
  181. Detto, M.; Levine, J.M.; Pacala, S.W. Maintenance of High Diversity in Mechanistic Forest Dynamics Models of Competition for Light. Ecol. Monogr. 2022, 92, e1500. [Google Scholar] [CrossRef]
  182. Tomao, A.; Bonet, J.A.; Castano, C.; de-Miguel, S. How Does Forest Management Affect Fungal Diversity and Community Composition? Current Knowledge and Future Perspectives for the Conservation of Forest Fungi. For. Ecol. Manag. 2020, 457, 117678. [Google Scholar] [CrossRef]
  183. Zanne, A.E.; Abarenkov, K.; Afkhami, M.E.; Aguilar-Trigueros, C.A.; Bates, S.; Bhatnagar, J.M.; Treseder, K.K. Fungal Functional Ecology: Bringing a Trait-Based Approach to Plant-Associated Fungi. Biol. Rev. 2020, 95, 409–433. [Google Scholar] [CrossRef]
  184. Wahab, A.; Muhammad, M.; Munir, A.; Abdi, G.; Zaman, W.; Ayaz, A.; Reddy, S.P.P. Role of Arbuscular Mycorrhizal Fungi in Regulating Growth, Enhancing Productivity, and Potentially Influencing Ecosystems Under Abiotic and Biotic Stresses. Plants 2023, 12, 3102. [Google Scholar] [CrossRef] [PubMed]
  185. Luo, S.; Phillips, R.P.; Jo, I.; Fei, S.; Liang, J.; Schmid, B.; Eisenhauer, N. Higher productivity in forests with mixed mycorrhizal strategies. Nat. Commun. 2023, 14, 1377. [Google Scholar] [CrossRef]
  186. Singh, A.; Kumar, R.; Singh, D. Mycorrhizal Fungi as Biocontrol Agent for Soil Borne Pathogens: A Review. J. Pharmacogn. Phytochem. 2019, 8, 281–284. [Google Scholar]
  187. Moles, A.T. Being John Harper: Using Evolutionary Ideas to Improve Understanding of Global Patterns in Plant Traits. J. Ecol. 2018, 106, 1–18. [Google Scholar] [CrossRef]
  188. Hassani, M.A.; Durán, P.; Hacquard, S. Microbial Interactions Within the Plant Holobiont. Microbiome 2018, 6, 58. [Google Scholar] [CrossRef] [PubMed]
  189. Song, X.; Li, Y.; Cao, X.; Qi, Y. MicroRNAs and Their Regulatory Roles in Plant–Environment Interactions. Annu. Rev. Plant Biol. 2019, 70, 489–525. [Google Scholar] [CrossRef] [PubMed]
  190. Bonfante, P. The Future Has Roots in the Past: The Ideas and Scientists That Shaped Mycorrhizal Research. New Phytol. 2018, 220, 982–995. [Google Scholar] [CrossRef] [PubMed]
  191. Chen, M.; Arato, M.; Borghi, L.; Nouri, E.; Reinhardt, D. Beneficial Services of Arbuscular Mycorrhizal Fungi–From Ecology to Application. Front. Plant Sci. 2018, 9, 1270. [Google Scholar] [CrossRef] [PubMed]
  192. Bennett, A.E.; Groten, K. The Costs and Benefits of Plant–Arbuscular Mycorrhizal Fungal Interactions. Annu. Rev. Plant Biol. 2022, 73, 649–672. [Google Scholar] [CrossRef] [PubMed]
  193. Sun, J. The Understanding of Mycorrhizae Networks: A Historical Approach. Confluence 2022, 1, 2. [Google Scholar] [CrossRef]
  194. Anthony, M.A.; Crowther, T.W.; Van Der Linde, S.; Suz, L.M.; Bidartondo, M.I.; Cox, F.; Averill, C. Forest Tree Growth Is Linked to Mycorrhizal Fungal Composition and Function Across Europe. ISME J. 2022, 16, 1327–1336. [Google Scholar] [CrossRef]
  195. Simard, S.W.; Roach, W.J.; Defrenne, C.E.; Pickles, B.J.; Snyder, E.N.; Robinson, A.; Lavkulich, L.M. Harvest Intensity Effects on Carbon Stocks and Biodiversity Are Dependent on Regional Climate in Douglas-Fir Forests of British Columbia. Front. For. Glob. Change 2020, 3, 88. [Google Scholar] [CrossRef]
  196. Roach, W.J.; Simard, S.W.; Defrenne, C.E.; Pickles, B.J.; Lavkulich, L.M.; Ryan, T.L. Tree Diversity, Site Index, and Carbon Storage Decrease with Aridity in Douglas-Fir Forests in Western Canada. Front. For. Glob. Change 2021, 4, 682076. [Google Scholar] [CrossRef]
  197. Defrenne, C.E.; Philpott, T.J.; Guichon, S.H.; Roach, W.J.; Pickles, B.J.; Simard, S.W. Shifts in Ectomycorrhizal Fungal Communities and Exploration Types Relate to the Environment and Fine-Root Traits Across Interior Douglas-Fir Forests of Western Canada. Front. Plant Sci. 2019, 10, 643. [Google Scholar] [CrossRef]
  198. Robinson, A.J.; Defrenne, C.E.; Roach, W.J.; Dymond, C.C.; Pickles, B.J.; Simard, S.W. Harvesting Intensity and Aridity Are More Important Than Climate Change in Affecting Future Carbon Stocks of Douglas-Fir Forests. Front. For. Glob. Change 2022, 5, 934067. [Google Scholar] [CrossRef]
  199. Birch, J.D.; Lutz, J.A.; Hogg, E.H.; Simard, S.W.; Pelletier, R.; LaRoi, G.H.; Karst, J. Decline of an Ecotone Forest: 50 Years of Demography in the Southern Boreal Forest. Ecosphere 2019, 10, e02698. [Google Scholar] [CrossRef]
  200. Beck, J.L.; Cale, J.A.; Rodriguez-Ramos, J.C.; Kanekar, S.S.; Karst, J.; Cahill, J.F.; Erbilgin, N. Changes in Soil Fungal Communities Following Anthropogenic Disturbance Are Linked to Decreased Lodgepole Pine Seedling Performance. J. Appl. Ecol. 2020, 57, 1292–1302. [Google Scholar] [CrossRef]
  201. Modi, D.; Simard, S.; Lavkulich, L.; Hamelin, R.C.; Grayston, S.J. Stump Removal and Tree Species Composition Promote a Bacterial Microbiome That May Be Beneficial in the Suppression of Root Disease. FEMS Microbiol. Ecol. 2021, 97, fiaa213. [Google Scholar] [CrossRef]
  202. Hooper, R. The Wisdom of the Woods. New Sci. 2021, 250, 39–43. [Google Scholar] [CrossRef]
  203. Becquer, A.; Guerrero-Galán, C.; Eibensteiner, J.; Houdinet, G.; Bücking, H.; Zimmermann, S.; Garcia, K. The ectomycorrhizal contribution to tree nutrition. Adv. Bot. Res. 2019, 89, 77–126. [Google Scholar]
  204. Usman, M.; Ho-Plágaro, T.; Frank, H.E.; Calvo-Polanco, M.; Gaillard, I.; Garcia, K.; Zimmermann, S.D. Mycorrhizal Symbiosis for Better Adaptation of Trees to Abiotic Stress Caused by Climate Change in Temperate and Boreal Forests. Front. For. Glob. Change 2021, 4, 742392. [Google Scholar] [CrossRef]
  205. Policelli, N.; Horton, T.R.; Hudon, A.T.; Patterson, T.R.; Bhatnagar, J.M. Back to Roots: The Role of Ectomycorrhizal Fungi in Boreal and Temperate Forest Restoration. Front. For. Glob. Change 2020, 3, 97. [Google Scholar] [CrossRef]
  206. Razgulin, S.M. Mycorrhizal Complexes and Their Role in the Ecology of Boreal Forests (Review). Biol. Bull. 2022, 49, 704–712. [Google Scholar] [CrossRef]
  207. Beiler, K.; Durall, D.; Simard, S.; Kretzer, M. Architecture of the wood-wide web: Rhizopogon spp. genets link multiple Douglas-fir cohorts. New Phytol. 2010, 185, 543–553. [Google Scholar] [CrossRef] [PubMed]
  208. Southam, H.; Stafl, N.; Guichon, S.H.; Simard, S.W. Characterizing the Ectomycorrhizal Fungal Community of Whitebark Pine in Interior British Columbia: Mature Trees, Natural Regeneration and Planted Seedlings. Front. For. Glob. Change 2022, 4, 750701. [Google Scholar] [CrossRef]
  209. Cornell, J.B. Deep Nature Play: A Guide to Wholeness, Aliveness, Creativity, and Inspired Learning; Crystal Clarity Publishers: Los Angeles, CA, USA, 2018. [Google Scholar]
  210. Nicholas, E. Seeing the Forest for the Trees: Exploring the Forest Aspect of the Tree of Life Process to Sustain and Nourish Socioecological Activism. Int. J. Narrat. Ther. Community Work 2021, 1, 1–9. [Google Scholar]
  211. Fishel, S.R. The Global Tree: Forests and the Possibility of a Multispecies IR. Rev. Int. Stud. 2023, 49, 223–240. [Google Scholar] [CrossRef]
  212. DellaSala, D.A.; Mackey, B.; Norman, P.; Campbell, C.; Comer, P.J.; Kormos, C.F.; Keith, H.; Rogers, B. Mature and old-growth forests contribute to large-scale conservation targets in the conterminous United States. Front. For. Glob. Change 2022, 5, 979528. [Google Scholar] [CrossRef]
  213. Lindenmayer, D.B.; Laurance, W.F. The Ecology, Distribution, Conservation and Management of Large Old Trees. Biol. Rev. 2017, 92, 1434–1458. [Google Scholar] [CrossRef] [PubMed]
  214. Carreon-Ortiz, H.; Valdez, F. A New Mycorrhized Tree Optimization Nature-Inspired Algorithm. Soft Comput. 2022, 26, 4797–4817. [Google Scholar] [CrossRef]
  215. Stan, K.; Sanchez-Azofeifa, A. Tropical Dry Forest Diversity, Climatic Response, and Resilience in a Changing Climate. Forests 2019, 10, 443. [Google Scholar] [CrossRef]
  216. Álvarez-Yépiz, J.C.; Martínez-Yrízar, A.; Fredericksen, T.S. Resilience of Tropical Dry Forests to Extreme Disturbance Events. For. Ecol. Manag. 2018, 426, 1–6. [Google Scholar] [CrossRef]
  217. Anjos, L.J.; de Toledo, P.M. Measuring Resilience and Assessing Vulnerability of Terrestrial Ecosystems to Climate Change in South America. PLoS ONE 2018, 13, e0194654. [Google Scholar] [CrossRef]
  218. Kijowska-Oberc, J.; Staszak, A.M.; Kamiński, J.; Ratajczak, E. Adaptation of Forest Trees to Rapidly Changing Climate. Forests 2020, 11, 123. [Google Scholar] [CrossRef]
  219. Baltzer, J.L.; Day, N.J.; Walker, X.J.; Greene, D.; Mack, M.C.; Alexander, H.D.; Johnstone, J.F. Increasing Fire and the Decline of Fire Adapted Black Spruce in the Boreal Forest. Proc. Natl. Acad. Sci. USA 2021, 118, e2024872118. [Google Scholar] [CrossRef] [PubMed]
  220. Simard, S. Finding the Mother Tree: Uncovering the Wisdom and Intelligence of the Forest; Penguin: London, UK, 2021. [Google Scholar]
  221. Genre, A.; Lanfranco, L.; Perotto, S.; Bonfante, P. Unique and Common Traits in Mycorrhizal Symbioses. Nat. Rev. Microbiol. 2020, 18, 649–660. [Google Scholar] [CrossRef] [PubMed]
  222. Wohlleben, P. The Power of Trees: How Ancient Forests Can Save Us If We Let Them; Greystone Books Ltd: Vancouver, BC, Canada, 2023. [Google Scholar]
  223. Wall, C.B.; Egan, C.P.; Swift, S.I.; Hynson, N.A. Three Decades Post-Reforestation Has Not Led to the Reassembly of Arbuscular Mycorrhizal Fungal Communities Associated with Remnant Primary Forests. Mol. Ecol. 2020, 29, 4234–4247. [Google Scholar] [CrossRef] [PubMed]
  224. Sapsford, S.J.; Paap, T.; Hardy, G.E.St.J.; Burgess, T.I. Anthropogenic Disturbance Impacts Mycorrhizal Communities and Abiotic Soil Properties: Implications for an Endemic Forest Disease. Front. For. Glob. Change 2021, 3, 593243. [Google Scholar] [CrossRef]
  225. Gorzelak, M.A.; Asay, A.K.; Pickles, B.J.; Simard, S.W. Inter-Plant Communication Through Mycorrhizal Networks Mediates Complex Adaptive Behaviour in Plant Communities. AoB Plants 2015, 7, plv050. [Google Scholar] [CrossRef] [PubMed]
  226. Frąc, M.; Hannula, S.E.; Bełka, M.; Jędryczka, M. Fungal Biodiversity and Their Role in Soil Health. Front. Microbiol. 2018, 9, 707. [Google Scholar] [CrossRef]
  227. Ma, X.; Zhu, B.; Nie, Y.; Liu, Y.; Kuzyakov, Y. Root and Mycorrhizal Strategies for Nutrient Acquisition in Forests Under Nitrogen Deposition: A Meta-Analysis. Soil Biol. Biochem. 2021, 163, 108418. [Google Scholar] [CrossRef]
  228. Winagraski, E.; Kaschuk, G.; Monteiro, P.H.R.; Auer, C.G.; Higa, A.R. Diversity of Arbuscular Mycorrhizal Fungi in Forest Ecosystems of Brazil: A Review. Cerne 2019, 25, 25–35. [Google Scholar] [CrossRef]
  229. Soka, G.E.; Ritchie, M.E. Arbuscular Mycorrhizal Spore Composition and Diversity Associated with Different Land Uses in a Tropical Savanna Landscape, Tanzania. Appl. Soil Ecol. 2018, 125, 222–232. [Google Scholar] [CrossRef]
  230. Fall, A.F.; Nakabonge, G.; Ssekandi, J.; Founoune-Mboup, H.; Badji, A.; Balde, I.; Ndiaye, M. Diversity of Arbuscular Mycorrhizal Fungi Associated with Maize in the Eastern Part of Uganda. Biol. Life Sci. Forum 2022, 15, 12. [Google Scholar] [CrossRef]
  231. Lugo, M.A.; Ontivero, R.E.; Iriarte, H.J.; Yelikbayev, B.; Pagano, M.C. The Diversity of Arbuscular Mycorrhizal Fungi and Their Associations in South America: A Case Study of Argentinean and Brazilian Cattle Raising Productive Ecosystems: A Review. Diversity 2023, 15, 1006. [Google Scholar] [CrossRef]
  232. Vieira, L.C.; Silva, D.K.A.; Escobar, I.E.C.; Silva, J.M.D.; Moura, I.A.; Oehl, F.; Silva, G.A.D. Changes in an Arbuscular Mycorrhizal Fungi Community Along an Environmental Gradient. Plants 2020, 9, 52. [Google Scholar] [CrossRef] [PubMed]
  233. Nouhra, E.R.; Palfner, G.; Kuhar, F.; Pastor, N.; Smith, M.E. Ectomycorrhizal Fungi in South America: Their Diversity in Past, Present and Future Research. In Mycorrhizal Fungi in South America; Springer: Berlin/Heidelberg, Germany, 2019; pp. 73–95. [Google Scholar]
  234. Hanif, M.; Ashraf, Z.; Bashir, S.; Riaz, F.; Amanat, R.; Yousaf, N.; Sarwar, S. Ectomycorrhizal Fungi as Biofertilizers in Forestry. In Arbuscular Mycorrhizal Fungi in Agriculture-New Insights; IntechOpen: London, UK, 2023. [Google Scholar]
  235. Wu, T.; Tissue, D.T.; Su, W.; Li, X.; Yang, S.; Liu, X.; Liu, J. Long-Term Field Translocation Differentially Affects Arbuscular Mycorrhizal and Ectomycorrhizal Trees in a Sub-Tropical Forest. Agric. For. Meteorol. 2023, 342, 109724. [Google Scholar] [CrossRef]
  236. Liu, Y.; Li, X.; Kou, Y. Ectomycorrhizal Fungi: Participation in Nutrient Turnover and Community Assembly Pattern in Forest Ecosystems. Forests 2020, 11, 453. [Google Scholar] [CrossRef]
  237. Zhang, Z.; Yuan, Y.; Liu, Q.; Yin, H. Plant Nitrogen Acquisition from Inorganic and Organic Sources via Root and Mycelia Pathways in Ectomycorrhizal Alpine Forests. Soil Biol. Biochem. 2019, 136, 107517. [Google Scholar] [CrossRef]
  238. Li, X.; Qu, Z.; Zhang, Y.; Ge, Y.; Sun, H. Soil Fungal Community and Potential Function in Different Forest Ecosystems. Diversity 2022, 14, 520. [Google Scholar] [CrossRef]
  239. Högberg, M.N.; Skyllberg, U.; Högberg, P.; Knicker, H. Does Ectomycorrhiza Have a Universal Key Role in the Formation of Soil Organic Matter in Boreal Forests? Soil Biol. Biochem. 2020, 140, 107635. [Google Scholar] [CrossRef]
  240. Männistö, M.; Vuosku, J.; Stark, S.; Saravesi, K.; Suokas, M.; Markkola, A.; Rautio, P. Bacterial and Fungal Communities in Boreal Forest Soil Are Insensitive to Changes in Snow Cover Conditions. FEMS Microbiol. Ecol. 2018, 94, fiy123. [Google Scholar] [CrossRef] [PubMed]
  241. Ho-Plágaro, T.; García-Garrido, J.M. Molecular Regulation of Arbuscular Mycorrhizal Symbiosis. Int. J. Mol. Sci. 2022, 23, 5960. [Google Scholar] [CrossRef]
  242. Miyauchi, S.; Kiss, E.; Kuo, A.; Drula, E.; Kohler, A.; Sánchez-García, M.; Morin, E.; Andreopoulos, B.; Barry, K.W.; Bonito, G.; et al. Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits. Nat. Commun. 2020, 11, 5125. [Google Scholar] [CrossRef]
  243. Shi, J.; Wang, X.; Wang, E. Mycorrhizal Symbiosis in Plant Growth and Stress Adaptation: From Genes to Ecosystems. Annu. Rev. Plant Biol. 2023, 74, 569–607. [Google Scholar] [CrossRef]
  244. Magurno, F.; Malicka, M.; Posta, K.; Wozniak, G.; Lumini, E.; Piotrowska-Seget, Z. Glomalin Gene as Molecular Marker for Functional Diversity of Arbuscular Mycorrhizal Fungi in Soil. Biol. Fertil. Soils 2019, 55, 411–417. [Google Scholar] [CrossRef]
  245. Stewart, J.E.; Kim, M.S.; Klopfenstein, N.B. Molecular Genetic Approaches Toward Understanding Forest-Associated Fungi and Their Interactive Roles Within Forest Ecosystems. Curr. For. Rep. 2018, 4, 72–84. [Google Scholar] [CrossRef]
  246. Valadares, R.B.S.; Marroni, F.; Sillo, F.; Oliveira, R.R.M.; Balestrini, R.; Perotto, S. A Transcriptomic Approach Provides Insights on the Mycorrhizal Symbiosis of the Mediterranean Orchid Limodorum abortivum in Nature. Plants 2021, 10, 251. [Google Scholar] [CrossRef] [PubMed]
  247. Martin, F.M.; van der Heijden, M. The mycorrhizal symbiosis: Research frontiers in genomics, ecology, and agricultural application. New Phytol. 2024, 242, 1486–1506. [Google Scholar] [CrossRef] [PubMed]
  248. Terhonen, E.; Blumenstein, K.; Kovalchuk, A.; Asiegbu, F.O. Forest Tree Microbiomes and Associated Fungal Endophytes: Functional Roles and Impact on Forest Health. Forests 2019, 10, 42. [Google Scholar] [CrossRef]
  249. Shi, L.; Dossa, G.G.O.; Paudel, E.; Zang, H.; Xu, J.; Harrison, R.D. Changes in Fungal Communities Across a Forest Disturbance Gradient. Appl. Environ. Microbiol. 2019, 85, e00080-19. [Google Scholar] [CrossRef] [PubMed]
  250. Vannier, N.; Mony, C.; Bittebiere, A.K.; Michon-Coudouel, S.; Biget, M.; Vandenkoornhuyse, P. A Microorganisms’ Journey Between Plant Generations. Microbiome 2018, 6, 79. [Google Scholar] [CrossRef] [PubMed]
  251. Bai, B.; Liu, W.; Qiu, X.; Zhang, J.; Zhang, J.; Bai, Y. The Root Microbiome: Community Assembly and Its Contributions to Plant Fitness. J. Integr. Plant Biol. 2022, 64, 230–243. [Google Scholar] [CrossRef]
  252. Riechers, M.; Balázsi, Á.; Betz, L.; Jiren, T.S.; Fischer, J. The Erosion of Relational Values Resulting From Landscape Simplification. Landsc. Ecol. 2020, 35, 2601–2612. [Google Scholar] [CrossRef]
  253. Steidinger, B.S.; Crowther, T.W.; Liang, J.; Van Nuland, M.E.; Werner, G.D.A.; Reich, P.B.; Nabuurs, G.J.; De-Miguel, S.; Zhou, M.; Picard, N.; et al. Climatic Controls of Decomposition Drive the Global Biogeography of Forest-Tree Symbioses. Nature 2019, 569, 404–408. [Google Scholar] [CrossRef] [PubMed]
  254. Phillips, M. Mycorrhizal Planet: How Symbiotic Fungi Work with Roots to Support Plant Health and Build Soil Fertility; Chelsea Green Publishing: Chelsea, VT, USA, 2017. [Google Scholar]
  255. Guiry, E.J.; Buckley, M.; Orchard, T.J.; Hawkins, A.L.; Needs-Howarth, S.; Holm, E.; Szpak, P. Deforestation Caused Abrupt Shift in Great Lakes Nitrogen Cycle. Limnol. Oceanogr. 2020, 65, 1921–1935. [Google Scholar] [CrossRef]
  256. Nickerson, M.A.; Pitt, A.L.; Tavano, J.J.; Hecht, K.A.; Mitchell, J.C. Forest Removal and the Cascade of Effects Corresponding with an Ozark Hellbender Population Decline. Bull. Fla. Mus. Nat. Hist. 2017, 54, 148–164. [Google Scholar] [CrossRef]
  257. Szatten, D.; Habel, M. Effects of Land Cover Changes on Sediment and Nutrient Balance in the Catchment with Cascade-Dammed Waters. Remote Sens. 2020, 12, 3414. [Google Scholar] [CrossRef]
  258. McCann, K.S.; Cazelles, K.; MacDougall, A.S.; Fussmann, G.F.; Bieg, C.; Cristescu, M.; Fryxell, J.M.; Gellner, G.; Lapointe, B.; Gonzalez, A. Landscape Modification and Nutrient-Driven Instability at a Distance. Ecol. Lett. 2021, 24, 398–414. [Google Scholar] [CrossRef] [PubMed]
  259. Wang, Z.; Zhou, Z.; Wang, C. Defoliation-induced tree growth declines are jointly limited by carbon source and sink activities. Sci. Total Environ. 2021, 762, 143077. [Google Scholar] [CrossRef] [PubMed]
  260. Muler, A.E.; Rother, D.C.; Brancalion, P.S.; Naves, R.P.; Rodrigues, R.R.; Pizo, M.A. Can overharvesting of a non-timber-forest-product change the regeneration dynamics of a tropical rainforest? The case study of Euterpe edulis. For. Ecol. Manag. 2014, 324, 117–125. [Google Scholar] [CrossRef]
  261. Garcia_Florez, L.; Vanclay, J.K.; Glencross, K.; Nichols, J.D. Understanding 48 years of changes in tree diversity, dynamics and species responses since logging disturbance in a subtropical rainforest. For. Ecol. Manag. 2017, 393, 29–39. [Google Scholar] [CrossRef]
  262. Baird, A.; Pope, F. ‘Can’t see the forest for the trees’: The importance of fungi in the context of UK tree planting. Food Energy Secur. 2022, 11, e371. [Google Scholar] [CrossRef]
  263. Faria, D.; Morante-Filho, J.C.; Baumgarten, J. The Breakdown of Ecosystem Functionality Driven by Deforestation in a Global Biodiversity Hotspot. Biol. Conserv. 2023, 283, 110126. [Google Scholar] [CrossRef]
  264. Liebhold, A.M.; Brockerhoff, E.G.; Kalisz, S.; Nuñez, M.A.; Wardle, D.A.; Wingfield, M.J. Biological Invasions in Forest Ecosystems. Biol. Invasions 2017, 19, 3437–3458. [Google Scholar] [CrossRef]
  265. Boers, N.; Marwan, N.; Barbosa, H.M.; Kurths, J. A Deforestation-Induced Tipping Point for the South American Monsoon System. Sci. Rep. 2017, 7, 41489. [Google Scholar] [CrossRef] [PubMed]
  266. Ayyam, V.; Palanivel, S.; Chandrakasan, S. Coastal Ecosystems of the Tropics-Adaptive Management; Springer: Singapore, 2019. [Google Scholar]
  267. Bhattarai, K.; Conway, D.; Bhattarai, K.; Conway, D. Forestry and Environment. In Contemporary Environmental Problems in Nepal. Geographic Perspectives; Springer: Dordrecht, Netherlands, 2021; pp. 663–754. [Google Scholar]
  268. Raimi, M.O.; Abiola, I.; Alima, O.; Omini, D.E. Exploring How Human Activities Disturb the Balance of Biogeochemical Cycles: Evidence from the Carbon, Nitrogen and Hydrologic Cycles. Nitrogen. Hydrol. Cycles 2021, 2, 3–44. [Google Scholar]
  269. Valtera, M.; Schaetzl, R.J. Pit-Mound Microrelief in Forest Soils: Review of Implications for Water Retention and Hydrologic Modelling. For. Ecol. Manag. 2017, 393, 40–51. [Google Scholar] [CrossRef]
  270. Chen, X.; Liang, Z.; Zhang, Z.; Zhang, L. Effects of Soil and Water Conservation Measures on Runoff and Sediment Yield in Red Soil Slope Farmland Under Natural Rainfall. Sustainability 2020, 12, 3417. [Google Scholar] [CrossRef]
  271. Szeman, I.; Wenzel, J. What Do We Talk About When We Talk About Extractivism? Text. Pract. 2021, 35, 505–523. [Google Scholar] [CrossRef]
  272. Alaoui, A.; Diserens, E. Mapping Soil Compaction–A Review. Curr. Opin. Environ. Sci. Health 2018, 5, 60–66. [Google Scholar] [CrossRef]
  273. Veldkamp, E.; Schmidt, M.; Powers, J.S.; Corre, M.D. Deforestation and Reforestation Impacts on Soils in the Tropics. Nat. Rev. Earth Environ. 2020, 1, 590–605. [Google Scholar] [CrossRef]
  274. Shimamoto, C.Y.; Padial, A.A.; da Rosa, C.M.; Marques, M.C. Restoration of ecosystem services in tropical forests: A global meta-analysis. PLoS ONE 2018, 13, e0208523. [Google Scholar] [CrossRef]
  275. Herbohn, J.; Ota, L.; Gregorio, N.; Chazdon, R.; Fisher, R.; Baynes, J.; Applegate, G.; Page, T.; Carias, D.; Romero, C.; et al. The community capacity curve applied to reforestation: A framework to support success. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2023, 378, 20210079. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  276. Carrière, S.D.; Martin-StPaul, N.K.; Cakpo, C.B.; Patris, N.; Gillon, M.; Chalikakis, K.; Davi, H. The Role of Deep Vadose Zone Water in Tree Transpiration During Drought Periods in Karst Settings–Insights from Isotopic Tracing and Leaf Water Potential. Sci. Total Environ. 2020, 699, 134332. [Google Scholar] [CrossRef] [PubMed]
  277. Jamali, D.; Karam, C. Corporate Social Responsibility in Developing Countries as an Emerging Field of Study. Int. J. Manag. Rev. 2018, 20, 32–61. [Google Scholar] [CrossRef]
  278. Zheng, H.; Wang, L.; Peng, W.; Zhang, C.; Li, C.; Robinson, B.E.; Daily, G.C. Realizing the Values of Natural Capital for Inclusive, Sustainable Development: Informing China’s New Ecological Development Strategy. Proc. Natl. Acad. Sci. USA 2019, 116, 8623–8628. [Google Scholar] [CrossRef] [PubMed]
  279. Gorwa, R. The Platform Governance Triangle: Conceptualising the Informal Regulation of Online Content. Internet Policy Rev. 2019, 8, 1–22. [Google Scholar] [CrossRef]
  280. Howes, M.; Wortley, L.; Potts, R. Environmental Sustainability: A Case of Policy Implementation Failure? Sustainability 2017, 2, 165. [Google Scholar] [CrossRef]
  281. O’Faircheallaigh, C. Shaping Projects, Shaping Impacts: Community-Controlled Impact Assessments and Negotiated Agreements. Third World Q. 2017, 38, 1181–1197. [Google Scholar] [CrossRef]
  282. Heywood, P.M. Rethinking Corruption: Hocus-Pocus, Locus and Focus. Slav. East Eur. Rev. 2017, 95, 21–48. [Google Scholar] [CrossRef]
  283. White, R. Global Harms and the Natural Environment. In The Palgrave Handbook of Social Harm; Palgrave Macmillan: Singapore, 2021; pp. 89–114. [Google Scholar]
  284. Szablowski, D.; Campbell, B. Struggles Over Extractive Governance: Power, Discourse, Violence, and Legality. Extr. Ind. Soc. 2019, 6, 635–641. [Google Scholar] [CrossRef]
  285. Gray, S.J.; Hellman, N.; Ivanova, M.N. Extractive Industries Reporting: A Review of Accounting Challenges and the Research Literature. Abacus 2019, 55, 42–91. [Google Scholar] [CrossRef]
  286. Banerjee, S.B. Transnational Power and Translocal Governance: The Politics of Corporate Responsibility. Hum. Relat. 2018, 71, 796–821. [Google Scholar] [CrossRef]
  287. Singh, R.L.; Singh, P.K. Global Environmental Problems. In Principles and Applications of Environmental Biotechnology for a Sustainable Future; Springer: Singapore, 2017; pp. 13–41. [Google Scholar]
  288. Kumari, R.; Banerjee, A.; Kumar, R.; Kumar, A.; Saikia, P.; Khan, M.L. Deforestation in India: Consequences and Sustainable Solutions. In Forest Degradation Around the World; IntechOpen: London, UK, 2019; pp. 1–18. [Google Scholar]
  289. Sheikh, H.; Mitchell, P.; Foth, M. More-Than-Human Smart Urban Governance: A Research Agenda. Digit. Geogr. Soc. 2023, 4, 100045. [Google Scholar] [CrossRef]
  290. Pickles, B.J.; Simard, S.W. Mycorrhizal Networks and Forest Resilience to Drought. In Mycorrhizal Mediation of Soil; Elsevier: Amsterdam, The Netherlands, 2017; pp. 319–339. [Google Scholar]
  291. Sonter, L.J.; Herrera, D.; Barrett, D.J.; Galford, G.L.; Moran, C.J.; Soares-Filho, B.S. Mining Drives Extensive Deforestation in the Brazilian Amazon. Nat. Commun. 2017, 8, 1013. [Google Scholar] [CrossRef] [PubMed]
  292. Garg, S.; Paliwal, R. Green Technologies for Restoration of Damaged Ecosystem. In Soil Health Restoration and Management; Springer: Singapore, 2020; pp. 357–380. [Google Scholar]
  293. Abe, C.A.; Lobo, F.L.; Novo, E.M.L.D.M.; Costa, M.; Dibike, Y. Modeling the Effects of Land Cover Change on Sediment Concentrations in a Gold-Mined Amazonian Basin. Reg. Environ. Change 2019, 19, 1801–1813. [Google Scholar] [CrossRef]
  294. De Jong, W.; Pokorny, B.; Katila, P.; Galloway, G.; Pacheco, P. Community Forestry and the Sustainable Development Goals: A Two Way Street. Forests 2018, 9, 331. [Google Scholar] [CrossRef]
  295. Feng, Y.; Su, H.; Tang, Z.; Wang, S.; Zhao, X.; Zhang, H.; Fang, J. Reduced Resilience of Terrestrial Ecosystems Locally Is Not Reflected on a Global Scale. Commun. Earth Environ. 2021, 2, 88. [Google Scholar] [CrossRef]
  296. Meng, Y.; Liu, X.; Ding, C.; Xu, B.; Zhou, G.; Zhu, L. Analysis of Ecological Resilience to Evaluate the Inherent Maintenance Capacity of a Forest Ecosystem Using a Dense Landsat Time Series. Ecol. Inform. 2020, 57, 101064. [Google Scholar] [CrossRef]
  297. Canarini, A.; Kaiser, C.; Merchant, A.; Richter, A.; Wanek, W. Root Exudation of Primary Metabolites: Mechanisms and Their Roles in Plant Responses to Environmental Stimuli. Front. Plant Sci. 2019, 10, 157. [Google Scholar] [CrossRef] [PubMed]
  298. Koshila Ravi, R.; Anusuya, S.; Balachandar, M.; Muthukumar, T. Microbial Interactions in Soil Formation and Nutrient Cycling. In Mycorrhizosphere and Pedogenesis; Springer: Singapore, 2019; pp. 363–382. [Google Scholar]
  299. Garcia, K.; Delaux, P.-M.; Cope, K.; Ane, J.-M. Molecular signals required for the establishment and maintenance of ectomycorrhizal symbioses. New Phytol. 2015, 208, 79–87. [Google Scholar] [CrossRef] [PubMed]
  300. Marín, C.; Bueno, C.G. A Systematic Review of South American and European Mycorrhizal Research: Is there a Need for Scientific Symbiosis. In Mycorrhizal Fungi in South America; Springer: Cham, Switzerland, 2019; pp. 97–110. [Google Scholar] [CrossRef]
  301. Muneer, M.A.; Wang, P.; Zaib-un-Nisa; Lin, C.; Ji, B. Potential role of common mycorrhizal networks in improving plant growth and soil physicochemical properties under varying nitrogen levels in a grassland ecosystem. Glob. Ecol. Conserv. 2020, 24, e01352. [Google Scholar] [CrossRef]
  302. Thurner, M.A.; Caldararu, S.; Engel, J.; Rammig, A.; Zaehle, S. Modelled forest ecosystem carbon–nitrogen dynamics with integrated mycorrhizal processes under elevated CO2. Biogeosciences 2024, 21, 1391–1410. [Google Scholar] [CrossRef]
  303. Hannula, E.S.; Morriën, E. Will fungi solve the carbon dilemma? Geoderma 2022, 413, 115767. [Google Scholar] [CrossRef]
  304. Mansourian, S.; Parrotta, J.; Balaji, P.; Bellwood-Howard, I.; Bhasme, S.; Bixler, R.P.; Yap, S.L. Putting the Pieces Together: Integration for Forest Landscape Restoration Implementation. Land Degrad. Dev. 2020, 31, 419–429. [Google Scholar] [CrossRef]
  305. Isaac, M.E.; Borden, K.A. Nutrient Acquisition Strategies in Agroforestry Systems. Plant Soil 2019, 444, 1–19. [Google Scholar] [CrossRef]
  306. Siqueira-Gay, J.; Sonter, L.J.; Sánchez, L.E. Exploring Potential Impacts of Mining on Forest Loss and Fragmentation within a Biodiverse Region of Brazil’s Northeastern Amazon. Resour. Policy 2020, 67, 101662. [Google Scholar] [CrossRef]
  307. Hailu, F. Climate Change as a Trigger for Desertification and Possible Alternatives to Reduce Biodiversity Loss. J. Selva Andin. Biosph. 2023, 11, 94–111. [Google Scholar]
  308. Karvonen, J.; Halder, P.; Kangas, J.; Leskinen, P. Indicators and tools for assessing sustainability impacts of the forest bioeconomy. For. Ecosyst. 2017, 4, 2. [Google Scholar] [CrossRef]
  309. Bebbington, A.J.; Sauls, L.A.; Rosa, H.; Fash, B.; Bebbington, D.H. Conflicts over Extractivist Policy and the Forest Frontier in Central America. Eur. Rev. Lat. Am. Caribb. Stud. 2018, 106, 103–132. [Google Scholar] [CrossRef]
  310. Jo, I.; Fei, S.; Oswalt, C.M.; Domke, G.M.; Phillips, R.P. Shifts in dominant tree mycorrhizal associations in response to anthropogenic impacts. Sci. Adv. 2019, 5, eaav6358. [Google Scholar] [CrossRef]
  311. Nocentini, S.; Buttoud, G.; Ciancio, O.; Corona, P. Managing Forests in a Changing World: The Need for a Systemic Approach. A Review. For. Syst. 2017, 26, eR01. [Google Scholar] [CrossRef]
  312. Boyno, G.; Rezaee Danesh, Y.; Demir, S.; Teniz, N.; Mulet, J.M.; Porcel, R. The Complex Interplay Between Arbuscular Mycorrhizal Fungi and Strigolactone: Mechanisms, Sinergies, Applications and Future Directions. Int. J. Mol. Sci. 2023, 24, 16774. [Google Scholar] [CrossRef] [PubMed]
  313. Pérez-Izquierdo, L.; Rincón, A.; Lindahl, B.D.; Buée, M. Fungal Community of Forest Soil: Diversity, Functions, and Services. In Forest Microbiology; Academic Press: Cambridge, MA, USA, 2021; pp. 231–255. [Google Scholar]
  314. Green, S.M.; Dungait, J.A.; Tu, C.; Buss, H.L.; Sanderson, N.; Hawkes, S.J.; Quine, T.A. Soil Functions and Ecosystem Services Research in the Chinese Karst Critical Zone. Chem. Geol. 2019, 527, 119107. [Google Scholar] [CrossRef]
  315. Menge, E.M. Evaluating the Impact of Land-Use Change on Arbuscular Mycorrhizal Fungi (AMF) Diversity and Function. Int. J. Sci. Res. Arch. 2023, 10, 546–556. [Google Scholar] [CrossRef]
  316. Menge, E.M. Investigating the Ecological Role of Arbuscular Mycorrhizal Fungi (AMF) in Natural Ecosystems. Int. J. Sci. Res. Arch. 2023, 10, 524–534. [Google Scholar] [CrossRef]
  317. Zavahir, J.S.; Wijepala, P.C.; Seneviratne, G. Role of Microbial Communities in Plant–Microbe Interactions, Metabolic Cooperation, and Self-Sufficiency Leading to Sustainable Agriculture. In Role of Microbial Communities for Sustainability; Springer: Singapore, 2021; pp. 1–35. [Google Scholar]
  318. Kaupper, T.; Hetz, S.; Kolb, S.; Yoon, S.; Horn, M.A.; Ho, A. Deforestation for Oil Palm: Impact on Microbially Mediated Methane and Nitrous Oxide Emissions, and Soil Bacterial Communities. Biol. Fertil. Soils 2020, 56, 287–298. [Google Scholar] [CrossRef]
  319. Argüelles-Moyao, A.; Galicia, L. Assisted Migration and Plant Invasion: Importance of Belowground Ecology in Conifer Forest Tree Ecosystems. Can. J. For. Res. 2023, 54, 110–121. [Google Scholar] [CrossRef]
  320. Di Sacco, A.; Hardwick, K.A.; Blakesley, D.; Brancalion, P.H.; Breman, E.; Cecilio Rebola, L.; Antonelli, A. Ten Golden Rules for Reforestation to Optimize Carbon Sequestration, Biodiversity Recovery and Livelihood Benefits. Glob. Change Biol. 2021, 27, 1328–1348. [Google Scholar] [CrossRef]
  321. Davies, S.J.; Abiem, I.; Salim, K.A.; Aguilar, S.; Allen, D.; Alonso, A.; Yap, S.L. ForestGEO: Understanding Forest Diversity and Dynamics Through a Global Observatory Network. Biol. Conserv. 2021, 253, 108907. [Google Scholar] [CrossRef]
  322. Garcia, S.; Abildtrup, J.; Stenger, A. How Does Economic Research Contribute to the Management of Forest Ecosystem Services? Ann. For. Sci. 2018, 75, 53. [Google Scholar] [CrossRef]
  323. Löf, M.; Madsen, P.; Metslaid, M.; Witzell, J.; Jacobs, D.F. Restoring Forests: Regeneration and Ecosystem Function for the Future. New For. 2019, 50, 139–151. [Google Scholar] [CrossRef]
  324. Trogisch, S.; Liu, X.; Rutten, G.; Xue, K.; Bauhus, J.; Brose, U.; Bruelheide, H. The Significance of Tree-Tree Interactions for Forest Ecosystem Functioning. Basic Appl. Ecol. 2021, 55, 33–52. [Google Scholar] [CrossRef]
  325. Baskent, E.Z.; Borges, J.G.; Kašpar, J.; Tahri, M. A Design for Addressing Multiple Ecosystem Services in Forest Management Planning. Forests 2020, 11, 1108. [Google Scholar] [CrossRef]
  326. Ogle, K.; Liu, Y.; Vicca, S.; Bahn, M. A hierarchical, multivariate meta-analysis approach to synthesising global change experiments. New Phytol. 2021, 231, 2382–2394. [Google Scholar] [CrossRef]
  327. Song, J.; Wan, S.; Piao, S.; Knapp, A.K.; Classen, A.T.; Vicca, S.; Ciais, P.; Hovenden, M.J.; Leuzinger, S.; Beier, C.; et al. A meta-analysis of 1,119 manipulative experiments on terrestrial carbon-cycling responses to global change. Nat. Ecol. Evol. 2019, 3, 1309–1320. [Google Scholar] [CrossRef]
  328. La Notte, A.; D’Amato, D.; Mäkinen, H.; Paracchini, M.L.; Liquete, C.; Egoh, B.; Crossman, N.D. Ecosystem Services Classification: A Systems Ecology Perspective of the Cascade Framework. Ecol. Indic. 2017, 74, 392–402. [Google Scholar] [CrossRef]
  329. Kučera, A.; Samec, P.; Bajer, A.; Skene, K.R.; Vichta, T.; Vranová, V.; Datta, R. Forest Soil Water in Landscape Context. In Soil Moisture Importance; IntechOpen: London, UK, 2020; p. 45. [Google Scholar]
  330. Busch, J.; Ferretti-Gallon, K. What Drives Deforestation and What Stops It? A Meta-Analysis. Rev. Environ. Econ. Policy 2017, 11, 3–23. [Google Scholar] [CrossRef]
  331. Desbureaux, S.; Damania, R. Rain, forests and farmers: Evidence of drought induced deforestation in Madagascar and its consequences for biodiversity conservation. Biol. Conserv. 2018, 221, 357–364. [Google Scholar] [CrossRef]
  332. Yousuf, S.; Naqash, N.; Singh, R. Nutrient Cycling: An Approach for Environmental Sustainability. In Environmental Microbiology: Advanced Research and Multidisciplinary Applications; Bentham Science Publisher: Sharjah, United Arab Emirates, 2022; p. 77. [Google Scholar]
  333. Swamy, L.; Drazen, E.; Johnson, W.R.; Bukoski, J.J. The Future of Tropical Forests Under the United Nations Sustainable Development Goals. J. Sustain. For. 2018, 37, 221–256. [Google Scholar] [CrossRef]
  334. Osaki, M.; Tsuji, N.; Kato, T.; Yamanaka, M.D.; Sulaiman, A.; Silsigia, S.; Wetadewi, R.I. Natural Capital-Based Societies in the Tropics. In Tropical Peatland Eco-Management; Springer: Singapore, 2021; pp. 197–245. [Google Scholar]
  335. Kusters, K.; De Graaf, M.; Ascarrunz, N.; Benneker, C.; Boot, R.; Van Kanten, R.; Zagt, R. Formalizing Community Forest Tenure Rights: A Theory of Change and Conditions for Success. For. Policy Econ. 2022, 141, 102766. [Google Scholar] [CrossRef]
  336. Pokorny, B.; Sotirov, M.; Kleinschmit, D.; Kanowski, P. Forests as a Global Commons: International Governance and the Role of Germany. In Report to the Science Platform Sustainability 2030; Universität Freiburg: Freiburg, Germany, 2019; pp. 1–67. [Google Scholar]
  337. Seddon, N.; Chausson, A.; Berry, P.; Girardin, C.A.; Smith, A.; Turner, B. Understanding the Value and Limits of Nature-Based Solutions to Climate Change and Other Global Challenges. Philos. Trans. R. Soc. B 2020, 375, 20190120. [Google Scholar] [CrossRef] [PubMed]
  338. Ingram, V.; van Den Berg, J.; Van Oorschot, M.; Arets, E.; Judge, L. Governance Options to Enhance Ecosystem Services in Cocoa, Soy, Tropical Timber and Palm Oil Value Chains. Environ. Manag. 2018, 62, 128–142. [Google Scholar] [CrossRef] [PubMed]
  339. Chiasson, G.; Angelstam, P.; Axelsson, R.; Doyon, F. Towards Collaborative Forest Planning in Canadian and Swedish Hinterlands: Different Institutional Trajectories? Land Use Policy 2019, 83, 334–345. [Google Scholar] [CrossRef]
  340. Barnard, P.; Moomaw, W.R.; Fioramonti, L.; Laurance, W.F.; Mahmoud, M.I.; O’Sullivan, J.; Ziervogel, G. World Scientists’ Warnings Into Action, Local to Global. Sci. Prog. 2021, 104, 00368504211056290. [Google Scholar] [CrossRef] [PubMed]
  341. Liang, J.; Gamarra, J.G. The Importance of Sharing Global Forest Data in a World of Crises. Sci. Data 2020, 7, 424. [Google Scholar] [CrossRef] [PubMed]
  342. Pal, P. An Assessment of Forest Diversity: Challenges and Management. In Agro-Biodiversity and Agri-Ecosystem Management; Springer: Singapore, 2022; pp. 11–26. [Google Scholar]
  343. Mansourian, S. Governance and Forest Landscape Restoration: A Framework to Support Decision-Making. J. Nat. Conserv. 2017, 37, 21–30. [Google Scholar] [CrossRef]
  344. Deacon, R.T. Assessing the Relationship between Government Policy and Deforestation 1. In The Economics of Land Use; Routledge: London, UK, 2017; pp. 517–534. [Google Scholar]
  345. Moraes, I.; Azevedo-Ramos, C.; Pacheco, J. Public Forests Under Threat in the Brazilian Amazon: Strategies for Coping Shifts in Environmental Policies and Regulations. Front. For. Glob. Change 2021, 4, 631756. [Google Scholar] [CrossRef]
  346. Viljur, M.; Abella, S.R.; Adámek, M.; Alencar, J.B.R.; Barber, N.A.; Beudert, B.; Burkle, L.A.; Cagnolo, L.; Campos, B.R.; Chao, A.; et al. The effect of natural disturbances on forest biodiversity: An ecological synthesis. Biol. Rev. 2022, 97, 1930–1947. [Google Scholar] [CrossRef] [PubMed]
  347. Ibáñez, B.; Gómez-Aparicio, L.; Ávila, J.M.; Pérez-Ramos, I.M.; García, L.V.; Marañón, T. Impact of tree decline on spatial patterns of seedling-mycorrhiza interactions: Implications for regeneration dynamics in Mediterranean forests. For. Ecol. Manag. 2015, 353, 1–9. [Google Scholar] [CrossRef]
  348. Urruth, L.M.; Bassi, J.B.; Chemello, D. Policies to Encourage Agroforestry in the Southern Atlantic Forest. Land Use Policy 2022, 112, 105802. [Google Scholar] [CrossRef]
  349. Karger, D.N.; Kessler, M.; Lehnert, M.; Jetz, W. Limited Protection and Ongoing Loss of Tropical Cloud Forest Biodiversity and Ecosystems Worldwide. Nat. Ecol. Evol. 2021, 5, 854–862. [Google Scholar] [CrossRef]
  350. Njana, M.A.; Mbilinyi, B.; Eliakimu, Z. The Role of Forests in the Mitigation of Global Climate Change: Empirical Evidence from Tanzania. Environ. Chall. 2021, 4, 100170. [Google Scholar] [CrossRef]
  351. Fort, T.; Pauvert, C.; Zanne, A.E.; Ovaskainen, O.; Caignard, T.; Barret, M.; Vacher, C. Maternal Effects and Environmental Filtering Shape Seed Fungal Communities in Oak Trees. BioRxiv 2019, 691121. [Google Scholar] [CrossRef]
  352. Cholewińska, O.; Keczyński, A.; Kusińska, B.; Jaroszewicz, B. Species Identity of Large Trees Affects the Composition and the Spatial Structure of Adjacent Trees. Forests 2021, 12, 1162. [Google Scholar] [CrossRef]
  353. Zhao, F.; Liu, J.; Zhu, W.; Zhang, B.; Zhu, L. Spatial Variation of Altitudinal Belts as Dividing Index Between Warm Temperate and Subtropical Zones in the Qinling-Daba Mountains. J. Geogr. Sci. 2020, 30, 642–656. [Google Scholar] [CrossRef]
  354. Jewaria, P.K.; Hänninen, H.; Li, X.; Bhalerao, R.P.; Zhang, R. A Hundred Years After: Endodormancy and the Chilling Requirement in Subtropical Trees. New Phytol. 2021, 231, 565–570. [Google Scholar] [CrossRef] [PubMed]
  355. Ballarin, F.; Li, S. Diversification in Tropics and Subtropics Following the Mid-Miocene Climate Change: A Case Study of the Spider Genus Nesticella. Glob. Change Biol. 2018, 24, e577–e591. [Google Scholar] [CrossRef] [PubMed]
  356. Li, Y.; Liu, X.; Xu, W.; Bongers, F.J.; Bao, W.; Chen, B.; Ma, K. Effects of Diversity, Climate and Litter on Soil Organic Carbon Storage in Subtropical Forests. For. Ecol. Manag. 2020, 476, 118479. [Google Scholar] [CrossRef]
  357. Weißbecker, C.; Heintz-Buschart, A.; Bruelheide, H.; Buscot, F.; Wubet, T. Linking Soil Fungal Generality to Tree Richness in Young Subtropical Chinese Forests. Microorganisms 2019, 7, 547. [Google Scholar] [CrossRef] [PubMed]
  358. Frelich, L.E.; Johnstone, J.; Kuuluvainen, T. Boreal Forests. In Future Forests; Elsevier: Amsterdam, The Netherlands, 2024; pp. 221–242. [Google Scholar]
  359. Molinari, C.; Lehsten, V.; Blarquez, O.; Carcaillet, C.; Davis, B.A.; Kaplan, J.O.; Bradshaw, R.H. The Climate, the Fuel and the Land Use: Long-Term Regional Variability of Biomass Burning in Boreal Forests. Glob. Change Biol. 2018, 24, 4929–4945. [Google Scholar] [CrossRef] [PubMed]
  360. Pohjanmies, T.; Triviño, M.; Le Tortorec, E.; Mazziotta, A.; Snäll, T.; Mönkkönen, M. Impacts of Forestry on Boreal Forests: An Ecosystem Services Perspective. Ambio 2017, 46, 743–755. [Google Scholar] [CrossRef]
  361. Kuuluvainen, T.; Gauthier, S. Young and Old Forest in the Boreal: Critical Stages of Ecosystem Dynamics and Management Under Global Change. For. Ecosyst. 2018, 5, 26. [Google Scholar] [CrossRef]
Figure 1. Global forest loss: deforestation versus forest degradation.
Figure 1. Global forest loss: deforestation versus forest degradation.
Plants 13 01231 g001
Figure 2. Interrelationship between the different ‘external’ actors that guarantee the survival of forest biodiversity.
Figure 2. Interrelationship between the different ‘external’ actors that guarantee the survival of forest biodiversity.
Plants 13 01231 g002
Table 1. Analysis of environmental research keywords: frequency, contextual themes, and potential implications in forest ecosystem studies.
Table 1. Analysis of environmental research keywords: frequency, contextual themes, and potential implications in forest ecosystem studies.
KeywordFrequency
(n = 1472)
Contextual ThemesPotential Implications
Mother trees: Guardians of ecosystem resilience46Ecosystem management, Forest resilienceImportance of key species in ecosystem recovery
The hypothesis of Suzanne Simard33Mycorrhizal networks, Inter-species communicationFoundation for understanding forest symbiotic relationships
Symbiotic relationships55Biodiversity, Ecosystem healthRole in ecosystem stability and resilience
Fungi, plants, carbohydrates, and water51Nutrient cycles, Water dynamicsCritical aspects of forest ecosystems’ functioning
Impact of deforestation, extraction and biodiversity77Deforestation impacts, Biodiversity lossEffects on global biodiversity and climate
Underground biodiversity and mycorrhiza networks49Soil health, MycorrhizaeRole of soil biodiversity in nutrient exchange
Arbuscular mycorrhizae32Plant-fungi interactionImportance in plant nutrition and soil health
Endomycorrhizas and ectomycorrhizas57Types of mycorrhizal fungiDifferences in symbiosis and ecosystem roles
Mycorrhizae and genetic engineering10Biotechnology applicationsPotential for enhancing plant resilience
Biotechnology and mycorrhizae19Biotech in ecosystem managementInnovations in sustainable forestry practices
Molecular research of mycorrhizal fungi16Scientific advancementsContributions to understanding mycorrhizal functions
Nitrogen collection34Nitrogen cycle, Plant adaptationEfficiency of Nitrogen Uptake and ecosystem nutrient cycling
Coopetition in the Forest19Inter-species relationshipsCompetitive and cooperative dynamics in forest ecosystems
Dynamic ecosystem and biodiversity63Ecosystem dynamics, Biodiversity importanceImpact of diversity on ecosystem resilience
Forest resilience65Response to disturbancesStrategies for enhancing forest recovery and sustainability
Resilience and disruption47Effects of environmental stressorsMechanisms of ecosystem adaptation and survival
Healthy Forests52Indicators of forest healthRelationship with biodiversity and ecosystem services
Overexploitation and depletion of resources68Resource managementConsequences of unsustainable extractivism
Forest biological diversity58Species diversity, Genetic diversityRole in ecosystem functionality and resilience
Tropical forests42Biodiversity hotspotsChallenges and conservation priorities
Subtropical forests30Ecosystem services, Climate regulationImportance in global ecological balance
Boreal forests28Carbon sequestration, BiodiversityRole in Climate Mitigation and biodiversity conservation
Natural Capital and extractivism37Economic valuation, Resource extractionImpact on ecosystem services and sustainability
Deforestation and alteration of biodiversity75Habitat destruction, Species extinctionLong-term effects on global biodiversity
Interrelation and exchange of nutrients in networks47Nutrient Cycle, Ecosystem interdependenceBasis for forest productivity and health
Disorganized development versus organized development25Sustainable development, Land use planningEffects on forest conservation and resource use
Nitrogen-fixing microorganisms34Nitrogen cycle, Soil fertilityContribution to ecosystem nutrient dynamics
Impairment of cascade nutrient exchange21Pollution, Soil degradationImpact on ecosystem nutrient cycles and productivity
Vadose zone and hydric sequences16Water cycle, Soil moistureInfluence on plant growth and ecosystem dynamics
Modification of water cycles38Climate change, DeforestationEffects on hydrological systems and forest health
Cascading ecological effects30Ecosystem interconnectionsConsequences of disruptions in ecological networks
Importance of public policies56Policy interventions, Conservation strategiesRole in regulating extractivism and protecting forests
Regulation of the extractivist framework39Legal frameworks, GovernanceApproaches to sustainable resource management
Institutions and governance48Policy effectiveness, Institutional rolesImpact on environmental regulation and enforcement
Extractivism vs. Sustainability33Economic models, Environmental sustainabilityChallenges in balancing resource use with conservation
Regulation of extractivism phenomena22Policy development, Environmental law
Table 2. Synthesis of some characteristics of boreal, tropical, and subtropical forests.
Table 2. Synthesis of some characteristics of boreal, tropical, and subtropical forests.
Forest RegionBoreal ForestsTropical ForestsSubtropical Forest
LocationLocated in the north of the northern hemisphere.
Russia (Siberia, European part); Canada (Yukon, British Columbia, to Newfoundland and Labrador); United States (Alaska); Sweden (North and center); Finland (North and East); Norway (North); Iceland
Estonia; Latvia; Lithuania
Kazakhstan (North); Mongolia (North).
Approximately 85 countries contain tropical forest ecosystems that cover 18 million km2.
Brazil (Amazon rainforest); Indonesia (Sumatra, Borneo, New Guinea); Democratic Republic of the Congo (Congo Forest); Peru (Amazon rainforest); Colombia (Amazon Region); Venezuela (Amazon jungle, Orinoco Forests); Malaysia (Peninsular and island); Papua New Guinea; Bolivia (Amazon rainforest); Madagascar
India (Northeast, western Ghats); Australia (Northern Queensland); Mexico (South, Yucatan Peninsula, Chiapas); Thailand
It is normally located between 23.5° and 35° latitude in both hemispheres.
United States (Southeast, Florida, Georgia); China (South, Yunnan); Australia (East Coast, New South Wales, Queensland); India (Northeast, Western Ghats); Brazil (South, Paraná, São Paulo); Argentina (North, Misiones); Mexico (South, Chiapas, Veracruz); South Africa (East Coast, KwaZulu-Natal); Japan (South, Kyushu); New Zealand (North Island, Northland).
ClimateExtreme cold with temperatures that can drop to −45 degrees Celsius and short growing seasons.Warm and humid with year-round growing seasons.Generally warm with high humidity. Two different seasons: a hot and humid summer and a cooler and drier winter.
VegetationForest soils are usually low in fertility and acidic, with a thin A horizon. These forests are dominated by conifers, spruce, pine, and larch, along with birch and poplar.Various plant species and dense vegetation. Generally, tropical forest ecosystems extend further towards the poles, where humidity is adequate.Diverse and dense, with a variety of trees, shrubs, and undergrowth. Evergreen broadleaf dominates these forests.
Species DiversityLower species diversityExtremely high species diversityThe high diversity of species varies depending on the specific region.
Dominant FaunaMoose, caribou, wolves, bears, owls.Jaguars, monkeys, various birds, insects, and species of mushrooms.Monkeys, tigers, snakes and numerous species of birds.
Impact on BiodiversityInfluenced by recurrent disturbances (fires, insect infestations). Habitat fragmentation causes species to be moved.It houses the greatest biodiversity on the planet, which is why they are the true thermometer of the planet. This forest helps stabilize the world’s climateThese forests play a crucial role in the maintenance of biodiversity. They serve as vital refuges for migratory species. Help stabilize the global climate
Carbon StorageImportant for carbon storageCarbon storage and oxygen production.Important carbon reservoirs
Importance of the EcosystemOne of the world’s leading providers of ecosystem services. Storage of carbon and fresh water.High biodiversity, ecological services, and climate balanceIt is important to maintain ecological and climatic balance.
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

Bas, T.G.; Sáez, M.L.; Sáez, N. Sustainable Development versus Extractivist Deforestation in Tropical, Subtropical, and Boreal Forest Ecosystems: Repercussions and Controversies about the Mother Tree and the Mycorrhizal Network Hypothesis. Plants 2024, 13, 1231. https://doi.org/10.3390/plants13091231

AMA Style

Bas TG, Sáez ML, Sáez N. Sustainable Development versus Extractivist Deforestation in Tropical, Subtropical, and Boreal Forest Ecosystems: Repercussions and Controversies about the Mother Tree and the Mycorrhizal Network Hypothesis. Plants. 2024; 13(9):1231. https://doi.org/10.3390/plants13091231

Chicago/Turabian Style

Bas, Tomas Gabriel, Mario Luis Sáez, and Nicolas Sáez. 2024. "Sustainable Development versus Extractivist Deforestation in Tropical, Subtropical, and Boreal Forest Ecosystems: Repercussions and Controversies about the Mother Tree and the Mycorrhizal Network Hypothesis" Plants 13, no. 9: 1231. https://doi.org/10.3390/plants13091231

APA Style

Bas, T. G., Sáez, M. L., & Sáez, N. (2024). Sustainable Development versus Extractivist Deforestation in Tropical, Subtropical, and Boreal Forest Ecosystems: Repercussions and Controversies about the Mother Tree and the Mycorrhizal Network Hypothesis. Plants, 13(9), 1231. https://doi.org/10.3390/plants13091231

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