Next Article in Journal
Understanding the Taxonomic Complexes and Species Delimitation within Sambucus L. (Viburnaceae)
Next Article in Special Issue
Marine Noise Effects on Juvenile Sparid Fish Change among Species and Developmental Stages
Previous Article in Journal
Long-Term Ringing Data on Migrating Passerines Reveal Overall Avian Decline in Europe
Previous Article in Special Issue
Circular Bedforms Due to Pit Foraging of Greater Flamingo Phoenicopterus roseus in a Back-Barrier Intertidal Habitat
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Project “Biodiversity MARE Tricase”: A Species Inventory of the Coastal Area of Southeastern Salento (Ionian Sea, Italy)

by
Valerio Micaroni
1,2,*,†,
Francesca Strano
1,2,*,†,
Fabio Crocetta
3,
Davide Di Franco
4,
Stefano Piraino
5,6,7,
Cinzia Gravili
5,7,
Fabio Rindi
8,
Marco Bertolino
9,
Gabriele Costa
9,10,
Joachim Langeneck
7,
Marzia Bo
7,9,
Federico Betti
9,
Carlo Froglia
11,
Adriana Giangrande
5,
Francesco Tiralongo
12,13,
Luisa Nicoletti
14,
Pietro Medagli
5,
Stefano Arzeni
5 and
Ferdinando Boero
15,16,17
1
School of Biological Sciences, Victoria University of Wellington, Wellington 6140, New Zealand
2
MARE Outpost, University of Salento, 73039 Tricase, Italy
3
Department of Integrative Marine Ecology (EMI), Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Naples, Italy
4
Institute for Ecology, Diversity and Evolution, Goethe University Frankfurt, 60325 Frankfurt am Main, Germany
5
Department of Biological and Environmental Sciences and Technologies-DiSTeBA, University of Salento, 73100 Lecce, Italy
6
Museo di Biologia Marina “Pietro Parenzan”, 73010 Porto Cesareo, Italy
7
Consorzio Nazionale Interuniversitario per le Scienze del Mare (CoNISMa), U.L.R di Lecce, Department of Biological and Environmental Sciences and Technologies-DiSTeBA, University of Salento, 73100 Lecce, Italy
8
Department of Life and Environmental Sciences, Polytechnic University of Marche, 60131 Ancona, Italy
9
Department for the Earth, Environment and Life Sciences, University of Genoa, 16132 Genoa, Italy
10
Department of Earth and Environmental Sciences, University of Milano-Bicocca, 20126 Milan, Italy
11
Institute of Marine Sciences, National Research Council, 60125 Ancona, Italy
12
Ente Fauna Marina Mediterranea, Scientific Organization for Research and Conservation of Marine Biodiversity, 96012 Avola, Italy
13
Department of Biological, Geological and Environmental Sciences, University of Catania, 95124 Catania, Italy
14
Italian National Institute for Environmental Protection and Research, 00144 Rome, Italy
15
Istituto per lo Studio Degli Impatti Antropici e Sostenibilità in Ambiente Marino (IAS), Consiglio Nazionale delle Ricerche, Italy Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Naples, Italy
16
Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Naples, Italy
17
Consorzio Nazionale Interuniversitario per le Scienze del Mare (CoNISMa), 00198 Rome, Italy
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Diversity 2022, 14(11), 904; https://doi.org/10.3390/d14110904
Submission received: 20 September 2022 / Revised: 20 October 2022 / Accepted: 20 October 2022 / Published: 26 October 2022
(This article belongs to the Special Issue Biodiversity in Mediterranean Sea Ecosystems)

Abstract

:
Biodiversity is a broad concept that encompasses the diversity of nature, from the genetic to the habitat scale, and ensures the proper functioning of ecosystems. The Mediterranean Sea, one of the world’s most biodiverse marine basins, faces major threats, such as overexploitation of resources, pollution and climate change. Here we provide the first multi-taxa inventory of marine organisms and coastal terrestrial flora recorded in southeastern Salento (Ionian Sea, Italy), realized during the project “Biodiversity MARE Tricase”, which provided the first baseline of species living in the area. Sampling was carried out by SCUBA and free diving, fishing gears, and citizen science from 0 to 70 m. Overall, 697 taxa were found between March 2016 and October 2017, 94% of which were identified to the species level. Of these, 19 taxa represented new records for the Ionian Sea (36 additional new records had been reported in previous publications on specific groups, namely Porifera and Mollusca Heterobranchia), and two findings represented the easternmost records in the Mediterranean Sea (Helicosalpa virgula and Lampea pancerina). For eight other taxa, our findings represented the only locality in the Ionian Sea, besides the Straits of Messina. In addition to the species list, phenological events (e.g., blooms, presence of reproductive traits and behaviour) were also reported, with a focus on gelatinous plankton. Our results reveal that even for a relatively well-known area, current biodiversity knowledge may still be limited, and targeted investigations are needed to fill the gaps. Further research is needed to understand the distribution and temporal trends of Mediterranean biodiversity and to provide baseline data to identify ongoing and future changes.

1. Introduction

Biodiversity is the most valuable resource on Earth [1]. In marine ecosystems, increased diversity of structural elements and functional traits are correlated with optimal resource use, which consequently increases and stabilizes energy and matter flows [2]. Conversely, biodiversity loss is associated with decreased productivity, recovery potential, and ecosystem stability [3]. Marine biodiversity provides key ecosystem goods and services such as food, raw materials, pharmaceuticals, genetic information, climate regulation, tourism, recreation, and many others [4]. Recent estimates (2011) of global ecosystem services ranged between US$125 and US$145 trillion/year, with coastal marine ecosystems as the most valuable biome, accounting for 22–27% of the total ecosystem services [5]. Nowadays, the importance of marine biodiversity is recognised by the scientific community, decision makers and citizens [6]. For instance, the European Union chose “Biodiversity is maintained” as the first descriptor of good environmental status in its Marine Strategy Framework Directive (2008/56/EC).
The Mediterranean Sea is a biodiversity hotspot, hosting more than 17,000 species, 20% of which are endemic [7]. This is particularly relevant considering that the Mediterranean Sea covers only 0.82% of the world’s ocean surface area [8]. Humans have benefited from Mediterranean marine ecosystems and their services for millennia, profoundly affecting their biodiversity [9]. Historically, coastal urbanisation pressure, habitat degradation and overexploitation of resources have been the main drivers of biodiversity changes [10]. However, following the industrial revolution and the demographic explosion of the last century, new threats have emerged, and these changes have dramatically accelerated [9]. Recent anthropogenic threats include industrial pollution, eutrophication, microplastics, and non-indigenous species [7]. Furthermore, climate change is altering the distribution, phenology and physiology of many animals, algae, and plants [11,12,13,14,15]. On the one hand, the gradual rise in global temperatures is promoting the spread of warm-water organisms in the Mediterranean, leading to the so-called process of “tropicalization” [16]. On the other hand, extreme thermal events, also called marine heatwaves, have already caused several mass mortalities in the Mediterranean Sea and will likely worsen in the future [13,17,18,19]. Although the Mediterranean basin is one of the most studied seas in the world, there are still important gaps in basic knowledge, such as taxonomy, distribution, abundance, and temporal trends of occurrence of most taxa [7,20]. There are many regional-scale databases, but the knowledge of local and small-scale biodiversity is lacking [21]. This gap hinders the reliable estimates of current changes in biodiversity patterns and the prediction of future scenarios. Hence, there is an urgent need for biodiversity data at a high taxonomic resolution, including species inventories and long-term data series [22,23].
The MARE Outpost was established in Tricase (southeastern Salento, Apulia, Italy) to monitor the local coastal and marine biodiversity and to investigate the phenology and behaviour of marine organisms [24,25]. The remarkable biological uniqueness of this stretch of coastline has been recognized since the 1970s [26,27] and was confirmed by recent findings [28]. Due to its naturalistic importance, Tricase Porto is included in a forthcoming Marine Protected Area that will extend from Otranto to Leuca [29]. Following the institution of the MARE Outpost, the project “Biodiversity MARE Tricase” was initiated to inventory the coastal and marine biodiversity of the area and promote public environmental knowledge and awareness [24].
In the last 50 years, several species lists have been published for the area, but they were all almost exclusively limited to specific taxonomic groups (Mollusca Heterobranchia, [30,31]; shell-bearing Mollusca [32]; Porifera [26,33,34]; Hydrozoa [35]; Polychaeta [36]; Macroalgae [37]), or specific habitats (e.g, caves, [38,39]).
The main aim of this work was to increase current knowledge on the biodiversity of the Central Mediterranean Sea, providing the first multi-taxa species inventory of the coastal area of the southeastern Salento peninsula (Ionian Sea). In addition to the species list, data on depth distribution and phenology are provided, with a special focus on gelatinous plankton.

2. Materials and Methods

2.1. Study Sites and Sampling Methods

Samplings were carried out on the southeastern coast of the Salento Peninsula, in the Otranto Channel (Ionian Sea), between March 2016 and October 2017. Samplings were mostly conducted in an area of ~33 km2 (Figure 1), having as the northern boundary the latitude 39°59′30.7″ N, the southern boundary the latitude 39°54′13.5″ N, the western boundary the coastline, and the eastern boundary a bathymetric depth of 70 m (the depth limit for local fishermen). In addition to the area described above, four additional sites were investigated: Acquaviva’s cave, Bortone’s cave, Ciolo’s cave and the Castro’s mussel farm (Figure 1). The specific sampling location with coordinates (available for 63% of the specimens recorded) is provided in Supplementary Material.
The sampling area is characterised by different substrate and habitat types. A steep rocky substrate, mainly consisting of limestone bedrock, is found from the surface to about 18 m depth. At higher depths, the slope decreases and patches of coralligenous banks (up to 3 m high) alternate with sand and mud down to about 70 m [27]. The area is also characterised by many karst freshwater springs and marine karst caves [40].
Sampling activities focused on the following ecological categories: hard and soft bottom phyto- and zoobenthos, gelatinous zooplankton, nekton, and terrestrial coastal vegetation. Sampling was carried out by free diving to sample benthic organisms, gelatinous plankton, and nekton from 0 to 20 m; by SCUBA diving, to sample benthos and nekton between 0 and 45 m; with fishing gear (set nylon trammel nets, set monofilament gillnets, pole and line and long line) to sample nekton, benthos, and substrates from both catch and bycatch between 0 and 70 m; by citizen scientists (i.e., locals, bathers, divers, and fishermen) to sample between the intertidal and 20 m.
Sampling in SCUBA and free diving was mainly carried out using a visual collection technique [41]. Compared to traditional sampling methods (quadrats, transects, substrate scraping), this visually oriented technique is equivalent in terms of species yields, but it is advantageous in terms of processing time and effort [12]. Samples of specimens of visible size (>5 mm) were collected physically and/or photographically. In addition, pieces of rocky and biogenic substrate were collected for subsequent screening and sorting in the laboratory under a dissecting microscope (Leica MZ6) to search for sessile and vagile organisms. In target stations, soft sediment (detritus) was collected to search for vagile organisms (mainly molluscs).
Sampling with artisanal and recreational fishing gear involved the visually oriented collection of visible catch and bycatch, and the screening of pieces of rocky and biogenic substrate that were collected by the nets for subsequent screening and sorting in the laboratory.
Citizen scientists sampling involved the physical and/or photographical collection of specimens by members of the public, such as locals, tourists, bathers, spear fishers, diving shops, and local fish shops.
In situ and laboratory photos were taken using cameras: Canon Power-Shot D30, Sony Rx100, Nikon AW130, and Sony A7 II. Overall, 134 sampling sessions were carried out. For most of the collected organisms, phenological traits (i.e., seasonality, presence of reproductive structures, mating behaviour) were also noted by stereoscope/light microscope observation and recorded.

2.2. Organism Preservation and Species Identification

Specimens that could not be identified in situ or from photographic material were sampled and brought to the field station, where they were photographed in vivo, and fixed in EtOH and/or formalin 10% as reference material, following the protocol for “Invertebrate Specimen Processing Procedures: Methods of Fixation and Preservation” of the Department of Invertebrate Zoology of the Smithsonian National Museum of Natural History.
Preliminary identification of taxa was made using available taxonomic guides [42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57] together with specific literature and original descriptions. Successively, samples and photographic materials were analysed by experienced taxonomists for accurate species identification. Nomenclature follows the World Register of Marine Species [58], and AlgaeBase [59], although authorities are only reported in tables (see below).

3. Results

3.1. General Description of Marine Biodiversity in the Area

The study area was characterized by rocky substrates from the surface to about 18 m. Below, the slope decreased, and rocky outcrops alternated with sand. In the supralittoral zone, Melarhaphe neritoides (Gastropoda) and Ligia italica (Isopoda) were abundant everywhere, along with algae such as Cladophora dalmatica and Cladophora laetevirens (Figure 2a). Algae such as Ellisolandia elongata and molluscs such as Lepidochitona caprearum and Patella rustica were common in the intertidal zone. The fucalean brown alga Ericaria amentacea was common in the infralittoral fringe (0–0.5 m), although it formed dense and continuous belts in a limited number of places. Algae such as Dictyota dichotoma (very common and abundant everywhere from 0 to 30 m), Jania rubens and species of the Laurencia complex (Laurencia cfr. obtusa, Laurencia glandulifera, Palisada perforata) were well represented in the upper infralittoral zone, from 0 to 3 m (Figure 2b). Then, from 3 to 13 m, the contribution of the Laurencia complex decreased, and other algae became abundant, such as Padina pavonica, Halimeda tuna and Flabellia petiolata (Figure 2c). Together with these algae, the sponges Sarcotragus spinosulus and Chondrosia reniformis were very common between 1 and 7 m.
At 14–18 m, coralligenous formations started. Calcareous algae such as Peyssonnelia heteromorpha, Peyssonnelia rosa-marina and Peyssonnelia squamaria, were very abundant in this habitat. Here, widespread sponges were Petrosia (Petrosia) ficiformis, Agelas oroides, Axinella cannabina, A. damicornis, A. polypoides, A. verrucosa and Acanthella acuta. Very abundant were the bryozoans Schizoretepora serratimargo, which formed large (>100 cm) bioconstructions in the upper mesophotic zone (40–60 m), Schizobrachiella sanguinea, and Adeonella pallasii. Patches of Posidonia oceanica were found from 15–18 m, interspersed with coralligenous formations (Figure 2d).
The Rio area was characterized by the presence of wastewater treatment plant discharges, so it was likely more eutrophic than its surroundings and hosted a different algal assemblage. In particular, Colpomenia sinuosa, Gelidium spinosum and Ellisolandia elongata were abundant (Figure 2e). In addition, Ericaria amentacea formed very dense belts in spring, with much longer fronds than in other areas.
The copious karst caves scattered around the coast hosted distinctive communities and high biodiversity. Very common species were Paractaea monodi, Herbstia condyliata (Brachyura), Polycyathus muellerae (Anthozoa) and Prostheceraeus giesbrechtii (Polycladida) feeding on Pycnoclavella sp. (Ascidiacea). In addition, a high diversity of encrusting and massive sponges such as Aplysina cavernicola, Fasciospongia cavernosa, and species of the genera Haliclona, Petrosia, and Plakina were found (Figure 2f).

3.2. Overall Species Inventory

Overall, we sampled and recorded 1032 specimens belonging to 697 taxa, 655 of which were identified at the species level (94% of taxa), 11 at the species complex level, 28 at the genus level, and 3 at the family level—538 taxa are firstly reported here, while 159 were reported in Micaroni et al. [30] and Costa et al. [33]. The complete list of species is reported in Table 1 and Supplementary Material Table S1; the list of recorded and identified specimens with additional metadata (depth, site, coordinates, substrate, sampling method, and notes) is reported in Table S2.
The most diverse phyla were Mollusca (144), Porifera (112), Chordata (108), Cnidaria (85), Arthropoda (62), Rhodophyta (52) and Annelida (33) (Figure 3a). Among Mollusca, the most diverse classes were Gastropoda (107) and Bivalvia (30), while the most diverse orders were Nudibranchia (29), Littorinimorpha (19), and Neogastropoda (19). Most Chordata belonged to the classes Actinopterygii (89, mostly Perciformes: 64) and Ascidiacea (9). Regarding cnidarians, most taxa belonged to the classes Hydrozoa (49) and Anthozoa (31) (Figure 3b).
Of all identified taxa, 55 represented new records for the Ionian Sea (36 of which were reported in Micaroni et al. [30] and Costa et al. [33]) (Table 1; Figure 3b, Figure 4 and Figure 5). Most of the new records belonged to the phyla Porifera (23, Costa et al., 2019), Mollusca (13), Cnidaria (7, of which 5 belonged to the class Anthozoa and 2 to the class Hydrozoa), Platyhelminthes (4, all from the order Polycladida), and Annelida (3). For other 8 taxa, our finding represented the only location in the Ionian Sea other than the Strait of Messina, considered by many authors to be a different biogeographical sector [16,60,61,62] (Table 1). Furthermore, records of Helicosalpa virgula (Chordata: Thaliacea) and Lampea pancerina (Ctenophora: Tentaculata) account for the easternmost sightings in the Mediterranean Sea (Table 1).
Polycladida (Platyhelminthes) was the taxonomic group with a higher proportion of new records on the total number of taxa, with 80% of the species found being new records for the Ionian Sea (4 out of 5 taxa), followed by Nemertea (50%, 1 out of 2), Thaliacea (33%, 1 out of 3), Heterobranchia (28%, 13 out of 47), Porifera (21%, 23 out of 112), and Anthozoa (16%, 5 out of 31) (Figure 3c). Similar results were found comparing the proportion of new records in this study to the total number of taxa found in the Italian Ionian Sea by the checklist of the Italian marine fauna [60,61], with Polycladida (Platyhelminthes), Nemertea, Anthozoa, Porifera, Thaliacea, and Heterobranchia being the taxa with the highest proportion of new records (Figure 6a).
The majority of taxa (48.8%) were recorded between 0 and 10 m, whereas 29.2% of taxa were sampled between 11 and 25 m and 21.9% from 26 to 70 m. The highest percentage of new records (10%) has been reported for the depth range 11–25 m (Figure 7).
For 63 of the taxa found, phenology traits were also reported. These included the presence of reproductive structures (31), the occurrence of seasonal organisms (25), and instances of reproductive behaviour (6) (Table 1 and Table S1).
Overall, we found 9 non-indigenous species (NIS), including two polychaetes (Lysidice collaris and Hydroides elegans), two crustaceans (Callinectes sapidus and Percnon gibbesi), two hydroids (Clytia linearis and Eudendrium merulum), and one ascidian, macroalga and ctenophore (Botrylloides niger, Caulerpa cylindracea and Mnemiopsis leidyi) (Table 1). None of these represent a new record for the area.
Most specimens were collected by SCUBA diving (32%), free diving (31%) and by artisanal fishers’ fishing gear (29%), while citizen science and recreational fishing gear, provided only 3% and 1% of the specimens, respectively. Regarding SCUBA and free diving, 79% of the specimens were collected physically either using the visual collection technique or by sampling substrate (biogenic substrate, pieces of rocks, and soft sediment), while the remaining 21% was only recorded photographically (mainly fish and organisms that could be identified only by the external morphology). Regarding sampling with fishing gears, most specimens were collected by set nylon trammel nets (63%), that were left 3–6 days in the water, and set monofilament gillnets (15%), that were left <24 h in the water (Table S2).
As for sampling substrate, most specimens we collected from rocky substrate (34%), coralligenous formations and rubble (22%), soft sediments including mud and sand (7%), while 9% were pelagic (Table S2).
Regarding the terrestrial near-shore vegetation, 81 species were found, 79 of which referred to the division Magnoliophyta and 2 to the division Polypodiophyta. Most species belonged to the order Asterales (16), Lamiales (13), Caryophyllales (10) and Poales (8). Regarding families, the most speciose ones were Asteraceae (13), Poaceae (8), Plantaginaceae (5), Apiaceae (4), and Crassulaceae (4). None of these species represent a new record for the area (Table S1).

3.3. Observations on Gelatinous Zooplankton

Gelatinous plankton blooms mostly occurred in spring and early summer, when complex communities developed. These communities were mainly composed of thaliaceans, scyphozoan and hydrozoan jellyfish, siphonophores, ctenophores, alciopid polychaetes and pterotracheid molluscs. Minor blooms involving fewer species also occurred throughout the year (Table 1 and Table S1).
Thaliaceans were very abundant in spring. Salpa fusiformis was the most abundant species and formed very dense blooms between March and April 2016; occasional isolated specimens were also found in autumn (November 2016). Salpa maxima bloomed later than S. fusiformis (April–May 2016). Isolate blastozooids of a rare helicosalpid (Helicosalpa virgula) were recorded on the 27 April 2016.
Regarding cnidarians, scyphozoan jellyfish mostly occurred in spring–summer. In 2016, Aurelia solida and Chrysaora hysoscella bloomed throughout April and May. Other scyphozoans were rarer, and only isolated specimens were found, and in particular Rhizostoma pulmo (February and June), and Cotylorhiza tuberculata (July–August). Regarding hydrozoan jellyfish, we found blooms of Aequorea forskalea and Oceania armata (April), and isolated specimens of Geryonia proboscidalis (April) and Olindias muelleri (September). Siphonophores were very common during the salp blooms in April and May, particularly Halistemma rubrum, Nanomia bijuga, Forskalia formosa, and Hippopodius hippopus.
As for ctenophores, the only blooming species was Mnemiopsis leidyi which occurred from November 2016 to January 2017. Other species were reported occasionally, including Leucothea multicornis (April–September), Lampea pancerina (April 2016, preying on Salpa fusiformis), and Cestum veneris (one specimen, May 2016).
Table 1. Complete list of marine species found during the project “Biodiversity MARE Tricase” with indication of depth or depth range (when multiple specimens were found) at which taxa were recorded during this study. For phenology, Rep. behav., reproductive behaviour; Rep. structures, reproductive structures. In the column New Record, * indicates a new record for the Ionian Sea, ‡ indicates that the only other record in the Ionian Sea is from the Messinian Strait, † indicates the easternmost record in the Mediterranean Sea, # indicates new species for science. For the records that were already reported in a separate publication, the reference is given at the end of the species name.
Table 1. Complete list of marine species found during the project “Biodiversity MARE Tricase” with indication of depth or depth range (when multiple specimens were found) at which taxa were recorded during this study. For phenology, Rep. behav., reproductive behaviour; Rep. structures, reproductive structures. In the column New Record, * indicates a new record for the Ionian Sea, ‡ indicates that the only other record in the Ionian Sea is from the Messinian Strait, † indicates the easternmost record in the Mediterranean Sea, # indicates new species for science. For the records that were already reported in a separate publication, the reference is given at the end of the species name.
TaxaDepthPhenologyNew Record
Kingdom BACTERIA
Phylum CYANOBACTERIA
Class CYANOPHYCEAE
Order NOSTOCALES
Family RIVULARIACEAE
Rivularia ind Roth ex Bornet & Flahault, 18860 m-
Kingdom CHROMISTA
Phylum FORAMINIFERA
Class GLOBOTHALAMEA
Order ROTALIIDA
Family HOMOTREMATIDAE
Miniacina miniacea (Pallas, 1766)30 m-
Order TEXTULARIIDA
Family TEXTULARIIDAE
Textularia ind Defrance, 182425 m-
Phylum RADIOZOA
Class POLYCYSTINA
Order COLLODARIA
Collozoum ind Haeckel, 1862 sensu Brandt, 19050–5 mOccurrence (VI–VII)
Phylum OCHROPHYTA
Class PHAEOPHYCEAE
Order CUTLERIALES
Family CUTLERIACEAE
Cutleria multifida (Turner) Greville1 m-
Zanardinia typus (Nardo) P.C.Silva5 m-
Order DICTYOTALES
Family DICTYOTACEAE
Dictyopteris polypodioides (A.P.De Candolle) J.V.Lamouroux1 m-
Dictyota cf. implexa (Desfontaines) J.V.Lamouroux20 m-
Dictyota dichotoma (Hudson) J.V.Lamouroux0–15 m-
Padina pavonica (Linnaeus) Thivy1–10 m-
Order ECTOCARPALES
Family SCYTOSIPHONACEAE
Colpomenia sinuosa (Mertens ex Roth) Derbès & Solier10 m-
Scytosiphon lomentaria (Lyngbye) Link1 m-
Order FUCALES
Family SARGASSACEAE
Cystoseira compressa (Esper) Gerloff & Nizamuddin1 m-
Cystoseira foeniculacea (Linnaeus) Greville20 m-
Ericaria amentacea (C.Agardh) Molinari & Guiry0–1 m-
Sargassum vulgare C.Agardh10 m-
Order SPHACELARIALES
Family CLADOSTEPHACEAE
Cladostephus hirsutus (Linnaeus) Boudouresque & M.Perret-Boudouresque ex Heesch & al.3 m-
Family SPHACELARIACEAE
Sphacelaria sp.20 m-
Family STYPOCAULACEAE
Halopteris scoparia (Linnaeus) Sauvageau10 m-
Order SPOROCHNALES
Family SPOROCHNACEAE
Nereia filiformis (J.Agardh) Zanardini40 m-
Phylum CILIOPHORA
Class HETEROTRICHEA
Order HETEROTRICHIDA
Family FOLLICULINIDAE
Folliculinidae ind (T.S. Wright, 1859) Dons, 193470 m-
Class OLIGOHYMENOPHOREA
Order SESSILIDA
Family ZOOTHAMNIIDAE
Zoothamnium niveum Ehrenberg, 183810 m-*
Kingdom PLANTAE
Phylum RHODOPHYTA
Class COMPSOPOGONOPHYCEAE
Order ERYTHROPELTALES
Family ERYTHROTRICHIACEAE
Erythrotrichia carnea (Dillwyn) J.Agardh0 m-
Class FLORIDEOPHYCEAE
Order BONNEMAISONIALES
Family BONNEMAISONIACEAE
Asparagopsis taxiformis (Delile) Trevisan de Saint-Léon1 m-
Order CERAMIALES
Family CALLITHAMNIACEAE
Callithamnion granulatum (Ducluzeau) C.Agardh0 m-
Crouania attenuata (C.Agardh) J.Agardh10 m-
Family CERAMIACEAE
Ceramium cf. virgatum Roth0 m-
Ceramium diaphanum (Lightfoot) Roth0 m-
Gayliella mazoyerae T.O.Cho, Fredericq & Hommersand2 m-
Family DASYACEAE
Dasya rigidula (Kützing) Ardissone20 m-
Family DELESSERIACEAE
Hypoglossum hypoglossoides (Stackhouse) Collins & Hervey1 m-
Family RHODOMELACEAE
Chondria sp. (Montagne)0 m-
Herposiphonia secunda (C.Agardh) Ambronn20 m-
Laurencia cf. microcladia Kützing20 m-
Laurencia cf. obtusa (Hudson) J.V.Lamouroux1 m-
Laurencia glandulifera (Kützing) Kützing1 m-
Osmundaria volubilis (Linnaeus) R.E.Norris30 m-
Osmundea truncata (Kützing) K.W.Nam & Maggs0 m-
Palisada perforata (Bory) K.W.Nam2 m-
Polysiphonia opaca (C.Agardh) Moris & De Notaris0 m-
Polysiphonia sertularioides (Grateloup) J.Agardh0 m-
Vertebrata fruticulosa (Wulfen) Kuntze1 mRep. structures (IV)
Xiphosiphonia pennata (C.Agardh) Savoie & G.W.Saunders0 m-
Family WRANGELIACEAE
Wrangelia penicillata (C.Agardh) C.Agardh10 m-
Order CORALLINALES
Family CORALLINACEAE
Ellisolandia elongata (J.Ellis & Solander) K.R.Hind & G.W.Saunders0–1 m-
Jania rubens (Linnaeus) J.V.Lamouroux2 m-
Jania virgata (Zanardini) Montagne10–18 m-
Family LITHOPHYLLACEAE
Amphiroa rigida J.V.Lamouroux2 m-
Lithophyllum byssoides (Lamarck) Foslie0 m-
Lithophyllum cf. incrustans Philippi3 m-
Lithophyllum stictiforme (J.E. Areschoug) Hauck5–10 m-
Tenarea tortuosa (Esper) Me.Lemoine1 m-
Titanoderma trochanter (Bory) Benhissoune, Boudouresque, Perret-Boudouresque & Verlaque1 m-
Family MASTOPORACEAE
Pneophyllum fragile Kützing0 m-
Order GELIDIALES
Family GELIDIACEAE
Gelidium spinosum (S.G.Gmelin) P.C.Silva1 m-
Family PTEROCLADIACEAE
Pterocladiella capillacea (S.G.Gmelin) Santelices & Hommersand0 m-
Order GIGARTINALES
Family CYSTOCLONIACEAE
Hypnea musciformis (Wulfen) J.V.Lamouroux2 m-
Family GIGARTINACEAE
Chondracanthus acicularis (Roth) Fredericq0 m-
Family PHYLLOPHORACEAE
Phyllophora crispa (Hudson) P.S.Dixon30 m-
Schottera nicaeensis (J.V.Lamouroux ex Duby) Guiry & Hollenberg1 m-
Family RHIZOPHYLLIDACEAE
Contarinia squamariae (Meneghini) Denizot5 m-
Family SPHAEROCOCCACEAE
Sphaerococcus coronopifolius Stackhouse7–10 m-
Order HALYMENIALES
Family HALYMENIACEAE
Halymenia floresii (Clemente) C.Agardh15 m-
Order NEMALIALES
Family GALAXAURACEAE
Tricleocarpa fragilis (Linnaeus) Huisman & R.A.Townsend10 m-
Family LIAGORACEAE
Liagora viscida (Forsskål) C.Agardh0–2 m-
Order NEMASTOMATALES
Family NEMASTOMATACEAE
Predaea ollivieri Feldmann22 m-
Family SCHIZYMENIACEAE
Platoma cyclocolpum (Montagne) F.Schmitz3 mRep. structures (VIII)
Order PEYSSONNELIALES
Family PEYSSONNELIACEAE
Peyssonnelia heteromorpha (Zanardini) Athanasiadis10 m-
Peyssonnelia rosa-marina Boudouresque & Denizot20 m-
Peyssonnelia rubra (Greville) J.Agardh0 m-
Peyssonnelia squamaria (S.G.Gmelin) Decaisne ex J.Agardh5–20 m-
Order RHODYMENIALES
Family CHAMPIACEAE
Gastroclonium clavatum (Roth) Ardissone1 m-
Family RHODYMENIACEAE
Botryocladia sp.30 m-
Irvinea boergesenii (Feldmann) R.J.Wilkes, L.M.McIvor & Guiry30 m-
Phylum CHLOROPHYTA
Class PYRAMIMONADOPHYCEAE
Order PALMOPHYLLALES
Family PALMOPHYLLACEAE
Palmophyllum crassum (Naccari) Rabenhorst4 m-
Class ULVOPHYCEAE
Order BRYOPSIDALES
Family BRYOPSIDACEAE
Bryopsis cf. pennata J.V.Lamouroux1 m-
Bryopsis cupressina J.V.Lamouroux0 m-
Family CAULERPACEAE
Caulerpa cylindracea Sonder8–45 m-
Caulerpa prolifera (Forsskål) J.V.Lamouroux15 m-
Family CODIACEAE
Codium bursa (Olivi) C.Agardh8 m-
Codium cf. vermilara (Olivi) Delle Chiaje5–10 m-
Codium coralloides (Kützing) P.C.Silva8–10 m-
Family HALIMEDACEAE
Halimeda tuna (J.Ellis & Solander) J.V.Lamouroux10–25 m-
Family UDOTEACEAE
Flabellia petiolata (Turra) Nizamuddin10–15 m-
Pseudochlorodesmis furcellata (Zanardini) Børgesen3 m-
Order CLADOPHORALES
Family ANADYOMENACEAE
Anadyomene stellata (Wulfen) C.Agardh1–20 m-
Family CLADOPHORACEAE
Chaetomorpha linum (O.F.Müller) Kützing0 m-
Cladophora dalmatica Kützing0 m-
Cladophora laetevirens (Dillwyn) Kützing0 m-
Family VALONIACEAE
Valonia utricularis (Roth) C.Agardh2 m-
Order DASYCLADALES
Family POLYPHYSACEAE
Acetabularia acetabulum (Linnaeus) P.C.Silva3–10 m-
Order ULVALES
Family ULVACEAE
Ulva linza Linnaeus0 m-
Phylum TRACHEOPHYTA
Class MAGNOLIOPSIDA
Order ALISMATALES
Family CYMODOCEACEAE
Cymodocea nodosa (Ucria) Ascherson6 m-
Family POSIDONIACEAE
Posidonia oceanica (Linnaeus) Delile10–22 m-
Kingdom ANIMALIA
Phylum CTENOPHORA
Class TENTACULATA
Order CESTIDA
Family CESTIDAE
Cestum veneris Lesueur, 18133 mOccurrence (V)
Order CYDIPPIDA
Family LAMPEIDAE
Lampea pancerina (Chun, 1879)3 mOccurrence (IV)‡†
Order LOBATA
Family BOLINOPSIDAE
Mnemiopsis leidyi A. Agassiz, 18651–5 mOccurrence (XI–I)
Family LEUCOTHEIDAE
Leucothea multicornis (Quoy & Gaimard, 1824)0–3 mOccurrence (IV–IX)
Phylum PORIFERA
Class CALCAREA
Order CLATHRINIDA
Family CLATHRINIDAE
Clathrina clathrus (Schmidt, 1864) [33]40 m-
Order LEUCOSOLENIDA
Family SYCETTIDAE
Sycon raphanus Schmidt, 1862 [33]70 m-
Class DEMOSPONGIAE
Order AGELASIDA
Family AGELASIDAE
Agelas oroides (Schmidt, 1864) [33]20–42 m-
Family HYMERHABDIIDAE
Hymerhabdia oxytrunca Topsent, 1904 [33]20 m-*
Prosuberites longispinus Topsent, 1893 [33]20 m-
Order AXINELLIDA
Family AXINELLIDAE
Axinella cannabina (Esper, 1794) [33]20–50 m-
Axinella damicornis (Esper, 1794) [33]20–35 m-
Axinella polypoides Schmidt, 1862 [33]10 m-
Axinella verrucosa (Esper, 1794) [33]20–40 m-
Family RASPAILIIDAE
Didiscus stylifer Tsurnamal, 1969 [33]20 m-
Eurypon cinctum Sarà, 1960 [33]20 m-*
Eurypon clavatum (Bowerbank, 1866) [33]20 m-
Eurypon coronula (Bowerbank, 1874) [33]20 m-*
Eurypon gracile Bertolino, Calcinai & Pansini, 2013 [33]20 m-
Eurypon major Sarà & Siribelli, 1960 [33]20 m-
Eurypon obtusum Vacelet, 1969 [33]20 m-*
Eurypon viride (Topsent, 1889) [33]20 m-
Raspaciona aculeata (Johnston, 1842) [33]20 m-
Raspailia (Raspailia) viminalis Schmidt, 1862 [33]70 m-*
Family STELLIGERIDAE
Halicnemia geniculata Sarà, 1958 [33]20 m-*
Order BIEMNIDA
Family RHABDEREMIIDAE
Rhabderemia gallica van Soest & Hooper, 1993 [33]20 m-*
Rhabderemia minutula (Carter, 1876) [33]20 m-
Order BUBARIDA
Family BUBARIDAE
Bubaris carcisis Vacelet, 1969 [33]20 m-
Bubaris vermiculata (Bowerbank, 1866) [33]20 m-
Monocrepidium vermiculatum Topsent, 1898 [33]20 m-*
Rhabdobaris implicata Pulitzer-Finali, 1983 [33]20 m-*
Family DESMANTHIDAE
Desmanthus incrustans (Topsent, 1889) [33]20 m-
Family DICTYONELLIDAE
Acanthella acuta Schmidt, 1862 [33]25–30 m-
Dictyonella incisa (Schmidt, 1880) [33]10 m-
Dictyonella obtusa (Schmidt, 1862) [33]22 m-
Order CHONDRILLIDA
Family CHONDRILLIDAE
Chondrilla nucula Schmidt, 1862 [33]5–25 m-
Order CHONDROSIIDA
Family CHONDROSIIDAE
Chondrosia reniformis Nardo, 1847 [33]2–20 mSpawning (VII)
Order CLIONAIDA
Family CLIONAIDAE
Cliona amplicavata Rützler, 1974 [33]20 m-*
Cliona burtoni Topsent, 1932 [33]20 m-*
Cliona celata Grant, 1826 [33]5 m-
Cliona schmidtii (Ridley, 1881) [33]10 m-
Cliona viridis (Schmidt, 1862) [33]5–20 m-
Cliothosa hancocki (Topsent, 1888) [33]20 m-
Spiroxya heteroclita Topsent, 1896 [33]20 m-
Spiroxya sarai (Melone, 1965) [33]20 m-
Family SPIRASTRELLIDAE
Diplastrella bistellata (Schmidt, 1862) [33]20 m-
Diplastrella boeroi Bertolino, Costa & Pansini, 2019 [33]20 m-#
Spirastrella cunctatrix Schmidt, 1868 [33]20 m-
Spirastrella regina Bertolino, Costa & Pansini, 2020 [33]20 m-#
Order DICTYOCERATIDA
Family DYSIDEIDAE
Dysidea avara (Schmidt, 1862) [33]20 m-
Dysidea fragilis (Montagu, 1814) [33]20 m-
Family IRCINIIDAE
Ircinia variabilis (Schmidt, 1862) [33]10 m-
Sarcotragus foetidus Schmidt, 1862 [33]5–10 m-
Sarcotragus spinosulus Schmidt, 1862 [33]12 m-
Family THORECTIDAE
Fasciospongia cavernosa (Schmidt, 1862) [33]5–20 m-
Scalarispongia scalaris (Schmidt, 1862) [33]10 m-
Order HAPLOSCLERIDA
Family CHALINIDAE
Haliclona (Reniera) mediterranea Griessinger, 1971 [33]5 m-
Haliclona (Rhizoniera) sarai (Pulitzer-Finali, 1969) [33]5 m-
Haliclona (Soestella) mucosa (Griessinger, 1971) [33]7 m-*
Haliclona (Soestella) valliculata (Griessinger, 1971) [33]5 m-*
Family PETROSIIDAE
Petrosia (Petrosia) clavata (Esper, 1794) [33]20 m-
Petrosia (Petrosia) ficiformis (Poiret, 1789) [33]7–40 m-
Petrosia (Strongylophora) pulitzeri Pansini, 1996 [33]7 m-*
Petrosia (Strongylophora) vansoesti Boury-Esnault, Pansini & Uriz, 1994 [33]5 m-*
Family PHLOEODICTYIDAE
Oceanapia perforata (Sarà, 1960) [33]7 m-*
Order POECILOSCLERIDA
Family COELOSPHAERIDAE
Lissodendoryx (Anomodoryx) cavernosa (Topsent, 1892) [33]20 m-
Family CRAMBEIDAE
Crambe crambe (Schmidt, 1862) [33]5 m-
Family CRELLIDAE
Crella sp. Gray, 1867 [33]20 m-
Family ESPERIOPSIDAE
Ulosa digitata (Schmidt, 1866) [33]10 m-
Family HYMEDESMIIDAE
Hamigera hamigera (Schmidt, 1862) [33]3 m-
Hemimycale columella (Bowerbank, 1874) [33]6 m-
Phorbas dives (Topsent, 1891) [33]20 m-
Phorbas fictitius (Bowerbank, 1866) [33]20 m-
Phorbas tenacior (Topsent, 1925) [33]20 m-
Family MICROCIONIDAE
Clathria (Clathria) coralloides (Scopoli, 1772) [33]70 m-
Clathria (Clathria) toxistricta Topsent, 1925 [33]70 m-
Clathria (Clathria) toxivaria (Sarà, 1959) [33]20 m-
Family MYCALIDAE
Mycale (Mycale) lingua (Bowerbank, 1866) [33]20 m-
Mycale (Mycale) massa (Schmidt, 1862) [33]20 m-
Order SUBERITIDA
Family HALICHONDRIIDAE
Axinyssa aurantiaca (Schmidt, 1864) [33]20 m-
Halichondria (Halichondria) cf. panicea (Pallas, 1766) [33]20 m-
Halichondria (Halichondria) contorta (Sarà, 1961) [33]10 m-*
Spongosorites intricatus (Topsent, 1892) [33]20 m-
Family SUBERITIDAE
Aaptos aaptos (Schmidt, 1864) [33]4–10 m-
Protosuberites epiphytum (Lamarck, 1815) [33]20 m-
Terpios gelatinosus (Bowerbank, 1866) [33]20 m-
Order TETHYIDA
Family TETHYIDAE
Tethya aurantium (Pallas, 1766) [33]20 m-
Tethya citrina Sarà & Melone, 1965 [33]20 m-
Family TIMEIDAE
Timea stellata (Bowerbank, 1866) [33]20 m-
Timea unistellata (Topsent, 1892) [33]20 m-
Order TETRACTINELLIDA
Family ANCORINIDAE
Ancorina cerebrum Schmidt, 1862 [33]20 m-*
Dercitus (Stoeba) plicatus (Schmidt, 1868) [33]20 m-
Jaspis incrustans (Topsent, 1890) [33]20 m-
Jaspis johnstonii (Schmidt, 1862) [33]20 m-
Stelletta grubii Schmidt, 1862 [33]20 m-
Stelletta mediterranea (Topsent, 1893) [33]20 m-*
Stelletta stellata Topsent, 1893 [33]20 m-
Family CALTHROPELLIDAE
Calthropella (Corticellopsis) stelligera (Schmidt, 1868) [33]--*
Family GEODIIDAE
Erylus discophorus (Schmidt, 1862) [33]20 m-
Geodia cydonium (Linnaeus, 1767) [33]20 m-
Penares euastrum (Schmidt, 1868) [33]20 m-
Penares helleri (Schmidt, 1864) [33]20 m-
Family PACHASTRELLIDAE
Pachastrella monilifera Schmidt, 1868 [33]20 m-
Triptolemma simplex (Sarà, 1959) [33]20 m-
Family TETILLIDAE
Tetilla sp. Schmidt, 1868 [33]20 m-
Family THOOSIDAE
Alectona millari Carter, 1879 [33]20 m-
Delectona madreporica Bavestrello, Calcinai, Cerrano & Sarà, 1997 [33]20 m-*
Family VULCANELLIDAE
Poecillastra compressa (Bowerbank, 1866) [33]20 m-
Order VERONGIIDA
Family APLYSINIDAE
Aplysina aerophoba (Nardo, 1833) [33]20 m-
Aplysina cavernicola (Vacelet, 1959) [33]70 m-
Family IANTHELLIDAE
Hexadella racovitzai Topsent, 1896 [33]15 m-
Class HOMOSCLEROMORPHA
Order HOMOSCLEROPHORIDA
Family OSCARELLIDAE
Oscarella cf. tuberculata (Schmidt, 1868) [33]5–15 m-*
Family PLAKINIDAE
Corticium candelabrum Schmidt, 1862 [33]20 m-
Plakina dilopha Schulze, 1880 [33]20 m-*
Plakina reducta (Pulitzer-Finali, 1983) [33]20 m-
Plakina trilopha Schulze, 1880 [33]20 m-
Plakortis simplex Schulze, 1880 [33]20 m-
Phylum CNIDARIA
Class ANTHOZOA
Order ACTINIARIA
Family ACTINIIDAE
Actinia mediterranea Schmidt, 19710 m -
Anemonia viridis (Forsskål, 1775)10 m-
Condylactis aurantiaca (Delle Chiaje, 1825)28 m-
Paranemonia cinerea (Contarini, 1844)3 m-*
Family AIPTASIIDAE
Aiptasia mutabilis (Gravenhorst, 1831)3 m-
Exaiptasia diaphana (Rapp, 1829)8 m-
Family HALCAMPIDAE
Halcampoides purpureus (Studer, 1879)4 m-*
Family HORMATHIIDAE
Calliactis parasitica (Couch, 1842)20–50 m-
Family PHYMANTHIDAE
Phymanthus pulcher (Andrès, 1883)23 m-*
Order ALCYONACEA
Family ALCYONIIDAE
Alcyonium cf. coralloides (Pallas, 1766)45 m-
Alcyonium palmatum Pallas, 176660 m-
Family CORALLIIDAE
Corallium rubrum (Linnaeus, 1758)60 m-
Family CORNULARIIDAE
Cornularia cornucopiae (Pallas, 1766)5–70 m-*
Family GORGONIIDAE
Eunicella cavolini (Koch, 1887)40 m-
Leptogorgia sarmentosa (Esper, 1789)30 m-
Family PLEXAURIDAE
Paramuricea clavata (Risso, 1826)55 m-
Order ANTIPATHARIA
Family MYRIOPATHIDAE
Antipathella subpinnata (Ellis & Solander, 1786)80 m-
Order PENICILLARIA
Family ARACHNACTIDAE
Arachnanthus cf. oligopodus (Cerfontaine, 1891)4 m-
Order PENNATULACEA
Family PENNATULIDAE
Pteroeides griseum (Bohadsch, 1761)70 m-
Family VIRGULARIIDAE
Virgularia mirabilis (Müller, 1776)70 m-*
Order SCLERACTINIA
Family CARYOPHYLLIIDAE
Caryophyllia (Caryophyllia) cf. inornata (Duncan, 1878)3 m-
Paracyathus pulchellus (Philippi, 1842)70 m-
Phyllangia americana mouchezii (Lacaze-Duthiers, 1897)40 m-
Polycyathus muellerae (Abel, 1959)4 m-
Family DENDROPHYLLIIDAE
Balanophyllia (Balanophyllia) europaea (Risso, 1826)4–15 m-
Family POCILLOPORIDAE
Madracis pharensis (Heller, 1868)15 m-
Family SCLERACTINIA INCERTAE SEDIS
Cladocora caespitosa (Linnaeus, 1767)8 m-
Order SPIRULARIA
Family CERIANTHIDAE
Cerianthus membranaceus (Gmelin, 1791)10–20 m-
Order ZOANTHARIA
Family EPIZOANTHIDAE
Epizoanthus ind Gray, 186760 m-
Family PARAZOANTHIDAE
Parazoanthus axinellae (Schmidt, 1862)21 m-
Savalia savaglia (Bertoloni, 1819)60 m-
Class HYDROZOA
Order ANTHOATHECATA
Family CORYNIDAE
Coryne pintneri Schneider, 189710–60 mRep. structures (VII)
Family EUDENDRIIDAE
Eudendrium merulum Watson, 198525 m-
Eudendrium moulouyensis Marques, Peña Cantero & Vervoort, 20005 mRep. structures (IX)
Eudendrium racemosum (Cavolini, 1785)20 m-
Family OCEANIIDAE
Corydendrium parasiticum (Linnaeus, 1767)1 m-
Oceania armata Kölliker, 18531 mMedusa, Eggs (IV)
Rhizogeton nudus Broch, 19103 m-
Turritopsis dohrnii (Weismann, 1883)2–70 mMedusa (VII-IX)
Family PANDEIDAE
Amphinema rugosum (Mayer, 1900)25 m-
Family PENNARIIDAE
Pennaria disticha Goldfuss, 18203 m-
Family PROBOSCIDACTYLIDAE
Proboscidactyla ornata (McCrady, 1859)70 mMedusa (VI)*
Family TUBULARIIDAE
Ectopleura wrighti Petersen, 197920 m-
Family ZANCLEIDAE
Halocoryne epizoica Hadzi, 191710–20 mMedusa (VI)
Zanclea giancarloi Boero, Bouillon & Gravili, 200070 m-
Order LEPTOTHECATA
Family AEQUOREIDAE
Aequorea forskalea Péron & Lesueur, 18100–5 mMedusa (IV)
Family AGLAOPHENIIDAE
Aglaophenia elongata Meneghini, 184511–50 m-
Aglaophenia kirchenpaueri (Heller, 1868)50 mRep. structures (IV)
Aglaophenia octodonta (Heller, 1868)1–5 mRep. structures (IV)
Aglaophenia tubiformis Marktanner-Turneretscher, 189011 mRep. structures (V)
Family CAMPANULARIIDAE
Clytia hemisphaerica (Linnaeus, 1767)11 m-
Clytia hummelincki (Leloup, 1935)5 m-
Clytia linearis (Thorneley, 1900)30 m-
Obelia dichotoma (Linnaeus, 1758)3–4 m-
Orthopyxis integra (MacGillivray, 1842)0 m-
Family HALECIIDAE
Halecium petrosum Stechow, 19195 m-
Halecium pusillum Sars, 18563 m-
Family HALOPTERIDIDAE
Antennella secundaria (Gmelin, 1791)3–11 m-
Antennella siliquosa (Hincks, 1877)15 m-
Family HEBELLIDAE
Anthohebella parasitica (Ciamician, 1880)1–2 m-
Scandia gigas (Pieper, 1884)10 m-
Family KIRCHENPAUERIIDAE
Kirchenpaueria pinnata (Linnaeus, 1758)0–20 m-
Family LAFOEIDAE
Filellum serpens (Hassall, 1848)--
Family LAODICEIDAE
Laodicea undulata (Forbes & Goodsir, 1853)45 m-
Family PLUMULARIIDAE
Monotheca obliqua (Johnston, 1847)2 m-
Nemertesia ramosa (Lamarck, 1816)70 m-
Plumularia posidoniae (Picard, 1952)12 m-
Plumularia setacea (Linnaeus, 1758)3–5 m-
Family SERTULARELLIDAE
Sertularella ellisii (Deshayes & Milne Edwards, 1836)3–60 mRep. structures (VI)
Sertularella gayi (Lamouroux, 1821)70 m-
Sertularella mediterranea Hartlaub, 190150 m-
Family SERTULARIIDAE
Dynamena disticha (Bosc, 1802)2 m-
Family SYNTHECIIDAE
Synthecium evansi (Ellis & Solander, 1786)70 m-
Order LIMNOMEDUSAE
Family GERYONIIDAE
Geryonia proboscidalis (Forsskål, 1775)3 mMedusa (IV)
Family OLINDIIDAE
Olindias muelleri Haeckel, 18797 mMedusa (IX)
Order SIPHONOPHORAE
Family AGALMATIDAE
Halistemma rubrum (Vogt, 1852)0 mOccurrence (IV)*
Nanomia bijuga (Delle Chiaje, 1844)5 mOccurrence (IV)
Family FORSKALIIDAE
Forskalia formosa Keferstein & Ehlers, 18601–2 mOccurrence (IV)
Family HIPPOPODIIDAE
Hippopodius hippopus (Forsskål, 1776)1 mOccurrence (IV-V)
Family PRAYIDAE
Rosacea cymbiformis (Delle Chiaje, 1830)0–5 mOccurrence (IV-V)
Class SCYPHOZOA
Order CORONATAE
Family NAUSITHOIDAE
Nausithoe ind Kölliker, 185370 m-
Order RHIZOSTOMEAE
Family CEPHEIDAE
Cotylorhiza tuberculata (Macri, 1778)1 mMedusa (VII)
Family RHIZOSTOMATIDAE
Rhizostoma pulmo (Macri, 1778)2 mMedusa (II; VI)
Order SEMAEOSTOMEAE
Family PELAGIIDAE
Chrysaora hysoscella (Linnaeus, 1767)0–2 mMedusa (IV-V)
Family ULMARIDAE
Aurelia solida Browne, 19050–5 mMedusa (IV-V)
Phylum HEMICHORDATA
Class GRAPTOLITHOIDEA
Order RHABDOPLEUROIDEA
Family RHABDOPLEURIDAE
Rhabdopleura recondita Beli, Cameron and Piraino, 201870 m-
Phylum ECHINODERMATA
Class ASTEROIDEA
Order FORCIPULATIDA
Family ASTERIIDAE
Coscinasterias tenuispina (Lamarck, 1816)6 m-
Marthasterias glacialis (Linnaeus, 1758)3–15 m-
Order PAXILLOSIDA
Family ASTROPECTINIDAE
Astropecten aranciacus (Linnaeus, 1758)10–34 m-
Order SPINULOSIDA
Family ECHINASTERIDAE
Echinaster (Echinaster) sepositus (Retzius, 1783)60 m-
Order VALVATIDA
Family CHAETASTERIDAE
Chaetaster longipes (Bruzelius, 1805)70 m-
Family GONIASTERIDAE
Peltaster placenta (Müller & Troschel, 1842)45 m-
Family OPHIDIASTERIDAE
Hacelia attenuata Gray, 184025 m-
Ophidiaster ophidianus (Lamarck, 1816)10 m-
Class CRINOIDEA
Order COMATULIDA
Family ANTEDONIDAE
Antedon mediterranea (Lamarck, 1816)45 m-
Class ECHINOIDEA
Order ARBACIOIDA
Family ARBACIIDAE
Arbacia lixula (Linnaeus, 1758)1–12 m-
Order CAMARODONTA
Family ECHINIDAE
Echinus melo Lamarck, 181650 m-
Family PARECHINIDAE
Paracentrotus lividus (Lamarck, 1816)1–10 m-
Psammechinus microtuberculatus (Blainville, 1825)34 m-
Family TOXOPNEUSTIDAE
Sphaerechinus granularis (Lamarck, 1816)8 m-
Order CIDAROIDA
Family CIDARIDAE
Cidaris cidaris (Linnaeus, 1758)70 m-
Stylocidaris affinis (Philippi, 1845)70 m-
Order CLYPEASTEROIDA
Family FIBULARIIDAE
Echinocyamus pusillus (O.F. Müller, 1776)18 m-
Order DIADEMATOIDA
Family DIADEMATIDAE
Centrostephanus longispinus (Philippi, 1845)50 m-
Class HOLOTHUROIDEA
Order HOLOTHURIIDA
Family HOLOTHURIIDAE
Holothuria (Holothuria) tubulosa Gmelin, 17917 m-
Holothuria (Panningothuria) forskali Delle Chiaje, 18232 m-
Holothuria (Platyperona) sanctori Delle Chiaje, 18234 m-
Order SYNALLACTIDA
Family STICHOPODIDAE
Parastichopus regalis (Cuvier, 1817)60 m-
Class OPHIUROIDEA
Order AMPHILEPIDIDA
Family OPHIOTRICHIDAE
Ophiothrix fragilis (Abildgaard in O.F. Müller, 1789)30–50 m-
Order OPHIACANTHIDA
Family OPHIODERMATIDAE
Ophioderma longicaudum (Bruzelius, 1805)10 m-
Phylum CHORDATA
Class ACTINOPTERYGII
Order ANGUILLIFORMES
Family CONGRIDAE
Conger conger (Linnaeus, 1758)2–4 m-
Family MURAENIDAE
Muraena helena Linnaeus, 17588–11 m-
Order ATHERINIFORMES
Family ATHERINIDAE
Atherina boyeri Risso, 18102 m-
Atherina hepsetus Linnaeus, 17582 m-
Order AULOPIFORMES
Family SYNODONTIDAE
Synodus saurus (Linnaeus, 1758)1–10 m-
Order BELONIFORMES
Family BELONIDAE
Belone belone (Linnaeus, 1760)1 m-
Order CLUPEIFORMES
Family CLUPEIDAE
Sardina pilchardus (Walbaum, 1792)25 m-
Sardinella aurita Valenciennes, 1847--
Family ENGRAULIDAE
Engraulis encrasicolus (Linnaeus, 1758)1–5 m-
Order GADIFORMES
Family MERLUCCIIDAE
Merluccius merluccius (Linnaeus, 1758)--
Family PHYCIDAE
Phycis phycis (Linnaeus, 1766)30 m-
Order LOPHIIFORMES
Family LOPHIIDAE
Lophius ind Linnaeus, 175860 m-
Order MUGILIFORMES
Family MUGILIDAE
Chelon auratus (Risso, 1810)2 m-
Chelon labrosus (Risso, 1827)1 m-
Order PERCIFORMES
Family APOGONIDAE
Apogon imberbis (Linnaeus, 1758)5 m-
Family BLENNIIDAE
Aidablennius sphynx (Valenciennes, 1836)1 m-
Coryphoblennius galerita (Linnaeus, 1758)0 m-
Lipophrys trigloides (Valenciennes, 1836)1 m-
Microlipophrys canevae (Vinciguerra, 1880)1 m-
Parablennius gattorugine (Linnaeus, 1758)8–11 m-
Parablennius incognitus (Bath, 1968)2 m-
Parablennius rouxi (Cocco, 1833)10 m-
Parablennius sanguinolentus (Pallas, 1814)0–3-
Parablennius zvonimiri (Kolombatovic, 1892)3 m-
Family CARANGIDAE
Lichia amia (Linnaeus, 1758)1 mSperm (XI)
Seriola dumerili (Risso, 1810)2 m-
Trachinotus ovatus (Linnaeus, 1758)3 m-
Trachurus trachurus (Linnaeus, 1758)60 m-
Family CENTRACANTHIDAE
Spicara maena (Linnaeus, 1758)--
Spicara smaris (Linnaeus, 1758)7–25 mRep. behav. (IV)
Family GOBIIDAE
Gobius cobitis Pallas, 18140–3-
Gobius geniporus Valenciennes, 18377 m-
Gobius incognitus Kovačić & Sanda, 20161–11 m-
Family LABRIDAE
Coris julis (Linnaeus, 1758)1–15 m-
Labrus merula Linnaeus, 175820 m-
Symphodus doderleini Jordan, 18903 m-
Symphodus mediterraneus (Linnaeus, 1758)25 m-
Symphodus ocellatus (Linnaeus, 1758)2 m-
Symphodus roissali (Risso, 1810)2 m-
Symphodus rostratus (Bloch, 1791)5 m-
Symphodus tinca (Linnaeus, 1758)3 mRep. behav. (VI-VII)
Thalassoma pavo (Linnaeus, 1758)1–5 m-
Xyrichtys novacula (Linnaeus, 1758)18 m-
Family MULLIDAE
Mullus barbatus barbatus Linnaeus, 175860 m-
Mullus surmuletus Linnaeus, 175860 m-
Family POMACENTRIDAE
Chromis chromis (Linnaeus, 1758)1–20 mRep. behav. (VIII)
Family POMATOMIDAE
Pomatomus saltatrix (Linnaeus, 1766)--
Family SCARIDAE
Sparisoma cretense (Linnaeus, 1758)3 m-
Family SCIAENIDAE
Sciaena umbra Linnaeus, 175823 m-
Family SCOMBRIDAE
Auxis rochei rochei (Risso, 1810)--
Euthynnus alletteratus (Rafinesque, 1810)1 m-
Sarda sarda (Bloch, 1793)20 m-
Scomber colias Gmelin, 178918 m-
Scomber scombrus Linnaeus, 175860 m-
Family SERRANIDAE
Anthias anthias (Linnaeus, 1758)40 m-
Epinephelus costae (Steindachner, 1878)30 m-
Epinephelus marginatus (Lowe, 1834)4 m-
Serranus cabrilla (Linnaeus, 1758)4–15 m-
Serranus hepatus (Linnaeus, 1758)7–25 m-
Serranus scriba (Linnaeus, 1758)2–18 m-
Family SPARIDAE
Boops boops (Linnaeus, 1758)1–10 m-
Dentex dentex (Linnaeus, 1758)--
Diplodus puntazzo (Walbaum, 1792)5–15 m-
Diplodus sargus (Linnaeus, 1758)7 m-
Diplodus vulgaris (Geoffroy Saint-Hilaire, 1817)5–15 m-
Lithognathus mormyrus (Linnaeus, 1758)7 m-
Oblada melanura (Linnaeus, 1758)1 m-
Pagellus acarne (Risso, 1827)20 m-
Pagellus bogaraveo (Brünnich, 1768)0–3-
Pagellus erythrinus (Linnaeus, 1758)20 m-
Pagrus pagrus (Linnaeus, 1758)0–3-
Sarpa salpa (Linnaeus, 1758)30 m-
Sparus aurata Linnaeus, 17582 m-
Spondyliosoma cantharus (Linnaeus, 1758)0–2 m-
Family SPHYRAENIDAE
Sphyraena sphyraena (Linnaeus, 1758)30 m-
Family TRACHINIDAE
Trachinus araneus Cuvier, 182925 m-
Family TRIPTERYGIIDAE
Tripterygion tripteronotum (Risso, 1810)0–3-
Family URANOSCOPIDAE
Uranoscopus scaber Linnaeus, 175830 m-
Order PLEURONECTIFORMES
Family BOTHIDAE
Bothus podas (Delaroche, 1809)1–4 m-
Family SOLEIDAE
Microchirus ocellatus (Linnaeus, 1758)20 m-
Solea solea (Linnaeus, 1758)20 m-
Order SCORPAENIFORMES
Family DACTYLOPTERIDAE
Dactylopterus volitans (Linnaeus, 1758)--
Family SCORPAENIDAE
Scorpaena maderensis Valenciennes, 18333–15 m-
Scorpaena notata Rafinesque, 181020 m-
Scorpaena porcus Linnaeus, 175816 m-
Scorpaena scrofa Linnaeus, 175825 m-
Family TRIGLIDAE
Chelidonichthys lastoviza (Bonnaterre, 1788)--
Order TETRAODONTIFORMES
Family BALISTIDAE
Balistes capriscus Gmelin, 178915 m-
Order ZEIFORMES
Family ZEIDAE
Zeus faber Linnaeus, 175867 m-
Class ASCIDIACEA
Order APLOUSOBRANCHIA
Family CLAVELINIDAE
Pycnoclavella ind Garstang, 189115 m-*
Family DIDEMNIDAE
Diplosoma spongiforme (Giard, 1872)1–60 m-
Family POLYCITORIDAE
Polycitor crystallinus (Renier, 1804)30 m-
Family POLYCLINIDAE
Aplidium ind Savigny, 181615 m-
Order PHLEBOBRANCHIA
Family ASCIDIIDAE
Ascidia mentula Müller, 17764 m-
Order STOLIDOBRANCHIA
Family PYURIDAE
Halocynthia papillosa (Linnaeus, 1767)5–30 m-
Microcosmus ind Heller, 187720 m-
Pyura tessellata (Forbes, 1848)60 m-
Family STYELIDAE
Botrylloides niger Herdman, 18861–3 m-
Class ELASMOBRANCHII
Order MYLIOBATIFORMES
Family DASYATIDAE
Dasyatis pastinaca (Linnaeus, 1758)20 m-
Order RAJIFORMES
Family RAJIDAE
Raja brachyura Lafont, 187120 m-
Raja miraletus Linnaeus, 175867 mEggs (V)
Order TORPEDINIFORMES
Family TORPEDINIDAE
Torpedo marmorata Risso, 18105 m-
Class LEPTOCARDII
Family BRANCHIOSTOMATIDAE
Branchiostoma lanceolatum (Pallas, 1774)7–11 m-
Class MAMMALIA
Order CETARTIODACTYLA
Family DELPHINIDAE
Tursiops truncatus (Montagu, 1821)0 m-
Class REPTILIA
Order TESTUDINES
Family CHELONIIDAE
Caretta caretta (Linnaeus, 1758)2 m-
Class THALIACEA
Order SALPIDA
Family SALPIDAE
Helicosalpa virgula (Vogt, 1854)†3 mOccurrence (IV)*†
Salpa fusiformis Cuvier, 18040–5 mOccurrence (III–IV)
Salpa maxima Forskål, 17750–5 mOccurrence (IV–V)
Phylum NEMATODA
Class CHROMADOREA
Order RHABDITIDA
Family ANISAKIDAE
Anisakis ind Dujardin, 1845--
Phylum ARTHROPODA
Class COLLEMBOLA
Family NEANURIDAE
Anurida maritima (Guérin-Méneville, 1836)0 m-
Class HEXANAUPLIA
Family SACCULINIDAE
Sacculina ind Thompson, 18361 m-
Order LEPADIFORMES
Family LEPADIDAE
Lepas (Anatifa) pectinata Spengler, 17930 m-
Order SIPHONOSTOMATOIDA
Family PENNELLIDAE
Pennella ind Oken, 1815--
Class MALACOSTRACA
Order AMPHIPODA
Family CAPRELLIDAE
Caprella ind Lamarck, 18013–5 m-
Phtisica marina Slabber, 17695 m-
Pseudoprotella phasma (Montagu, 1804)5 m-
Family ISCHYROCERIDAE
Jassa marmorata Holmes, 19052 m-
Family PHRONIMIDAE
Phronima sedentaria (Forskål, 1775)3 m-
Order DECAPODA
Family ALPHEIDAE
Alpheus dentipes Guérin, 1832-Eggs (VI)
Synalpheus gambarelloides (Nardo, 1847)--
Family CALAPPIDAE
Calappa granulata (Linnaeus, 1758)40–60 mEggs (II)
Family CARCINIDAE
Xaiva biguttata (Risso, 1816)7 m-
Family DIOGENIDAE
Calcinus tubularis (Linnaeus, 1767)1 m-
Clibanarius erythropus (Latreille, 1818)1 m-
Dardanus arrosor (Herbst, 1796)70 m-
Dardanus calidus (Risso, 1827 in [Risso, 1826–1827])20–50 mEggs (VIII)
Diogenes pugilator (P. Roux, 1829) complex7 m-
Paguristes eremita (Linnaeus, 1767)--
Family DORIPPIDAE
Medorippe lanata (Linnaeus, 1767)60 m-
Family DROMIIDAE
Dromia personata (Linnaeus, 1758)5–50 mEggs (VIII)
Family EPIALTIDAE
Acanthonyx lunulatus (Risso, 1816)1 m-
Herbstia condyliata (Fabricius, 1787)4 m-
Pisa cf. armata (Latreille, 1803)70 m-
Pisa cf. nodipes Leach, 181560 m-
Family ERIPHIIDAE
Eriphia verrucosa (Forskål, 1775)2 mEggs (VIII)
Family GALATHEIDAE
Galathea squamifera Leach, 1814 [in Leach, 1813–1815]5 m-
Family GONEPLACIDAE
Goneplax rhomboides (Linnaeus, 1758)60 m-
Family GRAPSIDAE
Pachygrapsus marmoratus (Fabricius, 1787)0 mEggs (VI)
Family HOMOLIDAE
Homola barbata (Fabricius, 1793)60 mEggs (VI)
Family INACHIDAE
Macropodia ind Leach, 1814 [in Leach, 1813–1815]20 m-
Family LEUCOSIIDAE
Ebalia edwardsii O.G. Costa, 1838 [in O.G. Costa & A. Costa, 1838–1871]25 m-
Ilia nucleus (Linnaeus, 1758)7 m-
Family MAJIDAE
Maja crispata Risso, 1827 in [Risso, 1826–1827]--
Maja squinado (Herbst, 1788)50 mEggs (VI;IX)
Neomaja goltziana (d’Oliveira, 1889)--
Family PAGURIDAE
Cestopagurus timidus (P. Roux, 1830 [in P. Roux, 1828–1830])5 m-
Pagurus anachoretus Risso, 1827 in [Risso, 1826–1827]--
Family PALAEMONIDAE
Brachycarpus biunguiculatus (H. Lucas, 1846)5 m-
Palaemon cf. serratus (Pennant, 1777)1 mEggs (VI)
Palaemon elegans Rathke, 18360–1 m-
Pontonia pinnophylax (Otto, 1821)10 m-
Family PALINURIDAE
Palinurus elephas (Fabricius, 1787)70 m-
Family PARTHENOPIDAE
Spinolambrus macrochelos (Herbst, 1790 [in Herbst, 1782–1790])70 m-
Family PENAEIDAE
Penaeus kerathurus (Forskål, 1775)20 m-
Family PERCNIDAE
Percnon gibbesi (H. Milne Edwards, 1853)1 m-
Family PILUMNIDAE
Pilumnus hirtellus (Linnaeus, 1761)50 m-
Pilumnus spinifer H. Milne Edwards, 183450 mEggs (V)
Pilumnus villosissimus (Rafinesque, 1814)0 m-
Family POLYBIIDAE
Liocarcinus vernalis (Risso, 1827 in [Risso, 1826–1827])0 m-
Family PORTUNIDAE
Callinectes sapidus Rathbun, 1896--
Portunus hastatus (Linnaeus, 1767)2–30 m-
Family PROCESSIDAE
Processa ind Leach, 1815 [in Leach, 1815–1875]3 m-
Family SCYLLARIDAE
Scyllarides latus (Latreille, 1803)60 mEggs (VI)
Family STENOPODIDAE
Stenopus spinosus Risso, 1827 in [Risso, 1826–1827]3 m-
Family XANTHIDAE
Paractaea monodi Guinot, 19695 m-
Xantho granulicarpus Forest in Drach & Forest, 19530 m-
Xantho poressa (Olivi, 1792)0 m-
Order ISOPODA
Family GNATHIIDAE
Gnathia ind Leach, 1814--
Family IDOTEIDAE
Idotea metallica Bosc, 18020 m-
Family LIGIIDAE
Ligia italica Fabricius, 17980 m-
Order STOMATOPODA
Family SQUILLIDAE
Squilla mantis (Linnaeus, 1758)60 m-
Phylum PLATYHELMINTHES
Order POLYCLADIDA
Family EURYLEPTIDAE
Prostheceraeus giesbrechtii Lang, 18844–16 m-
Family PLANOCERIDAE
Planocera ceratommata (Palombi, 1936)8 m-*
Family PSEUDOCEROTIDAE
Pseudoceros maximus-type A Lang, 188415 m-*
Pseudoceros velutinus (Blanchard, 1847)2 m-*
Thysanozoon brocchii (Risso, 1818)8 m-*
Class MONOGENEA
Order MAZOCRAEIDEA
Family HEXOSTOMATIDAE
Hexostoma thynni (Delaroche, 1811) Rafinesque, 1815--
Phylum MOLLUSCA
Class BIVALVIA
Order ADAPEDONTA
Family HIATELLIDAE
Hiatella arctica (Linnaeus, 1767)1 m-
Order ARCIDA
Family ARCIDAE
Arca noae Linnaeus, 175820 m-
Barbatia barbata (Linnaeus, 1758)--
Family GLYCYMERIDIDAE
Glycymeris bimaculata (Poli, 1795)18 m-
Family NOETIIDAE
Striarca lactea (Linnaeus, 1758)50 m-
Order CARDIIDA
Family CARDIIDAE
Laevicardium crassum (Gmelin, 1791)18 m-
Papillicardium papillosum (Poli, 1791)10 m-
Family TELLINIDAE
Moerella donacina (Linnaeus, 1758)18 m-
Peronaea planata (Linnaeus, 1758)18 m-
Order CARDITIDA
Family CARDITIDAE
Cardita calyculata (Linnaeus, 1758)--
Order GALEOMMATIDA
Family LASAEIDAE
Lasaea rubra (Montagu, 1803)--
Order GASTROCHAENIDA
Family GASTROCHAENIDAE
Rocellaria dubia (Pennant, 1777)2–5 m-
Order LIMIDA
Family LIMIDAE
Lima lima (Linnaeus, 1758)4 m-
Limaria tuberculata (Olivi, 1792)5 m-
Order MYTILIDA
Family MYTILIDAE
Lithophaga lithophaga (Linnaeus, 1758)2 m-
Musculus costulatus (Risso, 1826)--
Mytilus galloprovincialis Lamarck, 18191 m-
Order OSTREIDA
Family GRYPHAEIDAE
Neopycnodonte cochlear (Poli, 1795)4 m-
Family PINNIDAE
Pinna nobilis Linnaeus, 17583–20 m-
Family PTERIIDAE
Pteria hirundo (Linnaeus, 1758)50 m-
Order PECTINIDA
Family ANOMIIDAE
Anomia ephippium Linnaeus, 175820 m-
Family PECTINIDAE
Aequipecten opercularis (Linnaeus, 1758)20 m-
Manupecten pesfelis (Linnaeus, 1758)--
Mimachlamys varia (Linnaeus, 1758)10 m-
Palliolum incomparabile (Risso, 1826)50 m-
Pecten jacobaeus (Linnaeus, 1758)--
Talochlamys multistriata (Poli, 1795)--
Family SPONDYLIDAE
Spondylus gaederopus Linnaeus, 175830 m-
Order VENERIDA
Family VENERIDAE
Pitar mediterraneus (Aradas & Benoit, 1872)60 m-
Venus verrucosa Linnaeus, 1758--
Class CEPHALOPODA
Order MYOPSIDA
Family LOLIGINIDAE
Loligo vulgaris Lamarck, 179830 m-
Order OCTOPODA
Family OCTOPODIDAE
Octopus vulgaris Cuvier, 1797 complex2–30 m-
Order SEPIIDA
Family SEPIIDAE
Sepia officinalis Linnaeus, 17585–30 m-
Class GASTROPODA
Family CERITHIIDAE
Bittium latreillii (Payraudeau, 1826)10 m-
Bittium reticulatum (da Costa, 1778)--
Cerithium lividulum Risso, 18261 m-
Cerithium renovatum Monterosato, 1884 complex--
Cerithium vulgatum Bruguière, 1792 complex1 m-
Family SILIQUARIIDAE
Petalopoma elisabettae Schiaparelli, 200240 m-
Family LIMAPONTIIDAE
Ercolania viridis (A. Costa, 1866) [30]0 m-*
Family OMALOGYRIDAE
Ammonicera fischeriana (Monterosato, 1869)--
Omalogyra cf. simplex (Costa O. G., 1861)--
Family PATELLIDAE
Patella caerulea Linnaeus, 17580 m-
Patella rustica Linnaeus, 1758 complex0 m-
Family PLAKOBRANCHIDAE
Bosellia mimetica Trinchese, 1891 [30]21 mEggs (VI)
Elysia timida (Risso, 1818) [30]7 m-
Elysia viridis (Montagu, 1804) [30]10 m-
Thuridilla hopei (Vérany, 1853) [30]7 m-
Family PYRAMIDELLIDAE
Folinella excavata (Phillippi, 1836)--
Order APLYSIIDA
Family APLYSIIDAE
Aplysia depilans Gmelin, 1791 [30]2 mRep. behav. (IX)
Aplysia fasciata Poiret, 1789 [30]3 mRep. behav. (VII)
Aplysia punctata (Cuvier, 1803) [30]10 mRep. behav. (II)
Order CEPHALASPIDEA
Family AGLAJIDAE
Aglaja tricolorata Renier, 1807 [30]34 m-
Family BULLIDAE
Bulla striata Bruguière, 1792 [30]10 m-
Family HAMINOEIDAE
Haminoea ind Turton & Kingston [in Carrington], 1830 [30]1–40 m-
Weinkauffia turgidula (Forbes, 1844) [30]40 m-
Order LEPETELLIDA
Family FISSURELLIDAE
Diodora graeca (Linnaeus, 1758)1 m-
Emarginula sicula J.E. Gray, 18253 m-
Family HALIOTIDAE
Haliotis tuberculata Linnaeus, 17582–10 m-
Family SCISSURELLIDAE
Scissurella costata d’Orbigny, 1824--
Order LITTORINIMORPHA
Family APORRHAIDAE
Aporrhais pespelecani (Linnaeus, 1758)3 m-
Family CALYPTRAEIDAE
Calyptraea chinensis (Linnaeus, 1758)50 m-
Crepidula moulinsii Michaud, 182920 m-
Family CARINARIIDAE
Carinaria lamarckii Blainville, 18173 m-
Family CASSIDAE
Semicassis undulata (Gmelin, 1791)--
Family CHARONIIDAE
Charonia seguenzae (Aradas & Benoit, 1872)11 m-
Family CYMATIIDAE
Monoplex corrugatus (Lamarck, 1816)10 m-
Family CYPRAEIDAE
Luria lurida lurida (Linnaeus, 1758)4 m-
Naria spurca spurca (Linnaeus, 1758)4 m-
Family LITTORINIDAE
Melarhaphe neritoides (Linnaeus, 1758)0 mEggs (XI)
Family RISSOIDAE
Alvania hirta (Monterosato, 1884)--
Alvania lineata Risso, 1826--
Alvania mamillata Risso, 1826--
Manzonia crassa (Kanmacher, 1798)--
Family RISSOINIDAE
Rissoina bruguieri (Payraudeau, 1826)--
Family TONNIDAE
Tonna galea (Linnaeus, 1758)20–60 m-
Family VELUTINIDAE
Lamellaria perspicua (Linnaeus, 1758)3 m-
Family VERMETIDAE
Dendropoma petraeum (Monterosato, 1884) complex--
Thylacodes arenarius (Linnaeus, 1758)70 m-
Order NEOGASTROPODA
Family BUCCINIDAE
Euthria cornea (Linnaeus, 1758)--
Family COLUMBELLIDAE
Columbella rustica (Linnaeus, 1758)1 m-
Family CONIDAE
Conus ventricosus Gmelin, 17912 m-
Family COSTELLARIIDAE
Pusia tricolor (Gmelin, 1791)4 m-
Family FASCIOLARIIDAE
Fusinus fioritae Russo & Pagli, 201940 m-
Tarantinaea lignaria (Linnaeus, 1758)1 m-
Family MITRIDAE
Episcomitra zonata (Marryat, 1818)--
Isara cornea (Lamarck, 1811)--
Family MURICIDAE
Bolinus brandaris (Linnaeus, 1758)30 m-
Hexaplex trunculus (Linnaeus, 1758) complex1–50 mEggs (VI–VII)
Hirtomurex squamosus (Bivona e Bernardi, 1838)50 m-
Muricopsis cristata (Brocchi, 1814)30 m-
Ocinebrina cf. corallina/aegeensis 40 m-
Stramonita haemastoma (Linnaeus, 1767)0 m-
Family NASSARIIDAE
Tritia corniculum (Olivi, 1792) complex1 m-
Tritia incrassata (Strøm, 1768) complex1 m-
Tritia pellucida (Risso, 1826)5 m-
Family PISANIIDAE
Aplus dorbignyi (Payraudeau, 1826) complex--
Pisania striata (Gmelin, 1791)20 m-
Order NUDIBRANCHIA
Family AEOLIDIIDAE
Berghia coerulescens (Laurillard, 1832) [30]1 m-
Spurilla neapolitana (Delle Chiaje, 1841) [30]4 m-
Family CALYCIDORIDIDAE
Diaphorodoris papillata Portmann & Sandmeier, 1960 [30]30 m-*
Family CHROMODORIDIDAE
Felimare picta (Philippi, 1836) [30]8–18 m-
Felimare tricolor (Cantraine, 1835) [30]14 m-
Felimare villafranca (Risso, 1818) [30]10 m-
Felimida krohni (Vérany, 1846) [30]40 m-
Felimida luteorosea (Rapp, 1827) [30]40 m-
Family DENDRODORIDIDAE
Dendrodoris grandiflora (Rapp, 1827) [30]4 m-
Family DISCODORIDIDAE
Peltodoris atromaculata Bergh, 1880 [30]18–30 mEggs (VI)
Platydoris argo (Linnaeus, 1767) [30]22 m-
Family DORIDIDAE
Doris ocelligera (Bergh, 1881) [30]40 m-*
Family DOTIDAE
Doto acuta Schmekel & Kress, 1977 [30]2 m-*
Doto cf. koenneckeri Lemche, 1976 [30]2 m-*
Doto paulinae Trinchese, 1881 [30]2 m-*
Doto pygmaea Bergh, 1871 [30]0 mEggs (VII)*
Family EUBRANCHIDAE
Eubranchus exiguus (Alder & Hancock, 1848) [30]0 m-*
Family FACELINIDAE
Cratena peregrina (Gmelin, 1791) [30]21 - 25 m-
Facelina annulicornis (Chamisso & Eysenhardt, 1821) [30]4 m-*
Family FIONIDAE
Fiona pinnata (Eschscholtz, 1831) [30]0 mEggs (V)*
Family FLABELLINIDAE
Calmella cavolini (Vérany, 1846) [30]1 m-
Flabellina affinis (Gmelin, 1791) [30]10 m-
Family ONCHIDORIDIDAE
Onchidorididae ind Gray, 1827 [30]70 m-
Family PHYLLIDIIDAE
Phyllidia flava Aradas, 1847 [30]23 m-
Family POLYCERIDAE
Kaloplocamus ramosus (Cantraine, 1835) [30]70 m-
Polycera quadrilineata (O. F. Müller, 1776) [30]40 m-
Family SAMLIDAE
Luisella babai (Schmekel, 1972) [30]22 m-
Family TRINCHESIIDAE
Trinchesia caerulea (Montagu, 1804) [30]2 m-
Family TRITONIIDAE
Tritonia manicata Deshayes, 1853 [30]1 m-
Order PLEUROBRANCHIDA
Family PLEUROBRANCHAEIDAE
Pleurobranchaea meckeli (Blainville, 1825) [30]34 m-
Order RUNCINIDA
Family RUNCINIDAE
Runcina adriatica T. E. Thompson, 1980 [30]20–39 m-*
Runcina cf. brenkoae T. E. Thompson, 1980 [30]2 m-*
Runcina cf. ornata (Quatrefages, 1844) [30]20 m-*
Runcina ferruginea Kress, 1977 [30]40 m-
Order TROCHIDA
Family CALLIOSTOMATIDAE
Calliostoma conulus (Linnaeus, 1758)4–60 m-
Family COLLONIIDAE
Homalopoma sanguineum (Linnaeus, 1758)--
Family TROCHIDAE
Jujubinus exasperatus (Pennant, 1777) complex--
Jujubinus striatus (Linnaeus, 1758) complex1 m-
Phorcus turbinatus (Born, 1778)0 m-
Steromphala nebulosa (Philippi, 1849)3 m-
Family TURBINIDAE
Bolma rugosa (Linnaeus, 1767)--
Order UMBRACULIDA
Family UMBRACULIDAE
Umbraculum umbraculum ([Lightfoot], 1786) [30]1–3 m-
Class POLYPLACOPHORA
Order CHITONIDA
Family ACANTHOCHITONIDAE
Acanthochitona fascicularis (Linnaeus, 1767)20 m-
Family CALLOCHITONIDAE
Callochiton septemvalvis (Montagu, 1803)20 m-
Family CHITONIDAE
Rhyssoplax olivacea (Spengler, 1797)10 m-
Family LEPIDOCHITONIDAE
Lepidochitona caprearum (Scacchi, 1836)1 mEggs (V)
Phylum ANNELIDA
Order MYZOSTOMIDA
Family MYZOSTOMATIDAE
Myzostoma glabrum Graff, 187760 m-*
Order SIPUNCULA
Family PHASCOLOSOMATIDAE
Phascolosoma (Phascolosoma) granulatum Leuckart, 18280–1 m-
Class CLITELLATA
Order RHYNCHOBDELLIDA
Family PISCICOLIDAE
Branchellion torpedinis Savigny, 1822--*
Pontobdella muricata (Linnaeus, 1758)--
Class POLYCHAETA
Family OPHELIIDAE
Armandia polyophthalma Kükenthal, 18877 m-
Family ORBINIIDAE
Phylo foetida (Claparède, 1868)18 m-
Order AMPHINOMIDA
Family AMPHINOMIDAE
Hermodice carunculata (Pallas, 1766)5–25 mEggs (VIII)
Order ECHIUROIDEA
Family BONELLIIDAE
Bonellia viridis Rolando, 18225–15 m-
Order EUNICIDA
Family DORVILLEIDAE
Dorvillea rubrovittata (Grube, 1855)35 m-
Family EUNICIDAE
Leodice harassii (Audouin & Milne Edwards, 1833)70 m-
Lysidice collaris Grube, 187070 m-
Lysidice ninetta Audouin & H Milne Edwards, 183315 m-
Order PHYLLODOCIDA
Family HESIONIDAE
Psamathe fusca Johnston, 183670 m-
Family NEREIDIDAE
Ceratonereis (Composetia) costae (Grube, 1840)20 m-
Family PHYLLODOCIDAE
Alciopini ind Ehlers, 18645 mOccurrence (IV)
Family POLYNOIDAE
Harmothoe cf. impar (Johnston, 1839)35 m-
Harmothoe pagenstecheri Michaelsen, 189625 m-*
Lepidonotus clava (Montagu, 1808)70 m-
Family SIGALIONIDAE
Sigalion mathildae Audouin & Milne Edwards in Cuvier, 18307 m-
Family SYLLIDAE
Paraehlersia ferrugina (Langerhans, 1881)20 m-
Pseudosyllis brevipennis Grube, 186370 m-
Order SABELLIDA
Family SABELLIDAE
Sabella spallanzanii (Gmelin, 1791)3–20 m-
Family SERPULIDAE
Hydroides elegans (Haswell, 1883) [nomen protectum]60 m-
Hydroides pseudouncinata Zibrowius, 196870 m-
Protula ind Risso, 182610–70 m-
Spirobranchus triqueter (Linnaeus, 1758)60 m-
Spirorbis ind Daudin, 180010 m-
Vermiliopsis infundibulum (Philippi, 1844)50–70 mEggs (VII)
Vermiliopsis labiata (O. G. Costa, 1861)20 m-
Vermiliopsis striaticeps (Grube, 1862)18 m-
Order TEREBELLIDA
Family CIRRATULIDAE
Cirriformia tentaculata (Montagu, 1808)18 m-
Dodecaceria concharum Örsted, 184370 m-
Family TEREBELLIDAE
Streblosoma ind M. Sars in G.O. Sars, 187235 m-
Phylum NEMERTEA
Class HOPLONEMERTEA
Order POLYSTILIFERA
Family DREPANOPHORIDAE
Gibsonnemertes spectabilis (Quatrefages, 1846)70 m-*
Class PILIDIOPHORA
Order HETERONEMERTEA
Family LINEIDAE
Notospermus geniculatus (Delle Chiaje, 1828)4 m-
Phylum BRYOZOA
Class GYMNOLAEMATA
Order CHEILOSTOMATIDA
Family ADEONIDAE
Adeonella pallasii (Heller, 1867)20 m-
Reptadeonella violacea (Johnston, 1847)30 m-
Family AETEIDAE
Aetea anguina (Linnaeus, 1758)0–5 m-
Family BEANIIDAE
Beania magellanica (Busk, 1852)70 m-
Family BITECTIPORIDAE
Schizomavella ind Canu & Bassler, 191770 m-
Family BUGULIDAE
Bugulina calathus (Norman, 1868)50 m-
Family CANDIDAE
Caberea boryi (Audouin, 1826)20–30 m-
Family CELLARIIDAE
Cellaria salicornioides Lamouroux, 1816--
Family FLUSTRIDAE
Chartella ind Gray, 184870 m-*
Family HIPPALIOSINIDAE
Hippaliosina depressa (Busk, 1854)10 m-
Family MICROPORIDAE
Calpensia nobilis (Esper, 1796)5–50 m-
Family MYRIAPORIDAE
Myriapora truncata (Pallas, 1766)10–70 m-
Family PHIDOLOPORIDAE
Reteporella couchii (Hincks, 1878)25 m-
Reteporella grimaldii (Jullien, 1903)20 m-
Schizoretepora serratimargo (Hincks, 1886)10–25 m-
Family SCHIZOPORELLIDAE
Schizobrachiella sanguinea (Norman, 1868)10 m-
Order CTENOSTOMATIDA
Family MIMOSELLIDAE
Mimosella gracilis Hincks, 185115 m-
Family VESICULARIIDAE
Amathia semiconvoluta Lamouroux, 1824--
Family WALKERIIDAE
Walkeria ind Fleming, 182330 m-
Class STENOLAEMATA
Order CYCLOSTOMATIDA
Family FRONDIPORIDAE
Frondipora verrucosa (Lamouroux, 1821)60 m-
Phylum BRACHIOPODA
Class RHYNCHONELLATA
Order TEREBRATULIDA
Family MEGATHYRIDIDAE
Argyrotheca cuneata (Risso, 1826)70 m-

4. Discussion

Biodiversity is currently a central theme of global environmental policies and conservation strategies (e.g., EU’s Marine Strategy Framework Directive). However, a sound understanding of biodiversity should be considered at the foundation of any conservation policy. Despite that, our 18-month study showed that the knowledge of Mediterranean biodiversity can still be significantly improved.
This study provides the first species inventory (marine organisms and coastal flora) of the southeastern Salento coastal area and enriches the current basic knowledge information on the biodiversity of the Ionian and the central Mediterranean Sea. Overall, 696 taxa were identified, among which Mollusca, Porifera and Chordata were the most represented, accounting for more than half of the full species inventory. Despite that, the groups with the highest percentages of new records were Polycladida (Platyhelminthes), Nemertea, and Thaliacea, with the relative percentage of new records of 80%, 50% and 33%, respectively.
For some groups, these results reflect the knowledge gaps in their taxonomy and ecology. Some taxa are poorly studied and lack Mediterranean experts, leading to inaccurate estimates of species occurrence. Moreover, the scientific community nowadays tends to overlook descriptive research and biodiversity records [63]. For example, for polyclad platyhelminths and nemerteans, reference monographs for the Mediterranean Sea date back to the end of the 19th century, when they were studied in the Gulf of Naples [64,65]. Similarly, for the phylum Ctenophora, most of the records from Italy come from the Gulf of Naples and the Strait of Messina, the latter being the only location where most ctenophores have been reported in the Ionian Sea (Figure 6b) [66]. Some groups, like anthozoans, have been poorly surveyed in the Ionian Sea, which explains why one tenth of the species found by this study represented new records for the area [67]. For other groups (i.e., Heterobranchia and Porifera), the high proportion of new records and new species (sponges) likely reflects the lack of expert work in the area and the difficulty of taxonomic identification (for an in-depth discussion on these two groups, see [30,33]).
Comparing our species inventory with other works in the central and eastern Mediterranean Sea, the results vary by taxonomic group. However, species inventories at a very small spatial scale, such as ours, are rare, so comparisons are made with caution. Regarding sponges, we reported 112 taxa, while Evcen & Cinar [68] reported 116 taxa of sponges for the whole coast of Turkey, and Voultsiadou et al. [69] reported 81 taxa for the Aegean Sea. The fact that the coastlines of these areas are about two orders of magnitude longer than our study area suggests that the southeastern Salento has a relatively high diversity of sponges, as suggested by Sarà [26]. Regarding hydrozoans, Morri et al. [70] reported 38 taxa for Lebanon, raising the total number of hydrozoans in the Levant Sea to 70. Morri & Bianchi [71] reported 31 taxa for the Aegean Islands of Kos, raising to 67 the number of hydroids known from the Aegean Sea and nearby areas. Also in this case, considering that these areas are several orders of magnitude larger than southeastern Salento, our finding of 48 taxa represents a relatively high number, suggesting a high diversity in the class Hydrozoa. Regarding anthozoans, Vafidis et al. [72] found 21 taxa belonging to the orders Actiniaria, Corallimorpharja, and Scleractinia in the northern Aegean Sea, while we reported 16 of them, which could be comparable considering the smaller area investigated by our study. Also for molluscs, our species list is comparable to the one realised by Giacobbe & Renda [73] for Capo D’Armi, Sicily. They reported 133 taxa, compared to 144 taxa found in our study. The higher number of our species could be explained by the broader area and depth range of our study. Finally, regarding bony fishes, our list only reports 89 species, while Al-Hassan & El-Silini [74] reported 201 species for the coast of Benghazi, Libya, and Saad [75] reported 224 species for the coast of Syria. These large differences can be related to the larger survey areas in Al-Hassan & El-Silini [74], and to the higher sampling effort focused specifically on this group of organisms.
Comparing our species number with the total number of species in the Mediterranean Sea [7], the groups with a proportionally higher number of species were Anthozoa (19%), Porifera and Echinodermata (16%), Osteichthyes (~14%) and Decapoda (13%) (Table 2). Similarly, compared to the checklist for Italian waters, we recorded 24% of Anthozoa, 22% of Porifera, 20% of Echinodermata and Osteichthyes and 17% of Decapoda. Finally, compared to the checklist of the Italian Ionian Sea, we recorded 78% of Anthozoa, 58% of Porifera, 31% of Echinodermata, 29% of Hydrozoa and 25% of Osteichthyes (Table 2). However, it is important to emphasize that the known distribution for many marine taxa is directly related to the distribution of taxonomists and does not reflect the true distribution of the species [76,77]. Therefore, caution is needed in interpreting the numerical comparisons made in this and the previous paragraph.
Out of a total of 697 taxa, we reported only 9 NIS. Considering other areas of the Apulia region, this is a considerable low number of NIS [78]. NIS are often opportunistic species that proliferate in heavily impacted ecosystems [79]. The low numbers of NIS we reported in this study may reflect the overall good environmental conditions and lack of major anthropogenic disturbances in the Tricase coastal area.
Our results also depend on sampling methodologies. For instance, we reported only 32 species of annelids, while there are 152 taxa of hard-substrate polychaetes reported in the Otranto channel [36]. This was probably the result of not having performed ad hoc sampling, e.g., [80,81]. Importantly, this work is not intended to be an exhaustive inventory of species in the area, but a baseline. Future in-depth studies on single groups of fauna and flora will be necessary and will likely disclose further diversity of this stretch of coast.
Besides taxonomic groups, the highest proportion of new records was found within the group of gelatinous zooplankton (i.e., scyphozoan and hydrozoan jellyfish, siphonophores, thaliaceans, and ctenophores). Gelatinous plankton is often the dominant macrozooplankton of oceanic systems, and an important component of marine ecosystems, with particular significance for fisheries management and the tourism industry [82,83]. Despite its importance, gelatinous plankton remains one of the less studied and understood marine groups [84]. The reason lies mainly in the difficulty of sampling animals with fragile gelatinous bodies and in their irregular occurrence as adult forms, which makes it difficult to plan sampling campaigns [85,86]. Marine stations, such as the MARE Outpost, offer a significant advantage for the study of these organisms since they allow continuous surveillance of the coastal area and easy sampling by SCUBA and free diving. In addition, citizen science could also offer substantial help in the study of gelatinous plankton, as it can enable monitoring programs on large geographic and temporal scales, while increasing biodiversity awareness among the general public, e.g., [86,87,88,89,90,91].
Other taxonomic groups appeared to be relatively well studied, with no new records despite the high number of taxa reported. Among these, we found fishes (Osteichthyes), macroalgae, shelled molluscs, decapods (Crustacea), and echinoderms. Fishes are particularly well studied in the Mediterranean Sea, also because of their commercial interest [7,92]. Shelled molluscs are well-known partly due to contributions from amateur shell collectors, who far outnumber professional researchers [93].
Increased knowledge of species distribution and phenology is critical to understand the effects of climate change and human actions on ecosystems and assessing good environmental status, as required by the Marine Strategy Framework Directive. Therefore, long-term biodiversity monitoring and observation are needed to improve our knowledge of biodiversity changes. There is also a need for new taxonomists who can identify and research marine organisms [94]. Inspired by the seminal work of Salvatore Lo Bianco [95] in the Gulf of Naples, this work is an important addition to local and regional biodiversity knowledge and a baseline for future biodiversity monitoring in the Ionian and Mediterranean Sea.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/d14110904/s1, Table S1: Complete list of marine species and coastal plants found during the project Biodiversity MARE Tricase with the indication of the depth or depth range at which the taxa were recorded, the number of specimens sampled and recorded, phenology, whether the taxa is a non-indigenous species, whether the taxa is a new record for the area, and the reference for records already published in previous publications by the same authors [30,33]; Table S2: Complete list of marine specimens recorded and identified during the project Biodiversity MARE Tricase with relative metadata and notes.

Author Contributions

Conceptualization: V.M., F.S., S.P. and F.B. (Ferdinando Boero); Supervision: F.B. (Ferdinando Boero) and S.P.; Investigation: V.M. and F.S.; Taxonomic identification: F.C., D.D.F., C.G., F.R., M.B. (Marco Bertolino), G.C., J.L., M.B. (Marzia Bo), F.B. (Federico Betti), C.F., A.G., F.T., L.N., P.M. and S.A.; Writing—Original Draft Preparation, V.M., F.S.; Writing—Review & Editing, all the authors. All authors have read and agreed to the published version of the manuscript.

Funding

The project “Biodiversity MARE Tricase” was partially funded by the PADI Foundation Grant 2017 (28815) and by the Italian Zoological Union (UZI), and the Scientific Committee for the Italian Fauna (CSFI) through a prize for the best poster on the Italian Fauna at the National Joint Conference of the Italian Society of Ecology (SItE), the Italian Zoological Union (UZI), and the Italian Society of Biogeography (SIB).

Institutional Review Board Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the Supplementary Materials, Tables S1 and S2.

Acknowledgments

This work was possible thanks to the establishment of Avamposto MARE. A special thanks to Antonio Errico and Salvatore Baglivo (“Magna Grecia Mare” Association), Antonio Coppola (Former Mayor of Tricase), Maurizio Raeli and Biagio Di Terlizzi (CIHEAM Bari). We would like to thank the community of Tricase, starting from the “Deep Water Divers” (Salvatore Bortone and Anna Rita Chiuri), “Ittiturismo Anime Sante” (Daniele, Francesco, and Rocco Cazzato), “Masseria Nonno Tore (Irene Vaglio and Carlo Panico)”, Alessandro, Marco and Rocco Ferrarese, and Lucio Cazzato and Giulio, for their precious help. We would also thank the trainees, Emanuele Astoricchio (Italy), Laura Basconi (Italy), Anna Berti (Italy), Jessica de Felice (Italy), Jade Sourisse (France), Olivier Vangheluwe (France), and the work-linked training students Maria Assunta Corciulo, Giacomo Luzzati and Noemi Marra. Thanks also to Egidio Trainito for his scientific support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Tilman, D.; Isbell, F.; Cowles, J.M. Biodiversity and ecosystem functioning. Annu. Rev. Ecol. Evol. Syst. 2014, 45, 471–493. [Google Scholar] [CrossRef]
  2. Bertness, M.D.; Bruno, J.F.; Silliman, B.R.; Stachowicz, J.J. Marine Community Ecology and Conservation; Sinauer Associates, Inc.: Sunderland, MA, USA, 2014. [Google Scholar]
  3. Worm, B.; Barbier, E.B.; Beaumont, N.; Duffy, J.E.; Folke, C.; Halpern, B.S.; Jackson, J.B.C.; Lotze, H.K.; Micheli, F.; Palumbi, S.R.; et al. Impacts of Biodiversity Loss on Ocean Ecosystem Services. Science 2006, 314, 787–790. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Beaumont, N.J.; Austen, M.C.; Atkins, J.P.; Burdon, D.; Degraer, S.; Dentinho, T.P.; Derous, S.; Holm, P.; Horton, T.; Van Ierland, E.; et al. Identification, definition and quantification of goods and services provided by marine biodiversity: Implications for the ecosystem approach. Mar. Pollut. Bull. 2007, 54, 253–265. [Google Scholar] [CrossRef]
  5. Costanza, R.; de Groot, R.; Sutton, P.; van der Ploeg, S.; Anderson, S.J.; Kubiszewski, I.; Farber, S.; Turner, R.K. Changes in the global value of ecosystem services. Glob. Environ. Chang. 2014, 26, 152–158. [Google Scholar] [CrossRef]
  6. Rands, M.R.W.; Adams, W.M.; Bennun, L.; Butchart, S.H.M.; Clements, A.; Coomes, D.; Entwistle, A.; Hodge, I.; Kapos, V.; Scharlemann, J.P.W.; et al. Biodiversity Conservation: Challenges Beyond. Science 2010, 329, 1298–1303. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Coll, M.; Piroddi, C.; Steenbeek, J.; Kaschner, K.; Ben Rais Lasram, F.; Aguzzi, J.; Ballesteros, E.; Bianchi, C.N.; Corbera, J.; Dailianis, T.; et al. The Biodiversity of the Mediterranean Sea: Estimates, Patterns, and Threats. PLoS ONE 2010, 5, e11842. [Google Scholar] [CrossRef] [Green Version]
  8. Bianchi, C.N.; Morri, C. Marine biodiversity of the Mediterranean Sea: Situation, problems and prospects for future research. Mar. Pollut. Bull. 2000, 40, 367–376. [Google Scholar] [CrossRef]
  9. Lotze, H.K.; Coll, M.; Dunne, J.A. Historical changes in marine resources, food-web structure and ecosystem functioning in the Adriatic Sea, Mediterranean. Ecosystems 2011, 14, 198–222. [Google Scholar] [CrossRef]
  10. Coll, M.; Piroddi, C.; Albouy, C.; Ben Rais Lasram, F.; Cheung, W.W.; Christensen, V.; Karpouzi, V.S.; Guilhaumon, F.; Mouillot, D.; Paleczny, M.; et al. The Mediterranean Sea under siege: Spatial overlap between marine biodiversity, cumulative threats and marine reserves. Glob. Ecol. Biogeogr. 2012, 21, 465–480. [Google Scholar] [CrossRef]
  11. Hughes, L. Biological consequences of global warming: Is the signal already apparent? Trends Ecol. Evol. 2000, 15, 56–61. [Google Scholar] [CrossRef]
  12. Puce, S.; Bavestrello, G.; Di Camillo, C.G.; Boero, F. Long-term changes in hydroid (Cnidaria, Hydrozoa) assemblages: Effect of Mediterranean warming? Mar. Ecol. 2009, 30, 313–326. [Google Scholar] [CrossRef]
  13. Rivetti, I.; Fraschetti, S.; Lionello, P.; Zambianchi, E.; Boero, F. Global Warming and Mass Mortalities of Benthic Invertebrates in the Mediterranean Sea. PLoS ONE 2014, 9, e115655. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Boero, F.; Brotz, L.; Gibbons, M.J.; Piraino, S.; Zampardi, S. Impacts and effects of ocean warming on jellyfish. In Explaining Ocean Warming: Causes, Scale, Effects and Consequences; Laffoley, D., Baxter, J.M., Eds.; IUCN: Gland, Switzerland, 2016; pp. 213–237. ISBN 978-2-8317-1806-4. [Google Scholar]
  15. Gravili, C.; Cozzoli, F.; Boero, F. The historical reconstruction of distribution of the genus Halecium (Hydrozoa: Haleciidae): A biological signal of ocean warming? Mar. Biol. Res. 2017, 13, 587–601. [Google Scholar] [CrossRef]
  16. Bianchi, C.N. Biodiversity issues for the forthcoming tropical Mediterranean Sea. Hydrobiologia 2007, 580, 7–21. [Google Scholar] [CrossRef]
  17. Garrabou, J.; Coma, R.; Bensoussan, N.; Bally, M.; Chevaldonné, P.; Cigliano, M.; Diaz, D.; Harmelin, J.G.; Gambi, M.C.; Kersting, D.K.; et al. Mass mortality in Northwestern Mediterranean rocky benthic communities: Effects of the 2003 heat wave. Glob. Chang. Biol. 2009, 15, 1090–1103. [Google Scholar] [CrossRef]
  18. Galli, G.; Solidoro, C.; Lovato, T. Marine heat waves hazard 3D maps, and the risk for low motility organisms in a warming Mediterranean Sea. Front. Mar. Sci. 2017, 4, 136. [Google Scholar] [CrossRef] [Green Version]
  19. Smith, K.E.; Burrows, M.T.; Hobday, A.J.; King, N.G.; Moore, P.J.; Gupta, A.S.; Thomsen, M.S.; Wernberg, T.; Smale, D.A. Biological Impacts of Marine Heatwaves. Annu. Rev. Mar. Sci. 2022, 15, 12.1–12.27. [Google Scholar] [CrossRef]
  20. Giangrande, A. Biodiversity, conservation, and the ‘taxonomic impediment’. Aquat. Conserv. Mar. Freshw. Ecosyst. 2003, 13, 451–459. [Google Scholar] [CrossRef]
  21. Kim, K.C.; Byrne, L.B. Biodiversity loss and the taxonomic bottleneck: Emerging biodiversity science. Ecol. Res. 2006, 21, 794–810. [Google Scholar] [CrossRef] [Green Version]
  22. Visser, M.; Both, C. Shifts in phenology due to global climate change: The need for a yardstick. Proc. R. Soc. B 2005, 272, 2561–2569. [Google Scholar] [CrossRef]
  23. Boero, F.; Kraberg, A.C.; Krause, G.; Wiltshire, K.H. Time is an affliction: Why ecology cannot be as predictive as physics and why it needs time series. J. Coast. Res. 2015, 101, 12–18. [Google Scholar] [CrossRef]
  24. Micaroni, V.; Strano, F.; Di Franco, D.; Langeneck, J.; Gravili, C.; Bertolino, M.; Costa, G.; Rindi, F.; Froglia, C.; Crocetta, F.; et al. Project “Biodiversity MARE Tricase”: Biodiversity research, monitoring and promotion at MARE Outpost (Apulia, Italy). Rend. Lincei Sci. Fis. Nat. 2018, 29, 599–604. [Google Scholar] [CrossRef]
  25. Strano, F.; Micaroni, V.; Beli, E.; Mercurio, S.; Scarì, G.; Pennati, R.; Piraino, S. On the larva and the zooid of the pterobranch Rhabdopleura recondita Beli, Cameron and Piraino, 2018 (Hemichordata, Graptolithina). Mar. Biodivers. 2019, 49, 1657–1666. [Google Scholar] [CrossRef] [Green Version]
  26. Sarà, M. Specie nuove di Demospongiae provenienti dal coralligeno pugliese. Boll. Mus. Ist. Biol. Univ. Genova. 1969, 37, 89–96. [Google Scholar]
  27. Parenzan, P. Puglia Marittima; Congedo Editore: Galatina, Lecce, Italy, 1983. [Google Scholar]
  28. Beli, E.; Aglieri, G.; Strano, F.; Maggioni, D.; Telford, M.J.; Piraino, S.; Cameron, C.B. The zoogeography of extant rhabdopleurid hemichordates (Pterobranchia: Graptolithina), with a new species from the Mediterranean Sea. Invertebr. Syst. 2018, 32, 100–110. [Google Scholar] [CrossRef]
  29. Fraschetti, S.; D’Ambrosio, P.; Micheli, F.; Pizzolante, F.; Bussotti, S.; Terlizzi, A. Design of marine protected áreas in a human-dominated seascape. Mar. Ecol. Prog. Ser. 2009, 375, 13–24. [Google Scholar] [CrossRef]
  30. Micaroni, V.; Strano, F.; Di Franco, D.; Crocetta, F.; Grech, D.; Piraino, S.; Boero, F. Project “Biodiversity MARE Tricase”: A biodiversity inventory of the coastal area of Tricase (Ionian Sea, Italy)—Mollusca: Heterobranchia. Eur. Zool. J. 2018, 85, 180–193. [Google Scholar] [CrossRef] [Green Version]
  31. Furfaro, G.; Vitale, F.; Licchelli, C.; Mariottini, P. Two Seas for One Great Diversity: Checklist of the Marine Heterobranchia (Mollusca; Gastropoda) from the Salento Peninsula (South-East Italy). Diversity 2020, 12, 171. [Google Scholar] [CrossRef]
  32. Trono, D. Nuovi dati sulla malacofauna del Salento (Puglia meridionale). Boll. Malacol. 2006, 42, 58. [Google Scholar]
  33. Costa, G.; Bavestrello, G.; Micaroni, V.; Pansini, M.; Strano, F.; Bertolino, M. Sponge community variation along the Apulian coasts (Otranto Strait) over a pluri-decennial time span. Does water warming drive a sponge diversity increasing in the Mediterranean Sea? J. Mar. Biol. Assoc. UK 2019, 99, 1519–1534. [Google Scholar] [CrossRef]
  34. Strano, F.; Micaroni, V.; Costa, G.; Bertocci, I.; Bertolino, M. Shallow-water sponge grounds along the Apulian coast (central Mediterranean Sea). Mar. Biodivers. 2020, 50, 1–12. [Google Scholar] [CrossRef]
  35. Gravili, C.; De Vito, D.; Di Camillo, C.G.; Martell, L.; Piraino, S.; Boero, F. The non-Siphonophoran Hydrozoa (Cnidaria) of Salento, Italy with notes on their life-cycles: An illustrated guide. Zootaxa 2015, 3908, 1–187. [Google Scholar] [CrossRef] [PubMed]
  36. Giangrande, A.; Delos, A.L.; Fraschetti, S.; Musco, L.; Licciano, M.; Terlizzi, A. Polychaete assemblages along a rocky shore on the South Adriatic coast (Mediterranean Sea): Patterns of spatial distribution. Mar. Biol. 2003, 143, 1109–1116. [Google Scholar] [CrossRef]
  37. Bottalico, A.; Alongi, G.; Perrone, C. Macroalgal diversity of Santa Cesarea-Castro (Salento Peninsula, southeastern Italy). Anales Jard. Bot. Madrid 2016, 73, 1–12. [Google Scholar] [CrossRef] [Green Version]
  38. Bussotti, S.; Denitto, F.; Guidetti, P.; Belmonte, G. Fish assemblages in shallow marine caves of the Salento Peninsula (Southern Apulia, SE Italy). Mar. Ecol. 2002, 23, 11–20. [Google Scholar] [CrossRef]
  39. Onorato, M.; Belmonte, G. Submarine caves of the Salento pensinsula: Faunal aspects. Thalass. Salentina 2018, 39, 47–72. [Google Scholar]
  40. Onorato, R.; Denitto, F.; Belmonte, G. Le grotte marine del Salento: Classificazione, localizzazione e descrizione. Thalass. Salentina 1999, 23, 67–116. [Google Scholar]
  41. Boero, F.; Fresi, E. Zonation and evolution of a rocky bottom hydroid community. Mar. Ecol. 1986, 7, 123–150. [Google Scholar] [CrossRef]
  42. Zariquiey Alvarez, R. Crustáceos Decápodos Ibéricos. Investig. Pesq. 1968, 32, 1–510. [Google Scholar]
  43. Falciai, L.; Bernucci, P.; Minervini, R. Guía de los Crustáceos Decápodos de Europa; Omega: Barcelona, Spain, 1995. [Google Scholar]
  44. Louisy, P. Guide D’identification Des Poissons Marins: Europe De l’ouest et Méditerranée; Editions Eugen Ulmer: Paris, France, 2002; ISBN 2-84138-651-1. [Google Scholar]
  45. Barnich, R.; Fiege, D. The Aphroditoidea (Annelida: Polychaeta) of the-Mediterranean Sea. Senckenberg Naturf. Gesell. Abhandl. 2003, 559, 1–167. [Google Scholar]
  46. Bouillon, J.; Medel, M.D.; Pagès, F.; Gili, J.M.; Boero, F.; Gravili, C. Fauna of the Mediterranean hydrozoa. Sci. Mar. 2004, 68, 5–438. [Google Scholar] [CrossRef] [Green Version]
  47. Trainito, E.; Baldacconi, R. Atlante di Flora e Fauna del Mediterraneo; Il Castello srl.: Milan, Italy, 2004. [Google Scholar]
  48. Gofas, S.; Salas, C.; Moreno, D. Moluscos Marinos de Andalucía; Universidad de Málaga, Servicio de Publicaciones e Intercambio Científico: Málaga, Spain, 2011; Volume 2. [Google Scholar]
  49. Pansini, M. Fauna d’Italia: Porifera; 1. Calcarea, Demospongiae (Partim), Hexactinellida, Homoscleromorpha; Calderini: Bologna, Italy, 2011. [Google Scholar]
  50. Cormaci, M.; Furnari, G.; Catra, M.; Alongi, G.; Giaccone, G. Flora marina bentonica del Mediterraneo: Phaeophyceae. Boll. Accad. Gioenia Sci. Nat. Catania 2012, 45, 1–510. [Google Scholar]
  51. Cormaci, M.; Furnari, G.; Alongi, G. Flora marina bentonica del Mediterraneo: Chlorophyta. Boll. Accad. Gioenia Sci. Nat. 2014, 47, 11–436. [Google Scholar]
  52. Cormaci, M.; Furnari, G.; Alongi, G. Flora marina bentonica del Mediterraneo: Rhodophyta (Rhodymeniophycidae escluse). Boll. Accad. Gioenia Sci. Nat. Catania 2017, 50, 1–391. [Google Scholar]
  53. Cormaci, M.; Furnari, G.; Alongi, G. Flora marina bentonica del Mediterraneo: Rhodophyta -Rhodymeniophycidae, I. Acrosymphytales, Bonnemaisoniales, Gelidiales, Gigartinales, Gracilariales. Boll. Accad. Gioenia Sci. Nat. Catania 2020, 53, 11–346. [Google Scholar] [CrossRef]
  54. Cormaci, M.; Furnari, G.; Alongi, G. Flora marina bentonica del Mediterraneo: Rhodophyta—Rhodymeniophycidae II. Halymeniales, Nemastomatales, Peyssonneliales, Plocamiales, Rhodymeniales, Sebdeniales. Boll. Accad. Gioenia Sci. Nat. Catania 2021, 54, 9–342. [Google Scholar] [CrossRef]
  55. Chimenz Gusso, C.; Nicoletti, L.; Bondanese, C. Briozoi; Società Italiana di Biologia Marina: Genova, Italy, 2014; p. 336. [Google Scholar]
  56. Trainito, E.; Doneddu, M. Nudibranchi del Mediterraneo; Il Castello srl.: Milan, Italy, 2014; pp. 10–241. [Google Scholar]
  57. Brunetti, R.; Mastrototaro, F. Ascidiacea of the European Waters; Calderini: Bologna, Italy, 2017. [Google Scholar]
  58. Bernot, J.; Daly, M.; De Grave, S.; Hughes, L.; Neubauer, T.A.; Ahyong, S.; Bailly, N.; Bieler, R.; Boyko, C.B.; Brandão, S.N.; et al. World Register of Marine Species. Available online: https://www.marinespecies.org (accessed on 19 September 2022).
  59. Guiry, M.D.; Guiry, G.M. Algaebase. World-Wide Electronic Publication. National University of Ireland, Galway. 2022. Available online: http://www.algaebase.org (accessed on 19 September 2022).
  60. Relini, G. Checklist della flora e della fauna dei mari italiani. Parte I Biol. Mar. Mediterr. 2008, 15, 1–385. [Google Scholar]
  61. Relini, G. Checklist della flora e della fauna dei mari italiani. Parte II Biol. Mar. Mediterr. 2010, 17, 387–828. [Google Scholar]
  62. Crocetta, F.; Renda, W.; Vazzana, A. Alien Mollusca along the Calabrian shores of the Messina Strait area and a review of their distribution in the Italian seas. Boll. Malacol. 2009, 45, 15–30. [Google Scholar]
  63. Boero, F. Observational articles: A tool to reconstruct ecological history based on chronicling unusual events. F1000Research 2013, 2, 168. [Google Scholar] [CrossRef] [Green Version]
  64. Lang, A. Die Polycladen (Seeplanarien) des Golfes von Neapel und der angrenzenden Meeresabschnitte. Eine Monographie. In Fauna und Flora des Golfes von Neapel; W. Engelmann: Leipzig, Germany, 1884. [Google Scholar]
  65. Bürger, O. Die Nemertinen des Golfes von Neapel und der Angrenzenden Meeres–Abschnitte, Fauna und Flora des Golfes von Neapel; Verlag von R. Friedländer & Sohn: Berlin, Germany, 1895; Volume 22. [Google Scholar]
  66. Avian, M.; Boero, F.; Mills, C.; Rossi, L.; Rottini-Sandrini, L. Cnidaria, Ctenophora. In Checklist delle Specie Della Fauna Italiana; Minelli, A., Ruffo, S., La Posta, S., Eds.; Calderini: Bologna, Italy, 1995; Volume 3. [Google Scholar]
  67. Morri, C.; Esposito, F.; Pessani, D. Anthozoa. In Checklist Della Flora e Della Fauna dei Mari Italiani, Parte 1; Relini, G., Ed.; Società Italiana Di Biologia Marina: Genova, Italy, 2008. [Google Scholar]
  68. Evcen, A.; Cinar, M.E. Sponge (Porifera) species from the Mediterranean coast of Turkey (Levantine Sea, eastern Mediterranean), with a checklist of sponges from the coasts of Turkey. Turk. J. Zool. 2012, 36, 460–474. [Google Scholar] [CrossRef]
  69. Voultsiadou, E. Sponge Diversity in the Aegean Sea: Check List and New Information. Ital. J. Zool. 2005, 72, 53–64. [Google Scholar] [CrossRef]
  70. Morri, C.; Puce, S.; Bianchi, C.N.; Bitar, G.; Zibrowius, H.; Bavestrello, G. Hydroids (Cnidaria: Hydrozoa) from the Levant Sea (mainly Lebanon), with emphasis on alien species. J. Mar. Biol. Assoc. UK 2009, 89, 49–62. [Google Scholar] [CrossRef]
  71. Morri, C.; Bianchi, C.N. Hydroids (Cnidaria: Hydrozoa) from the Aegean Sea, mostly epiphytic on algae. Cah. Biol. Mar. 1999, 40, 283. [Google Scholar]
  72. Vafidis, D.; Koukouras, A.; Voultsiadou-Koukoura, E. Actiniaria, Corallimorpharja, and Scleractinia (Hexacorallia, Anthozoa) of the Aegean Sea, with a checklist of the eastern Mediterranean and Black Sea species. Isr. J. Ecol. Evol. 1997, 43, 55–70. [Google Scholar]
  73. Giacobbe, S.; Renda, W. Mollusc diversity in Capo d’Armi (Central Mediterranean Sea) subtidal cliff: A first, tardy, report. Biodivers. J. 2018, 9, 25–34. [Google Scholar]
  74. Al-Hassan, L.A.; El-Silini, O.A. Check-list of bony fishes collected from the Mediterranean coast of Benghazi, Libya. Rev. Biol. Mar. Oceanogr. 1999, 34, 291–301. [Google Scholar]
  75. Saad, A. Check-list of bony fish collected from the coast of Syria. Turkish J. Fish. Aquat. Sci. 2005, 5, 99–106. [Google Scholar]
  76. Giangrande, A.; Licciano, M. Factors influencing latitudinal pattern of biodiversity: An example using Sabellidae (Annelida, Polychaeta). Biodivers. Conserv. 2004, 13, 1633–1646. [Google Scholar] [CrossRef]
  77. Van Soest, R.W.; Boury-Esnault, N.; Vacelet, J.; Dohrmann, M.; Erpenbeck, D.; De Voogd, N.J.; Santodomingo, N.; Vanhoorne, B.; Kelly, M.; Hooper, J.N. Global diversity of sponges (Porifera). PLoS ONE 2012, 7, e35105. [Google Scholar] [CrossRef]
  78. Gravili, C.; Belmonte, G.; Cecere, E.; Denitto, F.; Giangrande, A.; Guidetti, P.; Longo, C.; Mastrototaro, F.; Moscatello, S.; Petrocelli, A.; et al. Nonindigenous species along the Apulian coast, Italy. Chem. Ecol. 2010, 26, 121–142. [Google Scholar] [CrossRef]
  79. Molnar, J.L.; Gamboa, R.L.; Revenga, C.; Spalding, M.D. Assessing the global threat of invasive species to marine biodiversity. Front. Ecol. Environ. 2008, 6, 485–492. [Google Scholar] [CrossRef]
  80. Fraschetti, S.; Giangrande, A.; Terlizzi, A.; Miglietta, M.P.; Della Tommasa, L.; Boero, F. Spatio-temporal variation of hydroids and polychaetes associated with Cystoseira amentacea (Fucales: Phaeophyceae). Mar. Biol. 2002, 140, 949–957. [Google Scholar]
  81. Giangrande, A.; Delos, A.L.; Musco, L.; Licciano, M.; Pierri, C. Polychaete assemblages of rocky shore along the South Adriatic coast (Mediterranean Sea). Cah. Biol. Mar. 2004, 45, 85–95. [Google Scholar]
  82. Purcell, J.E. Pelagic cnidarians and ctenophores as predators: Selective predation, feeding rates, and effects on prey populations. Annu. l’Instit. Oceanogr. 1997, 73, 125–137. [Google Scholar]
  83. Shiganova, T.A.; Bulgakova, Y.V. Effects of gelatinous plankton on Black Sea and Sea of Azov fish and their food resources. ICES J. Mar. Sci. 2000, 57, 641–648. [Google Scholar] [CrossRef]
  84. Purcell, J.E.; Arai, M.N. Interactions of pelagic cnidarians and ctenophores with fish: A review. Hydrobiologia 2001, 451, 27–44. [Google Scholar] [CrossRef]
  85. Raskoff, K.A.; Sommer, F.A.; Hamner, W.M.; Cross, K.M. Collection and culture techniques for gelatinous zooplankton. Biol. Bull. 2003, 204, 68–80. [Google Scholar] [CrossRef] [Green Version]
  86. Boero, F.; Bouillon, J.; Gravili, C.; Miglietta, M.P.; Parsons, T.; Piraino, S. Gelatinous plankton: Irregularities rule the world (sometimes). Mar. Ecol. Prog. Ser. 2008, 356, 299–310. [Google Scholar] [CrossRef]
  87. Boero, F.; Belmonte, G.; Bracale, R.; Fraschetti, S.; Piraino, S.; Zampardi, S. A salp bloom (Tunicata, Thaliacea) along the Apulian coast and in the Otranto Channel between March–May 2013. F1000Research 2013, 2, 181. [Google Scholar] [CrossRef]
  88. Giovos, I.; Kleitou, P.; Poursanidis, D.; Batjakas, I.; Bernardi, G.; Crocetta, F.; Doumpas, N.; Kalogirou, S.; Kampouris, T.; Keramidas, I.; et al. Citizen-science for monitoring marine invasions and stimulating public engagement—A case project from the eastern Mediterranean. Biol. Invasions 2019, 21, 3707–3721. [Google Scholar] [CrossRef]
  89. Magalhães, C.; Martins, A.; Dos Santos, A. New approaches to study jellyfish: From autonomous apparatus to citizen science. In Zooplankton Ecology, 1st ed.; Maria Alexandra Teodosio, M.A., Barbosa, A.M.B., Eds.; CRC Press: Boca Raton, FL, USA, 2020; pp. 227–251. [Google Scholar]
  90. Ringvold, H.; Hatlevik, A.; Hevrøy, J.; Hughes, M.; Aukan, N. Encounters with the rare genus Helicosalpa (Chordata, Thaliacea, Salpida), using citizen science data. Mar. Biol. Res. 2020, 16, 369–379. [Google Scholar] [CrossRef]
  91. Tiralongo, F.; Crocetta, F.; Riginella, E.; Lillo, A.O.; Tondo, E.; Macali, A.; Mancini, E.; Russo, F.; Coco, S.; Paolillo, G.; et al. 2020 Snapshot of rare, exotic and overlooked fish species in the Italian seas: A citizen science survey. J. Coast. Res. 2020, 164, 101930. [Google Scholar]
  92. Relini, G.; Lanteri, L. Osteichthyes. In Checklist Della Flora e Della Fauna dei Mari Italiani, Parte 2; Relini, G., Ed.; Società Italiana Di Biologia Marina: Genova, Italy, 2010. [Google Scholar]
  93. Crocetta, F.; Gofas, S.; Salas, C.; Tringali, L.P.; Zenetos, A. Local ecological knowledge versus published literature: A review of non-indigenous Mollusca in Greek marine waters. Aquat. Invasions 2017, 12, 415–434. [Google Scholar] [CrossRef]
  94. European Academies’ Science Advisory Council. Marine Sustainability in an Age of Changing Oceans and Seas; European Academies’ Science Advisory Council: Brussels, Belgium, 2016; Volume 28. [Google Scholar]
  95. Lo Bianco, S. Notizie biologiche riguardanti specialmente il periodo di maturità sessuale degli animali del golfo di Napoli. Pubbl. Stn. Zool. Napoli 1909, 19, 513–761. [Google Scholar]
Figure 1. Map of the southeastern tip of the Salento Peninsula (Italy). The Tricase Area is highlighted in gray; black dots indicate the additional study sites. In the bottom right corner: the location of the study area in the Mediterranean Sea. After Micaroni et al. [49].
Figure 1. Map of the southeastern tip of the Salento Peninsula (Italy). The Tricase Area is highlighted in gray; black dots indicate the additional study sites. In the bottom right corner: the location of the study area in the Mediterranean Sea. After Micaroni et al. [49].
Diversity 14 00904 g001
Figure 2. Marine habitats found in the coastal area of Tricase. (a) Intertidal zone, (b) upper infralittoral (2–4 m), (c) lower infralittoral (10–13 m), (d) coralligenous formation with Posidonia oceanica patches (17–22 m), (e) eutrophic infralittoral, (f) cave environment.
Figure 2. Marine habitats found in the coastal area of Tricase. (a) Intertidal zone, (b) upper infralittoral (2–4 m), (c) lower infralittoral (10–13 m), (d) coralligenous formation with Posidonia oceanica patches (17–22 m), (e) eutrophic infralittoral, (f) cave environment.
Diversity 14 00904 g002
Figure 3. General description of the taxonomic composition and new records found by this study. (a) Relative contribution of each phylum to the total number of taxa. (b) Total number of taxa and new records (in red) for each major taxonomic group. (c) Percentage proportion of new records for the Ionian Sea out of the total number of taxa found in this study. Het., Heterobranchia. * indicates taxonomic groups that have been already included in previous publications [30,33].
Figure 3. General description of the taxonomic composition and new records found by this study. (a) Relative contribution of each phylum to the total number of taxa. (b) Total number of taxa and new records (in red) for each major taxonomic group. (c) Percentage proportion of new records for the Ionian Sea out of the total number of taxa found in this study. Het., Heterobranchia. * indicates taxonomic groups that have been already included in previous publications [30,33].
Diversity 14 00904 g003
Figure 4. Photos of selected new records in the field. (a) Halcampoides purpureus on sand in Matrona Cave at 4 m; (b) Planocera ceratommata under a boulder on a rocky reef at 8 m; (c) Pseudoceros maximus-type A under a boulder on a rocky reef at 15 m; (d) Thysanozoon brocchii on a vertical wall in the Bortone’s cave at 8 m; (e) Pycnoclavella sp. at the entrance of Matrona Cave, 15 m; (f) colonies of Zoothamnium niveum at the edge between a rocky cliff and sand, 10 m. The scale bars correspond to 1 cm.
Figure 4. Photos of selected new records in the field. (a) Halcampoides purpureus on sand in Matrona Cave at 4 m; (b) Planocera ceratommata under a boulder on a rocky reef at 8 m; (c) Pseudoceros maximus-type A under a boulder on a rocky reef at 15 m; (d) Thysanozoon brocchii on a vertical wall in the Bortone’s cave at 8 m; (e) Pycnoclavella sp. at the entrance of Matrona Cave, 15 m; (f) colonies of Zoothamnium niveum at the edge between a rocky cliff and sand, 10 m. The scale bars correspond to 1 cm.
Diversity 14 00904 g004
Figure 5. Photos of selected new records under a dissection microscope, in vivo. (a) Branchellion torpedinis; (b) Harmothoe pagenstecheri; (c) Myzostoma glabrum; (d) Chartella ind; (e) nectophore of Halistemma rubrum; (f) Proboscidactyla ornata; (g) Gibsonnemertes spectabilis; (h) Helicosalpa virgula; (i) Zoothamnium niveum.
Figure 5. Photos of selected new records under a dissection microscope, in vivo. (a) Branchellion torpedinis; (b) Harmothoe pagenstecheri; (c) Myzostoma glabrum; (d) Chartella ind; (e) nectophore of Halistemma rubrum; (f) Proboscidactyla ornata; (g) Gibsonnemertes spectabilis; (h) Helicosalpa virgula; (i) Zoothamnium niveum.
Diversity 14 00904 g005
Figure 6. Comparison with the check list of the Italian marine fauna [60,61]. (a) Percentage proportion of new records found by this study to the total taxa reported in the Italian Ionian Sea by Relini [60,61]. (b) The proportion of taxa for which the only Ionian record in Relini [60,61] comes from the Strait of Messina biogeographic sector. Het., Heterobranchia. * indicates taxonomic groups that have already been included in previous publications [30,33].
Figure 6. Comparison with the check list of the Italian marine fauna [60,61]. (a) Percentage proportion of new records found by this study to the total taxa reported in the Italian Ionian Sea by Relini [60,61]. (b) The proportion of taxa for which the only Ionian record in Relini [60,61] comes from the Strait of Messina biogeographic sector. Het., Heterobranchia. * indicates taxonomic groups that have already been included in previous publications [30,33].
Diversity 14 00904 g006
Figure 7. Total number of taxa and new records (in red) found by this study per depth strata.
Figure 7. Total number of taxa and new records (in red) found by this study per depth strata.
Diversity 14 00904 g007
Table 2. Comparison of the results of this study with the total number of taxa in the Mediterranean Sea [7], Italian waters [60,61] and Italian Ionian Sea [60,61], for selected taxonomic groups. Numbers represent the number of taxa, while the percentage of taxa found by this study out of the total number of species known for the area is given in brackets. * this figure also includes Chondrichthyes.
Table 2. Comparison of the results of this study with the total number of taxa in the Mediterranean Sea [7], Italian waters [60,61] and Italian Ionian Sea [60,61], for selected taxonomic groups. Numbers represent the number of taxa, while the percentage of taxa found by this study out of the total number of species known for the area is given in brackets. * this figure also includes Chondrichthyes.
Our StudyMediterranean SeaItalian WatersItalian Ionian Sea
Porifera112681 (16%)509 (22%)193 (58%)
Gastropoda1071564 (7%)1155 (9%)763 (14%)
Osteichthyes89* 650 (14%)442 (20%)351 (25%)
Macrophyte881131 (8%)949 (9%)736 (12%)
Hydrozoa49457 (11%)346 (14%)171 (29%)
Decapoda49383 (13%)293 (17%)212 (23%)
Annelida331172 (3%)951 (3%)577 (6%)
Anthozoa31164 (19%)128 (24%)40 (78%)
Bivalvia29400 (7%)340 (9%)227 (13%)
Echinodermata24154 (16%)120 (20%)77 (31%)
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Micaroni, V.; Strano, F.; Crocetta, F.; Di Franco, D.; Piraino, S.; Gravili, C.; Rindi, F.; Bertolino, M.; Costa, G.; Langeneck, J.; et al. Project “Biodiversity MARE Tricase”: A Species Inventory of the Coastal Area of Southeastern Salento (Ionian Sea, Italy). Diversity 2022, 14, 904. https://doi.org/10.3390/d14110904

AMA Style

Micaroni V, Strano F, Crocetta F, Di Franco D, Piraino S, Gravili C, Rindi F, Bertolino M, Costa G, Langeneck J, et al. Project “Biodiversity MARE Tricase”: A Species Inventory of the Coastal Area of Southeastern Salento (Ionian Sea, Italy). Diversity. 2022; 14(11):904. https://doi.org/10.3390/d14110904

Chicago/Turabian Style

Micaroni, Valerio, Francesca Strano, Fabio Crocetta, Davide Di Franco, Stefano Piraino, Cinzia Gravili, Fabio Rindi, Marco Bertolino, Gabriele Costa, Joachim Langeneck, and et al. 2022. "Project “Biodiversity MARE Tricase”: A Species Inventory of the Coastal Area of Southeastern Salento (Ionian Sea, Italy)" Diversity 14, no. 11: 904. https://doi.org/10.3390/d14110904

APA Style

Micaroni, V., Strano, F., Crocetta, F., Di Franco, D., Piraino, S., Gravili, C., Rindi, F., Bertolino, M., Costa, G., Langeneck, J., Bo, M., Betti, F., Froglia, C., Giangrande, A., Tiralongo, F., Nicoletti, L., Medagli, P., Arzeni, S., & Boero, F. (2022). Project “Biodiversity MARE Tricase”: A Species Inventory of the Coastal Area of Southeastern Salento (Ionian Sea, Italy). Diversity, 14(11), 904. https://doi.org/10.3390/d14110904

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