Next Article in Journal
Population Genetic Structure and Phylogeography of Co-Distributed Pachymeniopsis Species (Rhodophyta) along the Coast of Korea and Japan
Previous Article in Journal
Diversity and Abundance of Roadkilled Bats in the Brazilian Atlantic Forest
Previous Article in Special Issue
Diversity of Seahorse Species (Hippocampus spp.) in the International Aquarium Trade
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Black Coral Distribution in the Italian Seas: A Review

by
Michela Ingrassia
1,* and
Letizia Di Bella
2
1
CNR-IGAG (Istituto di Geologia Ambientale e Geoingegneria), UOS Roma, P.le A. Moro, 5, 00185 Roma, Italy
2
Dipartimento di Scienze della Terra, Sapienza Università di Roma, P.le A. Moro, 5, 00185 Roma, Italy
*
Author to whom correspondence should be addressed.
Diversity 2021, 13(7), 334; https://doi.org/10.3390/d13070334
Submission received: 4 June 2021 / Revised: 5 July 2021 / Accepted: 17 July 2021 / Published: 20 July 2021
(This article belongs to the Special Issue Review Papers on Marine Diversity)

Abstract

:
Antipatharian corals are important structural and complex members of benthic communities inhabiting the Italian seafloor. In this study, the distribution of black corals in Italy is reported and mapped for the first time. This review has permitted the identification of occurrences of such vulnerable marine ecosystems along the Italian coasts in a bathymetric range of 42 m to 790 m. Black corals appear to be most conspicuous and widely distributed in the mesophotic zone (from around 60 to 300 m depth), with a major occurrence on the rocky bottom and shoals. This review also highlights that these communities suffer direct damage from anthropogenic impacts (fishing activity and lost garbage). Finally, this study provides evidence that the reported Italian submarine sites associated with the occurrence of black corals probably represent only a small portion of their real distribution. This finding urges the need to increase monitoring efforts to support the protection and the conservation of these pristine species assemblages.

1. Introduction

Black corals (Cnidaria: Anthozoa: Hexacorallia: Antipatharia) are characterized by arborescent vertical or monopodial growth forming three-dimensional habitats supporting high levels of biodiversity [1,2]. Antipatharian corals have been considered for a long time to be among the rarest and sporadic coral species in the Mediterranean Sea [3]. To date, it is well known that these corals are able to form dense aggregations forming pristine underwater forests [4].
Within the Italian seas, five species of black corals have been reported: Antipathes dichotoma Pallas, 1766 and Antipathes fragilis, Gravier, 1918 (both Antipathidae), Leiopathes glaberrima (Esper, 1972) (Leiopathidae), Antipathella subpinnata (Ellis & Solander, 1786) (Myriopathidae), and Parantipathes larix (Esper, 1788) (Schizopathidae). Actually, the latter was lost and its taxonomic position is highly dubious [5]. Such corals are mainly found in a water depth of 60 m to 300 m [4,6], forming characteristic ecological niches hosting rich associated fauna and attracting numerous species of commercial interest [1,7].
Because of their rarity, black corals low growth rates, and low recovery ability, are considered extremely sensitive and listed as indicator species of vulnerable marine ecosystems (VMEs). For this reason, they are mentioned in several international agreements concerning marine ecosystem conservation (CITES Appendix II [available at http://www.cites.org]; European Community 1999), in Annex III of the Berna Convention, in Annex II of the Barcelona Convention for the Mediterranean species, and are also categorized as “threatened” by the International Union for Conservation of Nature (IUCN) Red List of Mediterranean Anthozoa [8] (with the millennial life span L. glaberrima being the only one listed as “endangered”). The main anthropogenic impact affecting these corals is represented by fishing as artisanal and recreational activities and bottom trawling, which may cause the resuspension of fine sediments [4,9,10]. Rare activities related to the commercial fisheries of precious corals for the jewelry industry is also reported [11].
Review studies on deep coral assemblages in the Mediterranean Sea have mainly been limited to scleractinian corals (i.e., Lophelia and Madrepora [12,13]), while few studies were exclusively focused on the distribution of black corals in the Italian seas [4,5,14,15,16,17]. The Italian seas have an average depth of about 1500 m, and a maximum depth of about 5000 m. The main Italian seas are the Tyrrhenian, Adriatic, and Ionian, and the other seas are represented by the Ligurian and Corsica seas, and the Otranto, Messina, and Sicily straits. The seawater temperatures range from 12 °C to 13 °C during the cold season, and from 26 °C to 28 °C in the warm season. Temperatures at the seafloor are constant and range from 12 °C to 13 °C [18]. During the last decades, the temperatures of the Italian seas have significantly increased [19], which resulted in dramatic changes in biodiversity composition [18]. To date, 29 Italian Marine Protected Areas (MPAs) have been established, but this number strongly needs to be updated [20].
The aim of this study is to present a review of the knowledge on the occurrence of black corals in the Italian seas, providing the first comprehensive distribution map of these species. The distribution of black corals may be considered the first step towards defining a more complete overview regarding the present knowledge on these vulnerable species. This study also highlights the need for the conservation programs protecting black corals in the Italian seas.

2. Distribution Dataset and Methods

Table 1 shows dataset of black coral distribution in the Italian Seas. This dataset was created using all the available scientific literature and reports, starting from 1973 until today. For each site, when available, the following information was reported: region, ID (number code referred to the code reported in Figure 1), sites, sea, coral species, minimum and maximum depth, setting, substrate, anthropogenic impact, reference. The type of setting is based on the classification used by Gori et al. [6], whereas the substrate types were referred to those reported in the related scientific articles. The categories related to anthropogenic impact are represented by fishing activity (trawl and ghost nets, longlines, lines, ropes, other fishing gear) and lost garbage (e.g., plastic and metal objects).
All the sites reported in Table 1 were used to create the first distribution map of black corals in the Italian seas (Figure 1).
In the reported studies remotely operated vehicles (ROVs) and multibeam echosounders (MBES) were used for the identification of black coral specimens and the description of the geomorphological characteristics of the substrate [4,5,14,15,16,17].

3. Results

3.1. The Distribution of Black Corals in the Italian Seas

This study shows the occurrence of black-coral communities composed of A. subpinnata (34%), L. glaberrima (33%), A. dichotoma (17%), P. larix (15%), and A. fragilis (1%) in 59 Italian sites (Figure 2), which are reported from the Ligurian, Tuscany, Latium, Campanian, Apulian, Calabrian, Sicily, and Sardinia regions (Table 1).
The majority of these sites are located in the Sicily region (23 sites) followed by the Apulian (8 sites), Ligurian and Sardinia (6 sites), Campanian (5 sites), Calabrian and Tuscan regions (4 sites), and Latium (3 sites). Black coral communities were not reported from the central–northern Adriatic Sea.
The bathymetric distribution of black corals in the Italian seas ranges from 42 m to 790 m depth. The shallowest record is found in the Calabrian Region and the deepest one in the Apulian. In the first case, the identified coral is represented by A. dichotoma, and in the second one, by L. glaberrima.
The analysis of their bathymetric distribution (Figure 3) highlights that the corals A. dichotoma and L. glaberrima have a deeper distribution (depth ranges (min 250 m–max 243 m, respectively), whereas A. subpinnata has a shallower one (medium depth of 115 m).
In addition, L. glaberrima shows the most bathymetric tolerance, ranging from 45 m to 730.5 m water depth. In detail, 62% of the Italian submarine sites are characterized by the occurrence of mixed black coral communities, which are most frequent in depths ranging from 50 m to 200 m.
In the Italian seas, black corals were found in different environmental settings, varying from shelf, shelf edge and upper slope, offshore banks and seamounts, and deep areas (Figure 4a). In detail, A. subpinnata displays the widest distribution, occurring in all above-mentioned settings with a maximum frequency on the shelf. Antipathes dichotoma, L. glaberrima, and P. larix are reported from the shelf, shelf edge and upper slope, offshore banks and seamounts, and deep areas. Parantipathes larix and A. dichotoma mainly occur in the shelf edge and upper slope, whereas L. glaberrima in the deep areas. Antipathes fragils is only reported from the shelf. The black corals observed in the Italian seas are settled on different exposed substrates represented by the rocky bottom, deep rocky banks, rocks encrusted by coralline algae, shoal, terrace, and vertical rocky walls (Figure 4b). The most common substrate types associated with these corals is represented by rocky bottom. A minor percentage, excluding A. fragils, were also associated with shoal, deep rocky banks, and rocks encrusted by coralline algae. Finally, in very few cases they were occurring on terraces and vertical rocky walls (Figure 4b).

3.2. Anthropogenic Impact

The analysis of all the reported sites (Table 1) has permitted the identification of the different anthropogenic impacts affecting the Italian sites where the black corals are settled (Figure 5).
These sites, representing 29% of the total, are found in water depths ranging from 45 m to 730.5 m (with a medium depth of 200 m), and are associated with the rocky bottom, deep rocky banks, and shoal substrates. The items affecting the black coral communities are represented by two main categories (Table 1): fishing activity (trawl and ghost nets, longlines, lines, ropes, other fishing litter) and lost garbage (e.g., plastic and metal objects). A total of 83% of debris impacting the Italian sites is associated with fishing activity, whereas a few exceptions are related to lost garbage (Table 1).

4. Discussion

Black corals have for a long time been considered to be rarest corals in the Mediterranean Sea [3]. The recent increase in the use of modern technological tools, such as ROVs, has permitted the documentation of the great variability of the coral communities occurring in Mediterranean environments e.g., [2,27,44,45]. Exploration of the submarine environment by ROV has represented a turning point in the updating knowledge on benthic communities, providing a valuable tool for the understanding of their geographical and bathymetrical distribution, and their morphological description and ecological aspects [17,46].
Our study is focused on the distribution analysis of the antipatharian corals already reported in the Italian seas. This first step highlighting the presence of the black corals should be considered more common than what supposed. The present review strongly supports the idea proposed by Bo et al. [47], that black corals are among the most conspicuous and widely distributed organisms of mesophotic Mediterranean coral communities (especially in a depth range from 60 m to 150 m). It is also confirmed that the majority occur on rocky bottom and shoals [45]. This statement could be due to the occurrence, in the mesophotic zone, of more favorable environmental factors able to enhance coral growth (which are lower levels of competition for space, food supply, temperature, currents rich in suspended matter, heterogeneity of substrate, rate of sedimentation [47]). According to present knowledge e.g., [1,45,47,48,49], currents rich in suspended matter are probably the major environmental factor influencing black coral settlement and composition in the Italian seas.
Nevertheless, it is important to consider that shallow water was investigated more by manned submersibles, ROVs, and multibeam echo-sounders than deep water. Deep marine environments could represent an optimal habitat for the settlement of black corals [47]. Such environments are more sheltered from physical damages (e.g., strong storm induced waves [50]), and they are less influenced by seasonal variability. In fact, during the summer, the effect of high irradiance induces strong water-column stratification resulting in a depletion of food supply [51]. In addition, considering the worldwide black coral distribution [52], it is possible to assert that they are typically found in deeper waters, below the photic zone [53], with over 75% of described species occurring down to a 50 m depth [54]. This evidence accentuates the need of increasing knowledge regarding their ecological aspects, which to date are still scarse [49]. Distribution of antipatharian corals along the rocky bottom and shoals may be favored by the combination of both biotic and abiotic factors. The geomorphological characteristics associated with these substrates create a very high variability at a small spatial scale, promoting benthic biodiversity. In addition, low sediment accumulation rate and high bottom current acceleration increase the food supply [43,55,56], favoring the development of the black coral communities.
According to Bo et al., [17], the most frequent black coral species occurring in the Italian seas is A. subpinnata [5], followed by L. glaberrima, A. dichotoma, P. larix, and A. fragilis. The frequencies of some of these corals (e.g., L. glaberrima) may depend on a nutrient enrichment due to anthropogenic eutrophication [57]. Nevertheless, from available data, black corals occur in the vicinity of all the small Italian islands (Favignana, Montecristo, Elba, Capraia, Capri, western Pontine Archipelago, Aeolian islands, Pantelleria, Linosa, Carloforte, and Tremiti islands; Figure 1). In this regard, the theory of island biogeography proposed by MacArthur [58] helps to explain this result. According to this theory, the species richness of natural communities is influenced by different factors, such as habitat heterogeneity and rate of competition. These are both linked to the surface area of the island, larval dispersion and anthropogenic impact. Moreover, the distance from nutrition sources (such as a river mouth) and the degree of their isolation strongly influenced the amount of food supply. In the proximity of topographic structures such as islands or archipelagos marine currents commonly undergo a velocity increase, providing the right amount of nutrients and representing an optimal marine environment for the growth of black corals.

Anthropogenic Factors Affecting Black Corals

Black corals represent useful indicator species of deep-water marine ecosystems and play an important ecological role as ecosystem engineers [17,49,59]; direct damage linked to anthropogenic impact is frequently reported from the Italian seas e.g., [24,42].
Probably, the occurrence of black corals in Italy on specific types of substrate (mainly rocky bottoms and isolated shoals) as well as their bathymetric distribution (within 50 m and 300 m depth), makes them more exposed to fishing activities, causing damage to vulnerable marine ecosystems. Furthermore, this impact represents a considerable concern, considering their specific characteristics such as 3D structure, long lived species, slow growth rates, and recovery ability [24,60,61]. Fishing impacts (including ghost nets) can lead to the direct removal or partial damage to coral colonies. The skeletons of the damaged corals may become overgrown by various fast growing organisms [4,62]. This kind of damage can have far-reaching and long lasting effects on the population dynamics of Mediterranean black corals, especially when their low growth rates are considered [42]. Despite of the distance from the coast, it is well known that rocky bottoms and isolated shoals are considered important targets for fishermen [24]. In addition, other factors are well known to influence fishing efforts [24,63,64], such as their depth, topography, and the fact that they could represent a refuge for many commercial species. The different entities of fishing disturbance could also be linked to different coral morphologies. In fact, the morphological characteristics (arborescent and erect structures) and the grade of flexibility of black corals may increase their resistance to mechanical friction, showing different mechanical responses to their entanglement [24,43,65].
Finally, it is also important to highlight that in the last decades, all seas have experienced significant changes due to pollution and global warming [66]. These changes can result in mass coral mortality events and quantitative alterations in the composition of benthic communities [67].
Despite all this evidence, the only Italian MPA, containing black coral forests, is the Tremiti Islands Marine Protected Area [7]. All these findings indicate the need for actions focused on the implementation of effective management and proper conservation measures to preserve the Italian antipatharian corals.

5. Conclusions

This study presents an update of the current knowledge regarding the black coral distribution across Italian seas. For the first time, a distribution map is given of black corals occurring in the Italian seas. An analysis of their distribution shows a major bathymetric interval from 60 m to about 150 m (mesophotic zone) and wide occurrences along all the Italian coasts, except for the central–northern Adriatic Sea. It is also highlighted that the Italian sites where black corals occur probably represent only a small portion of their real number. This suspicion suggests the need of further investigations, especially in the deep marine environment. Considering that black corals are indicator species of vulnerable marine ecosystems, and that some of the reported sites are affected by anthropogenic impacts, targeted conservation and management measures should be adopted in order to preserve their pristine species assemblages in the Italian seas.

Author Contributions

M.I. and L.D.B. contributed the editing of present versions of manuscript. The authors participated in the review study and writing of the present versions of the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The Editor and the anonymous reviewers are gratefully acknowledged for their useful comments which helped us to improve the final version of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bo, M.; Bavestrello, G.; Canese, S.; Giusti, M.; Salvati, E.; Angiolillo, M.; Greco, S. Characteristics of a black coral meadow in the twilight zone of the central Mediterranean Sea. Mar. Ecol. Prog. Ser. 2009, 397, 53–61. [Google Scholar] [CrossRef]
  2. Bo, M.; Canese, S.; Spaggiari, C.; Pusceddu, A.; Bertolino, M.; Angiolillo, M.; Giusti, M.; Loreto, M.F.; Salvati, E.; Greco, S.; et al. Deep Coral Oases in the South Tyrrhenian Sea. PLoS ONE 2012, 7, e49870. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Opresko, D.M.; Försterra, G.; Hofrichter, R. Orden Antipatharia (corales negros o espinosos). El Mar Mediterraneo (Fauna, Flora, Ecologia); Hofrichter, R., Ed.; Omega: Barcelona, Spain, 2004; pp. 506–509. [Google Scholar]
  4. Bo, M.; Canese, S.; Bavestrello, G. Discovering Mediterranean black coral forests: Parantipathes larix (Anthozoa: Hexacorallia) in the Tuscan Archipelago, Italy. Ital. J. Zool. 2013, 81, 112–125. [Google Scholar] [CrossRef] [Green Version]
  5. Bo, M.; Bavestrello, G. Mediterranean Black Coral Communities. In Mediterranean Cold-Water Corals: Past, Present and Future; Springer: Cham, Switzerland, 2019; pp. 249–251. [Google Scholar]
  6. Gori, A.; Bavestrello, G.; Grinyó, J.; Dominguez-Carrió, C.; Ambroso, S.; Bo, M. Animal forests in deep coastal bottoms and continental shelf of the Mediterranean Sea. In Marine Animal Forests: The Ecology of Benthic Biodiversity Hotspots; Springer: Berlin/Heidelberg, Germany, 2017; pp. 207–233. [Google Scholar]
  7. Chimienti, G.; De Padova, D.; Mossa, M.; Mastrototaro, F. A mesophotic black coral forest in the Adriatic Sea. Sci. Rep. 2020, 10, 1–15. [Google Scholar] [CrossRef] [PubMed]
  8. Bo, M.; Numa, C.; Otero, M.D.M.; Orejas, C.; Garrabou, J.; Cerrano, C.; Kružić, P.; Antoniadou, C.; Aguilar, R.; Kipson, S.; et al. Overview of the Conservation Status of Mediterranean Anthozoa; IUCN: Gland, Switzerland, 2017. [Google Scholar]
  9. Deidun, A.; Tsounis, G.; Balzan, F.; Micallef, A. Records of black coral (Antipatharia) and red coral (Corallium rubrum) fishing activities in the Maltese Islands. Mar. Biodivers. Rec. 2010, 3. [Google Scholar] [CrossRef]
  10. Bo, M.; Barucca, M.; Biscotti, M.A.; Brugler, M.R.; Canapa, A.; Canese, S.; Bavestrello, G. Phylogenetic relationships of Medi-terranean black corals (Cnidaria: Anthozoa: Hexacorallia) and implications for classification within the order Antipatharia. Invertebr. Syst. 2018, 32, 1102–1110. [Google Scholar] [CrossRef]
  11. Opresko, D.M. Three new species of Leiopathes (Cnidaria: Anthozoa: Antipatharia) from Southern Australia. Rec. Aust. Mus. 1998, 31, 99–111. [Google Scholar]
  12. Tursi, A.; Mastrototaro, F.; Matarrese, A.; Maiorano, P.; D’Onghia, G. Biodiversity of the white coral reefs in the Ionian Sea (Central Mediterranean). Chem. Ecol. 2004, 20, 107–116. [Google Scholar] [CrossRef]
  13. Taviani, M.; Freiwald, A.; Zibrowius, H. Deep Coral Growth in the Mediterranean Sea: An overview. Erlangen Earth Conference Series; Springer: Berlin/Heidelberg, Germany, 2006; pp. 137–156. [Google Scholar]
  14. Vafidis, D.; Koukouras, A. Antipatharia, Ceriantharia and Zoantharia (Hexacorallia, Anthozoa) of the Aegean Sea with a check list of the Mediterranean and Black Sea Species. Ann. Inst. Oceanogr. 1998, 74, 115–126. [Google Scholar]
  15. Opresko, D.M. Redescription of Antipathes dichotoma Pallas, 1766 (Cnidaria: Anthozoa: Antipatharia). Zool. Med. Leiden 2003, 77, 481–493. [Google Scholar]
  16. Morri, C.; Esposito, F.; Pessani, D. Checklist della flora e della fauna dei mari italiani (Parte I). Anthozoa Biol. Mar. Mediterr. 2008, 15, 92–101. [Google Scholar]
  17. Bo, M.; Tazioli, S.; Spanò, N.; Bavestrello, G. Antipathella subpinnata (Antipatharia, Myriopathidae) in Italian seas. Ital. J. Zool. 2008, 75, 185–195. [Google Scholar] [CrossRef]
  18. Danovaro, R.; Boero, F. Italian Seas. In World Seas: An Environmental Evaluation; Elsevier BV: Amsterdam, The Netherlands, 2019; pp. 283–306. [Google Scholar]
  19. 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]
  20. Villa, F.; Tunesi, L.; Agardy, T. Zoning Marine Protected Areas through Spatial Multiple-Criteria Analysis: The Case of the Asinara Island National Marine Reserve of Italy. Conserv. Biol. 2002, 16, 515–526. [Google Scholar] [CrossRef]
  21. Terzin, M.M.G.; Matterson, K.; Coppari, M.; Bavestrello, G.; Abbiati, M.; Costantini, F. Population genomic structure of the black coral Antipathella subpinnata in Mediterranean Vulnerable Marine Ecosystems. In Coral Reefs; Springer: Berlin/Heidelberg, Germany, 2021; pp. 1–16. [Google Scholar]
  22. Coppari, M.; Mestice, F.; Betti, F.; Bavestrello, G.; Castellano, L.; Bo, M. Fragmentation, re-attachment ability and growth rate of the Mediterranean black coral Antipathella subpinnata. Coral Reefs 2019, 38, 1–14. [Google Scholar] [CrossRef]
  23. Coppari, M.; Ferrier-Pagès, C.; Castellano, M.; Massa, F.; Olivari, E.; Bavestrello, G.; Povero, P.; Bo, M. Seasonal variation of the stable C and N isotopic composition of the mesophotic black coral Antipathella subpinnata (Ellis & Solander, 1786). Estuarine Coast. Shelf Sci. 2020, 233, 106520. [Google Scholar] [CrossRef]
  24. Bo, M.; Bava, S.; Canese, S.; Angiolillo, M.; Cattaneo-Vietti, R.; Bavestrello, G. Fishing impact on deep Mediterranean rocky habitats as revealed by ROV investigation. Biol. Conserv. 2014, 171, 167–176. [Google Scholar] [CrossRef]
  25. Greenpeace. I tesori sommersi del Canale di Sicilia. NO TRIVELLE TOUR 2012. 2012. Available online: www.greenpeace.it (accessed on 21 June 2021).
  26. Massi, D.; Vitale, S.; Titone, A.; Milisenda, G.; Gristina, M.; Fiorentino, F. Spatial distribution of the black coral Leiopathes glaberrima (Esper, 1788) (Antipatharia: Leiopathidae) in the Mediterranean: A prerequisite for protection of Vulnerable Marine Ecosystems (VMEs). Eur. Zool. J. 2018, 85, 169–178. [Google Scholar] [CrossRef] [Green Version]
  27. Bo, M.; Bavestrello, G.; Canese, S.; Giusti, M.; Angiolillo, M.; Cerrano, C.; Salvati, E.; Greco, S. Coral assemblage off the Calabrian Coast (South Italy) with new observations on living colonies of Antipathes dichotoma. Ital. J. Zool. 2011, 78, 231–242. [Google Scholar] [CrossRef]
  28. Aguilar, R.; Pastor, X.; Garcia, S.; Marin, P.; Ubero, J. Importance of seamounts-like features for Mediterranean marine habitats and threatened species. Rapp. Comm. Int. Mer Méditerr. 2013, 40, 716. [Google Scholar]
  29. Arena, P.; Li Greci, F. Indagine sulle condizioni faunistiche e sui rendimenti di pesca dei fondali batiali della Sicilia occidentale e della bordura settentrionale dei banchi della soglia Siculo-Tunisina. Quad. Lab. Tecnol. Pesca 1973, 1, 157–201. [Google Scholar]
  30. Santin, A.; Aguilar, R.; Akyol, O.; Begburs, C.R.; Benoit, L.; Chimienti, G.; Tiralongo, F. New records of rare species in the Mediterranean Sea (March 2021). Mediterr. Mar. Sci. 2021, 22, 199–217. [Google Scholar]
  31. Romagnoli, B.; Grasselli, F.; Costantini, F.; Abbiati, M.; Romagnoli, C.; Innangi, S.; Di Martino, G.; Tonielli, R. Evaluating the distribution of priority benthic habitats through a remotely operated vehicle to support conservation measures off Linosa Island (Sicily Channel, Mediterranean Sea). Aquat. Conserv. Mar. Freshw. Ecosyst. 2021. [Google Scholar] [CrossRef]
  32. Bo, M.; Bavestrello, G. Distribuzione, Ecologia e conservazione dei coralli neri (Anthozoa, Antipatharia) del Mediterraneo; BMIB: Genova, Italy, 2013; p. 75. [Google Scholar]
  33. Ingrassia, M.; Macelloni, L.; Bosman, A.; Chiocci, F.L.; Cerrano, C.; Martorelli, E. Black coral (Anthozoa, Antipatharia) forest near the western Pontine Islands (Tyrrhenian Sea). Mar. Biodivers. 2016, 46, 285–290. [Google Scholar] [CrossRef]
  34. Gaino, E.; Scoccia, F. Gamete spawning in Antipathella subpinnata (Anthozoa, Antipatharia): A structural and ultrastructural investigation. Zoomorphology 2010, 129, 213–219. [Google Scholar] [CrossRef]
  35. Angiolillo, M.; Gori, A.; Canese, S.; Bo, M.; Priori, C.; Bavestrello, G.; Salvati, E.; Erra, F.; Greenacre, M.; Santangelo, G. Distribution and population structure of deep-dwelling red coral in the Northwest Mediterranean. Mar. Ecol. 2016, 37, 294–310. [Google Scholar] [CrossRef]
  36. Giusti, M.; Innocenti, C.; Canese, S. Predicting suitable habitat for the gold coral Savalia savaglia (Bertoloni, 1819) (Cnidaria, Zoantharia) in the South Tyrrhenian Sea. Cont. Shelf Res. 2014, 81, 19–28. [Google Scholar] [CrossRef]
  37. D’Onghia, G.; Calculli, C.; Capezzuto, F.; Carlucci, R.; Carluccio, A.; Maiorano, P.; Pollice, A.; Ricci, P.; Sion, L.; Tursi, A. New records of cold-water coral sites and fish fauna characterization of a potential network existing in the Mediterranean Sea. Mar. Ecol. 2016, 37, 1398–1422. [Google Scholar] [CrossRef]
  38. Carlier, A.; Le Guilloux, E.; Olu, K.; Sarrazin, J.; Mastrototaro, F.; Taviani, M.; Clavier, J. Trophic relationships in a deep Med-iterranean cold-water coral bank (Santa Maria di Leuca, Ionian Sea). Mar. Ecol. Prog. Ser. 2009, 397, 125–137. [Google Scholar] [CrossRef]
  39. Mastrototaro, F.; D’Onghia, G.; Corriero, G.; Matarrese, A.; Maiorano, P.; Panetta, P.; Gherardi, M.; Longo, C.; Rosso, M.A.; Sciuto, F.; et al. Biodiversity of the white coral bank off Cape Santa Maria di Leuca (Mediterranean Sea): An update. Deep Sea Res. Part II Top. Stud. Oceanogr. 2010, 57, 412–430. [Google Scholar] [CrossRef]
  40. Vertino, A.; Savini, A.; Rosso, A.; Di Geronimo, I.; Mastrototaro, F.; Sanfilippo, R.; Gay, G.; Etiope, G. Benthic habitat characterization and distribution from two representative sites of the deep-water SML Coral Province (Mediterranean). Deep Sea Res. Part II Top. Stud. Oceanogr. 2010, 57, 380–396. [Google Scholar] [CrossRef]
  41. Chimienti, G.; Mastrototaro, F. Searching for black corals: The exploration of Tremiti islands MPA. Rapp. Comm. Mer. Médit. 2019, 42, 268. [Google Scholar]
  42. Bo, M.; Bavestrello, G.; Angiolillo, M.; Calcagnile, L.; Canese, S.; Cannas, R.; Cau, A.; D’Elia, M.; D’Oriano, F.; Follesa, M.C.; et al. Persistence of Pristine Deep-Sea Coral Gardens in the Mediterranean Sea (SW Sardinia). PLoS ONE 2015, 10, e0119393. [Google Scholar] [CrossRef] [Green Version]
  43. Cau, A.; Follesa, M.C.; Moccia, D.; Alvito, A.; Bo, M.; Angiolillo, M.; Canese, S.; Paliaga, E.M.; Orrù, P.E.; Sacco, F.; et al. Deepwater corals biodiversity along roche du large ecosystems with different habitat complexity along the south Sardinia continental margin (CW Mediterranean Sea). Mar. Biol. 2015, 162, 1865–1878. [Google Scholar] [CrossRef]
  44. Gori, A.; Rossi, S.; Linares, C.; Berganzo, E.; Orejas, C.; Dale, M.R.; Gili, J.-M. Size and spatial structure in deep versus shallow populations of the Mediterranean gorgonian Eunicella singularis (Cap de Creus, northwestern Mediterranean Sea). Mar. Biol. 2011, 158, 1721–1732. [Google Scholar] [CrossRef]
  45. Angiolillo, M.; Canese, S. Deep Gorgonians and Corals of the Mediterranean Sea. In Corals in a Changing World; IntechOpen: London, UK, 2018. [Google Scholar]
  46. Tazioli, S.; Bo, M.; Boyer, M.; Rotinsulu, H.; Bavestrello, G. Ecological observations of some common antipatharian corals in the marine park of Bunaken (North Sulawesi, Indonesia). Zool. Stud. 2007, 46, 227–241. [Google Scholar]
  47. Bo, M.; Montgomery, A.D.; Opresko, D.M.; Wagner, D.; Bavestrello, G. Antipatharians of the Mesophotic Zone: Four Case Studies. In Coral Reefs of the Eastern Tropical Pacific; Springer: Berlin/Heidelberg, Germany, 2019; pp. 683–708. [Google Scholar]
  48. Genin, A.; Dayton, P.K.; Lonsdale, P.F.; Spiess, F.N. Corals on seamount peaks provide evidence of current acceleration over deep-sea topography. Nat. Cell Biol. 1986, 322, 59–61. [Google Scholar] [CrossRef]
  49. Bo, M.; Di Camillo, C.G.; Addamo, A.M.; Valisano, L.; Bavestrello, G. Growth strategies of whip black corals (Cnidaria: An-tipatharia) in the Bunaken Marine Park (Celebes, Indonesia). Mar. Biodivers. Rec. 2009, 2e54, 1–6. [Google Scholar] [CrossRef]
  50. Hiscock, K. Water movement. In Sublittoral Ecology. The Ecology of Shallow Sublittoral Benthos; Earll, R., Erwin, D.G., Eds.; Clarendon Press: Oxford, UK, 1983; pp. 58–96. [Google Scholar]
  51. Coma, R.; Ribes, M.; Gili, J.-M.; Zabala, M. Seasonality in coastal benthic ecosystems. Trends Ecol. Evol. 2000, 15, 448–453. [Google Scholar] [CrossRef]
  52. Cerrano, C.; Bastari, A.; Calcinai, B.; Di Camillo, C.; Pica, D.; Puce, S.; Valisano, L.; Torsani, F. Temperate mesophotic ecosystems: Gaps and perspectives of an emerging conservation challenge for the Mediterranean Sea. Eur. Zool. J. 2019, 86, 370–388. [Google Scholar] [CrossRef] [Green Version]
  53. Wagner, D.; Luck, D.G.; Toonen, R. The Biology and Ecology of Black Corals (Cnidaria: Anthozoa: Hexacorallia: Antipatharia). Adv. Mar. Biol. 2012, 63, 67–132. [Google Scholar]
  54. Cairns, S.D. Deep-water corals: An overview with special reference to diversity and distribution of deep-water scleractinian corals. Bull. Mar. Sci. 2007, 81, 311–322. [Google Scholar]
  55. Wilson, S.K.; Graham, N.A.J.; Polunin, N.V. Appraisal of visual assessments of habitat complexity and benthic composition on coral reefs. Mar. Biol. 2007, 151, 1069–1076. [Google Scholar] [CrossRef]
  56. Davies, A.; Duineveld, G.C.A.; Lavaleye, M.S.S.; Bergman, M.J.N.; Van Haren, H.; Roberts, M. Downwelling and deep-water bottom currents as food supply mechanisms to the cold-water coral Lophelia pertusa (Scleractinia) at the Mingulay Reef Complex. Limnol. Oceanogr. 2009, 54, 620–629. [Google Scholar] [CrossRef] [Green Version]
  57. Etnoyer, P.J.; Wagner, D.; Fowle, H.A.; Poti, M.; Kinlan, B.; Georgian, S.E.; Cordes, E.E. Models of habitat suitability, size, and age-class structure for the deep-sea black coral Leiopathes glaberrima in the Gulf of Mexico. Deep Sea Res. Part II Top. Stud. Oceanogr. 2018, 150, 218–228. [Google Scholar] [CrossRef]
  58. MacArthur, R.H.; Wilson, E.O. The Theory Ofisland Biogeography; Princeton University Press: Princeton, NJ, USA, 1967; p. 224. [Google Scholar]
  59. De Clippele, L.H.; Huvenne, V.A.I.; Molodtsova, T.N.; Roberts, J.M. The Diversity and Ecological Role of Non-scleractinian Corals (Antipatharia and Alcyonacea) on Scleractinian Cold-Water Coral Mounds. Front. Mar. Sci. 2019, 6, 6. [Google Scholar] [CrossRef]
  60. Prouty, N.; Roark, E.; Buster, N.; Ross, S. Growth rate and age distribution of deep-sea black corals in the Gulf of Mexico. Mar. Ecol. Prog. Ser. 2011, 423, 101–115. [Google Scholar] [CrossRef] [Green Version]
  61. Roark, E.B.; Guilderson, T.P.; Dunbar, R.B.; Fallon, S.; Mucciarone, D.A. Extreme longevity in proteinaceous deep-sea corals. Proc. Natl. Acad. Sci. USA 2009, 106, 5204–5208. [Google Scholar] [CrossRef] [Green Version]
  62. Mortensen, P.; Buhl-Mortensen, L. Deep-water corals and their habitats in The Gully, a submarine canyon off Atlantic Canada. Erlangen Earth Conf. Ser. 2006, 247–277. [Google Scholar]
  63. Purroy, A.; Requena, S.; Gili, J.M.; Canepa, A.; Sardá, R. Spatial assessment of artisanal fisheries and their potential impact on the seabed: The Cap de Creus regional case study (northwestern Mediterranean Sea). Sci. Mar. 2014, 78, 449–459. [Google Scholar] [CrossRef] [Green Version]
  64. Deidun, A.; Andaloro, F.; Bavestrello, G.; Canese, S.; Consoli, P.; Micallef, A.; Romeo, T.; Bo, M. First characterisation of aLeiopathes glaberrima(Cnidaria: Anthozoa: Antipatharia) forest in Maltese exploited fishing grounds. Ital. J. Zool. 2014, 1–10. [Google Scholar] [CrossRef] [Green Version]
  65. Van De Water, J.A.; Coppari, M.; Enrichetti, F.; Ferrier-Pagès, C.; Bo, M. Local Conditions Influence the Prokaryotic Com-mu-nities Associated With the Mesophotic Black Coral Antipathella subpinnata. Front. Microbiol. 2020, 11, 2423. [Google Scholar] [CrossRef] [PubMed]
  66. D’Onghia, G.; Mastrototara, F.; Matarrese, A.; Politou, C.-Y.; Mytilineou, C. Biodiversity of the Upper Slope Demersal Community in the Eastern Mediterranean: Preliminary Comparison Between Two Areas With and Without Trawl Fishing. J. Northwest Atl. Fish. Sci. 2003, 31, 263–273. [Google Scholar] [CrossRef]
  67. Cerrano, C.; Bavestrello, G.; Bianchi, C.N.; Cattaneo-Vietti, R.; Bava, S.; Morganti, C.; Morri, C.; Picco, P.; Sara, G.; Schiaparelli, S.; et al. A catastrophic mass-mortality episode of gorgonians and other organisms in the Ligurian Sea (North-western Mediterranean), summer 1999. Ecol. Lett. 2000, 3, 284–293. [Google Scholar] [CrossRef]
Figure 1. Distribution map of black corals in the Italian seas (red lines: 50-m isobaths; blue lines: 100-m isobaths; grey lines: isobaths of each 200 m interval). Number codes refer to the ID codes reported in Table 1.
Figure 1. Distribution map of black corals in the Italian seas (red lines: 50-m isobaths; blue lines: 100-m isobaths; grey lines: isobaths of each 200 m interval). Number codes refer to the ID codes reported in Table 1.
Diversity 13 00334 g001
Figure 2. Percentages of black coral species observed in the Italian Seas.
Figure 2. Percentages of black coral species observed in the Italian Seas.
Diversity 13 00334 g002
Figure 3. Bathymetric distribution of five black corals in the Italian seas (Outliers are marked with circles and the mean with x symbol).
Figure 3. Bathymetric distribution of five black corals in the Italian seas (Outliers are marked with circles and the mean with x symbol).
Diversity 13 00334 g003
Figure 4. (a) Different settings and (b) substrate types where black corals were observed in the Italian seas.
Figure 4. (a) Different settings and (b) substrate types where black corals were observed in the Italian seas.
Diversity 13 00334 g004
Figure 5. Map of the Italian black coral communities that are affected or unaffected by anthropogenic impact.
Figure 5. Map of the Italian black coral communities that are affected or unaffected by anthropogenic impact.
Diversity 13 00334 g005
Table 1. Dataset of the Italian submarine sites associated with black corals reported in the available scientific literature. Codes used for the black corals: AS, Antipathella subpinnata; AD, Antipathes dichotoma; AF, Antipathes fragilis; LG, Leiopathes glaberrima; PL, Parantipathes larix. Code nd means “no data”.
Table 1. Dataset of the Italian submarine sites associated with black corals reported in the available scientific literature. Codes used for the black corals: AS, Antipathella subpinnata; AD, Antipathes dichotoma; AF, Antipathes fragilis; LG, Leiopathes glaberrima; PL, Parantipathes larix. Code nd means “no data”.
RegionIDSiteSeaCoralMin DepthMax DepthSettingSubstrateAnthropogenic ImpactReference
Ligurian1Banco di S. LuciaSE Ligurian SeaAS, AD, LG, PL140210Offshore banks and seamountsDeep rocky banksFishing activity[4,21]
Sicily2Mantice ShoalWestern Ligurian SeaAS70150Shelf edge and upper slopeDeep rocky banksFishing activity[4]
3Portofino Secca dell’IsuelaLigurian SeaAS5660ShelfShoalnd[17,22,23]
4BordigheraWest Ligurian SeaAS6363Shelfndnd[22]
5Wreck RavennaLigurian SeaAS7590ShelfRocky bottomnd[20]
6Punta FaroLigurian SeaAS6377ShelfShoalnd[23]
37Marco BankWestern SicilyLG240260Offshore banks and seamountsDeep rocky banksFishing activity[24]
38Graham ShoalStrait of SicilyLG95150Offshore banks and seamountsShoalnd[25]
39Favignana and Talbot Shoal Strait of SicilyLG100100Offshore banks and seamountsShoalnd[26]
40Filicudi Aeolian islandsTyrrhenian SeaAD75300Shelf edge and upper slopeRocks encrusted by coralline algaend[27,28]
41Filicudi Aeolian islandsTyrrhenian SeaLG300300Deep areasRocky bottomnd[27,28]
42Cape San Vito SicilyTyrrhenian SeaLG275286Deep areasndnd[26,27]
43Messina StraitSecche di FavazzinaAS5570 Rocky bottomnd[20]
44Pantelleria AS70100Offshore banks and seamountsndnd[20]
45Northern Levanzo IslandTyrrhenian SeaAS235250Deep areasndnd[29]
46StromboliTyrrhenian SeaAS5258ShelfRocky bottomnd[20]
47StromboliTyrrhenian SeaLG187345Deep areasRocky bottomnd[30]
48NE StromboliTyrrhenian SeaAD, PL129,202349, 202Shelf edge and upper slopeRocky bottomnd[30]
49LinosaSicily channelAS160160ShelfBench terracend[31]
50LinosaSicily channelLG200200Shelf edge and upper slopeBench terracend[31]
51NE LipariTyrrhenian SeaAS83130ShelfRocks encrusted by coralline algaend[30]
52NE LipariTyrrhenian SeaAS612612Deep areasRocky bottomnd[30]
53NE LipariTyrrhenian SeaPL129158ShelfRocks encrusted by coralline algaend[30]
54NE LipariTyrrhenian SeaAD129218Shelf edge and upper slopeRocks encrusted by coralline algaend[30]
55SW LipariTyrrhenian SeaAD207298Shelf edge and upper slopeRocky bottomnd[30]
56SalinaTyrrhenian SeaPL129345Shelf edge and upper slope, deep areasRocky bottomnd[30]
57PanareaTyrrhenian SeaLG187345Deep areasVertical rocky wallsnd[30]
58SE PanareaTyrrhenian SeaAD, PL351,349351,349Deep areasVertical rocky wallsnd[30]
59NW FilicudiTyrrhenian SeaAD, LG647647Deep areasRocky bottomnd[30]
Campanian14Vedove Shoal (Capri)Tyrrhenian SeaLG240260Deep areasDeep rocky banksLost garbage[24]
15Bay of NaplesTyrrhenian SeaAD, AS200200Shelf edge and upper slopeRocks encrusted by coralline algaend[17,27]
16Naple GulfTyrrhenian SeaAF, AS80100ShelfRocky bottomnd[17,32]
17Capri IslandTyrrhenian SeaAS 7070ShelfShoalFishing activity[17,27]
18Capri IslandTyrrhenian SeaLG160260Shelf edge and upper slopeRocky bottomnd[17,27]
Latium11Western Pontine ArchipelagoTyrrhenian seaLG, PL194220Offshore banks and seamountsRocky bottomFishing activity[33]
12Western Pontine ArchipelagoTyrrhenian seaAD, LG, PL145155Shelf edge and upper slope Rocky bottomFishing activity[33]
13Western Pontine ArchipelagoTyrrhenian seaLG, PL130138ShelfRocky bottomFishing activity and lost garbage[33]
Tuscany7Montecristo Natural reserveTyrrhenian seaAS, PL, LG108200Shelf edge and upper slopeShoalnd[4]
8Mezzo CanaleTyrrhenian SeaAS7070Shelfndnd[34]
9Capraia IslandTyrrhenian SeaAS7590ShelfRocky bottomnd[17]
10ElbaTyrrhenian SeaAS6094ShelfRocks encrusted by coralline algaend[35]
Calabrian19ScillaTyrrhenian SeaAS50100ShelfRocky bottomnd[1]
20Golfo di S. EufemiaTyrrhenian SeaAD
PL
AS
70120ShelfShoalnd[2]
21Vibo MarinaTyrrhenian SeaAD90132ShelfShoalFishing activity[27]
22FavazzinaTyrrhenian sea northern border Messina StraitAS6272ShelfRocky bottomnd[36]
Apulia23Vieste Adriatic sea LG350350Deep areasRocky bottomFishing activity[37]
24GallipoliAdriatic seaAS7070ShelfRocky bottomnd[17]
25S. Maria di LeucaIonian SeaLG671790Deep areasRocky bottomFishing activity[12,27,38,39]
26S. Maria di LeucaIonian SeaAD630640Deep areasRocky bottomFishing activity[39,40]
27Torre InserraglioIonian SeaLG4545ShelfndFishing activity[37]
28Tremiti IslandsAdriatic SeaAS5180Shelfndnd[7,34,41]
29Porto cesareoIonian seaLG100236Shelf edge and upper slopeRocky bottomFishing activity[37]
30Porto cesareoIonian seaLG5050ShelfRocky bottomFishing activity[37]
31Capo CominoEastern coasts of SardiniaAS5454Shelfndnd[17]
Sardinia32SW coasts of SardiniaWestern Mediterranean SeaAD, PL, LG210210Shelf edge and upper slopeShoalFishing activity[42]
33Rocky pinnacles off CarloforteSardinian Sea AD, AS, LG,
PL
120170Shelf edge and upper slopeRocky bottomFishing activity and lost gabage[43]
34Northern edge of Skerki Bank Sardinian ChannelLG520650Deep areasndnd[29]
35Western Carloforte IslandSardinian SeaLG70130Shelfndnd[35]
36Posada canyonSardinian SeaAS152156Deep areasndnd[21]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ingrassia, M.; Di Bella, L. Black Coral Distribution in the Italian Seas: A Review. Diversity 2021, 13, 334. https://doi.org/10.3390/d13070334

AMA Style

Ingrassia M, Di Bella L. Black Coral Distribution in the Italian Seas: A Review. Diversity. 2021; 13(7):334. https://doi.org/10.3390/d13070334

Chicago/Turabian Style

Ingrassia, Michela, and Letizia Di Bella. 2021. "Black Coral Distribution in the Italian Seas: A Review" Diversity 13, no. 7: 334. https://doi.org/10.3390/d13070334

APA Style

Ingrassia, M., & Di Bella, L. (2021). Black Coral Distribution in the Italian Seas: A Review. Diversity, 13(7), 334. https://doi.org/10.3390/d13070334

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