35 results on '"Pronzato, R"'
Search Results
2. Body Polarity and Mineral Selectivity in the Demosponge Chondrosia reniformis
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Bavestrello, G, Benatti, U, Calcinai, B, Cattaneo-Vietti, R, Cerrano, C, Favre, A, Giovine, M, Lanza, S, Pronzato, R, Sara, M, and BioStor
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- 1998
3. Tubulin posttranslational modifications induced by cadmium in the sponge Clathrina clathrus
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Ledda, F.D., Ramoino, P., Ravera, S., Perino, E., Bianchini, P., Diaspro, A., Gallus, L., Pronzato, R., and Manconi, R.
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- 2013
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4. Sponge shape as a taxonomic character ; the case of Spongia officinalis and Spongia agaricina
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Pronzato, R M and BioStor
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- 1999
5. Global diversity of sponges (Porifera: Spongillina) in freshwater
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Manconi, R. and Pronzato, R.
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- 2008
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6. The Keratosa in a collection of Mediterranean sponges mainly from the Italian coasts
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Pulitzer-Finali, G, Pronzato, R, and BioStor
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- 1981
7. Algoritmi, strutture e agire sociale
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Pronzato, Riccardo
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algorithms, digital platforms, structure, agency, hegemony, digital sociology ,thema EDItEUR::J Society and Social Sciences::JH Sociology and anthropology::JHB Sociology ,thema EDItEUR::J Society and Social Sciences::JB Society and culture: general::JBC Cultural and media studies - Abstract
This book examines the everyday relationships with algorithmic media at the sociological level, taking into consideration both structural and social actor-related dimensions. Specifically, drawing on a critical review of multiple theoretical contributions and the analysis of two empirical cases involving university students and healthcare professionals, it discusses how algorithmic media exert hegemonic power in contemporary society. Within this power, however, it is highlighted a dialectical, symbiotic, and fluid relationship between structure and agency, in which the structures activated and reproduced by algorithmic media can become spaces of action and reflection for users. In the conclusions, it is argued that sociology itself can offer tools to facilitate a critical understanding of technologies and the development of activities that can counter the hegemonic power of platforms.
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- 2024
8. Sponges architecture by colour: new insights into the fibres morphogenesis, skeletal spatial layout and morpho-anatomical traits of a marine horny sponge species (Porifera)
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Stocchino, G. A., primary, Cubeddu, T., additional, Pronzato, R., additional, Sanna, M. A., additional, and Manconi, R., additional
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- 2021
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9. Radiospongilla
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Manconi, R., Cubeddu, T., and Pronzato, R.
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Haplosclerida ,Radiospongilla ,Animalia ,Demospongiae ,Spongillidae ,Biodiversity ,Taxonomy ,Porifera - Abstract
Radiospongilla cfr. philippinensis (Annandale, 1909) Figs 1 a, 2, 3, 4, 5; Tables 1, 2, 3 Material examined. Four specimens NTM ZOO 5052, NTM ZOO 5056, NTM ZOO 5063, NTM ZOO 5069. Dry shore of a billabong, Mamukala Wetlands, 12��38���S 132��35���E, 7 km East of the South Alligator River, South off the Arnhem Highway, Kakadu National Park (Fig. 1, site a), 10.vii.1998, R. Manconi leg. Some slides and stubs (DTRG-FW571a, b, c, d) are deposited in the authors��� collection. Additional material. NTM Z001431, Tom Lagoon, NT, 16��22���S 134��50���E, Latz leg., 3.i.1971, large clusters on roots (DTRG-FW706); NTM Z001435, unknown location, Stn n. FW-0016 (DTRG-FW707) Comparative material. Radiospongilla sceptroides, AM Z2837, neotype, Merrika River, Nadgee Faunal Reserve near Womboyne (37��15���S, 149��55���E), New South Wales, Australia, on large rock, 0.5 m depth, 6.iii.1958, leg. F. Hersey, det. Penney & Racek (DTRG-FW542). Spongilla philippinensis, BMNH 34.4.28.1 box 13.III. C, alcohol, leg. L.E. Cheesman, Lake Sentani, Dutch New Guinea (DTRG-FW382). Spongilla sceptroides Haswell, BMNH 86.8. 27.665, box 13.III. C, alcohol, Brisbane, Australia (DTRG-FW387), BMNH 86.8.27.658, box 5, dry, leg. von Lendenfeld, Kakalum River, Australia (DTRG-FW409). Spongilla cerebellata Bowerbank, 1863, schizotype, Bowerbank collection, leg. Brudley, Dominion of Nizam (DTRG- FW412). Description. Growth form encrusting (5���6 mm in diameter, 2���5 mm thick) to cushion-shaped (3.5 cm in diameter, 1 cm thick). Consistency extremely fragile (dry specimens are, at present, completely fragmented due to their extremely fragile consistency). Colour whitish in dry condition. Oscules scattered. Ectosomal skeleton with no special architecture. Choanosomal skeleton irregularly reticulate network, with ascending paucispicular primary fibres and vague secondary tracts. Spongin scanty. Megascleres acanthoxeas of two size classes straight to slightly bent, from stout [232���302 (266��17) x 6���13 (9.28��0.96) ��m] to slender [188���226 (208��13) x 2.9���5.8 (5.24��1.06) ��m] ornamented by large, straight to curved variably dense small spines except at the tips. Microscleres absent. Gemmules subspherical (600���750 ��m in diameter) single to grouped (2���3) scattered in the skeletal network at the sponge basal portion. Foramen in a more or less conical depression, simple, without collar, with brown, slender porus tube. Gemmular theca trilayered with gemmuloscleres in a single layer more or less radially embedded (NTM ZOO 5052, 5056, 5063, 5069) to in double layer both tangentially arranged at theca surface and radially embedded in it (NTM Z001431, NTM Z001435). Outer gemmular surface hispid due to the emerging distal apices of gemmuloscleres. Pneumatic layer with vague chambers of spongin to with welldeveloped polygonal chambers. Inner layer sublayered of compact spongin. Gemmuloscleres [122���174 (148��12) x 2.3���8.7 (5.25��2.26) ��m] straight to slightly curved of two types from slender acanthoxeas abruptly pointed with few small scattered spines except at the tips, to stout acanthostrongyles with large straight spines scattered along the axis, and curved spines densely clustered at the tips. Habitat. Several dry sponges were discovered along the shore of an almost dry billabong in shaded areas on the painted metallic piers of a bird-watching platform and on surrounding dry timbers and bushes between the platform and the path (Fig. 2). Data confirm the typical growth mode of this species on natural and artificial substrata (Racek 1969). Geographic distribution. The geographic range of R. philippinensis is from the Philippines to northern Australia (Tables 1���2). The present record in Kakadu National Park confirms the presence of this species in coastal tropical-subtropical areas of the north, western and southern Australia (Racek 1969). On the other hand R. streptasteriformis Stanisic, 1979 is apparently endemic to the Northern Territory (Tables 1���2) (Stanisic 1979) whereas R. pedderensis Osborne, Forteath & Stanisic, 2008 is endemic to Tasmania (Osborne et al. 2008). The doubtful presence in Australia of R. crateriformis (Potts, 1882) is discussed by Racek (1969). The biogeographic pattern of the speciose Radiospongilla (18 species) is in the Australasian, Afrotropical, Neotropical, Nearctic, Oriental, and Palaearctic regions (Fig. 5) (Penney & Racek 1968; Manconi & Pronzato 2002, 2007). Remarks. In his synopsis on Australian freshwater sponges Racek (1969) clarified the taxonomic status of Radiospongilla philippinensis (previously a junior synonym of R. sceptroides) as a valid species (Penney & Racek 1968). On the basis of comparative analysis of specimens from Kakadu National Park bearing gemmules with a single layer of radial gemmuloscleres are here ascribed to R. cfr. philippinensis (Table 3) because they diverge from descriptions of Philippine and other Australian material (Annandale 1909ab). Also additional material from the NTM bearing gemmules with two layers of gemmuloscleres i.e. tangentially and radially arranged in the gemmular theca is here ascribed to R. cfr. philippinensis (Table 3). Radiospongilla Radiospongilla philippinensis cfr. philippinensis Gemmuloscleres acanthostrongyles acanthostrongyles acanthostrongyles acanthostrongyles ��m 80���122 x 31 105���180 x 4���5 acanthoxeas acanthoxeas 102���149 x 4.5���7 122���174 x 2.3���8.7 Gemmular tangential spicules in irregularly radial irregularly radial theca single layer spicules in single tangential and radial spicules in spicules in single layer double layer layer References *Annandale 1909ab Racek 1969 Present paper Present paper # Gee, 1931b GENUS Pectispongilla ANNANDALE , 1909, Published as part of Manconi, R., Cubeddu, T. & Pronzato, R., 2016, Australian freshwater sponges with a new species of Pectispongilla (Porifera: Demospongiae: Spongillida), pp. 61-76 in Zootaxa 4196 (1) on pages 65-69, DOI: 10.11646/zootaxa.4196.1.3, http://zenodo.org/record/167679, {"references":["Racek, A. A. (1969) The freshwater sponges of Australia (Porifera: Spongillidae). Australian Journal of Marine and Freshwater Research, 20, 267 - 310.","Stanisic, J. (1979) Freshwater sponges from the Northern Territory (Porifera: Spongillidae). Proceedings of the Linnean Society of North South Wales, 103 (2), 123 - 130.","Osborn, A. W., Forteath, G. N. R. & Stanisic, J. (2008) A new species of freshwater sponge (Porifera: Spongillidae) of the genus Radiospongilla from Lake Pedder in Tasmania. Papers and Proceedings of the Royal Society of Tasmania, 142 (2), 39 - 44.","Penney, J. T. & Racek, A. A. (1968) Comprehensive revision of a world-wide collection of freshwater sponges (Porifera: Spongillidae). United States National Museum Bulletin, 272, 1 - 184.","Manconi, R. & Pronzato, R. (2002) Spongillina n. subord. Lubomirskiidae, Malawispongiidae n. fam., Metaniidae, Metschnikowiidae, Palaeospongillidae, Potamolepidae, Spongillidae. In: J. Hooper & R. W. M. van Soest (Eds.), Vol. 1. Systema Porifera. A guide to the classification of sponges. Kluwer Academic / Plenum Publisher: New York, pp. 921 - 1019. http: // dx. doi. org / 10.1007 / 978 - 1 - 4615 - 0747 - 5 _ 97","Manconi, R. & Pronzato, R. (2007) Gemmules as a key structure for the adaptive radiation of freshwater sponges: a morphofunctional and biogeographical study. In: Custodio M. R., Lobo-Hajdu G., Hajdu, E. & Muricy, G. (Eds.), Porifera research: biodiversity, innovation and sustainability. Serie Livros. Museu Nacional: Rio de Janeiro, pp. 61 - 77.","Gee, N. G. (1931 b) Freshwater sponges of the Philippine Islands. The Philippine Journal of Science, 46 (1), 61 - 74."]}
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- 2016
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10. Pectispongilla gagudjuensis Manconi, Cubeddu & Pronzato, 2016, n. sp
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Manconi, R., Cubeddu, T., and Pronzato, R.
- Subjects
Haplosclerida ,Pectispongilla ,Animalia ,Demospongiae ,Spongillidae ,Biodiversity ,Pectispongilla gagudjuensis ,Taxonomy ,Porifera - Abstract
Pectispongilla gagudjuensis n. sp. Manconi & Pronzato Figs 1 b, 6, 7, 8, 9; Tables 1, 2, 4 Material. Type material NTM ZOO 2024, NTM ZOO 2680, NTM ZOO 4338, NTM ZOO 4339, NTM ZOO 4340 from a small unnamed dry creek, 12��43���S 132��46���E (Fig. 1, site b) along the Kakadu Highway, North of Malabanjbanjdju, Kakadu National Park, Alligator River Region, Northern Territory, 11.vii.1998, leg. Luca Pronzato. Some slides and stubs (DTRG-FW568 a, b, c, d, e) are deposited in the authors��� collection. Comparative material. Pectispongilla botryoides NTM Z001405 (DTRG-FW646) and part of the latter as AM Z3504 (DTRG-FW701), Tanami Gorge, 19��58���S 129��39���E, Camel Waterhole, Northern Territory, 25.v.1970, leg. P. Latz, S. Parker & D. Howe, det. A.A. Racek; AM Z2905, Manchester Lake, Queensland, 6.ix.61, det. A.A. Racek (DTRG-FW700). P. aurea var. subspinosa , syntype, BMNH 14.11.24.34 (ex ZEV 3790/7), Kochi (ex- Cochin), Ernakulam, Kerala, SW India (DTRG-FW401); USNM 34578, Penney collection 90124, schizosyntype, dry, Kochi (ex-Cochin), Ernakulam, Kerala, SW India (DTRG-FW553); ZMB 7981 from BMNH 14.11.24.34, alcohol, Kochi (ex-Cochin), Ernakulam, Kerala, SW India (DTRG-FW515). Etymology. The specific epithet refers to the native word Gagudju (from which Kakadu) derived from the name of one of the ca. thirty old native languages of the flood plain area in the Arnhem Land. Diagnosis. Pectispongilla gagudjuensis n. sp. is characterised by two types of short skeletal megascleres (acanthostrongyles and acanthoxeas), absence of microscleres, free gemmules, mature botryoidal gemmuloscleres with disto-lateral apices as irregular concavities grouped to form a botryum, and growth form as a small hollow cup in dry condition. Description. Growth form encrusting as minute almost flat cushions (max. 1 cm in diameter) scattered and strictly adhering to substrata by basal spongin plate. Surface smooth. Consistency hard and fragile. Colour white. Oscul e apical, single, central, large (300���350 ��m in diameter). Ectosomal skeleton compact and dense arrangement of spicules more or less tangential. Choanosomal skeleton vaguely reticulate network of spicules joined by scanty spongin. Spongin scanty except for basal spongin plate and gemmular theca. Megascleres of two types. Dominant acanthostrongyles [90���168 (135��19) x 8���13 (10��4) ��m] almost straight to notably bent (boomerang-like shaped), spiny by few scattered short spines sometimes more dense at the tips. Acanthoxeas (mucronate acanthostrongyles?) [130���205 (163��19) x 5���12 (8.5��1.9) ��m] less frequent, gradually to abruptly pointed, with short spines from scattered to more dense at the tips. Microscleres absent. Gemmules free (up to 8 for each specimen), small (200���350 ��m in diameter), subspherical after rehydration with gemmuloscleres more or less radially embedded. Foramen single with a short tube and a well developed collar. Gemmular theca thick, trilayered. Outer layer with a variable amount of compact spongin, as a honeycomb-like surface due to the partial emergence of distal botryoidal apices of gemmuloscleres. Pneumatic layer as an irregular network of anastomosing thin spongin fibres. Inner layer of sublayered compact spongin. Gemmuloscleres botryoidal (mature) to pseudo-botryoidal (immature) [26���46 (36��4) x 2���3 (2.9��0.29) ��m] with smooth, straight to slightly bent shafts and a range of variable shape at the convex side of each tip according with the age of the spicules. Immature gemmuloscleres with disto-lateral arrangement of simple small spines in rows (pseudo-botryum); botryum-like tips in growing spicules with a progressive increase of siliceous webs joining spines one to each other; true botryoidal tips with a cluster of well developed rounded concavities in more aged gemmuloscleres. Remarks. A comparative analysis of Pectispongilla gagudjuensis n. sp. showed that it matches only in part diagnostic traits of the other species of the genus (Table 4). The skeletal megascleres are shorter than the other species of the genus and the gemmules are the largest of the genus. Microscleres are absent in P. gagudjuensis n. sp., whereas microscleres of P. aurea Annandale, 1909 and P. subspinosa Annandale, 1912 are smooth to microspined oxeas (Penney & Racek 1968, p. 78���79) and those of P. stellifera Annandale, 1915 range from microspined oxeas to subspherical tubercled spherasters (Penney & Racek 1968, p. 79). Compared with the Australian P. botryoides Haswell, (1882) and the other species of the genus the gemmuloscleres of the new species have the shorter shafts. Moreover the gemmuloscleres of P. gagudjuensis are characterized by displaying the entire range of the various tip morphs (Fig. 8) hitherto recorded in the other four species of Pectispongilla i.e. from small spines in rows (immature gemmuloscleres) up to well developed botryoidal-like apices (mature spicules). The peculiar body architecture deeply diverges from Pectispongilla species and all other Spongillida i.e. reduced in dry condition to an almost hollow cup with megascleres to form the body wall and containing only free gemmules and a few spicular tracts. This morpho-functional trait has never been hitherto described for the family Spongillidae and is comparable only to the Baikalian Swartschewskia papyracea (Dybowsky, 1880) in dry condition. This body architecture, closely adhering to the substratum by a thin spongin basal plate, indicates its functional role as a protective device for gemmules during the long, harsh dry season. Its morpho-functional role is comparable to that performed by the gemmular cages of megascleres enveloping the gemmular theca found in other genera of Spongillida. P. gagudjuensis however diverges in the depth of the gemmular cage architecture described for other genera (e.g. Corvospongilla Annandale, 1911; Heterorotula Penney & Racek, 1968; Uruguayella Bonetto & Ezcurra De Drago, 1969; Pachyrotula Volkmer-Ribeiro & R��tzler, 1997). In synthesis, exclusive traits of P. gagudjuensis n. sp. in comparison with those of the other Pectispongilla species are as follows: i) single apical oscular aperture, ii) presence of free gemmules in the hollow internal space of the dry body, iii) megascleres of two types i.e. acanthoxeas and dominant acanthostrongyles, iv) short length of megascleres (ca. half of those of other species), v) largest gemmules of the genus, vi) shorter shafts of gemmuloscleres in the genus (see Annandale 1915 and Penney & Racek 1968). The diagnosis of the genus is here emended adding the presence of spiny strongyles among megascleres. Genus Pectispongilla Habitat. Lotic, temporary creek. Several dry, scattered small specimens under pebbles, cobbles, and boulders, from 1 to 6 per substratum. Sponges were absent from the surveyed horizontal rocky bed and timbers. Encrusting bryozoans, with statoblasts, on the same substrata but not strictly associated to the sponges, were also collected and preserved together with the sponges. Geographic distribution. P. gagudjuensis n. sp. is known only from the type locality. The disjunct Oriental, Australasian, and far east Palaearctic biogeographic pattern of Pectispongilla (5 species) seems to indicate Gondwanan origins and is restricted to the south-western Indian sub-region and Australia with an enclave in Korea and Japan (Annandale 1911, 1915; Penney & Racek 1968; Racek 1969; Manconi & Pronzato 2002, 2007, 2015) (Fig. 9). P. botryoides Haswell, 1882 is reported exclusively from Australia (Tables 1���2). Two species P. aurea Annandale, 1909 and P. stellifera Annandale, 1915 are endemic to restricted areas in the SW-Indian subregion, while P. subspinosa Annandale, 1911 is known from SW-India, Japan, and Korea (Tables 1���2)., Published as part of Manconi, R., Cubeddu, T. & Pronzato, R., 2016, Australian freshwater sponges with a new species of Pectispongilla (Porifera: Demospongiae: Spongillida), pp. 61-76 in Zootaxa 4196 (1) on pages 69-74, DOI: 10.11646/zootaxa.4196.1.3, http://zenodo.org/record/167679, {"references":["Penney, J. T. & Racek, A. A. (1968) Comprehensive revision of a world-wide collection of freshwater sponges (Porifera: Spongillidae). United States National Museum Bulletin, 272, 1 - 184.","Annandale, N. (1915) Notes on freshwater sponges of the genus Pectispongilla and its allies. Records of the Indian Museum, 11, 171 - 178.","Haswell, W. A. (1882) On Australian freshwater sponges. Proceedings of the Linnean Society of North South Wales, 7, 208 - 210.","Annandale, N. (1911) Freshwater sponges, hydroids and polyzoa. Porifera. In: A. E. Shipley (Ed.), Fauna of British India, Including Ceylon and Burma. Taylor & Francis: London, pp. 27 - 126, 241 - 245","Racek, A. A. (1969) The freshwater sponges of Australia (Porifera: Spongillidae). Australian Journal of Marine and Freshwater Research, 20, 267 - 310.","Manconi, R. & Pronzato, R. (2002) Spongillina n. subord. Lubomirskiidae, Malawispongiidae n. fam., Metaniidae, Metschnikowiidae, Palaeospongillidae, Potamolepidae, Spongillidae. In: J. Hooper & R. W. M. van Soest (Eds.), Vol. 1. Systema Porifera. A guide to the classification of sponges. Kluwer Academic / Plenum Publisher: New York, pp. 921 - 1019. http: // dx. doi. org / 10.1007 / 978 - 1 - 4615 - 0747 - 5 _ 97","Manconi, R. & Pronzato, R. (2007) Gemmules as a key structure for the adaptive radiation of freshwater sponges: a morphofunctional and biogeographical study. In: Custodio M. R., Lobo-Hajdu G., Hajdu, E. & Muricy, G. (Eds.), Porifera research: biodiversity, innovation and sustainability. Serie Livros. Museu Nacional: Rio de Janeiro, pp. 61 - 77."]}
- Published
- 2016
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11. Biodiversity assessment in Western Mediterranean marine protected areas (MPAs): Porifera of Posidonia oceanica meadows (Asinara Island MPA) and marine caves (Capo Caccia–Isola Piana MPA) of Sardinia
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Padiglia, A., primary, Cadeddu, B., additional, Ledda, F. D., additional, Bertolino, M., additional, Costa, G., additional, Pronzato, R., additional, and Manconi, R., additional
- Published
- 2018
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12. Sponges of Posidonia oceanica meadows (Sardinia, W-Mediterranean Sea)
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Padiglia, A., Cadeddu, B., Demurtas, D., Bertolino, M., Manconi, R., and Pronzato, R.
- Published
- 2015
13. Long-term turnover of the sponge fauna in Faro Lake (North-East Sicily, Mediterranean Sea)
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Marra, M. V., primary, Bertolino, M., additional, Pansini, M., additional, Giacobbe, S., additional, Manconi, R., additional, and Pronzato, R., additional
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- 2016
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14. Hard bottoms
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BIANCHI C. N, PRONZATO R, CATTANEO VIETTI R, BENEDETTI CECCHI L, MORRI C, PANSINI M, CHEMELLO R, MILAZZO M, PEIRANO A, SALVATI E, BENZONI F, CALCINAI B, CERRANO C, BAVESTRELLO G., FRASCHETTI, Simonetta, TERLIZZI, Antonio, GAMBI M.C., DAPPIANO M., BIANCHI C., N, Pronzato, R, CATTANEO VIETTI, R, BENEDETTI CECCHI, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, Simonetta, Terlizzi, Antonio, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, and Bavestrello, G.
- Published
- 2004
15. Hard bottoms. In: Mediterranean marine benthos: a manual of methods for its sampling and study
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Bianchi, CN, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, MILAZZO, MARIO MARCELLO, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, Bavestrello, G, Bianchi, C, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, and Bavestrello, G
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Hard bottoms, sampling methods ,BIO/07 - ECOLOGIA ,BIO/05 - ZOOLOGIA - Published
- 2003
16. I fondi duri
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BIANCHI CN, PRONZATO R, CATTANEO VIETTI R, BENEDETTI CECCHI L, MORRI C, PANSINI M, CHEMELLO R, MILAZZO M, PEIRANO A, SALVATI E, BENZONI F, CALCINAI B, CERRANO C, BAVESTRELLO G., FRASCHETTI, Simonetta, TERLIZZI, Antonio, GAMBI MC, DAPPIANO M Eds, Bianchi, Cn, Pronzato, R, CATTANEO VIETTI, R, BENEDETTI CECCHI, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, Simonetta, Terlizzi, Antonio, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, and Bavestrello, G.
- Published
- 2003
17. The other side of rarity: recent habitat expansion and increased abundance of the horny spongeIrcinia retidermata(Demospongiae: Dictyoceratida) in the southeast Aegean
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Bianchi, C. N., primary, Morri, C., additional, and Pronzato, R., additional
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- 2014
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18. INSITU OBSERVATIONS ON CONTRACTION BEHAVIOR AND DIEL ACTIVITY OF HALCAMPOIDES-PURPUREA VAR MEDITERRANEA (CNIDARIA, ANTHOZOA) IN A MARINE CAVE
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BOERO, Ferdinando, CICOGNA F, PESSANI D, PRONZATO R., Boero, Ferdinando, Cicogna, F, Pessani, D, and Pronzato, R.
- Published
- 1991
19. Bacteria with antimicrobial properties isolated from the Mediterranean sponges Chondrilla nucula and Petrosia ficiformis
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Chelossi, E., Pantile, R., Pronzato, R., Milanese, M., Hentschel, Ute, Chelossi, E., Pantile, R., Pronzato, R., Milanese, M., and Hentschel, Ute
- Abstract
Bacteria were isolated seasonally from the Mediterranean sponges Chondrilla nucula and Petrosia ficiformis and screened for antibacterial activities. Selected isolates were taxonomically identified by 16S rRNA gene sequencing. A total of 416 different bacterial strains were isolated, 60 (14.4%) of which displayed variable degrees of antimicrobial activity. Of the bioactive strains, 58.3% were able to inhibit Staphylococcus aureus, 6.7% were active against Bacillus subtilis, 11.7% against both Enterococcus faecalis and Escherichia coli, 38.3% against Pseudoalteromonas atlantica and 33.3% against Pseudomonas elongata. 16S rRNA gene sequence analysis showed that 2 isolates, 1 from seawater samples and 1 from P. ficiformis, were most closely related to Bacillus subtilis (99% similarity) and that another isolate from P. ficiformis was most closely related to a previously described sponge-associated Alphaproteobacterium NW001 (98% similarity). Two isolates from C. nucula were most closely related to Brachybacterium paraconglomeratum (99% similarity) and Shewanella algae (89% similarity). The high percentage of bioactive isolates derived from the 2 sponges suggests that marine microorganisms, whether animal-associated or planktonic, are promising sources for drug discovery.
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- 2007
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20. Biodiversity assessment in Western Mediterranean marine protected areas (MPAs): Porifera of Posidonia oceanicameadows (Asinara Island MPA) and marine caves (Capo Caccia–Isola Piana MPA) of Sardinia
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Padiglia, A., Cadeddu, B., Ledda, F. D., Bertolino, M., Costa, G., Pronzato, R., and Manconi, R.
- Abstract
AbstractThis paper focuses on a faunistic inventory and the biogeographic pattern of Sardinian Porifera in a scarcely investigated Italian sea belonging to the Eastern Algero-Provençal Basin. The composition and structure of sponge fauna were studied in two priority habitats in two Marine Protected Areas (MPAs) of the North-Western Sardinian Sea. Shallow-water surveys investigated Posidonia oceanicameadows at five sites in the Asinara Island MPA and three karstic submerged caves in the Capo Caccia–Isola Piana MPA. The annotated checklist shows notably high values of taxonomic richness, confirming that P. oceanicameadows and karstic caves are key habitats for Porifera assemblages. Indeed, the sponge taxa recorded (n = 77) with 59 cave-dwelling and 45 taxa in seagrass meadows represent over 10% of the total Mediterranean sponge fauna, despite the small areas investigated, restricted biotopes and low sampling effort. This suggests that species richness is underestimated in circum-Sardinia seas. Internationally protected species (n = 6), rare species (n = 5) and Mediterranean endemic species (n = 14) were recorded. Previously investigated Posidoniameadows and caves share comparable values of species richness and endemicity with the Sardinian biotopes. The geographic range of species indicates that the biogeographic affinity of the NW Sardinian Sea sponge fauna is dominated by Atlanto-Mediterranean species. The three caves harbour a notably homogeneous sponge community, as indicated by the ca. 50% of shared species and high similarity index (> 83%). By contrast, the composition varies markedly among the five Posidoniameadows, which share only five species and display similarity values ranging ca. 20–60%. Unexpectedly when comparing these contrasting biotopes, faunal similarity is relatively low (< 40% shared species); indeed, Posidoniameadows harbour a notable number of cave-dwelling species in intermatte shaded microhabitats.
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- 2018
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21. Hard bottoms. In: Mediterranean marine benthos: a manual of methods for its sampling and study
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Bianchi, C, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, Bavestrello, G, Bianchi, CN, MILAZZO, MARIO MARCELLO, Bianchi, C, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, Bavestrello, G, Bianchi, CN, and MILAZZO, MARIO MARCELLO
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- 2003
22. Cap. 6: I fondi duri
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Bianchi, C, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, Bavestrello, G, Bianchi, CN, Bianchi, C, Pronzato, R, Cattaneo-Vietti, R, Benedetti Cecchi, L, Morri, C, Pansini, M, Chemello, R, Milazzo, M, Fraschetti, S, Terlizzi, A, Peirano, A, Salvati, E, Benzoni, F, Calcinai, B, Cerrano, C, Bavestrello, G, and Bianchi, CN
- Published
- 2003
23. Global diversity of sponges (Porifera: Spongillina) in freshwater
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Manconi, R., primary and Pronzato, R., additional
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- 2007
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24. Bacteria with antimicrobial properties isolated from the Mediterranean sponges Chondrilla nucula and Petrosia ficiformis
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Chelossi, E, primary, Pantile, R, additional, Pronzato, R, additional, Milanese, M, additional, and Hentschel, U, additional
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- 2007
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25. The other side of rarity: recent habitat expansion and increased abundance of the horny sponge Ircinia retidermata (Demospongiae: Dictyoceratida) in the southeast Aegean.
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Bianchi, C. N., Morri, C., and Pronzato, R.
- Subjects
SPONGES (Invertebrates) ,MARINE habitats ,MARINE ecology ,BIOLOGICAL extinction - Abstract
Environmental change is commonly considered as a driver for the extinction of rare species. This belief, long established on land, may not apply to marine species. Dramatic environmental change in the shallow marine ecosystems of Kos, an island in the Aegean (east Mediterranean Sea) caused algal reefs to shift to sponge reefs. Among the sponge species that gained supremacy on Kos reefs, the Mediterranean endemicIrcinia retidermatawas previously a rare species. Comparing surveys carried out in 1981 and 2013 by the same method (time-based visual census along random paths by scuba diving), in the same sites, by the same people, showed thatI. retidermataincreased its overall abundance by one order of magnitude, and expanded its occurrence to all the habitats examined. This outcome contradicts the current common belief that rare species in semi-enclosed seas are prone to extinction. Besides being the state preceding final extinction, rarity could represent the source of variation that marine ecosystems need in order to face environmental change. However, for many marine invertebrates, and especially sponges, inferred rarity may simply be the result of insufficient investigation. This study represents an attempt to assess change with time in a rare sponge species’ abundance using visual census by scuba diving. [ABSTRACT FROM AUTHOR]
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- 2014
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26. Body Polarity and Mineral Selectivity in the Demosponge Chondrosia reniformis
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Bavestrello, G., primary, Benatti, U., additional, Calcinai, B., additional, Cattaneo-Vietti, R., additional, Cerrano, C., additional, Favre, A., additional, Giovine, M., additional, Lanza, S., additional, Pronzato, R., additional, and Sara, M., additional
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- 1998
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27. Ultrastructural evidence of bacterial damage to Spongia officinalis fibres (Porifera, Demospongiae)
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Gaino, E, primary and Pronzato, R, additional
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- 1989
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28. Epibiontic sponges on the bivalve Pinna nobilis
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Corriero, G, primary and Pronzato, R, additional
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- 1987
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29. Biodiversity of Nearctic inland water: discovery of the genus Heterorotula (Porifera, Spongillida, Spongillidae) in the Appalachian Mountains, with biogeographical implications and description of new species.
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Manconi R, Copeland J, Kunigelis S, and Pronzato R
- Abstract
This paper reports the discovery of a small population of sponges in the Pigeon River of eastern Tennessee, USA, which were morphologically distinct from Spongillida of North America. A morphological comparative analysis resulted in the first Nearctic record of the genus Heterorotula with the description of a new species Heterorotulalucasi sp. nov. diverging from all other known species by its unique combinations of diagnostic morphotraits of spicules and gemmules. The new record enlarges the geographic range of the genus which has been known until now only from Australia, New Zealand, New Caledonia, Japan (as an alien species), and from subequatorial Brazil (as subfossil remains). The discovery of a biogeographic enclave of Heterorotula in the southeastern United States contributes to the understanding of Porifera inland water biodiversity, biogeographic patterns, and adaptive morphotraits in the Nearctic and globally. Data confirm that the Appalachian region (Ordovician-Permian origin) of Tennessee and, in general, of North America have high levels of diversity and endemicity., (Renata Manconi, John Copeland, Stan Kunigelis, Roberto Pronzato.)
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- 2022
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30. Relationship between bacterial phylotype and specialized metabolite production in the culturable microbiome of two freshwater sponges.
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Clark CM, Hernandez A, Mullowney MW, Fitz-Henley J, Li E, Romanowski SB, Pronzato R, Manconi R, Sanchez LM, and Murphy BT
- Abstract
Microbial drug discovery programs rely heavily on accessing bacterial diversity from the environment to acquire new specialized metabolite (SM) lead compounds for the therapeutic pipeline. Therefore, knowledge of how commonly culturable bacterial taxa are distributed in nature, in addition to the degree of variation of SM production within those taxa, is critical to informing these front-end discovery efforts and making the overall sample collection and bacterial library creation process more efficient. In the current study, we employed MALDI-TOF mass spectrometry and the bioinformatics pipeline IDBac to analyze diversity within phylotype groupings and SM profiles of hundreds of bacterial isolates from two Eunapius fragilis freshwater sponges, collected 1.5 km apart. We demonstrated that within two sponge samples of the same species, the culturable bacterial populations contained significant overlap in approximate genus-level phylotypes but mostly nonoverlapping populations of isolates when grouped lower than the level of genus. Further, correlations between bacterial phylotype and SM production varied at the species level and below, suggesting SM distribution within bacterial taxa must be analyzed on a case-by-case basis. Our results suggest that two E. fragilis freshwater sponges collected in similar environments can exhibit large culturable diversity on a species-level scale, thus researchers should scrutinize the isolates with analyses that take both phylogeny and SM production into account to optimize the chemical space entering into a downstream bacterial library., (© 2022. The Author(s).)
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- 2022
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31. Minimalist barcodes for sponges: a case study classifying African freshwater Spongillida.
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Erpenbeck D, Steiner M, Schuster A, Genner MJ, Manconi R, Pronzato R, Ruthensteiner B, van den Spiegel D, van Soest RWM, and Wörheide G
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- Animals, DNA Barcoding, Taxonomic standards, Porifera classification, DNA Barcoding, Taxonomic methods, Phylogeny, Porifera genetics
- Abstract
African sponges, particularly freshwater sponges, are understudied relative to demosponges in most other geographical regions. Freshwater sponges (Spongillida) likely share a common ancestor; however, their evolutionary history, particularly during their radiation into endemic and allegedly cosmopolitan groups, is unclear. Freshwater sponges of at least 58 species of 17 genera and four families are described from Central and Eastern Africa, but the diversity is underestimated due to limited distinguishable morphological features. The discovery of additional cryptic species is very likely with the use of molecular techniques such as DNA barcoding. The Royal Museum of Central Africa (MRAC, Tervuren, Belgium) hosts one of the largest collections of (Central) African freshwater sponge type material. Type specimens in theory constitute ideal targets for molecular taxonomy; however, the success is frequently hampered by DNA degradation and deamination, which are a consequence of suboptimal preservation techniques. Therefore, we genotyped African demosponge holotype material of the MRAC with specific short primers suitable for degenerated tissue and compare the results with the current, morphology-based classification. Our results demonstrate the utility of minimalistic barcodes for identification of sponges, potentially enabling efficient identification of individuals in taxonomic or metabarcoding studies, and highlight inconsistencies in the current freshwater sponge classification.
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- 2019
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32. Long-term experimental in situ farming of Crambe crambe (Demospongiae: Poecilosclerida).
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Padiglia A, Ledda FD, Padedda BM, Pronzato R, and Manconi R
- Abstract
Background: The marine sponge Crambe crambe was chosen as an experimental model of sustainable shallow-water mariculture in the Sardinian Sea (Western Mediterranean) to provide biomass with high potential in applied research., Methods: Explants were cultured in four long-term experiments (19 and 31 months at ca. 2.5 m depth), to determine the suitability of new culture techniques by testing substrata and seeding time (season), and monitoring survival and growth. Explants were excised and grown in an experimental plant close to the wild donor sponge population. Percentage growth rate (GR%) was measured in terms of surface cover area, and explant survival was monitored in situ by means of a digital photo camera., Results: Explant survival was high throughout the trial, ranging from 78.57% to 92.85% on travertine tiles and from 50% to 71.42% on oyster shells. A few instances of sponge regression were observed. Explant cover area correlated positively with season on two substrata, i.e., tiles and shells. The surface cover area and GR% of explants were measured in the starting phase and monitored up to the end of the trial. High GR% values were observed both on tiles (>21%) and on oyster shells (>15%)., Discussion: The data on the behaviour and life-style of cultured fragments, together with an increase >2,400% in cover area, demonstrate that in situ aquaculture is a viable and sustainable method for the shallow-water biomass supply of Crambe crambe ., Competing Interests: The authors declare there are no competing interests.
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- 2018
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33. How Environmental Factors Affect the Production of Guanidine Alkaloids by the Mediterranean Sponge Crambe crambe.
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Ternon E, Perino E, Manconi R, Pronzato R, and Thomas OP
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- Animals, Light, Metabolome, Temperature, Alkaloids biosynthesis, Guanidines metabolism, Porifera metabolism
- Abstract
Most marine sponges are known to produce a large array of low molecular-weight metabolites which have applications in the pharmaceutical industry. The production of so-called specialized metabolites may be closely related to environmental factors. In this context, assessing the contribution of factors like temperature, nutrients or light to the metabolomes of sponges provides relevant insights into their chemical ecology as well as the supply issue of natural sponge products. The sponge Crambe crambe was chosen as a model due to its high content of specialized metabolites belonging to polycyclic guanidine alkaloids (PGA). First results were obtained with field data of both wild and farmed specimens collected in two seasons and geographic areas of the North-Western Mediterranean. Then, further insights into factors responsible for changes in the metabolism were gained with sponges cultivated under controlled conditions in an aquarium. Comparative metabolomics showed a clear influence of the seasons and to a lesser extent of the geography while no effect of depth or farming was observed. Interestingly, sponge farming did not limit the production of PGA, while ex situ experiments did not show significant effects of several abiotic factors on the specialized metabolome at a one-month time scale. Some hypotheses were finally proposed to explain the very limited variations of PGA in C. crambe placed under different environmental conditions., Competing Interests: The authors declare no conflict of interest.
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- 2017
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34. A new species of Agelas from the Zanzibar Archipelago, western Indian Ocean (Porifera, Demospongiae).
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Manconi R, Pronzato R, and Perino E
- Abstract
A new sponge species (Demospongiae: Agelasida: Agelasidae) is described from the eastern coast of Unguja Island in the Zanzibar Archipelago. Agelas sansibarica sp. n. is compared to all other Agelas species described so far. The new species differs from its congeners mainly in its three categories of verticillate spicules (acanthostyles, acanthostrongyles, and acanthoxeas) and their sizes. Acanthostrongyles, well represented in the spicular complement, are an exclusive trait of the new species widening the morphological range of the genus. Summarizing on spicular complement and spicular morphotraits of 36 species belonging to the genus Agelas: i) 32 species show only acanthostyles from Indo-Pacific (n = 14), Atlantic (n = 17), and Mediterranean (n = 1); ii) three Indo-Pacific species show acanthostyles and acanthoxeas; iii) one species Agelas sansibarica sp. n. from the western Indian Ocean is characterised by the unique trait of three categories of verticillate spicules (acanthostyles, acanthostrongyles and acanthoxeas). A key for the Indo-Pacific species is supplied together with short descriptions, illustrations, and geographic range; literature on chemical bioprospecting of the genus Agelas is also provided.
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- 2016
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35. An overview of the Mediterranean cave-dwelling horny sponges (Porifera, Demospongiae).
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Manconi R, Cadeddu B, Ledda F, and Pronzato R
- Abstract
The present synthesis focuses on the so called 'horny sponges' recorded from marine caves of the Mediterranean Sea. The main aim is to provide a list of all recorded species, diagnostic keys to their identification up to family and genus level, and exhaustive, formally uniform descriptions at the species level contributing to sharing of information on the faunistics and taxonomy of Mediterranean cave-dwelling species, including habitat preferences. The majority of species was recorded in 105 Mediterranean marine caves hosting four orders of horny sponges belonging to 9 families, 19 genera and 40 species. Species endemic to the Mediterranean Sea harboured in marine caves are 14 with an endemicity value of 35%. For each species morphological descriptions are supported by illustrations both original and from the literature, including the diagnostic traits of the skeleton by light and scanning electron microscopy giving further characterization at the specific level. A detailed map together with a list of all caves harbouring horny sponges is also provided with geographic coordinates.
- Published
- 2013
- Full Text
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