232 results on '"Bello, Giambattista"'
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2. Occurrence of an egg mass of Thysanoteuthis rhombus (Cephalopoda: Teuthida) in the Strait of Messina (Italy), locus typicus of the species
- Author
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Biagi, Vinicio, Bello, Giambattista, and BioStor
- Published
- 2009
3. Micro-anatomical structure of the first spine of the dorsal fin of Atlantic bluefin tuna, Thunnus thynnus (Osteichthyes: Scombridae)
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Santamaria, Nicoletta, Bello, Giambattista, Passantino, Letizia, Di Comite, Mariasevera, Zupa, Rosa, Pousis, Chrysovalentinos, Vassallo-Agius, Robert, Cicirelli, Vincenzo, Basilone, Gualtiero, Mangano, Salvatore, and Corriero, Aldo
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- 2018
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4. Notes on the life cycle of Scaeurgus unicirrhus (Cephalopoda : Octopodidae)
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Bello, Giambattista and BioStor
- Published
- 2007
5. Sepia elegans (Cephalopoda: Sepiidae): a new host record for the parasite Nybelinia lingualis (Cestoda: Tentaculariidae)
- Author
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Bello, Giambattista and BioStor
- Published
- 2004
6. Struttura di popolazioni di Arca noae (Bivalvia, Arcidae) insediate su sustrati diversi nell'Adriatico meridionale
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Bello, Giambattista, Paparella, Pasqua, and BioStor
- Published
- 2001
7. The feeding ecology of the velvet belly, Etmopterus spinax (Chondrichthyes: Squalidae), of the Adriatic Sea on the basis of its stomach contents
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Bello, Giambattista and BioStor
- Published
- 1999
8. The biogeography of Mediterranean cephalopods
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Bello, Giambattista
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- 2003
9. Teuthopagous predators as collectors of oceanic cephalopods: The case of the Adriatic Sea
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Bello, Giambattista and BioStor
- Published
- 1996
10. Cephalopods in the stomach contents of Galeus melastomus (Selachii, Scyliorhinidae) from the Adriatic Sea
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Bello, Giambattista and BioStor
- Published
- 1995
11. The original descriptions of the Mediterranean cephalopods. I: Sepioidea
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Bello, Giambattista and BioStor
- Published
- 1995
12. Cephalopods preyed on by loggerhead turtles, Caretta caretta (Reptilia: Cheloniidae), from the eastern Tyrrhenian Sea
- Author
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Bello, Giambattista, Bentivegna, Flegra, Travaglini, Andrea, Bello, Giambattista, Bentivegna, Flegra, and Travaglini, Andrea
- Abstract
This study presents the results of the examination of cephalopod remains extracted from the digestive tract of 40 loggerhead turtles, Caretta caretta, stranded along the Campanian coasts (Southern Italy, eastern Tyrrhenian Sea). We retrieved the remains of 23 cephalopods from 16 turtles (frequency of occurrence = 40%). They belonged to Sepia officinalis (19 specimens) and Octopus vulgaris (2 specimens), both of them benthic neritic species, and Histioteuthis reversa (2 specimens), an oceanic species. Accordingly, loggerheads appear to feed both on the bottom, seemingly in shallow waters, and in the open seawater column; both on muscular items (S. officinalis and O. vulgaris) and ammoniacal ones (H. reversa). This is the first record of H. reversa as a prey of the loggerhead turtle., Ova studija prikazuje rezultate istraživanja ostataka plijena izvađenih iz probavila 40 glavatih želvi, Caretta caretta, nasukanih duž obala Kampanije (južna Italija, istočno Tirensko more). Iz 16 kornjača izvadili smo ostatke 23 glavonošca (učestalost pojavljivanja = 40%). Pripadali su vrstama Sepia officinalis (19 primjeraka) i Octopus vulgaris (2 primjerka), koje su obje bentoske neritičke vrste, kao i oceanskoj vrsti Histioteuthis reversa (2 primjerka). Prema tome, čini se da se glavate želve hrane na dnu, vjerovatno u plitkim vodama, kao i u stupcu otvorenih morskih voda; i to mišićavim plijenom (S. officinalis i O. vulgaris) kao i plijenom bogatim amonijakom (H. reversa). Ovo je prvi zapis vrste H. reversa kao plijena glavate želve.
- Published
- 2023
13. Adult of Ancistrocheirus lesueurii caught in the Straits of Messina (Cephalopoda: Ancistrocheiridae)
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Bello, Giambattista, Potoschi, Antonio, Berdar, Adolfo, and BioStor
- Published
- 1994
14. Cephalopods from trawlable grounds of the Gulf of Castellammare
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Bello, Giambattista, Pipitone, Carlo, Arculeo, Marco, and BioStor
- Published
- 1994
15. Histioteuthis bonnellii (Cephalopoda: Histioteuthidae) in the Adriatic Sea: Evidence from predator stomach contents
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Bello, Giambattista and BioStor
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- 1994
16. Stomach content of a specimen of Stenella coeruleoalba (Cetacea: Delphinidae) from the Ionian Sea
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Bello, Giambattista and BioStor
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- 1993
17. Tremoctopus violaceus (Cephalopoda: Tremoctopodidae) in the stomach content of a swordfish from the Adriatic Sea
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Bello, Giambattista and BioStor
- Published
- 1993
18. Corrigendum: The significance of cephalopod beaks as a research tool: An update
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Xavier, José C., primary, Golikov, Alexey V., additional, Queirós, José P., additional, Perales-Raya, Catalina, additional, Rosas-Luis, Rigoberto, additional, Abreu, José, additional, Bello, Giambattista, additional, Bustamante, Paco, additional, Capaz, Juan C., additional, Dimkovikj, Valerie H., additional, González, Ángel F., additional, Guímaro, Hugo, additional, Guerra-Marrero, Airam, additional, Gomes-Pereira, José N., additional, Hernández-Urcera, Jorge, additional, Kubodera, Tsunemi, additional, Laptikhovsky, Vladimir, additional, Lefkaditou, Evgenia, additional, Lishchenko, Fedor, additional, Luna, Amanda, additional, Liu, Bilin, additional, Pierce, Graham J., additional, Pissarra, Vasco, additional, Reveillac, Elodie, additional, Romanov, Evgeny V., additional, Rosa, Rui, additional, Roscian, Marjorie, additional, Rose-Mann, Lisa, additional, Rouget, Isabelle, additional, Sánchez, Pilar, additional, Sánchez-Márquez, Antoni, additional, Seixas, Sónia, additional, Souquet, Louise, additional, Varela, Jaquelino, additional, Vidal, Erica A. G., additional, and Cherel, Yves, additional
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- 2023
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19. Cephalopod remains from the stomach of a Risso's dolphin, Grampus griseus (Cetacea: Delphinidae), stranded along the eastern Tyrrhenian coast
- Author
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Bello, Giambattista, Bentivegna, Flegra, and BioStor
- Published
- 1996
20. The Mediterranean teuthofauna: Towards a biogeographical coverage by regional census. I: Generalities
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Bello, Giambattista and BioStor
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- 1994
21. Case 2874. Chtenopteryx Appellöf, 1890 (Mollusca, Cephalopoda): proposed confirmation as the correct original spelling
- Author
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Bello, Giambattista, Giannuzzi-Savelli, Riccardo, and BioStor
- Published
- 1993
22. The significance of cephalopod beaks as a research tool: An update
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Xavier, José C., primary, Golikov, Alexey V., additional, Queirós, José P., additional, Perales-Raya, Catalina, additional, Rosas-Luis, Rigoberto, additional, Abreu, José, additional, Bello, Giambattista, additional, Bustamante, Paco, additional, Capaz, Juan C., additional, Dimkovikj, Valerie H., additional, González, Angel F., additional, Guímaro, Hugo, additional, Guerra-Marrero, Airam, additional, Gomes-Pereira, José N., additional, Hernández-Urcera, Jorge, additional, Kubodera, Tsunemi, additional, Laptikhovsky, Vladimir, additional, Lefkaditou, Evgenia, additional, Lishchenko, Fedor, additional, Luna, Amanda, additional, Liu, Bilin, additional, Pierce, Graham J., additional, Pissarra, Vasco, additional, Reveillac, Elodie, additional, Romanov, Evgeny V., additional, Rosa, Rui, additional, Roscian, Marjorie, additional, Rose-Mann, Lisa, additional, Rouget, Isabelle, additional, Sánchez, Pilar, additional, Sánchez-Márquez, Antoni, additional, Seixas, Sónia, additional, Souquet, Louise, additional, Varela, Jaquelino, additional, Vidal, Erica A. G., additional, and Cherel, Yves, additional
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- 2022
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23. Comportamento di tre femine di Argonauta argo in acquario (Cephalopoda: Argonautidae)
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Bello, Giambattista, Rizzi, E, and BioStor
- Published
- 1990
24. The deep-water squid Octopoteuthis sicula Rüppell, 1844 (Cephalopoda: Octopoteuthidae) as the single species of the genus occurring in the Mediterranean Sea
- Author
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Jereb, Patrizia, Cannas, Rita, Maiorano, Porzia, Bello, Giambattista, Garibaldi, Fulvio, Mereu, Marco, Ancona, Francesco G., Ammendolia, Giovanni, Battaglia, Pietro, Duysak, Önder, Hoving, Hendrik Jan T., Lefkaditou, Eugenia, Lipinski, Marek R., Melis, Riccardo, Peristeraki, Panagiota N., Ragonese, Sergio, Romeo, Teresa, Salman, Alp, Santos, Begonia M., Villari, Alberto, and Cuccu, Danila
- Published
- 2016
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25. The significance of cephalopod beaks as a research tool: An update
- Author
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Xavier, José C., Golikov, Alexey V., Queirós, José P., Perales-Raya, Catalina, Rosas-Luis, Rigoberto, Abreu, José, Bello, Giambattista, Bustamante, Paco, Capaz, Juan C., Dimkovikj, Valerie H., González, Angel F., Guímaro, Hugo, Guerra-Marrero, Airam, Gomes-Pereira, José N., Kubodera, Tsunemi, Laptikhovsky, Vladimir, Lefkaditou, Evgenia, Lishchenko, Fedor, Luna, Amanda, Liu, Bilin, Pierce, Graham J., Pissarra, Vasco, Reveillac, Elodie, Romanov, Evgeny V., Rosa, Rui, Roscian, Marjorie, Rose-Mann, Lisa, Rouget, Isabelle, Sánchez, Pilar, Sánchez-Márquez, Antoni, Seixas, Sónia, Souquet, Louise, Varela, Jaquelino, Vidal, Erica A. G., Cherel, Yves, Xavier, José C., Golikov, Alexey V., Queirós, José P., Perales-Raya, Catalina, Rosas-Luis, Rigoberto, Abreu, José, Bello, Giambattista, Bustamante, Paco, Capaz, Juan C., Dimkovikj, Valerie H., González, Angel F., Guímaro, Hugo, Guerra-Marrero, Airam, Gomes-Pereira, José N., Kubodera, Tsunemi, Laptikhovsky, Vladimir, Lefkaditou, Evgenia, Lishchenko, Fedor, Luna, Amanda, Liu, Bilin, Pierce, Graham J., Pissarra, Vasco, Reveillac, Elodie, Romanov, Evgeny V., Rosa, Rui, Roscian, Marjorie, Rose-Mann, Lisa, Rouget, Isabelle, Sánchez, Pilar, Sánchez-Márquez, Antoni, Seixas, Sónia, Souquet, Louise, Varela, Jaquelino, Vidal, Erica A. G., and Cherel, Yves
- Abstract
The use of cephalopod beaks in ecological and population dynamics studies has allowed major advances of our knowledge on the role of cephalopods in marine ecosystems in the last 60 years. Since the 1960’s, with the pioneering research by Malcolm Clarke and colleagues, cephalopod beaks (also named jaws or mandibles) have been described to species level and their measurements have been shown to be related to cephalopod body size and mass, which permitted important information to be obtained on numerous biological and ecological aspects of cephalopods in marine ecosystems. In the last decade, a range of new techniques has been applied to cephalopod beaks, permitting new kinds of insight into cephalopod biology and ecology. The workshop on cephalopod beaks of the Cephalopod International Advisory Council Conference (Sesimbra, Portugal) in 2022 aimed to review the most recent scientific developments in this field and to identify future challenges, particularly in relation to taxonomy, age, growth, chemical composition (i.e., DNA, proteomics, stable isotopes, trace elements) and physical (i.e., structural) analyses. In terms of taxonomy, new techniques (e.g., 3D geometric morphometrics) for identifying cephalopods from their beaks are being developed with promising results, although the need for experts and reference collections of cephalopod beaks will continue. The use of beak microstructure for age and growth studies has been validated. Stable isotope analyses on beaks have proven to be an excellent technique to get valuable information on the ecology of cephalopods (namely habitat and trophic position). Trace element analyses is also possible using beaks, where concentrations are significantly lower than in other tissues (e.g., muscle, digestive gland, gills). Extracting DNA from beaks was only possible in one study so far. Protein analyses can also be made using cephalopod beaks. Future challenges in research using cephalopod beaks are also discussed.
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- 2022
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26. The significance of cephalopod beaks as a research tool: An update
- Author
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European Commission, Ministerio de Ciencia e Innovación (España), Institut Universitaire de France, Universidad de Las Palmas de Gran Canaria, Agencia Estatal de Investigación (España), Fundação para a Ciência e a Tecnologia (Portugal), Xavier, José C., Golikov, Alexey, Queirós, José P., Perales-Raya, Catalina, Rosas-Luis, Rigoberto, Abreu, José, Bello, Giambattista, Bustamante, Paco, Capaz, Juan C., Dimkovikj, Valerie H., González, Ángel F., Guímaro, Hugo, Guerra-Marrero, Airam, Gomes-Pereira, José N., Kubodera, Tsunemi, Laptikhovsky, Vladimir, Lefkaditou, E., Lishchenko, Fedor, Luna, Amanda, Liu, Bilin, Pierce, Graham J., Pissarra, Vasco, Reveillac, Elodie, Romanov, Evgeny V., Rosa, Rui, Roscian, Marjorie, Rose-Mann, Lisa, Rouget, Isabelle, Sánchez Zalacaín, Pilar, Sánchez-Márquez, Antoni, Seixas, Sonia, Souquet, Louise, Varela, Jaquelino, Vidal, Erica A. G., Cherel, Yves, European Commission, Ministerio de Ciencia e Innovación (España), Institut Universitaire de France, Universidad de Las Palmas de Gran Canaria, Agencia Estatal de Investigación (España), Fundação para a Ciência e a Tecnologia (Portugal), Xavier, José C., Golikov, Alexey, Queirós, José P., Perales-Raya, Catalina, Rosas-Luis, Rigoberto, Abreu, José, Bello, Giambattista, Bustamante, Paco, Capaz, Juan C., Dimkovikj, Valerie H., González, Ángel F., Guímaro, Hugo, Guerra-Marrero, Airam, Gomes-Pereira, José N., Kubodera, Tsunemi, Laptikhovsky, Vladimir, Lefkaditou, E., Lishchenko, Fedor, Luna, Amanda, Liu, Bilin, Pierce, Graham J., Pissarra, Vasco, Reveillac, Elodie, Romanov, Evgeny V., Rosa, Rui, Roscian, Marjorie, Rose-Mann, Lisa, Rouget, Isabelle, Sánchez Zalacaín, Pilar, Sánchez-Márquez, Antoni, Seixas, Sonia, Souquet, Louise, Varela, Jaquelino, Vidal, Erica A. G., and Cherel, Yves
- Abstract
The use of cephalopod beaks in ecological and population dynamics studies has allowed major advances of our knowledge on the role of cephalopods in marine ecosystems in the last 60 years. Since the 1960’s, with the pioneering research by Malcolm Clarke and colleagues, cephalopod beaks (also named jaws or mandibles) have been described to species level and their measurements have been shown to be related to cephalopod body size and mass, which permitted important information to be obtained on numerous biological and ecological aspects of cephalopods in marine ecosystems. In the last decade, a range of new techniques has been applied to cephalopod beaks, permitting new kinds of insight into cephalopod biology and ecology. The workshop on cephalopod beaks of the Cephalopod International Advisory Council Conference (Sesimbra, Portugal) in 2022 aimed to review the most recent scientific developments in this field and to identify future challenges, particularly in relation to taxonomy, age, growth, chemical composition (i.e., DNA, proteomics, stable isotopes, trace elements) and physical (i.e., structural) analyses. In terms of taxonomy, new techniques (e.g., 3D geometric morphometrics) for identifying cephalopods from their beaks are being developed with promising results, although the need for experts and reference collections of cephalopod beaks will continue. The use of beak microstructure for age and growth studies has been validated. Stable isotope analyses on beaks have proven to be an excellent technique to get valuable information on the ecology of cephalopods (namely habitat and trophic position). Trace element analyses is also possible using beaks, where concentrations are significantly lower than in other tissues (e.g., muscle, digestive gland, gills). Extracting DNA from beaks was only possible in one study so far. Protein analyses can also be made using cephalopod beaks. Future challenges in research using cephalopod beaks are also discussed
- Published
- 2022
27. Species-specific variation in cuttlebone δ[sup.13]C and δ[sup.18]O for three species of Mediterranean cuttlefish
- Author
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Dance, Michael A., Bello, Giambattista, Furey, Nathan B., and Rooker, Jay R.
- Subjects
Company distribution practices ,Biological sciences - Abstract
Stable carbon (δ[sup.13]C) and oxygen (δ[sup.18]O) isotopes in cuttlebones of three species of Mediterranean cuttlefish (Sepia elegans, S. officinalis, and S. orbignyana) with different life histories were contrasted. Cuttlebone δ[sup.13]C and δ[sup.18]O were quantified at both the core and edge (representing early life and recent deposition, respectively) for all three species sampled from the southern Adriatic Sea in 2010 (n = 28). For S. officinalis, cuttlebone δ[sup.13]C and δ[sup.18]O values were both lower relative to S. elegans and S. orbignyana at the core by approximately 1.0-2.0 and 3.0 %e, respectively. Differences between core and edge in cuttlebone δ[sup.13]C and δ[sup.18]O were also observed for S. officinalis with observed values at the cuttlebone edge (recent) exceeding core (early life) values by 2.5 %o for δ[sup.13]C and 1.4 %o for δ[sup.18]O. Differences in isotopic composition across S. officinalis cuttlebones are possibly reflective of ontogenetic migrations from nearshore nurseries (lower seawater δ[sup.13]C and δ[sup.18]O values) to offshore overwintering habitats (higher seawater δ[sup.13]C and δ[sup.18]O values). Overall, results from this study suggest that cuttlebone δ[sup.13]C and δ[sup.18]O hold promise as natural tags for determining the degree of spatial connectivity between nearshore and offshore environments used by cuttlefish., Introduction Marine organisms often utilize both nearshore and offshore environments to complete their life cycle (Gillanders et al. 2003), and determining the degree of spatial connectivity among life stages is [...]
- Published
- 2014
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- View/download PDF
28. Boletzkyola Bello 2020, gen. nov
- Author
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Bello, Giambattista
- Subjects
Cephalopoda ,Mollusca ,Animalia ,Boletzkyola ,Biodiversity ,Sepiolida ,Sepiolidae ,Taxonomy - Abstract
Boletzkyola gen. nov. urn:lsid:zoobank.org:act: AA294852-E5A5-40E6-A8F4-288A22290823 Figs 10���11 (the generic name used in the captions is the former one) Type species Sepiola knudseni Adam, 1984, here designated. Diagnosis Sepiolinae with fins rounded; their length about half mantle length. Suckers biseriate on all arms. Tentacle club suckers in 8 longitudinal rows. Mantle-head occipital band narrow (not reaching over the ocular globes). A single cordiform photophore on ventral surface of ink sac. Ventral mantle margin slightly sinuate, without any deep funnel indentation. Hectocotylus (male left arm I) tripartite: basal part with one incomplete transverse row of suckers (only the ventral one is present); copulatory apparatus with three ventral modified suckerless pedicels enlarged and lengthened into thick, bluntly pointed horn-like structures; distal part with several suckers missing proximally in ventral row and four enlarged suckers in dorsal row. Female bursa copulatrix pouch-like with wide opening. Included species Boletzkyola knudseni (Adam, 1984) gen. et comb. nov. Etymology This genus is named in honour of Sigurd von Boletzky (formerly Observatoire Arago / CNRS, Banyulssur-Mer, France; presently retired) for his outstanding contribution to the study of cephalopods, including Sepiolinae, and to the enhancement of Mediterranean teuthology; it is formed by his family name and the diminutive suffix - ola. Gender feminine. Discussion of affinities Boletzkyola gen. nov. differs from all other genera and species-groups in Sepiolinae because of its unique cordiform visceral light organ (different from that of Rondeletiola; see below). It differs from all genera with a copulatory apparatus involving dorsal modified pedicels. As for the other species sharing the character state ���only ventral modified pedicels in the copulatory apparatus���, i.e., all nominal Euprymna species, the modified ventral pedicels of Boletzkyola gen. nov. display a modification (thick horn-like instead of papilla-like) and, more importantly, its hectocotylus distal part suckers are carried by regular pedicels (i.e., not columnar). The affinity with Rondeletiola, fostered by the presence of similar visceral light organs, is just apparent. In fact, those organs are quite different from each other (see Remarks in the description of Group C hectocotylus). Furthermore, the copulatory apparatus and the bursa copulatrix of this genus differ completely from those of Rondeletiola. Remarks The hectocotylus of Boletzkyola gen. nov. is the least modified among Sepiolinae, hence may be primitive. In addition, the morphology of its visceral light organ may reflect incomplete development of the two-kidney-shaped arrangement that is typical of the subfamily. Both traits, as well as the small body size of Boletzkyola knudseni gen. et comb. nov. ��� seemingly the smallest among Sepiolinae: males mature at 8.5 mm mantle length ��� suggests that the evolution of this species might have been fostered by heterochronic development., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 37-38, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797
- Published
- 2020
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29. Adinaefiola Bello 2020, gen. nov
- Author
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Bello, Giambattista
- Subjects
Cephalopoda ,Adinaefiola ,Mollusca ,Animalia ,Biodiversity ,Sepiolida ,Sepiolidae ,Taxonomy - Abstract
Adinaefiola gen. nov. urn:lsid:zoobank.org:act: D156F532-3035-4FF0-AA5D-3FF6F39D5531 Figs 14���15 (the generic name used in the captions is the former one) Type species Sepiola ligulata Naef, 1912, here designated. Diagnosis Sepiolinae with fins rounded; their length about half mantle length. Suckers biseriate on all arms. Tentacle club suckers in 8 longitudinal rows. Mantle-head occipital band narrow (not reaching over the ocular globes). A pair of kidney-shaped photophores on ventral surface of ink sac. Gladius present, reduced. Ventral mantle margin with deep funnel indentation and markedly sinuate margin. Hectocotylus (male left arm I) tripartite: basal part either with three suckers, two ventral and one dorsal, or two ventral suckers only; copulatory apparatus with modified suckerless pedicels: two ventral pedicels horn- or tubercle-like, two dorsal pedicels separate from ventral ones, fused with each other and distally directed between the two rows of suckers of distal part, additional dorsal pedicels projecting toward right arm I; distal part with some enlarged suckers in either ventral or both rows. Female bursa copulatrix roughly ear-shaped, devoid of cover. Included species Adinaefiola ligulata (Naef, 1912) gen. et comb. nov., A. aurantiaca (Jatta, 1896) gen. et comb. nov. and A. pfefferi (Grimpe, 1921) gen. et comb. nov. Etymology This generic name is created to honour the memory of Adolf Naef (1883���1949), founder of modern teuthology and a major scholar of Sepiolinae; it derives from the combination of Adi, the name that the scientist was called by his family members, with surname, Naef, and the diminutive suffix - iola. Gender feminine. Discussion of affinities Adinaefiola gen. nov. fits in the clade of NE Atlantic-Mediterranean Sepiolinae, characterized by the open-type bursa copulatrix and the extant, though reduced, gladius. Its affinities with Sepiola, as understood here, are mainly limited to the same type of light organs, kidney-shaped, and the same type of bursa copulatrix, character state shared by all NE Atlantic-Mediterranean Sepiolinae (Rondeletiola, Sepietta and Sepiola). It differs from Sepiola (the genus in which its species were previously placed) in that the modified sucker pedicels in the dorsal row of the copulatory apparatus are separate from the ventral ones. Moreover, the ventral mantle margin is indented and enlarged suckers are also present in the ventral row of the hectocotylus distal part, whereas neither of these two character states occurs in Sepiola s.s. Remarks Adinaefiola gen. nov. is established to accommodate the species ligulata, aurantiaca and pfefferi, which should be removed from Sepiola because of their sound differences from the true members of that genus (see above). Adinaefiola aurantiaca gen. et comb. nov. and A. pfefferi gen. et comb. nov. are clearly sister species ��� the former Mediterranean and the latter from the NE Atlantic (Goud & de Heij 2012) ��� both of which ostensibly differ from A. ligulata gen. et comb. nov. Nevertheless, the three species in this new genus, in addition to the symplesiomorphic character state ���dorsal pedicels of copulatory apparatus separate from ventral pedicels���, share a few synapomorphies: the 2 nd and 3 rd modified dorsal pedicels of the hectocotylus are fused with each other and protruding in the middle of the arm; additional modified dorsal pedicels in the copulatory apparatus are separate from the first two, and are mesially directed; and the ventral mantle margin has a deep funnel indentation. In turn, A. aurantiaca and A. pfefferi have a unique muscular ridge projecting laterally from the hectocotylus basal part, which ends in a toothlike structure merging with the ventral pedicels of the copulatory apparatus; this is a synapomorphic character state of the two species., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 36-37, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797
- Published
- 2020
- Full Text
- View/download PDF
30. Lusepiola Bello 2020, gen. nov
- Author
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Bello, Giambattista
- Subjects
Cephalopoda ,Mollusca ,Animalia ,Lusepiola ,Biodiversity ,Sepiolida ,Sepiolidae ,Taxonomy - Abstract
Lusepiola gen. nov. urn:lsid:zoobank.org:act: 1520B148-44E4-4B35-9BA1-8F7C91086E18 Figs 8A, 13 (the generic name used in the captions is the former one) Type species Sepiola birostrata Sasaki, 1918, here designated. Diagnosis Sepiolinae with fins rounded with large anterior lobe, which may reach the anterior mantle margin; their length about �� to �� mantle length. Suckers biseriate on all arms. Tentacle club suckers in 4 to 8 longitudinal rows. Mantle-head occipital band narrow (not reaching over the ocular globes). A pair of kidney-shaped photophores on ventral surface of ink sac. Gladius absent. Ventral mantle margin slightly sinuate, without any deep funnel indentation. Hectocotylus (male left arm I) tripartite: basal part with four regular suckers in two rows; copulatory apparatus with modified sucker-less pedicels: two ventral pedicels horn-like, aligned, directed distally and slightly laterally, and two dorsal pedicels flattened, fused with each other and directed ventrally, adhering to the oral arm surface and to the base of both ventral horns to form a concave pad; distal part with sucker pedicels of both rows leaf-like, lengthened, widened, triangular- or squarish-shaped, flattened promixo-distally, their bases inserted transversally on arm oral surface, except for distalmost suckers with regular short pedicels; in several preserved specimens distal part rotated towards right dorsal arm. Female bursa copulatrix pouch-like. Included species Lusepiola birostrata (Sasaki, 1918) gen. et comb. nov. and L. trirostrata (Voss, 1962) gen. et comb. nov. Etymology This genus is dedicated to Chung Cheng Lu (Museum of Victoria, Melbourne, Australia and National Chung Hsing University, Taichung, Taiwan), in recognition of his enormous contribution to teuthology, including Sepiolinae systematics; its name derives from the combination of Lu���s family name with Sepiola, a closely related genus. Gender feminine. Discussion of affinities Lusepiola gen. nov., Euprymna, Eumandya gen. nov. and Boletzkyola gen. nov. all possess a closed bursa copularix, a clear indication of their affinity. However, Lusepiola gen. nov. differs from the other three genera because the formation of its hectocotylus copulatory apparatus involves modified sucker pedicels from both the ventral and dorsal rows. It differs from Sepiola s.s., from which its species were removed, primarily because of the different type of bursa copulatrix; moreover, the basal part of its hectocotylus bears four suckers (two complete rows) instead of three. The peculiarly modified pedicels in the distal part of the hectocotylus separates Lusepiola gen. nov. from all other sepioline genera. Remarks The species in this genus, namely L. birostrata gen. et comb. nov. and L. trirostrata gen. et comb. nov., are distributed in the western Pacific from the Okhotsk Sea to Singapore (Reid & Jereb 2005; Okutani 2015)., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on page 41, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797, {"references":["Okutani T. 2015. Cuttlefishes and Squids of the World (New Edition). Tokai University Press, Tokay."]}
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- 2020
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31. Sepiola Leach 1817
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Bello, Giambattista
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Cephalopoda ,Mollusca ,Animalia ,Biodiversity ,Sepiolida ,Sepiolidae ,Sepiola ,Taxonomy - Abstract
Sepiola Leach, 1817 Figs 8B, 19���20 Sepiola Leach, 1817: 137. Type species Sepiola rondeletii Leach, 1817, by monotypy. Diagnosis Sepiolinae with fins rounded; their length about half mantle length. Suckers biseriate on arms I to III and at least proximally on arm IV. Tentacle club suckers in 4 to 8 longitudinal rows. Mantle-head occipital band narrow (not reaching over the ocular globes). A pair of kidney-shaped photophores on ventral surface of ink-sac. Gladius present, reduced. Ventral mantle margin slightly sinuate, without any deep funnel indentation. Hectocotylus (male left arm I) tripartite: basal part with three suckers, two ventral and one dorsal; copulatory apparatus with transverse formation of two ventral and two dorsal modified suckerless pedicels, all four of them lengthened and fused with each other throughout their length (few additional dorsal modified pedicels may be present mesially to transverse formation); distal part with some enlarged suckers in dorsal row. Female bursa copulatrix roughly ear-shaped, devoid of cover. Included species Sepiola rondeletii Leach, 1817, S. affinis Naef, 1912, S. atlantica d���Orbigny, 1842, S. boletzkyi Bello & Salman, 2015, S. bursadhaesa Bello, 2013, S. intermedia Naef, 1912, S. robusta Naef, 1912, S. steenstrupiana Levy, 1912 and S. tridens de Heij & Goud, 2010. Remarks The revised diagnosis of the genus Sepiola reported above was formulated to comply with the rearrangement of Sepiolinae according to the present results. It dismisses several species previously included in Sepiola, namely S. aurantiaca, S. birostrata, S. knudseni, S. ligulata, S. pfefferi and S. trirostrata, which are better placed in different genera. The revised genus Sepiola includes all the species in the Sepiola atlantica -group sensu Naef 1923 (see also Bello 2013; Bello & Salman 2015). Hence, the atlantica -group coincides with the genus Sepiola as revised in this paper. The overall distribution of these species ranges from the north-eastern Atlantic Ocean to the Mediterranean Sea., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 35-36, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797, {"references":["Naef A. 1923. Die Cephalopoden. Fauna und Flora des Golfes von Neapel 35 (1): 1 - 863. [English translation by Mercado A. 1972; Smithsonian Institution, Washington D. C.: 1 - 917]"]}
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- 2020
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32. Euprymna Steenstrup 1887
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Bello, Giambattista
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Cephalopoda ,Mollusca ,Animalia ,Biodiversity ,Sepiolida ,Sepiolidae ,Euprymna ,Taxonomy - Abstract
Euprymna Steenstrup, 1887 Fig. 7 Euprymna Steenstrup, 1887a: 43. Type species Inioteuthis morsei Verrill, 1881, by subsequent designation. Diagnosis Sepiolinae with fins rounded; their length about half mantle length. Arm suckers in 4, exceptionally 8 longitudinal rows. Tentacle club with numerous minute suckers in a few tens of longitudinal rows. Mantle-head occipital band broad, extending over the ocular globes.A pair of kidney-shaped photophores on ventral surface of ink-sac. Gladius absent. Ventral mantle margin slightly sinuate, without any deep funnel indentation. Hectocotylus (male left arm I) thicker than right arm I, bipartite: proximal part, occupying 1���5 to �� of arm, with regular suckers, except for 1���3 modified pedicels (may bear vestigial suckers), lengthened papilla-like, in 3 rd to 5 th position of ventral sucker row; distalmost part, occupying �� to *���5 of arm distally, with lengthened columnar sucker pedicels, closely packed to form longitudinal palisades, bearing at tip embedded suckers that are partially covered by fleshy caps, number of palisades proximally equal to that of regular sucker rows but reduced toward arm extremity. Female bursa copulatrix pouch-like. Included species Euprymna morsei (Verrill, 1881), E. albatrossae, Voss, 1962, E. berryi Sasaki, 1929, E. brenneri Sanchez et al., 2019, E. hoylei Adam, 1986, E. hyllebergi, Nateewathana, 1997, E. megaspadicea Kubodera & Okutani, 2002, E. penares (Gray, 1849), E. scolopes Berry, 1913, E. stenodactyla (Grant, 1833) and E. tasmanica (Pfeffer, 1884). Remarks Some nominal tetraseriate sucker species are deemed unresolved (cf. Norman & Lu 1997). The biseriate sucker arm E. parva, E. pardalota and E. phenax, were removed from this genus to be placed into Eumandya gen. nov. (see above). The species in Euprymna are distributed in tropical and temperate waters of the Indo-West Pacific region (Norman & Lu 1997; Nateewathana 1997; Kubodera & Okutani 2002; Reid 2011)., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 39-40, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797, {"references":["Steenstrup J. 1887 a. Notae Teuthologicae. 6. Species generis Sepiolae Maris Mediterranei. Oversigt over det Kongelige Danske Videnskabernes Selskabs Forhandlinger 1887: 47 - 66.","Verrill A. E. 1881. The Cephalopods of the Northeastern Coast of America. Part II. The smaller cephalopods, including the \" squids \" and the octopi, with other allied forms. Transactions of the Connecticut Academy of Sciences 5 (6): 259 - 446.","Sasaki M. 1929. A monograph of the dibranchiate cephalopods of the Japanese and adjacent waters. Journal of the College of Agriculture, Hokkaido Imperial University 20 suppl: 1 - 357.","Sanchez G., Jolly J., Reid A., Sugimoto C., Azama C., Marletaz F., Simakov O. & Rokhsar D. S. 2019. New bobtail squid (Sepiolidae: Sepiolinae) from the Ryukyu islands revealed by molecular and morphological analysis. Communications Biology 2: 465. https: // doi. org / 10.1038 / s 42003 - 019 - 0661 - 6","Nateewathana A. 1997. The Sepiolidae (Cephalopoda) of the Andaman Sea, Thailand, with description of Euprymna hyllebergi sp. nov. Phuket Marine Biological Center Special Publication 17: 465 - 481.","Norman M. D. & Lu C. C. 1997. Redescription of the southern dumpling squid Euprymna tasmanica and a revision of the genus Euprymna (Cephalopoda: Sepiolidae). Journal of the Marine Biological Association of the United Kingdom 77: 1109 - 1137. https: // doi. org / 10.1017 / S 0025315400038662","Reid A. 2011. Euprymna pardalota sp. nov. (Cephalopoda: Sepiolidae), a new dumpling squid from northern Australia. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 27: 135 - 142."]}
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- 2020
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33. Eumandya Bello 2020, gen. nov
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Bello, Giambattista
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Cephalopoda ,Mollusca ,Animalia ,Biodiversity ,Sepiolida ,Sepiolidae ,Eumandya ,Taxonomy - Abstract
Eumandya gen. nov. urn:lsid:zoobank.org:act: 6FB7B832-3CFA-4914-842A-A526390BFCFD Fig. 9 (the generic name used in the caption is the former one) Type species Euprymna pardalota Reid, 2011, here designated. Diagnosis Sepiolinae with fins rounded; their length about half mantle length.Arm suckers in two longitudinal rows. Tentacle club suckers in 6 to 14 longitudinal rows. Mantle-head occipital band broad, extending over the ocular globes. A pair of kidney-shaped photophores on ventral surface of ink-sac. Gladius absent. Ventral mantle margin faintly sinuate or with slightly deep funnel indentation. Hectocotylus (male left arm I) bipartite: proximal part, occupying �� to �� of arm, with regular suckers, except for pedicel of 3 rd sucker in ventral row lengthened, papilla-like (may bear vestigial sucker at its tip); distalmost part, occupying ⅓ to �� of arm distally, with lengthened columnar sucker pedicels, closely packed longitudinally bearing reduced suckers and not connected with each other by any web. Female bursa copulatrix pouch-like. Included species Euprymna pardalota (Reid, 2011) gen. et comb. nov., E. parva (Sasaki, 1914) gen. et comb. nov. and E. phenax (Voss, 1962) gen. et com. nov. Etymology This genus is named in honour of Amanda Reid (Australian Museum Research Institute, Sydney) for her outstanding contribution in the field of cephalopod taxonomy, including Sepiolinae. The generic name is derived by the combination of Mandy, the diminutive name by which she is known to her friends and colleagues, and the prefix Eu - in order to keep the assonance with the sister genus Euprymna. Gender feminine. Discussion of affinities The members of Eumandya gen. nov., namely parva, pardalota and phenax, were formerly assigned to Euprymna because of the palisaded distalmost part of the hectocotylus, which, despite minor differences, is a unique feature of the clade (Eumandya gen. nov., Euprymna). In addition to the readily evident difference in number of longitudinal sucker rows on arms, i.e., biseriate arrangement in Eumandya gen. nov. vs tetraseriate arrangement in Euprymna, minor differences include the lack of well-developed fleshy caps on the columnar suckers and the lack of lengthwise connections between the ventral columnar pedicels in the former genus. An additional sign of possible hectocotylian primordiality in Eumandya gen. nov. is the presence of one-single-modified-stalk in the copulatory apparatus; in most Euprymna s.s. species it is composed of two or three papillae. Remarks Eumandya pardalota gen. et comb. nov. and E. parva gen. et comb. nov. are deemed sister species (Reid, pers. com.; Sanchez et al. 2019). The latter authors rightly removed parva from Sepiola, as previously understood, based on both morphological features and genetic analyses (Sanchez et al. 2019). Their decision is congruous with both the absence of modified dorsal sucker pedicels in the formation of the copulatory apparatus of the hectocotylus and the presence of palisaded suckers in its distalmost part, which characters do not pertain to Sepiola. The distribution of the members of Eumandya gen. nov. is limited to the eastern Indian-western Pacific Oceans., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 38-39, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797, {"references":["Reid A. 2011. Euprymna pardalota sp. nov. (Cephalopoda: Sepiolidae), a new dumpling squid from northern Australia. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 27: 135 - 142.","Sanchez G., Jolly J., Reid A., Sugimoto C., Azama C., Marletaz F., Simakov O. & Rokhsar D. S. 2019. New bobtail squid (Sepiolidae: Sepiolinae) from the Ryukyu islands revealed by molecular and morphological analysis. Communications Biology 2: 465. https: // doi. org / 10.1038 / s 42003 - 019 - 0661 - 6"]}
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- 2020
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34. Sepietta Naef 1912
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Bello, Giambattista
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Cephalopoda ,Mollusca ,Animalia ,Biodiversity ,Sepiolida ,Sepiolidae ,Sepietta ,Taxonomy - Abstract
Sepietta Naef, 1912 Fig. 18 Sepietta Naef, 1912: 248. Type species Sepiola oweniana d���Orbigny in F��russac & d���Orbigny, 1841, by monotypy. Diagnosis Sepiolinae with fins rounded or bluntly angled laterally; their length about half mantle length. Suckers biseriate on all arms. Tentacle club suckers in 12 or more longitudinal rows. Mantle-head occipital band narrow (not reaching over the ocular globes). Ventral mantle margin slightly sinuate, without any deep funnel indentation. Gladius present, reduced. Visceral photophores absent. Hectocotylus (male left arm I) tripartite: basal part with three or four suckers, two ventral and one or two dorsal; copulatory apparatus with transverse formation of two ventral and two dorsal modified suckerless pedicels of various degrees of development, all four of them fused at their bases, ventral-most one longest and hook-shaped; distal part with some proximal suckers of dorsal row enlarged, wide space between the two sucker rows (Naef 1923). Female bursa copulatrix roughly ear-shaped, devoid of cover. Included species Sepietta oweniana (d���Orbigny in F��russac & d���Orbigny, 1841), S. neglecta Naef, 1916 and S. obscura Naef, 1916. Remarks This is a well-established genus distributed in the NE Atlantic Ocean and the Mediterranean. Its most evident character is the lack of any visceral light organ, which is a derived condition, i.e., light organs secondarily lost. Sepietta oweniana and S. neglecta are sister species (Bello 2019a) and are distinguished from S. obscura, in addition to hectocotylian characters, by their fin shape (that is bluntlyangled in the former ones and rounded in the latter), as well as by the number of longitudinal sucker rows on tentacle clubs (fewer in the latter) and the occurrence of only three suckers in the basal part of the S. obscura hectocotylus. Sepietta obscura, contrary to the other two species, dwells in shallow depths and has a narrower distribution, in the Atlantic Lusitanian waters and the Mediterranean Sea (Bello 2019a)., Published as part of Bello, Giambattista, 2020, Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera, pp. 1-53 in European Journal of Taxonomy 655 on pages 42-43, DOI: 10.5852/ejt.2020.655, http://zenodo.org/record/3888797, {"references":["Naef A. 1923. Die Cephalopoden. Fauna und Flora des Golfes von Neapel 35 (1): 1 - 863. [English translation by Mercado A. 1972; Smithsonian Institution, Washington D. C.: 1 - 917]","Naef A. 1916. Ueber neue Sepioliden aus dem Golf von Neapel. Pubblicazioni della Stazione Zoologica di Napoli 1: 1 - 10."]}
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- 2020
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35. On the purported representation of Haliphron atlanticus (Cephalopoda: Octopoda: Alloposidae) on Mycenaean funerary gold ornaments
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Bello, Giambattista
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The common octopus, Octopus vulgaris Cuvier, 1797, is widely depicted in Minoan and Mycenaean craftworks from the Late Bronze Age (ca. 1900-1100 BC). Some octopus-shaped funerary gold ornaments from a Mycenaean grave, all of them displaying seven arms, were supposed to portray the so-called seven-armed octopus, Haliphron atlanticus Steenstrup, 1861 (Octopoda: Argonautoidea: Alloposidae). Here it is shown that in fact those octopus-like ornaments cannot represent H. atlanticus because of morphological as well as biogeographical and ecological reasons.
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- 2020
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36. Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera
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Bello, Giambattista and Bello, Giambattista
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The subfamily Sepiolinae (Mollusca: Cephalopoda: Sepiolidae), currently containing the genera Sepiola Leach, 1817, Euprymna Steenstrup, 1887, Inioteuthis Verrill, 1881, Rondeletiola Naef, 1921 and Sepietta Naef, 1912, is characterized by the hectocotylization of the left dorsal arm, i.e., its transformation into a copulatory organ thanks to modifications of sucker/pedicel elements. The hectocotylus morphology varies to a great extent across genera and species. In particular, one to several pedicels in its proximal third lose their sucker and become highly and diversely modified in shape to constitute a copulatory apparatus. An evolutionary gradient was observed in the copulatory apparatus morphology, from the simple modification into a papilla of just one pedicel from the third element of the ventral sucker row (some nominal species of Euprymna) to a quite complex structure involving several variously modified pedicels from both the ventral and dorsal sucker rows (Inioteuthis). In some species, elements in the distal portion of the hectocotylus may also be highly modified, such as the columnar suckers in Euprymna. The hectocotylian diversity allows to distinguish nine groups of species that do not match the current generic subdivision of Sepiolinae. Additional morphological characters (number of sucker rows on arms, female bursa copulatrix, occurrence and shape of visceral light organs, etc.) corroborate the subdivision of Sepiolinae into nine subtaxa, i.e., genera. Accordingly, a cladogram is drawn to describe the possible phylogenetic relationships among the nine clades. To comply with these results, all current genera are redefined and four new genera are described, namely Adinaefiola gen. nov., Boletzkyola gen. nov., Eumandya gen. nov. and Lusepiola gen. nov.
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- 2020
37. Non-indigenous cephalopods in the Mediterranean Sea: a review
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Bello, Giambattista, Andaloro, Franco, Battaglia, Pietro, Bello, Giambattista, Andaloro, Franco, and Battaglia, Pietro
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The present review critically assesses the records of cephalopods that have entered the Mediterranean Sea in the last few decades. It includes 13 species, namely Sepia dollfusi, Stoloteuthis leucoptera, Sepioteuthis lessoniana, Architeuthis dux, Cranchia scabra, Taonius pavo, Megalocranchia sp., Teuthowenia megalops, Cycloteuthis sirventi, Taningia danae, Octopus cyanea, Amphioctopus sp. and Tremoctopus gracilis. The presence of Sepia pharaonis needs to be confirmed, whereas that of Sepia gibba and Spirula spirula is excluded. The arrivals from the Atlantic Ocean through the Strait of Gibraltar are related to the entrance surface current, which either carried passively planktonic paralarvae or favoured in some other way the entrance of subadult and adult stray specimens. As a matter of fact, all Atlantic cephalopods are pelagic oegopsid squids, with the exception of the nekto-benthic sepiolid S. leucoptera; all of them have been found only in the western Mediterranean basin. None of them seemingly established a stable population there, apart from the latter species. On the contrary, the cephalopods entering the Mediterranean from the Red Sea through the Suez Canal (Lessepsian migrants) lead a benthic mode of life. At least two of them, namely S. lessoniana and Amphioctopus sp., set up stable populations in the eastern basin. Lastly the occurrences of the pelagic octopod T. gracilis are ascribed, in the literature, to human-mediated transfer., U ovom radu autori kritički procjenjuju nalaze glavonožaca koji su ušli u Sredozemno more u posljednjih nekoliko desetljeća, što uključuje 13 vrsta, a to su: Sepia dollfusi, Stoloteuthis leucopte-ra, Sepioteuthis lessoniana, Architeuthis dux, Cranchia scabra, Taonius pavo, Megalocranchia sp., Teuthowenia megalops, Cycloteuthis sirventi, Taningia danae, Octopus cyanea, Amphioctopus sp. i Tremoctopus gracilis. Prisutnost vrste Sepia pharaonis treba biti potvrđena, dok je prisutnost Sepia gibba i Spirula spirula isključena. Dolasci vrsta iz Atlantskog oceana kroz Gibraltarski tjesnac povezani su s ulaznom površinskom strujom koja je nosila pasivno planktonske paralarve ili je na neki drugi način favorizirala ulaz subadultnih i odraslih zalutalih primjeraka. Zapravo su svi atlantski glavonošci pelagične lignje, s izuzetkom nekto-bentoskog sepiolida S. leucoptera. Čini se da nijedna vrsta od navedenih tamo nije uspostavila stabilnu populaciju, osim potonje navednih vrsta. Naprotiv, glavonošci koji ulaze u Sredozemno more iz Crvenog mora kroz Sueski kanal (lesepsijski migranti) vode bentoski način života. Ipak, dvije vrste S. lessoniana i Amphioctopus sp., uspostavile su stabilne populacije u istoč-nom dijelu. Konačno, pojave pelagične hobotnice T. gracilis pripisuju se, u literaturi, prijenosu posredovanim antropogenim utjecajem.
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38. Multiple-Phase Biometric Relationships and Sexual Maturity in the Atlantic Bluefin Tuna, Thunnus thynnus (Osteichthyes: Scombridae)
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Bello, Giambattista, primary, Santamaria, Nicoletta, additional, and Corriero, Aldo, additional
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- 2021
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39. Non-indigenous cephalopods in the Mediterranean Sea
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Bello, Giambattista, primary, Andaloro, Franco, additional, and Battaglia, Pietro, additional
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- 2020
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40. Elenco dei cefalopodi del Golfo di Taranto
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Bello, Giambattista and BioStor
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- 1987
41. Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera
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BELLO, Giambattista, primary
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- 2020
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42. Bregmaceros nectabanus Whitley, 1941 (Teleostei: Bregmacerotidae), a new Lessepsian migrant in the Adriatic Sea
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Dulčić, Jakov, primary, Bello, Giambattista, additional, and Dragičević, Branko, additional
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- 2020
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43. The Mediterranean Sepiolidae (Mollusca Cephalopoda) diversity
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Bello, Giambattista, primary
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- 2019
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44. Erratum to: The deep-water squid Octopoteuthis sicula Rüppell, 1844(Cephalopoda: Octopoteuthidae) as the single species of the genus occurring in the Mediterranean Sea
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Jereb, Patrizia, Cannas, Rita, Maiorano, Porzia, Bello, Giambattista, Garibaldi, Fulvio, Mereu, Marco, Ancona, Francesco G., Ammendolia, Giovanni, Battaglia, Pietro, Duysak, Önder, Hoving, Hendrik Jan T., Lefkaditou, Eugenia, Lipinski, Marek R., Melis, Riccardo, Peristeraki, Panagiota N., Ragonese, Sergio, Romeo, Teresa, Salman, Alp, Santos, Maria Begoña, Villari, Alberto, and Cuccu, Danila
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- 2016
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45. Global patterns of species richness in coastal cephalopods
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Rosa, Rui, Pissarra, Vasco, Borges, Francisco O., Xavier, Jose, Gleadall, Ian G., Golikov, Alexey, Bello, Giambattista, Morais, Liliane, Lishchenko, Fedor, Roura, Álvaro, Judkins, Heather, Ibáñez, Christian M., Piatkowski, Uwe, Vecchione, Michael, Villanueva, Roger, Rosa, Rui, Pissarra, Vasco, Borges, Francisco O., Xavier, Jose, Gleadall, Ian G., Golikov, Alexey, Bello, Giambattista, Morais, Liliane, Lishchenko, Fedor, Roura, Álvaro, Judkins, Heather, Ibáñez, Christian M., Piatkowski, Uwe, Vecchione, Michael, and Villanueva, Roger
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Within the context of global climate change and overfishing of fish stocks, there is some evidence that cephalopod populations are benefiting from this changing setting. These invertebrates show enhanced phenotypic flexibility and are found from polar regions to the tropics. Yet, the global patterns of species richness in coastal cephalopods are not known. Here, among the 370 identified-species, 164 are octopuses, 96 are cuttlefishes, 54 are bobtails and bottletails, 48 are inshore squids and 8 are pygmy squids. The most diverse ocean is the Pacific (with 213 cephalopod species), followed by the Indian (146 species) and Atlantic (95 species). The least diverse are the Southern (15 species) and the Arctic (12 species) Oceans. Endemism is higher in the Southern Ocean (87%) and lower in the Arctic (25%), which reflects the younger age and the "Atlantification" of the latter. The former is associated with an old lineage of octopuses that diverged around 33 Mya. Within the 232 ecoregions considered, the highest values of octopus and cuttlefish richness are observed in the Central Kuroshio Current ecoregion (with a total of 64 species), followed by the East China Sea (59 species). This pattern suggests dispersal in the Central Indo-Pacific (CIP) associated with the highly productive Oyashio/Kuroshio current system. In contrast, inshore squid hotspots are found within the CIP, namely in the Sunda Shelf Province, which may be linked to the occurrence of an ancient intermittent biogeographic barrier: a land bridge formed during the Pleistocene which severely restricted water flow between the Pacific and Indian Oceans, thereby facilitating squid fauna differentiation. Another marked pattern is a longitudinal richness cline from the Central (CIP) toward the Eastern Indo-Pacific (EIP) realm, with central Pacific archipelagos as evolutionary dead ends. In the Atlantic Ocean, closure of the Atrato Seaway (at the Isthmus of Panama) and Straits of Gibraltar (Mediterranean Sea) are
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- 2019
46. Global Patterns of Species Richness in Coastal Cephalopods
- Author
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Ministerio de Educación y Cultura (España), Fundação para a Ciência e a Tecnologia (Portugal), Japan Science and Technology Agency, Rosa, Rui, Pissarra, Vasco, Borges, Francisco O., Xavier, José C., Gleadall, Ian G., Golikov, Alexey, Bello, Giambattista, Morais, Liliane, Lishchenko, Fedor, Roura, Álvaro, Judkins, Heather, Ibáñez, Christian Marcelo, Piatkowski, Uwe, Vecchione, Michael, Villanueva, Roger, Ministerio de Educación y Cultura (España), Fundação para a Ciência e a Tecnologia (Portugal), Japan Science and Technology Agency, Rosa, Rui, Pissarra, Vasco, Borges, Francisco O., Xavier, José C., Gleadall, Ian G., Golikov, Alexey, Bello, Giambattista, Morais, Liliane, Lishchenko, Fedor, Roura, Álvaro, Judkins, Heather, Ibáñez, Christian Marcelo, Piatkowski, Uwe, Vecchione, Michael, and Villanueva, Roger
- Abstract
Within the context of global climate change and overfishing of fish stocks, there is some evidence that cephalopod populations are benefiting from this changing setting. These invertebrates show enhanced phenotypic flexibility and are found from polar regions to the tropics. Yet, the global patterns of species richness in coastal cephalopods are not known. Here, among the 370 identified-species, 164 are octopuses, 96 are cuttlefishes, 54 are bobtails and bottletails, 48 are inshore squids and 8 are pygmy squids. The most diverse ocean is the Pacific (with 213 cephalopod species), followed by the Indian (146 species) and Atlantic (95 species). The least diverse are the Southern (15 species) and the Arctic (12 species) Oceans. Endemism is higher in the Southern Ocean (87%) and lower in the Arctic (25%), which reflects the younger age and the “Atlantification” of the latter. The former is associated with an old lineage of octopuses that diverged around 33 Mya. Within the 232 ecoregions considered, the highest values of octopus and cuttlefish richness are observed in the Central Kuroshio Current ecoregion (with a total of 64 species), followed by the East China Sea (59 species). This pattern suggests dispersal in the Central Indo-Pacific (CIP) associated with the highly productive Oyashio/Kuroshio current system. In contrast, inshore squid hotspots are found within the CIP, namely in the Sunda Shelf Province, which may be linked to the occurrence of an ancient intermittent biogeographic barrier: a land bridge formed during the Pleistocene which severely restricted water flow between the Pacific and Indian Oceans, thereby facilitating squid fauna differentiation. Another marked pattern is a longitudinal richness cline from the Central (CIP) toward the Eastern Indo-Pacific (EIP) realm, with central Pacific archipelagos as evolutionary dead ends. In the Atlantic Ocean, closure of the Atrato Seaway (at the Isthmus of Panama) and Straits of Gibraltar (Mediterranean Sea) are
- Published
- 2019
47. First record of paralarvae of Scaeurgus unicirrhus (Cephalopoda: Octopodidae)
- Author
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Bello, Giambattista
- Published
- 2004
48. Sulla cattura e liberazione di un grampo, Grampus griseus, nel mare Ionio (Mammalia, Cetacea)
- Author
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Cataldini, G, Bello, Giambattista, and BioStor
- Published
- 1987
49. Dokumentirani nalazi vrste Gaidropsarus granti (Osteichthyes: Lotidae) u Jadranskom moru i pregled njezinih pojavljivanja u Sredozemnom moru: da li se radi o autohtonoj ili novopridošloj vrsti ribe?
- Author
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BELLO, Giambattista
- Subjects
Gaidropsarus granti ,Lotidae ,Adriatic Sea ,Mediterranean ,new records ,Jadransko more ,Sredozemlje ,novi nalazi - Abstract
Gaidropsarus granti (Osteichthyes: Lotidae) is a rare fish that was recorded for the first time in the Mediterranean Sea in 1989. The Mediterranean records have been documented for the Ligurian Sea, the Levant Sea close to Rhodes, off the Sardinian coasts and for the northern Ionian Sea south of the Straits of Messina. Additional reports referred its presence in the Alboran Sea, in the southern Adriatic Sea and west of Malta, though without any additional information. The present paper reports the occurrence of G. granti in the Adriatic Sea (eastern Mediterranean) thanks to the examination of eight specimens collected in its south-western part, between February 1997 and October 2017. Six of them had been trawled at depths from 190 to 290 m, mainly in a channel within coral banks, while two were caught by hook at 420 m depth on coral banks. Their total length ranged from 21.0 to 32.3 cm. Four dissected individuals were adult, three males and one female. The stomach of two individuals contained only galatheid shrimps of the genus Munida, some of which were identified as M. rutllanti. According to interviews with fishermen based in the area where G. granti specimens were trawled, this conspicuous fish was unknown to them until the 1997 captures. Afterwards, it became well known to all of them, because few specimens are presently caught every once in a while. It is discussed whether G. granti is a native Mediterranean species or a fish that entered this sea a few decades ago. Both hypotheses have some support. The autochthonous origin hypothesis is mainly based on both G. granti distribution throughout the Mediterranean and its unavailability to old fishing gear uncapable of fishing on deep, rough grounds. The contrasting allochthonous hypothesis is backed by the total lack of Mediterranean records prior to 1989 coupled with its quite long larval pelagic phase., Gaidropsarus granti (Osteichthyes: Lotidae) je rijetka riba koja je prvi put zabilježena u Sredozemnom moru 1989. godine. Nalazi u Sredozemnom moru su dokumentirani za Ligursko more, Levantinsko more blizu Rodosa, s obale Sardinije i sjevernije Jonsko more južno od Messine. Dodatna izvješća ukazala su na njegovu prisutnost u Alboranskom moru, u južnom Jadranu i zapadno od Malte, iako bez ikakvih dodatnih informacija. U ovom radu prikazana je pojava G. granti u Jadranskom moru (istočni dio Sredozemnog mora) zahvaljujući ispitivanju osam uzoraka sakupljenih u jugozapadnom dijelu, u razdoblju između veljače 1997. i listopada 2017. godine. Šest primjeraka je ulovljeno na dubinama od 190 do 290 m, uglavnom u kanalu između koraljnih grebena, dok su dva uzorka uhvaćena udicom na dubini od 420 m na koraljnom grebenu. Njihova ukupna duljina kretala se od 21,0 do 32,3 cm. Četiri izdvojena primjerka su bila odrasle jedinke, tri mužjaka i jedna ženka. Želudci dvaju primjeraka su sadržavali samo rakove roda Munidae, od kojih su neki identificirani kao M. rutllanti. Sudeći po intervjuima s ribarima sa područja gdje su bili ulovljeni uzorci G. granti, ta lako prepoznatljiva riba bila je nepoznata do 1997. godine. Nakon toga, postala je uobičajena i prepoznata od strane ribara jer se od tada sporadično lovi. Vode se rasprave o tome da li je G. granti autohtona sredozemna vrsta ili novopridošla vrsta koja je tu dospjela prije nekoliko desetljeća. Obje hipoteze imaju uporište. Hipoteza o autohtonom podrijetlu uglavnom se temelji na zastupljenosti G. granti diljem Sredozemlja i relativne nedostupnosti starijim ribolovnim alatima neadekvatnim za ribolov na dubokim i grubim terenima. Oprečnu hipotezu podupire potpuni nedostatak nalaza u Sredozemnom moru prije 1989. godine zajedno s prilično dugom larvalnom pelagičkom fazom.
- Published
- 2018
50. Global Patterns of Species Richness in Coastal Cephalopods
- Author
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Rosa, Rui, primary, Pissarra, Vasco, additional, Borges, Francisco O., additional, Xavier, José, additional, Gleadall, Ian G., additional, Golikov, Alexey, additional, Bello, Giambattista, additional, Morais, Liliane, additional, Lishchenko, Fedor, additional, Roura, Álvaro, additional, Judkins, Heather, additional, Ibáñez, Christian M., additional, Piatkowski, Uwe, additional, Vecchione, Michael, additional, and Villanueva, Roger, additional
- Published
- 2019
- Full Text
- View/download PDF
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