CORSICABENTHOS 1

Une campagne orgnanisée par :

MNHN - Muséum national d'Histoire naturelle

Cette campagne bénéficie du financement de :

AFB - Agence Française de la Biodiversité
CdC - Collectivité de Corse

Programme

La Planète Revisitée : Corse 2019-2021

Informations générales

Chef de mission

Le Gall Line

Date et lieu de départ

Date et lieu d'arrivée

Etape	Date de départ	Date d'arrivée	Départ	Arrivée	Navire
CAMPAGNE	06/05/2019	24/05/2019
POST CAMPAGNE

Objectifs :

Pour cette première année, un volet marin se déroule du 6 au 26 mai 2019 dans le Parc naturel marin du cap Corse et de l’Agriate afin d’inventorier algues et invertébrés marins.

Travaux effectués :

Les mollusques, crustacés et algues ont constitué la cible principale de l’échantillonnage. Les prospections se sont concentrées dans la tranche de 0 à 30 mètres de profondeur avec des incursions dans la tranche de 30 à 50 mètres par des plongeurs qualifiés. Différentes méthodes d’exploration ont été déployées : la pêche à pied, des plongées couplées à des méthodes de prélèvement ciblant les organismes de petites tailles (paniers de brossage, aspirateur sous-marin, dragues à main pour capturer la faune vagile des herbiers de posidonies) et le déploiement de petits engins de pêche (dragues) pouvant aller jusqu’à 100 mètres de profondeur.

Remerciements :

Bibliographie (8) [+] [-]

Exporter les bibliographies

Fassio G., Russini V., Buge B., Schiaparelli S., Modica M.V., Bouchet P. & Oliverio M. 2020. High cryptic diversity in the kleptoparasitic genus Hyalorisia Dall, 1889 (Littorinimorpha: Capulidae) with the description of nine new species from the Indo-West Pacific. Journal of Molluscan Studies 86(4): 401-421. DOI:10.1093/mollus/eyaa028
Résumé [+] [-]
Species in the family Capulidae (Littorinimorpha: Capuloidea) display a wide range of shell morphologies. Several species are known to live in association with other benthic invertebrates—mostly bivalves and sabellid worms, but also other gastropods—and are believed to be kleptoparasitic ﬁlter feeders that take advantage of the water current produced by the host. This peculiar trophic ecology, implying a sedentary lifestyle, has resulted in highly convergent shell forms. This is particularly true for the genus Hyalorisia Dall, 1889, which occurs in deep water in the Caribbean and Indo-West Paciﬁc provinces, with two nominal species recognized so far. Combining morphological, ecological and molecular data, we assessed the diversity of the genus, its phylogenetic position inside the family and its association with its bivalve host, the genus Propeamussium de Gregorio, 1884 (Pectinoidea), resulting in the description of nine new cryptic species. When sympatric, species of Hyalorisia are associated with different host species, but the same species of Propeamussium may be the host of several allopatric species of Hyalorisia.

Campagnes accessibles citées (17) [+] [-]
AURORA 2007, CONCALIS, CORSICABENTHOS 1, EBISCO, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.3, MADEEP, MAINBAZA, MIRIKY, NanHai 2014, PANGLAO 2004, PANGLAO 2005, SALOMON 2, ZhongSha 2015

Codes des collections associés: IM (Mollusques)
Fassio G., Stefani M., Russini V., Buge B., Bouchet P., Treneman N., Malaquias M.A.E., Schiaparelli S., Modica M.V. & Oliverio M. 2022. Neither slugs nor snails: a molecular reappraisal of the gastropod family Velutinidae. Zoological Journal of the Linnean Society 197(4): 924-964. DOI:10.1093/zoolinnean/zlac091
Résumé [+] [-]
Abstract The systematics of the marine mollusc family Velutinidae has long been neglected by taxonomists, mainly because their often internal and fragile shells offer no morphological characters. Velutinids are usually undersampled owing to their cryptic mantle coloration on the solitary, social or colonial ascidians on which they feed and lay eggs. In this study, we address the worldwide diversity and phylogeny of Velutinidae based on the largest molecular dataset (313 specimens) to date, accounting for > 50% of the currently accepted genera, coupled with morphological and ecological data. Velutinids emerge as a diverse group, encompassing four independent subfamily-level lineages, two of which are newly described herein: Marseniopsinae subfam. nov. and Hainotinae subfam. nov. High diversity was found at genus and species levels, with two newly described genera (Variolipallium gen. nov. and Pacifica gen. nov.) and ≥ 86 species in the assayed dataset, 58 of which are new to science (67%). Velutinidae show a remarkable morphological plasticity in shell morphology, mantle extension and chromatic patterns. This variability is likely to be the result of different selective forces, including habitat, depth and trophic interactions.

Campagnes accessibles citées (23) [+] [-]
ATIMO VATAE, BIOMAGLO, BIOPAPUA, CEAMARC-AA, CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, GUYANE 2014, ILES DU SALUT, KANACONO, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, PANGLAO 2004, PAPUA NIUGINI, SAKIZAYA 2019, SANTO 2006, Tuhaa Pae 2013, ZhongSha 2015

Codes des collections associés: IM (Mollusques)
Fedosov A.E., Zaharias P., Lemarcis T., Modica M.V., Holford M., Oliverio M., Kantor Y.I. & Puillandre N. 2024. Phylogenomics of Neogastropoda: The Backbone Hidden in the Bush, in Whelan N. (Ed.), Systematic Biology: syae010. DOI:10.1093/sysbio/syae010
Résumé [+] [-]
Abstract The molluskan order Neogastropoda encompasses over 15,000 almost exclusively marine species playing important roles in benthic communities and in the economies of coastal countries. Neogastropoda underwent intensive cladogenesis in the early stages of diversification, generating a “bush” at the base of their evolutionary tree, which has been hard to resolve even with high throughput molecular data. In the present study to resolve the bush, we use a variety of phylogenetic inference methods and a comprehensive exon capture dataset of 1817 loci (79.6% data occupancy) comprising 112 taxa of 48 out of 60 Neogastropoda families. Our results show consistent topologies and high support in all analyses at (super)family level, supporting monophyly of Muricoidea, Mitroidea, Conoidea, and, with some reservations, Olivoidea and Buccinoidea. Volutoidea and Turbinelloidea as currently circumscribed are clearly paraphyletic. Despite our analyses consistently resolving most backbone nodes, 3 prove problematic: First, the uncertain placement of Cancellariidae, as the sister group to either a Ficoidea-Tonnoidea clade or to the rest of Neogastropoda, leaves monophyly of Neogastropoda unresolved. Second, relationships are contradictory at the base of the major “core Neogastropoda” grouping. Third, coalescence-based analyses reject monophyly of the Buccinoidea in relation to Vasidae. We analyzed phylogenetic signal of targeted loci in relation to potential biases, and we propose the most probable resolutions in the latter 2 recalcitrant nodes. The uncertain placement of Cancellariidae may be explained by orthology violations due to differential paralog loss shortly after the whole genome duplication, which should be resolved with a curated set of longer loci.

Campagnes accessibles citées (23) [+] [-]
ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, CORSICABENTHOS 1, DongSha 2014, EXBODI, ILES DU SALUT, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, NanHai 2014, PAPUA NIUGINI, TAIWAN 2013, Tuhaa Pae 2013, ZhongSha 2015

Codes des collections associés: IM (Mollusques)
Giannuzzi-Savelli, Riccardo, Pusateri, Francesco, Prkić Jakov, Bartolini S., Russini V., Fassio G. & Oliverio M. 2020. Revision of Mediterranean and NE Atlantic Raphitomidae (Gastropoda, Conoidea) 8: The genus Leufroyia Monterosato, 1884. Zoosystema 42(22): 433. DOI:10.5252/zoosystema2020v42a22
Résumé [+] [-]
The four recent species of the genus Leufroyia Monterosato, 1884 are revised based on an integrative taxonomy approach: L. leufroyi (Michaud, 1828), L. concinna (Scacchi, 1836), L. erronea Monterosato, 1884 and L. villaria (Pusateri & Giannuzzi-Savelli, 2008).

Campagnes accessibles citées (1) [+] [-]
CORSICABENTHOS 1

Codes des collections associés: IM (Mollusques)
Guerra-García J.M., Revanales T., Saenz-Arias P., Navarro-Barranco C., Ruiz-Velasco S., Pastor-Montero M., Sempere-Valverde J., Chebaane S., Vélez-Ruiz A., Martínez-Laiz G., Santos-Simón M., Ferrario J., Marchini A., Nour O.M., Gouillieux B., Hosie A.M., Gerovasileiou V., Carvalho S., Balistreri P., Sirchia B., Ruvolo V., Mancini E., Bonifazi A., Tempesti J., Tiralongo F., Ignoto S., Fernandez-Gonzalez V., Vázquez-Luis M., Cabezas M.D.P. & Ros M. 2023. Quick spreading of the exotic amphipod Laticorophium baconi (Shoemaker, 1934): another small stowaway overlooked?. Mediterranean Marine Science 24(3): 644-655. DOI:10.12681/mms.35817
Résumé [+] [-]
Studies of non-indigenous species (NIS) often tend to focus on medium and large-sized taxa with potential for remarkable ecological and/or economic impact, whereas the early detection of small invertebrates is often delayed due to taxonomic challenge, lack of consistent, standardised monitoring efforts and limited funding. This study represents the first records of the marine amphipod Laticorophium baconi (Shoemaker, 1934) in Morocco, Tunisia, Corsica (France), Italy, Greece, Egypt, Saudi Arabia and New Caledonia (France). Furthermore, it reports an expansion of its known distribution in Portugal (earliest and northernmost record for the country and first record for Macaronesia), Spain (earliest record for Atlantic and Mediterranean European waters), and Australia (first record for Indian Ocean). Recreational boating and commercial shipping, mainly through hull fouling and secondarily ballast waters, are proposed as vectors for introduction and secondary spread of L. baconi. The following traits, analysed during the present study, could contribute to its invasive potential: (i) quick and extensive spread of the species worldwide, (ii) high densities in marinas, harbours, hull fouling and other artificial habitats, including aquaculture facilities and floating debris, (iii) high ability for short-term colonisation of empty artificial niches, (iv) diet based on detritus suggesting an opportunistic feeding behaviour, and (v) population survival during seasonal fluctuations in different regions. Taxonomic expertise and scientific collaboration, based on multidisciplinary networks of experts, are crucial for the early detection, distribution updates, and risk assessment of small and overlooked stowaways in marine environments.

Campagnes accessibles citées (4) [+] [-]
CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, KOUMAC 2.3

Codes des collections associés: IU (Crustacés)
Kantor Y.I., Fedosov A.E., Kosyan A.R., Puillandre N., Sorokin P.A., Kano Y., Clark R. & Bouchet P. 2022. Molecular phylogeny and revised classification of the Buccinoidea (Neogastropoda). Zoological Journal of the Linnean Society 194(3): 789-857. DOI:10.1093/zoolinnean/zlab031
Résumé [+] [-]
Abstract The superfamily Buccinoidea is distributed across the oceans of the world from the Arctic Ocean to the Antarctic and from intertidal to abyssal depths. It encompasses 3351 recent species in 337 genera. The latest taxonomic account recognized eight full families. For the first time, the monophyly of the superfamily and the relationships among the families are tested with molecular data supplemented by anatomical and radula data. Five genetic markers were used: fragments of mitochondrial COI, 16S rRNA, 12S rRNA and nuclear Histone 3 (H3) and 28S rRNA genes (for 225 species of 117 genera). Our analysis recovered Buccinoidea monophyletic in Bayesian analyses. The relationships between the formerly recognized families and subfamilies are drastically revised and a new classification of the superfamily is here proposed, now including 20 taxa of family rank and 23 subfamilies. Five new families (Chauvetiidae, Dolicholatiridae, Eosiphonidae, Prodotiidae and Retimohniidae) and one subfamily of Nassariidae (Tomliniinae) are described. Austrosiphonidae and Tudiclidae are resurrected from synonymy and employed in a new taxonomical extension. All but 40 recent genera are reclassified. Our results demonstrate that anatomy is rather uniform within the superfamily. With exceptions, the rather uniform radular morphology alone does not allow the allocation of genera to a particular family without additional molecular data.

Campagnes accessibles citées (42) [+] [-]
ATIMO VATAE, AURORA 2007, BIOPAPUA, BOA1, CEAMARC-AA, CHALCAL 2, CONCALIS, CORSICABENTHOS 1, Restreint, Restreint, DongSha 2014, EBISCO, GUYANE 2014, ILES DU SALUT, INHACA 2011, KANACONO, KARUBENTHOS 2, KARUBENTHOS 2012, KAVALAN 2018, KOUMAC 2.1, KOUMAC 2.3, MADIBENTHOS, MAINBAZA, MIRIKY, MUSORSTOM 4, Restreint, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, Restreint, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2000, TAIWAN 2004, TARASOC, TERRASSES, Tuhaa Pae 2013, Restreint, ZhongSha 2015

Codes des collections associés: IM (Mollusques)
Nocella E., Zvonareva S.S., Fassio G., Pica D., Buge B., Villa R., Puillandre N., Modica M.V. & Oliverio M. 2024. Spicy food for the egg-cowries: the evolution of corallivory in the Ovulidae (Gastropoda: Cypraeoidea). Frontiers in Marine Science 10: 1323156. DOI:10.3389/fmars.2023.1323156
Résumé [+] [-]
Introduction Host-parasite associations provide very useful models to study adaptive processes. We investigated the interaction between carnivorous marine gastropods, the Ovulidae or egg-cowries, and their cnidarian food targets. Ovulidae (Fleming, 1828), is a family of specialized carnivorous caenogastropods that feed by browsing on octocorals (Anthozoa: Octocorallia: Malacalcyonacea and Scleralcyonacea) or, to a much lesser degree, on antipatharians (Anthozoa: Hexacorallia: Antipatharia) and Stylasteridae (Hydrozoa: Hydroidolina: Anthoathecata). Very scanty information is available on the phylogenetic relationships and the degree of specificity of the relationship with the cnidarians of this corallivorous lineage, especially for deep-water taxa. Methods To assess taxonomic identifications and investigate cnidarian/ovulid relationships in the context of their evolution, we generated an extensive molecular dataset comprising two mitochondrial ( cox1 and 16S rDNA ) and one nuclear gene ( 28S rDNA ) from 524 specimens collected worldwide. The coral hosts of the ovulid species have been identified by integrating literature data with new records, employing morphological and/or molecular (the mitochondrial 16S rDNA and mtMSH , and the nuclear ITS2) markers. Results We obtained a molecular phylogenetic framework for the Ovulidae, time-calibrated with nine reliable fossil records. An ancestral state reconstruction allowed to identify Hexacorallia or Hydroidolina as the most likely ancestral cnidarian host for the Ovulidae. Discussion Our phylogenetic hypothesis revealed the existence of groups that do not completely correspond to the currently employed subfamilial arrangement. Concerning trophic ecology, while only pediculariines ( Pedicularia and allied) are associated with hydrozoans (Stylasteridae), our results suggest that some ovulid lineages shifted independently between octocorals and hexacorals.

Campagnes accessibles citées (26) [+] [-]
ATIMO VATAE, AURORA 2007, BIOMAGLO, CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, SPANBIOS, ZhongSha 2015

Codes des collections associés: IK (Cnidaires), IM (Mollusques)
Zaharias P., Kantor Y.I., Fedosov A.E. & Puillandre N. 2024. Coupling DNA barcodes and exon-capture to resolve the phylogeny of Turridae (Gastropoda, Conoidea). Molecular Phylogenetics and Evolution 191: 107969. DOI:10.1016/j.ympev.2023.107969
Campagnes accessibles citées (38) [+] [-]
ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, BOA1, CONCALIS, CORSICABENTHOS 1, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, MIRIKY, MUSORSTOM 9, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2004, TAIWAN 2013, TARASOC, TERRASSES, ZhongSha 2015

Codes des collections associés: IM (Mollusques)

Liste des photos

Liste des participants

Par étape :

CAMPAGNE (06/05/2019 - 24/05/2019): Aurelle, Didier (Polyvalence, Université de Provence, Aix-Marseille); Tri; Barbeyron, Tristan (Bactéries, Station Biologique de Roscoff); Plongée - Collecte; Boiteux, Benoît (Logistique, Muséum national d'Histoire naturelle); Bouchet, Philippe (Malacologie, Muséum national d'Histoire naturelle); Caballer, Manuel (Malacologie, Muséum national d'Histoire naturelle); Plongée - collecte - tri - photo; Chambard, Cyril (Logistique, Muséum national d'Histoire naturelle); Chauffeur - tamisage; Corbari, Laure (Carcinologie, Muséum national d'Histoire naturelle); Tri - Photo; De Bettignies, Thibaut (Algologie, UMS PatriNat (OFB-CNRS-MNHN)); Plongée - collecte - tri; Devauchelle, Gilles (Malacologie, Muséum national d'Histoire naturelle); Barcoding moléculaire - photo; Devauchelle, Mireille (Logistique, Muséum national d'Histoire naturelle); Chauffeur; Duchaud, Eric (Bactéries, Institut National de Recherche et Agronomie); Plongée - Collecte; Duris, Zdenek (Carcinologie, University of Ostrava); Plongée - collecte - tri - photo; Enderlin, Olivier (Pédagogie, Muséum national d'Histoire naturelle); Fassio, Giulia (Malacologie, Sapienza Università di Roma); Barcoding moléculaire; Frutos Parralejo, Maria Inmaculada (Carcinologie, University of Lodz); Tri; Gouilleux, Benoît (Polyvalence, Station Marine d'Arcachon); Plongée - Collecte; Héros, Virginie (Malacologie, Muséum national d'Histoire naturelle); Collecte - Tri; Janson, Anne-Laure (Polyvalence, UMS PatriNat (OFB-CNRS-MNHN)); Tri; Kantor, Arseniy (Logistique ); Tamisage; Kantor, Yuri (Malacologie, Severtsov Institute of Ecology and Evolution); Barcoding moléculaire; Krygelmans, Anouchka (Polyvalence, Muséum national d'Histoire naturelle); Plongée - Collecte; Latrèche, Abderhamane (Logistique, Muséum national d'Histoire naturelle); Chauffeur - tamisage; Le Gall, Line (Algologie, Muséum national d'Histoire naturelle); Chef de mission; Le Gall, Michel (Logistique, Muséum national d'Histoire naturelle); Collectes à la drague; Leblond, Alice (Communication, Muséum national d'Histoire naturelle); Lepareur, Fanny (Polyvalence, UMS PatriNat (OFB-CNRS-MNHN)); Collecte - Tri; Lozouet, Pierre (Malacologie, Muséum national d'Histoire naturelle); Collecte - Tri - Photo; Maestrati, Philippe (Malacologie, Muséum national d'Histoire naturelle); Tri - Photo; Modica, Maria Vittoria (Malacologie, Université de Montpellier); Barcoding moléculaire; Oliverio, Marco (Polyvalence, Sapienza Università di Roma); Plongée - Collecte; Otero Ferrer, Francisco ( Universidad de Las Palmas); Plongée - Collecte; Popoff, Madeleine (Carcinologie, Muséum national d'Histoire naturelle); Tri; Puillandre, Nicolas (Malacologie, Muséum national d'Histoire naturelle); Barcoding moléculaire; Quinet, Béatrice (Malacologie, Muséum national d'Histoire naturelle); Tri; Rabiller, Michael (Pédagogie, Muséum d'Histoire naturelle de La Rochelle); Ratti, Claudia (Polyvalence, Muséum national d'Histoire naturelle); Tamisage - Tri; Sabroux, Romain (Carcinologie, Muséum national d'Histoire naturelle); Tri; Sartoretto, Stéphane ( Institut français de recherche pour l'exploitation de la mer); Plongée - Collecte; Soubzmaigne, Sébastien (Logistique, Muséum national d'Histoire naturelle); Chauffeur - tamisage; Steyker, Tanya (Polyvalence ); Tri; Strong, Ellen (Malacologie, National Museum of Natural History, Smithsonian Institution); Barcoding moléculaire; Thomas, François (Bactéries, Station Biologique de Roscoff); Plongée - Collecte; Urban-Dehoux, Danièle (Malacologie, Muséum national d'Histoire naturelle); Tri; Utge, José (Algologie, Muséum national d'Histoire naturelle); Plongée - Collecte; Vassard, Emmanuel (Polyvalence, Muséum national d'Histoire naturelle); Plongée - Collecte; Warén, Anders (Malacologie, Muséum national d'Histoire naturelle); Collecte - Tri

POST CAMPAGNE ( - ): Marani, Gilberto ( Muséum national d'Histoire naturelle); Numérisation

Cartographie des stations de collectes

Fichier GoogleEarth (.kml) des points de collectes

Liste des stations

Station/collecte	Latitude	Longitude	Date	Profondeurs
CM01	42°44,4'N	09°27,7'E	20190506 06/05/2019	0 m
CM02	42°45,2'N	09°28,0'E	20190506 06/05/2019	0 m
CQ01	42°42,4'N	09°27,6'E	20190506 06/05/2019	37-32 m
CQ02	42°44,7'N	09°28,0'E	20190506 06/05/2019	19 m
CR01	42°42,4'N	09°27,6'E	20190506 06/05/2019	37-32 m
CR02	42°44,7'N	09°28,0'E	20190506 06/05/2019	19 m
CS01	42°42,4'N	09°27,6'E	20190506 06/05/2019	28 m
CS02	42°44,7'N	09°28,0'E	20190506 06/05/2019	19 m
CS03	42°44,7'N	09°28,0'E	20190506 06/05/2019	19 m
CD01	42°56,4'N	09°31,4'E	20190507 07/05/2019	71 m
CD02	42°56,6'N	09°30,4'E	20190507 07/05/2019	60 m
CD03	42°55,1'N	09°31,5'E	20190507 07/05/2019	80 m
CD04	42°55,5'N	09°32,0'E	20190507 07/05/2019	90 m
CF01	42°45,2'N	09°28,4'E	20190507 07/05/2019	23 m
CM03	42°43,1'N	09°14,7'E	20190507 07/05/2019	0 m
CM04	42°43,0'N	09°15,4'E	20190507 07/05/2019	0 m
CQ03	43°00,2'N	09°28,4'E	20190507 07/05/2019	21-19 m
CR03	42°45,4'N	09°28,4'E	20190507 07/05/2019	28 m
CR04	43°00,2'N	09°28,4'E	20190507 07/05/2019	21-19 m
CS04	42°59,8'N	09°27,2'E	20190507 07/05/2019	11 m
CS05	43°00,2'N	09°28,4'E	20190507 07/05/2019	22 m
CD05	42°53,5'N	09°32,0'E	20190508 08/05/2019	110 m
CD06	42°53,7'N	09°32,0'E	20190508 08/05/2019	60 m
CD07	42°53,6'N	09°30,3'E	20190508 08/05/2019	40 m
CM05	42°52,8'N	09°28,7'E	20190508 08/05/2019	0 m
CQ04	42°43,7'N	09°27,9'E	20190508 08/05/2019	41-39 m
CR05	42°43,7'N	09°27,9'E	20190508 08/05/2019	41-39 m
CR06	42°42,7'N	09°27,6'E	20190508 08/05/2019	22 m
CS06	42°43,7'N	09°27,9'E	20190508 08/05/2019	32 m
CS07	42°42,7'N	09°27,5'E	20190508 08/05/2019	17 m
CQ05	42°44,2'N	09°28,0'E	20190509 09/05/2019	32-22 m
CR07	42°44,1'N	09°28,1'E	20190509 09/05/2019	50 m
CR08	42°45,3'N	09°28,7'E	20190509 09/05/2019	53 m
CR09	42°42,4'N	09°27,3'E	20190509 09/05/2019	4 m
CS08	42°45,3'N	09°28,7'E	20190509 09/05/2019	53 m
CD08	42°58,9'N	09°32,9'E	20190510 10/05/2019	90 m
CD09	42°58,2'N	09°31,2'E	20190510 10/05/2019	60 m
CD10	42°51,9'N	09°30,6'E	20190510 10/05/2019	80 m
CD11	42°51,0'N	09°31,0'E	20190510 10/05/2019	90 m
CD12	42°41,7'N	09°27,2'E	20190510 10/05/2019	10 m
CM06	42°54,8'N	09°28,3'E	20190510 10/05/2019	0 m
CM07	42°57,0'N	09°27,4'E	20190510 10/05/2019	0 m
CQ06	42°44,2'N	09°28,0'E	20190510 10/05/2019	33 m
CQ07	42°41,6'N	09°27,2'E	20190510 10/05/2019	2-6 m
CQ08	42°41,7'N	09°27,1'E	20190510 10/05/2019	6-5 m
CR10	42°44,2'N	09°28,0'E	20190510 10/05/2019	38-32 m
CR11	42°41,4'N	09°27,2'E	20190510 10/05/2019	19-18 m
CR12	42°41,6'N	09°27,2'E	20190510 10/05/2019	2-6 m
CR13	42°41,7'N	09°27,1'E	20190510 10/05/2019	6-5 m
CS09	42°44,2'N	09°28,0'E	20190510 10/05/2019	29 m
CS10	42°41,4'N	09°27,2'E	20190510 10/05/2019	19-18 m
CD13	42°40,0'N	09°27,3'E	20190511 11/05/2019	7 m
CD14	42°39,9'N	09°27,4'E	20190511 11/05/2019	15 m
CD15	42°39,7'N	09°29,3'E	20190511 11/05/2019	70 m
CD16	42°40,9'N	09°29,1'E	20190511 11/05/2019	70 m
CD17	42°38,0'N	09°28,5'E	20190511 11/05/2019	5 m
CF02	42°43,3'N	09°14,9'E	20190511 11/05/2019	17 m
CM08	42°08,7'N	09°33,2'E	20190511 11/05/2019	0 m
CM09	42°07,5'N	09°30,9'E	20190511 11/05/2019	0 m
CQ09	42°47,2'N	09°19,8'E	20190511 11/05/2019	40-36 m
CQ10	42°43,3'N	09°14,9'E	20190511 11/05/2019	17 m
CR14	42°47,2'N	09°19,8'E	20190511 11/05/2019	44-40 m
CR15	42°43,3'N	09°14,9'E	20190511 11/05/2019	17 m
CR16	42°08,7'N	09°33,2'E	20190511 11/05/2019	2-1 m
CR17	42°08,7'N	09°32,5'E	20190511 11/05/2019	2 m
CR18	42°07,8'N	09°32,2'E	20190511 11/05/2019	9 m
CR19	42°07,5'N	09°31,1'E	20190511 11/05/2019	4-2 m
CS11	42°47,2'N	09°19,8'E	20190511 11/05/2019	41 m
CS12	42°43,3'N	09°14,9'E	20190511 11/05/2019	17 m
CS13	42°08,7'N	09°33,2'E	20190511 11/05/2019	2-1 m
CS14	42°08,7'N	09°32,5'E	20190511 11/05/2019	2 m
CS15	42°07,5'N	09°31,1'E	20190511 11/05/2019	4-2 m
CB01	42°41,6'N	09°27,2'E	20190512 12/05/2019	10 m
CD18	42°44,4'N	09°28,8'E	20190512 12/05/2019	60 m
CD19	42°44,4'N	09°28,1'E	20190512 12/05/2019	20 m
CD20	42°43,3'N	09°27,7'E	20190512 12/05/2019	30 m
CD21	42°42,4'N	09°27,5'E	20190512 12/05/2019	10 m
CM10	42°38,2'N	09°27,7'E	20190512 12/05/2019	0 m
CR20	42°41,6'N	09°27,2'E	20190512 12/05/2019	10 m
CM11	42°38,5'N	09°27,6'E	20190513 13/05/2019	0 m
CM12	42°46,4'N	09°28,6'E	20190513 13/05/2019	0 m
CB02	42°46,1'N	09°20,0'E	20190514 14/05/2019	26 m
CB03	42°43,0'N	09°15,9'E	20190514 14/05/2019	29 m
CD22	42°41,8'N	09°18,3'E	20190514 14/05/2019	10 m
CD23	42°43,0'N	09°18,6'E	20190514 14/05/2019	30 m
CD24	42°42,9'N	09°16,8'E	20190514 14/05/2019	60 m
CM13	41°56,9'N	09°24,2'E	20190514 14/05/2019	0 m
CM14	41°57,1'N	09°24,4'E	20190514 14/05/2019	0 m
CM15	41°56,9'N	09°24,4'E	20190514 14/05/2019	0 m
CM16	41°56,3'N	09°24,6'E	20190514 14/05/2019	0 m
CM17	41°57,2'N	09°24,5'E	20190514 14/05/2019	0 m
CM18	42°37,0'N	09°28,9'E	20190514 14/05/2019	0 m
CQ11	42°46,1'N	09°20,0'E	20190514 14/05/2019	15 m
CQ12	42°43,0'N	09°15,9'E	20190514 14/05/2019	28 m
CR21	42°46,1'N	09°20,0'E	20190514 14/05/2019	29-16 m
CR22	42°43,3'N	09°14,8'E	20190514 14/05/2019	15 m
CR23	42°43,0'N	09°15,9'E	20190514 14/05/2019	28 m
CS16	42°46,2'N	09°20,0'E	20190514 14/05/2019	22 m
CS17	42°43,0'N	09°15,9'E	20190514 14/05/2019	29 m
CB04	42°49,8'N	09°18,4'E	20190515 15/05/2019	21 m
CD25	42°43,7'N	09°19,3'E	20190515 15/05/2019	35 m
CD26	42°44,1'N	09°19,3'E	20190515 15/05/2019	60 m
CD27	42°44,4'N	09°19,4'E	20190515 15/05/2019	70 m
CD28	42°44,9'N	09°19,2'E	20190515 15/05/2019	100 m
CM19	42°39,4'N	09°26,9'E	20190515 15/05/2019	0 m
CQ13	42°47,2'N	09°19,8'E	20190515 15/05/2019	40-36 m
CQ14	42°49,8'N	09°18,4'E	20190515 15/05/2019	40 m
CR24	42°47,2'N	09°19,8'E	20190515 15/05/2019	52-50 m
CR25	42°49,8'N	09°18,4'E	20190515 15/05/2019	15 m
CS18	42°47,2'N	09°19,8'E	20190515 15/05/2019	37 m
CS19	42°49,8'N	09°18,4'E	20190515 15/05/2019	15 m
CD29	42°56,8'N	09°19,9'E	20190516 16/05/2019	60 m
CD30	43°00,1'N	09°18,7'E	20190516 16/05/2019	110 m
CD31	42°57,7'N	09°20,1'E	20190516 16/05/2019	30 m
CD32	42°56,8'N	09°19,9'E	20190516 16/05/2019	60 m
CD33	42°53,2'N	09°18,8'E	20190516 16/05/2019	33 m
CQ15	42°59,5'N	09°17,5'E	20190516 16/05/2019	32 m
CQ16	43°01,7'N	09°24,1'E	20190516 16/05/2019	23 m
CR26	42°59,5'N	09°17,5'E	20190516 16/05/2019	36 m
CR27	42°59,3'N	09°17,8'E	20190516 16/05/2019	37-21 m
CR28	43°01,7'N	09°24,4'E	20190516 16/05/2019	21 m
CR29	43°01,7'N	09°24,1'E	20190516 16/05/2019	23 m
CS20	42°59,3'N	09°17,8'E	20190516 16/05/2019	21 m
CS21	43°01,7'N	09°24,4'E	20190516 16/05/2019	21 m
CB05	42°42,3'N	09°19,2'E	20190517 17/05/2019	9 m
CQ17	42°46,0'N	09°20,0'E	20190517 17/05/2019	25 m
CR30	42°45,7'N	09°20,0'E	20190517 17/05/2019	18 m
CR31	42°46,0'N	09°20,0'E	20190517 17/05/2019	25 m
CR32	42°42,3'N	09°19,2'E	20190517 17/05/2019	9-3 m
CS22	42°45,7'N	09°20,0'E	20190517 17/05/2019	18 m
CS23	42°42,3'N	09°19,2'E	20190517 17/05/2019	3 m
CM20	42°40,5'N	09°17,4'E	20190518 18/05/2019	0 m
CB06	42°41,4'N	09°27,1'E	20190519 19/05/2019	18 m
CD34	42°47,5'N	09°30,9'E	20190519 19/05/2019	90 m
CD35	42°48,7'N	09°31,8'E	20190519 19/05/2019	100 m
CD36	42°49,7'N	09°30,7'E	20190519 19/05/2019	60 m
CD37	43°00,8'N	09°28,1'E	20190519 19/05/2019	40 m
CD38	43°01,8'N	09°26,5'E	20190519 19/05/2019	60 m
CD39	43°02,5'N	09°26,3'E	20190519 19/05/2019	70 m
CR33	42°44,2'N	09°28,0'E	20190519 19/05/2019	33 m
CR34	42°43,7'N	09°27,9'E	20190519 19/05/2019	33 m
CR35	42°41,4'N	09°27,1'E	20190519 19/05/2019	18 m
CR36	42°44,7'N	09°28,0'E	20190519 19/05/2019	18-16 m
CS24	42°43,7'N	09°27,9'E	20190519 19/05/2019	33 m
CS25	42°44,7'N	09°28,0'E	20190519 19/05/2019	16 m
CB07	42°42,7'N	09°27,4'E	20190520 20/05/2019	7-6 m
CD40	43°00,8'N	09°22,8'E	20190520 20/05/2019	25 m
CD41	42°59,8'N	09°18,6'E	20190520 20/05/2019	95 m
CD42	43°02,6'N	09°19,9'E	20190520 20/05/2019	60 m
CD43	43°02,8'N	09°18,4'E	20190520 20/05/2019	100 m
CD44	43°02,9'N	09°22,7'E	20190520 20/05/2019	60 m
CM21	42°02,4'N	09°29,1'E	20190520 20/05/2019	1-0 m
CR37	42°44,8'N	09°28,1'E	20190520 20/05/2019	21-20 m
CR38	42°42,7'N	09°27,3'E	20190520 20/05/2019	7-6 m
CR39	42°03,2'N	09°27,8'E	20190520 20/05/2019	5 m
CR40	42°02,8'N	09°29,6'E	20190520 20/05/2019	5 m
CR41	42°03,5'N	09°29,0'E	20190520 20/05/2019	5 m
CS26	42°44,8'N	09°28,1'E	20190520 20/05/2019	21 m
CS27	42°42,7'N	09°27,3'E	20190520 20/05/2019	7 m
CS28	42°02,8'N	09°29,6'E	20190520 20/05/2019	5 m
CS29	42°03,5'N	09°29,0'E	20190520 20/05/2019	5 m
CS30	42°02,3'N	09°28,1'E	20190520 20/05/2019	5 m
CD45	42°41,2'N	09°30,9'E	20190521 21/05/2019	150 m
CD46	42°41,7'N	09°30,5'E	20190521 21/05/2019	130 m
CD47	42°41,2'N	09°27,7'E	20190521 21/05/2019	50 m
CM22	42°57,6'N	09°27,3'E	20190521 21/05/2019	0 m
CQ18	43°01,2'N	09°24,5'E	20190521 21/05/2019	25 m
CR42	43°00,1'N	09°28,5'E	20190521 21/05/2019	17-15 m
CR43	43°01,3'N	09°24,5'E	20190521 21/05/2019	20-18 m
CS31	43°00,1'N	09°28,5'E	20190521 21/05/2019	16-15 m
CS32	43°01,3'N	09°24,5'E	20190521 21/05/2019	18 m
CD48	42°43,1'N	09°29,9'E	20190522 22/05/2019	130 m
CD49	42°42,8'N	09°29,5'E	20190522 22/05/2019	100 m
CD50	42°43,2'N	09°27,9'E	20190522 22/05/2019	60 m
CD51	42°42,9'N	09°27,5'E	20190522 22/05/2019	10 m
CM23	42°34,4'N	09°29,1'E	20190522 22/05/2019	1-0 m
CM24	42°35,8'N	09°28,6'E	20190522 22/05/2019	1-0 m
CM25	42°38,1'N	09°27,0'E	20190522 22/05/2019	1-0 m
CM26	42°58,0'N	09°20,9'E	20190522 22/05/2019	0 m
CQ19	42°59,9'N	09°17,2'E	20190522 22/05/2019	30 m
CQ20	42°58,5'N	09°19,8'E	20190522 22/05/2019	28 m
CR44	42°59,9'N	09°17,2'E	20190522 22/05/2019	38-35 m
CR45	42°59,6'N	09°17,6'E	20190522 22/05/2019	43-41 m
CR46	42°59,5'N	09°17,3'E	20190522 22/05/2019	29-28 m
CR47	42°58,5'N	09°19,8'E	20190522 22/05/2019	28-24 m
CS33	42°59,6'N	09°17,6'E	20190522 22/05/2019	41 m
CS34	42°59,5'N	09°17,3'E	20190522 22/05/2019	28 m
CQ21	42°44,8'N	09°08,5'E	20190523 23/05/2019	32 m
CQ22	42°44,4'N	09°08,2'E	20190523 23/05/2019	23 m
CR48	42°46,0'N	09°06,5'E	20190523 23/05/2019	51 m
CR49	42°44,8'N	09°08,5'E	20190523 23/05/2019	32-31 m
CR50	42°42,2'N	09°19,2'E	20190523 23/05/2019	3 m
CR51	42°44,4'N	09°08,2'E	20190523 23/05/2019	24-23 m
CS35	42°46,0'N	09°06,5'E	20190523 23/05/2019	51 m
CQ23	42°43,8'N	09°06,5'E	20190524 24/05/2019	21 m
CR52	42°43,8'N	09°06,5'E	20190524 24/05/2019	21-18 m
CS36	42°40,7'N	09°17,9'E	20190524 24/05/2019	2-1 m

Taxons par accès

Classe	Accès	Nombre de signalements