CORSICABENTHOS 2

Une campagne orgnanisée par :

MNHN - Muséum national d'Histoire naturelle

Cette campagne bénéficie du financement de :

CdC - Collectivité de Corse
OFB - Office français de la biodiversité

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	12/10/2020	31/10/2020
POST CAMPAGNE

Objectifs :

Travaux effectués :

Remerciements :

Bibliographie (5) [+] [-]

Exporter les bibliographies

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)
Goulding T.C., Strong E.E. & Quattrini A.M. 2023. Target‐capture probes for phylogenomics of the Caenogastropoda. Molecular Ecology Resources 23(6): 1372-1388. DOI:10.1111/1755-0998.13793
Résumé [+] [-]
AbstractTarget‐capture approaches have facilitated a rapid growth in the field of phylogenomics but few probe sets exist for molluscs, an exceptionally rich phylum with unparalleled ecological and morphological diversity. We designed and tested the first universal probe set using Phyluce to capture ultraconserved elements (UCEs) and exon loci from the Subclass Caenogastropoda ‐ one of six major lineages of gastropods. The probe set consists of 29,441 probes designed to target 1142 UCE loci and 1933 exon loci (3075 total). In silico analyses of our probe set yielded an average of 2110 loci from genomes and 1389 loci from transcriptomes of diverse caenogastropods, from which an average of 1669 and 849 loci were retained respectively after screening to remove those that matched multiple contigs. Phylogenetic analyses of the loci extracted from transcriptomes produced well‐supported trees very similar to those published based on transcriptomic analyses. Phylogenetic relationships estimated from loci extracted from genomes recover similar phylogenetic relationships, and indicate that the loci targeted with this probe set are informative for resolving deep phylogenetic relationships. An in vitro analysis of the probe set with the Epitoniidae, a diverse caenogastropod family of uncertain affinity and with poorly resolved evolutionary relationships, recovered a total of 2850 loci. Although preliminary, the analysis of loci captured by our probe set for a small number of epitoniid taxa produced a well‐resolved tree indicating that this probe set is also able to resolve relationships at shallower hierarchical scales. Together, the in silico and in vitro analyses indicate that target‐capture enrichment with this probe set is a useful tool for reconstructing phylogenetic relationships across taxonomic levels and evolutionary time scales.

Campagnes accessibles citées (12) [+] [-]
ATIMO VATAE, CORSICABENTHOS 2, KANACONO, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, SPANBIOS, ZhongSha 2015

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)
Nocella E., Fassio G., Zuccon D., Puillandre N., Modica M.V. & Oliverio M. 2024. From coral reefs into the abyss: the evolution of corallivory in the Coralliophilinae (Neogastropoda, Muricidae). Coral Reefs 43(5): 1285-1302. DOI:10.1007/s00338-024-02537-1
Résumé [+] [-]
In this study, we delved into the interaction between corallivorous marine gastropods, the muricid Coralliophilinae Chenu, 1859, and their cnidarian food targets. Coralliophilinae is a subfamily of specialised corallivorous caenogastropods that feed by browsing on octocorals or hexacorals. Only sparse information is available on the phylogenetic relationships and the degree of specificity of the trophic relationships within this corallivorous lineage. To address these gaps, we generated the largest molecular dataset to date, comprising two mitochondrial (cox1 and 16S rDNA) and one nuclear gene (ITS2 rDNA) from 586 specimens collected worldwide. The coral hosts of coralliophilines were identified through an integrative approach, combining literature data with new records, employing morphological and/or molecular markers, and incorporating data from DNA barcoding of the snail stomach content. Our comprehensive approach unveiled the existence of numerous cryptic species in Coralliophilinae, while the phylogeny showed that most of the currently accepted genera are not monophyletic. The molecular dating confirmed the origin of the Coralliophilinae in Middle Eocene, with diversification of most lineages during the Miocene. Our results indicate that the subfamily’s ancestor evolved in shallow waters in association with Scleractinia. Through the evolutionary history of Coralliophilinae, multiple host shifts to other cnidarian orders were observed, not correlated with changes in the depth range. The results of diversification analyses within the subfamily further suggest that the association with the host has influenced the evolutionary patterns of Coralliophilinae, but not vice versa.

Campagnes accessibles citées (27) [+] [-]
ATIMO VATAE, BIOMAGLO, CONCALIS, CORSICABENTHOS 2, CORSICABENTHOS 3, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KAVIENG 2014, LIFOU 2000, MADIBENTHOS, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SANTO 2006, TARASOC, TERRASSES, Tuhaa Pae 2013, Walters Shoal, 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)

Liste des photos

Organisme : 12 photos

Liste des participants

Par étape :

CAMPAGNE (12/10/2020 - 31/10/2020): Le Gall, Line (Algologie, Muséum national d'Histoire naturelle); Chef de mission

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
CM29	41°28,5'N	09°04,1'E	20201015 15/10/2020	0 m
CR86	41°25,7'N	09°15,9'E	20201024 24/10/2020	12-36 m
CD52	41°24,7'N	09°13,6'E	20201012 12/10/2020	38 m
CD53	41°25,6'N	09°14,7'E	20201012 12/10/2020	23 m
CD54	41°26,7'N	09°18'E	20201012 12/10/2020	80 m
CD55	41°22'N	09°13,5'E	20201012 12/10/2020	18-25 m
CM27	41°28,5'N	09°04,2'E	20201012 12/10/2020	1 m
CM28	41°28,5'N	09°04,1'E	20201012 12/10/2020	0 m
CQ24	41°27,5'N	09°03,6'E	20201012 12/10/2020	11 m
CQ25	41°28,5'N	09°04,1'E	20201012 12/10/2020	2 m
CR53	41°27,5'N	09°03,6'E	20201012 12/10/2020	3-11 m
CR54	41°28,5'N	09°04,3'E	20201012 12/10/2020	3 m
CR55	41°28,5'N	09°04,3'E	20201012 12/10/2020	10 m
CR56	41°28,4'N	09°04,2'E	20201012 12/10/2020	0-2 m
CS37	41°27,5'N	09°03,6'E	20201012 12/10/2020	10 m
CB08	41°29,2'N	09°17,2'E	20201013 13/10/2020	5-10 m
CD56	41°23,9'N	09°16,4'E	20201013 13/10/2020	32-36 m
CD57	41°24'N	09°18'E	20201013 13/10/2020	82-83 m
CD58	41°24,3'N	09°16,9'E	20201013 13/10/2020	71-71 m
CD59	41°26,7'N	09°17,9'E	20201013 13/10/2020	78 m
CD60	41°25,2'N	09°13,7'E	20201013 13/10/2020	13-13 m
CM30	41°30,2'N	09°16,5'E	20201013 13/10/2020	0-1 m
CM31	41°31,4'N	09°16,5'E	20201013 13/10/2020	0 m
CQ26	41°32,7'N	09°24'E	20201013 13/10/2020	16-19 m
CQ27	41°29,2'N	09°17,2'E	20201013 13/10/2020	12-12 m
CR57	41°32,7'N	09°24'E	20201013 13/10/2020	13-25 m
CR58	41°29,2'N	09°17,2'E	20201013 13/10/2020	16 m
CS38	41°32,7'N	09°24'E	20201013 13/10/2020	23 m
CS39	41°29,2'N	09°17,2'E	20201013 13/10/2020	16 m
CB09	41°30,5'N	09°23,6'E	20201014 14/10/2020	13-20 m
CD61	41°32,4'N	09°29,9'E	20201014 14/10/2020	118-118 m
CD62	41°32,9'N	09°30,8'E	20201014 14/10/2020	209-214 m
CD63	41°32,1'N	09°28,4'E	20201014 14/10/2020	101-102 m
CD64	41°29,7'N	09°17,8'E	20201014 14/10/2020	48-51 m
CQ28	41°30,6'N	09°23'E	20201014 14/10/2020	12 m
CR59	41°30,5'N	09°23,6'E	20201014 14/10/2020	13-29 m
CR60	41°30,6'N	09°23'E	20201014 14/10/2020	0-12 m
CS40	41°30,5'N	09°23,6'E	20201014 14/10/2020	26 m
CS41	41°30,6'N	09°23'E	20201014 14/10/2020	12 m
CB10	41°35,3'N	09°17,4'E	20201015 15/10/2020	6 m
CD65	41°25,2'N	09°14'E	20201015 15/10/2020	24-24 m
CD66	41°27,4'N	09°21,7'E	20201015 15/10/2020	91-91 m
CD67	41°31,3'N	09°21,6'E	20201015 15/10/2020	45-45 m
CD68	41°31,4'N	09°17,3'E	20201015 15/10/2020	13-15 m
CD69	41°28,2'N	09°16,3'E	20201015 15/10/2020	6-7 m
CR61	41°35,3'N	09°17,4'E	20201015 15/10/2020	6 m
CS42	41°35,3'N	09°17,4'E	20201015 15/10/2020	6 m
CB11	41°32,5'N	09°18,7'E	20201016 16/10/2020	13 m
CD70	41°33,1'N	09°28,4'E	20201016 16/10/2020	103-103 m
CD71	41°32,8'N	09°27,2'E	20201016 16/10/2020	89-90 m
CD72	41°33,7'N	09°23,7'E	20201016 16/10/2020	45-46 m
CD73	41°32,6'N	09°22,9'E	20201016 16/10/2020	45-47 m
CQ29	41°31,7'N	09°24,1'E	20201016 16/10/2020	30 m
CQ30	41°32,5'N	09°18,7'E	20201016 16/10/2020	12 m
CR62	41°31,7'N	09°24,1'E	20201016 16/10/2020	32-42 m
CR63	41°32,5'N	09°18,7'E	20201016 16/10/2020	13 m
CS43	41°31,7'N	09°24,1'E	20201016 16/10/2020	32 m
CS44	41°31,7'N	09°24,1'E	20201016 16/10/2020	38 m
CB12	41°25,8'N	09°15,8'E	20201017 17/10/2020	5-10 m
CD74	41°30,1'N	09°34,9'E	20201017 17/10/2020	394-397 m
CD75	41°29,5'N	09°33,3'E	20201017 17/10/2020	309-313 m
CD76	41°28,9'N	09°33,3'E	20201017 17/10/2020	281-288 m
CD77	41°27,2'N	09°33,3'E	20201017 17/10/2020	143-143 m
CD78	41°25,3'N	09°33,3'E	20201017 17/10/2020	101-102 m
CQ31	41°30,5'N	09°23,6'E	20201017 17/10/2020	23 m
CQ32	41°25,8'N	09°15,8'E	20201017 17/10/2020	29 m
CR64	41°30,6'N	09°23,9'E	20201017 17/10/2020	50 m
CR65	41°30,5'N	09°23,6'E	20201017 17/10/2020	23 m
CR66	41°25,8'N	09°15,8'E	20201017 17/10/2020	12 m
CR67	41°25,8'N	09°15,8'E	20201017 17/10/2020	25-28 m
CS45	41°30,6'N	09°23,9'E	20201017 17/10/2020	50 m
CS46	41°25,8'N	09°15,8'E	20201017 17/10/2020	10-25 m
CB13	41°20,3'N	09°14,5'E	20201018 18/10/2020	20-30 m
CB14	41°20,8'N	09°16,5'E	20201018 18/10/2020	20-25 m
CD79	41°21,5'N	09°19,5'E	20201018 18/10/2020	40-52 m
CD80	41°21,6'N	09°17,3'E	20201018 18/10/2020	64-67 m
CD81	41°22,6'N	09°17,2'E	20201018 18/10/2020	53-53 m
CD82	41°24,9'N	09°15,7'E	20201018 18/10/2020	14-15 m
CD83	41°20,1'N	09°17,7'E	20201018 18/10/2020	64 m
CM32	41°31,5'N	09°16,2'E	20201018 18/10/2020	0 m
CM33	41°38,5'N	09°21,4'E	20201018 18/10/2020	0 m
CM34	41°38,4'N	09°21,2'E	20201018 18/10/2020	0 m
CM35	41°28,3'N	09°04'E	20201018 18/10/2020	0-1 m
CQ33	41°20,3'N	09°14,5'E	20201018 18/10/2020	27 m
CQ34	41°20,8'N	09°16,5'E	20201018 18/10/2020	24 m
CR68	41°20,3'N	09°14,5'E	20201018 18/10/2020	30 m
CR69	41°20,3'N	09°14,5'E	20201018 18/10/2020	46 m
CR70	41°20,8'N	09°16,5'E	20201018 18/10/2020	25-27 m
CR71	41°22,6'N	09°13,3'E	20201018 18/10/2020	0 m
CS47	41°20,3'N	09°14,5'E	20201018 18/10/2020	44 m
CS48	41°20,8'N	09°16,5'E	20201018 18/10/2020	25 m
CB15	41°21,8'N	09°11,6'E	20201019 19/10/2020	15-18 m
CD84	41°21,3'N	09°14'E	20201019 19/10/2020	64-65 m
CD85	41°19,2'N	09°12,9'E	20201019 19/10/2020	75-75 m
CD86	41°20,4'N	09°11,4'E	20201019 19/10/2020	50-50 m
CD87	41°21'N	09°10,6'E	20201019 19/10/2020	73-73 m
CD88	41°21,8'N	09°09,6'E	20201019 19/10/2020	73-73 m
CM36	41°27,4'N	09°05,9'E	20201019 19/10/2020	0 m
CM37	41°26,8'N	09°06,5'E	20201019 19/10/2020	0 m
CM39	41°20,2'N	09°15,5'E	20201019 19/10/2020	0-1 m
CM40	41°20'N	09°15,6'E	20201019 19/10/2020	0-2 m
CQ35	41°18,6'N	09°15,4'E	20201019 19/10/2020	24 m
CQ36	41°21,8'N	09°11,6'E	20201019 19/10/2020	17 m
CR72	41°18,6'N	09°15,4'E	20201019 19/10/2020	15-32 m
CR73	41°21,8'N	09°11,6'E	20201019 19/10/2020	15 m
CS49	41°19'N	09°15,8'E	20201019 19/10/2020	30-33 m
CS50	41°21,8'N	09°11,6'E	20201019 19/10/2020	15 m
CC01	41°20,5'N	09°06,5'E	20201020 20/10/2020	74-75 m
CD89	41°21'N	09°09,5'E	20201020 20/10/2020	53-53 m
CD90	41°22,9'N	09°09,5'E	20201020 20/10/2020	48-48 m
CM41	41°20,4'N	09°15'E	20201020 20/10/2020	0-2 m
CM42	41°20,3'N	09°15,4'E	20201020 20/10/2020	0 m
CQ37	41°23,1'N	09°09'E	20201020 20/10/2020	15 m
CR74	41°20,4'N	09°10,9'E	20201020 20/10/2020	40-44 m
CR75	41°20,4'N	09°10,9'E	20201020 20/10/2020	10-16 m
CR76	41°23,1'N	09°09'E	20201020 20/10/2020	13-15 m
CR77	41°23,3'N	09°08,6'E	20201020 20/10/2020	5 m
CR78	41°23,4'N	09°09,1'E	20201020 20/10/2020	3 m
CR79	41°23,4'N	09°09,6'E	20201020 20/10/2020	0 m
CS51	41°20,4'N	09°10,9'E	20201020 20/10/2020	43 m
CS52	41°23,4'N	09°09,1'E	20201020 20/10/2020	3 m
CB16	41°23,5'N	09°06,2'E	20201021 21/10/2020	20-24 m
CD91	41°23,6'N	09°04,1'E	20201021 21/10/2020	60-60 m
CD92	41°24,2'N	008°59'E	20201021 21/10/2020	82-82 m
CD93	41°25,3'N	09°05'E	20201021 21/10/2020	53-53 m
CD94	41°24,5'N	09°04,1'E	20201021 21/10/2020	63-64 m
CM43	41°27,4'N	09°02,4'E	20201021 21/10/2020	0-1 m
CQ38	41°23,5'N	09°06,2'E	20201021 21/10/2020	22 m
CQ39	41°27,2'N	09°01,3'E	20201021 21/10/2020	22 m
CR80	41°23,5'N	09°06,2'E	20201021 21/10/2020	30-37 m
CR81	41°27,2'N	09°01,3'E	20201021 21/10/2020	22-26 m
CS53	41°23,4'N	09°06,2'E	20201021 21/10/2020	37 m
CS54	41°27,2'N	09°01,3'E	20201021 21/10/2020	26 m
CB17	41°27,8'N	008°57,4'E	20201023 23/10/2020	27-34 m
CD95	41°26,6'N	008°55'E	20201023 23/10/2020	72-72 m
CD96	41°28'N	008°52,6'E	20201023 23/10/2020	55 m
CD97	41°24,5'N	008°50'E	20201023 23/10/2020	147-147 m
CM44	41°27,6'N	09°02,8'E	20201023 23/10/2020	0-1 m
CQ40	41°26,8'N	008°54'E	20201023 23/10/2020	24 m
CQ41	41°27,8'N	008°57,5'E	20201023 23/10/2020	26 m
CR82	41°26,8'N	008°54'E	20201023 23/10/2020	25-34 m
CR83	41°27,5'N	09°03'E	20201023 23/10/2020	0-1 m
CR84	41°27,8'N	008°57,4'E	20201023 23/10/2020	27-35 m
CR85	41°27,3'N	09°01,2'E	20201023 23/10/2020	0-1 m
CS55	41°26,8'N	008°54'E	20201023 23/10/2020	34 m
CB18	41°25,7'N	09°15,9'E	20201024 24/10/2020	34 m
CC02	41°24,8'N	09°01,4'E	20201024 24/10/2020	80-82 m
CD98	41°25,4'N	09°03,7'E	20201024 24/10/2020	60 m
CD99	41°23,4'N	09°06,7'E	20201024 24/10/2020	50 m
CM45	41°27,6'N	09°02,8'E	20201024 24/10/2020	0-1 m
CR87	41°24,3'N	09°13,5'E	20201024 24/10/2020	1 m
CS56	41°25,7'N	09°15,9'E	20201024 24/10/2020	5-25 m
CB19	41°23,6'N	09°07,6'E	20201025 25/10/2020	26 m
CD100	41°20,9'N	09°10,6'E	20201025 25/10/2020	74-74 m
CD101	41°21,1'N	09°10,5'E	20201025 25/10/2020	74-74 m
CD102	41°19,7'N	09°17,5'E	20201025 25/10/2020	68-68 m
CD103	41°22,7'N	09°17,7'E	20201025 25/10/2020	46-50 m
CQ42	41°26,2'N	09°04,8'E	20201025 25/10/2020	22 m
CQ43	41°23,6'N	09°07,6'E	20201025 25/10/2020	10 m
CR88	41°26,2'N	09°04,8'E	20201025 25/10/2020	47-52 m
CR89	41°26,2'N	09°04,8'E	20201025 25/10/2020	21-22 m
CR90	41°23,6'N	09°07,6'E	20201025 25/10/2020	5-26 m
CS57	41°26,2'N	09°04,8'E	20201025 25/10/2020	50 m
CB20	41°35,8'N	09°21,7'E	20201026 26/10/2020	3 m
CD104	41°31,2'N	09°20,9'E	20201026 26/10/2020	58-59 m
CD105	41°33,7'N	09°23,7'E	20201026 26/10/2020	47-47 m
CD106	41°29,3'N	09°17,6'E	20201026 26/10/2020	39-45 m
CM46	41°24,4'N	09°13,5'E	20201026 26/10/2020	0 m
CQ44	41°36,8'N	09°22,3'E	20201026 26/10/2020	14 m
CQ45	41°35,9'N	09°21,7'E	20201026 26/10/2020	14 m
CR91	41°36,7'N	09°22,4'E	20201026 26/10/2020	23-25 m
CR92	41°35,8'N	09°21,7'E	20201026 26/10/2020	3 m
CR93	41°36,5'N	09°19,1'E	20201026 26/10/2020	0 m
CR94	41°35,9'N	09°21,7'E	20201026 26/10/2020	14 m
CS58	41°36,7'N	09°22,4'E	20201026 26/10/2020	25 m
CB21	41°37,3'N	09°18,6'E	20201027 27/10/2020	2-3 m
CB22	41°35,3'N	09°17,4'E	20201027 27/10/2020	4 m
CD107	41°24,8'N	09°12,6'E	20201027 27/10/2020	1 m
CD108	41°24,8'N	09°13,6'E	20201027 27/10/2020	2 m
CD109	41°25,4'N	09°13,6'E	20201027 27/10/2020	2 m
CD110	41°24,4'N	09°13,5'E	20201027 27/10/2020	5 m
CM47	41°28,5'N	09°04,3'E	20201027 27/10/2020	0 m
CR95	41°37,3'N	09°18,6'E	20201027 27/10/2020	1-3 m
CR96	41°35,3'N	09°17,4'E	20201027 27/10/2020	4 m
CS59	41°37,3'N	09°18,6'E	20201027 27/10/2020	2-3 m
CS60	41°35,3'N	09°17,4'E	20201027 27/10/2020	4 m
CC03	41°24,2'N	09°18,3'E	20201028 28/10/2020	85-85 m
CD111	41°27,9'N	09°17,2'E	20201028 28/10/2020	48-48 m
CD112	41°28,1'N	09°19,7'E	20201028 28/10/2020	80-80 m
CQ46	41°21,9'N	09°18,8'E	20201028 28/10/2020	27 m
CQ47	41°23,6'N	09°16,1'E	20201028 28/10/2020	26 m
CR97	41°21,9'N	09°18,8'E	20201028 28/10/2020	30-33 m
CR98	41°23,6'N	09°16,1'E	20201028 28/10/2020	20-22 m
CS61	41°21,9'N	09°18,8'E	20201028 28/10/2020	30-33 m
CS62	41°23,6'N	09°16,1'E	20201028 28/10/2020	18-22 m
CB23	41°24,8'N	09°13'E	20201029 29/10/2020	2 m
CD113	41°23'N	09°15,9'E	20201029 29/10/2020	37-37 m
CD114	41°21'N	09°16,4'E	20201029 29/10/2020	60-60 m
CD115	41°22,2'N	09°16,2'E	20201029 29/10/2020	9 m
CM48	41°24,8'N	09°12,6'E	20201029 29/10/2020	0 m
CM49	41°26,5'N	09°13,3'E	20201029 29/10/2020	0 m
CR100	41°26,5'N	09°13,7'E	20201029 29/10/2020	6 m
CR99	41°24,8'N	09°13'E	20201029 29/10/2020	2-4 m
CS63	41°24,8'N	09°13'E	20201029 29/10/2020	2 m
CS64	41°26,5'N	09°13,7'E	20201029 29/10/2020	6 m
CD116	41°20,1'N	09°08,1'E	20201030 30/10/2020	75-75 m
CD117	41°21,7'N	09°12,4'E	20201030 30/10/2020	35-40 m
CD118	41°23,1'N	09°16,8'E	20201030 30/10/2020	60-60 m
CD119	41°22,8'N	09°19'E	20201030 30/10/2020	55-55 m
CQ48	41°23,7'N	09°07,6'E	20201030 30/10/2020	26 m
CR101	41°20,4'N	09°10,8'E	20201030 30/10/2020	42 m
CR102	41°23,7'N	09°07,6'E	20201030 30/10/2020	14-25 m
CS65	41°20,4'N	09°10,8'E	20201030 30/10/2020	42 m
CS66	41°23,7'N	09°07,6'E	20201030 30/10/2020	10-14 m
CQ49	41°23,2'N	09°08,4'E	20201031 31/10/2020	32 m
CR103	41°23,2'N	09°08,4'E	20201031 31/10/2020	37 m
CR104	41°23,4'N	09°05,6'E	20201031 31/10/2020	43-50 m
CS67	41°23,2'N	09°08,4'E	20201031 31/10/2020	37 m

Taxons par accès

Classe	Accès	Nombre de signalements