Morphology of first zoeal stage of four genera of alvinocaridid shrimps from hydrothermal vents and cold seeps: Implications for ecology, larval biology and phylogeny.
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Alvinocaridid shrimps are endemic species inhabiting hydrothermal vents and/or cold seeps. Although indirect evidences (genetic and lipid markers) suggest that their larval stages disperse widely and support large scale connectivity, larval life and mechanisms underlying dispersal are unknown in alvinocaridids. Here we provide for the first time detailed descriptions of the first larval stage (zoea I) of four alvinocaridid species: Rimicaris exoculata and Mirocaris fortunata from the Mid-Atlantic Ridge, Alvinocaris muricola from the Congo Basin and Nautilocaris saintlaurentae from the Western Pacific. The larvae were obtained from onboard hatching of brooding females (either at atmospheric pressure or at habitat pressure in hyperbaric chambers) and from the water column near adult habitats, sampled with plankton pumps or sediment traps. Major characteristics of the alvinocaridid larvae include undeveloped mandible and almost complete absence of setation in the inner margin of the mouth parts and maxillipeds. Although the larvae are very similar between the four species studied, some morphological features could be used for species identification. In addition, undeveloped mouthparts and the large amount of lipid reserves strongly support the occurrence of primary lecithotrophy in the early stage of alvinocaridids. Although lecithotrophy in decapod crustaceans is usually associated with abbreviated larval development, as a mechanism of larval retention, morphological and physiological evidences suggest the occurrence of an extended and lecithotrophic larval stage in the Alvinocarididae. These traits permit the colonization of widely dispersed and fragmented environments of hydrothermal vents and cold seeps. Distribution of larval traits along the phylogenetic reconstruction of the Alvinocarididae and related families suggest that lecithotrophy/planktotrophy and extended/abbreviated development have evolved independently along related families in all potential combinations. However, the Alvinocarididae is the only taxa with a combination of lecithotrophy and extended larval development.
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Absence of direct association for some eggs within the brood - those of the inner area - and high abundance of lipid reserves maintained even after hatching in Rimicaris larvae suggest that a similar role is quite unlikely for eggs.
“However, absence of direct association for some eggs within the brood – those of the inner area – and high abundance of lipid reserves maintained even after hatching in Rimicaris larvae (Hernández-Ávila et al., 2015) suggest that a similar role is quite unlikely for eggs.”
From Is It First the Egg or the Shrimp? – Diversity and Variation in Microbial Communities Colonizing Broods of the Vent Shrimp Rimicaris exoculata During Embryonic Development (2019) · cites this paper as Hernández-Ávila et al., 2015
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MUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662 · cited 2× · see citing works
“For the phylogenetic reconstructions , the sequences were aligned using MUSCLE [ 42 ] .”
Folmer, O., Black, M., Hoeh, W., Lutz, R., & Vrijenhoek, R. (1994) · PubMed · doi:10.5281/zenodo.15145663 · Cited by 15,546 · see citing works
Isolation of plant DNA from fresh tissue
Doyle, J. J. (1990) · Focus eBooks · Cited by 10,802 · see citing works
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
Drummond, A. J., Suchard, M. A., Xie, D., & Rambaut, A. (2012) · Molecular Biology and Evolution · doi:10.1093/molbev/mss075 · Cited by 9,991 · see citing works
Keane, T., Creevey, C. J., Pentony, M. M., Naughton, T. J., & Mclnerney, J. O. (2006) · BMC Evolutionary Biology · doi:10.1186/1471-2148-6-29 · Cited by 1,070 · see citing works
A Classification of Living and Fossil Genera of Decapod Crustaceans
Grave, S. D., Pentcheff, N. D., Ahyong, S. T., Chan, T., Crandall, K. A., Dworschak, P. C., Felder, D. L., Feldmann, R. M., Fransen, C. H. J. M., Goulding, L. Y. D., et al. (2009) · DSpace Repository (Smithsonian) · Cited by 679 · see citing works
First molecular evidence for the existence of a Tardigrada + Arthropoda clade
Giribet, G., Carranza, S., Baguñà, J., Riutort, M., & Ribera, C. (1996) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a025573 · Cited by 661 · cited 2× · see citing works
“5 mM of each primer (18S1 Forward and 1498 Reverse [34]), 1.”
Mecoptera is paraphyletic: multiple genes and phylogeny of Mecoptera and Siphonaptera
Whiting, M. F. (2002) · Zoologica Scripta · doi:10.1046/j.0300-3256.2001.00095.x · Cited by 542 · see citing works
The Biology of Decapod Crustacean Larvae
Anger, K. (2001) · Helmholtz-Zentrum für Polar-und Meeresforschung (Alfred-Wegener-Institut) · Cited by 471 · see citing works
Fourment, M., & Gibbs, M. J. (2006) · BMC Evolutionary Biology · doi:10.1186/1471-2148-6-1 · Cited by 454 · see citing works
(1942) · Nature · doi:10.1038/150474a0 · Cited by 446 · see citing works
Accuracy and standardization of brachyuran larval descriptions
Clark, P. F., de Calazans, D. K., & Pohle, G. W. (1998) · Invertebrate Reproduction & Development · doi:10.1080/07924259.1998.9652627 · Cited by 280 · see citing works
Eusociality in a coral-reef shrimp
Duffy, J. E. (1996) · Nature · doi:10.1038/381512a0 · Cited by 279 · cited 1× · see citing works
“These features are associated with restricted larval dispersal due to the short development period and larval or postlarval retention [56,58,64,68].”
Desbruyères, D., Almeida, A. J., Biscoito, M., Comtet, T., Khripounoff, A., Bris, N. L., Sarradin, P., & Segonzac, M. (2000) · Springer eBooks · doi:10.1007/978-94-017-1982-7_19 · Cited by 193 · see citing works
Desbruyères, D., Almeida, A. J., Biscoito, M., Comtet, T., Khripounoff, A., Bris, N. L., Sarradin, P., & Segonzac, M. (2000) · Hydrobiologia · doi:10.1023/a:1004175211848 · Cited by 159 · see citing works
Decapod Crustacean Phylogenetics
(2010) · CRC Press eBooks · doi:10.1201/9781420092592 · Cited by 126 · see citing works
Shank, T. M., Black, M. B., Halanych, K. M., Lutz, R. A., & Vrijenhoek, R. C. (1999) · Molecular Phylogenetics and Evolution · doi:10.1006/mpev.1999.0642 · Cited by 123 · see citing works
Decapod crustacean phylogenetics
Berggren, M. (2010) · Marine Biology Research · doi:10.1080/17451001003604796 · Cited by 120 · see citing works
Larvae from afar colonize deep-sea hydrothermal vents after a catastrophic eruption
Mullineaux, L. S., Adams, D. K., Mills, S. W., & Beaulieu, S. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913187107 · Cited by 119 · cited 1× · see citing works
“Also larval morphology can bring important cues about the early life history of the species [20] and provide useful morphological features to help interpreting both phylogenies [21,22] and ecology [23,24].”
Ponsard, J., Cambon-Bonavita, M.-A., Zbinden, M., Lepoint, G., Joassin, A., Corbari, L., Shillito, B., Durand, L., Cueff-Gauchard, V., & Compère, P. (2013) · The ISME Journal · doi:10.1038/ismej.2012.87 · Cited by 110 · cited 2× · see citing works
“Some species such as Rimicaris exoculata harbour symbiotic bacteria in their gill chambers and within their guts, which supply nutrients to the shrimp in a complex mutualistic association [4], whereas other species depend on grazing on chemoautotrophic bacteria and detritus in their adult stage [2].”
Thermal Limit for Metazoan Life in Question: In Vivo Heat Tolerance of the Pompeii Worm
Ravaux, J., Hamel, G., Zbinden, M., Tasiemski, A., Boutet, I., Léger, N., Tanguy, A., Jollivet, D., & Shillito, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064074 · Cited by 102 · cited 1× · see citing works
“exoculata collected during the BICOSE cruise in January 2014 at the TAG site of the MAR were brought on board with pressure compensation in the PERISCOP chamber [27] and were maintained in the BALIST chamber [28] at 300 bars and 5°C during 24 hours.”
Ecology and Biogeography of the Hydrothermal Vent Fauna of the Mid-Atlantic Ridge
Gebruk, A. V., Galkin, S. V., Vereshchaka, A. L., Moskalev, L. I., & SOUTHWARD, A. J. (1997) · Advances in marine biology · doi:10.1016/s0065-2881(08)60016-4 · Cited by 92 · cited 2× · see citing works
“However, information about larval stages is scarce, limited to reports of post-larvae in plankton samples [9,10], estimations of larval development mode based on egg size [11], and on board observations of larvae hatched from brooding females [10, 12–17].”
Li, C. P., Grave, S. D., Chan, T., Lei, H. C., & Chu, K. H. (2011) · Zoologischer Anzeiger · doi:10.1016/j.jcz.2011.04.003 · Cited by 88 · cited 10× · see citing works
“[ 76 ] highlighted the larval similarities between Campylonotidae and Oplophoridae sensu lato ( Oplophoridae+ - Acantephyridae ) based on the absence of external setae in maxillule , occurrence of four well developed endites on the maxilla and presence of exopods in all pereiopods .”
InfluentialGuri, M., Durand, L., Cueff-Gauchard, V., Zbinden, M., Crassous, P., Shillito, B., & Cambon-Bonavita, M.-A. (2012) · The ISME Journal · doi:10.1038/ismej.2011.133 · Cited by 87 · cited 1× · see citing works
“This suggests the accumulation of new lipid reserves before the recruitment to the vents, which could supply, at least partially the period between the recruitment, maturity and the acquisition of symbiotic bacteria [16].”
Self-citationPhylogeny of the infraorder Caridea based on mitochondrial and nuclear genes (Crustacea: Decapoda)
Bracken‐Grissom, H. D., Grave, S. D., Felder, D. L., Martin, J., & Crandall, K. A. (2009) · doi:10.1201/9781420092592-20 · Cited by 87 · see citing works
Teixeira, S., Serrão, E. Á., & Arnaud‐Haond, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038521 · Cited by 80 · cited 2× · see citing works
“However, populations of these shrimps exhibit high genetic connectivity along the MidAtlantic Ridge [5], between different vent and cold seeps systems in the Atlantic [6] and in vents systems of the Western Pacific and Indian Oceans [7,8].”
Biogeography and Potential Exchanges Among the Atlantic Equatorial Belt Cold-Seep Faunas
Olu, K., Cordes, E. E., Fisher, C. R., Brooks, J. M., Sibuet, M., & Desbruyères, D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011967 · Cited by 80 · cited 2× · see citing works
“However , this species is also found in the Barbados Prism , the Gulf of Mexico and the Blake Diapir [ 52 ] .”
Komai, T., & Segonzac, M. (2005) · Journal of Natural History · doi:10.1080/00222930400002499 · Cited by 73 · see citing works
Beedessee, G., Watanabe, H., Ogura, T., Nemoto, S., Yahagi, T., Nakagawa, S., Nakamura, K., Takai, K., Koonjul, M., & Marie, D. E. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081570 · Cited by 68 · cited 3× · see citing works
“However, populations of these shrimps exhibit high genetic connectivity along the MidAtlantic Ridge [5], between different vent and cold seeps systems in the Atlantic [6] and in vents systems of the Western Pacific and Indian Oceans [7,8].”
Aznar-Cormano, L., Brisset, J., Chan, T., Corbari, L., Puillandre, N., Utge, J., Zbinden, M., Zuccon, D., & Samadi, S. (2015) · Genetica · doi:10.1007/s10709-014-9807-0 · Cited by 67 · see citing works
Teixeira, S., Olu, K., Decker, C., da Cunha, R. L., Fuchs, S., Hourdez, S., Serrão, E. Á., & Arnaud‐Haond, S. (2013) · Molecular Ecology · doi:10.1111/mec.12419 · Cited by 67 · cited 11× · see citing works
“[6] and confirmed by Vereshchaka et al.”
InfluentialOn the Larvae of certain Crustacea Macrura, mainly from Bermuda.
Gurney, R., & Lebour, M. V. (1941) · Journal of the Linnean Society of London Zoology · doi:10.1111/j.1096-3642.1941.tb02290.x · Cited by 66 · cited 11× · see citing works
“Polyphyletic taxa , such as Oplophoridae ( sensu lato ) ( Ophophoridae + Acanthephyridae ) [ 39 , 41 , 47 ] and Pasiphaeidae [ 39 ] , exhibit distinct larval trait combinations , which further support the genetic evidence that split them into monophyletic groups .”
InfluentialPond, D., Segonzac, M., Bell, M., Dixon, D., Fallick, A. E., & Sargent, J. (1997) · Marine Ecology Progress Series · doi:10.3354/meps157221 · Cited by 65 · see citing works
Cowen, J. P., Bertram, M., Wakeham, S. G., Thomson, R. E., Lavelle, J. W., Baker, E. T., & Feely, R. A. (2001) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/s0967-0637(00)00070-4 · Cited by 61 · see citing works
Pradillon, F., Schmidt, A., Peplies, J., & Dubilier, N. (2007) · Marine Ecology Progress Series · doi:10.3354/meps333103 · Cited by 60 · see citing works
Reproductive patterns of decapod crustaceans from hydrothermal vents
Dover, C. L. V., Williams, A. B., & Berg, C. J. (1985) · Bulletin of the Biological Society of Washington · Cited by 60 · see citing works
Ramírez-Llodra, E., Tyler, P. A., & Copley, J. (2000) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315400002174 · Cited by 59 · see citing works
Thaler, A. D., Plouviez, S., Saleu, W., Alei, F., Jacobson, A., Boyle, E. A., Schultz, T. F., Carlsson, J., & Dover, C. L. V. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101345 · Cited by 58 · see citing works
Live capture of megafauna from 2300 m depth, using a newly designed Pressurized Recovery Device
Shillito, B., Hamel, G., Duchi, C., Cottin, D., Sarrazin, J., Sarradin, P., Ravaux, J., & Gaill, F. (2008) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2008.03.010 · Cited by 58 · see citing works
Spatial and temporal patterns in larval supply at hydrothermal vents in the northeast Pacific Ocean
Meta×as, A. (2004) · Limnology and Oceanography · doi:10.4319/lo.2004.49.6.1949 · Cited by 57 · cited 1× · see citing works
“Also larval morphology can bring important cues about the early life history of the species [20] and provide useful morphological features to help interpreting both phylogenies [21,22] and ecology [23,24].”
Larval development of the snapping shrimpAlpheus heterochaelisSay, reared in the laboratory
Knowlton, R. E. (1973) · Journal of Natural History · doi:10.1080/00222937300770231 · Cited by 57 · cited 2× · see citing works
“For instance, three distant and diverse monophyletic families as Alpheidae, Pandalidae and Atyidae [39–41] have species with planktotrophic and extended development but also species with lecithotrophic and abbreviated development [65,81,82].”
Extensive deep-sea dispersal of postlarval shrimp from a hydrothermal vent
Herring, P. J., & Dixon, D. R. (1998) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/s0967-0637(98)00050-8 · Cited by 50 · see citing works
Occurrence and recent long-distance dispersal of deep-sea hydrothermal vent shrimps
Tokuda, G., Yamada, A., Nakano, K., Arita, N. O., & Yamasaki, H. (2005) · Biology Letters · doi:10.1098/rsbl.2005.0420 · Cited by 44 · cited 1× · see citing works
“[75] suggest monophyly of Alvinocarididae with Palaemonidae, however general phylogenetic reconstruction of carideans using both mitochondrial and nuclear genes support the phylogenetic relationship of Alvinocarididae with Oplophoridae, Acanthephyridae, Nematocarcinidae, Pasiphaeidae [39–41], and also Agostocarididae,…”
Characterization of vent fauna at the Mid-Cayman Spreading Center
Plouviez, S., Jacobson, A., Wu, M., & Dover, C. L. V. (2014) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2014.11.011 · Cited by 42 · see citing works
Vereshchaka, A. L., Kulagin, D. N., & Lunina, A. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129975 · Cited by 40 · see citing works
Ecological aspects of hydrothermal vent animals in captivity at atmospheric pressure
Miyake, H., Kitada, M., Tsuchida, S., Okuyama, Y., & Nakamura, K. (2007) · Marine Ecology · doi:10.1111/j.1439-0485.2006.00115.x · Cited by 40 · see citing works
Komai, T., & Segonzac, M. (2008) · Journal of Shellfish Research · doi:10.2983/0730-8000(2008)27[21:trothv]2.0.co;2 · Cited by 40 · see citing works
Phylogenetic analysis using rDNA reveals polyphyly of Oplophoridae (Decapoda : Caridea)
Chan, T., Lei, H. C., Li, C. P., & Chu, K. H. (2010) · Invertebrate Systematics · doi:10.1071/is09049 · Cited by 38 · cited 12× · see citing works
“Polyphyletic taxa, such as Oplophoridae (sensu lato) (Ophophoridae + Acanthephyridae) [39,41,47] and Pasiphaeidae [39], exhibit distinct larval trait combinations, which further support the genetic evidence that split them into monophyletic groups.”
InfluentialPressure vessels forin vivostudies of deep-sea fauna
Pradillon, F., Shillito, B., Chervin, J. C., Hamel, G., & Gaill, F. (2004) · High Pressure Research · doi:10.1080/08957950410001699818 · Cited by 36 · cited 1× · see citing works
“Larvae were maintained in the PICCEL chamber [29] at 300 bars and 8°C during 96 hours.”
Copley, J., & Young, C. M. (2006) · Marine Ecology Progress Series · doi:10.3354/meps315199 · Cited by 35 · cited 18× · see citing works
“Differences in larval morphology of alvinocaridid larvae with others caridean shrimps General characters in the Alvinocarididae first larvae include tiny rostrum hidden between the eyes , pterisgostomial spine present , setation absent in mouth parts ( except for scaphognathite and occasionally the tip of the endopod…”
InfluentialNye, V., Copley, J., & Tyler, P. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060319 · Cited by 32 · cited 1× · see citing works
“As other carideans, brooding females of alvinocaridids maintain their eggs below the abdomen during the embryonic development until the hatching, which is followed by a planktonic larval stage [15,17,18].”
The Abbreviated Larval Development of Caridina Singhalensis Ortmann, 1894 (Decapoda, Atyidae)
Benzie, J., & de Silva, P. K. (1983) · Journal of Crustacean Biology · doi:10.2307/1547857 · Cited by 31 · see citing works
Anger, K., & Schuh, M. (1992) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(92)90280-4 · Cited by 30 · cited 2× · see citing works
“These features are associated with restricted larval dispersal due to the short development period and larval or postlarval retention [56,58,64,68].”
Ramírez-Llodra, E., & Segonzac, M. (2006) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315406014378 · Cited by 30 · cited 1× · see citing works
“As other carideans, brooding females of alvinocaridids maintain their eggs below the abdomen during the embryonic development until the hatching, which is followed by a planktonic larval stage [15,17,18].”
Bolaños, J., Cuesta, J. A., Hernández, G., Hernández, J., & Felder, D. L. (2004) · Scientia Marina · doi:10.3989/scimar.2004.68n3373 · Cited by 29 · see citing works
Thatje, S., Lovrich, G. A., & Anger, K. (2003) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2003.09.010 · Cited by 29 · see citing works
Zelnio, K. A., & Hourdez, S. (2009) · Proceedings of the Biological Society of Washington · doi:10.2988/07-28.1 · Cited by 28 · see citing works
Komai, T., & Segonzac, M. (2003) · Institutional Archive of Ifremer (French Research Institute for Exploitation of the Sea) · doi:10.21411/cbm.a.b886ea84 · Cited by 27 · see citing works
Tyler, P. A., & Dixon, D. R. (2000) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315400002605 · Cited by 26 · see citing works
Pond, D. W., SARGENT, J. R., Fallick, A. E., Allen, C., Bell, M. V., & Dixon, D. R. (2000) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/s0967-0637(99)00050-3 · Cited by 23 · see citing works
Koyama, S., Nagahama, T., Ootsu, N., Takayama, T., Horii, M., Konishi, S., Miwa, T., Ishikawa, Y., & Aizawa, M. (2005) · Marine Biotechnology · doi:10.1007/s10126-004-3050-0 · Cited by 22 · cited 2× · see citing works
“Although Alvinocarididae early stages seem to tolerate large pressure variation, with larvae that can, in some cases, hatch and survive at atmospheric pressure ([12,13], present study), temperature tolerance may constrain the upper limit of the bathypelagic habitat [12].”
Bacardit, R., & Thatje, S. (2000) · Crustaceana · doi:10.1163/156854000504697 · Cited by 21 · see citing works
González-Gordillo, J. I., Schubart, C. D., & Anger, K. (2009) · Journal of Crustacean Biology · doi:10.1651/08-3110.1 · Cited by 19 · see citing works
Larval Stages of Pasiphaea Siv Ado and Some Other Pasiphaeidae (Decapoda)
Williamson, D. I. (1960) · Crustaceana · doi:10.1163/156854060x00339 · Cited by 19 · see citing works
Larvae of deep-sea chemosynthetic ecosystem animals in captivity
Miyake, H., Kitada, M., Itoh, T., Nemoto, S., Okuyama, Y., Watanabe, H., Tsuchida, S., Inoue, K., Kado, R., Ikeda, S., et al. (2010) · Station Biologique de Roscoff · doi:10.21411/cbm.a.6a25f44a · Cited by 18 · see citing works
Thatje, S., Smith, K., Marsh, L., & Tyler, P. (2015) · Aquatic Biology · doi:10.3354/sedao00011 · Cited by 15 · cited 1× · see citing works
“Lipid reserves in a lecithotrophic larvae or lacking of developed feeding structures has been documented previously in land crabs [56,57], symbiotic crabs [58], symmetric hermit crabs [59–61], galatheids [62,63], alpheid shrimps [64,65], freshwater shrimps (Atydae, [66]) and in some deep water Oplophoridae, Acanthephy…”
Terossi, M., Cuesta, J. A., Wehrtmann, I. S., & Mantelatto, F. L. M. (2010) · Zootaxa · doi:10.11646/zootaxa.2624.1.2 · Cited by 13 · see citing works
Psalidopus: the scissor-foot shrimps (Crustacea: Decapoda: Caridea)
Chace, F. A., & Holthuis, L. B. (1978) · Smithsonian contributions to zoology · doi:10.5479/si.00810282.277 · Cited by 13 · see citing works
Borowsky, R. L., & Borowsky, B. (1990) · Crustaceana · doi:10.1163/156854090x00516 · Cited by 12 · see citing works
Thatje, S., Tapella, F., Bacardit, R., Lovrich, G. A., & Romero, M. C. (2001) · Journal of Crustacean Biology · doi:10.1651/0278-0372(2001)021[0492:dakttz]2.0.co;2 · Cited by 12 · cited 1× · see citing works
“[76] highlighted the larval similarities between Campylonotidae and Oplophoridae sensu lato (Oplophoridae+Acantephyridae) based on the absence of external setae in maxillule, occurrence of four well developed endites on the maxilla and presence of exopods in all pereiopods.”
The prezoeal stage in various decapod crustaceans
Hong, S. Y. (1988) · Journal of Natural History · doi:10.1080/00222938800770651 · Cited by 11 · cited 2× · see citing works
“The absence of a cover layer over the appendices and telson confirms that larvae analyzed here are at first zoeal stage instead of a prezoea stage [50,51] that could occur just after hatching.”
Clark, P. F., & Ng, P. K. L. (2008) · doi:10.5281/zenodo.5341343 · Cited by 11 · see citing works
Recent advances in our understanding of the life history of bresiliid vent shrimps on the MAR
Dixon, D. R., Dixon, L. R. J., & POND, D. W. (1998) · Cahiers de biologie marine · doi:10.21411/cbm.a.7a5ba34 · Cited by 9 · see citing works
Campos, E., & Hernández‐Ávila, I. (2010) · Zootaxa · doi:10.11646/zootaxa.2691.1.2 · Cited by 8 · see citing works
HERRING, P. J. (1998) · Cahiers de biologie marine · doi:10.21411/cbm.a.f342c900 · Cited by 8 · see citing works
Konishi, K., & Imafuku, M. (2000) · Crustacean Research · doi:10.18353/crustacea.29.0_65 · Cited by 7 · see citing works
Saito, T., & Konishi, K. (2002) · Crustaceana · doi:10.1163/156854002760095642 · Cited by 7 · see citing works
McLaughlin, P. A., & Lemaitre, R. (2008) · Zootaxa · doi:10.11646/zootaxa.1911.1.3 · Cited by 7 · see citing works
Nanjo, N., & Konishi, K. (2009) · Crustacean Research · doi:10.18353/crustacea.38.0_77 · Cited by 6 · cited 2× · see citing works
“Additionally, in three genera of Oplophoridae (Systellaspis, Janicella and Oplophorus), two Acanthephyridae (Hymenodora and Acanthephyra) and two Pasiphaeidae (Pasiphaea and Parapasiphae) a first larval stage with undeveloped mouth parts has been described [67,69,77].”
A Late Embryo of the Deep Water Shrimp Psalidopus Barbouri Chace, 1939 (Decapoda, Caridea)
Martin, J. W. (1986) · Crustaceana · doi:10.1163/156854086x00476 · Cited by 3 · see citing works
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1 of the 81 references couldn’t be matched to a known paper.
Research works printed but not linked: 4
- [29]Pradillon F, Shillito B, Chervin J-C, Hamel G, Gaill F (2004) Pressure vessels for in vivo studies of deep-sea fauna. High Press Res 24: 237– 246.
- [30]Fouquet Y, Alix AS, Birot D, Chéron S, Charlou JL, Donval JP, et al (2015) Discovery of extensive hydrothermal fields in the Wallis and Futuna back-arc environment (SW Pacific). Marine Mineral Ressources in a Sustainable World. 13th SGA Biennial Meeting 2015, Proceedings, vol 3: 1223–1226.
- [45]Rabalais NN, Gore RH (1985) Abbreviated development in decapods In: Wenner AM, Schram FR, editors. Larval Growth. Rotterdam: Balkema pp. 67– 126.
- [54]Bauer R (2004) Remarkable shrimps: adaptations and natural history of Carideans: University Oklahoma Press.
Cited by
Sorted by citations
Sun, S., Hui, M., Wang, M., & Sha, Z. (2017) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2017.11.002 · Cited by 73 · see citing works
“The alvinocaridid shrimps are endemic to deep-sea hydrothermal vent and cold seep environments, and constitute the predominant faunal biomass of various hydrothermal and cold seep ecosystems (Nye et al., 2012; Yahagi et al., 2014; Hernandez-Avila et al., 2015).”
BackgroundZhang, J., Sun, Q.-L., Luan, Z., Lian, C., & Sun, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-02073-9 · Cited by 51 · see citing works
Zbinden, M., & Cambon‐Bonavita, M. (2020) · Marine Ecology Progress Series · doi:10.3354/meps13467 · Cited by 38 · see citing works
“Although knowledge on the reproduction and life cycle of R. exoculata has progressed in recent years (Hernandez-Avila et al. 2015, Hernandez-Avila 2016, Methou et al. 2019, 2020), there are still many unresolved questions.”
BackgroundMethodInfluentialGu, H., Sun, Q.-L., Jiang, S., Zhang, J., & Sun, L. (2018) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2018.03.016 · Cited by 36 · see citing works
A Crustin from Hydrothermal Vent Shrimp: Antimicrobial Activity and Mechanism
Wang, Y., Zhang, J., Sun, Y., & Sun, L. (2021) · Marine Drugs · doi:10.3390/md19030176 · Cited by 35 · see citing works
“Shrimps of the family Alvinocarididae inhabit the deep waters in Atlantic, Pacific, and Indian Oceans, especially the hydrothermal vents and cold seeps, where they are often found to be the dominant fauna [25,26].”
BackgroundMethou, P., Hernández-Ávila, I., Aube, J., Cueff-Gauchard, V., Gayet, N., Amand, L., Shillito, B., Pradillon, F., & Cambon-Bonavita, M.-A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00808 · Cited by 30 · see citing works
Le Bloa, S., Boidin-Wichlacz, C., Cueff-Gauchard, V., Rosa, R. D., Cuvillier-Hot, V., Durand, L., Methou, P., Pradillon, F., Cambon-Bonavita, M.-A., & Tasiemski, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01511 · Cited by 30 · see citing works
“After hatching, larvae undergo several molting events, still uncharacterized, to the juvenile stage A, while dispersing in the water column before their recruitment to a new hydrothermal vent field (5, 67).”
BackgroundLiao, Y., Grave, S. D., Ho, T. W., Ip, B. H. Y., Tsang, L. M., Chan, T., & Chu, K. H. (2017) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2017.07.021 · Cited by 28 · see citing works
“(4) Hernández-Ávila et al. (2015) 318 summarized selected larval features for a range of carideans, including pasiphaeids, generally 319 finding intra-familial consistency.”
BackgroundKersten, O., Smith, C. R., & Vetter, E. W. (2017) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2017.07.001 · Cited by 26 · see citing works
Sun, S., Sha, Z., & Wang, Y. (2018) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2018.10.001 · Cited by 22 · see citing works
A g-Type Lysozyme from Deep-Sea Hydrothermal Vent Shrimp Kills Selectively Gram-Negative Bacteria
Luo, J.-C., Zhang, J., & Sun, L. (2021) · Molecules · doi:10.3390/molecules26247624 · Cited by 21 · see citing works
Machon, J., Lucas, P., Ravaux, J., & Zbinden, M. (2018) · Chemical Senses · doi:10.1093/chemse/bjy041 · Cited by 19 · see citing works
Pereira, O. S., Shimabukuro, M., Bernardino, A. F., & Sumida, P. Y. G. (2020) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2020.103343 · Cited by 14 · see citing works
Brown, A., Thatje, S., Martinez, A., Pond, D. W., & Oliphant, A. (2019) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2019.03.011 · Cited by 12 · see citing works
“Indeed, Alvinocarididae hydrothermal vent shrimp share closer affinities with other deep-water shrimp families and non-hydrothermal vent shrimp families with both shallow-water and deep-water representatives, than with exclusively shallow-water shrimp families (Bracken et al., 2009; Li et al., 2011; Aznar-Cormano et a…”
BackgroundLife-history traits of alvinocaridid shrimps inhabiting chemosynthetic ecosystems around Japan
Methou, P., Nye, V., Copley, J., Watanabe, H., Nagai, Y., & Chen, C. (2023) · Marine Biology · doi:10.1007/s00227-023-04221-4 · Cited by 10 · see citing works
“…stages, with the O. loihi hatched larva exhibiting carapace sizes or total sizes similar to those seen in R. exoculata or M. fortunata hatched larva (Hernández-Ávila et al. 2015) despite larger mean egg sizes than O. loihi for these two species (Ramirez-Llodra et al. 2000; Methou et al. 2022b).”
Hernández‐Ávila, I., Cambon‐Bonavita, M., Sarrazin, J., & Pradillon, F. (2021) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2022.103827 · Cited by 10 · see citing works
Sun, S., Sha, Z., & Wang, Y. (2021) · Journal of Oceanology and Limnology · doi:10.1007/s00343-020-0266-4 · Cited by 10 · see citing works
Methou, P., Ogawa, N. O., Nomaki, H., Ohkouchi, N., Chen, C., & Schnabel, K. E. (2024) · Marine Ecology Progress Series · doi:10.3354/meps14611 · Cited by 8 · see citing works
Deep-sea ecosystems of the North Atlantic Ocean: discovery, status, function and future challenges
Allcock, A. L., Amon, D. J., Bridges, A. E. H., Colaço, A., Escobar-Briones, E. G., Hilário, A., Howell, K. L., Mestre, N. C., Muller-Karger, F. E., Priede, I. G., et al. (2025) · Deep Sea Research Part I Oceanographic Research Papers · doi:10.1016/j.dsr.2025.104580 · Cited by 6 · see citing works
A Mysterious World Revealed: Larval-Adult Matching of Deep-Sea Shrimps from the Gulf of Mexico
Varela, C., & Bracken‐Grissom, H. D. (2021) · Diversity · doi:10.3390/d13100457 · Cited by 6 · see citing works
Guéganton, M., Methou, P., Aubé, J., Noël, C., Rouxel, O., Cueff‐Gauchard, V., Gayet, N., Durand, L., Pradillon, F., & Cambon‐Bonavita, M. (2024) · Ecology and Evolution · doi:10.1002/ece3.70369 · Cited by 6 · see citing works
Dai, Q., Xu, T., Li, Y., Sun, Y., Lin, Y., Yahagi, T., Perez, M., Qian, P., & Qiu, J. (2025) · Integrative Zoology · doi:10.1111/1749-4877.12954 · Cited by 3 · see citing works
“Previous morphological observations (Hernández-Ávila, Cambon-Bonavita, and Pradillon 2015; Ramirez-Llodra and Segonzac 2006), along with analyses of fatty acid biomarkers and stable isotope analyses (Stevens et al. 2008), have shown that alvinocaridid shrimps produce larvae with well-developed eyes.”
Methou, P., Johnson, S. B., Sherrin, J., Shank, T. M., Chen, C., & Tunnicliffe, V. (2025) · Molecular Ecology · doi:10.1111/mec.70119 · Cited by 4 · see citing works
“Morphological features of their hatched larvae, including R. loihi , also support a long pelagic larval duration (PLD) (Hernández-Ávila et al. 2015; Methou et al. 2023).”
Bartilotti, C., & Santos, A. D. (2019) · PeerJ · doi:10.7717/peerj.7334 · Cited by 2 · see citing works
Three-dimensional management needs of deep-sea hydrothermal vent ecosystems
Gollner, S., Jaeckel, A. L., Robb, S., Sarrazin, J., Tunnicliffe, V., van der Grient, J., Amon, D. J., Bellanger, M., Blanchard, C., Colaço, A., et al. (2025) · Marine Policy · doi:10.1016/j.marpol.2025.106959 · Cited by 1 · see citing works
Portanier, E., Adrien Tran Lu, Y., Pradillon, F., Daguin‐Thiébaut, C., Ruault, S., Collins, P. C., Omnes, E., Fuchs, S., Carlsson, J., Jollivet, D., et al. (2026) · Conservation Biology · doi:10.1111/cobi.70284 · Cited by 1 · see citing works
Soundharapandiyan, N., Kannan, R. R., & Alphonse, C. R. W. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08700-1 · Cited by 1 · see citing works
“The majority of the faunal biomass is in a variety of hydrothermal ecosystems as the vent-endemic species of Alvinocarididae shrimps [5].”
BackgroundMethou, P., Chen, C., Watanabe, H., Cambon‐Bonavita, M., & Pradillon, F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.10.456763
“No size variation was found among first zoeal larval stages of four phylogenetically distinct alvinocaridids [45].”
BackgroundEffects of developmental mode on genome size in shrimps (Dendrobranchiata and Caridea)
de Moraes, I. R. R., Castilho, A. L., & Hultgren, K. M. (2025) · Journal of Crustacean Biology · doi:10.1093/jcbiol/ruaf040
Apremont, V. (2017) · doi:10.70675/d9f20765zc6ecz461bza22dz324ebafb09f8
“Cependant, il semblerait, après analyses moléculaires, que ces regroupements soient en réalité des juvéniles de Rimicaris chacei, la différenciatio e t e les deu esp es, au stade la ai e o e au stade ju ile ta t pas ais e ia des données de vidéos ou même des observations morphologiques (Hernández-Avila et al., 2015).”
BackgroundInfluentialMethou, P. (2019) · theses.fr (ABES) · doi:10.70675/bf7aab7fzc361z40c2z9ac6z34c7f7b317db · Cited by 1 · see citing works
- Authors
- Hernández-Ávila, I., Cambon-Bonavita, M.-A., & Pradillon, F.
- Affiliations
- Ifremer (FR)
- Corresponding author
- Pradillon, Florence
- ORCID
- Pradillon, Florence
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2015-12-28
- Volume
- 10
- Issue
- 12
- Pages
- e0144657
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC4694104
- OpenAlex
- W2198357860
- Cited by
- 37
- References
- 81
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 2 · 2023: 2 · 2021: 6 · 2020: 3 · 2019: 8 · 2018: 4 · 2017: 6
- FWCI
- 2.77
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Institutional Archive of Ifremer (French Research Institute for Exploitation of the Sea) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Greater South Information System
- Funders
- European Commission (2007–2013, FP7 2007-2013, FP7/2007, 603418, FP6-GOCE-CT-2003-505342)
- Agence Nationale de la Recherche (018-01, ANR-08-BLAN-0252)
- Campus France (FP7/2007-2013)
- Topics
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Marine Biology and Ecology Research
- Physical Sciences › Environmental Science › Ecology › Crustacean biology and ecology
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Subterranean biodiversity and taxonomy
- Keywords
- Alvinocarididae, zoea I, larval morphology, hydrothermal vents, cold seeps, Rimicaris exoculata, lecithotrophy, planktotrophy, larval dispersal, larval retention, mouthpart development, lipid reserves, phylogenetic evolution, Decapoda
- MeSH terms
- Animals, Larva, Marine Biology, Oceans and Seas, Phylogeny, Shellfish, Ecosystem, Decapoda, Hydrothermal Vents
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