Topical issue on Crayfish
Open Access
Review
Issue
Knowl. Manag. Aquat. Ecosyst.
Number 417, 2016
Topical issue on Crayfish
Article Number 33
Number of page(s) 15
DOI https://doi.org/10.1051/kmae/2016020
Published online 16 September 2016
  • Abe M. and Fukuhara H., 1996. Protogynous hermaphroditism in the brackish and freshwater isopod, Gnorimosphaeroma naktongense (Crustacea: Isopoda, Sphaeromatidae). Zool. Sci., 13(2), 325–329. [CrossRef]
  • Adams J., Greenwood P. and Naylor C., 1987. Evolutionary aspects of environmental sex determination. Int. J. Inver. Rep. Dev., 11, 123–135. [CrossRef]
  • Adiyodi R.G., 1984. Seasonal changes and the role of eyestalks in the activity of the androgenic gland of the crab, Paratelphusa hydrodromous (Herbst). Comp. Physiol. Ecol., 9, 427–431.
  • Aguilar M.B., Falchetto R., Shabanowitz J., Hunt D.F. and Huberman A., 1996. Complete primary structure of the molt-inhibiting hormone (MIH) of the Mexican crayfish Procambarus bouvieri (Ortmann). Peptides, 17, 367–374. [CrossRef] [PubMed]
  • Alfaro J., Muñoz N., Vargas M. and Komen J., 2003. Induction of sperm activation in open and closed thelycum penaeoid shrimps. Aquaculture, 216, 371–381. [CrossRef]
  • Alfaro J., Ulate K. and Vargas M., 2007. Sperm maturation and capacitation in the open thelycum shrimp Litopenaeus (Crustacea: Decapoda: Penaeoidea). Aquaculture, 270, 436–442. [CrossRef]
  • Almeida A.O. and Buckup L., 2000. Occurrence of protandric hermaphroditism in a population of the neotropical freshwater crayfish Parastacus brasiliensis (Parastacidae). J. Crustacean Biol., 20, 224–230. [CrossRef]
  • Anderson W.A. and Ellis R.A., 1967. Cytodifferentiation of the crayfish spermatozoon: acrosome formation, transformation of mitochondria and development of microtubules. Z. Zellforsch. Mik. Ana., 77, 80–94. [CrossRef]
  • Andrews E.A. 1906a. The annulus ventralis. Proc. Boston Soc. Nat. Hist., 32, 427–479.
  • Andrews E.A., 1906b. Egg-laying of crayfish. Am. Nat., 40, 343–356. [CrossRef]
  • Aungsuchawan S., Browdy C.L. and Withyachumnarnkul B., 2011. Sperm capacitation of the shrimp Litopenaeus vannamei. Aquacult. Res., 42, 188–195. [CrossRef]
  • Awari S.A. and Dube K., 1999. Histological and histochemical study of androgenic gland of Macrobrachium rosenbergii (DE MAN). J. Aquat. Trop., 14, 101–112.
  • Azzouna A., Greve P. and Martin G., 2004. Sexual differentiation traits in functional males with female genital apertures (male symbol fga) in the woodlice Armadillidium vulgare Latr. (Isopoda, Crustacea). Gen. Comp. Endocrinol., 138, 42–49. [CrossRef] [PubMed]
  • Barki A., Karplus I., Manor R. and Sagi A., 2006. Intersexuality and behavior in crayfish: The de-masculinization effects of androgenic gland ablation. Horm. Behav., 50, 322–331. [CrossRef]
  • Beach D. and Talbot P., 1987. Ultrastructural Comparison of Sperm from the Crayfishes Cherax tenuimanus and Cherax albidus. J. Crustacean Biol., 7, 205–218. [CrossRef]
  • Bell G., 1982. The masterpiece of nature. The evolution and genetics of sexuality. Univ. of California Pr., June, 1982.
  • Boecking D., Dircksen H. and Keller R., 2002. The crustacean peptides of the CHH/MIH/GIH family. In: Wiese K. (ed.), The Crustacean Nervous System. Springer-Verlag, Heidelberg, pp. 84–97.
  • Borg B. and van den Hurk R., 1983. Oocytes in the testes of the three-spined stickleback, Gasterosteus aculeatus. Copeia, 1983(1), 259–261.
  • Bracken-Grissom H.D., Ahyong S.T., Wilkinson R.D., Feldmann R.M., Schweitzer C.E., Breinholt J.W., Bendall M., Palero F., Chan T.Y., Felder D.L., Robles R., Chu K.H., Tsang L.M., Kim D., Martin J.W. and Crandall K.A., 2014. The emergence of lobsters: phylogenetic relationships, morphological evolution and divergence time comparisons of an ancient group (decapoda: achelata, astacidea, glypheidea, polychelida). Syst. Biol., 63, 457–479. [CrossRef] [PubMed]
  • Braga A., Suita de Castro A.L., Poersch H.L. and Wasielesky W., 2014. Spermatozoal capacitation of pink shrimp Farfantepenaeus paulensis. Aquaculture, 430, 207–210. [CrossRef]
  • Brook H.J., Rawlings T.A. and Davies R.W., 1994. Protogynous sex change in the intertidal isopod Gnorimosphaeroma oregonense (Crustacea: Isopoda). Biol. Bull., 187(1), 99–111. [CrossRef]
  • Browne R.A., 1992. Population genetics and ecology of Artemia: insights into parthenogenetic reproduction. Trends Ecol. Evol., 7, 232–237. [CrossRef] [PubMed]
  • Bunn J.J., Koenders A., Austin C.M. and Horwitz P., 2008. Identification of Hairy, Smooth And Hybrid Marron (Decapoda: Parastacidae) in the Margaret River: Morphology And Allozymes.
  • Buřič M., Kouba A. and Kozák P., 2009. Spring mating period in Orconectes limosus: the reason for movement. Aquat. Sci., 71, 473–477. [CrossRef]
  • Buřič M., Kouba A. and Kozák P. 2010. Intra-sex dimorphism in crayfish females. Zoology, 113, 301–307. [CrossRef]
  • Buřič M., Hulák M., Kouba A., Petrusek A. and Kozák P., 2011. A successful crayfish invader is capable of facultative parthenogenesis: A novel reproductive mode in decapod crustaceans. PloS One, 6, e20281. [CrossRef] [PubMed]
  • Buřič M., Kouba A. and Kozák P., 2013. Reproductive plasticity in freshwater invader: from long-term sperm storage to parthenogenesis. PloS one, 8, e77597. [CrossRef] [PubMed]
  • Buřič M., Veselý L. and Kouba A. 2015. Molting and growth of adult signal crayfish Pacifastacus leniusculus (Dana 1852): Effective investments due to seasonal morphological changes? European Crayfish Conference Research and Management, 9th–12th April, Landau, Germany, Abstract book, p. 61.
  • Carpenter A., 1978. Protandry in the freshwater shrimp, Paratya curvirostris (Heller, 1862) (Decapoda: Atyidae), with a review of the phenomenon and its significance in the Decapoda. J. R. Soc. N. Z., 8(4), 343–358. [CrossRef]
  • Chang E.S. and Sagi A., 2008. Male reproductive hormones. In: Mente E. (ed.), Reproductive biology of crustaceans. Science Publishers, Enfield, NH.
  • Charniaux-Cotton H., 1975. Hermaphroditism and gynandromorphism in malacostracan crustacea. In: Reinboth R. (ed.), Intersexuality in the Animal Kingdom. Springer, Berlin, Heidelberg, pp. 91–105.
  • Charniaux-Cotton H. and Payen G., 1985. Sexual differentiation. Mantel L.H. (ed.), In The Biology of Crustacea. Academic Press, Orlando, Florida, pp. 217–299.
  • Charniaux-Cotton H. and Payen G., 1988. Crustacean reproduction. In: Laufer H. and Downer R.G.H. (eds.), Endocrinology of Selected Invertebrate Types. A.R. Liss, New York, 279–303.
  • Crocker D.W., 1957. The crayfishes of New York (Decapoda: Astacidae). New York State Mus., Sci. Serv., Bull., 355, 1–97.
  • Crocker D.W. and Barr D.W., 1968. Handbook of the crayfishes of Ontario. published for Royal Ontario Museum by University of Toronto Press.
  • Cukerzis J., 1968. Interspecific relations between Astacus astacus L. and A. leptoductylus Esch. Pañstwowe Wydawnictwo Naukowe.
  • Dubé P. and Portelance B., 1992. Temperature and photoperiod effects on ovarian maturation and egg laying of the crayfish, Orconectes limosus. Aquaculture, 102, 161–168. [CrossRef]
  • Dudenhausen E.E. and Talbot P., 1983. An ultrastructural comparison of soft and hardened spermatophores from the crayfish Pacifastacus leniusculus Dana. Can. J. Zoolog., 61, 182–194. [CrossRef]
  • Duriš Z., Horká I. and Vavricek O., 2001. K populacni ekologii raku na Karvinsku (On population ecology of crayfish in the Karvina District). Biologie Ekologie, 8, 118–126.
  • Duriš z., Horká I. and Kozák P., 2015. Morphology and Anatomy of Crayfish. In: Kozák P. (ed.), Crayfish Biology and Culture. University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Vodnany, Czech Republic, pp. 165–200.
  • Felgenhauer B.E. and Abele L.G., 1991. Morphological diversity of decapod spermatozoa. In: Bauer R.T. and Martin J.W. (eds.), Crustacean Sexual Biology. Columbia University Press, New York, NY, pp. 322–341.
  • Filipova L., Kozubikova E. and Petrusek A., 2009. Allozyme variation in Czech populations of the invasive spiny-cheek crayfish Orconectes limosus (Cambaridae). Knowl. Manag. Aquat. Ecosyst., 10, 394–395.
  • Fingerman M., 1995. Endocrine Mechanisms in Crayfish, with Emphasis on Reproduction and Neurotransmitter Regulation of Hormone Release. Am. Zool., 35, 68–78. [CrossRef]
  • Ford A.T., Fernandes T.F., Rider S.A., Read P.A., Robinson C.D. and Davies I.M., 2004. Endocrine disruption in a marine amphipod? Field observations of intersexuality and de-masculinisation. Mar. Environ. Res., 58, 169–173. [CrossRef] [PubMed]
  • Foulks N.B. and Hoffman D.L., 1974. The effects of eyestalk ablation and B-ecdysone on RNA synthesis in the androgenic glands of the protandric shrimp, Pandalus platyceros Brandt. Gen. Comp. Endocrinol., 22, 439–447. [CrossRef] [PubMed]
  • Furrer S.C., Cantieni M. and Duvoisin N., 1999. Freshly hatched hybrids between Astacus astacus and Astacus leptodactylus differ in chela shape from purebred offspring. Freshw. Crayfish, 12, 90–97.
  • Gherardi F., 2007. Biological invaders in inland waters: Profiles, distribution and threats. Quarterly Rev. Biol., 44, 504–542.
  • Ghiselin M.T., 1969. The evolution of hermaphroditism among animals. Quarterly Rev. Biol., 189–208.
  • Golubev, A.P., Khmeleva, N.N., Alekhnovich, A.V., Roshchina, N.N. and Stolyarova, S.A., 2001. Influence of reproduction on variability of life history parameters in Artemia salina (Crustacea, Anostraca). Entomological Review, 81(1), 96.
  • González-Tizón A.M., Rojo V., Menini E., Torrecilla Z. and Martínez-Lage A., 2013. Karyological analysis of the shrimp (Decapoda: Palaemonidae). J. Crustacean Biol., 33, 843–848. [CrossRef]
  • Grave D.S., Pentcheff N.D., Ahyong S.T., Chan T.Y., Crandall K.A., Dworschak P.C., Felder D.L., Feldmann R.M., Fransen C.H.J.M., Goulding L.Y.D., Lemaitre R., Low M.E.Y., Martin J.W., Ng P.K.L., Schweitzer C.E., Tan S.H., Tshudy D. and Wetzer R., 2009. A classification of living and fossil genera of decapods crustaceans. Raff. Bull. Zool., 21, 1–109.
  • Gruner H.E., 1993. Crustacea. In: Gruner H.E. (ed.), Lehrbuch der Speziellen Zoologie. Band I, 4. Teil, Arthropoda. Jena, Gustav Fischer, pp. 448–1030.
  • Hajslova J., Pulkrabova J., Poustka J., Cajka T. and Randak T., 2007. Brominated flame retardants and related chlorinated persistent organic pollutants in fish from river Elbe and its main tributary Vltava. Chemosphere, 69, 1195–1203. [CrossRef] [PubMed]
  • Hamr P., 2002. Biology of freshwater crayfish. In: Holdich D. (ed.), Blackwell Publishing Ltd., Oxford.
  • Harshbarger, J.C., Coffey, M.J. and Young, M.Y., 2000. Intersexes in Mississippi river shovelnose sturgeon sampled below Saint Louis, Missouri, USA. Mar. Environ. Res., 50(1), 247–250. [CrossRef] [PubMed]
  • Hartnoll, R.G., 1977. Reproductive strategy in two British species of Alcyonium. In: Biology of benthic organisms: 11th European symposium on marine biology, Galway, 321–328.
  • Havelková M., Randák T., Žlábek V., Krijt J., Kroupová H., Pulkrabová J. and Svobodová Z., 2007. Biochemical markers for assessing aquatic contamination. Sensors-Basel, 7, 2599–2611. [CrossRef]
  • Hebert P.D.N. and Crease T., 1983. Clonal diversity in populations of Daphnia pulex reproducing by obligate parthenogenesis. Heredity, 51(1), 353–369. [CrossRef]
  • Hobbs H.H.Jr., 1972. Crayfishes (Astacidae) of North and Middle America. Biota of freshwater ecosystems, identification manual 9. US Environmental Protection Agency, Washington, DC.
  • Hobbs, H.H.Jr., Hobbs, H.H.III. and Daniel, M.A. 1977. A review of the troglobitic decapod crustaceans of the Americas. Smithsonian Institution Press., No. 244.
  • Hobbs H.H.J.Jr., 1989. An illustrated checklist of the American crayfishes (Decapoda: Astacidae, Cambaridae, and Parastacidae). Washington, D.C.: Smithsonian Institution Press.
  • Hoffman D.L., 1968. Seasonal Eyestalk Inhibition on the Androgenic Glands of a Protandric Shrimp. Nature, 218, 170–172. [CrossRef]
  • Hogger J.B., 1988. Ecology, population biology and behaviour. Freshwater crayfish: biology, management and exploitation. Croom Helm, London.
  • Holdich D.M., 2002. Background and Functional Morphology. In: Holdich D.M. (ed.), Biology of freshwater crayfish, Blackwell, Oxford, Chapter 1, p. 29.
  • Horwitz P., 1988. Secondary sexual characteristics of females of the freshwater crayfish genus Engaeus (Decapoda, Parastacidae). Crustaceana, 54, 25–32. [CrossRef]
  • Imgrund J.A., 1998. Population Genetic Analysis of the Freshwater Crayfish, Cherax tenuimanus. IUCN 2001. IUCN Red List Categories and Criteria: Version 3.1., IUCN Species Survival Commission. IUCN, Gland, Switzerland and Cambridge, UK.
  • Jamieson B.G.M. and Tudge C.C., 2000. Crustacea-Decapoda. In: Jamieson B.G.M. (ed.), Progress in Male Gamete Ultrastructure and Phylogeny, Reproductive Biology of the Invertebrates. Chichester, 9, 1–95.
  • Jamieson B.G.M., Ausio J. and Justine J.-L., 1995a. Advances in spermatozoal phylogeny and taxonomy. Mémoires du Muséum National d’Histoire Naturelle (Paris), 166, 343–358.
  • Jamieson B.G.M., Guinot D. and Richer de Forges B., 1995b. Phylogeny of the Brachyura (Crustacea, Decapoda): evidence from spermatozoal ultrastructure. In: Jamieson B.G.M., Ausio J. and Justine J.L. (eds.), Advances in spermatozoal phylogeny and taxonomy. Mémoires du Méusum National d’Histoire Naturelle (Paris), 166, 265–283.
  • Jelić M., Klobucar G., Bláha M. and Maguire I., 2013. Noble and narrow-clawed crayfish hybridisation experiment in natural habitat. Regional European Crayfish meeting (CrayCro). September 26–28, Rovinj, Croatia.
  • Jobling S., Nolan M., Tyler C.R., Brighty G. and Sumpter J.P., 1998. Widespread sexual disruption in wild fish. Environ. Sci. Technol., 32(17), 2498–2506. [CrossRef]
  • Johnson S.G., 1992. Spontaneous and hybrid origins of parthenogenesis in Campeloma decisum (freshwater prosobranch snail). Heredity, 68(3), 253–261. [CrossRef]
  • Jokela J., Lively C.M., Dybdahl M.F. and Fox J.A., 1997. Evidence for a cost of sex in the freshwater snail Potamopyrgus antipodarum. Ecology, 78, 452–460. [CrossRef]
  • Jones D.R., 2016. A New Crayfish of the Genus Cambarus (Decapoda: Cambaridae) From the Flint River Drainage in Northern Alabama and South Central Tennessee, USA. Zootaxa, 4103, 43–53. [CrossRef] [PubMed]
  • Karplus I., Sagi A., Khalaila I. and Barki A., 2003. The Influence of Androgenic Gland Implantation on the Agonistic Behavior of Female Crayfish (Cherax quadricarinatus) in Interactions with Males. Behaviour, 140, 649–663. [CrossRef]
  • Katakura Y., 1989. Endocrine and genetic control of sex differentiation in the Malacostracan Crustacea. Invertebr. Reprod. Dev., 16, 177–181. [CrossRef]
  • Keller R., 1992. Crustacean neuropeptides: Structures, functions and comparative aspects. Experientia, 48, 439–448. [CrossRef]
  • Keller R., Kegel G., Reichwein B., Sedlmeier D. and Soyez D., 1999. Biological effects of neurohormones of the CHH/MIH/GIH peptide family in crustaceans. In: Roubos E.W., Wendelaar-Bonga S.E., Vaudry H. and DeLoof A. (eds.), Recent Developments in Comparative Endocrinology and Neurobiology. Shaker, Maastricht, pp. 209–212.
  • Khalaila I., Manor R., Weil S., Granot Y., Keller R. and Sagi A., 2002. The eyestalk-androgenic gland-testis endocrine axis in the crayfish Cherax quadricarinatus. Gen. Comp. Endocrinol., 127, 147–156. [CrossRef] [PubMed]
  • King D.S., 1964. Fine structure of the androgenic gland of the crab, Pachygrapsus crassipes. Gen. Comp. Endocrinol., 4, 533–544. [CrossRef] [PubMed]
  • Kouba A., Kuklina I., Niksirat H., Máchová J. and Kozák P., 2012. Tolerance of signal crayfish (Pacifastacus leniusculus) to Persteril 36 supports use of peracetic acid in astaciculture. Aquaculture, 350, 71–74. [CrossRef]
  • Kouba A., Petrusek A. and Kozák P., 2014. Continental-wide distribution of crayfish species in Europe: update and maps. Knowl. Manag. Aquat. Ecosyst., 413, 5. [CrossRef] [EDP Sciences]
  • Kouba A., Niksirat H. and Bláha M., 2015. Comparative ultrastructure of spermatozoa of the redclaw Cherax quadricarinatus and the yabby Cherax destructor (Decapoda, Parastacidae). Micron, 69, 56–61. [CrossRef]
  • Kozák P., Hulák M., Policar T. and Tichy F., 2007. Studies of annual gonadal development and gonadal ultrastructure in spiny-cheek crayfish (Orconectes limosus). BFPP/Bull. Fr. Pêche Piscic., 384, 15–26. [CrossRef] [EDP Sciences]
  • Kulkarni G.K., Nagabhushanam R. and Joshi P.K., 1984. Neuroendocrine control of reproduction in the male penaeid prawn, Parapenaeopsis hardwickii (Miers) (Crustacea, Decapoda, Penaeidae). Hydrobiologia, 108, 281–289. [CrossRef]
  • Lawrence C., 2002. Margaret River Marron: morphology and hybrids. In: Molony, B. (ed.), Scientific Workshop on the Margaret River Marron, Perth, Australie, 20–23.
  • Lawrence C.S., Morrissy N.M., Vercoe P.E. and Williams I.H., 2000. Hybridization in australian freshwater crayfish production of all-male progeny. J. World Aquacult. Soc., 31, 651–658. [CrossRef]
  • Liu L. and Laufer H., 1996. Isolation and characterization of sinus gland neuropeptides with both mandibular organ inhibiting and hyperglycemic effects from the spider crab Libinia emarginata. Arch. Insect. Biochem., 32, 375–385. [CrossRef]
  • López Greco L.S. and Lo Nostro F.L., 2008. Structural changes in the spermatophore of the freshwater ‘red claw’ crayfish Cherax quadricarinatus (Von Martens, 1898) (Decapoda, Parastacidae). Acta Zool-Stockholm., 89, 149–155. [CrossRef]
  • MacDonald L., Bulach B., Stamper R. and Ziemba R., 2006. Hybridization Between the Crayfishes Orconectes juvenilis and Orconectes cristavarius in the Kentucky River Basin: Morphological Evidence.
  • Maguire I., Špelić I., Jelić M. and Klobučar G., 2013. Is it Possible to Detect Narrow-clawed and Noble crayfish Probable Hybrids Using Multivariate Discriminant Analysis of Morphometric Data? Freshwater Crayfish, 19, 219–227. [CrossRef]
  • Malek S.R.A. and Bawab F.M., 1971. Tanning in the spermatophore of a crustacean (Penaeus trisulcatus). Experientia, 27, 1098–1098. [CrossRef]
  • Manor R., Aflalo E.D., Segall C., Weil S., Azulay D., Ventura T. and Sagi A., 2004. Androgenic gland implantation promotes growth and inhibits vitellogenesis in Cherax quadricarinatus females held in individual compartments. Invertebr. Reprod. Dev., 45, 151–159. [CrossRef]
  • Martin G., Sorokine O., Moniatte M., Bulet P., Hetru C. and Van Dorsselaer A., 1999. The structure of a glycosylated protein hormone responsible for sex determination in the isopod, Armadillidium vulgare. Eur. J. Biochem., 262, 727–736. [CrossRef] [PubMed]
  • Martin J.W. and Davis G.E., 2001. An updated classification of the recent Crustacean. Science Series No. 39. Natural History Museum of Los Angeles County, 124.
  • Martin P., Kohlmann K. and Scholtz G., 2007. The parthenogenetic Marmorkrebs (marbled crayfish) produces genetically uniform offspring. Naturwissenschaften, 94, 843–846. [CrossRef] [PubMed]
  • Martin P., Dorn N.J., Kawai T., van der Heiden C. and Scholtz G., 2010. The enigmatic Marmorkrebs (marbled crayfish) is the parthenogenetic form of Procambarus fallax (Hagen, 1870). Contrib. Zool., 79, 107–118.
  • Martin P., Thonagel S. and Scholtz G., 2015. The parthenogenetic Marmorkrebs (Malacostraca: Decapoda: Cambaridae) is a triploid organism. J. Zool. Syst. Evol. Res., 54, 13–21. [CrossRef]
  • Martínez R.I., Llanos F.E. and Quezada A.E., 1994. Samastacus araucanius (Faxon, 1914): aspectos morfológicos de un nuevo registro para Chile (Crustacea, Decapoda, Parastacidae). Gayana Zool., 58, 9–15.
  • McLay C.L. and López Greco L.S., 2011. A hypothesis about the origin of sperm storage in the Eubrachyura, the effects of seminal receptacle structure on mating strategies and the evolution of crab diversity: How did a race to be first become a race to be last? Zool. Anz., 250, 378–406. [CrossRef]
  • Medina A., 1994. Spermiogenesis and sperm structure in the shrimp Parapenaeus longirostris (Crustacea: Dendrobranchiata): comparative aspects among decapods. Mar. Biol., 119, 449–460. [CrossRef]
  • Medley P.B. and Rouse D.B., 1993. Intersex australian red claw crayfish (Cherax quadricarinatus). J. Shellfish Res., 12, 93–94.
  • Medley P., Camus A., Tiersch T. and Avault J.W., 1994. Hermaphroditic Australian redclaw crayfish (Cherax quadricarinatus). Int. Assoc. Astacology, 10th Symposium, 50.
  • Michiels N.K., 1998. Mating conflicts and sperm competition in simultaneous hermaphrodites. In: Birkhead T.R. and Møller A.P. (eds.), Sperm competition and sexual selection. Academic Press, London, pp. 219–254.
  • Miyawaki M. and Taketomi Y., 1978. The Occurrence of an Extended Perinuclear Space in Androgenic Gland Cells of the Crayfish, Procambarus clarki. Cytologia, 43, 351–355. [CrossRef]
  • Mlinarec, J., Mcžić, M., Pavlica, M., Šrut, M., Klobučar, G., and Maguire, I., 2011. Comparative karyotype investigations in the European crayfish Astacus astacus and A. leptodactylus (Decapoda, Astacidae). Crustaceana, 84, 1497–1510. [CrossRef]
  • Moore J.E.S., 1898. The mollusks of the great African lakes. II. The anatomy of the Typhobias, with a description of the new genus (Batanalia). Q. J. Microsc. Sci. 41, 181–204.
  • Morrison J.P., 1954. The relationships of old and new world melanians. Smithsonian Inst., United States National Museum, 103, 357–394. [CrossRef]
  • Nagamine C.M., Knight A.W., Maggenti A. and Paxman G., 1980. Effects of androgenic gland ablation on male promary and secondary sexual characteristics in the Malaysian prawn Macrachium rosenbergii (De Man) (Decapoda, Palamonidae), with first evidence of induced feminization in a nonhermaphroditic decapod. Gen. Comp. Endocrinol., 41, 423–441. [CrossRef] [PubMed]
  • Nagaraju G.P., 2011. Reproductive regulators in decapod crustaceans: an overview. J. Exp. Biol., 214, 3–16. [CrossRef] [PubMed]
  • Niksirat H. and Kouba A., 2016, Subcellular localization of calcium deposits in the noble crayfish Astacus astacus spermatophore: Implications for post-mating spermatophore hardening and spermatozoon maturation. J. Morphol., 277, 445–452. [CrossRef] [PubMed]
  • Niksirat H., Kouba A., Pšenička M., Kuklina I. and Kozák P., 2013a. Ultrastructure of spermatozoa from three genera of crayfish Orconectes, Procambarus and Astacus (Decapoda: Astacoidea): New findings and comparisons. Zool. Anz., 252, 226–233. [CrossRef]
  • Niksirat H., Kouba A., Rodina M. and Kozák P., 2013b. Comparative ultrastructure of the spermatozoa of three crayfish species: Austropotamobius torrentium, Pacifastacus leniusculus, and Astacus astacus (Decapoda: Astacidae). J. Morphol., 274, 750–758. [CrossRef] [PubMed]
  • Niksirat H., Andersson L., James P., Kouba A. and Kozák P., 2014a. Proteomic profiling of the signal crayfish Pacifastacus leniusculus egg and spermatophore. Anim. Reprod. Sci., 149, 335–344. [CrossRef]
  • Niksirat H., Kouba A. and Kozák P., 2014b. Post-mating morphological changes in the spermatozoon and spermatophore wall of the crayfish Astacus leptodactylus: insight into a non-motile spermatozoon. Anim. Reprod. Sci., 149, 325–334. [CrossRef]
  • Niksirat H., Kouba A. and Kozák P., 2015a. Ultrastructure of egg activation and cortical reaction in the noble crayfish Astacus astacus. Micron, 68, 115–121. [CrossRef]
  • Niksirat H., James P., Andersson L., Kouba A. and Kozák P., 2015b. Label-free protein quantification in freshly ejaculated versus post-mating spermatophores of the noble crayfish Astacus astacus. J. Proteomics, 123, 70–77. [CrossRef]
  • Noro C., López-Greco L.S. and Buckup L., 2008. Gonad morphology and type of sexuality in Parastacus defossus Faxon 1898, a burrowing, intersexed crayfish from southern Brazil (Decapoda: Parastacidae). Acta Zool-Stockholm, 89, 59–67. [CrossRef]
  • O’Foighil, D., 1988. Random mating and planktotrophic larval development in the brooding hermaphroditic clam Lasaea australis (Lamarck, 1818). The Veliger, 31(3-4), 214–221.
  • Okuno A., Hasegawa Y. and Nagasawa H., 1997. Purification and Properties of Androgenic Gland Hormone from the Terrestrial Isopod Armadillidium vulgare. Zool. Sci., 14, 837–842. [CrossRef]
  • Okuno A., Hasegawa Y., Ohira T., Katakura Y. and Nagasawa H., 1999. Characterization and cDNA cloning of androgenic gland hormone of the terrestrial isopod Armadillidium vulgare, Biochem. Biophys. Res. Commun., 264, 419–423. [CrossRef] [PubMed]
  • Parker I.M., Simberloff D., Lonsdale W.M., Goodell K., Wonham M., Kareiva P.M., Williamson M.H., Von Holle B., Moyle P.B., Byers J.E. and Goldwasser L., 1999. Impact: Toward a Framework for Understanding the Ecological Effects of Invaders. Biol. Invasions, 1, 3–19. [CrossRef]
  • Parnes S., Khalaila I., Hulata G. and Sagi A., 2003. Sex determination in crayfish: are intersex Cherax quadricarinatus (Decapoda, Parastacidae) genetically females? Genet. Res., 82, 107–116. [CrossRef] [PubMed]
  • Parnes S., Raviv S. and Sagi A., 2008. Reproductive biology of crustaceans, Enfield, NH: Science Publishers.
  • Patoka J., Bláha M. and Kouba A., 2015. Cherax (Cherax) subterigneus, a new crayfish (Decapoda: Parastacidae) from West Papua, Indonesia. J. Crustacean Biol., 35, 830–838. [CrossRef]
  • Payen G.G., 1990. Roles of androgenic gland hormone in determining the sexual characters in crustacea. In: Gupta A.P. (ed.), Morphogenetic Hormones of Arthropods. Roles in Histogenesis, Organogenesis, and Morphogenesis. Rutgers University Press, New Jersey, pp. 431–452.
  • Perry W.L., Feder J.L. and Lodge D.M., 2001. Implications of hybridization between introduced and resident Orconectes crayfishes. Conserv. Biol., 15, 1656–1666. [CrossRef]
  • Perry W.L., Lodge D.M. and Feder J.L., 2002. Importance of hybridization between indigenous and nonindigenous freshwater species: An overlooked threat to North American biodiversity. Syst. Biol., 51, 255–275. [CrossRef] [PubMed]
  • Poljaroen J., Vanichviriyakit R., Tinikul Y., Phoungpetchara I., Linthong V., Weerachatyanukul W. and Sobhon P., 2010. Spermatogenesis and distinctive mature sperm in the giant freshwater prawn, Macrobrachium rosenbergii (De Man, 1879). Zool. Anz., 249, 81–94. [CrossRef]
  • Reynolds J.D. 2002. Growth and Reproduction. In: Holdich D.M. (ed.), Biology of Freshwater Crayfish. Blackwell Science, Oxford, pp. 152–191.
  • Reynolds J.D. and Souty-Grosset C., 2012. Crayfish as prime players in ecosystems: life- history strategies. In: Reynolds J.D. and Souty-Grosset C. (eds.), Management of Freshwater Biodiversity. Crayfish as bioindicators. Cambridge University Press, Cambridge, pp. 55–56.
  • Rudolph E. and Almeida A., 2000. On the sexuality of South American Parastacidae (Crustacea, Decapoda). Invertebr. Reprod. Dev., 37, 249–257. [CrossRef]
  • Rudolph E. and Crandall K., 2005. A new species of burrowing crayfish Virilastacus rucapihuelensis (Crustácea, Decapoda, Parastacidae) from southern Chile. Proc. Biol. Soc. Washington, 118, 765–776. [CrossRef]
  • Rudolph E. and Rivas H., 1988. Nuevo hallazgo de Samastacus araucanius (Faxon, 1914) (Decapoda: Parastacidae). Biota, 4, 73–78.
  • Rudolph E.H., 1995a. Partial protandric hermaphroditism in the Burrowing Crayfish Parastacus nicoleti (Philippi, 1882) (Decapoda: Parastacidae). J. Crustacean Biol., 15, 720–732. [CrossRef]
  • Rudolph E.H., 1995b. A case of gynandromorphism in the freshwater crayfish Samastacus spinifrons (Philippi, 1882)(Decapoda, Parastacidae). Crustaceana, 68, 705–711. [CrossRef]
  • Rudolph E.H., 2002. New records of intersexuality in the freshwater crayfish Samastacus spinifrons (Decapoda, Parastacidae). J. Crustacean Biol., 22, 377–389. [CrossRef]
  • Sagi A. and Khalaila I., 2001. The Crustacean Androgen: A Hormone in an Isopod and Androgenic Activity in Decapods. Am. Zool., 41, 477–484.
  • Sagi A., Khalaila I., Barki A., Hulata G. and Karplus I., 1996. Intersex red Claw crayfish, Cherax quadricarinatus (von Martens): Functional males with pre-Vitellogenic ovaries. Biol. Bull., 190, 16–23. [CrossRef]
  • Sagi A., Snir E. and Khalaila I., 1997. Sexual differentiation in decapod crustaceans: role of the androgenic gland. Invertebr. Reprod. Dev., 31, 55–61. [CrossRef]
  • Sagi A., Manor R., Segall C., Da Vis C. and Khalaila I., 2002. On intersexuality in the crayfish Cherax quadricarinatus: an inducible sexual plasticity model. Invertebr. Reprod. Dev., 41, 27–33. [CrossRef]
  • Sassaman C., 1995. Sex determination and evolution of unisexuality in the Conchostraca. Hydrobiologia, 298, 45–65. [CrossRef]
  • Scholtz G., Braband A., Tolley L., Reimann A., Mittmann B., Lukhaup C., Steuerwald F. and Vogt G., 2003. Ecology: Parthenogenesis in an outsider crayfish. Nature, 421, 806. [CrossRef] [PubMed]
  • Schulte-Oehlmann U., Oehlmann J., Bauer B., Fioroni P., Leffler U.-S., 1998. Toxico-kinetic and -dynamic aspects of TBT-induced imposex in Hydrobia ulvae compared with intersex in Littorina littorea (Gastropoda, Prosobranchia). In: O’Riordan R.M., Burnell G.M., Davies M.S. and Ramsay N.F. (eds.), Aspects of Littorinid Biology: Proceedings of the Fifth International Symposium on Littorinid Biology, Cork, Ireland, 7-13 September 1996. Springer Netherlands, Dordrecht, 215–225.
  • Simeo C.G., Kurtz K., Rotllant G., Chiva M. and Ribes E., 2010. Sperm ultrastructure of the spider crab Maja brachydactyla (Decapoda: Brachyura). J. Morphol., 271, 407–417. [CrossRef] [PubMed]
  • Simon J.C., Delmotte F., Rispe C. and Crease T., 2003. Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals. Biol. J. Linn. Soc., 79, 151–163. [CrossRef]
  • Skurdal J. and Taugbol T., 2002. Astacus. In: Holdich D.M. (ed.), Biology of freshwater crayfish. Blackwell Science Ltd., Oxford, UK, pp. 467–510.
  • Smith D.G., 1979. Brief Note New Locality Records of Crayfishes from the Middle Hudson River System.
  • Smith D.G., 1981. Evidence for Hybridization Between Two Crayfish Species (Decapoda: Cambaridae: Orconectes) with a Comment on the Phenomenon in Cambarid Crayfish. The American Midland Naturalist, University of Notre Dame, 105 (2), 405–407. [CrossRef]
  • Sokol A., 1988. The australian yabby. In: Holdich D.M. and Lowery R.S. (eds.), Freshwater Crayfish: Biology, Management and Exploitation. Croom-Helm, London, Sydney.
  • Suomalainen E., 1950. Parthenogenesis in animals. Adv. Genet., 3, 193–253. [PubMed]
  • Suomalainen E., Saura A. and Lokki J., 1987. Cytology and evolution in parthenogenesis. CRC, Boca Raton, FL.
  • Taketomi Y., 1986. Ultrastructure of the androgenic gland of the crayfish, Procambarus clarkii. Cell Biol. Int. Rep., 10, 131–136. [CrossRef]
  • Taketomi Y., Nishikawa S. and Koga S., 1996. Testis and Androgenic Gland during Development of External Sexual Characteristics of the Crayfish Procambarus clarkii. J. Crustacean Biol., 16, 24–34. [CrossRef]
  • Tan-Fermin J.D., 1991. Effects of unilateral eyestalk ablation on ovarian histology and oocyte size frequency of wild and pond-reared Penaeus monodon (Fabricius) broodstock. Aquaculture, 93, 77–86. [CrossRef]
  • Terauchi A., Tsutsumi H., Yang W.-J., Aida K., Nagasawa H. and Sonobe H., 1996. A Novel Neuropeptide with Molt-inhibiting Activity from the Sinus Gland of the Crayfish. Procambarus clarkii. Zool. Sci., 13, 295–298. [CrossRef]
  • Tirelli T., Pessani D., Silvestro D. and Tudge C., 2008. Reproductive Biology of Mediterranean Hermit Crabs: Fine Structure of Spermatophores and Spermatozoa of Diogenes pugilator (Decapoda: Anomura) and Its Bearing on a Sperm Phylogeny of Diogenidae. J. Crustacean Biol., 28, 534–542. [CrossRef]
  • Tudge C.C., 1995. ltrastructure and phylogeny of the spermatozoa of the infraorders Thalassinidea and Anomura (Decapoda, Crustacea). In: Jamieson B.G.M., Ausio J. and Justine J.-L. (eds.), I. Advances in spermatozoal phylogeny and taxonomy. Mémoires du Muséum National d’Histoire Naturelle Paris, 166, 251–263.
  • Tudge C.C., 2009. Spermatozoal morphology and its bearing on decapod phylogeny. In: Martin J.W., Crandall A. and Felder D.L. (eds.), Crustacean Issues: Decapod Crustacean Phylogenetics. Francis & Taylor/CRC Press, Boca Raton, pp. 101–119.
  • Turgeon, J., and Hebert, P.D., 1994. Evolutionary interactions between sexual and all-female taxa of Cyprinotus (Ostracoda: Cyprididae). Evolution, 1855–1865.
  • Uma K. and Subramoniam T., 1979. Histochemical characteristics of spermatophore layers of Scylla serrata (Forskal) (Decapoda: Portunidae). Int. J. Inver. Rep. Dev., 1, 31–40. [CrossRef]
  • Vanichviriyakit R., Kruevaisayawan H., Weerachatyanukul W., Tawipreeda P., Withyachumnarnkul B., Pratoomchat B., Chavadej J. and Sobhon P., 2004. Molecular modification of Penaeus monodon sperm in female thelycum and its consequent responses. Mol. Reprod. Dev., 69, 356–363. [CrossRef] [PubMed]
  • Velisek J., Kouba A. and Stara A., 2013. Acute toxicity of triazine pesticides to juvenile signal crayfish (Pacifastacus leniusculus). Neuro. Endocrinol. Lett., 2, 31–36.
  • Vogt V., 2002. Functional anatomy. In: Holdich D.M. (ed.), Biology of freshwater crayfish, Blackwell Science, Oxford. 53–151.
  • Vogt G., 2007. Exposure of the eggs to 17a-methyl testosterone reduced hatching success and growth and elicited teratogenic effects in postembryonic life stages of crayfish. Aquat. Toxicol., 85, 291–296. [CrossRef] [PubMed]
  • Vogt G., Tolley L. and Scholtz G., 2004. Life stages and reproductive components of the Marmorkrebs (marbled crayfish), the first parthenogenetic decapod crustacean. J. Morphol., 261, 286–311. [CrossRef] [PubMed]
  • Vogt G., Huber M., Thiemann M., van den Boogaart G., Schmitz O.J., and Schubart C.D., 2008. Production of different phenotypes from the same genotype in the same environment by developmental variation. J. Exp. Biol., 211, 510–523. [CrossRef] [PubMed]
  • Vogt G., Falckenhayn C., Schrimpf A., Schmid K., Hanna K., Panteleit J., Helm M., Schulz R. and Lyko F., 2015. The marbled crayfish as a paradigm for saltational speciation by autopolyploidy and parthenogenesis in animals. Biology Open, 4, 1583–1594. [CrossRef] [PubMed]
  • Wainwright G., Webster S.G., Wilkinson M.C., Chung J.S., Rees H.H., 1996. Structure and significance of mandibular organ-inhibiting hormone in the crab, Cancer pagurus. Involvement in multihormonal regulation of growth and reproduction. J. Biol. Chem., 271, 12749–12754. [CrossRef] [PubMed]
  • Werner B., 1955. On the development and reproduction of the anthomedusan Margelopsis haeckeli Hartlaub. Annals of the New York Academy of Sciences, 62(1), 3–29. [CrossRef]
  • Wetzel J.E., 2002. Form alteration of adult female crayfishes of the genus Orconectes (Decapoda: Cambaridae). Am. Midl. Nat., 147, 326–337. [CrossRef]
  • Wilder N.M., Okumura T., Suzuki Y., Fusetani N. and Aida K., 1994. Vitellogenin Production Induced by Eyestalk Ablation in Juvenile Giant Freshwater Prawn Macrobrachium rosenbergii and Trial Methyl Farnesoate Administration. Zool. Sci., 11, 45–53.
  • Winterbourn M., 1970. The New Zealand species of Potamopyrgus (Gastropoda: Hydrobiidae). Malacologia, 10(2), 283–321.
  • Yasuzumi G. and Lee K.J., 1966. Spermatogenesis in animals as revealed by electron microscopy. XVI. The microtubular structure and sites of thiamine pyrophosphatase activity in premature sperm of the Japanese crayfish. Z. Zellforsch. Mik. Ana., 73, 384–404. [CrossRef]
  • Yazicioglu B., Linhartova Z., Niksirat H. and Kozák P., 2014. First report of intersex in the signal crayfish Pacifastacus leniusculus (Dana, 1862). Crustaceana, 87, 1559–1566. [CrossRef]
  • Yue G.H., Wang G.L., Zhu B.Q., Wang C.M., Zhu Z.Y. and Lo L.C., 2008. Discovery of four natural clones in a crayfish species Procambarus clarkii. Int. J. Biol. Sci., 4, 279–282. [CrossRef] [PubMed]
  • Yue G.H., Li J., Bai Z., Wang C.M. and Feng F., 2010. Genetic diversity and population structure of the invasive alien red swamp crayfish. Biol. Invas., 12, 2697–2706. [CrossRef]
  • Zuber S.T., Muller K., Laushman R.H. and Roles A.J., 2012. Hybridization between an invasive and a native species of the crayfish genus Orconectes in North-Central Ohio. J. Crustacean Biol., 32, 962–971. [CrossRef]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.