EDP Sciences logo
Submit your paper
Search
Menu
All issues No 417 (2016) Knowl. Manag. Aquat. Ecosyst., 417 (2016) 33 References
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] [Google Scholar]
  • Adams J., Greenwood P. and Naylor C., 1987. Evolutionary aspects of environmental sex determination. Int. J. Inver. Rep. Dev., 11, 123–135. [CrossRef] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Andrews E.A. 1906a. The annulus ventralis. Proc. Boston Soc. Nat. Hist., 32, 427–479. [Google Scholar]
  • Andrews E.A., 1906b. Egg-laying of crayfish. Am. Nat., 40, 343–356. [CrossRef] [Google Scholar]
  • Aungsuchawan S., Browdy C.L. and Withyachumnarnkul B., 2011. Sperm capacitation of the shrimp Litopenaeus vannamei. Aquacult. Res., 42, 188–195. [CrossRef] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [PubMed] [Google Scholar]
  • 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] [Google Scholar]
  • Bell G., 1982. The masterpiece of nature. The evolution and genetics of sexuality. Univ. of California Pr., June, 1982. [Google Scholar]
  • 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. [Google Scholar]
  • Borg B. and van den Hurk R., 1983. Oocytes in the testes of the three-spined stickleback, Gasterosteus aculeatus. Copeia, 1983(1), 259–261. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [PubMed] [Google Scholar]
  • Browne R.A., 1992. Population genetics and ecology of Artemia: insights into parthenogenetic reproduction. Trends Ecol. Evol., 7, 232–237. [CrossRef] [PubMed] [Google Scholar]
  • 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. [Google Scholar]
  • Buřič M., Kouba A. and Kozák P., 2009. Spring mating period in Orconectes limosus: the reason for movement. Aquat. Sci., 71, 473–477. [Google Scholar]
  • Buřič M., Kouba A. and Kozák P. 2010. Intra-sex dimorphism in crayfish females. Zoology, 113, 301–307. [CrossRef] [Google Scholar]
  • 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. [Google Scholar]
  • Buřič M., Kouba A. and Kozák P., 2013. Reproductive plasticity in freshwater invader: from long-term sperm storage to parthenogenesis. PloS one, 8, e77597. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • Chang E.S. and Sagi A., 2008. Male reproductive hormones. In: Mente E. (ed.), Reproductive biology of crustaceans. Science Publishers, Enfield, NH. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • Crocker D.W., 1957. The crayfishes of New York (Decapoda: Astacidae). New York State Mus., Sci. Serv., Bull., 355, 1–97. [Google Scholar]
  • Crocker D.W. and Barr D.W., 1968. Handbook of the crayfishes of Ontario. published for Royal Ontario Museum by University of Toronto Press. [Google Scholar]
  • Cukerzis J., 1968. Interspecific relations between Astacus astacus L. and A. leptoductylus Esch. Pañstwowe Wydawnictwo Naukowe. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • Fingerman M., 1995. Endocrine Mechanisms in Crayfish, with Emphasis on Reproduction and Neurotransmitter Regulation of Hormone Release. Am. Zool., 35, 68–78. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • Gherardi F., 2007. Biological invaders in inland waters: Profiles, distribution and threats. Quarterly Rev. Biol., 44, 504–542. [Google Scholar]
  • Ghiselin M.T., 1969. The evolution of hermaphroditism among animals. Quarterly Rev. Biol., 189–208. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • Hamr P., 2002. Biology of freshwater crayfish. In: Holdich D. (ed.), Blackwell Publishing Ltd., Oxford. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • Hobbs H.H.J.Jr., 1989. An illustrated checklist of the American crayfishes (Decapoda: Astacidae, Cambaridae, and Parastacidae). Washington, D.C.: Smithsonian Institution Press. [Google Scholar]
  • Hoffman D.L., 1968. Seasonal Eyestalk Inhibition on the Androgenic Glands of a Protandric Shrimp. Nature, 218, 170–172. [CrossRef] [Google Scholar]
  • Hogger J.B., 1988. Ecology, population biology and behaviour. Freshwater crayfish: biology, management and exploitation. Croom Helm, London. [Google Scholar]
  • Holdich D.M., 2002. Background and Functional Morphology. In: Holdich D.M. (ed.), Biology of freshwater crayfish, Blackwell, Oxford, Chapter 1, p. 29. [Google Scholar]
  • Horwitz P., 1988. Secondary sexual characteristics of females of the freshwater crayfish genus Engaeus (Decapoda, Parastacidae). Crustaceana, 54, 25–32. [CrossRef] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • Johnson S.G., 1992. Spontaneous and hybrid origins of parthenogenesis in Campeloma decisum (freshwater prosobranch snail). Heredity, 68(3), 253–261. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Katakura Y., 1989. Endocrine and genetic control of sex differentiation in the Malacostracan Crustacea. Invertebr. Reprod. Dev., 16, 177–181. [CrossRef] [Google Scholar]
  • Keller R., 1992. Crustacean neuropeptides: Structures, functions and comparative aspects. Experientia, 48, 439–448. [CrossRef] [PubMed] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • King D.S., 1964. Fine structure of the androgenic gland of the crab, Pachygrapsus crassipes. Gen. Comp. Endocrinol., 4, 533–544. [CrossRef] [PubMed] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [PubMed] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Lawrence C., 2002. Margaret River Marron: morphology and hybrids. In: Molony, B. (ed.), Scientific Workshop on the Margaret River Marron, Perth, Australie, 20–23. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • Malek S.R.A. and Bawab F.M., 1971. Tanning in the spermatophore of a crustacean (Penaeus trisulcatus). Experientia, 27, 1098–1098. [CrossRef] [PubMed] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • Martin P., Kohlmann K. and Scholtz G., 2007. The parthenogenetic Marmorkrebs (marbled crayfish) produces genetically uniform offspring. Naturwissenschaften, 94, 843–846. [CrossRef] [PubMed] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • Medina A., 1994. Spermiogenesis and sperm structure in the shrimp Parapenaeus longirostris (Crustacea: Dendrobranchiata): comparative aspects among decapods. Mar. Biol., 119, 449–460. [CrossRef] [Google Scholar]
  • Medley P.B. and Rouse D.B., 1993. Intersex australian red claw crayfish (Cherax quadricarinatus). J. Shellfish Res., 12, 93–94. [Google Scholar]
  • Medley P., Camus A., Tiersch T. and Avault J.W., 1994. Hermaphroditic Australian redclaw crayfish (Cherax quadricarinatus). Int. Assoc. Astacology, 10th Symposium, 50. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • Morrison J.P., 1954. The relationships of old and new world melanians. Smithsonian Inst., United States National Museum, 103, 357–394. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • Nagaraju G.P., 2011. Reproductive regulators in decapod crustaceans: an overview. J. Exp. Biol., 214, 3–16. [CrossRef] [PubMed] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [PubMed] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Parnes S., Raviv S. and Sagi A., 2008. Reproductive biology of crustaceans, Enfield, NH: Science Publishers. [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Reynolds J.D. 2002. Growth and Reproduction. In: Holdich D.M. (ed.), Biology of Freshwater Crayfish. Blackwell Science, Oxford, pp. 152–191. [Google Scholar]
  • 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. [Google Scholar]
  • Rudolph E. and Almeida A., 2000. On the sexuality of South American Parastacidae (Crustacea, Decapoda). Invertebr. Reprod. Dev., 37, 249–257. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • Rudolph E. and Rivas H., 1988. Nuevo hallazgo de Samastacus araucanius (Faxon, 1914) (Decapoda: Parastacidae). Biota, 4, 73–78. [Google Scholar]
  • Rudolph E.H., 1995a. Partial protandric hermaphroditism in the Burrowing Crayfish Parastacus nicoleti (Philippi, 1882) (Decapoda: Parastacidae). J. Crustacean Biol., 15, 720–732. [CrossRef] [Google Scholar]
  • Rudolph E.H., 1995b. A case of gynandromorphism in the freshwater crayfish Samastacus spinifrons (Philippi, 1882)(Decapoda, Parastacidae). Crustaceana, 68, 705–711. [CrossRef] [Google Scholar]
  • Rudolph E.H., 2002. New records of intersexuality in the freshwater crayfish Samastacus spinifrons (Decapoda, Parastacidae). J. Crustacean Biol., 22, 377–389. [CrossRef] [Google Scholar]
  • Sagi A. and Khalaila I., 2001. The Crustacean Androgen: A Hormone in an Isopod and Androgenic Activity in Decapods. Am. Zool., 41, 477–484. [Google Scholar]
  • 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] [PubMed] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Sassaman C., 1995. Sex determination and evolution of unisexuality in the Conchostraca. Hydrobiologia, 298, 45–65. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Skurdal J. and Taugbol T., 2002. Astacus. In: Holdich D.M. (ed.), Biology of freshwater crayfish. Blackwell Science Ltd., Oxford, UK, pp. 467–510. [Google Scholar]
  • Smith D.G., 1979. Brief Note New Locality Records of Crayfishes from the Middle Hudson River System. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • Suomalainen E., 1950. Parthenogenesis in animals. Adv. Genet., 3, 193–253. [PubMed] [Google Scholar]
  • Suomalainen E., Saura A. and Lokki J., 1987. Cytology and evolution in parthenogenesis. CRC, Boca Raton, FL. [Google Scholar]
  • Taketomi Y., 1986. Ultrastructure of the androgenic gland of the crayfish, Procambarus clarkii. Cell Biol. Int. Rep., 10, 131–136. [CrossRef] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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. [Google Scholar]
  • Turgeon, J., and Hebert, P.D., 1994. Evolutionary interactions between sexual and all-female taxa of Cyprinotus (Ostracoda: Cyprididae). Evolution, 1855–1865. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • Vogt V., 2002. Functional anatomy. In: Holdich D.M. (ed.), Biology of freshwater crayfish, Blackwell Science, Oxford. 53–151. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • Wetzel J.E., 2002. Form alteration of adult female crayfishes of the genus Orconectes (Decapoda: Cambaridae). Am. Midl. Nat., 147, 326–337. [CrossRef] [Google Scholar]
  • 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. [Google Scholar]
  • Winterbourn M., 1970. The New Zealand species of Potamopyrgus (Gastropoda: Hydrobiidae). Malacologia, 10(2), 283–321. [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]
  • 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] [Google Scholar]

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.