Density, sex ratio, size structure and reproduction were analysed in populations of Viviparus contectus (Millet) from oxbows differently connected with the Bug River. The mean density was 20 ind./m2, the sex ratio was 1:1. Snails of size classes II (8.1-12.0 mm shell width and height), III (12.1–25.0 mm width and 12.1–20.0 mm height) and IV (25.1–35.0 mm and 20.1–35.0 mm) were the most numerous. The youngest snails (shell heightand width < 8 mm) were the least numerous. Smaller snails (class II) dominated in the spring. The proportion of classes III and IV increased in the summer and autumn. The number of embryos per female was the highest during the spring and summer - the period of intense reproduction. The number of embryos per female was the smallest (mean 6.8) in the oxbow isolated from the river; it was higher in the flow oxbows (13.6 and 14.2). In the isolated lake that number increased with the female's shell size. In the flow lakes the number of embryos washigh irrespective of the female's size; females from these lakes showed the highest fecundity in all size classes. Int he spring the mean number of embryos per female in classes II (11.5), III (12.4) and IV (14.6) was higher than in the largest females from the isolated lake. Similarly, in the summer the mean fecundity of females in class II(15.4 embryos/female) was higher than in the largest females in the lake isolated from the river (6.2).
REFERENCES(50)
1.
Browne R. A. 1978. Growth, mortality, fecundity, biomass and productivity of four lake populations of the Prosobranch snail, Viviparus georgianus. Ecology 59: 742-750. https://doi.org/10.2307/193877....
Chung E. Y., Kim S. Y., Park K. H., Park G. M. 2002. Sexual maturation, spawning and deposition of the egg capsules of the female purple shell, Rapana venosa (Gastropoda: Muricidae). Malacologia 44: 241-252.
Clench W. 1962. A catalogue of the Viviparidae of North America with notes on the distribution of Viviparus georgianus. Lea. Mus. Comparative Zoology, Harvard Univeristy Occas. Pap. Moll. 2: 261-288.
Czarnołęski M., Kozłowski J. 1998. Do Bertalanffy's growth curves result from optimal resource allocation? Ecol. Lett. 1: 5-7. https://doi.org/10.1046/j.1461....
De Bernardi R., Ravera K. W., Oregioni B. 1976. Demographic structure and biometric characteristics of Viviparus ater Cristofori and Jan (Gastropoda: Prosobranchia) from Lake Alserio (Northern Italy). J. Moll. Stud. 42: 310-318. https://doi.org/10.1093/oxford....
Eleutheriadis N., Lazaridou-Dimitriadou M. 1995. The life cycle, population dynamics, growth and secondary production of the snail Viviparus contectus (Millet) (Gastropoda, Prosobranchia) in the marshes of the river Strymonas, Serres, Macedonia, northern Greece. Malacologia 37: 41-52.
Eleutheriadis N., Lazaridou-Dimitriadou M. 2001. The life cycle, population dynamics, growth and secondary production of Bithynia graeca (Westerlund, 1879) (Gastropoda) in Lake Kerkini, northern Greece. J. Moll. Stud. 67: 319-328. https://doi.org/10.1093/mollus....
Falniowski A. 1989. Przodoskrzelne (Prosobranchia) Polski. I. Neritidae, Viviparidae, Valvatidae, Bithyniidae, Rissoidae, Aciculidae. Zeszyty naukowe UJ, Prace Zool. 35: 1-148.
Falniowski A., Kozik A., Szarowska M., Fiałkowski W., Mazan K. 1996. Allozyme and morphology evolution in European Viviparidae (Mollusca: Gastropoda: Architaenioglossa). J. Zool. Syst. Evol. Res. 34: 49-62. https://doi.org/10.1111/j.1439....
Fretter V., Graham A. 1978. The prosobranch molluscs of Britain and Denmark. Part 3 - Neritacea, Viviparacea, Valvatacea, terrestrial and freshwater Littorinacea and Rissoacea. J. Moll. Stud. 5 (suppl.): 101-152.
Jakubik B. 2003. Year-to-year stability of aggregations of Viviparus viviparus (Linnaeus 1758) in littoral zone of lowland, rheophilic reservoir (Central Poland). Pol. J. Ecol. 51: 53-66.
Jakubik B. 2006. Reproductive pattern of of Viviparus viviparus (Linnaeus 1758) (Gastropoda, Viviparidae) from littoral aggregations in a through-flow reservoir (Central Poland). Pol. J. Ecol. 54: 39-55.
Jakubik B. 2007. Egg number-female body weight relationship in freshwater snail (Viviparus viviparus L.) population in a reservoir. Pol. J. Ecol. 55: 325-336.
Jakubik B. in press. Reproduction as a variable life history trait in freshwater snail Viviparus viviparus (Linnaeus, 1758) (Gastropoda: Architaenioglossa: Viviparidae). Ekologia (Bratislava).
Jakubik B., Kufel L., Lewandowski K. 2006. Macrobenthos differentiation among ox-bow lakes of the Bug within the Bug River Valley Landscape Park. 2006. Teka Komisji Ochrony i Kształtowania Środowiska Przyrodniczego 3: 55-59.
Kozłowski J., Teriokhin A. T. 1999. Allocation of energy between growth and reproduction: the pontryagin maximum principle solution for the case of age- and season-dependent mortality. Evol. Ecol. Res. 1: 423-441.
Krodkiewska M., Strzelec M., Serafiński W. 1998. Potamopyrgus antipodarum (Gray)(Gastropoda, Prosobranchia) a dangerous newcomer in malacofauna of Poland. Przegl. Zool. 42: 53-60.
Middelfart P. 1996. Egg capsules and early development of ten muricid gastropods from Thai waters. Phuket Marine Biological Center Special Publication 16: 103-130.
Ribi G., Gebhardt M. 1986. Age-specific fecundity and size of offspring in the prosobranch snail, Viviparus ater. Oecologia (Berlin) 71: 18-24. https://doi.org/10.1007/BF0037....
Ribi G., Katoh M. 1998. Weak preference for conspecific mates in the hybridizing snails Viviparus ater and V. contectus (Mollusca Prosobranchia). Ethol. Ecol. & Evol., 10: 383-392. https://doi.org/10.1080/089270....
Ribi G., Porter A. H. 1995. Mating between two hybridizing species, Viviparus ater and V. contectus (Mollusca: Prosobranchia). Anim. Behav. 49: 1389-1398. https://doi.org/10.1006/anbe.1....
Samochwalenko T., Stańczykowska A. 1972. Fertility differentiation of two species of Viviparidae (Viviparus fasciatus Müll. and Viviparus viviparus L.) in some environments. Ekol. pol. 20: 479-492.
Skoog G. 1971. Variation in the distribution of Theodoxus fluviatilis on stony localites in the northern Baltic proper. Thalassia Yugoslavia 7: 363-372.
Stańczykowska A. 1959. Rozmieszczenie i dynamika liczebności żyworódki paskowanej Viviparus fasciatus Müll. na terenie łachy Konfederatka. Ekol. pol. B 5: 55-60.
Stańczykowska A. 1960b. Rozmieszczenie i dynamika liczebności mięczaków dennych na łasze wiślanej Konfederatka pod Wyszogrodem. Ekol. pol. A 8: 155-168.
Stańczykowska A., Magnin E., Dumouchel A. 1971. Etude de trois populations de Viviparus malleatus (Reeve) (Gastropoda, Prosobranchia) de la règion de Montrèal. I. Croissance, fècondite biomasse et production annuelle. Can. J. Zool. 49: 491-497. https://doi.org/10.1139/z71-07....
Stańczykowska A., Pliński M., Magnin E. 1972. Etude de trois populations de Viviparus malleatus (Reeve) (Gastropoda, Prosobranchia) de la region de Montrèal. II. Etude qualitative et quantitative de la nourriture. Can. J. Zool. 50: 1617-1624. https://doi.org/10.1139/z72-21....
Taki A. 1981. The fecundity of a mud snail, Cipangopaludina japonica. Verh. Internat. Verein. Limnol. 21: 1637-1639. https://doi.org/10.1080/036807....
Taylor P. M., Andrews E. B. 1991. Non-protein nitrogen excretion in the prosobranch gastropod Viviparus contectus. J. Moll. Stud. 57: 391-393. https://doi.org/10.1093/mollus....
Vincent B., Vaillancourt G., Harvey M. 1981. Cycle de développement, croissance, effectifs, biomasse et production de Bithynia tentaculata L. (Gastropoda: Prosobranchia) dans le Saint-Laurent (Québec). Can. J. Zool. 59: 1237-1250. https://doi.org/10.1139/z81-17....
Zettler M. L. 1996. The aquatic malacofauna (Gastropoda and Bivalvia) in the Catchment area of a North German Lowland River, the Warnow. Limnologia 26: 327-337.
Zhochov A. E. 1993. Age structure and seasonal dynamics of invasion of a pond snail, Viviparus viviparus, population with parthenitas of trematodes. Zool. Zh. 72: 17-25.
Life strategies of Viviparidae (Gastropoda: Caenogastropoda: Architaenioglossa) in various aquatic habitats: Viviparus viviparus (Linnaeus, 1758) and V. contectus (Millet, 1813) Beata Jakubik Folia Malacologica
Chromosome-Level Genome Assembly and Annotation of the Freshwater Snail Sinotaia angularis (O. F. Müller, 1774) Enjie Chua, Zhiqiang Wang, Jie Huang, Yanhong Wen, Xiaoyun Zhou, Fuguang Luo Animals
We process personal data collected when visiting the website. The function of obtaining information about users and their behavior is carried out by voluntarily entered information in forms and saving cookies in end devices. Data, including cookies, are used to provide services, improve the user experience and to analyze the traffic in accordance with the Privacy policy. Data are also collected and processed by Google Analytics tool (more).
You can change cookies settings in your browser. Restricted use of cookies in the browser configuration may affect some functionalities of the website.