Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-13T00:43:04.477Z Has data issue: false hasContentIssue false
  • English
  • Français

Short-term dynamics of cladocerans in a eutrophic shallow lake during a shift in the phytoplankton dominance

Published online by Cambridge University Press:  29 October 2009

Nelson Abrantes ,
António Nogueira  and
Fernando Gonçalves
Nelson Abrantes*
Affiliation:
CESAM & Department of Environment, University of Aveiro, 3810-193 Aveiro, Portugal
António Nogueira
Affiliation:
CESAM & Department of Environment, University of Aveiro, 3810-193 Aveiro, Portugal
Fernando Gonçalves
Affiliation:
CESAM & Department of Environment, University of Aveiro, 3810-193 Aveiro, Portugal
*
[email protected]
Get access

Abstract

The changes in the dynamics of cladocerans in Lake Vela (Portugal), as well as the morphologic and life history traits of the small-bodied cladoceran Ceriodaphnia pulchella, were studied intensively during one month characterized by deep and fast changes in the phytoplankton community: the beginning of the cyanobacteria dominance. Lake Vela, located in the Mediterranean region, is a polymictic shallow lake exhibiting characteristics typical of an advanced trophic status, namely the permanently turbid water, the reduction in biodiversity and the occurrence of cyanobacteria blooms. The density and composition of the cladocerans populations varied considerably during the short-term period analyzed. Coincident with the increase of cyanobacteria, the density of Daphnia longispina decreased drastically, associated with an increase of Bosmina longirostris and Chydorus sp. The constant density of C. pulchella, even during the cyanobacteria dominance, and the strong relationship found between weight and size, suggests that the low quality of phytoplanktonic food in Lake Vela did not play an important role in its fitness. Besides the small size of C. pulchella, this fact could be also related to its diversified diet. Nevertheless, a closer examination of the life history parameters of C. pulchella revealed a reduction in the fecundity, size at first reproduction, mean size of ovigerous females and maximum size of the population, which suggest an increase of the fish pressure after the decline of Daphnia. C. pulchella showed also a short-life cycle and a fast turnover of individuals, which constitutes also an advantage, allowing a fast adaptive response of the population.

Keywords

Mediterranean shallow lakesshort-term dynamicscladoceranscyanobacteriaCeriodaphnia pulchella
Type
Research Article
Information
Annales de Limnologie - International Journal of Limnology , Volume 45 , Issue 4 , 2009 , pp. 237 - 245
Copyright
© EDP Sciences, 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abrantes, N. and Goncalves, F., 2003. The dynamics of Ceriodaphnia pulchella (Cladocera) in laboratory. Acta Oecol. , 24, S245–S249. CrossRef
Abrantes, N., Antunes, S.C., Pereira, M.J. and Goncalves, F., 2006. Seasonal succession of cladocerans and phytoplankton and their interactions in a shallow eutrophic lake (Lake Vela, Portugal). Acta Oecol. , 29, 54–64. CrossRef
A.P.H.A., 1995. Standard Methods for the Examination of Water and Wastewater, 19th edn., American Public Health Association, Washington.
Amoros, C., 1984a. Introduction pratique à la systématique des organismes des eaux continentales françaises. Crustacés cladocères. Bull. Mens. Soc. Linn. Lyon , 3, 72–107. CrossRef
Amoros, C., 1984b. Introduction pratique à la systématique des organismes des eaux continentales françaises. Crustacés cladocères (suite). Bull. Mens. Soc. Linn. Lyon , 4, 120–144. CrossRef
Arnold, D.E., 1971. Ingestion, assimilation, survival, and reproduction by Daphnia pulex Fed 7 species of blue-green-algae. Limnol. Oceanogr. , 16, 906–920. CrossRef
Balseiro, E.G., Modenutti, B.E. and Queimalinos, C.P., 1992. The coexistence of bosmina and ceriodaphnia in a South Andes lake – An analysis of demographic responses. Freshwat. Biol. , 28, 93–101. CrossRef
Barros P., 1994. Implicações ecotoxicológicas de cianobactérias em cladóceros, University of Coimbra, Faculty of Sciences and Technology, Coimbra.
Becker, C. and Boersma, M., 2003. Resource quality effects on life histories of Daphnia. Limnol. Oceanogr. , 48, 700–706. CrossRef
Berzins, B. and Pejler, B., 1989. Rotifer occurrence and trophic degree. Hydrobiologia , 182, 171–180. CrossRef
Bird, D.F. and Prairie, Y.T., 1985. Practical guidelines for the use of zooplankton length-weight regression equations. J. Plankton Res. , 7, 955–960. CrossRef
Boersma, M., Spaak, P. and De Meester, L., 1998. Predator-mediated plasticity in morphology, life history, and behavior of Daphnia: The uncoupling of responses. Amer. Nat. , 152, 237–248.
Burns, C.W., 1969. Relation between filtering rate, temperature, and body size in 4 species of Daphnia. Limnol. Oceanogr. , 14, 693–700. CrossRef
Castro, B.B. and Goncalves, F., 2007. Seasonal dynamics of the crustacean zooplankton of a shallow eutrophic lake from the Mediterranean region. Fund. Appl. Limnol. , 169, 189–202. CrossRef
Castro, B.B., Marques, S.M. and Goncalves, F., 2007. Habitat selection and diel distribution of the crustacean zooplankton from a shallow Mediterranean lake during the turbid and clear water phases. Freshwat. Biol. , 52, 421–433. CrossRef
Christoffersen, K., Riemann, B., Klysner, A. and Sondergaard, M., 1993. Potential role of fish predation and natural-populations of zooplankton in structuring a plankton community in eutrophic lake water. Limnol. Oceanogr. , 38, 561–573. CrossRef
de Figueiredo, D.R., Antunes, S.C., Pereira, M.J. and Goncalves, F.G., 2004a. Chronic effects of Aphanizomenon flos-aquae on the survival and reproduction of daphnids. Fresenius Environ. Bull. , 13, 665–670.
de Figueiredo, D.R., Azeiteiro, U.M., Esteves, S.M., Goncalves, F.J.M. and Pereira, M.J., 2004b. Microcystin-producing blooms Coimbra a serious global public health issue. Ecotox. Environ. Safety , 59, 151–163. CrossRef
de Figueiredo, D.R., Reboleira, A., Antunes, S.C., Abrantes, N., Azeiteiro, U., Goncalves, F. and Pereira, M.J., 2006. The effect of environmental parameters and cyanobacterial blooms on phytoplankton dynamics of a Portuguese temperate lake. Hydrobiologia , 568, 145–157. CrossRef
DeMott W.R., 1989. The role of competition in zooplankton succession. In: Sommer U. (ed.), Plankton Ecology: Succession in Plankton Communities, Springer-Verlag, Berlin, 195–252.
DeMott, W.R., 1999. Foraging strategies and growth inhibition in five daphnids feeding on mixtures of a toxic cyanobacterium and a green alga. Freshwat. Biol. , 42, 263–274. CrossRef
DeMott, W.R., Gulati, R.D. and Van Donk, E., 2001. Daphnia food limitation in three hypereutrophic Dutch lakes: Evidence for exclusion of large-bodied species by interfering filaments of cyanobacteria. Limnol. Oceanogr. , 46, 2054–2060. CrossRef
Duncan, A., 1985. Body carbon in daphnids as an indicator of the food concentration available in the field. Adv. Limnol. , 21, 81–90.
Geitler L., 1932. Cyanophyceae von Europa. In: Kolkwitz R. (ed.), Dr. L. Rabenhorst's Kryptogamen-Flora von Deutschland, Österreich und der Schweiz, Akademische Verlagsgesellschaft, Leipzig, 1–1196.
Ghadouani, A., Pinel-Alloul, B. and Prepas, E.E., 2003. Effects of experimentally induced cyanobacterial blooms on crustacean zooplankton communities. Freshwat. Biol. , 48, 363–381. CrossRef
Ghadouani A., Pinel-Alloul B. and Prepas E.E., 2006. Could increased cyanobacterial biomass following forest harvesting cause a reduction in zooplankton body size structure? Can. J. Fish. Aquat. Sci., 63, 2308–2317.
Gliwicz, Z.M., 1994. Relative significance of direct and indirect effects of predation by planktivorous fish on zooplankton. Hydrobiologia , 272, 201–210. CrossRef
Goss, L.B. and Bunting, D.L., 1983. Daphnia development and reproduction – Responses to temperature. J. Thermal Biol. , 8, 375–380. CrossRef
Greenwood, T.L., Green, J.D., Hicks, B.J. and Chapman, M.A., 1999. Seasonal abundance of small cladocerans in Lake Mangakaware, Waikato, New Zealand. New Zeal. J. Mar. Fresh. , 33, 399–415. CrossRef
Gulati R.D. and DeMott W.R., 1996. The role of food quality for zooplankton: remarks on the state-of-the-art, perspectives and priorities. In: 1st International-Plankton-Ecology-Group Workshop on the Role of Food Quality for Zooplankton, Nieuwersluis, 38, 753–768.
Haney, J.F., 1987. Field studies on zooplankton-cyanobacteria interactions. New Zeal. J. Mar. Fresh. , 21, 467–475. CrossRef
Haney, J.F. and Hall, D.J., 1973. Sugar-coated Daphnia – Preservation technique for Cladocera. Limnol. Oceanogr. , 18, 331–333. CrossRef
Hessen D.O., Faafeng B.A. and Brettum P., 2003. Autotroph: herbivore biomass ratios; carbon deficits judged from plankton data. Hydrobiologia, 491, 167–175.
Hulsmann, S., 2001. Reproductive potential of Daphnia galeata in relation to food conditions: implications of a changing size-structure of the population. Hydrobiologia , 442, 241–252. CrossRef
Hulsmann S., Vijverberg J., Boersma M. and Mooij W.M., 2004. Effects of infochemicals released by gape-limited fish on life history traits of Daphnia: a maladaptive response? J. Plankton Res., 26, 535–543.
Jeppesen, E., Jensen, J.P., Sondergaard, M. and Lauridsen, T., 1999. Trophic dynamics in turbid and clearwater lakes with special emphasis on the role of zooplankton for water clarity. Hydrobiologia , 408, 217–231. CrossRef
Komárek J. and Anagnostidis K., 1999. Cyanoprokaryota 1, Teil: Chroococcales. Süßwasserflora von Mitteleuropa, Gustav Fischer Verlag, Jena.
Komárek J. and Fott B., 1983. Das Phytoplankton des Süßwassers, Systematik und Biologie. 7. Teil, 1. Hälfte, Chlorophyceae (Grünalgen). Ordnung: Chlorococcales, Schweizerbart'sche Verlagsbuchhandlung, Stuttgart.
Krammer K. and Lange-Bertalot H., 1986–1991. Bacillariophyceae. 1–4. Süßwasserflora von Mitteleuropa, Gustav Fischer Verlag, Stuttgart.
Lampert, W., 1978. Field-study on dependence of fecundity of Daphnia spec. on food concentration. Oecologia , 36, 363–369. CrossRef
Lampert, W., 1982. Further-studies on the inhibitory effect of the toxic blue-green Microcystis aeruginosa on the filtering rate of zooplankton. Arch. Hydrobiol. , 95, 207–220.
Lampert, W., 1987. Laboratory studies on zooplankton-Cyanobacteria interactions. New Zeal. J. Mar. Fresh. , 21, 483–490. CrossRef
Lampert, W., 1988. The relative importance of food limitation and predation in the seasonal cycle of two Daphnia species. Internationale Vereinigung für Theoretische und Angewandte Limnologie Verhandlungen , 23, 713–718.
Lampert, W., 1993. Phenotypic plasticity of the size at 1st reproduction in Daphnia – The importance of maternal size. Ecology , 74, 1455–1466. CrossRef
Lampert, W., 1994. Phenotypic plasticity of the filter screens in Daphnia – Adaptation to a low-food environment. Limnol. Oceanogr. , 39, 997–1006. CrossRef
Lampert, W. and Brendelberger, H., 1996. Strategies of phenotypic low-food adaptation in Daphnia: Filter screens, mesh sizes, and appendage beat rates. Limnol. Oceanogr. , 41, 216–223. CrossRef
Lund, J.W.G., Kipling, C. and Le Cren, E.D., 1958. The inverted microscope method of estimating algal numbers and the statistical basis of estimations by couting. Hydrobiologia , 11, 143–170. CrossRef
Machacek J., 1991. Indirect effect of planktivorous fish on the growth and reproduction of Daphnia galeata. Hydrobiologia, 225, 193–197.
Machacek, J., 2001. Daphnia galeata life history response to heterogeneous food conditions and dissolved chemicals in the Rimov Reservoir. Hydrobiologia , 442, 215–222. CrossRef
Müller-Navarra, D. and Lampert, W., 1996. Seasonal patterns of food limitation in Daphnia galeata: Separating food quantity and food quality effects. J. Plankton Res. , 18, 1137–1157. CrossRef
Nogueira A.J.A., 1992. Anamod – Extracção dos componentes modais de distribuições de frequência de variáveis biométricas, University of Coimbra, Faculty of Sciences and Technology, Coimbra.
Orcutt, J.D. and Porter, K.G., 1984. The synergistic effects of temperature and food concentration on life-history parameters of Daphnia. Oecologia , 63, 300–306. CrossRef
Paloheimo, J.E., 1974. Calculation of instantaneous birth-rate. Limnol. Oceanogr. , 19, 692–694. CrossRef
Pinel-Alloul, B., 1993. Zooplankton community structure in hardwater hypertrophic lakes of Alberta. Wat. Sci. Technol. , 27, 353–361.
Polishchuk, L.V. and Vijverberg, J., 2005. Contribution analysis of body mass dynamics in Daphnia. Oecologia , 144, 268–277. CrossRef
Radwan, S. and Popiolek, B., 1989. Percentage of Rotifers in spring zooplankton in lakes of different trophy. Hydrobiologia , 186, 235–238. CrossRef
Reede, T., 1995. Life-history shifts in response to different levels of fish Kairomones in Daphnia. J. Plankton Res. , 17, 1661–1667. CrossRef
Reinikainen M., Ketola M. and Walls M., 1994. Effects of the concentrations of toxic Microcystis aeruginosa and an alternative food on the survival of Daphnia pulex. Limnol. Oceanogr., 39, 424–432.
Repka S., 1996. Inter- and intraspecific differences in Daphnia life histories in response to two food sources: The green alga Scenedesmus and the filamentous cyanobacterium Oscillatoria. J. Plankton Res., 18, 1213–1223.
Repka S., 1997. Effects of food type on the life history of Daphnia clones from lakes differing in trophic state. I. Daphnia galeata feeding on Scenedesmus and Oscillatoria. Freshwat. Biol., 38, 675–683.
Rohrlack, T., Dittmann, E., Borner, T. and Christoffersen, K., 2001. Effects of cell-bound microcystins on survival and feeding of Daphnia spp. Appl. Environ. Microbiol. , 67, 3523–3529. CrossRef
Scourfield D.J. and Harding J.P., 1966. A key to the British freshwater Cladocera, 3rd edn., Freshwater Biological Association, Sciencific Publication 5, Ambleside.
Smolders, R., Baillieul, M. and Blust, R., 2005. Relationship between the energy status of Daphnia magna and its sensitivity to environmental stress. Aquat. Toxicol. , 73, 155–170. CrossRef
Sommer, U., Gliwicz, Z.M., Lampert, W. and Duncan, A., 1986. The PEG-model of seasonal succession of planktonic events in fresh waters. Arch. Hydrobiol. , 106, 433–471.
Stibor, H., 1992. Predator induced life-history shifts in a fresh-water Cladoceran. Oecologia , 92, 162–165. CrossRef
Tollrian R. and Dodson S.I., 1999. Inducible defences in cladocera: constrains, costs, and multipredator environments. In: Tollrian R. and Harvell C.D. (eds.), The Ecology and Evolution of Inducible Defenses, Princeton University Press, 177–202.
Vanni, M.J. and Lampert, W., 1992. Food quality effects on life-history traits and fitness in the generalist herbivore Daphnia. Oecologia , 92, 48–57. CrossRef
Vasconcelos, V.M., Evans, W.R., Carmichael, W.W. and Namikoshi, M., 1993. Isolation of microcystin-LR from a Microcystis (Cyanobacteria) waterbloom collected in the drinking-water reservoir for Porto, Portugal. J. Environ. Sci. Heal. A , 28, 2081–2094.
Vijverberg J. and Boersma M., 1997. Long-term dynamics of small-bodied and large-bodied cladocerans during the eutrophication of a shallow reservoir, with special attention for Chydorus sphaericus. Hydrobiologia, 360, 233–242.
Viroux, L., 2002. Seasonal and longitudinal aspects of microcrustacean (Cladocera, Copepoda) dynamics in a lowland river. J. Plankton Res. , 24, 281–292. CrossRef
Wetzel R.G., 1993. Limnologia, 2nd edn., Fundação Calouste Gulbenkian, Lisboa.