Abstract:We investigated the behaviour and life histories of large zooplankton in the Esch-sur-Suˆre reservoir (Luxembourg). We found that the decrease in size at maturity, as well as diurnal refuge in deep waters, were the adaptive responses (concurrently or alternatively) adopted by large zooplankters to cope with the increasing predation risk throughout the summer. Daphnia galeata initiated a more severe trade-off to cope with high summer predation relative to other cladoceran species. Diaphanosoma brachyurum and Da… Show more
“…Despite Eudiaptomus gracilis is often presented as a herbivorous species, its clearance rates on protozoa are similar to those of cladocerans such as Bosmina longirostris or Daphnia hyalina (Ju¨rgens et al, 1996;Jack & Gilbert, 1997). Contrary to what has happened in May, metazooplankton is not able to control protozoa and phytoplankton because it is itself controlled by juvenile fishes that move out into the pelagic zone at this time (Thys & Hoffmann, 2005). Reduced grazing pressure also beneficiated to phytoplankton whose biomass reached maximum values in mid-July.…”
Section: Seasonal Patterns Of Protozoa Developmentmentioning
The spatio-temporal distribution of the heterotrophic nanoflagellates (HNF) and ciliates was monitored in the reservoir of Esch-sur-Suˆre during the year 1999. Three main periods of protozoan development were observed, in early April, early May, and in July. On the basis of the seasonal dynamics, it appeared that the early spring development of protozoa was probably not controlled by resources or predators. The second protozoan development was progressively controlled by the increase of metazooplankton density that led to the clear water phase characterised by very low protozoan densities and biomasses. A summer development of protozoa was possible thanks to the development of bacteria and moderate metazooplankton densities due to the appearance of non-edible algae. Prorodontida, Halteriida and Strombidiida were the dominant ciliates in the upper part of the water column. A development of Tintinnida was moreover observed in spring whereas Philasterida and Sessilida developed in winter and summer. Ciliates occupied the entire water column in spring and were concentrated in the epilimnion and the metalimnion during the summer period where they fed on bacteria and algae.
“…Despite Eudiaptomus gracilis is often presented as a herbivorous species, its clearance rates on protozoa are similar to those of cladocerans such as Bosmina longirostris or Daphnia hyalina (Ju¨rgens et al, 1996;Jack & Gilbert, 1997). Contrary to what has happened in May, metazooplankton is not able to control protozoa and phytoplankton because it is itself controlled by juvenile fishes that move out into the pelagic zone at this time (Thys & Hoffmann, 2005). Reduced grazing pressure also beneficiated to phytoplankton whose biomass reached maximum values in mid-July.…”
Section: Seasonal Patterns Of Protozoa Developmentmentioning
The spatio-temporal distribution of the heterotrophic nanoflagellates (HNF) and ciliates was monitored in the reservoir of Esch-sur-Suˆre during the year 1999. Three main periods of protozoan development were observed, in early April, early May, and in July. On the basis of the seasonal dynamics, it appeared that the early spring development of protozoa was probably not controlled by resources or predators. The second protozoan development was progressively controlled by the increase of metazooplankton density that led to the clear water phase characterised by very low protozoan densities and biomasses. A summer development of protozoa was possible thanks to the development of bacteria and moderate metazooplankton densities due to the appearance of non-edible algae. Prorodontida, Halteriida and Strombidiida were the dominant ciliates in the upper part of the water column. A development of Tintinnida was moreover observed in spring whereas Philasterida and Sessilida developed in winter and summer. Ciliates occupied the entire water column in spring and were concentrated in the epilimnion and the metalimnion during the summer period where they fed on bacteria and algae.
“…However, we did not observe this migration pattern in this study, and most D. brachyurum individuals remained in the bottom layer during the night in reservoirs with D max >6 m. Adamczuk (2009) also reported that D. brachyurum did not perform migrations pattern. They seem less susceptible to fish predation as indicated by the low alteration of their vertical distribution (Thys and Hoffmann, 2005). Therefore, D. …”
“…Parental care behavior increases the competitiveness of peacock bass (Latini & Petrere, 2004), and, along with feeding plasticity could be important for successful colonization of lentic habitat. The lentic characteristics of reservoirs cause considerable water transparency and facilitate predation Thys & Hoffmann, 2005) by diurnal piscivores like the peacock bass (Novaes et al, 2004). Furthermore, abundant prey during the colonization phase (Agostinho et al, 1999) may also aid in the success of this species.…”
In order to investigate trophic interactions, the diets of peacock bass (Cichla kelberi) and dogfish (Galeocharax knerii) were studied in the Corumbá Reservoir between 1997 and 2000. This dietary study was performed to assess the niche breadth of each species and to determine the degree of niche overlap during different phases of reservoir colonization. During Period I, peacock bass were absent or recorded only in low numbers; during Periods II and III, peacock bass reached high abundances in the reservoir. Interactions between the species were weak during period I, but, during Periods II and III, they were found to interact intensively. The diet overlap was highest during Period II. The niche breadth fluctuated for both species in the different phases. Greater niche breadth was observed for dogfish during periods of low peacock abundance (i.e., Period I), and the lowest niche breadth value was observed during Period II. During the same period, the peacock bass exhibited a wide foraging niche. During Period III, the dogfish showed an increase of its niche breadth, while for the peacock bass a simultaneous decrease in the niche breadth, caused by increasing rates of cannibalism, was recorded. These results show that the presence of peacock bass induces changes in the diet of dogfish, probably due to a restricted number of prey items.
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