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THE EFFECTS OF THERMAL HABITAT AND MACROINVERTEBRATE PREDATION ON THE CRUSTACEAN ZOOPLANKTON COMMUNITY OF A SMALL BOREAL SHIELD LAKEMACPHEE, SHANNON 31 March 2009 (has links)
Climate change will affect all freshwater ecosystems via both direct physiological and indirect, biologically-mediated effects. Small lakes (< 10 ha) numerically dominate the Boreal Shield and represent an important habitat for aquatic biota. Small, shallow lakes are particularly responsive to climate-induced changes in thermal structure. Furthermore, biological interactions may be particularly important in small lakes where space, habitat heterogeneity, and thermal refugia are limited. Therefore, it is critical to understand and predict the consequences of climate change for community dynamics in small Boreal Shield lakes.
Using 10 years of monitoring data and a field experiment I tested for differences in crustacean zooplankton community structure between warm and cool lake habitats. I classified years from a small, shallow Boreal Shield lake as ‘warm’ or ‘cool’ based on several characteristics of lake thermal structure. Since macroinvertebrates are often the main predators in small, shallow lakes, I further tested for potential interactions between lake thermal structure and spatially-dependent macroinvertebrate predation using in situ mesocosms.
Body sizes of two ubiquitous crustacean zooplankton taxa, Leptodiaptomus minutus and Bosmina spp., were reduced in warm years, but no differences in abundance or diversity were detected at the annual scale. In contrast, in 15d enclosure experiments, crustacean zooplankton abundance and calanoid copepodid body size were reduced by the vertically-migrating predator Chaoborus punctipennis, but only in warm isothermal conditions. Zooplankton lowered their daytime depth distribution to avoid the surface-orienting notonectid predator, Buenoa macrotibialis, regardless of thermal habitat. No predation effect was detected in a hot (25ºC) isothermal habitat where both Chaoborus and notonectids were likely heat-stressed.
Differences in abundance effects between the enclosure and monitoring data are likely due to the scales at which the analyses were conducted. Over short timescales predator-prey dynamics depended on lake thermal structure. However, over annual timescales zooplankton response was averaged across periods of seasonal change in thermal structure and biological processes, which may dampen the short-term effects associated with strong predation in isothermal conditions. Therefore, the importance of macroinvertebrate predators in regulating crustacean zooplankton community structure may increase if small lakes become progressively more isothermal with future climate change. / Thesis (Master, Biology) -- Queen's University, 2009-03-31 13:29:35.975
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Fenotypová plasticita perloočky Daphnia cucullata ve dvou polabských tůních / Phenotypic plasticity of Daphnia cucullata in two lowland pondsVolemanová, Eva January 2010 (has links)
4 ABSTRACT Characteristic high helmets in Daphnia cucullata, which increase resistance of Daphnia against various invertebrate predators, can be induced by chemical cues released by these invertebrates but also by small-scale turbulence. I evaluated the response of D. cucullata to both factors in several clones originating from two riverine pools differing in their predator regime. In a large pool, the dominant invertebrate predator is the cladoceran Leptodora kindtii, and the Daphnia population there shows a typical cyclomorphosis. In the second (small) pool, Daphnia do not produce helmets, despite the presence of the phantom midge larvae Chaoborus flavicans. I compared phenotypic changes of Daphnia cucullata clones from these pools to Chaoborus kairomones and to a small-scale turbulence in laboratory experiments. Kairomones induced significantly longer helmets in clones from both pools; however, only clones form the large pool reacted also to turbulence. As all daphnids in the experiments responded to chemical cues from Chaoborus, I assume that either the kairomone dose under natural conditions in the small pool is too low to induce helmets or the phenotypic response of the local population is mediated by other factors. On the other hand, the variation of response to small-scale turbulence suggests that...
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Re-evaluation of north-temperate reservoir food web interactions and their assessmentDillon, Rebecca January 2020 (has links)
No description available.
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The Ecological Influence of the Non-Indigenous Zooplankter <i>Eubosmina coregoni</i> in Lake EcosystemsKirkpatrick, Heather 08 April 2011 (has links)
No description available.
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Alternative Stable States in Size-Structured Communities : Patterns, Processes, and MechanismsSchröder, Arne January 2008 (has links)
<p>Alternative stable states have been, based on theoretical findings, predicted to be common in ecological systems. Empirical data from a number of laboratory and natural studies strongly suggest that alternative stable states also occur in real populations, communities and ecosystems. Potential mechanisms involve population size-structure and food-dependent individual development. These features can lead to ontogenetic niche shifts, juvenile recruitment bottlenecks and emergent Allee effects; phenomena that establish destabilising positive feedbacks in a system and hence create alternative stable states.</p><p>I studied the consequences of population size-structure for community dynamics at different scales of system complexity. I performed laboratory and ecosystem experiments. Small poecilliid fishes and planktonic invertebrates with short generation times and life spans were used as model organisms. This allowed me to assess the long-term dynamics of the populations and communities investigated.</p><p>The main experimental results are: (a) An ontogenetic niche shift in individuals of the phantom midge <i>Chaoborus</i> made the population vulnerable to an indirect competitive recruitment bottleneck imposed by cladoceran mesozooplankton via rotifers. Consequentially the natural zooplankton food web exhibited two alternative attractors. (b) Body size determined the success of <i>Poecilia reticulata</i> invading resident population of <i>Heterandria formosa</i> and thus the type of alternative stable state that established. Small invaders were outcompeted by the residents, whereas large invaders excluded their competitor by predating on its recruits. (c) External juvenile and adult mortality altered the internal feedback structure that regulates a laboratory population of <i>H. formosa</i> in such a way that juvenile biomass increased with mortality. This biomass overcompensation in a prey population can establish alternative stable states with top-predators being either absent or present.</p><p>The major conclusion is that size-structure and individual growth can indeed lead to alternative stable states. The considerations of these ubiquitous features of populations offer hence new insights and deeper understanding of community dynamics. Alternative stable states can have tremendous consequences for human societies that utilise the ecological services provided by an ecological system. Understanding the effects of size-structure on alternative stability is thus crucial for sustainable exploitation or production of food resources.</p>
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Alternative Stable States in Size-Structured Communities : Patterns, Processes, and MechanismsSchröder, Arne January 2008 (has links)
Alternative stable states have been, based on theoretical findings, predicted to be common in ecological systems. Empirical data from a number of laboratory and natural studies strongly suggest that alternative stable states also occur in real populations, communities and ecosystems. Potential mechanisms involve population size-structure and food-dependent individual development. These features can lead to ontogenetic niche shifts, juvenile recruitment bottlenecks and emergent Allee effects; phenomena that establish destabilising positive feedbacks in a system and hence create alternative stable states. I studied the consequences of population size-structure for community dynamics at different scales of system complexity. I performed laboratory and ecosystem experiments. Small poecilliid fishes and planktonic invertebrates with short generation times and life spans were used as model organisms. This allowed me to assess the long-term dynamics of the populations and communities investigated. The main experimental results are: (a) An ontogenetic niche shift in individuals of the phantom midge Chaoborus made the population vulnerable to an indirect competitive recruitment bottleneck imposed by cladoceran mesozooplankton via rotifers. Consequentially the natural zooplankton food web exhibited two alternative attractors. (b) Body size determined the success of Poecilia reticulata invading resident population of Heterandria formosa and thus the type of alternative stable state that established. Small invaders were outcompeted by the residents, whereas large invaders excluded their competitor by predating on its recruits. (c) External juvenile and adult mortality altered the internal feedback structure that regulates a laboratory population of H. formosa in such a way that juvenile biomass increased with mortality. This biomass overcompensation in a prey population can establish alternative stable states with top-predators being either absent or present. The major conclusion is that size-structure and individual growth can indeed lead to alternative stable states. The considerations of these ubiquitous features of populations offer hence new insights and deeper understanding of community dynamics. Alternative stable states can have tremendous consequences for human societies that utilise the ecological services provided by an ecological system. Understanding the effects of size-structure on alternative stability is thus crucial for sustainable exploitation or production of food resources.
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Les rôles relatifs de la prédation et des ressources sur la distribution verticale du zooplancton à travers un gradient de prédation des poissons dans les lacs boréauxGignac Brassard, Sabrina January 2020 (has links) (PDF)
No description available.
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