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Predator Density (predator + density)
Selected AbstractsMortality dynamics and population regulation in Bemisia tabaciENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 2 2005Steven E. Naranjo Abstract Natural mortality is an important determinant of the population dynamics of a species, and an understanding of mortality forces should aid in the development of better management strategies for insect pests. An in situ, observational method was used to construct cohort-based life tables for Bemisia tabaci (Gennadius) Biotype B (Homoptera: Aleyrodidae) over 14 generations on cotton in central Arizona, USA, from 1997 to 1999. In descending order, median marginal rates of mortality were highest for predation, dislodgment, unknown causes, egg inviability, and parasitism. The highest mortality occurred during the 4th nymphal stadium, and the median rate of immature survival over 14 generations was 6.6%. Predation during the 4th nymphal stadium was the primary key factor. Irreplaceable mortality was highest for predation and dislodgment, with the absence of these mortality factors leading to the greatest increases in estimated net reproduction. There was little evidence of direct or delayed density-dependence for any mortality factor. Wind, rainfall, and predator densities were associated with dislodgment, and rates of predation were related to densities of Geocoris spp., Orius tristicolor (White), Chrysoperla carnea s.l. Stephens, and Lygus hesperus Knight. Simulations suggest that immigration and emigration play important roles in site-specific dynamics by explaining departures from observed population trajectories based solely on endogenous reproduction and mortality. By a direct measurement of these mortality factors and indirect evidence of adult movement, we conclude that efficient pest management may be best accomplished by fostering greater mortality during the 4th stadium, largely through a conservation of predators and by managing immigrating adult populations at their sources. [source] Interspecific interference and the functional response of four species of carnivorous stonefliesFRESHWATER BIOLOGY, Issue 9 2003J.M. Elliott Summary 1.,A previous study compared the functional responses to their prey and intraspecific interference in mature larvae of Perlodes microcephalus, Isoperla grammatica, Dinocras cephalotes and Perla bipunctata. The present study extends this work by assessing interspecific interference between pairs of these species in equal numbers (one, two or three larvae per species) to provide total predator densities of two, four or six larvae. Baetis larvae as prey were replaced as they were eaten, and their density per predator was varied between 20 and 200 larvae. 2.,The number of prey eaten by each competing species increased curvilinearly with prey density, the relationship being well described by a Type II model. Of the two constants in the model, handling time varied considerably between species, mean values being shortest for Perlodes, slightly higher for Isoperla, and much higher for Dinocras and Perla. It was not affected significantly either by predator density or the identity of the competing species. 3.,Attack rate also varied between species and decreased with predator density. This decrease was slight for Perlodes, and also for Dinocras and Perla in competition with Isoperla. The decrease in Dinocras and Perla was similar to that for intraspecific interference. 4.,The decrease in attack rate was described by a convex curve for Perlodes with the other three species and for Dinocras/Perla with Isoperla, but by a concave curve (negative power function) for Isoperla competing with the other three species, and for both Dinocras and Perla in competition with Perlodes. Prey consumption also decreased with predator density, the severity of competition with different species reflecting that for attack rate. 5.,A comparison with previous results for intraspecific interference showed that the latter was dominant for Perlodes in all contests and for Dinocras or Perla competing with Isoperla, whilst interspecific interference dominated for Isoperla in all contests and for Dinocras and Perla competing with Perlodes. Both types of interference were applicable to competition between Dinocras and Perla. Isoperla was the least, and Perlodes the most, aggressive of the four species with Dinocras and Perla intermediate. [source] Characteristics of woods used recently and historically by Lesser Spotted Woodpeckers Dendrocopos minor in EnglandIBIS, Issue 3 2010ELISABETH C. CHARMAN Lesser Spotted Woodpecker Dendrocopos minor numbers have declined greatly in England since the early 1980s for reasons that are not yet fully understood. It has been suggested that the species' decline may be linked to the increase in Great Spotted Woodpeckers Dendrocopos major, changes in woodland habitat quality (such as deadwood abundance) and landscape-scale changes in tree abundance. We tested some of these hypotheses by comparing the characteristics of woods in southern England where the species is still relatively numerous with those of woods used in the 1980s before the major decline. In each time period, habitat, predator and landscape information from woods known to be occupied by Lesser Spotted Woodpeckers was compared with those found to be unoccupied during surveys. Before the main period of decline, Lesser Spotted Woodpeckers used oak-dominated, mature, open woods with a large amount of standing deadwood. Habitat use assessed from recent data was very similar, the species being present in mature, open, oak-dominated woodlands. There was a strong relationship between wood use probability and the extent of woodland within a 3-km radius, suggesting selection for more heavily wooded landscapes. In recent surveys, there was no difference in deadwood abundance or potential predator densities between occupied and unoccupied woods. Habitat management should focus on creating and maintaining networks of connected woodlands in areas of mature, open woods. Finer-scale habitat selection by Lesser Spotted Woodpecker within woodlands should be assessed to aid development of beneficial management actions. [source] Phenotypic plasticity of anuran larvae: environmental variables influence body shape and oral morphology in Rana temporaria tadpolesJOURNAL OF ZOOLOGY, Issue 2 2002Miguel Vences Abstract Environmental variables shaped the morphology of tadpoles of the common frog, Rana temporaria, in various ways at the Pyrenean locality Circo de Piedrafita. Examining only specimens in similar developmental stages, those from small ponds (with higher temperature and higher tadpole density) had lower growth rates, lower relative tail height, lower relative body width and fewer labial keratodonts and keratodont rows. The variation in keratodonts may have been caused by heterochrony related to the slower growth rate. The number of lingual papillae also differed between ponds but was not related to pond size. Higher predator densities caused a higher percentage of damaged tails and a lower relative tail length in specimens with apparently intact tails, probably as a result of incomplete regeneration after mutilations earlier in development. [source] Optimal foraging when predation risk increases with patch resources: an analysis of pollinators and ambush predatorsOIKOS, Issue 5 2010Emily I. Jones Pollinators and their predators share innate and learned preferences for high quality flowers. Consequently, pollinators are more likely to encounter predators when visiting the most rewarding flowers. I present a model of how different pollinator species can maximize lifetime resource gains depending on the density and distribution of predators, as well as their vulnerability to capture by predators. For pollinator species that are difficult for predators to capture, the optimal strategy is to visit the most rewarding flowers as long as predator density is low. At higher predator densities and for pollinators that are more vulnerable to predator capture, the lifetime resource gain from the most rewarding flowers declines and the optimal strategy depends on the predator distribution. In some cases, a wide range of floral rewards provides near-maximum lifetime resource gains, which may favor generalization if searching for flowers is costly. In other cases, a low flower reward level provides the maximum lifetime resource gain and so pollinators should specialize on less rewarding flowers. Thus, the model suggests that predators can have qualitatively different top-down effects on plant reproductive success depending on the pollinator species, the density of predators, and the distribution of predators across flower reward levels. [source] Seasonal and habitat differences affect the impact of food and predation on herbivores: a comparison between gaps and understory of a tropical forestOIKOS, Issue 1 2007Lora A. Richards Herbivore populations are influenced by a combination of food availability and predator pressure, the relative contribution of which is hypothesized to vary across a productivity gradient. In tropical forests, treefall gaps are pockets of high productivity in the otherwise less productive forest understory. Thus, we hypothesize that higher light availability in gaps will increase plant resources, thereby decreasing resource limitation of herbivores relative to the understory. As a result, predators should regulate herbivore populations in gaps, whereas food should limit herbivores in the understory. We quantified potential food availability and compared arthropod herbivore and predator densities in large forest light gaps and in the intact understory in Panama. Plants, young leaves, herbivores and predators were significantly more abundant per ground area in gaps than in the understory. This pattern was similar when we focused on seven gap specialist plant species and 15 shade-tolerant species growing in gaps and understory. Consistent with the hypothesis, herbivory rates were higher in gaps than the understory. Per capita predation rates on artificial caterpillars indicated higher predation pressure in gaps in both the dry and late wet seasons. These diverse lines of evidence all suggest that herbivores experience higher predator pressure in gaps and more food limitation in the understory. [source] Habitat-dependent foraging in a classic predator,prey system: a fable from snowshoe haresOIKOS, Issue 2 2005Douglas W. Morris Current research contrasting prey habitat use has documented, with virtual unanimity, habitat differences in predation risk. Relatively few studies have considered, either in theory or in practice, simultaneous patterns in prey density. Linear predator,prey models predict that prey habitat preferences should switch toward the safer habitat with increasing prey and predator densities. The density-dependent preference can be revealed by regression of prey density in safe habitat versus that in the riskier one (the isodar). But at this scale, the predation risk can be revealed only with simultaneous estimates of the number of predators, or with their experimental removal. Theories of optimal foraging demonstrate that we can measure predation risk by giving-up densities of resource in foraging patches. The foraging theory cannot yet predict the expected pattern as predator and prey populations covary. Both problems are solved by measuring isodars and giving-up densities in the same predator,prey system. I applied the two approaches to the classic predator,prey dynamics of snowshoe hares in northwestern Ontario, Canada. Hares occupied regenerating cutovers and adjacent mature-forest habitat equally, and in a manner consistent with density-dependent habitat selection. Independent measures of predation risk based on experimental, as well as natural, giving-up densities agreed generally with the equal preference between habitats revealed by the isodar. There was no apparent difference in predation risk between habitats despite obvious differences in physical structure. Complementary studies contrasting a pair of habitats with more extreme differences confirmed that hares do alter their giving-up densities when one habitat is clearly superior to another. The results are thereby consistent with theories of adaptive behaviour. But the results also demonstrate, when evaluating differences in habitat, that it is crucial to let the organisms we study define their own habitat preference. [source] Oviposition habitat selection by mosquitoes in response to predator (Notonecta maculata) densityPHYSIOLOGICAL ENTOMOLOGY, Issue 2 2004Avi Eitam Abstract., Some species of mosquitoes can detect the presence of predatory notonectid bugs and avoid oviposition in predator pools. The oviposition response of two mosquito species, Culiseta longiareolata Macquart and Culex laticinctus Edwards (Diptera: Culicidae), to a range of densities of the predator, Notonecta maculata Fabricius (Heteroptera: Notonectidae), was tested here. Densities of 0, 1, 2 or 4 Notonecta were established in 30-L artificial pools. Both mosquito species oviposited less in predator pools, but the response was unrelated to predator density, whereas vulnerability of Culiseta immatures to predation was density-dependent. Thus, although mosquitoes can detect Notonecta at any density within the range tested, they may be unable to discriminate among predator densities. The avoidance of predator pools by Culiseta, as well as its vulnerability to predation, occurred to a lesser degree than in earlier studies. This may have been due to the mitigating effects of components of the biotic community. [source] Foraging behavior of an estuarine predator, the blue crab Callinectes sapidus in a patchy environmentECOGRAPHY, Issue 1 2000Mary E. Clark To define general principles of predator-prey dynamics in an estuarine subtidal environment, we manipulated predator density (the blue crab, Callinectes sapidus) and prey (the clam, Macoma balthica) patch distribution in large field enclosures in the Rhode River subestuary of the central Chesapeake Bay. The primary objectives were to determine whether predators forage in a way that maximizes prey consumption and to assess how their foraging success is affected by density of conspecifics. We developed a novel ultrasonic telemetry system to observe behavior of individual predators with unprecedented detail. Behavior of predators was more indicative of optimal than of opportunistic foraging. Predators appeared responsive to the overall quality of prey in their habitat. Rather than remaining on a prey patch until depletion, predators appeared to vary their patch use with quality of the surrounding environment. When multiple (two) prey patches were available, residence time of predators on a prey patch was shorter than when only a single prey patch was available. Predators seemed to move among the prey patches fairly regularly, dividing their foraging time between the patches and consuming prey from each of them at a similar rate. That predators more than doubled their consumption of prey when we doubled the number of prey (by adding the second patch) is consistent with optimizing behaviors - rather than with an opportunistic increase in prey consumption brought about simply by the addition of more prey. Predators at high density, however, appeared to interfere with each other's foraging success, reflected by their lower rates of prey consumption. Blue crabs appear to forage more successfully (and their prey to experience higher mortality) in prey patches located within 15,20 meters of neighboring patch, than in isolated patches. Our results are likely to apply, at least qualitatively, to other crustacean-bivalve interactions, including those of commercial interest; their quantitative applicability will depend on the mobility of other predators and the scale of patchiness they perceive. [source] Control of aphids on wheat by generalist predators: effects of predator density and the presence of alternative preyENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 3 2009Katja Oelbermann Abstract There is evidence for both positive and negative effects of generalist predators on pest populations and the various reasons for these contrasting observations are under debate. We studied the influence of a generalist predator, Pardosa lugubris (Walckenaer) (Araneae: Lycosidae), on an aphid pest species, Rhopalosiphum padi (L.) (Hemiptera: Aphididae; low food quality for the spider), and its host plant wheat, Triticum spec. (Poaceae). We focused on the role of spider density and the availability of alternative prey, Drosophila melanogaster Meigen (Diptera: Drosophilidae; high food quality). The presence of spiders significantly affected plant performance and aphid biomass. Alternative prey and spider density strongly interacted in affecting aphids and plants. High spider density significantly improved plant performance but also at low spider density plants benefited from spiders especially in the presence of alternative prey. The results suggest that generalist arthropod predators may successfully reduce plant damage by herbivores. However, their ability to control prey populations varies with predator nutrition, the control of low-quality prey being enhanced if alternative higher-quality prey is available. [source] Interspecific interference and the functional response of four species of carnivorous stonefliesFRESHWATER BIOLOGY, Issue 9 2003J.M. Elliott Summary 1.,A previous study compared the functional responses to their prey and intraspecific interference in mature larvae of Perlodes microcephalus, Isoperla grammatica, Dinocras cephalotes and Perla bipunctata. The present study extends this work by assessing interspecific interference between pairs of these species in equal numbers (one, two or three larvae per species) to provide total predator densities of two, four or six larvae. Baetis larvae as prey were replaced as they were eaten, and their density per predator was varied between 20 and 200 larvae. 2.,The number of prey eaten by each competing species increased curvilinearly with prey density, the relationship being well described by a Type II model. Of the two constants in the model, handling time varied considerably between species, mean values being shortest for Perlodes, slightly higher for Isoperla, and much higher for Dinocras and Perla. It was not affected significantly either by predator density or the identity of the competing species. 3.,Attack rate also varied between species and decreased with predator density. This decrease was slight for Perlodes, and also for Dinocras and Perla in competition with Isoperla. The decrease in Dinocras and Perla was similar to that for intraspecific interference. 4.,The decrease in attack rate was described by a convex curve for Perlodes with the other three species and for Dinocras/Perla with Isoperla, but by a concave curve (negative power function) for Isoperla competing with the other three species, and for both Dinocras and Perla in competition with Perlodes. Prey consumption also decreased with predator density, the severity of competition with different species reflecting that for attack rate. 5.,A comparison with previous results for intraspecific interference showed that the latter was dominant for Perlodes in all contests and for Dinocras or Perla competing with Isoperla, whilst interspecific interference dominated for Isoperla in all contests and for Dinocras and Perla competing with Perlodes. Both types of interference were applicable to competition between Dinocras and Perla. Isoperla was the least, and Perlodes the most, aggressive of the four species with Dinocras and Perla intermediate. [source] Dynamic models allowing for flexibility in complex life histories accurately predict timing of metamorphosis and antipredator strategies of preyFUNCTIONAL ECOLOGY, Issue 6 2009Andrew D. Higginson Summary 1.,The development of antipredator defences in the larval stage of animals with complex life cycles is likely to be affected by costs associated with creating and maintaining such defences because of their impact on the timing of maturation or metamorphosis. 2.,Various theoretical treatments have suggested that investment in defence should both increase or decrease with increasing resource availability, but a recent model predicts investment in defences should be highest at intermediate resource level and predator density. 3.,Previous models of investment in defence and timing of metamorphosis provide a poor match to empirical data. Here we develop a dynamic state-dependent model of investment in behavioural and morphological defences that enables us to allow flexibility in investment in defences over development, the timing of metamorphosis and the size of the organism at metamorphosis that were absent from previous theory. 4.,We show that the inclusion of this flexibility results in different predictions to those of the fixed investment approach used previously, especially when we allow metamorphosis to occur at the optimal time and state for the organism. 5.,Under these more flexible conditions, we predict that morphological defences should be insensitive to resource level whilst behavioural defences should either increase or decrease with increasing resources depending on the predation risk and the magnitude of the fitness benefits of large size at metamorphosis. 6.,Our work provides a formal framework in which we might progress in the study of how the use of antipredator defences is affected by their costs. Most of the predictions of our model in are in good accord with empirical results, and can be understood in terms of the underlying biological assumptions. The reasons why simpler models failed to match empirical observations can be explained, and our predictions that are a poor match help to target the circumstances which warrant future study. [source] Non-lethal effects of predation in birdsIBIS, Issue 1 2008WILL CRESSWELL Predators can affect individual fitness and population and community processes through lethal effects (direct consumption or ,density' effects), where prey is consumed, or through non-lethal effects (trait-mediated effects or interactions), where behavioural compensation to predation risk occurs, such as animals avoiding areas of high predation risk. Studies of invertebrates, fish and amphibians have shown that non-lethal effects may be larger than lethal effects in determining the behaviour, condition, density and distribution of animals over a range of trophic levels. Although non-lethal effects have been well described in the behavioural ecology of birds (and also mammals) within the context of anti-predation behaviour, their role relative to lethal effects is probably underestimated. Birds show many behavioural and physiological changes to reduce direct mortality from predation and these are likely to have negative effects on other aspects of their fitness and population dynamics, as well as affecting the ecology of their own prey and their predators. As a consequence, the effects of predation in birds are best measured by trade-offs between maximizing instantaneous survival in the presence of predators and acquiring or maintaining resources for long-term survival or reproduction. Because avoiding predation imposes foraging costs, and foraging behaviour is relatively easy to measure in birds, the foraging,predation risk trade-off is probably an effective framework for understanding the importance of non-lethal effects, and so the population and community effects of predation risk in birds and other animals. Using a trade-off approach allows us to predict better how changes in predator density will impact on population and community dynamics, and how animals perceive and respond to predation risk, when non-lethal effects decouple the relationship between predator density and direct mortality rate. The trade-off approach also allows us to identify where predation risk is structuring communities because of avoidance of predators, even when this results in no observable direct mortality rate. [source] Breeding success in a Houbara Bustard Chlamydotis [undulata] macqueenii population on the eastern fringe of the Jungar Basin, People's Republic of ChinaIBIS, Issue 2 2002O. Combreau Nesting success and chick survival of a migratory population of Houbara Bustard Chlamydotis [undulata] macqueenii were studied during three consecutive years (1998,2000) in the Xinjiang province of north-west China. A total of 45 nests was monitored and 85 broods comprising 227 chicks were captured, of which 82 chicks were radio-tracked. Start of laying varied between 6 and 17 April between years but the laying mode fell consistently between 26 and 30 April. Mean clutch size was 4.0 (sd = 0.8) (range 2,6) for early clutches and 3.3 (sd = 1.1) for late clutches (range 2,5). The average nesting success was 0.588 (sd = 0.270) but great variations were observed between years ,0.882 in 1998, 0.530 in 1999 and 0.351 in 2000. This was related to increased predation in 1999 and 2000, which is reflected by increased predator density (chiefly Corsac Fox Vulpes corsac and Long-legged Buzzards Buteo rufinus). The overall hatchability, defined as the proportion of eggs hatched in successful nests was 0.839 sd = 0.238). The average brood size at hatching varied from 2.9 (sd = 0.8) to 3.3 (sd = 0.9) according to years, and no significant decrease in brood size was observed in the first 5 days post-hatching. In 1999 and 2000 the brood size diminished sharply (14% and 27%, respectively) in prefledging chicks. A further severe decrease (37%) was observed in fledglings in 2000, probably due to predation by raptors. For the 3 years of the study, a successful female Houbara would bring on average 2.3 (sd = 0.9) chicks to fledging and would have lost 30.2% (sd = 14.9%) of its brood to adversity during the rearing process. The proportion of females that lost their entire brood was 0.181 in 1998, 0.708 in 1999 and 0.453 in 2000. For the 3 years of the study, only 55.3% (sd = 26.3%) of the females hatching eggs brought chicks to fledging. The overall chick production was 0.827 per breeding female per year and the probability of an egg laid producing a fledgling of 8 weeks old was 0.190. [source] BIOLOGY OF CHRYSOPA PHYLLOCHROMA WESMAEL (NEUROPTERA: CHRYSOPIDAE).INSECT SCIENCE, Issue 3 2004II: INTRASPECIFIC INTERFERENCE AND SEARCHING CAPACITY Abstract, The present study examined intraspecific interference and searching behavior of Chrysopa phyllochroma Wesmael (Neuroptera: Chrysopidae) for Aphis gossypii Glover (Homoptera: Aphididae) nymphs under laboratory and greenhouse conditions. The results were shown as follow: 1) In four different arenas (i.e. Petri dish, glass vessel, glass vessel with barriers in it, and cage with potted cotton plant), the predaceous efficiency of C. phyllochroma larvae varied with the predator density, the hunt constant (Q) and the intraspecific interference (m) increased with the prey density but decreased with the space heterogeneity; 2) In cage with potted cotton plant, the first- and second-instar green lacewing larvae consumed 13.6 and 29.4 cotton aphiddday respectively. The number of cotton aphids consumed by C. phyllochroma on lower leaves was significantly less than that on upper leaves; and 3) In cage with potted cotton plant, the percentage of the first- and second-instar green lacewing larvae located on upper leaves was significant less than that on lower leaves. [source] Predator behaviour and prey density: evaluating density-dependent intraspecific interactions on predator functional responsesJOURNAL OF ANIMAL ECOLOGY, Issue 1 2001Nilsson P. Anders Abstract 1In models of size-structured predator,prey systems, the effects are evaluated of gape-size limited predation on prey population growth and density when predators are non-interacting, cannibalistic, interfering, and cannibalistic and interfering. 2Predation from non-interacting predators markedly reduces prey density, compared with prey densities in the absence of predation. When density-dependent cannibalism between predators is introduced, predator density and therefore total functional response decrease, resulting in a decrease in predation pressure and higher prey densities. 3Size- and density-dependent interference between predators substantially decreases functional responses in the predators, and the prey population is thus allowed to grow more dense. Allowing for cannibalism between interfering predators also decreases predator density, but here the decreased number of predators does not have the releasing effect seen in solely cannibalistic predators. The interference between predators decreases with predator density, and per capita functional responses increase and compensate for the decrease in predator density. 4These theoretical results are compared with results from natural systems with pikeperch and northern pike. Both species are cannibalistic, and pike are also kleptoparasitic, mirroring the models. Results from introductions of the different piscivores into natural systems corroborate the outcome of the models, since introduction or increased densities of pikeperch have shown to have severe and long-lasting effects on prey, while pike have only initial, decreasing over time effects on prey stock. Thus, predator behaviour may seriously affect predator impact on prey, and size- and density-dependent interactions between predators may be a major key to the understanding of predator,prey dynamics and community composition in lakes. [source] Influence of non-crop plants on stink bug (Hemiptera: Pentatomidae) and natural enemy abundance in tomatoesJOURNAL OF APPLIED ENTOMOLOGY, Issue 8 2010C. G. Pease Abstract We investigated the effects of weed hosts on stink bug density and damage (Euschistus conspersus Uhler and Thyanta pallidovirens Stal), and a nectar bearing plant on natural enemies of stink bugs in the Sacramento Valley of California. Stink bug density and fruit damage were evaluated in processing tomatoes adjacent to weedy and cultivated borders. The density of E. conspersus was significantly greater in tomatoes adjacent to weedy borders in July but not during August/September. Thyanta pallidovirens was less abundant overall (19%), but was found in significantly greater densities adjacent to cultivated borders in July but not in August/September. Mean percent fruit damage by stink bugs was greater adjacent to the weedy border than the cultivated border, but this difference was not significant. Stink bug egg parasitism and generalist predator density were evaluated in fresh market tomatoes adjacent to a sweet alyssum (Lobularia maritima L.) border and an unplanted control border at three sites. Egg parasitism was significantly greater in the alyssum treatment for the 9,12 September sampling period. Jalysus wickhami VanDuzee (Hemiptera: Berytidae) density was significantly greater in the alyssum treatment in mid-June. No other significant differences in predator populations were detected. Results of these two studies show that habitat manipulations have the potential to reduce densities of E. conspersus in tomato, the first step in developing a farmscape management plan for stink bug control. [source] Morphological variation of perch Perca fluviatilis in humic lakes: the effect of predator density, competition and prey abundanceJOURNAL OF FISH BIOLOGY, Issue 4 2010J. Kekäläinen Between and within-lake variations in morphology of perch Perca fluviatilis were studied in four humic lakes in eastern Finland. Perca fluviatilis were more streamlined and smaller headed in a lake with the highest abundance of cyprinids, but lowest abundance of predators (Lake Tuopanjärvi), indicating adaptation to planktivorous feeding and low predator density. Highest bodied fish were found from a lake with the lowest cyprinid but highest predator abundance (Lake Koppelojärvi), which conversely indicates adaptation to more effective predator avoidance. Furthermore, the length of the paired fins was longest in Lake Kinnasjärvi and Lake Tuopanjärvi, where the abundance of benthic macroinvertebrates was lowest, suggesting selection for more effective benthivory. Clear morphological differences of P. fluviatilis between habitats were found only in Lake Kinnasjärvi, whereas in Lake Koppelojärvi and Lake Tuopanjärvi only the length of the paired fins differed and in Lake Harkkojärvi no differences were found. Taken together, these results suggest that inter and intrapopulation morphological differences are probably highly dependent on different biotic factors (i.e. predation risk, resource availability and competition). Spatial and temporal variations in these factors may have a great effect on body morphology of P. fluviatilis. [source] Terrestrial carnivores and human food production: impact and managementMAMMAL REVIEW, Issue 2-3 2008PHILIP J. BAKER ABSTRACT 1The production of food for human consumption has led to an historical and global conflict with terrestrial carnivores, which in turn has resulted in the extinction or extirpation of many species, although some have benefited. At present, carnivores affect food production by: (i) killing human producers; killing and/or eating (ii) fish/shellfish; (iii) game/wildfowl; (iv) livestock; (v) damaging crops; (vi) transmitting diseases; and (vii) through trophic interactions with other species in agricultural landscapes. Conversely, carnivores can themselves be a source of dietary protein (bushmeat). 2Globally, the major areas of conflict are predation on livestock and the transmission of rabies. At a broad scale, livestock predation is a customary problem where predators are present and has been quantified for a broad range of carnivore species, although the veracity of these estimates is equivocal. Typically, but not always, losses are small relative to the numbers held, but can be a significant proportion of total livestock mortality. Losses experienced by producers are often highly variable, indicating that factors such as husbandry practices and predator behaviour may significantly affect the relative vulnerability of properties in the wider landscape. Within livestock herds, juvenile animals are particularly vulnerable. 3Proactive and reactive culling are widely practised as a means to limit predation on livestock and game. Historic changes in species' distributions and abundance illustrate that culling programmes can be very effective at reducing predator density, although such substantive impacts are generally considered undesirable for native predators. However, despite their prevalence, the effectiveness, efficiency and the benefit:cost ratio of culling programmes have been poorly studied. 4A wide range of non-lethal methods to limit predation has been studied. However, many of these have their practical limitations and are unlikely to be widely applicable. 5Lethal approaches are likely to dominate the management of terrestrial carnivores for the foreseeable future, but animal welfare considerations are increasingly likely to influence management strategies. The adoption of non-lethal approaches will depend upon proof of their effectiveness and the willingness of stakeholders to implement them, and, in some cases, appropriate licensing and legislation. 6Overall, it is apparent that we still understand relatively little about the importance of factors affecting predation on livestock and how to manage this conflict effectively. We consider the following avenues of research to be essential: (i) quantified assessments of the loss of viable livestock; (ii) landscape-level studies of contiguous properties to quantify losses associated with variables such as different husbandry practices; (iii) replicated experimental manipulations to identify the relative benefit of particular management practices, incorporating (iv) techniques to identify individual predators killing stock; and (v) economic analyses of different management approaches to quantify optimal production strategies. [source] Optimal foraging when predation risk increases with patch resources: an analysis of pollinators and ambush predatorsOIKOS, Issue 5 2010Emily I. Jones Pollinators and their predators share innate and learned preferences for high quality flowers. Consequently, pollinators are more likely to encounter predators when visiting the most rewarding flowers. I present a model of how different pollinator species can maximize lifetime resource gains depending on the density and distribution of predators, as well as their vulnerability to capture by predators. For pollinator species that are difficult for predators to capture, the optimal strategy is to visit the most rewarding flowers as long as predator density is low. At higher predator densities and for pollinators that are more vulnerable to predator capture, the lifetime resource gain from the most rewarding flowers declines and the optimal strategy depends on the predator distribution. In some cases, a wide range of floral rewards provides near-maximum lifetime resource gains, which may favor generalization if searching for flowers is costly. In other cases, a low flower reward level provides the maximum lifetime resource gain and so pollinators should specialize on less rewarding flowers. Thus, the model suggests that predators can have qualitatively different top-down effects on plant reproductive success depending on the pollinator species, the density of predators, and the distribution of predators across flower reward levels. [source] Being high is better: effects of elevation and habitat on arctic ground squirrel demographyOIKOS, Issue 2 2005Elizabeth A. Gillis We investigated the effect of local environment on the demography and population dynamics of arctic ground squirrels (Spermophilus parryii plesius) by comparing reproduction, survival, and population trends of squirrels living in low elevation boreal forest and high elevation alpine tundra sites in southwestern Yukon Territory, Canada. Contrary to the trend for most birds and mammals, reproduction was significantly lower at the lower elevation and females living at higher elevation did not delay the age at which they first reproduced. Even though survival in the boreal forest was lower in summer than in the alpine, it was higher over winter so annual adult female survival was similar between sites. Sensitivity analysis of model parameters revealed that in the forest, population growth rate (,) was most sensitive to small changes in adult active season survival whereas for the alpine population, , was most sensitive to changes in juvenile winter survival. In their respective habitats, these parameters also showed high year to year variation and thus contributed greatly to the population trends observed. Even though ground squirrels persisted in the boreal forest, the measured demographic rates indicate the forest was sink habitat (,<1) and may have relied on nearby grassy meadows for immigrants. In contrast, the alpine habitat maintained a ground squirrel population in the absence of immigration (,=1). The variation in demographic rates between ground squirrels living at high and low elevation may arise from phenotypic responses of squirrels to different habitat structure. Arctic ground squirrels rely on sight to detect predators from a safe distance, and the boreal forest, with its lower visibility and higher predator density, appears to be suboptimal habitat. [source] Oviposition habitat selection by mosquitoes in response to predator (Notonecta maculata) densityPHYSIOLOGICAL ENTOMOLOGY, Issue 2 2004Avi Eitam Abstract., Some species of mosquitoes can detect the presence of predatory notonectid bugs and avoid oviposition in predator pools. The oviposition response of two mosquito species, Culiseta longiareolata Macquart and Culex laticinctus Edwards (Diptera: Culicidae), to a range of densities of the predator, Notonecta maculata Fabricius (Heteroptera: Notonectidae), was tested here. Densities of 0, 1, 2 or 4 Notonecta were established in 30-L artificial pools. Both mosquito species oviposited less in predator pools, but the response was unrelated to predator density, whereas vulnerability of Culiseta immatures to predation was density-dependent. Thus, although mosquitoes can detect Notonecta at any density within the range tested, they may be unable to discriminate among predator densities. The avoidance of predator pools by Culiseta, as well as its vulnerability to predation, occurred to a lesser degree than in earlier studies. This may have been due to the mitigating effects of components of the biotic community. [source] |