Olfactory assessment of predation risk in the aquatic environment

The aquatic environment is well suited for the transmission of chemical information. Aquatic animals have evolved highly sensitive receptors for detecting these cues. Here, I review behavioural evidence for the use of chemical cues by aquatic animals for the assessment of predation risk. Chemical cues are released during detection, attack, capture and ingestion of prey. The nature of the cue released depends on the stage of the predation sequence in which cues are released. Predator odours, disturbance pheromones, injury-released chemical cues and dietary cues all convey chemical information to prey Prey use these cues to minimize their probability of being taken on to the next stage of the sequence. The evolution of specialized epidermal alarm substance cells in fishes in the superorder Ostariophysi represent an amplification of this general phenomenon. These cells carry a significant metabolic cost. The cost is offset by the fitness benefit of the chemical attraction of predators. Attempts of piracy by secondary predators interrupt predation events allowing prey an opportunity for escape. In conclusion, chemical cues are widely used by aquatic prey for risk assessment and this has resulted in the evolution of specialized structures among some taxa.     

Experimental evidence for predation risk sensitive oviposition by a mosquito, Culiseta longiareolata

1. Females should choose to oviposit in habitats where risk of predation and competition are low. The ovipositional responses of a mosquito, Culiseta longiareolata, to a predator and to species sharing the same trophic level as this mosquito (controphic species) were assessed experimentally in outdoor artificial pools. 2. The predator, larval Anax imperator, which strongly reduced larval C. longiareolata survival, resulted in a 52% reduction of C. longiareolata egg rafts. The controphic species (primarily Daphnia magna), which had a small but statistically significant negative effect on the survival of C. longiareolata larvae, did not have a statistically significant influence on the number of egg rafts. 3. Laboratory trials indicated that only a small fraction of the reduced number of egg rafts seen in predator pools may be due to consumption of the egg rafts by A. imperator. 4. The experimental evidence indicates that the reduced number of C. longiareolata egg rafts found in the presence of A. imperator is due largely to oviposition habitat selection, i.e. C. longiareolata females choose pools with low risk of predation for their offspring.     

Landscape-dependent response to predation risk by forest birds

Knowing how forest loss and associated fragmentation actually impact individual birds is essential to our understanding of consequences at the population level. We conducted a landscape-level experiment to test whether deforestation affects the trade-off between foraging and antipredatory behaviour of black-capped chickadees ( Poecile atricapilla ) in 24 landscapes (range 8–88% forest cover, 500-m radius) during two winters. At a field-forest edge in the centre of each landscape, we used the maximum distance ventured into the open by flocks to get sunflower seeds placed on the snow-covered fields, as a measure of risk-taking. In the more deforested landscapes, chickadees ventured farther (up to the maximum of 40 m) into the open. Edge density and proportion of conifers in the forest had no influence on risk-taking. However, where ad libitum food was available for a few weeks prior to the experiment (in 12 of the 24 landscapes), chickadees ventured four meters or less away from the forest edge, regardless of the level of deforestation. We conclude that landscape deforestation increases energy stress, which in turn promotes risk-taking, and may therefore increase winter mortality through greater exposure to predators.     

Experimental evidence for the adaptive value of sexual reproduction

It is generally believed that recombination by sexual reproduction is unfavourable in constant environments but is of adaptive value under changing environmental conditions. To test this theory, experimental populations of yeast (Saccharomyces cerevisiae) were set up and maintained at different levels of environmental heterogeneity. Recombination was estimated by determining sporulation rates. Sporulation rates first increased in populations living in highly variable environments, but after some time began to decrease. The decrease started last and was slowest in populations which were maintained under the same conditions for a sufficiently long time, to allow some adaptation of the gene pool to the respective environment. Patterns of genotypic variability could not be interpreted in such simple terms, but there was a statistically significant correlation between sporulation rate and genotypic variability. This correlation is to be expected because recombination generates genotypic variability. Summing up, recombination by sexual reproduction is advantageous in changing environments if the population can track the changes in the environment by changing its genotypic structure.     

Dynamic rodent behavioral response to predation risk: implications for disease ecology

Oecologia - Prey modify their behavior in response to variation in predation risk, and such modifications can affect trophic processes such as disease transmission. However, variation in predation...     

Experimental evidence for edge-related predation in a fragmented agricultural landscape

Abstract This study tested the hypothesis that increased predation of experimental nests occurs close to a forest edge in a fragmented agricultural landscape. Artificial nests and eggs of willie wagtails Rhipidura leucophrys and superb fairy-wrens Malurus cyaneus were used in experiments to assess the extent and nature of predation occurring throughout the known breeding seasons of these species. Predators were identified by the imprints they left in plasticine eggs, and by remote photography. Surveys of avian predators were undertaken to investigate the relationship between predation intensity and predator distribution and abundance. Avian predators accounted for almost all predation for which a predator could be identified (96%). Five of seven predator species photographed attacking wagtail nests were corvids or artamids. Fairy-wren nests suffered relatively low rates of predation (29%) compared to wagtail nests (87%). Increased predation at the habitat edge was recorded for wagtail nests only; predation was correlated with the distribution and abundance of predatory avian species. The different extent and pattern of predation on fairy-wren nests could be explained by problems in detecting predation by mammals, and by possible failure of avian predators to locate the cryptic nests.     

Invertebrate eggs can fly: evidence of waterfowl-mediated gene flow in aquatic invertebrates

Waterfowl often have been assumed to disperse freshwater aquatic organisms between isolated wetlands, but no one has analyzed the impact of this transport on the population structure of aquatic organisms. For three cladocerans (Daphnia ambigua, Daphnia laevis, and Sida crystallina) and one bryozoan (Cristatella mucedo), we estimated the genetic distances between populations across North America using sequences of several mitochondrial DNA genes and genotypic frequencies at allozyme and microsatellite loci. Waterfowl movements across North America (estimated from band recovery data) explained a significant proportion of the gene flow occurring between populations across the continent for three of the four species, even after controlling for geographic distances between localities. The fourth species, S. crystallina, has propagules less likely to survive desiccation or ingestion by birds. Differences in the capacity to exploit bird-mediated transport are likely to have important consequences for the ecology of aquatic communities and the spread of invasive species.     

Toxicity of synthetic detergents to fish and aquatic invertebrates

Synthetic detergents are reported to be acutely toxic to fish in concentrations between 0.4 and 40 mg/1. Factors affecting toxicity include the molecular structure of the detergent, water hardness, temperature and dissolved oxygen concentration; the age and species of the test fish, and acclimation to low concentrations of detergent. Some of these factors appear to be of only limited importance. Gill damage is the most obvious acute toxic effect; the immediate cause of death may be asphyxiation, but detergents may also be toxic internally. Lethal effects not related to gill damage have not been investigated. Sublethal effects include retardation of growth, alteration of feeding behaviour and inhibition of chemoreceptor organs. Low levels of detergents may also increase the uptake of other pollutants. Invertebrates, especially in their juvenile stages, are extremely sensitive to detergents: concentrations below 0.1 mg/1 interfere with growth and development in some species. The interactions between detergents and proteins, and their influence on membrane permeability may be the basis of the biological action of detergents. Detergents in natural waters are usually partially degraded, and a maximum permissible concentration of 0.5 mg/1 would probably be harmless under most conditions.     

Mass regulation in response to predation risk can indicate population declines

In theory, survival rates and consequent population status might be predictable from instantaneous behavioural measures of how animals prioritize foraging vs. avoiding predation. We show, for the 30 most common small bird species ringed in the UK, that one quarter respond to higher predation risk as if it is mass-dependent and lose mass. Half respond to predation risk as if it only interrupts their foraging and gain mass thus avoiding consequent increased starvation risk from reduced foraging time. These mass responses to higher predation risk are correlated with population and conservation status both within and between species (and independently of foraging habitat, foraging guild, sociality index and size) over the last 30 years in Britain, with mass loss being associated with declining populations and mass gain with increasing populations. If individuals show an interrupted foraging response to higher predation risk, they are likely to be experiencing a high quality foraging environment that should lead to higher survival. Whereas individuals that show a mass-dependent foraging response are likely to be in lower quality foraging environments, leading to relatively lower survival.     

Adaptive plasticity in nest-site selection in response to changing predation risk

Birds selecting a nest site have to find the best compromise between the risk of encountering predation, the availability of food near to the nest and microclimatic requirements. As the optimal solution of this problem will vary with changes in predator abundance, we ask whether birds are capable of assessing such changes and of adjusting their nest-site choice accordingly. The reproductive success of dusky warblers Phylloscopus fuscatus , breeding in a mosaic of bushland and tundra habitat in the Russian Far East, varied greatly depending on the abundance of a nest predator, the Siberian chipmunk Tamias sibiricus . Using artificial nests we analysed which strategies dusky warblers should follow to avoid nest predation by chipmunks. We then compared the nest sites which dusky warblers actually had chosen in years with very high chipmunk densities (1998 and 1999) with those chosen in 1997, when chipmunks were almost absent from the study area. We found that safe nest-sites were preferred over those offering other advantages (microclimate, proximity to food) when the risk of predation was high, and we could not detect any confounding factor that might alternatively have caused these striking between-year differences. Our study suggests that even a short-lived passerine may be capable of choosing its nest site according to the actual predation risk. We show that such behavioural plasticity can lead to a paradoxical situation where better-protected nest-sites (selected in years and areas with high risk), on average, suffer greater predation than sites offering low safety. Thus, behavioural plasticity, if undetected, may result in serious misinterpretation of nest-predation patterns. A review of the literature suggests that adaptive plasticity in nest placement may be more widespread than is currently recognized.     

A simple trickle chamber for rearing aquatic invertebrates

A chamber for laboratory rearing of aquatic invertebrates is described. The animals are reared in plastic dishes, through which a recirculating water volume is passed. The design ensures identical water quality in a high number of parallels. The chamber is constructed for rearing the freshwater amphipod Gammarus pulex, but can be used in studies of growth, reproduction etc. of other aquatic invertebrates as well.     

Crawl-out behaviour in response to predation cues in an aquatic gastropod: insights from artificial selection

Local adaptation to predation often occurs in populations experiencing stable predator regimes. Under such conditions, prey species may respond by fine-tuning their behavioural defences towards a local optimum, although it is often difficult to ascertain whether such local adaptation is due to selection on fixed traits, developmental plasticity that is dependent on relatively long term exposure to environmental cues or phenotypic plasticity that can respond rapidly to a changing environment. Here we investigate whether anti-predator behaviour in two populations of the freshwater gastropod Lymnaea stagnalis responded to artificial selection. Previous work had shown that populations of this species showed a higher level of innate avoidance behaviour (crawling above the water line) in the presence of predatory fish compared with sites lacking this predation threat. By selectively breeding from high and low response selection lines, we demonstrated that this crawl-out behaviour responds rapidly to artificial selection: high response selection lines showed a significant increase and low response selection lines a significant decrease in avoidance compared with non-selected control lines. This suggests that the crawl out response in this species is heritable, and that there is potential for a response to selection in natural populations, which may produce the divergence in the plasticity of crawl out behaviour found between gastropod populations experiencing high and low predation intensity.     

Experimental test for adaptive differentiation of ginseng populations reveals complex response to temperature

Background and Aims Local climatic adaptation can influence species' response to climate change. If populations within a species are adapted to local climate, directional change away from mean climatic conditions may negatively affect fitness of populations throughout the species' range. Methods Adaptive differentiation to temperature was tested for in American ginseng (Panax quinquefolius) by reciprocally transplanting individuals from two populations, originating at different elevations, among temperature treatments in a controlled growth chamber environment. Fitness-related traits were measured in order to test for a population × temperature treatment interaction, and key physiological and phenological traits were measured to explain population differences in response to temperature. Key Results Response to temperature treatments differed between populations, suggesting genetic differentiation of populations. However, the pattern of response of fitness-related variables generally did not suggest 'home temperature' advantage, as would be expected if populations were locally adapted to temperature alone. Conclusions Failure consistently to detect a 'home temperature' advantage response suggests that adaptation to temperature is complex, and environmental and biotic factors that naturally covary with temperature in the field may be critical to understanding the nature of adaptation to temperature.     

Leaf-eating invertebrates as competitors of aquatic hyphomycetes

Summary Leaf-eating invertebrates selectively ingest leaf areas rich in fungal cells. The effect of this process on coincident and cumulative species diversity (species numbers and evenness) of the fungi was studied on 3 substrates (oak leaves, larch and spruce needles) in 2 hardwater and 2 softwater streams. Cumulative species number of colonizing fungi follows the equation S=k·A ^z(A=area below decay curve of the substrate, k=substrate-specific constant, Z=0.47). Higher feeding activity means faster weight loss of the substrate which leads to lower species richness of the fungi. The opposite is true for early successional stages on larch needles. Evenness of the fungi (distribution of individuals among species) is negatively correlated with feeding intensity by invertebrates, as measured by increased decay rates. The overall effect of leaf-eating invertebrates on aquatic hyphomycetes resembles that of potent competitors preempting substrate otherwise used by a late successional tail of relatively rare fungi.     

A study of the hatching process in aquatic invertebrates

Summary The hatching process was observed in eggs of Notonecta melaena. A thick outer egg membrane ruptured at the cephalic end by pressure from within, exerted by the expansion of an inner egg membrane which forms a blister over the head. The osmotic nature of this expansion is demonstrated. The pronymph then drank water and its head pushed forward. At the same time, the blister membrane broke. The pronymph then emerged by a combination of a swelling of its body and a worm-like expansion and contraction in the abdominal region. The body swelled from a copious ingestion and absorption of water. The appendages did not participate in any way during hatching. At the termination of the emergence, a second inner membrane was ruptured. Shortly thereafter the pronymph underwent an ecdysis and swam away as a fully formed nymph.The eggs of Ranatra absona hatched in a somewhat similar manner, but the blister membrane was broken only after the head pushed against it. Also, the second inner membrane was ruptured long before the emergence of the nymph had been completed. In addition, there was no pronymphal stage and no ecdysis immediately after emergence.The eggs of Amnicola (?) hydrobioides are described. They were laid at an advanced stage of development. The young were very small (ca. 350 × 270 µ) and were surrounded by single egg membranes whose diameters were about % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaGOmaKaaGm% aaliaabaGaaGymaaqaaiaaikdaaaaaaa!385B!\[2{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace}\!\lower0.7ex\hbox{$2$}}\] times that of the young. Hatching was through a mechanical tearing motion by the foot and proboscis, but the tearing reflex set in only after the egg membrane collapsed. Evidence is presented which suggests that the collapse was caused by the enzymatic softening of the membrane.

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Sumario Eclosión se observa en los huevos de Notonecta melaena. La membrana exterior del huevo se rompe en la extremidad cefálica por presión desde el interior. Esta presión se deriva de la expansión de una membrana interior, que forma sobre la cabeza una ampolla. Es demonstrado que ésta expansión es de tipo osmótico.. Entoncces la proninfa bebe agua y empuja hacia adelante. Al mismo tiempo la membrana la de ampolla se rompe. Entonces sale la proninfa por combinación la de hinchazón del cuerpo y la expansón y abreviatura del abdomen,, como de la un gusano. El cuerpo se hincha debido a la gran imbibición de agua. Las patas no participan en algunas de estas acciones. Al final de la eclosión la segunda membrana interior se rompe. Poco tiempo despues la proninfa vierte su esqueleto exterior y nada como una ninfa verdadera.Los huevos de Ranatra absona se rompen de una manera semejante, pero la membrana dela ampolla se rompe despures de que la cabeza la ha empujado. Además, la segunda membrana interior se rompe despues de que la ninfa ha salido completamente. Tampoco hay etapa proninfal y no hay muda de esqueleto exterior immediatemente despues de la salida.Los huevos de Amnicola (?) hydroboides han sido descritos. Ellos son puestos en un estado avanzado de desarrollo. Los jóvenes son muy pequeños (ca. 350 × 270 µ) y están circundados por membranas únicas que tienen diámetros cerca de% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaGOmaKaaGm% aaliaabaGaaGymaaqaaiaaikdaaaaaaa!385B!\[2{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace}\!\lower0.7ex\hbox{$2$}}\] veces más que los de los jóvenes. Eclosión es por causa de una rotura mecánica de la membrana por accion del pie y probóscide, pero la acción refleja de rotura occure solamente despues de un hundimiento de la membrana del huevo. Se han presentado evidencias que indican que este hundimiente es ocasionado por un ablandamiento enzimático de la membrana.