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Type II Functional Response (type + ii_functional_response)
Selected AbstractsExperimental demonstration of population extinction due to a predator-driven Allee effectJOURNAL OF ANIMAL ECOLOGY, Issue 3 2010Andrew M. Kramer Summary 1. Allee effects may result in negative growth rates at low population density, with important implications for conservation and management of exploited populations. Theory predicts prey populations will exhibit Allee effects when their predator exhibits a Type II functional response, but empirical evidence linking this positively density-dependent variation in predator-induced individual mortality to population growth rate and probability of extinction is lacking. 2. Here, we report a demonstration of extinction due to predator-driven Allee effects in an experimental Daphnia-Chaoborus system. A component Allee effect caused by higher predation rates at low Daphnia density led to positive density dependence in per capita growth rate and accelerated extinction rate at low density. 3. A stochastic model of the process revealed how the critical density below which population growth is negative depends on the mechanistic details of the predator,prey interaction. 4. The ubiquity of predator,prey interactions and saturating functional responses suggests predator-driven Allee effects are potentially important in determining extinction risk of a large number of species. [source] Does Holling's disc equation explain the functional response of a kleptoparasite?JOURNAL OF ANIMAL ECOLOGY, Issue 4 2001R. W. G. Caldow Summary 1Type II functional responses, which can be described by Holling's disc equation, have been found in many studies of predator/prey and host/parasite interactions. However, an increasing number of studies have shown that the assumptions on which the disc equation is based do not necessarily hold. We examine the functional response of kleptoparasitically feeding Arctic skuas (Stercorarius parasiticus L.) to the abundance of fish-carrying auks and, by examination of the assumptions of the disc equation, test whether it can explain the function. 2The rate at which individual skuas make successful chases is a decelerating function of the abundance of auks. However, it would appear that this is not determined by factors that influence their probability of success, but by the rate at which they initiate chases. This too is a decelerating function of the abundance of auks. Arctic skuas have a Type II functional response. 3Although Arctic skuas exhibited a direct numerical response there was no evidence that components of predation connected to the density of predators (direct prey stealing, or increased host avoidance) had any effect on the rate at which individual skuas made chases or were successful in their chases. We conclude that the observed functional response is free from any effects of interference. 4We suggest that abnormally high levels of foraging effort expended by breeding skuas and their poor breeding success in the years of observation argue against the limit to the observed functional response being determined by skuas' energetic requirements. 5Several of the assumptions underlying the disc equation do not hold. The duration of chases (handling time) was not a constant; it decreased with increasing host abundance. Moreover, the chase duration predicted by the disc equation, if handling time limited the functional response, was far in excess of that observed. Furthermore, the observed rate of decline in the searching time per victim with increasing host abundance suggested that skuas' instantaneous rate of discovery was also not constant. Possible reasons for these observations are discussed. The basic disc equation may describe Arctic skuas' functional response, but it cannot explain it. [source] Shorebird predation of horseshoe crab eggs in Delaware Bay: species contrasts and availability constraintsJOURNAL OF ANIMAL ECOLOGY, Issue 3 2007S. GILLINGS Summary 1Functional responses , the relationship between resource intake rate and resource abundance , are widely used in explaining predator,prey interactions yet many studies indicate that resource availability is crucial in dictating intake rates. 2For time-stressed migrant birds refuelling at passage sites, correct decisions concerning patch use are crucial as they determine fattening rates and an individual's future survival and reproduction. Measuring availability alongside abundance is essential if spatial and temporal patterns of foraging are to be explained. 3A suite of shorebird species stage in Delaware Bay where they consume horseshoe crab Limulus polyphemus eggs. Several factors including spawning activity and weather give rise to marked spatial and temporal variation in the abundance and availability of eggs. We undertook field experiments to determine and contrast the intake rates of shorebird species pecking for surface and probing for buried eggs. 4Whether eggs were presented on the sand surface or buried, we demonstrate strong aggregative responses and rapid depletion (up to 80%). Depletion was greater at deeper depths when more eggs were present. No consistent give-up densities were found. Type II functional responses were found for surface eggs and buried eggs, with peck success twice as high in the former. Maximum intake rates of surface eggs were up to 83% higher than those of buried eggs. 5Caution is needed when applying functional responses predicted on the basis of morphology. Our expectation of a positive relationship between body size and intake rate was not fully supported. The smallest species, semipalmated sandpiper, had the lowest intake rate but the largest species, red knot, achieved only the same intake rate as the mid-sized dunlin. 6These functional responses indicate that probing is rarely more profitable than pecking. Currently, few beaches provide egg densities sufficient for efficient probing. Areas where eggs are deposited on the sand surface are critical for successful foraging and ongoing migration. This may be especially true for red knot, which have higher energetic demands owing to their larger body size yet appear to have depressed intake rates because they consume smaller prey than their body size should permit. [source] Does aggregation benefit bark beetles by diluting predation?ECOLOGICAL ENTOMOLOGY, Issue 2 2004Links between a group-colonisation strategy, the absence of emergent multiple predator effects Abstract., 1. Aggregation in bark beetles (Coleoptera: Scolytidae) aids in mate attraction and resource procurement when colonising well-defended plants; however, some species colonise primarily poorly defended plants, and intraspecific competition increases mortality. The hypothesis that decreased risk of predation was a potential benefit to aggregation in such circumstances was tested, using the pine engraver, Ips pini (Say) and its two major predators Thanasimus dubius (F.) (Coleoptera: Cleridae) and Platysoma cylindrica (Paykull) (Coleoptera: Histeridae). Both single- and multiple-predator effects, across a range of prey densities, were tested. 2. Both male and female colonisation events increased with herbivore density, in an asymptotic fashion. 3. Predators decreased the number of colonisers in a density-dependent manner, consistent with a type II functional response. 4. The proportional impact of predators decreased with increased herbivore colonisation densities. These findings indicate that predator dilution may be a viable benefit to aggregation. 5. Total emergence of the herbivore also increased with density, although the net replacement rate during one generation was independent of initial arrival density. This was likely due to larval predation, which negates potential relationships between per capita reproductive success and establishment density. 6. Each predator species decreased I. pini's net replacement rate by approximately 42%, and their combined effect was approximately 70%. 7. Overall, these predators modified their prey's establishment and adult mortality relationships in additive manners. This is somewhat surprising, given the potential for emergent effects due to interactions between multiple predators foraging within a common habitat. The persistence of additivity, rather than risk reduction or enhancement to the prey, may increase the predator-swamping benefit to aggregation for this herbivore. 8. The effects of these predators are substitutable, and likely exert equivalent selective pressures to mask signals at the whole-plant level. [source] Functional response of Picromerus bidens: effects of host plantJOURNAL OF APPLIED ENTOMOLOGY, Issue 3 2007K. Mahdian Abstract:, The influence of three solanaceous plants (tomato, sweet pepper and eggplant) on the functional response of the predatory bug Picromerus bidens to densities of fourth-instar larvae of the beet armyworm Spodoptera exigua was assessed. Logistic regression indicated a type II functional response on all host plants. Over all prey densities, P. bidens killed significantly fewer fourth instars of S. exigua on tomato than on sweet pepper or eggplant (1.96 ± 0.17 vs. 4.37 ± 0.19 and 3.90 ± 0.15 larvae per predator per 24 h respectively). A higher theoretical maximum predation rate was estimated on sweet pepper (11.1 prey larvae per day) and eggplant (7.4) than on tomato (5.4). The mean number of prey killed per day by P. bidens females ranged from 0.78 at a density of one prey on tomato to 8.45 at a density of 24 prey on sweet pepper. The data indicated that the estimates of handling time (Th) and attack rate (a) were highly affected by host plant. Based on asymptotic 95% confidence intervals, a lower attack coefficient was found on tomato (0.02 h,1) than on sweet pepper or eggplant (0.07 and 0.11 h,1 respectively). On the other hand, handling times were significantly longer on tomato (4.42 h) and eggplant (3.23 h) than on sweet pepper (2.15 h). This laboratory study suggests that plant characteristics influence the ability of P. bidens to respond to changes in prey density. [source] Functional response of juvenile pink and chum salmon: effects of consumer size and two types of zooplankton preyJOURNAL OF FISH BIOLOGY, Issue 2 2007J. H. Moss Feeding rate experiments were conducted for pink salmon Oncorhynchus gorbuscha fry [mean fork length (LF) 39 mm], juveniles (103,104 mm LF) and juvenile chum salmon Oncorhynchus keta (106,107 mm LF). Fishes were presented with small copepod (Tisbi sp.) or larger mysid shrimp (Mysidopsis bahia) prey at varying densities ranging from 1 to 235 prey l,1 in feeding rate experiments conducted at water temperatures ranging from 10·5 to 12·0° C under high light levels and low turbidity conditions. Juvenile pink and chum salmon demonstrated a type II functional response to mysid and copepod prey. Mysid prey was readily selected by both species whereas the smaller bodied copepod prey was not. When offered copepods, pink salmon fry fed at a higher maximum consumption rate (2·5 copepods min,1) than larger juvenile pink salmon (0·4 copepods min,1), whereas larger juvenile chum salmon exhibited the highest feeding rate (3·8 copepods min,1). When feeding on mysids, the maximum feeding rate for larger juvenile pink (12·3 mysids min,1) and chum (11·5 mysids min,1) salmon were similar in magnitude, and higher than feeding rates on copepods. Functional response models parameterized for specific sizes of juvenile salmon and zooplankton prey provide an important tool for linking feeding rates to ambient foraging conditions in marine environments, and can enable mechanistic predictions for how feeding and growth should respond to spatial-temporal variability in biological and physical conditions during early marine life stages. [source] | ||||||||||