A New View of the Predation Cycle of a Planktivorous Fish, White Crappie (Pomoxis annularis)

1986 ◽  
Vol 43 (10) ◽  
pp. 1894-1899 ◽  
Author(s):  
W. John O'Brien ◽  
Barbara I. Evans ◽  
Gregory L. Howick

Predators are often categorized as either cruise or ambush feeding strategists. We present evidence that white crappie (Pomoxis annularis) are neither. Instead, the crappie swim intermittently and search only when stationary. If the crappie searched while swimming, one would expect the run speeds to be slower than the pursuit speeds, but no difference was found between these two measurements. Assuming that prey are located while swimming, a foreshortening of runs prior to pursuit would also be expected, but again, none was detectable. The duration of the search pause appears to be related to the detectability of the prey. Crappie also search during the pause immediately following the attack and ingestion of a prey item. The observation that the probabilities of detecting and pursuing a prey following a run or an attack do not differ significantly supports this conclusion. Also, the duration of the pause following a run or attack does not differ significantly over a wide range of temperatures. If these views are correct, white crappie could not forage optimally by either deleting located prey items from the diet or minimizing handling time. What they appear to be doing is creatively managing their search time.

2021 ◽  
Vol 2021 (5) ◽  
Author(s):  
Damon J. Binder ◽  
Shai M. Chester ◽  
Max Jerdee ◽  
Silviu S. Pufu

Abstract We study the space of 3d $$ \mathcal{N} $$ N = 6 SCFTs by combining numerical bootstrap techniques with exact results derived using supersymmetric localization. First we derive the superconformal block decomposition of the four-point function of the stress tensor multiplet superconformal primary. We then use supersymmetric localization results for the $$ \mathcal{N} $$ N = 6 U(N)k × U(N + M)−k Chern-Simons-matter theories to determine two protected OPE coefficients for many values of N, M, k. These two exact inputs are combined with the numerical bootstrap to compute precise rigorous islands for a wide range of N, k at M = 0, so that we can non-perturbatively interpolate between SCFTs with M-theory duals at small k and string theory duals at large k. We also present evidence that the localization results for the U(1)2M × U (1 + M)−2M theory, which has a vector-like large-M limit dual to higher spin theory, saturates the bootstrap bounds for certain protected CFT data. The extremal functional allows us to then conjecturally reconstruct low-lying CFT data for this theory.


2005 ◽  
Vol 62 (6) ◽  
pp. 1076-1094 ◽  
Author(s):  
J. Matías Braccini ◽  
Bronwyn M. Gillanders ◽  
Terence I. Walker

Abstract Sources of variation in dietary composition were examined in the piked spurdog (Squalus megalops). The species is an opportunistic predator that consumes a wide range of prey items. When importance of prey was measured by weight or occurrence, S. megalops preyed largely on molluscs and teleosts. However, when number of prey was considered, the main items were crustaceans. A bootstrap analysis showed that considerable variability can be expected in the importance of prey items in the species' overall diet. Regional, seasonal, and ontogenetic differences in dietary composition were found, but there were no differences between mature and immature sharks or between males and females. The spatial and temporal variation in diet exhibited by S. megalops and the intrinsic natural variability of the dietary composition of this opportunistic predator suggest that studies that infer predator–prey interactions from overall diet are likely to miss information on the ecological relationships among species and thus account for only part of these interactions.


2015 ◽  
Vol 11 (1) ◽  
pp. 20140603 ◽  
Author(s):  
Katharina C. Engel ◽  
Lisa Männer ◽  
Manfred Ayasse ◽  
Sandra Steiger

Same-sex sexual behaviour (SSB) has been documented in a wide range of animals, but its evolutionary causes are not well understood. Here, we investigated SSB in the light of Reeve's acceptance threshold theory. When recognition is not error-proof, the acceptance threshold used by males to recognize potential mating partners should be flexibly adjusted to maximize the fitness pay-off between the costs of erroneously accepting males and the benefits of accepting females. By manipulating male burying beetles' search time for females and their reproductive potential, we influenced their perceived costs of making an acceptance or rejection error. As predicted, when the costs of rejecting females increased, males exhibited more permissive discrimination decisions and showed high levels of SSB; when the costs of accepting males increased, males were more restrictive and showed low levels of SSB. Our results support the idea that in animal species, in which the recognition cues of females and males overlap to a certain degree, SSB is a consequence of an adaptive discrimination strategy to avoid the costs of making rejection errors.


Author(s):  
Azadeh Farazmand ◽  
Masood Amir-Maafi

Abstract In this research, functional responses of Amblyseius swirskii Athias-Henriot preying on different Tetranychus urticae Koch nymphal densities (2, 4, 8, 16, 32, 64, and 128) were studied at eight constant temperatures (15, 20, 25, 27.5, 30, 32.5, 35 and 37.5°C) in a circular Petri dish (3-cm diameter × 1-cm height) under lab conditions. At all temperatures, the logistic regression showed a type II functional response. A nonlinear relationship was found between temperature and attack rate and the reciprocal of handling time. The reciprocal of handling time decreased exponentially with increasing temperature. In contrast, the attack rate grew rapidly with increasing temperatures up to an optimum, showing a decreasing trend at higher temperatures. In order to quantify the functional response of A. swirskii over a broad range of temperatures and to gain a better estimation of attack rate and handling time, a temperature-settled functional response equation was suited to our data. Our model showed that the number of prey consumed increased with rising prey density. Also, the predation rates increased with increasing temperatures but decreased at extremely high temperatures. Based on our model, the predation rate begins at the lower temperature threshold (11.73°C) and reaches its peak at upper temperature threshold (29.43°C). The coefficient of determination (R2) of the random predator model was 0.99 for all temperatures. The capability of A. swirskii to search and consume T. urticae over a wide range of temperatures makes it a good agent for natural control of T. urticae in greenhouses.


2015 ◽  
Vol 370 (1675) ◽  
pp. 20140289 ◽  
Author(s):  
Ulrich D. Kadolsky ◽  
Andrew J. Yates

What effect does the spatial distribution of infected cells have on the efficiency of their removal by immune cells, such as cytotoxic T lymphocytes (CTL)? If infected cells spread in clusters, CTL may initially be slow to locate them but subsequently kill more rapidly than in diffuse infections. We address this question using stochastic, spatially explicit models of CTL interacting with different patterns of infection. Rather than the effector : target ratio, we show that the relevant quantity is the ratio of a CTL's expected time to locate its next target (search time) to the average time it spends conjugated with a target that it is killing (handling time). For inefficient (slow) CTL, when the search time is always limiting, the critical density of CTL (that required to control 50% of infections, C * ) is independent of the spatial distribution and derives from simple mass-action kinetics. For more efficient CTL such that handling time becomes limiting, mass-action underestimates C * , and the more clustered an infection the greater is C * . If CTL migrate chemotactically towards targets the converse holds— C * falls, and clustered infections are controlled most efficiently. Real infections are likely to spread patchily; this combined with even weak chemotaxis means that sterilizing immunity may be achieved with substantially lower numbers of CTL than standard models predict.


2019 ◽  
Vol 56 (4) ◽  
pp. 296-302 ◽  
Author(s):  
L. Garbin ◽  
J. I. Diaz ◽  
A. Morgenthaler ◽  
A. Millones ◽  
L. Kuba ◽  
...  

SummaryAnisakids are usually acquired through the diet. Cormorant pellets are useful to detect both parasite larval stages, and prey items which could act as intermediate hosts in the environment. The current study provides information about the feeding habits of both birds and mammals, and the diversity of parasites circulating in the environment. The objective of the study was to identify Anisakidae larvae and prey items in pellets from the Imperial shag Phalacrocorax atriceps and the Red-legged cormorant P. gaimardi, suggesting possible parasite–prey associations. A total of 92 P. atriceps’ and 82 P. gaimardi’s pellets were collected from both Punta León, and Isla Elena bird colonies, respectively, during the period from 2006 to 2010. Pellets were preserved in ethanol and hard prey item remnants, and nematode larvae were studied using standard techniques. Prey item occurrence, nematode prevalence, and mean intensity were calculated. A correspondence analysis was performed to evaluate the larvae-prey association. Contracaecum spp., Pseudoterranova spp,, Anisakis spp., Terranova spp., and Hysterothylacium spp. third-stage larvae (L3) were identifi ed in pellets. Pseudoterranova spp. and Anisakis spp. L3 predominated in the environment of Punta León, whereas Contracaecum spp. and Hysterothylacium spp. L3 predominated in the Puerto Deseado area. The highest larvae-prey association was that of Contracaecum spp. L3 with Engraulis anchoita, followed by with Odontestes sp. in P. atriceps’ pellets. Contracaecum spp. L3 were significantly related to both sprats, Sprattus fueguensis and Ramnogaster arcuatta, in P. gaimardi’s pellets. It was verifi ed that E. anchovy is the main gateway of Contracaecum spp. L3 in P. atriceps. Odonthestes sp. might act as an intermediate/paratenic host of Contracaecum spp. L3 in the area. Both sprats might play a role as intermediate/paratenic hosts of C. australe, being the main gateway into P. gaimardi in the area. Thus, pellet analysis can be postulated as a good tool for indicating parasite-host associations between anisakids, and the prey items which act as intermediate hosts.


Behaviour ◽  
1976 ◽  
Vol 56 (1-2) ◽  
pp. 44-67 ◽  
Author(s):  
Glenn Hausfater

Abstract1. A group of 32 yellow baboons (Papio cynocephalus) in the Masai-Amboseli National Park, Kenya, caught and ate 45 vertebrate prey items during 2519.19 hours of observation. 2. Eighty percent of the prey items were mammals and the most frequently eaten species were African hares (Lepus capensis), vervet monkeys (Cercopithecus aethiops) and neonate gazelle (Cazella granti and G. thomsoni) in that order. The details of predatory behavior for each prey species are described. 3. Rates of predation were significantly higher during the long dry season than during other months of the year, although no correlation was found between total monthly rainfall and monthly rates of predation. A lognormal model however provided a good fit to the monthly rate of predation data suggesting that the rate of predation by Amboseli baboons was affected by several factors that acted multiplicatively with respect to each other and were themselves related to rainfall or dryness. 4. A mean of 2.3 individuals fed directly from the carcass of each prey item. A mean of 3.5 individuals per prey item fed directly or indirectly, i.e., on scraps, from each carcass. In general, both the number of individuals who fed from each carcass and the duration of their feeding bouts was dependent upon the gross body size of the prey item. Adult males fed directly from the carcass of prey items for about three times more minutes than expected from their number in the group; other classes of individuals fed directly from prey carcasses for only one-fourth as many minutes as expected. In general, an adult male would be expected to feed on each category of vertebrate prey at least once per year, while individuals of all other age-sex classes would be expected to feed on most prey categories only once every two years. 5. The most frequent social behavior around prey items was agonistic bouts; no cooperation, simultaneous feeding or specific begging gestures were observed. 6. Estimates of the total number of prey killed annually by Amboseli baboons indicate that baboon predation probably has a negligible effect on prey populations other than vervet monkeys. 7. It is speculated that the need for vitamin B12 underlies baboon predatory behavior, and perhaps that of other primate species as well.


1980 ◽  
Vol 58 (6) ◽  
pp. 1168-1173 ◽  
Author(s):  
T. E. Quinney ◽  
P. C. Smith

Foraging behaviour and efficiency of adult and newly fledged juvenile great blue herons, Ardea herodius L., were studied at the Gaspereau River estuary. Nova Scotia, in July and August 1977 and 1978. Pace and strike rates of adults and juveniles were similar, whereas capture and probe rates differed markedly. Adults captured prey more successfully than juveniles but the ability of the latter improved with age. Foraging success of adults was greater in flocks of more than five individuals. In contrast, juvenile success does not seem related to flock size. Ninety-eight percent of the identified prey were flounder Liopsetta putnmi Gill. Handling time of small prey items was the same for adults and juveniles but juveniles took much longer to swallow medium-sized prey than adults did.


2000 ◽  
Vol 48 (1) ◽  
pp. 59 ◽  
Author(s):  
V. W. Framenau ◽  
L. A. Finley ◽  
K. Allan ◽  
M. Love ◽  
D. Shirley ◽  
...  

Multiple prey capture, the behaviour of a predator attacking prey whilst handling a previously caught item, occurs in a variety of spiders that do not build webs. The effects of recent feeding history on the frequency of multiple prey attacks, handling time, ingestion rate, and intercatch intervals were examined experimentally in the wolf spider Lycosa lapidosa McKay. Juvenile spiders were subjected to two different feeding regimes (starvation for 14 and 28 days) and then provided with two different prey types (blowflies, Lucilia cuprina, and crickets, Acheta domestica). These two starvation levels or prey types had little effect on the frequency (75%) of multiple prey attacks. Spiders ingested approximately half the weight of any captured prey, regardless of how many prey items they attacked. At the same time, the handling time per prey item decreased with an increasing number of prey attacked. This indicates a more efficient ingestion rate when more prey are consumed. While the attacking time for the first prey was the same for all treatments, the first intercatch interval was longer for spiders that were starved longer. Chronically starved L. lapidosa appear to secure a previously caught item rather than optimise their capture rate by attacking further available prey.


Behaviour ◽  
2010 ◽  
Vol 147 (8) ◽  
pp. 933-951 ◽  
Author(s):  

AbstractForaging efficiency of predators can be evaluated by using optimality or profitability models which incorporate prey choice, handling time and pursuit or search time. Optimality of a diet could vary based on the age, sex, size, predation risk, or foraging experience of the predator. This study tested the effects of a predator's age and foraging experience by observing prey capture attempts and success rate, and by calculating diet profitability for adult and neonate Sceloporus jarrovii and adult Sceloporus virgatus. Prey availability was assessed in order to determine prey preference and profitability. Neonates showed an increased number of prey capture attempts, but success rate was similar for neonates and adults of both species. Total diet profitability of neonates was lower than adults of either species, which could be a result of poor prey choice or gape limitation (although body size showed no direct effect). Overall, the diets of all three groups were less profitable than would be expected based on the types of prey in the environment, although this is likely due to low availability (from the lizard's perspective) of highly profitable items. Lizards seem to be eating prey items in the same proportion as they are found in the environment.


Sign in / Sign up

Export Citation Format

Share Document