Fine-scale substrate use by a small sit-and-wait predator

Substrate choice is one of the most important decisions thatsit-and-wait predators must make. Not only may it dictate theprey available but also the cover for the predator which mayconceal it from prey or its own predators. However, while ona particular substrate the behavior and use of that substratemay vary widely. When naïve, newly emerged crab spiderlingsMisumena vatia (Thomisidae) occupied flowering goldenrod Solidagocanadensis, their behavior differed markedly on inflorescenceswith relatively sparse and densely packed flower heads as wellas on experimentally thinned and unthinned inflorescences. Initially,the spiderlings most often hunted at the thinned sites and hidamong the dense flower heads at the unthinned sites, a differencethat disappeared in all broods tested after 2–3 h, possiblybecause of the growing hunger of the initially concealed individuals.Prey capture (dance flies) in the thinned sites initially significantlyexceeded that in unthinned sites but subsequently did not differ.However, spiderlings encountered their principal predator, thejumping spider Pelegrina insignis, significantly more oftenon unthinned than thinned inflorescences. Even though usagepatterns initially differed strikingly, spiderlings did notdiffer in their rates of quitting the two types of sites. Theseresults suggest a trade-off between foraging and predator avoidancethat changes in response to increasing hunger over time.     

The impact of a sit-and-wait predator: separating consumption and prey emigration

Reviews of the impact of invertebrate predators in enclosure/exclosure experiments suggest that much of the apparent depletion of prey is due to prey emigration induced by the predators. However, these generalisations derive mainly from studies of invertebrate predators that are predominantly active searchers (usually stoneflies) and of prey with strong avoidance responses (mainly mayflies).
We examined the impact of a large sit-and-wait predator, the nymph of the dragonfly Cordulegaster boltonii , which has recently invaded Broadstone Stream as a new top predator. Field enclosure/exclosure experiments were conducted to assess the impact of the invader on the benthos. Depletion of prey varied seasonally and among taxa, and was highest when prey density and encounter rates were high. Mobile prey, although least likely to show a statistically significant response because of high exchange rates, were those most strongly depleted.
Experimental channels were used to separate the relative contribution of consumption and emigration to total impact for the two most depleted prey species. Depletion of prey was due solely to consumption and predators did not induce emigration. We therefore urge caution in making generalisations about the impacts of invertebrate predators, since sit-and-wait and searching predators potentially have very different impacts.     

Foraging in the ant-lionMyrmeleon mobilis hagen 1888 (neuroptera: Myrmeleontidae): Behavioral flexibility of a sit-and-wait predator

The relative effects of foraging benefits (food intake) and costs (disturbance = pit destruction) on growth rate and foraging behavior of larvae of the ant-lionMyrmeleon mobilis were investigated. In a laboratory experiment second-instar larvae were subjected to combinations of three rates of feeding and three rates of disturbance. Pit relocations were generally rare but occurred more often in starved larvae. Disturbance rate had no significant effect on pit relocation rate. Feeding rate was a major determinant of the energy allocated in pit construction and maintenance (positive relationship). In a second experiment third-instar larvae encountered changing rates of disturbance. Pit size was reduced as a response to increased rates of disturbance. Disturbance had no detectable effect on growth. In general,M. mobilis larvae were cost-conservative, foragers.     

Utilization of different prey type patches in the Ural owl(Strix uralensis): a sit-and-wait predator

To quantify the pattern of allocation of foraging activity ofa sit-and-wait forager among feeding sites of different profitability,I conducted an experimental study of patch utilization behaviorof Ural owls (Strix uralensis) in an experimental flight cage.The owls were allowed to search among four patches containingequal numbers of mice, two with the large Japanese field mouse(Apodemus speciosus) and two with the small Japanese field mouse(A. argenteus). Patches with A. speciosus were more profitablethan those with A. argenteus, and owls visited more profitablepatches more frequently. Visiting frequency to richer patchesdid not increase with experience; however, owls changed searchtime according to experience. Search time in a patch becamelonger in later visits than in earlier visits during a givennight according to an owl’s sampling experience amongpatches. Furthermore, owls stayed longer in richer patches thanin poor ones if they had caught mice in both types of patches.Search time had great variance. Mean search time that endedwith attack was longer than that ended without attack (giveup). In effect, Ural owls improved their resource utilizationpattern as they accumulated experience in the environment. [BehavEcol 1991;2:99–105J]     

Colour-associated foraging success and population genetic structure in a sit-and-wait predator Nephila maculata (Araneae: Tetragnathidae)

Giant wood spiders, Nephila maculata (Fabricius 1793), typically have a greenish cephalothorax and a dark abdomen decorated with striking yellow bands and spots. However, in Taiwan and neighbouring coastal islands we also found some morphologically indistinguishable individuals that were totally dark. As insects are attracted to ultraviolet (UV) light, we compared the UV reflectance property and insect-catching ability of the two morphs to see whether variation in colour affected foraging success. We also examined the population genetic structure to estimate indirectly the level of gene flow between these two colour morphs. Body surface UV reflection rate was measured from six areas of the spider with a spectrometer. To compare the insect-catching ability of different morphs, we recorded the spiders' body colour, orb size and insect-interception rates. The typical morph of N. maculata reflected significantly more UV in four of the six areas examined and caught significantly more insects than the melanic morph. We estimated population genetic structure by allozyme electrophoresis, using 20 loci from 17 enzymes. The population differentiation index (F_ST) derived from all eight polymorphic loci was 0.023, indicating a minimum level of genetic differentiation. These results indicate that the two morphs ofN. maculata may be members of an interbreeding population, and melanics have lower foraging success because of a lower body surface reflectance.     

Costs and benefits of within-group spatial position: a feeding competition model

An animal's within-group spatial position has several important fitness consequences. Risk of predation, time spent engaging in antipredatory behavior and feeding competition can all vary with respect to spatial position. Previous research has found evidence that feeding rates are higher at the group edge in many species, but these studies have not represented the entire breadth of dietary diversity and ecological situations faced by many animals. In particular the presence of concentrated, defendable food patches can lead to increased feeding rates by dominants in the center of the group that are able to monopolize or defend these areas. To fully understand the tradeoffs of within-group spatial position in relation to a variety of factors, it is important to be able to predict where individuals should preferably position themselves in relation to feeding rates and food competition. A qualitative model is presented here to predict how food depletion time, abundance of food patches within a group, and the presence of prior knowledge of feeding sites affect the payoffs of different within-group spatial positions for dominant and subordinate animals. In general, when feeding on small abundant food items, individuals at the front edge of the group should have higher foraging success. When feeding on slowly depleted, rare food items, dominants will often have the highest feeding rates in the center of the group. Between these two extreme points of a continuum, an individual's optimal spatial position is predicted to be influenced by an additional combination of factors, such as group size, group spread, satiation rates, and the presence of producer-scrounger tactics.     

Active foragers vs. sit-and-wait predators: a simple model

I propose a simple model for the decision of when to leave a foraging site in a variable environment for a predator that does not deplete its local resources. Active foraging is favored when the cost of moving is small or the difference between good and poor sites is large. The model corresponds to the behavior of two guilds of web-spinning spiders.     

Food selection by a sit-and-wait predator,the monkfish,Lophius upsicephalus,off Namibia (South West Africa)

Synopsis We investigated prey selection by the monkfish, Lophius upsicephalus. This sit-and-wait predator preferentially selected prey types that would be expected to react to the lure of the illicium. Prey size selection was dependent on predator size, with larger predators feeding on a wider range of prey sizes.     

The effect of predation risk on the predatory behaviour of a sit-and-wait predator,Ranatra dispar (Heteroptera: Nepidae), the water stick insect

Two primary defence behaviours, fore-leg extension to enhance crypsis and swimming to bottom and remaining motionless, of a predatory water bug,Ranatra dispar, are described along with their subsequent effect on foraging behaviour. It was hypothesised that hungry predators would respond less and for a shorter duration compared with recently fed individuals when exposed to a model threat stimulus, thereby tending to take a higher risk of predation during feeding than satiated animals. A greater proportion of animals responded overall with the leg extension response compared with the swimming response, although the mean duration of the former was significantly shorter than the latter response. A significantly higher proportion of nonfasted predators responded, and for a longer duration than fasted individuals. The type of model used significantly effected the proportion of animals that responded with leg extensions but not on its duration. In contrast, both number of animals and the duration of the swim/motionless behaviour were significantly effected by stimulus type. The subsequent effect of these 2 behavioural responses on feeding behaviour was examined and showed that although about the same number of predators removed prey from their mouthparts during both responses, significantly more prey were dropped, and therefore lost, during swimming. The results clearly indicate the significant effects that defensive behaviours have on time budgets in foraging behaviour.     

Visual fields, eye movements, and scanning behavior of a sit-and-wait predator, the black phoebe (Sayornis nigricans)

Foraging mode influences the dominant sensory modality used by a forager and likely the strategies of information gathering used in foraging and anti-predator contexts. We assessed three components of visual information gathering in a sit-and-wait avian predator, the black phoebe (Sayornis nigricans): configuration of the visual field, degree of eye movement, and scanning behavior through head-movement rates. We found that black phoebes have larger lateral visual fields than similarly sized ground-foraging passerines, as well as relatively narrower binocular and blind areas. Black phoebes moved their eyes, but eye movement amplitude was relatively smaller than in other passerines. Black phoebes may compensate for eye movement constraints with head movements. The rate of head movements increased before attacking prey in comparison to non-foraging contexts and before movements between perches. These findings suggest that black phoebes use their lateral visual fields, likely subtended by areas of high acuity in the retina, to track prey items in a three-dimensional space through active head movements. These head movements may increase depth perception, motion detection and tracking. Studying information gathering through head movement changes, rather than body posture changes (head-up, head-down) as generally presented in the literature, may allow us to better understand the mechanisms of information gathering from a comparative perspective.     

A regional analysis of weather mediated competition between a parasitoid and a coccinellid predator of oleander scale

The regulation of an asexual population of the oleander scale [Aspidiotus nerii Bouchè (Hemiptera: Diaspididae)] on California bay tree [Umbellularia californica (Hopk. & Arn.) Nut.] by two natural enemies; an idiobiont, ectoparasitoid Aphytis chilensis Howard (Hymenoptera: Aphelinidae) and a coccinellid predator (Rhysobius lophanthae (Blaisd.) (Coleoptera: Coccinellidae), was examined using a general weather-driven, tri-trophic, physiologically based age-mass structured demographic model. The model is of intermediate complexity and was parameterized using extensive laboratory data and field observations from Albany, CA. Temperature-dependent physiological indices were estimated from the laboratory data and used to scale per capita growth, fecundity and survivorship rates from maximal values in a time varying environment. The tri-trophic model was integrated in a GIS (geographic information system) and the species dynamics examined across years and across the ecological zones of California. Field data and simulation results suggested the coccinellid predator was the most important regulating agent of oleander scale in the mild climate of Albany. However, multiple linear regression analysis of simulation data across all ecological zones of California shows that the parasitoid A. chilensis is the most important agent in suppressing oleander scale densities in warmer climates, while the predator R. lophanthae increases scale density an average of 9.7% across all regions.     

On the economics of sit-and-wait foraging: site selection and assessment

We present two models of optimal resource exploitation for sit-and-waitforagers. The first model assumes immediate recognition of sitequality and that site quality does not change over time. Thismodel predicts a forager's minimum acceptable site quality.We present a graphical analysis to show how (1) the distributionof site qualities, (2) the travel time between sites, (3) costof search, and (4) expected duration of the foraging processinfluence the minimum acceptable rate. Our second model allowssite qualities to change and relaxes the assumption of immediaterecognition. This model defines conditions of (1) state duration,(2) recognition time, (3) site abundance, and (4) cost of searchwhere the optimal policy is to stay put in a site regardlessof experience. We discuss the implications of these models forthe design and interpretation of field experiments of site useand habitat selection.     

Spatial scale of aggregation in three acarine predator species with different degrees of polyphagy

Aggregative responses by the predatory mites, Phytoseiulus persimilis, Typhlodromus occidentalis, and Amblyseius andersoni (Acari: Phytoseiidae), to spatial variation in the density of mobile stages of Tetranychus urticae (Acari: Tetranychidae) were studied over different spatial scales on greenhouse roses. Significant spatial variations in prey numbers per leaflet, per leaf, per branch or per plant were present in all experimental plots. None of the predator species responded to prey numbers per plant, and all searched randomly among plants. Within a plant, the oligophagous P. persimilis searched randomly among branches, but aggregated strongly among leaves within a branch and among leaflets within a leaf. The narrowly polyphagous T. occidentalis searched randomly among leaflets within a leaf and amond leaves within a branch, but aggregated strongly among leaflets or leaves within a plant. The boradly polyphagous A. andersoni searched randomly among leaflets within a leaf, a branch or a plant, and among leaves within a branch or a plant, but distributed themselves more often on branches with lower prey densities. Thus, specialist predators aggregate strongly at lower spatial levels but show random search at higher spatial levels, whereas generalist predators show random search at lower spatial levels but aggregate at higher spatial levels. This is the first empirical evidence demonstrating the relation between the degree of polyphagy and the spatial scale of aggregation. It is also concluded that both the prey patch size (i.e. grain) and predator foraging range (i.e. extent) are important for analyzing spatial scales of predator aggregation. The importance of studying spatial scale of aggregation is also discussed in relation to predator-prey metapopulation dynamics.     

Testing predictions of foraging theory for a sit-and-wait forager, Anolis gingivinus

Research in foraging theory has been dominated by studies ofactive foragers choosing among patches and among prey withina patch. Studies of central-place foraging have mainly focusedon loading decisions of an animal provisioning a central place.The problem faced by a sit-and-wait forager that encountersprey at a distance has received little attention. In this studywe tested foraging theory predictions for such foragers, Anolisgingivinus females in the West Indies island of Anguilla. Wepresented lizards with antlion larvae at various distances.Experiment 1 showed that an individual's probability of pursuingprey decreases with the prey's distance and is best describedby a sigmoidal function (which may be as steep as a step function).This function's inflection point defines a cutoff distance.Experiment 3 tested how cutoff distance changes as a functionof prey size. Cutoff distances were greater for larger prey,as predicted for an energy-maximizing forager. Experiments 2and 4 tested how cutoff distance changes as a function of preyabundance. As predicted, cutoff distance were greater at a sitewhere prey abundance was lower. Furthermore, cutoff distancesdecreased immediately following prey augmentation and returnedto previous values within one day of ending augmentation. Thus,moles' foraging behavior is a dynamic process, consistent withthe qualitative predictions of foraging theory. We attributethe success of this study in supporting fundamental foragingtheory predictions to the lizards exhibiting natural behaviorunder field conditions and to particular advantages of studyingsit-and-wait foragers.     

Costs and benefits of colony aggregation in the social wasp, Polistes annularis

Females of the social wasp, Polistes annularis, nest in largeaggregations onriverside cliffs in central Texas. Aggregationsoccur where there is an overhang under which wasps build theirnests. Colony aggregations appear to occur partly because individualfemales do notdisperse far from the natal site where most coloniesare successful. In most taxa greater reproductive success nearthe natal nest site is related to unique physical features orto advantages ofbeing in a group. In P. annularis, the physicalfactors and not the social factors appear to be most important.Advantages to remaining near the natal nest site include protectionprovided by the cliff overhang from rain and afternoon sun.Central colonies are as likely to suffer predation as are peripheralcolonies, which indicates an absence of selfish herd advantagesto being in the center of the group. A cost of being in a denseaggregation is often increased reproductive competition, andthis is the case for P. annularis. Colonies in the center ofthe aggregation suffer high usurpation rates by unrelated femalesand in 1 of 3 years produced fewer reproductives than edge colonies.