Metabolic consequences of feeding and fasting on nutritionally different diets in the wolf spider Pardosa prativaga

We investigated whether spiders fed lipid-rich rather than protein-rich prey elevate metabolism to avoid carrying excessive lipid deposits, or whether they store ingested lipids as a buffer against possible future starvation. We fed wolf spiders (Pardosa prativaga) prey of different lipid:protein compositions and measured the metabolic rate of spiders using closed respirometry during feeding and fasting. After a 16-day feeding period, spider lipid:protein composition was significantly affected by the lipid:protein composition of their prey. Feeding caused a large and fast increase in metabolism. The cost of feeding and digestion was estimated to average 21% of the ingested energy irrespective of diet. We found no difference in basal metabolic rate between dietary treatments. During starvation and decreased gradually, and the larger lipid stores in spiders fed lipid-rich prey appeared to extend survival of these spiders under starvation compared to spiders fed protein-rich prey. The results show that these spiders do not adjust metabolism in order to maintain a constant body composition when prey nutrient composition varies. Instead, lipids are stored efficiently and help to prepare the spiders for the long periods of food deprivation that may occur as a consequence of their opportunistic feeding strategy.     

A comparison of prey lengths among spiders

Summary Field observations and laboratory experiments were carried out to determine the influence of body length of preys on the acceptance rate by spiders. Feeding experiments with 13 spider species and a model prey (crickets) reveal a decreasing acceptance rate with increasing prey size. Prey sizes of 50–80% of the spiders' size yielded the highest acceptance rates, crickets of double the spiders' size were accepted by two species only. By fitting the acceptance rate Y versus prey size X by Y(x)=Y(0) (1-x²), two coefficients could be calculated: Y(0), the size-independent palatibility of the prey and , a coefficient of size-induced refusal of the prey. These values describe the degree of specialisation towards (a) crickets and (b) large prey, respectively. Further comparison showed (a) that labidognath (= araneomorph) spiders do not necessarily subdue larger prey items than orthognath (=mygalmorph) spiders and (b) that webbuilding spiders are superior to non-webbuilding spiders in respect of catching large prey. A modified model of the generalized pattern of the length relations of predator and prey is given with special reference to spiders and compared to other polyphagous predator groups.     

The effects of temperature on feeding in zooplanktivorous walleye,Stizostedion vitreum,larvae

Synopsis We examined the prey capture process in walleye larvae (9.8–18.0 mm mean length) feeding on zooplankton (density 1501^–1) in laboratory aquaria at 15,18.5 and 22°C. Larvae were starved for 8 h prior to the experiment and only allowed to feed for 10 min during the experiment in order to minimize the influence of gut processing or satiation on feeding behaviour. Prey consumption (g min^–1) increased exponentially and prey capture success (%) increased logarithmically with mean walleye length. Prey consumption and attack rate (strikes min^–1) increased significantly with increasing temperature. The effect of temperature on capture success was slight (2% increase from 15 to 22°C) and not significant. Walleye showed positive electivity for medium-sized prey (0.3–0.6 mm body width, mostlyCeriodaphnia quadrangula), negative electivity for small prey (0.3 mm, mostly cyclopoid copepods) and neutral electivity for large prey (0.6 mm, mostlyDaphnia sp.). Neither prey species electivity nor prey size electivity were significantly affected by temperature. However, prey size electivity did show a fairly large effect size with respect to temperature and we suggest that this relationship should be examined further. These results indicate that temperature affects prey capture in walleye larvae primarily by influencing attack rate.     

Effects of satiation on feeding and swimming behaviour of planktivores

Hunger affects the feeding and swimming behaviour in fish. After 36 h of food deprivation, the feeding and swimming behaviour of Pseudorasbora parva (Cyprinidae) was studied under different prey densities (0.5, 1, 2, 5, 10 and 25 of Daphnia pulex per liter). The initial feeding rates showed marked variations in relation to prey availability. Under high prey densities, the initial feeding rate of fish was higher and subsequently decreased faster, when compared to those feeding under low prey densities. At higher prey densities, two factors were involved: that of higher prey encounter rates and also the attainment of food satiation at a faster rate. Across all prey densities, the feeding rates of fish reached a plateau after satiation. The swimming speed of fish was found to be negatively related to the prey density and a significant change in swimming speed was noted as being directly related to the level of satiation. It was found that the increasing satiation level greatly influenced the handling time and reactive volume of predator, which finally caused reduced feeding rates.     

The Effect of Feeding History on Prey Capture Behaviour in the Orbweb Spider Argiope keyserlingi Karsch (Araneae: Araneidae)

The prey capture behaviour of the orb-web spider Argiope keyserlingi Karsch was examined experimentally by subjecting spiders to two different feeding regimes (food deprived and food satiated) and three types of prey: Drosophila, blowflies (Lucilia cuprina) and bees (Apis mellifera). The attack behaviour of the spiders was influenced by both their foraging history and the type of prey. Food deprived spiders attacked Drosophila and bees more frequently than food satiated spiders, and food satiated spiders travelled more slowly to any of the prey types than food deprived spiders. Furthermore, Drosophila were never wrapped in silk but only grasped with the chelicerae, whereas both blowflies and bees were always wrapped. This provides experimental confirmation that feeding history affects the decision of orb-web spiders to accept or reject any given prey.     

Changes in body weight of two species of predatory mites (Acarina: Phytoseiidae) as a consequence of feeding in an interactive system

Changes in body weight of two species of predatory mites,Phytoseiulus persimilis Athias-Henriot andAmblyseius degenerans (Berlese), when each species was feeding alone on the prey miteTetranychus pacificus McGregor, were determined in the laboratory. The body weight of a starved adult femaleP. persimilis could increase 105.6% (13.05 g) to full satiation, whereasA. degenerans increased 43.2% (7.6 g). A simple model is used to describe the weight changes of each species. Changes in body weight also were determined when each of the two species fed with conspecifics at a high and low predator density. WithP. persimilis there was a reduction in body weight as well as in reproduction and in the number of prey killed when feeding at a high density of conspecifics. These reductions were not observed withA. degenerans. WhenP. persimilis fed with heterospecifics (A. degenerans), reductions in these three variables were less marked. The reductions are attributed primarily to the effect of sharing prey meals with conspecifics. Possible mechanisms for these reductions through meal-sharing are discussed.     

Quantitative evaluation of predation by spiders on the green rice leafhopper,Nephotettix cincticeps Uhler,by a sight-count method

A sight-count method for evaluation of predation by spiders on the green rice leafhopper, Nephotettix cincticeps was proposed and its applicability was tested under natural conditions. The number (n) of leafhoppers preyed on by spiders per rice hill per day was estimated by the formula: (1) where F is the frequency of predation observed per hill:P is given by dividing the time spent feeding on prey by 24 hours; and C refers to the total amount of feeding activity expressed in terms of the activity during the standard time interval. The total number (N) of prey attacked during the specified period can be given as follows: (2) With this method, the role of paddy-inhabiting spiders, Lycosa pseudoannulata, Oedothorax insecticeps, Tetragnatha spp, and Enoplognatha japonica, as predator of N. cincticeps was evaluated with reference to life tables of the prey. The advantages and limitation of the sight-count method were discussed as compared with other methods so far proposed.     

A specialized araneophagic predator's short‐term nutrient utilization depends on the macronutrient content of prey rather than on prey taxonomic affiliation

A specialist predator that has a specialized diet, prey‐specific prey‐capture behaviour and a preference for a particular type of prey may or may not be specialized metabolically. Previous studies have shown that jumping spiders of the genus Portia prey on other spiders using prey‐specific prey‐capture behaviour, prefer spiders as prey to insects and gain long‐term benefits in terms of higher survival and growth rates on spider diets than on insect diets. However, it is unclear whether there are substances uniquely present in spiders on which Portia depends, or, alternatively, spiders and insects all contain more or less the same nutrients but the relative amounts of these substances are such that Portia perform better on a spider diet. These questions are addressed by testing the hypothesis that prey specialization includes metabolic adaptations that allow Portia an enhanced nutrient extraction or nutrient utilization efficiency when feeding on spider prey compared with insect prey. Three groups of Portia quei Zabka are fed either their preferred spider prey or one of two types of flies (Drosophila melanogaster Meigen) that differ in nitrogen and lipid content. Portia quei shows a higher feeding rate of high‐protein flies than of high‐lipid flies and spiders but, after 5 days of feeding, there is no significant difference in growth between treatments, and the diets lead to significant changes in the macronutrient composition of P. quei as a result of variable extraction and utilization of the prey. The short‐term utilization of spider prey is similar to that of high‐lipid flies and both differ in several respects from the utilization of high‐protein flies. Thus, the short‐term nutrient utilization is better explained by prey macronutrient content than by whether the prey is a spider or not. The results suggest that spider prey may have a more optimal macronutrient composition for P. quei and that P. quei does not depend on spider‐specific substances.     

Hunger, partial consumption of prey and prey size preference in a carabid beetle

ABSTRACT.

• 1 Partial consumption of prey and prey size preference were studied in females of the carabid Notiophilus biguttatus F., using different size-classes of the springtail Orchesella cincta (L.) as prey.
• 2 Time to ingest a prey increases disproportionately with prey size, mainly as a consequence of satiation.
• 3 During consumption of a prey the predator's rate of ingestion decreases, partly because of diminishing returns from the prey over feeding time.
• 4 The hypothesis that the diminishing returns from the prey induce partial consumption was refuted.
• 5 Partial consumption in the beetle is due to gut limitation; its occurrence depends on prey size.
• 6 Average weight of prey remains in four prey size classes were close to weights expected from average intercatch intervals and estimates of hunger.
• 7 Prey choice depends on level of food deprivation.
• 8 Partial consumption of prey, prey size preference and profitability of prey in relation to hunger of the beetle are discussed.

     

Experimental assessment of trophic ecology in a generalist spider predator: Implications for biocontrol in Uruguayan crops

Conservative biological control promotes the use of native natural enemies to limit the size and growth of pest populations. Although spiders constitute one of the most important groups of native predators in several crops, their trophic ecology remains largely unknown, especially for several generalist taxa. In laboratory, we assessed the predatory behaviour of a wandering spider (the wolf spider Lycosa thorelli (Keyserling, 1877) against several arthropods varying in size and trophic positions, all found in South American soybean and rice crops. As prey we used the bug Piezodorus guildinii (Westwood, 1837) as well as larvae and adults of the moth Spodoptera frugiperda (Smith, 1797), both being considered important pests in Uruguayan crops. We also used several non-pest arthropods as prey, sarcophagid flies, carabid beetles and wolf spiders. All prey were attacked in more or less high, although not statistically differing, proportions. However, carabids were not consumed, and bugs were consumed in significantly lower proportions than flies. A negative correlation was found between prey size and acceptance rate. Immobilization times were longer against larvae when compared to moths and flies, while predatory sequences were longer for bugs when compared to flies, moths and spiders. In addition, we found a positive effect of prey size on predatory sequence length and complexity. Our results confirm the ability of spiders to attack and feed upon prey with different morphologies, included well-defended arthropods, and their potential use as natural enemies of several pests in South American crops.     

Tracing the evolutionary origin of a visual signal: the coincidence of wrap attack and web decorating behaviours in orb web spiders (Araneidae)

The silk decorations that adorn the webs of many orb-web spiders are thought to have a signal function, but the evolution of the decorating behaviour remains unresolved. The decoration signal is maintained apparently because it improves foraging efficiency, through either increased encounter rates with prey or reduced damage to the web. Recent investigations suggest that the decorations may originate in a regulation of the activity of the aciniform silk glands, which produce silk for both decorating the web and wrapping prey. This view predicts a link between decorating behaviour and a preference for restraining prey by wrapping with silk, which is evident among species of Argiope spiders. Here I compare the frequency of the wrap attack behaviour in four species of orb-web spiders that occupy the same habitat, but differ in their silk decorating behaviour: two species, Plebs bradleyi and Gea theridioides, build silk decorations, while the other two, Araneus hamiltoni and Backobourkia brounii do not. Spiders were presented with prey items that varied in the ease with which they could be captured, with houseflies being more easily subdued than house crickets. As predicted, the silk decorating species used wrap attacks significantly more often than non-decorating spiders, irrespective of the prey species. These data support the view that both behaviours are evolutionary linked. I propose that silk decorating originated from the evolution of wrap attacking, and that silken web decorations have later evolved into a signal and are now maintained for that function.     

Herbivore release through cascading risk effects

Predators influence prey through consumption, and through trait-mediated effects such as emigration in response to predation risk (risk effects). We studied top-down effects of (sub-) adult wolf spiders (Lycosidae) on arthropods in a meadow. We compared risk effects with the overall top-down effect (including consumption) by gluing the chelicers of wolf spiders to prevent them from killing the prey. In a field experiment, we created three treatments that included either: (i) intact (‘predation’) wolf spiders; (ii) wolf spiders with glued chelicers (‘risk spiders’); or (iii) no (sub-) adult wolf spiders. Young wolf spiders were reduced by their (sub-) adult congeners. Densities of sheetweb spiders (Linyphiidae), a known intraguild prey of wolf spiders, were equally reduced by the presence of risk and predation wolf spiders. Plant- and leafhoppers (Auchenorrhyncha) showed the inverse pattern of higher densities in the presence of both risk and predation wolf spiders. We conclude that (sub-) adult wolf spiders acted as top predators, which reduced densities of intermediate predators and thereby enhanced herbivores. Complementary to earlier studies that found trait-mediated herbivore suppression, our results demonstrate that herbivores can be enhanced through cascading risk effects by top predators.     

Distinct feeding strategies of generalist and specialist spiders

1. Feeding behaviour of generalist and specialist predators is determined by a variety of trophic adaptations. Specialised prey‐capture adaptations allow specialists to catch relatively large prey on a regular basis. As a result, specialists might be adapted to exploit each item of prey more thoroughly than do generalists. 2. It was expected that obligatory specialist cursorial spiders would feed less frequently than generalists but for a longer time and, thus, that their foraging pause would be longer. First, the feeding frequencies of three generalist spider species (Cybaeodamus taim, Harpactea hombergi, Hersiliola sternbergsi) were compared with those three phylogenetically related specialist species: myrmecophagous Zodarion rubidum, and araneophagous Nops aff. variabilis and Palpimanus orientalis. 3. Generalists captured more prey, exploited each item of prey for a significantly shorter time, and had a shorter foraging pause than was the case for specialists. Generalists also gained significantly less relative amount of prey mass than did specialists. 4. Second, the study compared the prey DNA degradation rate in the gut of generalists and specialists by means of PCR. The degradation rate was not significantly different between specialists and generalists: the detectability half‐life was estimated to exist for 14.3 days after feeding. 5. This study shows that the feeding strategies of cursorial generalist and obligatory specialist spiders are different. Obligatory specialists have evolved a feeding strategy that is based on thorough exploitation of a few large prey, whereas generalists have evolved a strategy that is based on short exploitation of multiple small items of prey.     

Are you what you eat? A highly transient and prey‐influenced gut microbiome in the grey house spider Badumna longinqua

Stable core microbial communities have been described in numerous animal species and are commonly associated with fitness benefits for their hosts. Recent research, however, highlights examples of species whose microbiota are transient and environmentally derived. Here, we test the effect of diet on gut microbial community assembly in the spider Badumna longinqua. Using 16S rRNA gene amplicon sequencing combined with quantitative PCR, we analyzed diversity and abundance of the spider's gut microbes, and simultaneously characterized its prey communities using nuclear rRNA markers. We found a clear correlation between community similarity of the spider's insect prey and gut microbial DNA, suggesting that microbiome assembly is primarily diet‐driven. This assumption is supported by a feeding experiment, in which two types of prey—crickets and fruit flies—both substantially altered microbial diversity and community similarity between spiders, but did so in different ways. After cricket consumption, numerous cricket‐derived microbes appeared in the spider's gut, resulting in a rapid homogenization of microbial communities among spiders. In contrast, few prey‐associated bacteria were detected after consumption of fruit flies; instead, the microbial community was remodelled by environmentally sourced microbes, or abundance shifts of rare taxa in the spider's gut. The reshaping of the microbiota by both prey taxa mimicked a stable core microbiome in the spiders for several weeks post feeding. Our results suggest that the spider's gut microbiome undergoes pronounced temporal fluctuations, that its assembly is dictated by the consumed prey, and that different prey taxa may remodel the microbiota in drastically different ways.     

Temperature dependency of predation: Increased killing rates and prey mass consumption by predators with warming

Temperature dependency of consumer–resource interactions is fundamentally important for understanding and predicting the responses of food webs to climate change. Previous studies have shown temperature‐driven shifts in herbivore consumption rates and resource preference, but these effects remain poorly understood for predatory arthropods. Here, we investigate how predator killing rates, prey mass consumption, and macronutrient intake respond to increased temperatures using a laboratory and a field reciprocal transplant experiment. Ectothermic predators, wolf spiders (Pardosa sp.), in the lab experiment, were exposed to increased temperatures and different prey macronutrient content (high lipid/low protein and low lipid/high protein) to assess changes in their killing rates and nutritional demands. Additionally, we investigate prey mass and lipid consumption by spiders under contrasting temperatures, along an elevation gradient. We used a field reciprocal transplant experiment between low (420 masl; 26°C) and high (2,100 masl; 15°C) elevations in the Ecuadorian Andes, using wild populations of two common orb‐weaver spider species (Leucauge sp. and Cyclosa sp.) present along the elevation gradient. We found that killing rates of wolf spiders increased with warmer temperatures but were not significantly affected by prey macronutrient content, although spiders consumed significantly more lipids from lipid‐rich prey. The field reciprocal transplant experiment showed no consistent predator responses to changes in temperature along the elevational gradient. Transplanting Cyclosa sp. spiders to low‐ or high‐elevation sites did not affect their prey mass or lipid consumption rate, whereas Leucauge sp. individuals increased prey mass consumption when transplanted from the high to the low warm elevation. Our findings show that increases in temperature intensify predator killing rates, prey consumption, and lipid intake, but the responses to temperature vary between species, which may be a result of species‐specific differences in their hunting behavior and sensitivity to temperature.     

Juvenile Snooks (Centropomidae) as Mimics of Mojarras (Gerreidae), with a Review of Aggressive Mimicry in Fishes

Aggressive mimicry has been proposed for several unrelated fish species both in freshwater and marine environments. I describe herein a few additional examples, including the first ones from brackish water. In one well documented case, juvenile snooks, Centropomus mexicanus (Centropomidae) join bottom-foraging groups of the superficially similar mojarras, Eucinostomus melanopterus (Gerreidae) and prey on small fishes and crustaceans under such disguise. Two other snook species and two species of groupers (Serranidae), are here suggested as additional instances of aggressive mimicry. Furthermore, I review published examples of aggressive mimicry in fishes and indicate trends in the relationships between the mimics, their feeding tactics, and their putative models. Three large families, Serranidae, Cichlidae, and Blenniidae display most of the examples of aggressive mimicry, serranids being largely represented by the genus Hypoplectrus and blenniids by the tribe Nemophini only. Three major trends are here indicated for aggressive mimics: (1) fish species that feed on prey smaller than themselves tend to mimic and join fish species harmless to their prospective prey; (2) fish species that feed on prey larger than themselves tend to mimic mostly beneficial fish species (cleaners) or, less frequently, join species harmless to their prospective prey; (3) fish species that feed on prey about their own size tend to mimic their prospective prey species, the perfect wolf in a sheep's clothes disguise type. The latter deceit is recorded mostly for scale and fin-feeding freshwater fishes.     

Holling's “hungry mantid” model for the invertebrate functional response considered as a Markov process. Part I: The full model and some of its limits

In this paper we give an analytical reformulation of Holling's (1966) simulation model for invertebrate predatory behaviour. To this end we represent a population of predators as a frequency distribution over a space of (physiological) states. The functional response of a predator is calculated from the (stable) equilibrium distribution of its state as a function of prey density.Starting from the general model various other models are obtained by limit processes, some of them new and some of them old. The more interesting of which will be studied in further papers in this series.List of Notation a rate constant of digestion - b maximum of rate constant of prey encounter in the mantid - b maximum pursuit duration in the mantid (_p(0)) - c satiation threshold for search - c satiation threshold for pursuit in the mantid: c=c(b-D_s/v)/b - D _m maximum sighting distance - D _p pursuit distance - D _s strike distance - expectation operator - f, f ₀ rate of change of satiation during search - f ₁ rate of change of satiation during prey handling - F functional response: number of prey eaten per unit of time by one predator - g rate constant of effective prey encounter in the gobbler and sucker - g₀ rate constant of prey encounter - g₁ probability of no prey loss from pursuit - g₂ probability of no prey escaping during pursuit - H Holling secretary correction factor in the sucker: fraction of the time spent searching - k _R density of R - k_T probability density of maximum prey handling time - K probability that maximum prey handling time is _e, i.e. pursuit duration is zero - K _R distribution function of R - N number of prey caught - p (marginal) density of S - p₀ density of S in search - p₁ simultaneous density of S and T - P probability - p ₁ marginal density of S in handling prey - q probability of strike success - R ratio of realized to maximum sighting distance - s, S satiation - satiation axis - t time - handling time axis - u eating speed - U homogeneous(0,1) random variable - v pursuit speed - V exponential(1) random variable - w prey weight - W exponential(_m) random variable - x prey density - ratio of maximum successful pursuit duration to meal duration (_pm/_e) - _pm - relative duration of successful pursuit (_p/_pm) - ratio of shortest to largest sighting distance - x_e - time already spent handling a prey item - rate of prey loss during prey handling - prey escape rate during pursuit - prey biomass density (xw) - , T maximum time still to be spent handling a prey item - _e meal duration - _m maximum handling time ( _e+ _p) - _p duration of successful pursuit - _pm maximum duration of successful pursuit (_p(0)) - hazard rate - _m maximum of hazard rate - scaled functional response (wF) - minimal i-state space     

Mechanisms of prey selection by predaceous stoneflies: roles of prey morphology,behavior and predator hunger

Summary Laboratory feeding experiments using Hesperoperla pacifica (Banks), Perlidae, and Megarcys signata (Hagen), Perlodidae, as predators and Baetis tricaudatus Dodds and Ephemerella altana Allen as prey indicate a strong effect of prey morphology and mobility and predator hunger on prey selection by stoneflies. Knowledge of both dietary composition and feeding behavior was necessary to fully understand prey selection by these stoneflies.Fasted stoneflies presented with live prey ate more E. altana while satiated stoneflies ate approximately equal numbers of the two mayfly species. This pattern of dietary composition was the result of a reduction of attack frequency on the slower swimming E. altana with predator satiation and a continued high attack rate on B. tricaudatus regardless of recent feeding history. In contrast, fasted H. pacifica fed fresh frozen mayflies ate more B. tricaudatus indicating the importance of differences in prey mobility in controlling dietary composition.The high degree of similarity in patterns of feeding and mechanisms underlying those patterns for H. pacifica and M. signata suggest that they may be using similar rules for choosing mayfly prey and we suggest that mayfly prey are ranked by stoneflies on the basis of handling times. A general mechanistic model for stoneflies feeding on mayflies is presented and discussed.     

Feeding by the aquatic heteropteran,Diplonychus rusticum (Belostomatidae): an effect of prey density on meal size

The behaviour of Diplonychus rusticum feeding on chironomid larvae has been investigated under laboratory conditions. Changes in the percentage of material extracted from prey indicated that feeding for the first two minutes enabled the predator to obtain approximately 33% of the available food; feeding for 10 minutes resulted in only 60% extraction. Comparing the percentage of each prey consumed by D. rusticum exposed to various prey densities, it was apparent that predators were more wasteful and ate less of each prey as chironomid density increased. Because the rate of food intake declined as a greater proportion of each prey was extracted, predators exposed to high chironomid densities reduced the amount of each prey consumed thereby conforming to a simple optimal feeding model.     

A continuous flow-chamber to study prey preferences of Golden Perch (Macquaria ambigua Richardson) larvae

This paper describes the use of a continuous-flow chamber for maintaining small and fragile fish larvae and their prey in a healthy state and under suitable conditions over a 24 h period for studies on prey preferences. Survival of golden perch (Macquaria ambigua Richardson) larvae and prey was high and ten replicates on food preferences were carried out simultaneously. The larvae preferred small Daphnia carinata King (780–860 m) over larger ones (2000–3120 and 3680–5440 m) and preferred cladocerans (Daphnia carinata King and Moina micrura Kurz) over calanoids (Boeckella de Guerne & Richard). The chamber is also suitable for studies on feeding behaviour and diet requirements of fish larvae.