Wasp Attacks and Spider Defence in the Orb Weaving Species <Emphasis Type="Italic">Zygiella x-notata</Emphasis>

Predator–prey relationships are generally based on arm-race. Wasps and spiders are both predators, which could be potential prey for each other. The orb weaver spider Zygiella x-notata is sometimes a prey for the wasp Vespula germanica. We observed the wasp hunting behaviour under natural conditions, and we tested the influence of the spider’s behaviour on the wasp attack success. Wasps were active predators during the reproductive period of the spider. Results showed that wasps located more easily male spiders than females particularly when they were engaged in mate guarding. Female location depended on the presence of a web, but also of prey or prey remains in the web. On the other hand, their location depend neither on the characteristics and the position of the retreat in the environment nor on the size of the web. After location, males were more often captured than females whatever their behaviour (mate guarding or not). Presence of prey remains or prey in the web did not increase the risk for the spider to be captured. There was also no influence of the retreat’s characteristics or of its position in the habitat on the risk for the spider to be captured; but wasp successful attacks were less numerous when silk was present around the entrance of the retreat or when the spider was completely inside. As prey and prey remains favoured location of spiders by the wasps, we tested spider web cleaning behaviour as a response to wasp predatory pressure. By throwing small polystyrene pellets in the webs, we observed that more 80% of the spiders rejected the pellets in less than one minute. Our data indicated that wasps were significant predators of Z. x-notata and wasp attack could have been a selective pressure that had favoured spider defensive behaviours such as web cleaning.     

Spiders Use Airborne Cues to Respond to Flying Insect Predators by Building Orb-Web with Fewer Silk Thread and Larger Silk Decorations

Orb-web spiders are an important group of trap-building animals that feed upon an array of insect prey and are themselves the prey of wasps and parasitoid flies. The purpose of this study was to examine whether spiders use airborne vibration cues to respond to these flying insect predators by changing their web-building behavior. While on its web waiting for prey, the orb-web spider Eriophora sagana was exposed to a vibrating tuning fork that emitted an airborne vibration signal. The signal mimicked the approach of flying insect predators and its effect on the subsequent web building was examined. No stimulus was provided during web building. A significant treatment effect was observed with respect to the total thread length (TTL) and area of the silk decoration (conspicuous white structure attached to the orb-webs of diurnal spiders) of their webs. While control spiders increased the TTL in their second web, the stimulus group spiders did not, providing the first evidence that orb-web spiders use airborne vibration cues to assess the predation risk and change their foraging activity. It also indicates that spiders remember an encounter with a predator on their webs and use this information later to adjust their web building. My findings imply that spiders devote less effort to foraging (i.e. web building) in response to the presence of their predators, which is considered to reduce their foraging efficiency. In contrast, the stimulus group spiders increased the area of their silk decoration significantly more in their second webs than did the control spiders. This is considered an experimental support for the hypothesis that silk decorations have an anti-predator function.     

Cues for web invasion and aggressive mimicry signalling in Portia (Araneae, Salticidae)

Portia is a web-invading araneophagic spider that uses aggressive mimicry to deceive its prey. The present paper is a first step toward clarifying experimentally the cues that govern Portia's decisions of whether to enter a web, whether to make signals once in a web, and whether to persist at signalling once started. The following conclusions are supported: cues from seeing a web elicit web entry, but volatile chemical cues from webs of prey spiders are not important; seeing a spider in a web increases Portia's inclination to enter the web; after web entry, cues from webs of prey spiders are sufficient to elicit signalling behaviour, even in the absence of other cues coming directly from the prey spider; seeing a prey spider or detecting vibrations on the web make Portia more prone to signal, but volatile chemical cues from prey spiders are not important; once Portia is on a web and signalling, seeing a moving spider and detecting vibrations on the web encourage Portia to persist in signalling; on the basis of visual cues alone, Portia can distinguish between quiescent spiders, insects and eggsacs.     

Are three‐dimensional spider webs defensive adaptations?

Spider webs result from complex behaviours that have evolved under many selective pressures. Webs have been primarily considered to be foraging adaptations, neglecting the potential role of predation risk in the evolution of web architecture. The ecological success of spiders has been attributed to key innovations in how spiders use silk to capture prey, especially the invention of chemically adhesive aerial two‐dimensional orb webs. However, araneoid sheet web weavers transformed the orb architecture into three‐dimensional webs and are the dominant group of aerial web‐building spiders world‐wide, both in numbers and described species diversity. We argue that mud‐dauber wasps are major predators of orbicularian spiders, and exert a directional selective pressure to construct three‐dimensional webs such that three‐dimensional webs are partly defensive innovations. Furthermore, patterns of diversification suggest that escape from wasp predators may have facilitated diversification of three‐dimensional web‐building spiders.     

Predator-induced plasticity in web-building behaviour

Many orb-web weaving spiders add conspicuous silken structures, called stabilimenta, to the hub of their webs, which are hypothesized to attract more prey. However, they may also attract predators. Orb spiders should therefore alter their web-building behaviour to minimize predation risk. We tested this hypothesis by experimentally examining web-building responses of the St Andrew cross spider, Argiope versicolor, to predation risk from one of its natural predators, the jumping spider Portia labiata. We randomly assigned A. versicolor juveniles to one of three treatments: (1) blank control (clean blotting paper: no odour from the predator or nonpredator); (2) predator odour cues from P. labiata; and (3) nonpredator control (odour cues from Leucauge decorata). Each individual of A. versicolor was monitored until it had built five consecutive webs (two webs before and three webs after the introduction of predator cues). When exposed to predator cues, the juveniles not only decreased the frequency of stabilimentum building but also refrained from increasing stabilimentum area, capture area and capture silk thread with subsequent webs compared with the blank control and the nonpredator control. Web-building traits, however, were not significantly different between the blank control and the nonpredator control. One plausible explanation is that A. versicolor juveniles can detect and discriminate between predators and nonpredators through olfactory cues and alter stabilimentum building and other web traits in response to the risk of predation. This is the first demonstration of an adaptive, plastic web-building behavioural response induced by chemical cues from a predator.     

Trophic structure of the spider community of a Mediterranean citrus grove: A stable isotope analysis

Spiders are dominant terrestrial predators that consume a large variety of prey and engage in intraguild predation. Although the feeding habits of certain species are well known, the trophic structure of spider assemblages still needs to be investigated. Stable isotope analysis enables characterisation of trophic relationships between organisms because it tracks the energy flow in food webs and indicates the average number of trophic transfers between a given species and the base of the web, thus being a useful tool to estimate the magnitude of intraguild predation in food webs. Using this technique, we studied the trophic groups of spiders and their links within the arthropod food web of a Mediterranean organic citrus grove. We assessed the trophic positions of the 25 most common spider species relative to other arthropod predators and potential prey in the four seasons of the year, both in the canopy and on the ground. The analyses showed great seasonal variation in the isotopic signatures of some arthropod species, as well as the existence of various trophic groups and a wide range of trophic levels among spiders, even in species belonging to the same family. Differences in δ¹⁵N between spiders and the most abundant prey in the grove usually spanned two trophic levels or more. Our findings provide field evidence of widespread intraguild predation in the food web and caution against using spider families or guilds instead of individual species when studying spider trophic interactions.     

Discrimination and release of unpalatable butterflies by Nephila clavipes, a neotropical orb-weaving spider

Abstract. 1. Nephila clavipes (L.), a common spider in neotropical forests, discriminates some unpalatable prey and releases them unharmed from its web. Release is not accidental but results from a specific behavioural sequence.
2. Field trials with twenty-seven butterfly species showed that spiders respond consistently to butterfly species and higher taxa. Ithomiinae and some Danainae are almost always released while Heliconiinae, Nymphalinae, Acraeinae, Pieridae and Papilionidae are usually eaten.
3. Paired tests showed that an immediately preceding experience with a different butterfly did not reveal any change in the spider's usual response to a particular butterfly.
4. Warning coloration is not involved in spider response. Spiders rejected the models but ate the mimics of two different butterfly species pairs. Distastefulness is probably signalled by chemical cues.
5. Some unpalatable butterflies stay motionless when entangled and while the spiders release them. Motionlessness in webs seems to be a requisite to allow recognition of their distastefulness without being bitten by the spider.
6. Spiders differ from vertebrates in the prey accepted and in rejection mechanics. Although there is no indication of learning, spiders may select butterflies for distastefulness, chemical signals and motionlessness, at the individual level.     

Predator kairomones change food web structure and function,regardless of cues from consumed prey

Predation risk in aquatic systems is often assessed by prey through chemical cues, either those released by prey or by the predator itself. Many studies on predation risk focus on simple pairwise interactions, with only a few studies examining community‐level and ecosystem responses to predation risk in species‐rich food webs. Further, of these few community‐level studies, most assume that prey primarily assess predation risk through chemical cues from consumed prey, even heterospecific prey, rather than just those released by the predator. Here, we compared the effects of different predation cues (predator presence with or without consumed prey) on the structure and functioning of a speciose aquatic food web housed in tropical bromeliads. We found that the mere presence of the top predator (a damselfly) had a strong cascading effect on the food web, propagating down to nutrient cycling. This predation risk cue had no effect on the identity of colonizing species, but strongly reduced the abundance and biomass of the macroinvertebrate colonists. As a result, bacterial biomass and nitrogen cycling doubled, with a concomitant decrease in bacterial production, but CO₂ flux was unaffected. These community and ecosystem effects of predator presence cues were not amplified by the addition of chemical cues from consumed prey. Our results show that some of the consequences of predation risk observed in controlled experiments with simplified food webs may be observed in a natural, species‐rich food web.     

Previous foraging success influences web building in the spider Stegodyphus lineatus (Eresidae)

Stegodyphus lineatus (Eresidae) is a desert spider that buildsan aerial capture web on bushes in the Negev desert in southernIsrael. Web building for spiders is costly in energy, time,and risk of predation. Spiders should trade-off these costswith the benefits in terms of prey capture. We tested the hypothesisthat the previous foraging success of the spider influencesthe effort invested in foraging. Specifically, we asked whetheran increase in food intake causes spiders to reduce web renewalactivity and web size. Alternatively, time constraints on foragingand development, resulting from a short growing season, couldinduce spiders to continue foraging even when supplemented withprey. The cost of web building was measured as time and massloss. To build an average size web (about 150 cm²), we calculatedthat a spider requires 6 h and that spiders lose 3%-7% of their weight.In field experiments, spiders responded differently to food supplementationin 2 different years. In 1994, they improved their condition comparedto individuals whose webs were removed to reduce foraging opportunitiesand compared to control spiders. In 1995, spiders tested earlier inthe season than the previous year did not improve their conditionin response to prey supplementation. Nonetheless, in both years, food-supplementedspiders built significantly smaller webs than food-deprived andcontrol spiders. This result was confirmed in a laboratory experiment whereprey intake was controlled. We conclude that for S. lineatus immediateforaging risks outweigh the potential time constraints on foraging.     

Caught in the web: Spider web architecture affects prey specialization and spider–prey stoichiometric relationships

Quantitative approaches to predator–prey interactions are central to understanding the structure of food webs and their dynamics. Different predatory strategies may influence the occurrence and strength of trophic interactions likely affecting the rates and magnitudes of energy and nutrient transfer between trophic levels and stoichiometry of predator–prey interactions. Here, we used spider–prey interactions as a model system to investigate whether different spider web architectures—orb, tangle, and sheet‐tangle—affect the composition and diet breadth of spiders and whether these, in turn, influence stoichiometric relationships between spiders and their prey. Our results showed that web architecture partially affects the richness and composition of the prey captured by spiders. Tangle‐web spiders were specialists, capturing a restricted subset of the prey community (primarily Diptera), whereas orb and sheet‐tangle web spiders were generalists, capturing a broader range of prey types. We also observed elemental imbalances between spiders and their prey. In general, spiders had higher requirements for both nitrogen (N) and phosphorus (P) than those provided by their prey even after accounting for prey biomass. Larger P imbalances for tangle‐web spiders than for orb and sheet‐tangle web spiders suggest that trophic specialization may impose strong elemental constraints for these predators unless they display behavioral or physiological mechanisms to cope with nutrient limitation. Our findings suggest that integrating quantitative analysis of species interactions with elemental stoichiometry can help to better understand the occurrence of stoichiometric imbalances in predator–prey interactions.     

Reducing predation of orb-web spiders by controlling common wasps (Vespula vulgaris) in a New Zealand beech forest

1. Introduced common wasps ( Vespula vulgaris ) reach high densities in the beech forests ( Nothofagus spp.) of the northern South Island, New Zealand, and may be having a severe impact on populations of native invertebrates. An experimental approach was used to test whether reducing the abundance of common wasps increases the probability of native invertebrates surviving. Garden orb-web spiders ( Eriophora pustulosa ) were used because they were easy to collect and could be trained to build webs on a standard frame. Thirty orb-web spiders were placed out on web-frames in each of four study sites in beech forest during periods of low, medium and high wasp abundance, and their rate of removal was measured over a 4-h period. Wasp numbers were reduced by poisoning in two study sites. Using wasp-abundance data from weekly Malaise trap samples in the poisoned and non-poisoned sites, the probability of spider survival over the entire wasp season was modelled and the level of wasp control necessary to protect natural populations of orb-web spiders was estimated.
2. Wasp abundance and the probability of spider survival were negatively correlated, and smaller spiders were likely to survive longer than larger spiders. At the peak of the wasp season, significantly more spiders survived in the poisoned areas than in the non-poisoned areas.
3. The probability of a spider surviving to the end of the wasp season was virtually nil in the non-poisoned sites (5.08 × 10^–18), but was also very unlikely in the poisoned areas (3.47 × 10^–5).
4. The survival model predicts that wasp abundance would need to be reduced by 80–89.5% over the entire wasp season to protect populations of orb-web spiders.
5. Extrapolation from the model predicts that the invertebrate taxa most vulnerable to wasp predation may have already been removed from the beech forest ecosystem during the 40 years of wasp occupation.     

Signaling by decorating webs: luring prey or deterring predators?

Many organisms convey false signals to mislead their prey orpredators. Some orb-weaving spiders build conspicuous structureson webs called decorations. Web decorations and spider colorationsare both suggested to be important signals involved in interactionsbetween spiders and other organisms. There are several hypothesesabout the functions of signaling by decorations, among whichprey attraction had received much support, but empirical evidenceregarding predator defense is controversial. In this study,we conducted field experiments to investigate the effects ofspider decoration and coloration on insect interception ratesof webs built by Argiope aemula and to evaluate whether presenceof decorations may decrease predation risk of spiders. Decoratedwebs with spiders present had the highest prey interceptionrate, followed by undecorated webs with spiders, and then undecoratedwebs without spiders. Such results indicated that decorationsof Argiope spiders functioned as visual lures, and so did spiders'bright body colorations. In the field, almost all wasp attackevents occurred on medium-sized spiders rather than on largeones. Moreover, medium-sized Arg. aemula on decorated webs receivedfar more attacks than those on undecorated webs. Results ofthis study thus show that the signals conveyed by decorationscan visually lure prey but at the cost of an increased predationrisk. Received 20 March 2007; revised 3 August 2007; accepted 5 August 2007.     

A virtual robot to model the use of regenerated legs in a web-building spider

The garden cross orb-spider, Araneus diadematus, shows behavioural responses to leg loss and regeneration that are reflected in the geometry of the web's capture spiral. We created a virtual spider robot that mimicked the web construction behaviour of thus handicapped real spiders. We used this approach to test the correctness and consistency of hypotheses about orb web construction. The behaviour of our virtual robot was implemented in a rule-based system supervising behaviour patterns that communicated with the robot's sensors and motors. By building the typical web of a nonhandicapped spider our first model failed and led to new observations on real spiders. We realized that in addition to leg position, leg posture could also be of importance. The implementation of this new hypothesis greatly improved the results of our simulation of a handicapped spider. Now simulated webs, like the real webs of handicapped spiders, had significantly more gaps in successive spiral turns compared with webs of nonhandicapped spiders. Moreover, webs built by the improved virtual spiders intercepted prey as well as the digitized real webs. However, the main factors that affected web interception frequency were prey size, size of capture area and individual variance; having a regenerated leg, surprisingly, was relatively unimportant for this trait. Copyright 1999 The Association for the Study of Animal Behaviour.     

Direct and indirect effects of predation and predation risk in old-field interaction webs

ABSTRACT Indirect effects emerge when a change in the abundance of one species indirectly affects another by changing the abundances of intermediate species-called density-mediated indirect effects-or they arise when one species modifies how two other species interact-called trait-mediated indirect effects. I report on field experiments that evaluated how grass and herb biomass in old-field interaction webs was influenced indirectly by a spider carnivore through its interactions with a generalist and a grass-specialist grasshopper species. I manipulated interaction pathways between the spider and the plants using different combinations of the grasshopper species. I changed the modality of predator-prey interactions to isolate density-mediated from trait-mediated effects using natural spiders (predation spiders) or spiders that were prevented from subduing prey by mouthpart manipulation (risk spiders). I found that indirect effects were stronger in speciose, reticulate food webs than in linear food chains owing to a trait-mediated effect, a diet shift by herbivores in response to predation risk. Spiders alone did not have significant effects on grasshopper densities in the field experiments, removing any possibility of density-mediated indirect effects. The study illustrates that ecologists should not underestimate the importance of behavioral ecology in determining community-level interactions.     

Prey analysis of four species of tropical orb-weaving spiders (Araneae: Araneidae) and a comparison with araneids of the temperate zone

Summary The actual prey in the orb webs of four araneid spiders (Nephila clavipes, Eriophora fuliginea, Argiope argentata, and A. savignyi) and the relative abundance of their potential prey (pitfall traps, yellow traps, and sweep-netting) was investigated over 1 year at different locations in Panama. The relative abundance of insects and spiders depends on seasonal fluctuations (Fig. 2) which are reflected by corresponding variations in the effectiveness of the webs. The main prey groups are Nematocera (50%–68%), winged Formicoidea (6%–15%) and Hymenoptera, Coleoptera, and Brachycera (4%–10% each) (Fig. 4-6). The remaining 10%–17% of the prey comes from up to 26 other groups (Table 2). Differences in prey size and prey composition between the spider species are small (Fig. 7). Most prey items are 1–2 mm long: only a few insects exceed 30 mm body length (Figs. 9–12). Relative to the available prey, some groups (e.g. Nematocera, Aphidoidea, Psocoptera) are caught selectively, while other groups (e.g. Heteroptera, Coleoptera, Brachycera, Orthoptera) are underrepresented in the prey spectrum and obviously avoid orb webs (Table 7). The differences in prey composition between araneids of the tropics and of the temperate zone are discussed (Table 8) and compared to those recorded in other studies (Table 9, 10). Most of these report large numbers of big prey items (Odonata, Lepidoptera, wasps/bees). It is pointed out that those studies do not take into account the total available prey in a spider's web but only that part which the spider selects from the web (mainly according to size). The importance of small prey items even for large spiders is explained and an obvious lack of niche partitioning among coexisting araneids is discussed (Table 11).     

Age-related sequential web building in the colonial spider Metepeira incrassata (Araneidae): an adaptive spacing strategy

Colonial orb-weaving spiders provide insight into the proximate mechanisms by which social animals space themselves within a group. We examined mechanisms for the temporal patterns of web building that determine individual positions in Metepeira incrassata (Araneidae) colonies. The spiders display a characteristic age-related sequence of daily web building, with larger spiders completing their webs significantly earlier than smaller ones. We used data on behavioural interactions, web building, prey capture and predator attacks to evaluate four hypotheses. (1) Larger spiders are better competitors and pre-empt optimal spatial positions. (2) Smaller spiders reduce competition with larger individuals by building webs later. (3) Prey captured by different size classes is available at different times. (4) Differential predation risk determines web-building times. Large individuals dominated behavioural interactions. Disturbances by larger spiders during web construction significantly delayed the completion of smaller individuals' webs and precipitated movements to new web sites. One prediction of the first hypothesis, that spatial needs translate into earlier building, was confirmed by significantly earlier web building by mature females with egg sacs (which are unable to move their egg sacs) compared with same-sized females without eggs (which can change locations freely). Experiments to determine whether the presence of large spiders inhibited the web building of smaller individuals were equivocal. Prey availability and risk of predation are not factors affecting web-building patterns. Sequential web building appears to be a result of both larger spiders competing to pre-empt space from one another and smaller individuals attempting to reduce conflict during web construction. Sequential web building is a proximate mechanism that influences spacing among colonial orb-weaving spiders and helps shape the typical hierarchical size distribution of spiders within the colony. Similar spacing mechanisms may be seen in colonial birds and marine invertebrates. Copyright 2000 The Association for the Study of Animal Behaviour.     

Web-building behaviour in the orb-weaving spider Zygiella x-notata: influence of experience

Zygiella x-notata is an orb-weaving spider that often renews its trap daily. Web building has associated costs and benefits, and building successive webs may have consequences for lifetime reproductive success. In the laboratory, we tested the ability of Z. x-notata to modify its building behaviour in response to various stages in predation (prey detection, capture and ingestion) experienced with a previous web. We determined which stages provided information for the spiders. Spiders that detected, captured and ingested prey and then rebuilt their web used less silk and made a smaller capture area than in the previous web. There was no effect of prey detection alone on the next web. Capture without feeding gave the same results as capture followed by feeding. The spiders that ate prey without detection and capture (feeding by hand) had the same energetic gains as spiders that caught prey but delayed building a new web. The spiders thus showed plasticity in web-building behaviour and in the amount of silk used (energetic investment) in the short term (from one web to the next). Changes in body condition may therefore influence web construction. Moreover, information gained during prey capture appeared to influence the size and structure of the next web. This ability should enable spiders to adapt their web building to maximize their fitness. Copyright 2000 The Association for the Study of Animal Behaviour.     

Stabilimenta of Philoponella vicina (Araneae: Uloboridae) and Gasteracantha cancriformis (Araneae: Araneidae): Evidence Against a Prey Attractant Function

Both the uloborid Philoponella vicina and the araneid Gasteracantha cancriformis spiders sometimes placed silk stabilimenta on non-orb "resting webs" that consisted of only one or a few lines. These webs completely lacked sticky silk, so their stabilimenta could not function to attract prey. Some non-orbs were built by spiders when their orb webs are damaged. These observations contradict the prey attraction camouflage hypothesis for stabilimentum function, but are compatible with the spider camouflage and web advertisement to avoid web destruction hypotheses.     

Contributions of detrital subsidies to aboveground spiders during secondary succession, revealed by radiocarbon and stable isotope signatures

Prey subsidies originating from detritus add nutrients and energy to arboreal communities. Measurement of this subsidy is required in the understanding of how food web dynamics respond to changes in surrounding environments. Shrub spiders are one of the key predators involved in food web coupling. We evaluate the effects of potential changes in prey availabilities during secondary succession on the contribution of subsidy from detrital food webs to shrub spiders and how different spider feeding guilds used the subsidy of prey from detrital food webs. We measured the relative importance of the subsidy for the spider feeding guilds, using the ratios of stable isotopes of C (δ¹³C), and N (δ¹⁵N) and C isotope discrimination (Δ¹⁴C). Diet age was calculated from Δ¹⁴C values, because old diet ages of spiders indicate that the spiders consume prey from detrital food sources. Dominant aerial prey (Diptera) had a distinctively old diet age compared with arboreal prey, which indicates that aerial prey were subsidized from detrital food webs. Sit-and-wait spiders tended to have an older diet age than active hunting spiders, which indicates that sit-and-wait spiders depended more on subsidies. Diet age varied only slightly for spiders in stands of different ages, indicating that rates at which spiders use grazing and detrital prey are probably determined more by foraging strategies and not by stand age. A dominance of sit-and-wait predators will lead to higher detrital subsidy inputs in shrub habitats. This study highlights the effect of shrub spider community structure (feeding guild composition) on the volume of the subsidy received from the detrital food web.     

Small-scale spatial pattern of web-building spiders (Araneae) in alfalfa: relationship to disturbance from cutting, prey availability, and intraguild interactions

Understanding the development of spatial patterns in generalist predators will improve our ability to incorporate them into biological control programs. We studied the small-scale spatial patterns of spider webs in alfalfa by analyzing the relationship between web locations over distances ranging from 4 to 66 cm. Using a coordinate-based spatial statistic (O-ring) and assuming a heterogeneous distribution of suitable web sites, we analyzed the impact of cutting and changes in spider abundance on web distribution. We analyzed the influence of small-scale variation in prey availability by comparing web distributions to the pattern of sticky-trap captures of Aphididae and Diptera described by a count-based spatial statistic (SADIE). Cutting of alfalfa reduced the overall density of web-building spiders but had no immediate impact on the spatial distribution of their webs. Availability of aphids was highest before the alfalfa was cut and was clumped at a scale of 66 cm. Spider webs, however, were not clumped at any scale or date. In contrast, webs were regularly distributed at smaller distances (<20 cm) immediately before and after cutting. Because cursorial and web-building spiders were most active during this period, we hypothesize that the development of small-scale regularity in web locations was driven by intraguild interactions. Our results suggest that intraguild interactions contribute to the development of small-scale spatial patterns of spider webs in alfalfa. Variation in prey availability may have more of an influence on web distribution in crops with a different vegetation structure or if patterns are studied at larger spatial scales.