Testing the Functions of Detritus Stabilimenta in Webs of Cyclosa fililineata and Cyclosa morretes (Araneae: Araneidae): Do They Attract Prey or Reduce the Risk of Predation?

Spiders of the genus Cyclosa often add prey remains and other debris to their orb‐webs. The function of silk decorations is generally associated with defense against predators or with the attraction of prey, but few studies have focused on stabilimenta containing detritus. In this study, we used artificial webs with and without the detritus stabilimenta of two species of Cyclosa to investigate whether these structures increase the number of insects intercepted. Artificial models of spiders and stabilimenta were used to compare the frequency of attacks against different shapes. We also conducted choice experiments in laboratory to determine whether detritus columns attracted Drosophila melanogaster (Diptera: Drosophilidae) and Trigona angustula (Hymenoptera: Apidae, Meliponinae) to the webs. The frequency of interception in artificial webs with a stabilimentum was similar to that of webs without such structure. The taxonomic composition and biomass of insects were also similar in both types of artificial webs. The choice experiments showed no significant tendency in attraction to webs with a stabilimentum. However, models of spiders were attacked at a higher frequency than those simulating detritus columns and silk decorations. These findings argue against the prey attraction hypothesis and suggest that the addition of stabilimenta to webs of Cyclosa could reduce the intensity of predation, possibly by disrupting the image of the spider's outline.     

Do stabilimenta in orb webs attract prey or defend spiders?

Orb-weaving spiders are ideal organisms for the study of conflictbetween behavioral investments in foraging and defense becausetheir webs provide physical manifestations of those investments.We examined the impact of including stabilimenta, designs ofbright-white noncapture silk, at the center of orb webs forforaging and defense in Argiope aurantia. Our findings suggestthat stabilimentum building is a defensive behavior, supportingthe "web advertisement" hypothesis that the high visibilityof stabilimenta can prevent birds from flying through webs.Yet, spiders often do not include stabilimenta in their webs,indicating that a serious cost is associated with them. We alsoshow, through comparison of paired webs with and without stabilimenta,that stabilimenta reduce the prey capture success of spidersby almost 30%. This demonstrates the potential impact that defensivebehaviors of spiders can have on their foraging success andsuggests that much of the variation in stabilimenta may be accountedfor by a cost—benefit trade-off made when including stabilimentain webs.     

The biology of Pholcus phalangioides (Araneae, Pholcidae): predatory versatility, araneophagy and aggressive mimicry

Predatory versatility occurs in Pholcus phalangioides (Fuesslin). In addition to building prey-catching space webs, P. phalangioides invades webs of other spiders and feeds on the occupants. It acts as an aggressive mimic by performing specialized vibratory behaviours to which the prey-spider responds as it normally would to its own prey. Prey (spiders and insects) is attacked by wrapping. Prey that trips over lines at the edge of a web of P. phalangioides , but fails to enter the web, is successfully attacked: P. phalangioides leans out of its web to throw silk over the prey, keeping as few as two legs on the silk. However, P. phalangioides does not attack prey that is completely away from webs. Occasionally, P. phalangioides feeds on eggs of other spiders and on ensnared insects it encounters in alien webs. Experimental evidence indicates that vision is of little or no importance in the predatory behaviour of P. phalangioides . Although P. phalangioides invades diverse types of webs, in addition to using its own web, its efficiency as a predator varies with web-type. It is most efficient as a predator of spiders and, especially, insects on its own web, and least efficient as a predator of amaurobiids on their cribellate sheet webs. Sensory, locomotory and other factors which influence differential predatory efficiency are discussed. The behaviour of P. phalangioides is compared to that of Portia , an araneophagic web-invading salticid, and the results of this study are discussed in relation to hypotheses concerning salticid evolution.     

Web tuning of an orb-web spider, Octonoba sybotides, regulates prey-catching behaviour

An uloborid spider (Oclonoba sybotides constructs two types of web which are distinguished by linear or spiral stabilimenta. Food-deprived spiders tend to construct webs with spiral stabilimenta and food-satiated spiders tend to construct webs with linear stabilimenta. I experimentally examined the influence of web type on the speed of a spider's response to small and large flies. The results indicated that web type rather than the spiders' energetic condition influences the response speed to small or large Drosophila flies. I also examined whether thread tension affects the response speed of spiders by increasing the tension of the radial threads. The results showed that spiders on an expanded web responded to small prey as quickly as spiders on webs with spiral stabilimenta. The tension of the radial threads may be regulated by the degree of distortion of the radial threads at the hub. O. sybotides seems to construct orb webs which induce different responses for smaller, less-profitable prey according to its energetic state. The spider appears to increase the tension of the radial threads so that it can sense smaller prey better when hungry.     

The multiple disguises of spiders: web colour and decorations, body colour and movement

Diverse functions have been assigned to the visual appearance of webs, spiders and web decorations, including prey attraction, predator deterrence and camouflage. Here, we review the pertinent literature, focusing on potential camouflage and mimicry. Webs are often difficult to detect in a heterogeneous visual environment. Static and dynamic web distortions are used to escape visual detection by prey, although particular silk may also attract prey. Recent work using physiological models of vision taking into account visual environments rarely supports the hypothesis of spider camouflage by decorations, but most often the prey attraction and predator confusion hypotheses. Similarly, visual modelling shows that spider coloration is effective in attracting prey but not in conveying camouflage. Camouflage through colour change might be used by particular crab spiders to hide from predator or prey on flowers of different coloration. However, results obtained on a non-cryptic crab spider suggest that an alternative function of pigmentation may be to avoid UV photodamage through the transparent cuticle. Numerous species are clearly efficient locomotory mimics of ants, particularly in the eyes of their predators. We close our paper by highlighting gaps in our knowledge.     

Effect of abiotic factors on the foraging strategy of the orb‐web spider Argiope keyserlingi (Araneae: Araneidae)

Abstract Environmental conditions such as light level, background contrast and temperature might influence a spider's prey capture success and risk of predation. Thus it may often be advantageous for spiders to adjust web‐building behaviour in response to variation in these environmental conditions. This hypothesis was examined in a study of the construction of webs and web decorations (conspicuous strands of silk at the hub of the web) of the orb‐web spider Argiope keyserlingi. Web decorations are thought to have one or more separate functions. They may attract prey, deter predators or advertise the web to oncoming birds, thus preventing web damage. In this series of experiments, relationships between weather parameters and the construction of webs and web decorations were considered. In complementary laboratory experiments, A. keyserlingi spiders were exposed to two different light levels (700 and 90 lx), background contrasts (black and white) and temperature conditions (20 and 26°C). Of the available weather parameters, only temperature was significantly related to web decorating behaviour but not to web size. In the laboratory, temperature also influenced web‐decorating behaviour, and spiders in dim light (700 lx) constructed larger webs and longer decorations. Background contrast did not significantly alter web size or web decorations. These data suggest that when prey availability is reduced at low temperatures, spiders may use web decorations to attract prey to the web. Similarly, in dim light, spiders may build more and larger decorations to increase the visual signal to approaching prey or to advertise the web to oncoming birds.     

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.     

Costs and benefits of facultative aggregating behaviour in the orb-spinning spider Gasteracantha minax Thorell (Araneae: Araneidae)

Abstract The potential costs and benefits of foraging in aggregations are examined for the orb-spinning spider Gasteracantha minax. Web-site tenacity is low in this species; individuals frequently move among sites, thereby joining aggregations of different sizes. Female spiders in aggregations suffered lower predation rates and attracted more males than their solitary counterparts. However, aggregated eggsacs, probably produced by females in aggregations, experienced higher rates of parasitism than solitary eggsacs. We found no evidence of higher prey capture success rates among spiders in aggregations. However, we demonstrate a novel way in which spiders can increase their foraging efficiency by decreasing silk investment. A spider spinning a web within an existing aggregation can attach the support threads of its web to those of other webs, thereby exploiting the silk produced by other spiders.     

Signal conflict in spider webs driven by predators and prey

Variation in the sensory physiologies of organisms can bias the receptions of signals, driving the direction of signal evolution. Sensory drive in the evolution of signals may be particularly important for organisms that confront trade-offs in signal design between the need for conspicuousness to allow effective transfer of information and the need for crypsis of the signal to unintended receivers. Several genera of orb-weaving spiders include conspicuous silk designs, stabilimenta, in the centre of their webs. Stabilimenta can be highly visible signals to predators, warning them of the presence of a noxious, sticky silk web. However, stabilimenta can also be used by prey as a signal in avoidance of webs, creating a trade-off in signal visibility. I argue that the derived spectral properties of stabilimentum silk have resulted in part from this conflict. The innate colour preferences of insects, their ability to learn colours, and the spectral properties of flowers all suggest that the reflectance spectra of stabilimenta renders them relatively cryptic to many insect prey, while maintaining their visibility to vertebrate predators.     

Developmental changes in barrier web structure under different levels of predation risk inNephila clavipes (Araneae: Tetragnathidae)

Individuals of the orb-weaving spider Nephila clavipesbuild complex webs with a region used for prey capture, the orb, and tangle webs opposite either face, the barrier webs. Barrier webs have been hypothesized to serve a variety of functions, including predator defense, and the primary function of the barrier web should be reflected in the relative size of the barrier to the orb under varying conditions of foraging success and predation risk. To investigate the effects of predation pressure and foraging success on barrier web structure, I conducted a comparative study in three disjunct populations that differed in predation risk and foraging success. Although both the orb web and the barrier webs are silk, there was no indication of a foraging-defense trade-off. Barrier web structure did not change during seasonal shifts in orb web size related to changes in preycapture rate, and barrier web silk density and orb radius were positively correlated. The hypothesis that the construction of barrier webs is in part a response to predation pressure was supported. Barrier webs do deflect attacks by some predators, and barrier webs built by small spiders, suffering frequent predation attempts, had a higher silk density than barrier webs built by larger individuals. Additionally, barrier web complexity decreased at a later age in areas with higher predation risk.     

Signalling conflict between prey and predator attraction

Predators may utilize signals to exploit the sensory biases of their prey or their predators. The inclusion of conspicuous silk structures called decorations or stabilimenta in the webs of some orb‐web spiders (Araneae: Araneidae, Tetragnathidae, Uloboridae) appears to be an example of a sensory exploitation system. The function of these structures is controversial but they may signal to attract prey and/or deter predators. Here, we test these predictions, using a combination of field manipulations and laboratory experiments. In the field, decorations influenced the foraging success of adult female St. Andrew’s Cross spiders, Argiope keyserlingi: inclusion of decorations increased prey capture rates as the available prey also increased. In contrast, when decorations were removed, prey capture rates were low and unrelated to the amount of available prey. Laboratory choice experiments showed that significantly more flies (Chrysomya varipes; Diptera: Calliphoridae) were attracted to decorated webs. However, decorations also attracted predators (adult and juvenile praying mantids, Archimantis latistylus; Mantodea: Mantidae) to the web. St. Andrew’s Cross spiders apparently resolve the conflicting nature of a prey‐ and predator‐attracting signal by varying their decorating behaviour according to the risk of predation: spiders spun fewer decorations if their webs were located in dense vegetation where predators had greater access, than if the webs were located in sparse vegetation.     

The biology of some Argiope species from New Guinea: predatory behaviour and stabilimentum construction (Araneae: Araneidae)

Three species of Argiope: A. picta, A. aemula and A. reinwardti were studied at Wau, New Guinea. The stabilimenta in 548 webs of these species were classified into 18 categories, and the frequency of occurrence of each category was recorded. The data from this study are compared with previous records on the variation in the form of the devices built by spiders of the genera Argiope and Gasteracantha and related to theories about stabilimentum function.
Studies of the predatory behaviour of the three species show that this is, in general, similar to that of Argiope argentata . Data are cited to show that the spiders discriminate lepidopterans from insects of similar size. Particular attention was paid to the question of whether the species interrupt predatory sequences, after the attack phase, with a stage during which they rest at the hub of the web before transporting the prey. Unlike Argiope argentata these species interrupt a high proportion of predatory sequences that are initiated by bite/wrap attacks. This aspect of their behaviour is evaluated and discussed.     

The evolution of novel animal signals: silk decorations as a model system

Contemporary animal signals may derive from an elaboration of existing forms or novel non-signalling traits. Unravelling the evolution of the latter is challenging because experiments investigating the maintenance of the signal may provide little insight into its early evolution. The web decorations, or stabilimenta of some orb web spiders represent an intriguing model system to investigate novel animal signals. For over 100 years, biologists have struggled to explain why spiders decorate their webs with additional threads of silk, producing a conspicuous signal on a construction whose function is to entangle unsuspecting prey. The numerous explanations for the maintenance of this behaviour starkly contrast with the absence of a plausible explanation for its evolutionary origin. Our review highlights the difficulties in resolving both the evolution and maintenance of animal signalling, and inferring the causative arrow-even from experimental studies. Drawing on recent research that focuses on physiological processes, we provide a model of the evolutionary progression of web-decorating behaviour.     

Foraging strategies in orb-spinning spiders: Ambient light and silk decorations in Argiope aetherea Walckenaer (Araneae: Araneoidea)

Abstract Many species of orb-spinning spiders construct silk decorations within the structure of the orb-web. The evolutionary significance of these decorations is poorly understood, but the silk decorations of many species reflect UV light, suggesting that they may function to attract insects. In these species, relatively more silk decoration may be required under dimmer light conditions in order to maintain a constant UV-reflecting signal, and hence level of insect attraction. We investigated experimentally whether the orb-spinning spider Argiope aetherea adjusts the amount of silk decoration added to the web according to light conditions. Consistent with the prey-attracting function, we found that spiders adjusted the quantity of silk decoration to their webs, adding more silk decoration when the web was located in dim light rather than bright light.     

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.     

Function of bright coloration in the wasp spider Argiope bruennichi (Araneae: Araneidae)

There are two major competing explanations for the counter-intuitive presence of bright coloration in certain orb-web spiders. Bright coloration could lure insect prey to the web vicinity, increasing the spider's foraging success. Alternatively, the markings could function as disruptive camouflage, making it difficult for the insect prey to distinguish spiders from background colour variation. We measured the prey capture rates of wasp spiders, Argiope bruennichi, that were blacked out, shielded from view using a leaf fragment, or left naturally coloured. Naturally coloured spiders caught over twice the number of prey as did either blacked-out or leaf-shielded spiders, and almost three times as many orthopteran prey. Spectrophotometer measurements suggest that the bright yellow bands on the spider's abdomen are visible to insect prey, but not the banding on the legs, which could disguise the spider's outline. Thus, our results provide strong support for the hypothesis that bright coloration in the wasp spider acts as a visual lure for insect prey and weak support for the hypothesis that the arrangement of the banding pattern across the spider's body disguises the presence of the spider on the web.     

Spinneret Microstructure of the Silk Spinning Apparatus in the Crab Spider, Misumenops tricuspidatus (Araneae: Thomisidae)

The silk spinning apparatus in the crab spider, Misumenops tricuspidatus was studied with the field emission scanning electron microscope (FESEM) and the main microstructural characteristics of the silk glands are presented. In spite of the fact that the crab spiders do not spin webs to trap a prey, they also have silk apparatus even though the functions are not fully defined. The crab spider, Misumenops tricuspidatus possesses only three types of silk glands which connected through the typical spinning tubes on the spinnerets. The spinning apparatus of Misumenops closely corresponds to that of wandering spiders such as jumping spiders or wolf spiders except some local variations. Anterior spinnerets comprise 2 pairs of the ampullates and 48 (±5) pairs of pyriform glands. Another 2 pairs of ampullate glands and nearly 20 (±3) pairs of aciniform glands were connected on the middle spinnerets. Additional 50 (±5) pairs of the aciniform glands were connected on the posterior spinnerets. The aggregate glands and the flagelliform glands which have the function of sticky capture thread production in orb‐web spiders as well as the tubuliform glands for cocoon production in females were not developed at both sexes of this spider, characteristically.     

Oldest true orb-weaving spider (Araneae: Araneidae)

The aerial orb web woven by spiders of the family Araneidae typifies these organisms to laypersons and scientists alike. Here we describe the oldest fossil species of this family, which is preserved in amber from Alava, Spain and represents the first record of Araneidae from the Lower Cretaceous. The fossils provide direct evidence that all three major orb web weaving families: Araneidae, Tetragnathidae and Uloboridae had evolved by this time, confirming the antiquity of the use of this remarkable structure as a prey capture strategy by spiders. Given the complex and stereotyped movements that all orb weavers use to construct their webs, there is little question regarding their common origin, which must have occurred in the Jurassic or earlier. Thus, various forms of this formidable prey capture mechanism were already in place by the time of the explosive Cretaceous co-radiation of angiosperms and their flying insect pollinators. This permitted a similar co-radiation of spider predators with their flying insect prey, presumably without the need for a 'catch-up lag phase' for the spiders.     

The common house spider alters the material and mechanical properties of cobweb silk in response to different prey

Many spiders depend upon webs to capture prey. Web function results from architecture and mechanical performance of the silk. We hypothesized that the common house spider, Achaearanea tepidariorum, would alter the mechanical performance of its cobweb in response to different prey by varying the structural and material properties of its silk. We fed spiders either large, high kinetic energy crickets or small, low kinetic energy pillbugs for 1 week and then examined their freshly spun silk. We separated mechanical performance into structural and material effects. We measured both types of properties for silk threads collected directly from cobwebs to test for "tuning" of silk performance to different aspects of prey capture. We compared silk from two different functional regions of the cobweb-sticky gumfooted threads that adhere directly to prey and supporting threads that maintain web integrity. Supporting threads from cricket-fed spiders were stiffer and tougher than supporting threads from pillbug-fed spiders. Both types of silk from cricket-fed spiders broke at higher loads than silk from pillbug-fed spiders. We explain this variation using a simple model of forces exerted by prey and spiders on single threads and propose potential mechanisms for this change in material properties. Two alternative, nonexclusive, hypotheses are suggested by our data. Spiders may tune silk to different types of prey by spinning threads that are able to hold prey without deforming permanently. Alternatively, as spider's body mass differed dramatically between the two feeding regimes, spiders may tune silk to their own body mass.