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.     

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.     

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.     

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.     

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.     

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.     

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 Influence of Energetic State on the Form of Stabilimentum Built by Octonoba sybotides (Araneae: Uloboridae)

The influence of food supply on the type of stabilimentum built by Octonoba sybotides, an uloborid spider, was investigated in a laboratory experiment. Spiders were separated into two groups that built distinct stabilimenta (linear or spiral), and then further subdivided into two different feeding groups (food-deprived and food-supplemented). Food-deprived spiders (a fruit fly every 10 d) tended to form spiral stabilimenta, whereas food-supplemented spiders (a fruit fly every 2 d) tended to form linear stabilimenta. Furthermore, there was a significant difference in the distribution of stabilimentum forms before and after egg production. After egg production, which involves a large expenditure of energy, spiders tended to form spiral stabilimenta. These results suggest that the spider's energetic state influences the type of stabilimentum built by O. sybotides , and that hunger induces the spider to form spiral stabilimenta.     

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.     

Conspicuous colouration attracts prey to a stationary predator

Abstract 1. Conspicuous body colouration is counter‐intuitive in stationary predators because sit‐and‐wait tactics frequently rely on concealed traps to capture prey. Consequently, bright colours and contrasting patterns should be rare in predators using traps as they may alert potential prey. Yet, some orb‐weaving spiders are brightly coloured and contrastingly patterned. How can conspicuousness of trap‐building sit‐and‐wait predators be favoured by natural selection? 2. Observations of spiny spiders Gasteracantha fornicata in north‐eastern Australia showed that the size of spiders relative to their orb webs correlated positively with relative prey numbers already captured in their webs. A possible explanation is that the relatively larger appearance of the yellow–black striped dorsal surface of this spider attracts more visually oriented prey items. Prey attracted to webs may get trapped, thereby increasing the spiders' foraging success. 3. To test this hypothesis for the function of conspicuous body colouration, a field experiment was conducted that documented the prey capture rates of spiny spiders after manipulating or sham‐manipulating their appearance. 4. As predicted, spiders that were dyed black on their striped dorsal surface caught relatively fewer prey items than did control spiders. Thus, conspicuous dorsal body colouration may be adaptive in spiny spiders because it increases foraging success and, presumably, survival rates and reproductive outputs. Overall, these data support the colour‐as‐prey‐attractant hypothesis in a stationary, trap‐building predator.     

Predator hunting mode influences patterns of prey use from grazing and epigeic food webs

Multichannel omnivory by generalist predators, especially the use of both grazing and epigeic prey, has the potential to increase predator abundance and decrease herbivore populations. However, predator use of the epigeic web (soil surface detritus/microbe/algae consumers) varies considerably for reasons that are poorly understood. We therefore used a stable isotope approach to determine whether prey availability and predator hunting style (active hunting vs. passive web-building) impacted the degree of multichannel omnivory by the two most abundant predators on an intertidal salt marsh, both spiders. We found that carbon isotopic values of herbivores remained constant during the growing season, while values for epigeic feeders became dramatically more enriched such that values for the two webs converged in August. Carbon isotopic values for both spider species remained midway between the two webs as values for epigeic feeders shifted, indicating substantial use of prey from both food webs by both spider species. As the season progressed, prey abundance in the grazing food web increased while prey abundance in the epigeic web remained constant or declined. In response, prey consumption by the web-building spider shifted toward the grazing web to a much greater extent than did consumption by the hunting spider, possibly because passive web-capture is more responsive to changes in prey availability. Although both generalist predator species engaged in multichannel omnivory, hunting mode influenced the extent to which these predators used prey from the grazing and epigeic food webs, and could thereby influence the strength of trophic cascades in both food webs.     

Dying from the lesser of three evils: facilitation and non‐consumptive effects emerge in a model with multiple predators

Prey modify their behaviour to avoid predation, but dilemmas arise when predators vary in hunting style. Behaviours that successfully evade one predator sometimes facilitate exposure to another predator, forcing the prey to choose the lesser of two evils. In such cases, we need to quantify behavioural strategies in a mix of predators. We model optimal behaviour of Atlantic cod Gadus morhua larvae in a water column, and find the minimal vulnerability from three common predator groups with different hunting modes; 1) ambush predators that sit‐and‐wait for approaching fish larvae; 2) cruising invertebrates that eat larvae in their path; and 3) fish which are visually hunting predators. We use a state‐dependent model to find optimal behaviours (vertical position and swimming speed over a diel light cycle) under any given exposure to the three distinct modes of predation. We then vary abundance of each predator and quantify direct and indirect effects of predation. The nature and strength of direct and indirect effects varied with predator type and abundance. Larvae escaped about half the mortality from fish by swimming deeper to avoid light, but their activity level and cumulative predation from ambush predators increased. When ambush invertebrates dominated, it was optimal to be less active but in more lit habitats, and predation from fish increased. Against cruising predators, there was no remedy. In all cases, the shift in behaviour allowed growth to remain almost the same, while total predation were cut by one third. In early life stages with high and size‐dependent mortality rates, growth rate can be a poor measure of the importance of behavioural strategies.     

Chemical Mediation of Prey Recognition by Spider-Hunting Wasps

Predator–prey interactions are important in maintaining the structure and dynamics of ecological communities. Both predators and prey use cues from a range of sensory modalities to detect and assess one another; identification of these cues is necessary to understand how selection operates to shape predator–prey interactions. Mud-dauber wasps (Sphecidae) provision their larval nests with paralyzed spiders, and different genera of wasps specialize on particular spider taxa. Sceliphron caementarium (Drury 1773) wasps preferentially capture spiders that build two-dimensional (2D) webs, rather than those that construct three-dimensional (3D) webs, but the basis of this preference is not clear. Wasps may choose spiders based on an assessment of their web architecture, as 3D webs may provide better defenses against wasp predation than do 2D webs. However, because many hymenopterans use chemical cues to locate and recognize prey, it is also possible that mud-dauber wasps rely on chemical cues associated with the spider and/or the web to assess prey suitability. When we offered foraging S. caementarium wasps 2D and 3D spiders both on and off their webs, we found that in both cases the wasps took 2D spiders and avoided 3D spiders, demonstrating that the web itself is not the impediment. Results of a series of behavioral choice assays involving filter paper discs containing spider cues and chemically manipulated spiders or spider dummies corroborated the importance of spider chemical cues in mediation of prey recognition by mud-dauber wasps. We also discuss the relative importance of visual and chemical cues for prey recognition by wasps, examine the anti-predator behaviors of 2D and 3D spiders, and consider the role of wasp predation in spider diversification.     

The Trochidae and Turbinidae of the Kermadec Ridge (Mollusca: Gastropoda)

Abstract

Taieria erebus (Gnaphosidae) was found to be a versatile predator: it captured insects both cursorially (away from webs) and kleptopar-asitically (on alien webs); it captured spiders in both the presence and absence of webs; and it also ate the eggs of host spiders (oophagy). When T. erebus invaded webs, it was as an aggressive mimic — it performed a repertoire of vibratory behaviours to lure the host spider. Although T. erebus pursued and captured spiders on diverse web-types, it was more effective as a predator when invading densely (rather than sparsely) woven cribellate and non-sticky webs, and was especially effective on non-cribellate sticky webs. Gnaphosids are traditionally referred to as hunting spiders, but T. erebus built a small prey-capture web. T. erebus also preyed on segestriid spiders, then used their webs to catch more prey, this being an unusual example of a spider using, as a tool for predation, the spinning-work of another species from an unrelated family. T. erebus used specialised behaviours to prey on nesting cursorial spiders. Prey was either grasped or stabbed; the venom of T. erebus was highly potent against spiders. Experiments indicated that vision was of little or no importance in the predatory behaviour of T. erebus. The behaviour of T. erebus is compared to that of Portia, a web-building salticid spider which is very versatile in its predatory behaviour and has acute vision. T. erebus is discussed in relation to hypotheses concerning gnaphosid and salticid evolution.     

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.     

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.     

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.     

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.     

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.     

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.