Antipredator Tactics of Amphibious Sea-Snakes (Serpentes, Laticaudidae)

Because the antipredator behavior that an animal displays depends upon the context in which it encounters the predator, apparent interspecific differences in antipredator tactics may result from ecological rather than behavioral differences among taxa. We approached 127 free-ranging laticaudid sea-snakes on small islands in Noumea Lagoon, New Caledonia, prodded the animals midbody, and recorded their responses. One species (Laticauda colubrina) usually remained immobile (relying on crypsis) whereas another (L. laticaudata) generally fled. However, multivariate analysis shows that the two species actually responded in very similar ways to any given stimulus; the species differed overall because colubrina was generally encountered on land during the day whereas laticaudata was more often encountered in the ocean at night. Thus, apparent interspecific differences in antipredator responses were secondary consequences of interspecific differences in the times and places that predators were encountered. Snakes were more likely to flee rather than remain immobile when rapid locomotion was possible (i.e. juveniles rather than adults; in water rather than on land) and pursuit by a predator was difficult (i.e. at night rather than during the day). These patterns suggest that snakes adjust their antipredator tactics in ways that maximize the chances of surviving the encounter, although the remarkable docility of these highly venomous snakes remains puzzling.     

Parental defence on the reef: antipredator tactics of coral‐reef fishes against egg‐eating seasnakes

On coral reefs in New Caledonia, the eggs of demersal‐spawning fishes are consumed by turtle‐headed seasnakes (Emydocephalus annulatus). Fish repel nest‐raiding snakes by a series of tactics. We recorded 232 cases (involving 22 fish species) of antipredator behaviour towards snakes on a reef near Noumea. Blennies and gobies focused their attacks on snakes entering their nests, whereas damselfish (Pomacentridae) attacked passing snakes, as well as nest‐raiders (reflecting territorial defence). Biting the snake was the most common form of attack, although damselfish and blennies also slapped snakes with the tail, or (blennies only) plugged the nest entrance with the parent fish's body. Gobies rarely defended the nest, although they sometimes bit or threw sand at the snake. A snake was more likely to flee if it was attacked before it began feeding rather than after it found the eggs (82% versus 3% repelled) and if bitten on the head rather than the body (68% versus 53%). Tail‐slaps were not effective, although plugging the burrow and throwing sand often caused snakes to flee. These strong patterns reflect phylogenetic variation in fish behaviour (e.g. damselfish detect a snake approach sooner than do substrate‐dwelling blennies and gobies) coupled with intraspecific variation in snake diets. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, 114 , 415–425.     

Meal Size Effects on Antipredator Behavior of Hatchling Trinket Snakes, Elaphe helena

Current foraging models limit the decision‐making process of animals to the food searching and consuming phase. The post‐consummatory phase of feeding may influence optimal meal size for some species as a morphologic change often results from feeding. In snakes, a single prey item can lead to abrupt increases in body mass, thus influencing locomotor performance. Identifying factors affecting locomotor performance can help predict behaviors that should maximize an animal's chance of evading predators. Although many snakes ingest large percentages of their body mass, not much work has examined the post‐consummatory effects of ingesting bulky prey differing in relative mass. I examined the locomotor performance and antipredator tactics of hatchling trinket snakes (Elaphe helena) after subjecting snakes to mice prey varying by relative mass differences of 20–35%, 50–59% or 70–79% of an individual hatchling's body mass. Snakes in treatment groups were compared with snakes in a control group (0%). Meal size‐affected locomotor parameters such as burst speed, endurance, and endurance times for hatchlings that ingested 50–59% and 70–79% of their body mass (p < 0.001). Recent feeding also affected the types of antipredator modes employed. Hatchlings in the 0% and 20–35% treatments exhibited behaviors that were categorized as active and threatening, while hatchlings in the 50–59% and 70–79% treatments exhibited stationary, neutral, and cryptic behaviors. Although snakes may become more reclusive following a meal, this study demonstrates that relative prey mass affects the ability of hatchling trinket snakes to flee from a predator. In turn, these results suggest that the post‐consummatory effects of foraging should be considered in optimal foraging models for organisms that consume a substantial portion of their body mass during a single feeding.     

Effects of sex, body size, temperature, and location on the antipredator tactics of free-ranging gartersnakes (Thamnophis sirtalis, Colubridae)

Gartersnakes (Thamnophis sirtalis parietalis) in southern Manitoba are subject to intense predation (primarily by crows) duringtheir spring breeding season. The huge numbers of snakes providea unique opportunity to quantify behavioral traits. We simulatedpredator attacks by "pecking" more than 500 free-ranging snakes,to explore the determinants of snake response. Snakes respondedto a human finger in the same way as they did to a more realisticstimulus (a model crow). A snake's response to attack dependedon several factors, which interacted in complex ways. The primaryinfluences on response were body temperature (warmer snakes tended to flee, whereas colder snakes remained cryptic or flattenedand/or gaped and struck) and sex (males were more likely toflee). Responses also depended on microhabitat (i.e., insidethe winter den versus in adjacent grassland) and on the snake'sprior activity (e.g., courting snakes often ignored our closeapproach). These factors interacted in significant ways; for example, snakes outside the den were smaller and warmer thanthose inside, male snakes were smaller and warmer than females,and mean body temperatures were higher in larger snakes withineach sex. Thus, a snake's body size and its location affectedits defensive response indirectly (via their influence on bodytemperature). Our results differ from those of previous studiesand suggest that antipredator responses in these animals dependin a flexible and complex way upon biotic and abiotic variables.Interactions among these variables also must be consideredbefore we can identify underlying causal processes.     

Correlated geographic variation in predation risk and antipredator behaviour within a wide‐ranging snake species (Notechis scutatus,Elapidae)

Geographic variation in antipredator behaviour within wide‐ranging species may be driven by both genetic and environmental influences. We quantified antipredator responses in neonatal (laboratory born, n = 555) and adult (field caught, n = 346) tiger snakes (Notechis scutatus) from 11 mainland and island sites in southern Australia. We used these data to test predictions from Bonnet et al.'s hypothesis that the vigour of antipredator responses in this species reflects behavioural plasticity (in turn, driven by an individual snake's exposure to predators during its lifetime) rather than by genetic variation in this trait. We used the number of predator taxa in each area as an index of predator risk. As predicted, adult snakes from predator‐rich areas had more vigorous defensive responses when handled, whereas neonatal behaviour (although also variable among populations) was unrelated to predator species richness. Adult males bit more readily than adult females (as expected from the greater predation exposure of males during mate searching) but no such sex difference was evident in neonates. Although alternative models remain possible, our data are most consistent with the hypothesis that geographic divergence in antipredator tactics within this species primarily reflects developmentally plastic responses to local predation risk.     

Intrinsic and Extrinsic Factors Influence Expression of Defensive Behavior in Plains Hog‐Nosed Snakes (Heterodon nasicus)

Animals failing to deter predation are eaten. Among the many deterrents to predation, antipredator behaviors are perhaps the most variable, ranging from active (fight or flight) to passive (immobility). We assessed variation in the expression of a passive defensive behavior, death‐feigning, in Plains Hog‐nosed Snakes (Heterodon nasicus) and predicted that intrinsic and extrinsic factors would influence the duration of this behavior and the latency to its onset. We simulated predatory attacks on 27 snakes encountered in the field, and analyzed the behavioral responses of snakes as a function of differences among individuals (sex and size) and environmental factors (temperature and microhabitat). Larger snakes death‐feigned for longer durations than smaller ones; this relationship was stronger for female snakes than for males. Death feints were initiated sooner when snakes were encountered at higher temperatures. Extrinsic factors had a greater influence on latency to death‐feigning behavior, whereas intrinsic factors more strongly influenced its duration. Because our results involved wild snakes, they provide an improved, highly relevant understanding of individual and environmental factors that regulate the expression of immobile defensive behavior. Furthermore, additional hypotheses can now be proposed that address the evolution of defensive behaviors that leave animals prone to attack.     

Antipredator behaviour of invasive geckos in response to chemical cues from snakes

Antipredator behaviours and the ability to appropriately assess predation risk contribute to increased fitness. Predator avoidance can be costly; however, so we expect prey to most strongly avoid predators that pose the greatest risk (i.e., prey should show threat sensitivity). For invasive species, effectively assessing the relative risk posed by predators in the new environment may help them establish in new environments. We examined the antipredator behaviour of introduced Asian house geckos, Hemidactylus frenatus (Schlegel), by determining if they avoided shelters scented with the chemical cues of native predatory snakes (spotted pythons, Antaresia maculosa [Peters]; brown tree snakes, Boiga irregularis [Merrem]; common tree snakes, Dendrelaphis punctulata [Grey]; and carpet pythons, Morelia spilota [Lacépède]). We also tested if Asian house geckos collected from vegetation vs. anthropogenic substrates (buildings) responded differently to the chemical cues of predatory snakes. Asian house geckos did not show a generalised antipredator response, that is, they did not respond to the chemical cues of all snakes in the same way. Asian house geckos avoided the chemical cues of carpet pythons more strongly than those of other snake species, providing some support for the threat‐sensitivity hypothesis. There was no difference in the antipredator behaviour of Asian house geckos collected from buildings vs. natural vegetation, suggesting that individuals that have invaded natural habitats have not changed their antipredator behaviour compared to urban individuals. Overall, we found some evidence indicating Asian house geckos are threat‐sensitive to some Australian predacious snakes.     

Phenotypic divergence between seasnake (Emydocephalus annulatus) populations from adjacent bays of the New Caledonian Lagoon

Populations of widespread species often differ in phenotypic traits, although rarely in such a dramatic fashion as revealed by research on turtle‐headed seasnakes (Emydocephalus annulatus). These snakes are highly philopatric, with mark–recapture studies showing that the interchange of individuals rarely occurs even between two adjacent bays (separated by < 1.2 km) in Noumea, New Caledonia. Data on > 500 field‐captured snakes from these two bays reveal significant differences between these two locations in snake morphology (mean body length, relative tail length, head shape), colour, ecology (body condition, growth rate, incidence of algal fouling), behaviour (antipredator tactics), and locomotor performance. For some traits, the disparity was very marked (e.g. mean swimming speeds differed by > 30%). The causal bases for these phenotypic divergences may involve founder effects, local adaptation, and phenotypic plasticity. The spatial divergence in phenotypic traits offers a cautionary tale both for researchers (sampling of only a few populations may fail to provide a valid overview of the morphology, performance, and behaviour of a species) and managers (loss of local populations may eliminate distinctive genetic variation). © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ??, ??–??.     

Comparative experimental tests of natricine antipredator displays, with special reference to the apparently unique displays in the Asian genus, Rhabdophis

Nuchal glands are unique organs known in only twelve Old World natricine species (three genera) including Rhabdophis tigrinus tigrinus. The glands of R. t. tigrinus contain a toxic secretion that may be derived from its toxic toad diet. A series of peculiar antipredator behaviors, for example neck arch, neck butt, and dorsal-facing posture, are exhibited by R. t. tigrinus, and a functional association between this behavior and the nuchal glands has been suggested. To investigate the ubiquitousness of these putatively unique displays among snakes, antipredator responses of 27 taxa of natricine snakes, both with and without nuchal glands, were studied using a common testing procedure. Three of four taxa with nuchal glands exhibited neck arch, neck butt, and dorsal-facing posture. None of the remaining 23 taxa, which do not possess the glands, showed neck arch and neck butt. Principal-components analysis indicated the association of the above three displays along with the behaviors termed neck flatten and head elevation, confirming the presence of a series of nuchal gland-related behaviors. These results support the assumption that the suite of peculiar displays is associated with the deterrent effects of the nuchal gland secretion.     

Behavioural variation in natural populations. III: Antipredator displays in the garter snake Thamnophis radix

Recently born garter snakes (Thamnophis radix) were subjected to a variety of threatening stimuli. The would crawl away from the investigator until high levels of lactate were attained, and then adopt one of a variety antipredator displays. These antipredator behaviours were surprisingly variable between individuals of a single population, but behaviours of individuals were consistent in replicate trials and in response to different stimuli. Snakes became more defensive when simulated predator attacks were more severe, but they became more offensive when tested at a lower temperature. Analysis of behavioural variation within and between 15 litters of full-sibling (172) snakes gave heritability estimates of 0.37 for single trials and 0.45 for the average of two replicate trials. This is the first study to examine the heritability of antipredator behaviour in any terrestrial vertebrate species.     

Bluffing and Waiting: Handling Effects and Post-Release Immobility in a Death-Feigning Snake (Natrix natrix)

Tonic immobility is a common response of animals to capture by a predator; in some cases, the behaviour is elaborated into death-feigning. Death-feigning is usually interpreted as a last-resort anti-predator tactic that depends on the predator ceasing or slowing its attack when the prey is apparently dead, thus buying time for the prey to escape if the predator's attention is directed elsewhere, even momentarily. I tested the effects of different handling regimes on the expression of death-feigning in the grass snake ( Natrix natrix ). In one test, degree of handling had a significant effect on frequency of death-feigning in small snakes, with snakes that received more handling feigning death more often. A second test showed that different initial handling regimes also affected the probability of death-feigning in large snakes, with snakes initially held by the tail feigning death least frequently and those initially held by the head most frequently. Thus, increased apparent threat to a vulnerable part of the body is more likely to result in death-feigning. It remains to be seen whether death-feigning can reduce the threat posed by real predators, but immobility is frequently carried over into the post-release period, during which the animal presumably weighs its chances and awaits an opportunity to escape. Regardless of cause, death-feigning snakes exhibited significantly more frequent and longer post-release immobility than did non-death-feigning snakes, which typically fled immediately upon release. Overall, small snakes feigned death less frequently than adults and were more likely to flee upon release, suggesting that immobility is a riskier anti-predator defence strategy for them.     

Generalization of predator recognition: Velvet geckos display anti-predator behaviours in response to chemicals from non-dangerous elapid snakes

Many prey species detect chemical cues from predators and modify their behaviours in ways that reduce their risk of predation. Theory predicts that prey should modify their anti-predator responses according to the degree of threat posed by the predator. That is, prey should show the strongest responses to chemicals of highly dangerous prey, but should ignore or respond weakly to chemicals from non-dangerous predators. However, if anti-predator behaviours are not costly, and predators are rarely encountered, prey may exhibit generalised antipredator behaviours to dangerous and non-dangerous predators. In Australia, most elapid snakes eat lizards, and are therefore potentially dangerous to lizard prey. Recently, we found that the nocturnal velvet gecko Oedura lesueurii responds to chemicals from dangerous and non-dangerous elapid snakes, suggesting that it displays gen-eralised anti-predator behaviours to chemicals from elapid snakes. To explore the generality of this result, we videotaped the be-haviour of velvet geckos in the presence of chemical cues from two small elapid snakes that rarely consume geckos: the nocturnal golden-crowned snake Cacophis squamulosus and the diurnal marsh snake Hemiaspis signata. We also videotaped geckos in tri-als involving unsceted cards (controls) and cologne-scented cards (pungency controls). In trials involving Cacophis and Hemi-aspis chemicals, 50% and 63% of geckos spent long time periods (> 3 min) freezing whilst pressed flat against the substrate, re-spectively. Over half the geckos tested exhibited anti-predator behaviours (tail waving, tail vibration, running) in response to Ca-cophis (67%) or Hemiaspis (63%) chemicals. These behaviours were not observed in control or pungency control trials. Our re-sults support the idea that the velvet gecko displays generalised anti-predator responses to chemical cues from elapid snakes. Generalised responses to predator chemicals may be common in prey species that co-occur with multiple, ecologically similar, dangerous predators.     

Size-based variation in antipredator behavior within a snake (Agkistrodon piscivorus) population

Variation in an animal's response to a predator likely reflectsthe complex interaction of factors that influence predationrisk. Due to their high degree of behavioral variation and simplifiedbauplan, snakes offer a unique model for investigating the influenceof sex and body size on antipredator behavior. We examined variationin antipredator behavior within a cottonmouth (Agkistrodon piscivorusleucostoma) population. Behavioral responses to human-inducedpredation risk were compared across a continuous scale of bodysize. Defensive responses significantly declined with increasingbody size. After controlling for body size, no differences betweenthe sexes were detected. Although this study suggests that variationin antipredator behavior is, in part, related to body size,some studies on snakes have not found this relationship. Likewise,some studies have demonstrated differences between sexes. Suchdisparate patterns of variation indicate a need for future comparativestudies examining the complex interaction of factors that mayinfluence predator–prey relationships.     

Evolution of coloration, urotomy and coral snake mimicry in the snake genus Scaphiodontophis (Serpentes: Colubridae)

The Neotropical hinged-tooth, coral snake mimics of the genus Scaphiodontophis are characterized by extremely long and disproportionately thick tails that are extremely fragile. Both the coloration and tail structure are putative antipredator devices. While all examples have components of the coloration that match those of the venomous coral snakes (family Elapidae), the range of variation is extreme, leading to controversy on the status of various populations, including nine named taxa. Individual, ontogenetic and geographic variation in scutellation and head, body and tail coloration were analysed to evaluate population status and possible evolutionary trends based on a sample of 183 examples from Mexico, Central America and Colombia. Variation in subcaudal counts show population differences (higher in Mexico and upper Central America) but are not congruent with geographic variation in coloration. Generally snakes from north of Nicaragua and from central and eastern Panama have a pattern of dyads (black-light-black bands separating red bands), those from Atlantic slope Nicaragua to western Panama a pattern of monads (light-black-light bands separating the red ones) and those from Colombia have both pattern types on the same snake. The dyads and/or monads may be present the length of the body and tail, restricted to the anterior part of the body or on the entire body or on the anterior part of the body and on the tail. Two or more of these variants may occur at a single geographic locality or only a single one may be present. Head and nuchal colour patterns (Z, A, V and Du) are relatively consistent geographically. The Adantic slope Guatemala, Belize and Honduras population have the A pattern, those of Nicaragua, Costa Rica and western Panama the V pattern, and those in Colombia a Du pattern. Other populations have the Z coloration. Intermediate conditions in coloration of the body and tail and head and neck are found at localities intermediate between the main pattern types, indicating intergradation among adjacent populations. Consequently, we regard these snakes as representative of a single species, Scaphiodontophis annulatus Dumeril and Bibron and the eight other names applied to various populations and individuals as synonyms. Analysis of colour pattern leads us to the conclusion that the tricolour pattern evolved from a uniform one through a lineate-spotted condition (usually present on the non-tricolour portions of the snake) through a bicolour red and black pattern to the dyadal condition. The monadal pattern in turn was derived from the dyadal one. The data further indicates that tricolour components first appeared anteriorly and progressively expanded posteriorly. The evolutionary sequence for the head and nuchal pattern appears to be A → Z → V → Du S. annulatus has a series of jaw and tooth specializations designed for rapid processing of hard-bodied prey found during diurnal foraging in the leaf-litter. Urotomy in this species involves intervertebral tail-breakage (pseudoautotomy) without regeneration. Evidence is presented supporting the long-tail multiple break hypothesis as applicable to Scaphiodontophis and other snakes with similar tail morphology (specialized pseudoautotomy). This is in contrast to snakes with similar tail morphology (specialized pseudoautotomy). This is in contrast to Coniophanes and other snakes with a high incidence of urotomy having long but unspecialized tails (unspecialized pseudoautotomy) without multiple breaks over time. All Scaphiodontophis colour patterns have a general resemblance to that of venomous coral snakes and offer protection from generalizing predators having innate or other triggered responses to coral snake colours. The aposematic effect is enhanced by tail thrashing and head twitching behaviours. The characteristic foraging pose of S. annulatus, which tends to expose the head and anterior body, makes even the incomplete tricolour pattern effective as an antipredator defence. No evidence supports the idea that tail thrashing or the incomplete tricolour pattern directs the predator attacks to the tail to expedite pseudoautotomy. Coral snake mimicry and specialized pseudoautotomy are shown not to be co-evolved and pseudautotomy seems to have evolved long before mimetic coloration in this genus.     

GENETIC BASIS OF ACTIVITY METABOLISM. I. INHERITANCE OF SPEED,STAMINA, AND ANTIPREDATOR DISPLAYS IN THE GARTER SNAKE THAMNOPHIS SIRTALIS

Recent conceptual advances in physiological ecology emphasize the potential selective importance of whole-animal performance. Empirical studies of locomotor performance in reptiles have revealed surprising amounts of individual variation in speed and stamina. The present study is the first in a series examining the genetic basis of variation in locomotor performance, activity metabolism, and associated behaviors in garter snakes. Maximal sprint crawling speed, treadmill endurance, and antipredator displays (Arnold and Bennett, 1984; exhibited as snakes reached exhaustion on the treadmill) were measured for approximately six offspring (presumed to be full siblings) from each of 46 wild-caught gravid garter snakes (Thamnophis sirtalis). Each character was measured on two days; all were individually repeatable. Correlations of these characters with body mass, snout–vent length, age at testing, litter size, dam mass, and dam snout–vent length were removed by computing residuals from multiple-regression equations. These residuals were used in subsequent genetic analyses. Approximate coefficients of variation of residuals were 17% for speed, 48% for endurance, and 31% for antipredator displays. Broad-sense heritabilities were significant for all characters: speed h² = 0.58; stamina h² = 0.70; antipredator display h² = 0.42. All three residual characters showed positive and statistically significant phenotypic correlations (r = 0.19–0.36). Genetic correlations (estimated and tested by restricted maximum likelihood) among residuals were positive and highly significant between speed and endurance (0.58), but nonsignificant between speed and antipredator display (0.43), and between endurance and antipredator display (0.26). All environmental correlations were nonsignificant. These data suggest that, contrary to expectations based on previous physiological studies, there may be no necessary evolutionary trade-off between speed and stamina in these animals. This tentative conclusion will have important implications for future theoretical studies of the evolution of locomotor performance and associated antipredator behaviors.     

Causes and consequences of aggregation by neonatal tiger snakes (Notechis scutatus,Elapidae)

Although snakes traditionally have been regarded as asocial animals, recent studies have revealed complex interactions among neonatal snakes and their mothers. We noticed frequent aggregation by captive neonatal Australian elapids (tiger snakes, Notechis scutatus), and conducted simple experiments to clarify the proximate causation of, and potential consequences of, aggregative behaviour. Litters of neonates exhibited statistically significant aggregation (clustering) in empty containers, especially if the test area was subjected to rapid cooling. Aggregation was most pronounced inside shelter‐sites, and familiar shelters (i.e. containing scent cues from the litter) attracted snakes more than did novel (unscented) shelters. Snakes in larger aggregations cooled more slowly (reflecting their higher combined mass and thus, thermal inertia) and higher body temperatures facilitated neonatal locomotor performance, retreat‐site location and anti‐predator tactics. Plausibly, aggregation in neonatal tiger snakes (and other reptiles) functions to retard cooling rates, with the result that the young snakes are better able to evade or repel attacks by predators.     

Can Wall Lizards Combine Chemical and Visual Cues to Discriminate Predatory from Non‐Predatory Snakes Inside Refuges?

The ability to use multiple cues in assessing predation risk is especially important to prey animals exposed to multiple predators. Wall lizards, Podarcis muralis, respond to predatory attacks from birds in the open by hiding inside rock crevices, where they may encounter saurophagous ambush smooth snakes. Lizards should avoid refuges with these snakes, but in refuges lizards can also find non‐saurophagous viperine snakes, which lizards do not need to avoid. We investigated in the laboratory whether wall lizards used different predator cues to detect and discriminate between snake species within refuges. We simulated predatory attacks in the open to lizards, and compared their refuge use, and the variation in the responses after a repeated attack, between predator‐free refuges and refuges containing visual, chemical, or visual and chemical cues of saurophagous or non‐saurophagous snakes. Time to enter a refuge was not influenced by potential risk inside the refuge. In contrast, in a successive second attack, lizards sought cover faster and tended to increase time spent hidden in the refuge. This suggests a case of predator facilitation because persistent predators in the open may force lizards to hide faster and for longer in hazardous refuges. However, after hiding, lizards spent less time in refuges with both chemical and visual cues of snakes, or with chemical cues alone, than in predator‐free refuges or in refuges with snake visual cues alone, but there were no differences in response to the two snake species. Therefore, lizards could be overestimating predation risk inside refuges. We discuss which selection pressures might explain this lack of discrimination of predatory from similar non‐predatory snakes.     

Do Experience and Body Size Play a Role in Responses of Larval Ringed Salamanders,Ambystoma annulatum,to Predator Kairomones? Laboratory and Field Assays

Prey may experience ontogenetic changes in vulnerability to some predators, either because of changes in morphology or experience. If prey match their level of antipredator behavior to the level of predatory threat, prey responses to predators should reflect the appropriate level of threat for their stage of development. For larval salamanders, responses to predators may change with body size because larger larvae are less vulnerable to predation by gape‐limited predators or because fleeing responses by large salamanders may be more effective than for smaller salamanders. In a field experiment, small larval ringed salamanders, Ambystoma annulatum, responded to chemical stimuli (‘kairomones’) from predatory newts, Notophthalmus viridescens, with an antipredator response (decreased activity). Laboratory‐reared larvae decreased their activity following exposure to newt kairomones, indicating that larval ringed salamanders do not require experience with newts to recognize them as predators. In both experiments, larvae distinguished between chemical stimuli from newts and stimuli from tadpoles (non‐predators) and a blank control. In a third experiment, field‐caught (experienced) larvae showed a graded response to newt kairomones based on their body size: small larvae tended to decrease their activity while larger larvae showed no change or an increase in activity. This graded response was not observed for neutral stimuli, indicating that it is predator‐specific. Therefore, ringed salamander larvae exhibit threat‐sensitive ontogenetic changes in their response to chemical stimuli from predatory newts.     

Probing,Assessment, and Management during Interactions between Ground Squirrels and Rattlesnakes

The predator-prey relationship between California ground squirrels (Spermophilus beecheyi) and northern Pacific rattlesnakes (Crotalus viridis) is a useful system for exploring conflict and assessment. Rattlesnakes are major predators of ground squirrel pups, but pose a less significant threat to adult squirrels. Adults approach, harass, and even attack rattlesnakes in defense of their pups. Two factors that may influence risk to both squirrel and snake during encounters are the size and body temperature of the rattlesnake. We used high-speed video to analyze the strikes of rattlesnakes of various sizes tested at different body temperatures. Results indicate that warmer snakes are more dangerous because they strike with higher velocity, greater accuracy, and less hesitation. Similarly, larger snakes are more dangerous because they can strike farther and at higher speeds, and keep their fangs embedded longer. Thus, ground squirrels would benefit from extracting information about a rattlesnake's size and temperature. The converse of our results is that cooler, smaller rattlesnakes may be more vulnerable. These snakes could mitigate their risk by avoiding dangerous adversaries and minimizing cues that divulge their weaknesses. Such tactics might explain the active probing that squirrels direct at rattlesnakes, which may function to overcome a snake's resistance to disclosing its vulnerability.