Sexual dimorphism of tail length in lacertid lizards: test of a morphological constraint hypothesis

Males of many lizard species have longer tails than similarly-sized females. We hypothesized that this dimorphism is induced by a longer non-autotomous tail part in males, which is associated with the presence of the copulatory organs at the tail base, and presumably reduces the males' ability to escape predation by tail shedding. A compensatory mechanism would be an increase of total tail length in males, to achieve equal lengths of the autotomous tail part in both sexes. A critical prediction of this 'morphological constraint' hypothesis is that the extent of dimorphism in total tail length increases with the magnitude of sexual differences in length of the non-autotomous tail base. We tested this prediction through a comparative study in a small clade of lacertid lizards. Within each of nine species, sexual differences in length of the non-autotomous tail base and in total tail length do not change with body size. All species, except one, exhibit a clear male-biased dimorphism in length of the non-breakable tail base. In all species studied, males have longer tails than females. We used the method of phylogenetically independent contrasts to explore the interspecific relation between dimorphism in length of the tail base and sexual differences in total tail length. Contrary to our prediction, we found no evidence for a positive correlation between the extent of dimorphism in both traits. Thus, constraints imposed by the male copulatory organs on tail autotomy do not seem to be a significant factor in the evolution of dimorphism in tail length in this clade of lacertid lizards.     

The m. caudifemoralis longus and its relationship to caudal autotomy and locomotion in lizards (Reptilia: Sauna)

Although the phenomenon of tail autotomy has traditionally been viewed in a purely adaptive light, functional constraints imposed by the locomotor system appear to have influenced the presence and extent of autotomy in lizards. Them. caudifemoralis longus is an unsegmented hind limb retractor that originates from the caudal vertebrae. It does not participate in autotomy and thus limits the proximal position of autotomic septa. Variation in the extent of the m. caudifemoralis is correlated with locomotor type. The muscle is large and originates from a long series of caudal vertebrae in fast moving lizards with powerful limb retraction, as exemplified by taxa capable of bipedal running. In slower lizards with sprawling postures, such as geckos, the m. caudifemoralis is small and restricted to the first few postsacral vertebrae. Autotomy is typically restricted or absent in the former lizards, while in the latter only the most proximal vertebrae are incapable of autotomy. In the evolution of existing patterns of caudal autotomy, functional demands intrinsic to the tail may be subservient to locomotor constraints imposed on the tail base by the m. caudifemoralis longus .     

Sex, Reproductive Status, and Cost of Tail Autotomy via Decreased Running Speed in Lizards

Autotomy, voluntary shedding of body parts to permit escape, is a theoretically interesting defense because escape benefit is offset by numerous costs, including impaired future escape ability. Reduced sprint speed is a major escape cost in some lizards. We predicted that tail loss causes decreased speed in males and previtellogenic females, but not vitellogenic females already slowed by mass gain. In the striped plateau lizard, Sceloporus virgatus , adults of both sexes are subject to autotomy, and females undergo large increases in body condition (mass/length) during vitellogenesis. Time required for running 1 m was similar in intact autotomized males and previtellogenic females, but increased by nearly half after autotomy. Vitellogenic females were slower than other lizards when intact, but their speed was unaffected by autotomy. Following autotomy, speeds of all groups were similar. Thus, speed costs of autotomy vary with sex and reproductive condition: decreased running speed is not a cost of autotomy in vitellogenic females or presumably gravid females. Costs of autotomy are more complex than previously known. Speed and other costs might interact in unforseen ways, making it difficult to predict whether strategies to compensate for diminished escape ability differ with reproductive condition in females.     

Patterns of sexual dimorphism in Mexican alligator lizards,Barisia imbricata

We compare morphological characteristics of male and female Barisia imbricata, Mexican alligator lizards, and find that mass, head length, coloration, incidence of scars from conspecifics, tail loss, and frequency of bearing the color/pattern of the opposite sex are all sexually dimorphic traits. Overall size (measured as snout–vent length), on the other hand, is not different between the two sexes. We use data on bite scar frequency and fecundity to evaluate competing hypotheses regarding the selective forces driving these patterns. We contend that sexual selection, acting through male‐male competition, may favor larger mass and head size in males, whereas large females are likely favored by natural selection for greater fecundity. In addition, the frequency of opposite‐sex patterning in males versus females may indicate that the costs of agonistic interactions among males are severe enough to allow for an alternative mating strategy. Finally, we discuss how sexual and natural selective forces may interact to drive or mask the evolution of sexually dimorphic traits.     

Tail Length and Mutual Mate Choice in Bearded Tits (Panurus biarmicus)

Direct sexual selection via mutual mate choice can result in both sexes showing conspicuous traits. We experimentally tested whether this hypothesis can explain tail length in the bearded tit (Panurus biarmicus). In this species, both sexes have a long, graduated tail. Males have, however, a longer tail than females, suggesting perhaps that females are choosier than males in selecting mates. We used two choice set‐ups for each sex: shortened vs. control tail individuals and elongated vs. control tail individuals. We found that direct sexual selection seems to operate differently in the two sexes. In both set‐ups, females spent more time with the male with the longest tail, and they also showed sexual display behaviour only towards these males. Males spent more time with control than with short‐tailed females, but they did not discriminate between control and long‐tailed females. Moreover, males displayed preference towards both short‐ and long‐tailed females. Thus, females preferred long‐tailed males, whereas males did not always prefer long‐tailed females. Our study suggests that mutual mate choice has played a role in the evolution of long tails in bearded tits. It also suggests that the sexual dimorphism in tail length has evolved because mate choice exerts a stronger sexual selection pressure on males than on females.     

Female choice, male interference, and sperm precedence in the red-spotted newt

Darwin first identified female choice and male—male competitionas forms of sexual selection resulting in the evolution of conspicuoussexual dimorphism, but it has proven challenging to separatetheir effects. Their effects on sexual selection become evenmore complicated when sperm competition occurs because spermprecedence may be either a form of cryptic female choice ora form of male—male competition. We examined the effectsof tail height on male—male competition and female choiceusing the sexually dimorphic red-spotted newt (Notophthalmusviridescens viridescens). Experiment 1 examined whether maletail height influenced male mating success. Males with deeptails were more successful at mating with females than thosewith shallow tails. Successful, deep-tailed males also were bigger(snout-vent length; SVL) than unsuccessful, shallow-tailed males,but they did not vary in tail length or body condition. Of these,only tail height and tail length are sexually dimorphic traits.Experiment 2 tested the hypothesis that the differential successof males with deeper tails was due to female choice by examiningboth simultaneous female preference for association and sequentialfemale choice. We found no evidence of female choice. When maleswere not competing to mate with females, tail height did notinfluence male mating success. Successful males did not havedifferent SVL and tail lengths than unsuccessful males. Thus,tail height in male red-spotted newts appears to be an intrasexuallyselected secondary sexual characteristic. Experiment 3 usedpaternity exclusion analyses based on molecular genetic markersto examine the effect of sperm precedence on sperm competitionin doubly-mated females. Sperm precedence likely does not havea pervasive and consistent effect on fertilization success becausewe found evidence of first, last, and mixed sperm usage.     

The relative importance of male tail length and nuptial plumage on social dominance and mate choice in the red-backed fairy-wren Malurus melanocephalus: evidence for the multiple receiver hypothesis

Understanding why males of many species exhibit two or more sexual ornaments depends upon identifying both the information conveyed and the intended receiver(s) for each signal. Here we focus on identifying the intended receivers for two sexual signals exhibited by male red-backed fairy-wrens Malurus melanocephalus , extent of nuptial plumage and tail length. In doing so we test the multiple receiver hypothesis, which predicts that each trait is directed toward a different type of receiver (e.g., males vs females). Male red-backed fairy-wrens in nuptial plumage exhibit reversed sexual dimorphism for tail length in the breeding season, when their tails are significantly shorter than those of females or males in eclipse plumage. Using both aviary-based experiments and indices of mate choice and social dominance from a natural population, we found that extent of nuptial plumage and age primarily affected female mate choice and that shorter tails were primarily associated with male:male dominance signaling. The field and aviary studies combined are consistent with the multiple receiver hypothesis, in that each trait appears to be directed primarily to a different set of receivers (plumage for females and tail length for males), though each trait may also signal information to the other set of receivers as well. We propose that sexual selection may favor shorter tail lengths in male red-backed fairy-wrens through social competition mechanisms.     

Frequency of tail loss reflects variation in predation levels,predator efficiency,and the behaviour of three populations of brown anoles

We investigated two predictions regarding the incidence of tail regeneration in lizards for three populations of brown anoles exposed to varying predation levels from the same predator (cats). Firstly although inefficient predators are likely to increase the incidence of regenerated tails (i.e. lizards can escape through tail autotomy), highly efficient predators will kill and eat the lizard and thus leave no evidence of autotomy. At the site with no cats, only 4% of anoles demonstrated signs of tail regeneration. This value was not significantly different from the site where feral cats (i.e. ‘efficient’ predators that would capture prey to eat, as supported by behavioural observation) were present (7%). By contrast, 25% of anoles present at the site with pet cats (well‐fed domesticated cats that caught and played with anoles, i.e. were ‘inefficient’ predators) exhibited regenerated tails. Secondly, more obvious lizards are more susceptible to predation attempts. Supporting this hypothesis, our data indicate a higher incidence of regenerated tails (28%) was recorded amongst adult males (which are territorial, occupying exposed positions) compared to females and subadult males (17%) or juveniles (1%). In conclusion, the behaviour of both the predator and the lizard influences the frequency of regenerated tails in brown anoles. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 103 , 648–656.     

Patterns of caudal-autotomy evolution in lizards

Using comparative techniques to account for phylogenetic effects, I examined patterns of evolution of caudal autotomy and foraging in 39 lizard species to test the hypothesis that caudal autotomy has co-evolved with morphology, locomotor performance, and foraging behaviour. There were significant positive associations between evolution of the point on the tail (distance from cloaca) at which tail loss occurs (an indirect measure of caudal autotomy) and evolution of each of the following: tail length, caudifemoralis longus (CFL) muscle length, and jump distance. The correlation with the evolution of sprint speed approached significance. These relationships primarily were due to the influence of tail-length evolution on autotomy-point evolution. With the effect of tail-length evolution removed, autotomy-point evolution was negatively correlated with the evolution of tail-loss frequency. The CFL restricts tail loss to portions of the tail posterior to the most distal point of its insertion in the tail. In addition, with the effect of tail-length evolution removed, CFL length co-evolved with sprint speed. These results indicate that tail morphology has co-evolved with caudal autotomy such that the evolution of the CFL has reduced caudal autotomy in certain groups of lizards.
Ambush foraging, the ability to lose the tail, intermediate CFL length, and low locomotor performance (i.e. slow sprint speed and short jump distance) are hypothesized to be the ancestral conditions in lizards using outgroup rooting. The diversification of lizard taxa has resulted in some lineages moving away from ancestral character states (i.e. family Teiidae, superfamily Varanoidea), while others are very similar or identical to their ancestors (i.e. superfamily Iguania).     

Is partial tail loss the key to a complete understanding of caudal autotomy?

Autotomy, the self‐amputation of limbs or appendages, is a dramatic anti‐predator tactic that has repeatedly evolved in a range of invertebrate and vertebrate groups. In lizards, caudal autotomy enables the individual to break away from the predator's grasp, with the post‐autotomy thrashing of the tail distracting the attacker while the lizard makes its escape. This drastic defensive strategy should be selectively advantageous when the benefit (i.e. survival) exceeds the subsequent costs associated with tail loss. Here, we highlight how the position of autotomy along the length of the tail may influence the costs and benefits of the tactic, and thus the adaptive advantage of the strategy. We argue that most studies of caudal autotomy in lizards have focused on complete tail loss and failed to consider variation in the amount of tail shed, and, therefore, our understanding of this anti‐predator behaviour is more limited than previously thought. We suggest that future research should investigate how partial tail loss influences the likelihood of surviving encounters with a predator, and both the severity and duration of costs associated with caudal autotomy. Investigation of partial autotomy may also enhance our understanding of this defensive strategy in other vertebrate and invertebrate groups.     

Growth and survivorship as proximate causes of sexual size dimorphism in peninsula dragon lizards Ctenophorus fionni

Males and females differ in body size in many animals, but the direction and extent of this sexual size dimorphism (SSD) varies widely. Males are larger than females in most lizards of the iguanian clade, which includes dragon lizards (Agamidae). I tested whether the male larger pattern of SSD in the peninsula dragon lizard, Ctenophorus fionni, is a result of sexual selection for large male size or relatively higher mortality among females. Data on growth and survivorship were collected from wild lizards during 1991–1994. The likelihood of differential predation between males and females was assessed by exposing pairs of male and female lizards to a predator in captivity, and by comparing the frequency of tail damage in wild‐caught males and females. Male and female C. fionni grew at the same rate, but males grew for longer than females and reached a larger asymptotic size (87 mm vs. 78 mm). Large males were under‐represented in the population because they suffered higher mortality than females. Predation may account for some of this male‐biased mortality. The male‐biased SSD in C. fionni resulted from differences in growth pattern between the sexes. The male‐biased SSD was not the result of proximate factors reducing female body size. Indeed SSD in this species remained male‐biased despite high mortality among large males. SSD in C. fionni is consistent with the ultimate explanation of sexual selection for large body size in males.     

Investigating the evolutionary effects of one feature on another: does muscle spread suppress caudal autotomy in lizards?

Hypotheses of secondary evolutionary change, where alteration in a particular feature is thought to result in change in another, can be tested in two main ways. First, phylogenies can be used to identify separate cases where one of the features changes and each case can then be examined to see whether the other change also actually takes place and if the perceived sequence of the alterations is appropriate. Secondly, the mechanism by which change in the second feature is supposed to be effected can be scrutinized and, in some cases, subjected to experimental investigation.
This approach was applied to a recent hypothesis, that backward spread of the caudifemoralis longus muscle in the tail base of lizards was the primary cause of loss of capacity to autotomize the tail. Some 23 to 25 independent cases of total autotomy loss in adult lizards were identified. In all but six of these there was no substantial spread of the muscle. In two of the remainder, the muscle appears to have spread ufiev autotomy loss, and another case cannot be tested properly as information about relationships is equivocal. The final three cases exhibit extension of the caudifemoralis longus before autotomy loss, but the latter is not found in related species that also inherit muscle extension, which suggests that other causal factors may be involved. In about 15 other cases, where autotomy becomes restricted to the tail base, there is no marked spread of the caudifemoralis longus. The proposed functional link between muscle extension and autotomy loss is also discussed and discounted     

Energetic and locomotor costs of tail loss in the Chinese skink, Eumeces chinensis

Caudal autotomy is a defense mechanism used by numerous lizards to evade predators, but this entails costs. We collected 294 adult Chinese skinks (Eumeces chinensis) from a population in Lishui (eastern China) to evaluate energetic and locomotor costs of tail loss. Of the 294 skinks, 214 (c. 73%) had previously experienced caudal autotomy. Neither the proportion of individuals with regenerated tails nor the frequency distribution of locations of the tail break differed between sexes. We successively removed four tail segments from each of the 20 experimental skinks (adult males) initially having intact tails. Lipid content in each removed tail segment was measured, and locomotor performance (sprint speed, the maximal length traveled without stopping and the number of stops in the racetrack) was measured for each skink before and after each tail-removing treatment. Another independent sample of 20 adult males with intact tails was measured for locomotor performance to serve as controls for successive measurements taken for the experimental lizards. Caudal lipids were disproportionately stored along the length of the tail, with most lipids being aggregated in its proximal portion. Tail loss significantly affected sprint speed, but not the maximal length of, or the number of stops during the sprint. However, the adverse influence of tail loss on sprint speed was not significant until more than 51% of the tail (in length) was lost. Our data show that partial tail loss due to predatory encounters or other factors may not severely affect energy stores or locomotor performance in E. chinensis. As tail breaks occurred more frequently in the proximal portion of the tail in skinks collected from the field, we conclude that caudal autotomy occurring in nature often incurs substantial energetic and locomotor costs in E. chinensis.     

Partial tail loss has no severe effects on energy stores and locomotor performance in a lacertid lizard, <Emphasis Type="Italic">Takydromus septentrionalis</Emphasis>

Many species of lizards use caudal autotomy as a defense strategy to avoid predation, but tail loss entails costs. These topics were studied experimentally in the northern grass lizard, Takydromus septentrionalis. We measured lipids in the three-tail segments removed from each of the 20 experimental lizards (adult females) initially having intact tails to evaluate the effect of tail loss on energy stores; we obtained data on locomotor performance (sprint speed, the maximal length traveled without stopping and the number of stops in the racetrack) for these lizards before and after the tail-removing treatments to evaluate the effect of tail loss on locomotor performance. An independent sample of 20 adult females that retained intact tails was measured for locomotor performance to serve as controls for successive measurements taken for the experimental lizards. The lipids stored in the removed tail was positively correlated with tailbase width when holding the tail length constant, indicating that thicker tails contained more lipids than did thinner tails of the same overall length. Most of the lipids stored in the tail were concentrated in the proximal portion of the tail. Locomotor performance was almost unaffected by tail loss until at least more than 71% of the tail (in length) was lost. Our data show that partial tail loss due to predatory encounters or other factors may not severely affect energy stores and locomotor performance in T. septentrionalis.     

The Proximate Causes of Sexual Size Dimorphism in Phrynocephalus przewalskii

Sexual size dimorphism (SSD) is a common phenomenon and is a central topic in evolutionary biology. Recently, the importance of pursuing an ontogenetic perspective of SSD has been emphasized, to elucidate the proximate physiological mechanisms leading to its evolution. However, such research has seldom focused on the critical periods when males and females diverge. Using mark-recapture data, we investigated the development of SSD, sex-specific survivorship, and growth rates in Phrynocephalus przewalskii (Agamidae). We demonstrated that both male and female lizards are reproductively mature at age 10–11 months (including 5 months hibernation). Male-biased SSD in snout-vent length (SVL) was only found in adults and was fully expressed at age 11 months (June of the first full season of activity), just after sexual maturation. However, male-biased SSD in tail length (TL), hind-limb length (LL), and head width (HW) were fully expressed at age 9–10 months, just before sexual maturation. Analysis of age-specific linear growth rates identified sexually dimorphic growth during the fifth growth month (age 10–11 months) as the proximate cause of SSD in SVL. The males experienced higher mortality than females in the first 2 years and only survived better than females after SSD was well developed. This suggests that the critical period of divergence in the sizes of male and female P. przewalskii occurs between 10 and 11 months of age (May to June during the first full season of activity), and that the sexual difference in growth during this period is the proximate cause. However, the sexual difference in survivorship cannot explain the male-biased SSD in SVL. Our results indicate that performance-related characteristics, such as TL, HW, and LL diverged earlier than SVL. The physiological mechanisms underlying the different growth patterns of males and females may reflect different energy allocations associated with their different reproductive statuses.     

Ornament evolution in dragon lizards: multiple gains and widespread losses reveal a complex history of evolutionary change

The expression in females of ornaments thought to be the target of sexual selection in males is a long-standing puzzle. Two main hypotheses are proposed to account for the existence of conspicuous ornaments in both sexes (mutual ornamentation): genetic correlation between the sexes and sexual selection on females as well as males. We examined the pattern of ornament gains and losses in 240 species of dragon lizards (Agamidae) in order to elucidate the relative contribution of these two factors in the evolution of mutual ornamentation. In addition, we tested whether the type of shelter used by lizards to avoid predators predicts the evolutionary loss or constraint of ornament expression. We found evidence that the origin of female ornaments is broadly consistent with the predictions of the genetic correlation hypothesis. Ornaments appear congruently in both sexes with some lineages subsequently evolving male biased sexual dimorphism, apparently through the process of natural selection for reduced ornamentation in females. Nevertheless, ornaments have also frequently evolved in both sexes independently. This suggests that genetic correlations are potentially weak for several lineages and sexual selection on females is responsible for at least some evolutionary change in this group. Unexpectedly, we found that the evolutionary loss of some ornaments is concentrated more in males than females and this trend cannot be fully explained by our measures of natural selection.     

The effects of tail loss on survival, growth, reproduction, and sex ratio of offspring in the lizard Uta stansburiana in the field

Tail autotomy is a defense against predators used by many lizard species but is associated with various costs, most of which have been measured only in the laboratory. We conducted a field experiment in which we induced tail autotomy to approximately half (58%) of a marked sample (n=326) of Uta stansburiana from western Texas in the fall, and left the other half with intact tails. The following spring we determined survival, measured growth, and brought females to the laboratory to allow them to oviposit their eggs, which we incubated until hatching. Based on past studies, we anticipated inferior survival, growth, and reproduction following tail autotomy. We also predicted that females with tail loss would be energetically compromised and would alter the sex ratio of their offspring toward more daughters (as predicted by the Trivers-Willard hypothesis). Tailless lizards experienced significantly reduced survivorship, but those that survived grew the same as their tailed counterparts. Tailed and tailless females produced clutches equivalent in number of eggs and total mass. Whereas tailed females showed a significant positive relationship between average egg mass and snout-vent length, tailless females did not. Contrary to our expectations, tailless females produced heavier hatchlings than tailed ones, and sex ratios of hatchlings were equivalent for tailed and tailless females. In this population, tail loss in subadults leads to an increased risk of death, but apparently does not impose an energetic handicap such that later growth and reproduction suffer. We suggest that because tailless females are faced with decreased reproductive value, they respond by growing as much and laying as many eggs of the same mass as tailed females, despite the fact that they are also regenerating the tail. In addition, they somehow produce larger hatchlings than tailed females. Nevertheless, tailless females probably end up with lower overall lifetime fitness than tailed females, and tail loss thus induces the conditional reproductive strategy ”make the best of a bad situation”. Because tailless females produce larger, not smaller, hatchlings, they do not produce more daughters as predicted; i.e., we found no evidence for the Trivers-Willard effect following tail autotomy. Received: 29 November 1998 / Accepted: 17 September 1999     

Determinants of age-dependent change in a secondary sexual character

Many secondary sexual characters vary in a systematic way with the age of individuals, with young and old individuals displaying at lower levels than individuals of intermediate age. Analyses quantifying the within-individual and among-individual components of phenotypic variation can help partition effects of phenotypic plasticity and selective mortality. We analysed phenotypic variation in the expression of a secondary sexual character, tail length, in male and female barn swallows Hirundo rustica from four European populations studied during 11-26 years, using linear mixed effect models to describe age-related expression. Tail length increased from yearlings to intermediate aged birds with a subsequent decrease at old age. In males, this age-related pattern was because of both within-subject and between-subject effects, with no difference among populations. Males having longer lifespan had shorter tails when young than those having shorter lifespan. Females showed similar patterns of age-related variation as males, with no difference among populations. The major difference between sexes was that the between-subject effects (i.e. disappearance effects or selection) were much more important for males compared to females for which lifetime variation in tail length was mainly because of a within-subject effect (i.e., a plastic response). These findings suggest that whereas males trade greater expression of the secondary sexual character at young age against longevity, that was not the case for females. This is consistent with tail length being more costly in males than in females, with the cost of long tails potentially being offset by elevated mating success, whereas that is not the case in females.     

No behavioural compensation for fitness costs of autotomy in a lizard

Abstract Antipredator mechanisms employed by animals are obviously beneficial if they increase survival, but their use may be costly and decrease fitness. Fitness costs of antipredator mechanisms may, in turn, be defrayed by behavioural compensation. We used lizards as a model to measure behavioural fitness costs of the antipredator mechanism, autotomy, as they commonly lose their tails when attacked by predators. In addition, we examined whether male skinks, Carlia jarnoldae (Scincidae), behaviourally compensate for tail loss by comparing the behaviour of tailed and tailless males in experimental enclosures, either alone, with a conspecific male or female, or with a predator. Tailless males experience several costs of autotomy including reduced energy stores, and loss of autotomy as a defence. We identified an additional cost of tail loss: reduced mating success. However, this species did not behaviourally compensate these costs. Instead, characteristics of the ecology of C. jarnoldae may minimize the costs of autotomy. This species experiences an extended breeding season, which means that they experience reduced mating success for only 20% of this breeding season. Additionally, the presence of inguinal fat stores which supply energy in addition to stores in the tail reduce energetic costs.     

Handling-related tail loss in an endangered skink: incidence, correlates and a possible solution

Caudal autotomy (tail loss) during capture and handling is widely reported among several families of lizards. Autotomy causes elevated stress levels in lizards, and imposes a significant fitness cost on autotomized individuals. Despite these detrimental impacts, conservation and ethical issues associated with handling-related tail loss have received little attention. We assessed the incidence and correlates of tail autotomy during capture and handling in an endangered skink, the alpine she-oak skink Cyclodomorphus praealtus . A significant proportion (9.3%) of lizards autotomized their tails during capture and handling. Medium-sized lizards were more likely to lose their tails during handling, and this effect was exacerbated at intermediate body temperatures. Probability of autotomy had a complex relationship with cumulative observer experience, independent of other risk factors. Based on the modelled relationship of autotomy with body temperature, we propose that alpine she-oak skinks be cooled immediately after capture to reduce rates of autotomy during subsequent handling.