Tail Autotomy Plays No Important Role in Influencing Locomotor Performance and Anti‐Predator Behavior in a Cursorial Gecko

We used the frog‐eyed sand gecko (Teratoscincus scincus) as a model system to evaluate the locomotor costs of tail loss, and to examine whether tailless geckos use alternative anti‐predator behavior to compensate for the costs of tail loss. Of the 16 field‐captured geckos, eight were used as experimental animals and the remaining ones as controls. Locomotor performance, activity level and anti‐predator behavior were measured for experimental geckos before and after the tail‐removing treatment. Control geckos never undergoing the tail‐removing manipulation were measured to serve as controls for the measurements taken at the same time for experimental geckos. Experimental geckos did not differ from controls in activity level before they underwent the tail‐removing manipulation, but became less active thereafter. The mean locomotor stamina of tailless geckos was reduced by about 30% of the mean value for tailed ones. However, as the maximum stamina predicted from the laboratory trials is seldom required in nature, we expect that the costs associated with the reduced locomotor stamina may be relatively minor in T. scincus. All other examined locomotor (overall speed, maximal speed and stride length) and behavioral (distance to refuge, approach distance and flight distance) traits were not affected by the tail‐removing manipulation. Overall, our results suggest that tail autotomy plays no important role in influencing locomotor performance and anti‐predator behavior in lizards where the tail has no direct role in locomotion but is used to direct predatory strikes away from the torso.     

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     

The Influence of Tail Autotomy on the Escape Response of the Cape Dwarf Gecko, Lygodactylus capensis

Tail autotomy as a defence against predators occurs in many species of lizard. Although tail autotomy may provide an immediate benefit in terms of survival it may nevertheless be costly due to other functions of the tail. For example, tail autotomy may affect the locomotory performance of lizards during escape. We investigated the influence of tail autotomy on the escape performance of the Cape Dwarf Gecko, Lygodactylus capensis, on a vertical and a horizontal surface. Autotomized geckos were significantly slower than intact geckos during vertical escape, whereas tail autotomy did not influence the horizontal escape speed. Backward falling of the autotomized geckos on the vertical platform may explain the reduced speed. In addition, tail autotomy did not significantly affect body curvature and stride length of the geckos. The observed decrease of escape speed on a vertical platform may influence the habitat use and behaviour of these geckos. Ecological consequences resulting from tail autotomy are discussed in light of these findings.     

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.     

Tail injuries increase the risk of mortality in free-living lizards (Uta stansburiana)

Summary Caudal autotomy is an effective anti-predator mechanism used by many lizard species. Fitness benefits of surviving a predatory attack are obvious, although lizards that autotomize their tails may be at greater risk during subsequent encounters with predators than lizards with complete tails. In previous laboratory studies, tail-less lizards were more vulnerable to capture by predators, but little is known about the relative survival of tailed versus tail-less lizards in nature. This study reports on significant associations between naturally incurred tail injuries and the subsequent risk of mortality in 7 populations of the lizard Uta stansburiana. I used standard mark-recapture techniques to document survival and quantified tail injuries by estimating tail completeness. I then used sampled randomization tests to compare intitial tail completeness values of surviving versus non-surviving lizards. I evaluated overall patterns by comparising the means of tail completeness values of survivors versus non-survivors among mark-recapture sequences. Lizards with incomplete tails suffered higher mortality in the field, although this was not true for every comparison considered (i.e., for every mark-recapture sequence analyzed), and the overall trend was much stronger for adult males than for either adult females or juveniles. Higher mortality among lizards with incomplete tails is presumably a consequence of increased vulnerability to capture by predators. Vulnerability to predation of tail-injured lizards may be confounded by reduced social status in this species, because social subordination can result in the occupation of an inferior home range.     

Flip,flop and fly: modulated motor control and highly variable movement patterns of autotomized gecko tails

Many animals lose and regenerate appendages, and tail autotomy in lizards is an extremely well-studied example of this. Whereas the energetic, ecological and functional ramifications of tail loss for many lizards have been extensively documented, little is known about the behaviour and neuromuscular control of the autotomized tail. We used electromyography and high-speed video to quantify the motor control and movement patterns of autotomized tails of leopard geckos (Eublepharis macularius). In addition to rhythmic swinging, we show that they exhibit extremely complex movement patterns for up to 30 min following autotomy, including acrobatic flips up to 3 cm in height. Unlike the output of most central pattern generators (CPGs), muscular control of the tail is variable and can be arrhythmic. We suggest that the gecko tail is well suited for studies involving CPGs, given that this spinal preparation is naturally occurring, requires no surgery and exhibits complex modulation.     

The regenerated tail of juvenile leopard geckos (Gekkota: Eublepharidae: Eublepharis macularius) preferentially stores more fat than the original

The tail of many species of lizard is used as a site of fat storage, and caudal autotomy is a widespread phenomenon among lizards. This means that caudal fat stores are at risk of being lost if the tail is autotomized. For fat-tailed species, such as the leopard gecko, this may be particularly costly. Previous work has shown that tail regeneration in juveniles of this species is rapid and that it receives priority for energy allocation, even when dietary resources are markedly reduced. We found that the regenerated tails of juvenile leopard geckos are more massive than their original counterparts, regardless of dietary intake, and that they exhibit greater amounts of skeleton, inner fat, muscle and subcutaneous fat than original tails (as assessed through cross-sectional area measurements of positionally equivalent stations along the tail). Autotomy and regeneration result in changes in tail shape, mass and the pattern of tissue distribution within the tail. The regenerated tail exhibits enhanced fat storage capacity, even in the face of a diet that results in significant slowing of body growth. Body growth is thus sacrificed at the expense of rapid tail growth. Fat stores laid down rapidly in the regenerating tail may later be used to fuel body growth or reproductive investment. The regenerated tail thus seems to have adaptive roles of its own, and provides a potential vehicle for studying trade-offs that relate to life history strategy.     

The effects of tail autotomy on survivorship and body growth of Uta stansburiana under conditions of high mortality

We examined the effects of tail autotomy on survivorship and body growth of both adult and juvenile Uta stansburiana by directly manipulating tail condition. Tail loss decreased neither survivorship nor rate of body growth for individuals in two natural populations. Lack of an influence of tail loss on survivorship in these two populations may be the result of high mortality. Under high mortality any differential effects of tail loss will be lower than in populations facing lower mortality. Growth experiments in the laboratory demonstrated that, under conditions of minimal environmental variation and social interactions, there is no tradeoff between body growth and tail regeneration as has been suggested for other species of lizards. One possible reason for this difference is that U. stansburiana does not use the tail as a storage organ for lipids. The original and regenerated tails are composed mainly of protein. In general, any differential body growth between tailed and tailless individuals may be due to social interactions and not a diversion of limited energy into tail regeneration.     

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.     

Population ecology of the velvet gecko,Oedura lesueurii in south eastern Australia: Implications for the persistence of an endangered snake

Abstract Ecological specialization, such as major dependence upon a single‐prey species, can render a predator taxon vulnerable to extinction. In such cases, understanding the population dynamics of that prey type is important for conserving the predator that relies upon it. In eastern Australia, the endangered broad‐headed snake Hoplocephalus bungaroides feeds largely on velvet geckos (Oedura lesueurii). We studied growth, longevity and reproduction in a population of velvet geckos in Morton National Park in south‐eastern Australia. We marked 458 individual geckos over a 3‐year period (1992–1995) and made yearly visits to field sites from 1995–2006 to recapture marked individuals. Female geckos grew larger than males, and produced their first clutch at age 4 years. Males can mature at 2 years, but male–male combat for females probably forces males to delay reproduction until age 3 years. Females lay a single clutch of two eggs in communal nests in November, and up to 22 females deposited eggs in a single nest. Egg hatching success was high (100%), and juveniles had high survival (76%) during their first 6 months of life. Velvet geckos are long‐lived, and the mean age of marked animals recaptured after 1995 was 6.1 years (males) and 8.4 years (females). Older females (7.5–9.5 years) were all gravid when last recaptured. Like other temperate‐climate gekkonids, O. lesueurii has a ‘slow’ life history, and population viability could be threatened by any factors that increase egg or adult mortality. Two such factors – the removal of ‘bush rocks’ for urban gardens, and the overgrowth of rock outcrops by vegetation – could render small gecko populations vulnerable to extinction. In turn, the reliance of predatory broad‐headed snakes on this slow‐growing lizard species may increase its vulnerability to extinction.     

The cannibalistic snail Agaronia propatula (Caenogastropoda,Mollusca) is reluctant to feed on autotomized ‘tails’ of conspecifics

Autotomy and cannibalism increase the complexity of the life history, population structure, and population dynamics of a species. Species in which autotomy is triggered by cannibalism have rarely been studied. It has been hypothesized that in the intertidal gastropod Agaronia propatula, autotomized tissues are highly attractive to cannibals and so increase the victim’s chance to escape. We tested the hypothesis by presenting autotomized ‘tails’ to foraging animals. The attack rates on autotomized ‘tails’ were lower than those on artificial objects reported previously. Autonomously moving autotomized ‘tails’ were more frequently ignored than non-moving and artificially moved ‘tail’ pieces. Thus, autotomized tissue repelled rather than attracted potential cannibals. Autotomy in A. propatula does not help to defend against cannibalism by offering the cannibal an attractive food item for consumption. It seems possible, though, that autotomized conspecifics are less attractive to cannibals than intact ones due to a repelling action of autotomized tissues.     

Tail loss reduces home range size and access to females in male lizards, Psammodromus algirus

Numerous lizard species use caudal autotomy as an antipredatordevice even though there must be significant costs during theperiod of tail regeneration. Strategies used by tailless individualsto enhance survival in natural populations are still poorlyunderstood. We experimentally examine tail loss in large, dominantmales of Psammodromus algirus in the middle of the breedingseason in the field. We report data showing home range reductionof large dominant males after autotomy, reduction in the numberof females in the home ranges of manipulated males, and a potentialincrease in mating opportunities of small subordinate maleswith complete tails. We conclude that changes in home rangeuse because of desertion of areas with less cover can resultin decreased predation risk at the cost of decreased accessto females.     

Some vaguely explored (but not trivial) costs of tail autotomy in lizards

Lizard tail autotomy is considered an efficient anti-predator strategy that allows animals to escape from a predator attack. However, since the tail also is involved in many alternative functions, tailless animals must cope with several costs following autotomy. Here we explicitly evaluate the consequences of tail autotomy for two costs that have been virtually unexplored: 1. we test whether the anatomical change that occurs after tail loss causes a reduction in the role of the tail as a distraction mechanism to predators; 2. we analyzed whether tail synthesis comprises an energetically costly process in itself, by directly comparing the cost of maintenance before and after autotomy. We found that original tails displace further and at greater velocity than regenerated tails, indicating that the anti-predation responses of a lizard probably changes according to whether its tail is original or regenerated. With regard to the energetic cost of tail synthesis, we observed a significant increase in the standard metabolic rate, which rose 36% in relation to the value recorded prior to tail loss. This result suggests that the energetic cost of tail synthesis itself could be enough to affect lizard fitness.     

Muscle activity in autotomized tails of a lizard (Gekko gecko): a naturally occurring spinal preparation

We quantified muscle activity in tails of lizards (Gekko gecko) during running and after autotomy of the tail. We chose different animals and varied where we broke the tails in order to obtain three experimental preparations having: no regenerated tissue or prior tail loss (non-regenerated), a large regenerated portion and a few original caudal vertebrae (partially regenerated), and only regenerated tissue (fully regenerated). All observed axial motor patterns were rhythmic. During running of intact animals, muscles in non-regenerated tails were activated in an alternating, unilateral pattern that was propagated posteriorly. After autotomy, non-regenerated tails had unilateral muscle activity that alternated between the left and right sides and propagated anteriorly. Autotomized, partially regenerated tails had unilateral, alternating muscle activity that lacked any longitudinal propagation. Autotomized, fully regenerated tails had periodic muscle activity that occurred simultaneously for both left and right sides and all longitudinal positions. Neither tactile stimulation nor removal of the tail tip prior to autotomizing the tail affected the motor pattern. Several features of the motor pattern of autotomized tails changed significantly with increased time after autotomy. Autotomized tails with one or more spinal segments moved longer and more vigorously than autotomized tails consisting entirely of regenerated (unsegmented) tissue.Abbreviations AREA rectified integrated area - CYCDUR cycle duration or time between the onsets of successive bursts for a single channel - DUTY duty factor = EMG duration/CYCDUR - EMG electromyogram - EMGDUR EMG duration - INTENSITY = AREA/EMGDUR - ISPL intersegmental phase lag = PLAG/number of intervening muscle segments - LAG among site lag time = difference in onset times of adjacent ipsilateral electrode sites - PLAG phase lag = LAG/CYCDUR - RELISPL relative intersegmental phase lag = RELPLAG/number of intervening muscle segments - RELPLAG relative phase lag = LAG/EMGDUR     

Autotomy reduces feeding, energy storage and growth of the sea star Stichaster striatus

We evaluated the effect of autotomy on feeding, energy storage and growth of juvenile Stichaster striatus kept in the laboratory for five months with a limited supply of the mussel Semimytilus algosus. Autotomy strongly decreased feeding, energy storage and growth. Intact juveniles showed a ∼ 3 fold higher feeding rate than autotomized individuals throughout the experiment. Intact juveniles also had a higher (∼ 5 fold) energy content per pyloric caeca in each arm. This was mainly due to higher lipid content, the main proximate constituent of pyloric caeca. Intact juveniles showed a greater growth rate and reached a greater size than autotomized individuals, more evident for underwater mass than radius length. The reduced capacity to feed reduced energy intake in autotomized individuals. However, low energy reserves along with low growth in autotomized sea stars, support the hypothesis that juveniles of this species allocate energy to regeneration to the detriment of growth. This was also supported by the ∼ 25% of arm length regeneration after 5 mo. Remaining small could increase risk of lethal predation, however, S. striatus may reduce predation risk by using crevices and kelp holdfasts as refuges from predators. Given the strong impact of autotomy on feeding, regeneration of arms to recover full capacity to forage and grow seems a better strategy for juvenile S. striatus, than merely growing.     

Why don't small snakes bask? Juvenile broad‐headed snakes trade thermal benefits for safety

Previous studies have suggested that most small Australian elapid snakes are nocturnal and rarely bask in the open because of the risk of predation by diurnal predatory birds. Because the physiology and behaviour of reptiles is temperature dependent, staying in refuges by day can entail high thermoregulatory costs, particularly for juveniles that must grow rapidly to maximise their chances of survival. We investigated whether the risk of predation deters juveniles of the endangered broad-headed snake ( Hoplocephalus bungaroides ) from basking, and if so, whether there are thermal costs associated with refuge use. To estimate avian attack rates on snakes, we placed 900 plasticine snake replicas in sunny locations and underneath small stones on three sandstone plateaus for 72 h. At the same time we quantified the thermal benefits of basking vs refuge use. On sunny days, juveniles could maintain preferred body temperatures for 4.7 h by basking but only for 2.0 h if they remained inside refuges. Our predation experiment showed that basking has high costs for juvenile snakes. Predators attacked a significantly higher proportion of exposed models (13.3%) than models under rocks (1.6%). Birds were the major predators of exposed models (75% of attacks), and avian predation did not vary across the landscape. By trading heat for safety, juvenile H. bungaroides decreased the potential time period that they could maintain preferred body temperatures by 57%. Thermal costs of refuge use may therefore contribute to the slow growth and late maturation of this endangered species. Our results support the hypothesis that nocturnal activity in elapid snakes has evolved to minimise the risk of avian predation.     

Ceratal autotomy and regeneration in the aeolid nudibranch Phidiana crassicornis and the role of predators

Abstract. Ceratal autotomy by the aeolid nudibranch Phidinna crassicornis is common in the field and was induced in the laboratory by mechanical and predatory stimuli. The ceras detaches from the body wall along an autotomy plane located at its basal constriction. Cerata released copious amounts of mucus during autotomy and exhibited a prolonged writhing response that continued for several hours after detachment. Regeneration of cerata autotomized in the field and in the laboratory was documented. Four days after autotomy, regenerating cerata appeared as small protuberances. By day 24 the regenerates acquired their mature structural organisation and vivid colour. The cerata subsequently increased in length and diameter and were indistin‐guishable from surrounding cerata by 41 to 43 days after autotomy. Regeneration rates of cerata induced to autotomize in the laboratory and regeneration of cerata autotomized in the field were similar, averaging 0.08 and 0.067 mdday, respectively. The sequence of morphological events involved with regeneration following experimental and natural induction of autotomy was identical. The kelp crab Pugettia productn induced autotomy by holding cerata with its chelae. This crab also fed on autotomized cerata and consumed locomotory and ceratal mucus. Ceratal autotomy may be an important mechanism of escape from this predatory crustacean. Other potential predators including hermit crabs and tidepool sculpins did not elicit defensive behaviour in P. crussicornis. Nematocysts were present in the enidosacs and their role in defense was investigated. Fired nematocysts were observed in podia of the asteroid Crossaster papposus following ceratal contact but were not seen in the podia of Pycnopodia helianthoides in a similar trial. For P. crassicornis, the cnidosacs may function primarily as a storage device for safe sequestering of nematoeysts that could pose a threat to the digestive system. They did not play a major defensive role against the predators tested, but may be important in the field against other predators.     

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.     

断尾对蓝尾石龙子能量储存和运动表现的影响

在许多蜥蜴种类中,尾自切是一种主要的逃避天敌捕食的防御性策略。虽然断尾使蜥蜴获得短期的生存利益,但同时也需为此承受多方面的代价。利用从丽水采集的117条蓝尾石龙子来评价该种动物断尾的能量和运动代价。81条(约69%)石龙子至少经历过1次尾自切。断尾个体中,原先断尾事件的发生频率在不同尾区间存在显著差别,但两性间无差别。将实验组17条具完整尾的石龙子依次切去3个尾段,然后测定断尾前后石龙子的运动表现以及每个尾段、身体各部分中的脂肪含量。另15条具完整尾的石龙子作为对照组,仅测量其运动表现。尾部的脂肪含量与尾基部宽呈正相关,说明具较粗尾部的石龙子一般具有相当较多的尾部储能。尾部脂肪含量随尾长呈非等比例分布,大部分脂肪集中于尾近基部端。断尾几乎不影响蓝尾石龙子的运动表现,仅当大部分尾部被切除时疾跑速有较小程度的降低。显示了蓝尾石龙子因遭遇天敌捕食攻击或其它因素作用而产生的部分断尾可能并不会导致严重的能量和运动代价。由于野外种群蓝尾石龙子个体的断尾情况主要发生在尾近基部或中部位置,因此可以认为自然条件下该种动物的尾自切通常会遭受明显的能量和运动代价。     

Tail development and regeneration throughout the life cycle of the four-toed salamander Hemidactylium scutatum

The salamander tail displays different functions and morphologies in the aquatic and terrestrial stages of species with complex life cycles. During metamorphosis the function of the tail changes; the larval tail functions in aquatic locomotion while the juvenile and adult tail exhibits tail autotomy and fat storage functions. Because tail injury is common in the aquatic environment, we hypothesized that mechanisms have evolved to prevent altered larval tail morphology from affecting normal juvenile tail morphology. The hypothesis that injury to the larval tail would not affect juvenile tail morphology was investigated by comparing tail development and regeneration in Hemidactylium scutatum (Caudata: Plethodontidae). The experimental design included larvae with uninjured tails and with cut tails to simulate natural predation. The morphological variables analyzed to compare normally developing and regenerating tails were 1) tail length, 2) number of caudal vertebrae, and 3) vertebral centrum length. Control and experimental groups do not differ in time to metamorphosis or snout-vent length. Tails of experimental individuals are shorter than controls, yet they display a significantly higher rate of tail growth and less resorption of tail tissue. Anterior to the site of tail injury, caudal vertebrae in juveniles display greater average centrum lengths. Results suggest that regenerative mechanisms are functioning not only to produce structures, but also to influence growth of existing structures. Further investigation of juvenile and adult stages as well as comparative analyses of tail morphology in salamanders with complex life cycles will enhance our understanding of amphibian development and of the evolution of amphibian life cycles. J Morphol 233:15–29, 1997. © 1997 Wiley-Liss, Inc.