Dynamics of Mara–Serengeti ungulates in relation to land use changes

Caudal autotomy, the ability to shed the tail, is common in lizards as a response to attempted predation. Since Arnold's substantial review of caudal autotomy as a defence in reptiles 20 years ago, our understanding of the costs associated with tail loss has increased dramatically. In this paper, we review the incidence of caudal autotomy among lizards (Reptilia Sauria) with particular reference to questions posed by Arnold. We examine tail break frequencies and factors that determine occurrence of autotomy in natural populations (including anatomical mechanisms, predation efficiency and intensity, microhabitat preference, sex and ontogenetic differences, as well as intraspecific aggression). We also summarize the costs associated with tail loss in terms of survivorship and reproduction, focusing on potential mechanisms that influence fitness (i.e. locomotion costs, behavioural responses and metabolic costs). Finally, we examine the factors that may influence the facility with which autotomy takes place, including regeneration rate, body form and adaptive behaviour. Taking Arnold's example, we conclude with proposals for future research.     

Spatial Biodiversity Patterns of Madagascar's Amphibians and Reptiles

Madagascar has become a model region for testing hypotheses of species diversification and biogeography, and many studies have focused on its diverse and highly endemic herpetofauna. Here we combine species distribution models of a near-complete set of species of reptiles and amphibians known from the island with body size data and a tabulation of herpetofaunal communities from field surveys, compiled up to 2008. Though taxonomic revisions and novel distributional records arose since compilation, we are confident that the data are appropriate for inferring and comparing biogeographic patterns among these groups of organisms. We observed species richness of both amphibians and reptiles was highest in the humid rainforest biome of eastern Madagascar, but reptiles also show areas of high richness in the dry and subarid western biomes. In several amphibian subclades, especially within the Mantellidae, species richness peaks in the central eastern geographic regions while in reptiles different subclades differ distinctly in their richness centers. A high proportion of clades and subclades of both amphibians and reptiles have a peak of local endemism in the topographically and bioclimatically diverse northern geographic regions. This northern area is roughly delimited by a diagonal spanning from 15.5°S on the east coast to ca. 15.0°S on the west coast. Amphibian diversity is highest at altitudes between 800–1200 m above sea-level whereas reptiles have their highest richness at low elevations, probably reflecting the comparatively large number of species specialized to the extended low-elevation areas in the dry and subarid biomes. We found that the range sizes of both amphibians and reptiles strongly correlated with body size, and differences between the two groups are explained by the larger body sizes of reptiles. However, snakes have larger range sizes than lizards which cannot be readily explained by their larger body sizes alone. Range filling, i.e., the amount of suitable habitat occupied by a species, is less expressed in amphibians than in reptiles, possibly reflecting their lower dispersal capacity. Taxonomic composition of communities assessed by field surveys is largely explained by bioclimatic regions, with communities from the dry and especially subarid biomes distinctly differing from humid and subhumid biomes.     

Late Quaternary reptile extinctions: size matters,insularity dominates

Aim A major Late Quaternary vertebrate extinction event affected mostly large‐bodied ‘megafauna’. This is well documented in both mammals and birds, but evidence of a similar trend in reptiles is scant. We assess the relationship between body size and Late Quaternary extinction in reptiles at the global level. Location Global. Methods We compile a body size database for all 82 reptile species that are known to have gone extinct during the last 50,000 years and compare them with the sizes of 10,090 extant reptile species (97% of known extant diversity). We assess the body size distributions in the major reptile groups: crocodiles, lizards, snakes and turtles, while testing and correcting for a size bias in the fossil record. We examine geographical biases in extinction by contrasting mainland and insular reptile assemblages, and testing for biases within regions and then globally by using geographically weighted models. Results Extinct reptiles were larger than extant ones, but there was considerable variation in extinction size biases among groups. Extinct lizards and turtles were large, extinct crocodiles were small and there was no trend in snakes. Lizard lineages vary in the way their extinction is related to size. Extinctions were particularly prevalent on islands, with 73 of the 82 extinct species being island endemics. Four others occurred in Australia. The fossil record is biased towards large‐bodied reptiles, but extinct lizards were larger than extant ones even after we account for this. Main conclusions Body size played a complex role in the extinction of Late Quaternary reptiles. Larger lizard and turtle species were clearly more affected by extinction mechanisms such as over exploitation and invasive species, resulting in a prevalence of large‐bodied species among extinct taxa. Insularity was by far the strongest correlate of recent reptile extinctions, suggesting that size‐biased extinction mechanisms are amplified in insular environments.     

An allometric comparison of the mitochondria of mammalian and reptilian tissues: The implications for the evolution of endothermy

Summary The effects of body size and phylogeny on metabolic capacities were examined by comparing the mitochondrial capacities of 6 mammalian and 4 reptilian species representing 100-fold body weight ranges. The mammals examined included 3 eutherian, 2 marsupial and a monotreme species and the reptiles 2 saurian, 1 crocodilian and 1 testudine species. The tissues examined were liver, kidney, brain, heart, lung and skeletal muscle. Allometric equations were derived for tissue weights, mitochondrial volume densities, internal mitochondrial membrane surface area densities, tissue mitochondrial membrane surface areas both per gram and per total tissue and summated tissue mitochondrial membrane surface areas. For the mammals and reptiles studied a 100% increase in body size resulted in average increases of 68% in internal organ size and 107% in skeletal muscle mass. Similarly, total organ mitochondrial membrane surface areas increase in mammals and reptiles by an average 54% and for skeletal muscle by an average 96%. These values are similar to increases in standard (54 and 71%) and maximum (73 and 77%) organismal metabolism values found by other authors for mammals and reptiles respectively. Although the allometric exponents (or rates of change with increasing body size) of the mitochondrial parameters in mammals and reptiles are statistically the same, in general the total amount of mitochondrial membrane surface area in the mammalian tissues are four times greater than found in the reptilian tissues. These differences were not the result of any single ‘quantum’ factor but are the result of the mammals having relatively larger tissues with a greater proportion of their volume occupied by mitochondria and to a lesser extent increases in the internal mitochondrial membrane surface area densities. Mitochondrial volume density from this present study would appear to be the major factor involved in changing weight specific metabolism of tissues both as a result of changes in body size and in the evolution of endothermy in mammals from reptiles.     

Effects of temperature on the metabolic response to feeding in Python molurus

As ectothermic vertebrates, reptiles undergo diurnal and seasonal changes in body temperature, which affect many biological functions. In conjunction with a general review regarding the effects of temperature on digestion in reptiles, we describe the effects of various temperatures (20-35 degrees C) on the metabolic response to digestion in the Burmese python (Python molurus). The snakes were fed mice amounting to 20% of their body weight and gas exchange (oxygen uptake and CO(2) production) were measured until digestion had ended and gas exchange returned to fasting levels. Elevated temperature was associated with a faster and larger metabolic increase after ingestion, and the time required to return to fasting levels was markedly longer at low temperature. The factorial increase between fasting oxygen consumption (VO(2)) and maximal VO(2) during digestion was, however, similar at all temperatures studied. Furthermore, the integrated SDA response was not affected by temperature suggesting the costs associated with digestion are temperature-independent. Other studies on reptiles show that digestive efficiency is only marginally affected by temperature and we conclude that selection of higher body temperatures during digestion (postprandial thermophilic response) primarily reduces the time required for digestion.     

An identification of invariants in life history traits of amphibians and reptiles

While many morphological, physiological, and ecological characteristics of organisms scale with body size, some do not change under size transformation. They are called invariant. A recent study recommended five criteria for identifying invariant traits. These are based on that a trait exhibits a unimodal central tendency and varies over a limited range with body mass (type I), or that it does not vary systematically with body mass (type II). We methodologically improved these criteria and then applied them to life history traits of amphibians, Anura, Caudata (eleven traits), and reptiles (eight traits). The numbers of invariant traits identified by criteria differed across amphibian orders and between amphibians and reptiles. Reproductive output (maximum number of reproductive events per year), incubation time, length of larval period, and metamorphosis size were type I and II invariant across amphibians. In both amphibian orders, reproductive output and metamorphosis size were type I and II invariant. In Anura, incubation time and length of larval period and in Caudata, incubation time were further type II invariant. In reptiles, however, only number of clutches per year was invariant (type II). All these differences could reflect that in reptiles body size and in amphibians, Anura, and Caudata metamorphosis (neotenic species go not through it) and the trend toward independence of egg and larval development from water additionally constrained life history evolution. We further demonstrate that all invariance criteria worked for amphibian and reptilian life history traits, although we corroborated some known and identified new limitations to their application.     

Conflicts between courtship and thermoregulation: the thermal ecology of amorous male garter snakes (Thamnophis sirtalis parietalis, colubridae)

Thermoregulatory behavior is an important component of daily activities for many reptiles, especially for small heliothermic (sun-basking) species that inhabit cold climates. However, the relative costs and benefits of thermoregulation depend on numerous factors, such that reptiles may sometimes accord a low priority to precise control of body temperatures. We observed and radio tracked garter snakes (Thamnophis sirtalis parietalis) in central Manitoba during the mating season (spring). Previous studies on this species have documented precise behavioral regulation of body temperatures during summer. In contrast, the courting snakes that we studied in springtime spent little time in overt thermoregulatory behavior. Body temperatures were extremely variable (both in outdoor enclosures and in the field) despite abundant opportunities for more precise thermal control. These small elongate reptiles cool so quickly (relative to the time periods needed for effective courtship) that any benefit to higher body temperatures would be transitory at best. Experiments show that hotter males are no better at obtaining matings or at detecting predators. Thus, male garter snakes concentrate on courtship rather than on basking. In the face of conflicting priorities, reptiles may often forgo precise thermoregulation because its benefits are too low, and its costs too high, compared with alternative behaviors.     

Physiological thermoregulation in a crustacean? Heart rate hysteresis in the freshwater crayfish Cherax destructor

Differential heart rates during heating and cooling (heart rate hysteresis) are an important thermoregulatory mechanism in ectothermic reptiles. We speculate that heart rate hysteresis has evolved alongside vascularisation, and to determine whether this phenomenon occurs in a lineage with vascularised circulatory systems that is phylogenetically distant from reptiles, we measured the response of heart rate to convective heat transfer in the Australian freshwater crayfish, Cherax destructor. Heart rate during convective heating (from 20 to 30 degrees C) was significantly faster than during cooling for any given body temperature. Heart rate declined rapidly immediately following the removal of the heat source, despite only negligible losses in body temperature. This heart rate 'hysteresis' is similar to the pattern reported in many reptiles and, by varying peripheral blood flow, it is presumed to confer thermoregulatory benefits particularly given the thermal sensitivity of many physiological rate functions in crustaceans.     

The Cardiovascular Control of Heat Exchange: Consequences of Body Size

For blood flow to be an effective agent for the control of heatexchange, it must occur in a region of the body where conductionresistance in the tissues is relatively high, and in an environmentwhere external resistance to heat exchange is relatively low.If either of these conditions is not met, control of heat exchangeby blood flow is not possible. Very small reptiles should notbe able to control heat exchange by blood flow in any environment,unless they control blood flow specifically to appendages. Verylarge reptiles should be able to control heat exchange by bloodflow only under certain conditions, such as in water, very highwinds, or intense radiative heating. Otherwise, they shouldhave little control. An optimum body size should exist for areptile's ability to control heat exchange using blood flow.In air, this optimum body size for alligators appears to beabout 5 kg. Theoretically, the optimum size should be substantiallylarger than 5 kg for reptiles heating and cooling in water.     

The adaptive significance of reptilian viviparity in the tropics: testing the maternal manipulation hypothesis

Abstract Phylogenetic transitions from oviparity to viviparity in reptiles generally have occurred in cold climates, apparently driven by selective advantages accruing from maternal regulation of incubation temperature. But why, then, are viviparous reptiles so successful in tropical climates? Viviparity might enhance fitness in the tropics via the same pathway as in the temperate zone, if pregnant female reptiles in the tropics maintain more stable temperatures than are available in nests (Shin's maternal manipulation hypothesis). Alternatively, viviparity might succeed in the tropics for entirely different reasons than apply in the temperate zone. Our data support the maternal manipulation hypothesis. In a laboratory thermal gradient, pregnant death adders (Acanthophis praelongus) from tropical Australia maintained less variable body temperatures (but similar mean temperatures) than did nonpregnant females. Females kept at a diel range of 25–31d?C (as selected by pregnant females) gave birth earlier and produced larger offspring (greater body length and head size) than did females kept at 23–33d?C (as selected by nonpregnant snakes). Larger body size enhanced offspring recapture rates (presumably reflecting survival rates) in the field. Thus, even in the tropics, reproducing female reptiles manipulate the thermal regimes experienced by their developing embryos in ways that enhance the fitness of their offspring. This similarity across climatic zones suggests that a single general hypothesis‐maternal manipulation of thermal conditions for embryogenesis‐may explain the selective advantage of viviparity in tropical as well as cold‐climate reptiles.     

Metabolic scaling of antibiotics in reptiles: Basis and limitations

The allometric equation y = a · x^b has been used to scale many morphological and physiological attributes relative to body mass. For instance, in eutherian mammals, the equation P_met = 70M_b^0.75 has been used to describe the relationship between metabolic rate (P_met) and body mass (M_b). Similar equations have been derived for squamate reptiles. Recently, this relationship between metabolic rate and body mass has been used in determining appropriate dosages and dosing intervals of antibiotics both intraspecifically for different sized reptiles and interspecifically for those reptiles in which antibiotic pharmacokinetic studies have not been performed. Although this is a simple mathematical process, a number of problems surface when this approach is examined closely. First, the mass constant (a) in reptiles varies from 1–5 for snakes and 6–10 for lizards. No such information is available for chelonians or crocodilians. Unless the mass constant for the unknown species approximates that of the known species, inappropriate dosages and intervals of administration will be calculated. Second, pharmacokinetic differences may exist between widely divergent species, independent of metabolic rate. Third, all available pharmacokinetic studies and metabolic allometric equations are derived from clinically healthy reptiles. Differences more than likely exist between healthy and ill reptiles in regard to uptake, distribution, and elimination of drugs and overall metabolism. While metabolic scaling of antibiotics is a potentially useful and practical tool in drug dosing, these limitations must be considered when dosing an ill reptile. Until more scientifically derived information is available for demonstrating the accuracy of metabolic scaling of antibiotics in reptiles, the clinician will need to understand the limitations of this approach. © 1996 Wiley-Liss, Inc.     

Physiological mechanisms of thermoregulation in reptiles: a review

The thermal dependence of biochemical reaction rates means that many animals regulate their body temperature so that fluctuations in body temperature are small compared to environmental temperature fluctuations. Thermoregulation is a complex process that involves sensing of the environment, and subsequent processing of the environmental information. We suggest that the physiological mechanisms that facilitate thermoregulation transcend phylogenetic boundaries. Reptiles are primarily used as model organisms for ecological and evolutionary research and, unlike in mammals, the physiological basis of many aspects in thermoregulation remains obscure. Here, we review recent research on regulation of body temperature, thermoreception, body temperature set-points, and cardiovascular control of heating and cooling in reptiles. The aim of this review is to place physiological thermoregulation of reptiles in a wider phylogenetic context. Future research on reptilian thermoregulation should focus on the pathways that connect peripheral sensing to central processing which will ultimately lead to the thermoregulatory response.     

The Uses of Anaerobiosis by Amphibians and Reptiles

Amphibians and reptiles rely upon anaerobic glycolysis to supporttheir energetic requirements under a variety of circumstances.Although adult frogs derive most of the energy for muscle contractionduring intense, short-term locomotion from glycolysis, anurantadpoles have a very low rate of lactate formation during 30sec of burst swimming; instead, they rely largely on the useof phosphocreatine stores. Among squamate reptiles, the rateof lactate formation during vigorous exercise is largely relatedto the duration of activity and to body temperature. Recentstudies have shown that fossorial, limbless reptiles do notdiffer from surface-dwelling, quadrupedal species in the rateof glycolysis during intense activity. The energetics of locomotiondiffers significantly between swimming and running turtles;thus the site of activity influences the role of anaerobiosisin movement. Lactate levels increase in some frogs during callingand nest building and in some reptiles during prey capture andingestion. However, voluntary locomotion and diving by reptilesare rarelyaccompanied by an increase in lactate levels. Freshwaterturtles rely heavily on glycolysis during aquatic hibernation.Thus, it can be concluded that amphibians and reptiles derivea significant proportion of their energetic requirements fromanaerobic metabolism only under selected circumstances whenthe benefits outweigh the costs associated with the accumulationof lactate.     

Blood flow to long bones indicates activity metabolism in mammals, reptiles and dinosaurs

The cross-sectional area of a nutrient foramen of a long bone is related to blood flow requirements of the internal bone cells that are essential for dynamic bone remodelling. Foramen area increases with body size in parallel among living mammals and non-varanid reptiles, but is significantly larger in mammals. An index of blood flow rate through the foramina is about 10 times higher in mammals than in reptiles, and even higher if differences in blood pressure are considered. The scaling of foramen size correlates well with maximum whole-body metabolic rate during exercise in mammals and reptiles, but less well with resting metabolic rate. This relates to the role of blood flow associated with bone remodelling during and following activity. Mammals and varanid lizards have much higher aerobic metabolic rates and exercise-induced bone remodelling than non-varanid reptiles. Foramen areas of 10 species of dinosaur from five taxonomic groups are generally larger than from mammals, indicating a routinely highly active and aerobic lifestyle. The simple measurement holds possibilities offers the possibility of assessing other groups of extinct and living vertebrates in relation to body size, behaviour and habitat.     

Body temperature null distributions in reptiles with nonzero heat capacity: seasonal thermoregulation in the American alligator (Alligator mississippiensis)

Regulation of body temperature may increase fitness of animals by ensuring that biochemical and physiological processes proceed at an optimal rate. The validity of current methods of testing whether or not thermoregulation in reptiles occurs is often limited to very small species that have near zero heat capacity. The aim of this study was to develop a method that allows estimation of body temperature null distributions of large reptiles and to investigate seasonal thermoregulation in the American alligator (Alligator mississippiensis). Continuous body temperature records of wild alligators were obtained from implanted dataloggers in winter (n=7, mass range: 1.6-53.6 kg) and summer (n=7, mass range: 1.9-54.5 kg). Body temperature null distributions were calculated by randomising behavioural postures, thereby randomly altering relative animal surface areas exposed to different avenues of heat transfer. Core body temperatures were predicted by calculations of transient heat transfer by conduction and blood flow. Alligator body temperatures follow regular oscillations during the day. Occasionally, body temperature steadied during the day to fall within a relatively narrow range. Rather than indicating shuttling thermoregulation, however, this pattern could be predicted from random movements. Average daily body temperature increases with body mass in winter but not in summer. Daily amplitudes of body temperature decrease with increasing body mass in summer but not in winter. These patterns result from differential exposure to heat transfer mechanisms at different seasons. In summer, alligators are significantly cooler than predictions for a randomly moving animal, and the reverse is the case in winter. Theoretical predictions show, however, that alligators can be warmer in winter if they maximised their sun exposure. We concluded that alligators may not rely exclusively on regulation of body temperature but that they may also acclimatise biochemically to seasonally changing environmental conditions.     

PROBLEMS OF THE ORIGIN OF REPTILES

The fossil records of the four living reptilian orders can be traced into the Triassic. The earlier ancestry of the turtles has not been established. Squamates and rhyncho-cephalians evolved from the Late Permian eosuchians; crocodiles from the thecodonts. The ancestry of the eosuchians and thecodonts is to be found in the central stock of Permo-Carboniferous reptiles, the captorhinomorphs. The earliest captorhino-morphs, from the Lower Pennsylvanian, are already fully developed reptiles. The limnoscelids and solenodonsaurids are more primitive forms, retaining features typical of anthracosaurian amphibians. Neither reptiles nor any appropriate ancestors are known prior to the Lower Pennsylvanian. Because of the absence of any true ancestors, the nature of the amphibian-reptilian transition must be studied on the basis of amphibians contemporary with the early reptiles. The Permian seymouriamorphs have long been accepted as relicts of the group which gave rise to reptiles, although Seymouria itself is specialized in many features of its anatomy. The Middle Pennsylvanian genus Gephyrostegus appears to resemble much more closely the anatomy expected in the ancestors of reptiles. This genus forms the basis for consideration of the anatomical, physiological and behavioural changes which culminated in the origin of reptiles. Study of the earliest known reptiles and their closest relatives among contemporary amphibians indicates that the initial adaptation leading to the emergence of the class was assumption of a terrestrial habit, with accompanying small body size. The small body size of the immediate ancestors of reptiles would have made it possible for them to produce sufficiently small eggs that they could develop in damp places on land without initially being supported and protected by extraembryonic membranes. The rapid increase in body size in all lineages of Pennsylvanian reptiles indicates the prior development of an amniotic egg. Fundamental to the emergence of reptiles was modification in the jaw mechanism from the kinetic inertial system of amphibians to a static pressure system. The latter was presumably developed in order for the developing reptiles to utilize more active terrestrial prey. This change in the jaw mechanism is reflected in the reorganization of the palate which serves as a morphological basis for denning the establishment of reptilian status. At approximately the same stage as the change in palatal structure, the definitive reptilian vertebral pattern was developed. The apparent closure of the otic notch and the probable reorientation of the stapes in the amphibian-reptilian transition presumably resulted from the decrease in relative skull size and do not appear to be related to any change in hearing ability. The tympanum probably maintained the same relative relationship with the squamosal and supratemporal throughout this transition. On the basis of the present fossil record, all adequately known Palaeozoic reptiles appear to have had a common ancestry among the predecessors of the known gephyro-stegids. The family Diadectidae is the only important group whose specific relationships cannot be established. On the basis of this study, the following taxonomic changes are suggested: the family Limnoscelidae should not be included among the captorhinomorphs. The seymouria-morph concept should be restricted to forms having the specializations of Seymouria, the discosauriscids and kotlassids. Gephyrostegids should be specifically excluded from the Seymouriamorpha and should be included in a separate taxon among the anthra-cosaurs of equal rank with embolomeres and seymouriamorphs.     

An exploration of differences in the scaling of life history traits with body mass within reptiles and between amniotes

Allometric relationships linking species characteristics to body size or mass (scaling) are important in biology. However, studies on the scaling of life history traits in the reptiles (the nonavian Reptilia) are rather scarce, especially for the clades Crocodilia, Testudines, and Rhynchocephalia (single extant species, the tuatara). Previous studies on the scaling of reptilian life history traits indicated that they differ from those seen in the other amniotes (mammals and birds), but so far most comparative studies used small species samples and also not phylogenetically informed analyses. Here, we analyzed the scaling of nine life history traits with adult body mass for crocodiles (n = 22), squamates (n = 294), turtles (n = 52), and reptiles (n = 369). We used for the first time a phylogenetically informed approach for crocodiles, turtles, and the whole group of reptiles. We explored differences in scaling relationships between the reptilian clades Crocodilia, Squamata, and Testudines as well as differences between reptiles, mammals, and birds. Finally, we applied our scaling relationships, in order to gain new insights into the degree of the exceptionality of the tuatara's life history within reptiles. We observed for none of the life history traits studied any difference in their scaling with body mass between squamates, crocodiles, and turtles, except for clutch size and egg weight showing small differences between these groups. Compared to birds and mammals, scaling relationships of reptiles were similar for time‐related traits, but they differed for reproductive traits. The tuatara's life history is more similar to that of a similar‐sized turtle or crocodile than to a squamate.     

The behavioral responses of amphibians and reptiles to microgravity on parabolic flights

In the present study, we exposed 53 animals from 23 different species of amphibians and reptiles to microgravity (mug). This nearly doubles the number of amphibians and reptiles observed so far in mug. The animals were flown on a parabolic flight, which provided 20-25s of mug, to better characterize behavioral reactions to abrupt exposure to mug. Highly fossorial limbless caecilians and amphisbaenians showed relatively limited movement in mug. Limbed quadrupedal reptiles that were non-arboreal in the genera Leiocephalus, Anolis, and Scincella showed the typical righting response and enormous amounts of body motion and tail rotation, which we interpreted as both righting responses and futile actions to grasp the substrate. Both arboreal and non-arboreal geckos in the genera Uroplatus, Palmatogecko, Stenodactylus, Tarentola, and Eublepharis instead showed a skydiving posture previously reported for highly arboreal anurans. Some snakes, in the genera Thamnophis and Elaphe, which typically thrashed and rolled in mug, managed to knot their own bodies with their tails and immediately became quiescent. This suggests that these reptiles gave stable physical contact, which would indicate that they were not falling, primacy over vestibular input that indicated that they were in freefall. The fact that they became quiet upon self-embrace further suggests a failure to distinguish self from non-self. The patterns of behavior seen in amphibians and reptiles in mug can be explained in light of their normal ecology and taxonomic relations.     

A new tale of lost tails: Correlates of tail breakage in the worm lizard Amphisbaena vermicularis

Predator–prey interactions are important evolutionary drivers of defensive behaviors, but they are usually difficult to record. This lack of data on natural history and ecological interactions of species can be overcome through museum specimens, at least for some reptiles. When facing aggressive interactions, reptile species may exhibit the defensive behavior of autotomy by losing the tail, which is also known as “urotomy”. The inspection of preserved specimens for scars of tail breakage can reveal possible ecological and biological correlates of urotomy. Herein, we investigated how the probability of urotomy in the worm lizard Amphisbaena vermicularis is affected by sex, body size, temperature, and precipitation. We found higher chances of urotomy for specimens with larger body size and from localities with warmer temperatures or lower precipitation. There was no difference in urotomy frequency between sexes. Older specimens likely faced – and survived – more predation attempts through their lifetime than smaller ones. Specimens from warmer regions might be more active both below‐ and aboveground, increasing the odds to encounter predators and hence urotomy. Probability of urotomy decreased with increased precipitation. Possibly, in places with heavier rainfall worm lizards come more frequently to the surface when galleries are filled with rainwater, remaining more exposed to efficient predators, which could result in less survival rates and fewer tailless specimens. This interesting defensive behavior is widespread in squamates, but yet little understood among amphisbaenians. The novel data presented here improve our understanding on the correlates of tail breakage and help us to interpret more tales of lost tails.     

Natural environment and thermal behaviour of Dimetrodon limbatus

This paper examines the body temperature variation of Dimetrodon during the different seasons of the year. The effect of the sail of Dimetrodon on its body temperature is also evaluated. It is shown that the sail of pelycosaurs provided an advantage to the reptile by warming it up quicker in the morning in cold environments. This would be a benefit, allowing Dimetrodon to prey on large reptiles, above 55kg, in the early morning while they were sluggish. From the results presented a climate similar to that of March for Cyprus could be representative of that of Permian period.