Are viviparous lizards from cool climates ever exclusively nocturnal? Evidence for extensive basking in a New Zealand gecko

Viviparity has evolved numerous times among squamate reptiles; however, the combination of viviparity and nocturnality is apparently rare among lizards. We used time‐lapse photography to examine evidence for diurnal activity in a viviparous lizard often described as nocturnal, the gecko Woodworthia ‘Otago/Southland’ from southern New Zealand (family Diplodactylidae). Evidence for diurnal emergence was extensive. Females have a higher incidence of basking compared to males, although no difference was detected between females in different reproductive conditions. Temperature loggers inserted into calibrated copper models were used to compare the body temperatures available to geckos in two basking positions and in two retreat types. Models in basking positions reached higher mean temperatures than models in retreats, although there was no significant effect of basking position or retreat type on model temperatures. Collectively, our results indicate that pregnant geckos that bask consistently could reduce gestation length by at least 14 days compared with females that remain in retreats. Extensive basking in this species adds to the growing evidence of diurno‐nocturnality in many New Zealand lepidosaurs, including other viviparous geckos. Our results lead us to question whether viviparity in lizards is ever compatible with ‘pure’ nocturnality in a cool climate. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, ●● , ●●–●●.     

Into the light: diurnality has evolved multiple times in geckos

Geckos are the only major lizard group consisting mostly of nocturnal species. Nocturnality is presumed to have evolved early in gecko evolution and geckos possess numerous adaptations to functioning in low light and at low temperatures. However, not all gecko species are nocturnal and most diurnal geckos have their own distinct adaptations to living in warmer, sunlit environments. We reconstructed the evolution of gecko activity patterns using a newly generated time‐calibrated phylogeny. Our results provide the first phylogenetic analysis of temporal activity patterns in geckos and confirm an ancient origin of nocturnality at the root of the gecko tree. We identify multiple transitions to diurnality at a variety of evolutionary time scales and transitions back to nocturnality occur in several predominantly diurnal clades. The scenario presented here will be useful in reinterpreting existing hypotheses of how geckos have adapted to varying thermal and light environments. These results can also inform future research of gecko ecology, physiology, morphology and vision as it relates to changes in temporal activity patterns. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, ●●, ●●–●●.     

Effects of substrate structure on speed and acceleration capacity in climbing geckos

We studied the effects of substrate structure on locomotor performance in a climbing gecko, Hemidactylus garnoti . We quantified three performance traits (acceleration capacity, instantaneous speed, and final speed) on three substrates: (i) smooth wood, (ii) a cloth surface, and (iii) a wire mesh. While acceleration capacity and instantaneous speed were highest on the wooden surface, final speed did not differ significantly among substrates. Using scanning electron microscopy (SEM) pictures, we estimated that 98% of the wooden surface is available for adhesion by the setae on the toepads, while this percentage is much lower for the mesh and cloth (41 and 37%, respectively). We suggest that when a gecko climbs up a gap-filled substrate, such as the wire mesh or cloth, adhesion will only happen between part of the toepad and the substrate, resulting in a diminished acceleration capacity. The higher acceleration capacity on the wooden substrate and the fact that the geckos tend to slip less often on this particular surface, may explain the difference in instantaneous speed. As for final speed, geckos might achieve similar final speeds on all three substrates by employing different locomotor strategies. Our results suggest that microhabitat use in nature might have a profound effect on locomotor performance and survival for climbing lizards such as geckos.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 85 , 385–393.     

How to climb a tree: lizards accelerate faster,but pause more,when escaping on vertical surfaces

Many species of lizards effectively traverse both two and three‐dimensional habitats. However, few studies have examined maximum locomotor performance on different inclines. Do maximum acceleration and velocity differ on a level and inclined surface? Do lizards pause more on an inclined surface? To address these questions, Sceloporus woodi lizards (N = 12) were run in the laboratory on a level trackway and a vertical tree trunk. This species is known to frequently utilize both vertical and horizontal aspects of its habitat. Average maximum acceleration on the vertical surface exceeded that on the level surface, although average maximum velocity exhibited the opposite pattern. The average number of pauses during level locomotion was lower compared to vertical locomotion. In addition, the average location of the first pause on the level surface was 0.51 m, which is farther than the average for vertical locomotion where the first pause was at 0.35 m. The combination of performance and pause data suggests that the relative lack of pausing during level locomotion allows individuals to reach higher maximum velocities on level surfaces because they accelerate over greater distances. The increased pausing when moving vertically could be a result of high energetic demands of vertical locomotion, or greater microhabitat complexity as a result of branching and/or refuges. The faster acceleration exhibited during vertical locomotion by S. woodi likely offsets the frequent pauses. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 83–90.     

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.     

Low cost of locomotion in lizards that are active at low temperatures

The nocturnality hypothesis of K. Autumn and coworkers states that nocturnal geckos have evolved a low energetic cost of locomotion (C(min)). A low C(min) increases maximum aerobic speed and partially offsets the decrease in maximum oxygen consumption caused by activity at low nocturnal temperatures. We tested whether a low C(min) is unique to nocturnal geckos or represents a more general pattern of convergent evolution among lizards that enables nocturnality and/or cold-temperature activity. We measured C(min) in four carefully selected lizard species from New Zealand (two nocturnal and two diurnal; n=5-9 individuals per species), including a nocturnal and diurnal gecko (a low C(min) is a gecko trait and is not related to nocturnality), a nocturnal skink (a low C(min) is related to being nocturnal), and a diurnal skink active at low temperatures (a low C(min) is related to being active at low body temperatures). The C(min) values of the four species measured in this study (range=0.21-2.00 mL O(2) g(-1) km(-1)) are lower than those of diurnal lizards from elsewhere, and the values are within or below the 95% confidence limits previously published for nocturnal geckos. A low C(min) increases the range of locomotor speeds possible at low temperatures and provides an advantage for lizards active at these temperatures. We accepted the hypothesis that nocturnal lizards in general have a low C(min) and provide evidence for a low C(min) in lizards from cool-temperate environments. The low C(min) in lizards living at high latitudes may enable extension of their latitudinal range into otherwise thermally suboptimal habitats.     

Secondarily diurnal geckos return to cost of locomotion typical of diurnal lizards

Previous studies showed that nocturnal geckos evolved a low energetic cost of locomotion (Cmin), which increases maximum aerobic speed and partially offsets the decrease in maximal oxygen consumption caused by activity at low nocturnal temperatures. Because the advantage of a low Cmin should apply at high diurnal temperatures as well as at low nocturnal temperatures, I hypothesized that Cmin remained low in geckos that have secondarily evolved diurnality. I measured Cmin in two secondarily diurnal gecko species, Rhoptropus bradfieldi (4.7 g+/-0.71 SE) and Phelsuma madagascariensis (23.9 g+/-3.7 SE), during steady exercise on a treadmill and rejected the hypothesis that secondarily diurnal geckos retain the low Cmin of their nocturnal ancestors. The Cmin in R. bradfieldi (2.468 mL O2 g-1 km-1+/-0.489 SE) and P. madagascariensis (1.389 mL O2 g-1 km-1+/-0.119 SE) returned to values typical of ancestrally diurnal lizards. This suggests that there is a trade-off that outweighs the performance advantage of low Cmin in a diurnal environment and that may cause an evolutionary association between Cmin and activity time (diurnality/nocturnality).     

Extant Lizard Tracks: Variation and Implications for Paleoichnology

In this study, I collected tracks and trackways from nine species of extant lizards representing all five major lizard clades. Previously, tracks from species of only two of these clades were described. Lizard tracks conventionally are regarded as having curved digit imprints that progressively increase in length from digit I to IV, with a smaller digit V directing antero-laterally. However, the zygodactylous feet of chameleons (Calumma parsonii and Furcifer pardalis), the posteriorly directed digit V in the pes of ground-dwelling geckos (Eublepharis macularius) and the rounded feet of blue-tongued skinks (Tiliqua scincoides) did not make “typical” lizard tracks, and demonstrate that even within a limited taxonomic sample there can be considerable variation in the morphologies of lizard tracks. Among the lizards examined, mode of locomotion and how the feet function have more influence on the morphology of tracks than does the phylogenetic affinities of the trackmaker. This preliminary neoichnological study increases the known variation in lizard tracks and aids in interpreting the fossil trackway record by providing comparative information that can be used to identify fossil tracks made by lizards.     

The development of cephalic armor in the tokay gecko (Squamata: Gekkonidae: Gekko gecko)

Armored skin resulting from the presence of bony dermal structures, osteoderms, is an exceptional phenotype in gekkotans (geckos and flap-footed lizards) only known to occur in three genera: Geckolepis, Gekko, and Tarentola. The Tokay gecko (Gekko gecko LINNAEUS 1758) is among the best-studied geckos due to its large size and wide range of occurrence, and although cranial dermal bone development has previously been investigated, details of osteoderm development along a size gradient remain less well-known. Likewise, a comparative survey of additional species within the broader Gekko clade to determine the uniqueness of this trait has not yet been completed. Here, we studied a large sample of gekkotans (38 spp.), including 18 specimens of G. gecko, using X-rays and high-resolution computed tomography for visualizing and quantifying the dermal armor in situ. Results from this survey confirm the presence of osteoderms in a second species within this genus, Gekko reevesii GRAY 1831, which exhibits discordance in timing and pattern of osteoderm development when compared with its sister taxon, G. gecko. We discuss the developmental sequence of osteoderms in these two species and explore in detail the formation and functionality of these enigmatic dermal ossifications. Finally, we conducted a comparative analysis of endolymphatic sacs in a wide array of gekkotans to explore previous ideas regarding the role of osteoderms as calcium reservoirs. We found that G. gecko and other gecko species with osteoderms have highly enlarged endolymphatic sacs relative to their body size, when compared to species without osteoderms, which implies that these membranous structures might fulfill a major role of calcium storage even in species with osteoderms.     

Posture, speed, and habitat structure: three-dimensional hindlimb kinematics of two species of padless geckos

Differences in habitat use are often correlated with differences in morphology and behavior, while animals in similar habitats often exhibit similarities in form and function. However, this has not been tested extensively among lizards, especially geckos. Most studies of gecko locomotion have focused on the ability to adhere to surfaces. However, there are several species of geckos that have either secondarily lost adhesive capabilities or simply lack the capability. We quantified the three-dimensional locomotor kinematics for two desert-dwelling padless geckos, Teratoscincus scincus and Eublepharis macularius, on a level trackway over a range of speeds. Our results indicate that T. scincus landed with a high relative hip height of 48.7 ± 2.4% of total limb length at footfall, while E. macularius exhibited hip heights averaging only 36.0 ± 1.8% of total limb length for footfall. The three-dimensional knee angle of T. scincus averaged 120.6 ± 3.9° at footfall, while E. macularius averaged only 101.6 ± 1.8° at footfall. In addition, the femur of E. macularius was elevated to a much greater extent (i.e., was closer to being perpendicular to the long axis of the body) than that of T. scincus and every other lizard that has been studied, suggesting they move with a “hyper-sprawled” posture. Both of these gecko species live in deserts, but T. scincus is psammophilic while E. macularius inhabits a rocky, more densely vegetated environment. Benefits of the more upright posture of T. scincus on open sandy habitat may include a greater field of view and more efficient locomotion. The more sprawled posture of E. macularius may lower its center of gravity and aid in balance while climbing on rocks or shrubs.     

Nesting in a thermally challenging environment: nest‐site selection in a rock‐dwelling gecko,Oedura lesueurii (Reptilia: Gekkonidae)

In egg‐laying species, maternal oviposition choice can influence egg survival and offspring phenotypes. According to the maternal‐preference offspring‐performance hypothesis, females should choose oviposition sites that are optimal for offspring fitness. However, in thermally challenging environments, maternal oviposition behaviour may be constrained by the limited availability of suitable oviposition sites. We investigated nest‐site selection in a nocturnal lizard [velvet gecko Oedura lesueurii (Duméril and Bibron)] that inhabits a thermally challenging environment in south‐eastern Australia. The viability of these gecko populations is critical for the persistence of an endangered snake species (Hoplocephalus bungaroides Wagler) that feeds heavily on velvet geckos. Female geckos chose nest sites nonrandomly, with 87% of nests (N = 30) being laid in deep crevices. By contrast, only 13% of clutches were laid under rocks, which were the most readily available potential nest sites. Nest success in crevices was high (100%), but no eggs hatched from nests under rocks. Temperatures in nest crevices remained relatively low and constant throughout the incubation period (mean = 22.7 °C, range 21.0–24.5 °C), whereas thermal regimes under rocks showed large diurnal fluctuations. Geckos selected crevices that were deeper, had less canopy cover, and were warmer than most available crevices; in 85% of cases, such crevices were used simultaneously by more than one female. The thermally distinctive attributes of nest sites, and their frequent communal use, suggest that nest sites are a scarce resource for female velvet geckos, and that the shading of rock outcrops through vegetation encroachment may influence nest success in this species. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 250–259.     

Patterns of plant visitation by nectar-feeding lizards

Geckos in the genus Hoplodactylus visit flowers to feed on nectar. I examined the patterns of flower visitation exhibited by two gecko species (H. maculatus and H. duvauceli) having access to two plant species: pohutukawa (Metrosideros excelsa: Myrtaceae) and flax (Phormium tenax: Agavaceae). Individual geckos were not observed to visit both plant species; individuals visiting flax tended to revisit the same plant. Geckos visiting pohutukawa were larger than those visiting flax and exhibited an early night peak in plant visitation, while lizards on flax displayed a more even pattern of activity throughout the night. On flax, geckos were more likely to be found on plants with a greater number of male flowers. Male flax flowers were of greater diameter than female flowers and produced nectar at higher rates and with greater concentrations of sugars. Experimental manipulation of pohutukawa nectar volumes suggested that the distribution of geckos is influenced by the pattern of nectar availability.     

An experimental investigation of the competitive displacement of a native gecko by an invading gecko: no role for parasites

On islands across the Pacific the invasion of the gecko Hemidactylusfrenatus has caused a decline in the abundance of a resident gecko, Lepidodactyluslugubris. In a previous study we demonstrated that the prevalence of the cestode Cylindrotaenia sp. is higher in the resident gecko on islands where it is sympatric with the invader than on islands where it occurs alone. In the present study we experimentally test whether the presence of the invading gecko causes an increase in parasites, particularly Cylindrotaenia sp., in the resident. In addition, we test whether the effect of the invader on parasite prevalence in the resident is mediated through an increase in corticosterone in the resident. Corticosterone is the primary glucocorticoid, or “stress” hormone in lizards, and chronic elevation in corticosterone may suppress some types of immune responses. After experimental manipulations of interspecific interactions (single vs. mixed species treatments) and intraspecific densities (high vs. low), we detected no difference in parasite prevalence or circulating corticosterone among the experimental treatments in either L. lugubris or H. frenatus. Circulating levels of corticosterone were higher in geckos␣sampled at night than geckos sampled during the day, indicating a circadian cycle in corticosterone levels in these nocturnal animals. Circulating levels of corticosterone were higher in experimental geckos than in geckos that had not been used in the experiment, and, in some groups, higher in geckos infected with cestodes than in uninfected geckos. Circulating levels of corticosterone did not differ between non-experimental H. frenatus and L. lugubris, but when geckos used in the experiment were compared, circulating levels of corticosterone were significantly higher in H.␣frenatus than in L. lugubris. Received: 17 March 1997 / Accepted: 5 December 1997     

Step on it: can footprints from tracking tunnels be used to identify lizard species?

There are few effective or efficient established methods for monitoring cryptic herpetofauna. Footprint tracking tunnels are routinely used to index small mammal populations, but also have potential for monitoring herpetofauna. We evaluated the utility of tracking tunnels for identification of New Zealand lizards using captive- and wild-sourced animals (four skink and eight gecko species). All skink prints that we obtained were indistinct or obscure, but we obtained relatively clear, measurable prints for all gecko species. We found that identification to species level was possible for the two gecko species for which we had a large sample—Naultinus gemmeus and Woodworthia ‘Otago large’—using linear discriminant analysis (the best model correctly assigned 96.1% of individuals). Our findings suggest that footprints from tracking tunnels may be used to distinguish between species of geckos. Additional research is needed to assess the ability to further discriminate intra- and inter-genera lizard footprints from tracking tunnels, and the utility of the technique for surveying and monitoring lizard populations.     

Gecko vision—visual cells,evolution, and ecological constraints

Geckos comprise both nocturnal and diurnal genera, and between these categories there are several transitions. As all geckos depend on their visual sense for prey capture, they are promising subjects for comparison of morphological modifications of visual cells adapted to very different photic environments. Retinae of 22 species belonging to 15 genera with different activity periods are examined electron microscopically. Scotopic and photopic vision in geckos is not divided between “classical” rods and cones, respectively; both are performed by one basic visual cell type. Independent of the activity periods of the individual species, the visual cells of geckos exhibit characteristics of cones at all levels of their ultrastructure. Thus, gecko retinae have to be classified as cone retinae. Only the large size and the shape of the photoreceptor outer segments in nocturnal geckos are reminiscent of rods; the outer segments are up to 60 μm in length and up to 10 μm in diameter. The visual cells of diurnal geckos have considerably smaller outer segments with lengths ranging from 6 to 12 μm and diameters ranging from 1.3 to 2.1 μm. Nocturnal and diurnal species differ in the structure of their ellipsoids. One type of visual cell in nocturnal geckos has modified mitochondria with either rudimentary cristae or no cristae at all, and one type of visual cell in diurnal geckos possesses an oil droplet. The visual cells of Phelsuma guentheri and Rhoptropus barnardi are intermediate between those of nocturnal and diurnal species.     

The relationship between habitat use and body shape in geckos

Geckos are a highly diverse group of lizards, with more than 1,700 species that exhibit a wide range of behaviors, ecologies, and sizes. However, no study has examined links between habitat use and body shape in pad-bearing geckos. We set out to answer a basic question using a data set of pad-bearing geckos (112 species, 103 pad-bearing, 9 padless, 42 genera): Do geckos that occur in different habitats also differ in body shape? Overall, we found that body shape was surprisingly similar among our sample of pad-bearing species, with the exception of the genus Uroplatus, which was clearly distinct from other geckos due to its depressed body and long limbs. However, the padless geckos differed in body shape from the pad-bearing geckos by having longer arms and legs and less rotund bodies. We found that about half of the pad-bearing species primarily inhabit trees, with the other half, divided approximately equally among rocks, the ground, and mixed habitats. We found no significant links between habitat use and body shape, nor any propensity for larger species to occupy different habitats than smaller species. Padless species tend to inhabit rock and ground substrates. Our results indicate that pad-bearing geckos have a relatively uniform body form, which contrasts with to their diversity in color, size, and behavior. Indeed, our data show that the general gecko body shape is suitable for a wide range of habitats, ranging from arboreal to terrestrial. This pattern is a departure from other ecomorphological studies and suggests that geckos may not easily fit into the mold of adaptive radiation, as suggested by prior studies.     

Do all geckos hatch in the same way? Histological and 3D studies of egg tooth morphogenesis in the geckos Eublepharis macularius Blyth 1854 and Lepidodactylus lugubris Duméril & Bibron 1836

The egg tooth of squamates evolved to facilitate hatching from mineralized eggshells. Squamate reptiles can assist their hatching with a single unpaired egg tooth (unidentates) or double egg teeth (geckos and dibamids). Egg tooth ontogeny in two gekkotan species, the leopard gecko Eublepharis macularius and the mourning gecko Lepidodactylus lugubris, was compared using microtomography, scanning electron microscopy, and light microscopy. Investigated species are characterized by different hardnesses of their eggshells. Leopard geckos eggs have a relatively soft and flexible parchment (leathery) shell, while eggshells of mourning geckos are hard and rigid. Embryos of both species, like other Gekkota, have double egg teeth, but the morphology of these structures differs between the investigated species. These differences in shape, localization, and spatial orientation were present from the earliest stages of embryonic development. In mourning gecko, anlagen of differentiating egg teeth change their position on the palate during embryonic development. Initially they are separated by condensed mesenchyme, but later in development, their enamel organs are connected. In leopard geckos, the localization of egg tooth germs does not change, but their spatial orientation does. Egg teeth of this species shift from inward to outward orientation. This is likely related to differences in structure and mechanical properties of eggshells in the studied species. In investigated species, two hatching mechanisms are possible during emergence of young individuals. We speculate that mourning geckos break the eggshell through puncturing action with egg teeth, similar to the pipping phase of chick and turtles embryos. Egg teeth of leopard geckos cut egg membranes similarly to most squamates. Our results also revealed differences in egg tooth implantation between Gekkota and Unidentata: gekkotan egg teeth are subthecodont (in shallow sockets), while those in unidentates are acrodont (attached to the top of the alveolar ridge). © 2020 Wiley Periodicals LLC     

Interactions between native and invasive gecko lizards in tropical Australia

Invasive geckos of the genus Hemidactylus (Gekkonidae) are spreading rapidly through urban environments in many tropical and subtropical parts of the world. The invaders have caused rapid declines in native gecko abundance in some areas, but their interactions with Australian native species remain unknown. In a small rural village near Darwin, we found that Hemidactylus frenatus is abundant around both lighted and unlighted buildings, but rarely found in surrounding bushland. It is sympatric with the larger Gehyra australis (Gekkonidae) in this disturbed site, and often forages on the same buildings, but is active mostly during the dry‐season (vs. wet‐season for G. australis) and is competitively subordinate to the larger native species. In laboratory encounters, H. frenatus fled from G. australis, and modified its refuge‐site use in the presence of the native lizard. In those same trials, the native gecko often attacked and rarely fled; and did not shift its refuge‐site selection. In field surveys, the two taxa frequently co‐occurred. However, substrate use of the invasive H. frenatus was modified by the presence of the native G. australis, consistent with competitive displacement. Our counts of H. frenatus were highest during the dry‐season, when G. australis (like most other small native reptiles) is relatively inactive. The invasive gecko thus appears to be exploiting a ‘vacant niche’ around buildings, rather than displacing the native gecko taxon. This outcome may reflect the size disparity between the native species and the invader; Hemidactylus frenatus may well have significant ecological impacts on smaller native lizards.     

Sexual dimorphism and interpopulation differences in lizard hind limb length: locomotor performance or chemical signalling?

Intraspecific variation in morphology has often been related to fitness differences through its effects on performance. In lizards, variation in hind limb length can be shaped by natural selection for increased locomotor performance, sexual selection on the number or size of femoral pores involved in chemical signalling, or both. Here, we analyse the selective forces involved in sexual dimorphism and differences in hind limb length between two populations of Psammodromus algirus living at different elevation. Males were more robust and had longer hind limbs and limb segments than females, and low‐elevation lizards had longer limbs than high‐elevation lizards. However, differences in locomotor performance were small and non‐significant, making natural selection for faster runs an unlikely explanation for the observed pattern. On the other hand, males had more femoral pores than females, and lizards had more pores at lower elevation, although the difference was significant only for males (which invest more in chemical signalling). In males, the number of pores, which remains constant along a lizard's life, was not correlated with hind limb length. However, femur length was positively correlated with mean pore size, allowing low‐elevation males to have larger than expected pores, which could increase the effectiveness with which they spread their signals in a dry and warm habitat where chemicals become volatile rapidly. Also, saturation of the sexual coloration of the head was higher for low‐elevation males, suggesting that sexual selection pressures may be more intense. Overall, our results indicate that sexual selection plays a significant role in shaping intraspecific variation in hind limb length. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104 , 318–329.     

Geographic variation in antisnake tactics: the evolution of scent-mediated behavior in a lizard

We used modern comparative methods to examine the evolution of scent-mediated antisnake behavior in the rock-dwelling velvet gecko (Oedura lesueurii). The selective agent is a snake species (broad-headed snake, Hoplocephalius bungaroides) that feeds primarily on velvet geckos by remaining sedentary in rock crevices for days or weeks, waiting to ambush lizards. The past and present distribution of this predator is well documented because of its threatened conservation status. We used this information to sample lizards from three populations distributed with snakes (sympatric) and three populations that appear never to have been distributed with snakes (allopatric) in each of two widespread but geographically distinct genetic groups of velvet gecko (as determined using allozyme electrophoresis). Wild-caught immature geckos from sympatric populations showed higher tongue-flick rates and stronger shifts in locomotion (increased duration of crawling and remaining stationary while pressed against the rock) toward snake-scented rocks than did lizards from allopatric populations. However, predation environment did not significantly affect a lizard's tendency to display other typical antisnake tactics such as tail waving or fleeing. These results were highly repeatable across the two sampled genetic groups of velvet gecko, despite demonstrable genetic divergence between groups. Experiments with hatchling lizards that had no experience with predators indicate that qualitative components of antisnake behaviors are probably inherited. The method of phylogenetically independent contrasts strongly suggests that the presence or absence of snakes has driven the evolution of behavior in velvet geckos. Collectively, these results provide support for an often suggested but speculative expectation that prey can adapt to predation pressure on a local scale.