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.     

Armored geckos: A histological investigation of osteoderm development in Tarentola (Phyllodactylidae) and Gekko (Gekkonidae) with comments on their regeneration and inferred function

Osteoderms are bone‐rich organs found in the dermis of many scleroglossan lizards sensu lato, but are only known for two genera of gekkotans (geckos): Tarentola and Gekko. Here, we investigate their sequence of appearance, mode of development, structural diversity and ability to regenerate following tail loss. Osteoderms were present in all species of Tarentola sampled (Tarentola annularis, T. mauritanica, T. americana, T. crombei, T. chazaliae) as well as Gekko gecko, but not G. smithii. Gekkotan osteoderms first appear within the integument dorsal to the frontal bone or within the supraocular scales. They then manifest as mineralized structures in other positions across the head. In Tarentola and G. gecko, discontinuous clusters subsequently form dorsal to the pelvis/base of the tail, and then dorsal to the pectoral apparatus. Gekkotan osteoderm formation begins once the dermis is fully formed. Early bone deposition appears to involve populations of fibroblast‐like cells, which are gradually replaced by more rounded osteoblasts. In T. annularis and T. mauritanica, an additional skeletal tissue is deposited across the superficial surface of the osteoderm. This tissue is vitreous, avascular, cell‐poor, lacks intrinsic collagen, and is herein identified as osteodermine. We also report that following tail loss, both T. annularis and T. mauritanica are capable of regenerating osteoderms, including osteodermine, in the regenerated part of the tail. We propose that osteoderms serve roles in defense against combative prey and intraspecific aggression, along with anti‐predation functions. J. Morphol. 276:1345–1357, 2015. © 2015 Wiley Periodicals, Inc.     

Morphology and morphometrics of the appendicular musculature in geckoes with different locomotor habits (Lepidosauria)

 In this study a ground-dwelling (Eublepharis macularius) and a highly specialised climbing (Gekko gecko) lizard were chosen as study objects. The fore- and hindlimbs of two individuals of each species were dissected, and muscle masses, mean fibre lengths, cross-sectional areas and moment arms were determined. Special attention was paid to general muscle architecture (origin, insertion, fibre orientation, etc.) and pennation angles. Using these variables (cross sectional areas and moment arms), maximal moments exertable across the shoulder/hip, elbow/knee and wrist/ankle were calculated for both species. In accordance with the biomechanical predictions related to the preferred locomotor substrate of each species (i.e. level running for E. macularius and climbing for G. gecko), the results of this study indicate that climbers such as G. gecko generally possess powerful retractor muscles crossing the shoulder and hip joints. Additionally, the specialised climber is able to exert higher flexion moments across the elbow, which prevents the animals from falling backwards. However, G. gecko appears to be constrained in its ankle extension capabilities by the presence of the adhesive toe pads. The level-running species, on the other hand, shows a relatively stronger development of the extensor muscles in the lower limbs, allowing these lizards to run in an erect posture. In general, both species show large similarities on a gross morphological level as expected when considering their phylogenetic relatedness. Adaptations to their preferred locomotor substrate only become apparent when considering the functional properties (i.e. joint moments) of the appendicular musculature. Accepted: 30 November 1998     

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, ●● , ●●–●●.     

Evolutionary patterns in the terebratulid genus Caryona Cooper (Brachiopoda,Jurassic of France)

The study of ontogenetic and morphological changes in different species of the brachiopod genus Caryona COOPER (Terebratulidae) from the Lower Callovian‐Lower Oxfordian of northern France shows a succession (and an interference) of processes which vary according to the characters studied. This is an example of “mosaic evolution”;. The ontogenetic changes result from heterochrony, especially acceleration and hypermorphism. The main phylogenetic tendency is peramorphosis in most characters. This evolutionary pattern agrees with phyletic gradualism.

Moreover, analysis of the internal characters demonstrates the limited value of these in discrimination of the various genera.     

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.     

Comparative studies on the structure and adhesion of setae in <Emphasis Type="Italic">G. gecko</Emphasis> and <Emphasis Type="Italic">G. swinhonis</Emphasis>

Scanning electron microscopy (SEM) and histological techniques were used to observe and study the setae structures of two gecko species (G. gecko and G. swinhonis) and the relationships between these structures and the adhesive forces. The SEM results showed that the setae of these two species were densely distributed in an orderly fashion, and branched with curved tips. The setae of G. gecko had cluster structures, each cluster containing 4–6 setae whose terminal branches curved towards the center of the toes at ∼ 10°, the tips of the branches like spatulae and densely arrayed at an interval of less than 0.2–0.3 μm. On the contrary, the branch tips in the setae of G. swinhonis were curled, and the terminal parts of setae curved towards the center of the toes at various angles. Usually the setae of these gecko species branch twice at the top at intervals greater than that of G. gecko. The histological observation found that inside the setae of these two species there were plenty of unevenly distributed contents, such as epithelia, fat cells, pigmental cells and muscle tissue, but no gland cells existed. The results of functional experiments suggested that modifying the structure of gecko’s setae could reduce its adhesive ability dramatically, demonstrating the positive correlation between the structure of the gecko’s setae and its adhesive ability. The above results provide important information in designing bio-mimic setae and bio-gecko robots.     

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.     

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.     

Cranial musculature of South American Gekkonidae

The cranial myology of 13 South American geckos was compared and analyzed for taxonomic significance. The general pattern emerges that muscles in this group do not vary substantially from those of other lizards, except that the geckonids have fewer muscle layers. The former condition is particularly important with respect to the adductor musculature of the jaw, given its fundamental role in the chewing process. A great variety of lizards, both those with the geckonid bauplan and those with other morphologies exhibit similar basic structures in the jaw adductor muscles, despite significant differences in diet. There appears to be no direct correlation between diet and the morphology of head musculature of lizards. It is hypothesized that differences between and within bauplans can be ascribed to phylogenetic factors rather than to functional characteristics such as diet and life-styles. Twenty characteristics reflecting minor variations in the Gekkotan bauplan were selected for comparison in performing a cladistic analysis rooted on the sphaerodactylinid geckoes Coleodactylus amazonicus and C. septentrionalis. Groupings of muscular characteristics resulting from this analysis lead to different interpretations of taxonomic relationships from those derived from previous studies on the taxa examined. © 1996 Wiley-Liss, Inc.     

DISPERSAL AND EVOLUTION OF THE PACIFIC BASIN GEKKONID LIZARDS GEHYRA OCEANICA AND GEHYRA MUTILATA

The Pacific island geckos Gehyra mutilata and Gehyra oceanica were studied on several Pacific Basin archipelagos to determine the degree that their distributions have been modified by humans (as commensals), through the analysis of protein variation using starch gel electrophoresis. Gehyra mutilata is an anthropophilic species that is widespread in the Pacific Basin and Southeast Asia. No protein variation was found in the Pacific Basin and southern Asia, although there were fixed allelic differences between populations of southern Asia and those further north. These results suggest possible recent human-aided transport across the Pacific from a population that experienced a genetic bottleneck in southern Asia. Gehyra oceanica, based on protein variation, consists of two natural groups in the Pacific, a northern (Micronesian) form and a southern (Melanesian and Polynesian) form. The northern form has very similar gene frequencies across its range in Micronesia. The southern form has its greatest allelic diversity in the south-central Pacific. F-statistics for G. oceanica in the south fall within the range of values in the literature for mainland Australian species of Gehyra that are not human commensals and for other island lizards that have been considered as natural dispersers. These values are consistent with the hypothesis that G. oceanica was naturally dispersed across the Pacific, prior to the arrival of humans and that the equatorial currents are a barrier to natural, north-south gene flow/dispersal in Pacific Basin lizards. However, human-aided dispersal within the northern and southern regions cannot be ruled out. By comparing the ecology of these two species, G. oceanica has the adaptations necessary for natural oversea dispersal, whereas G. mutilata has an ecology consistent with human-mediated dispersal, in support of the conclusions from the genetic data.     

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.     

Comparative studies on the structure and adhesion of setae in G. gecko and G. swinhonis

Scanning electron microscopy (SEM) and histological techniques were used to observe and study the setae structures of two gecko species (G. gecko and G. swinhonis) and the relationships between these structures and the adhesive forces. The SEM results showed that the setae of these two species were densely distributed in an orderly fashion, and branched with curved tips. The setae of G. gecko had cluster structures, each cluster containing 4-6 setae whose terminal branches curved towards the center of the toes at ~ 10o, the tips of the branches like spatulae and densely arrayed at an interval of less than 0.2―0.3 μm. On the contrary, the branch tips in the setae of G. swinhonis were curled, and the terminal parts of setae curved towards the center of the toes at various angles. Usually the setae of these gecko species branch twice at the top at intervals greater than that of G. gecko. The histological observation found that inside the setae of these two species there were plenty of unevenly distributed contents, such as epithelia, fat cells, pigmental cells and muscle tissue, but no gland cells existed. The results of functional experiments suggested that modifying the structure of gecko's setae could reduce its adhesive ability dramatically, demonstrating the positive correlation between the structure of the gecko's setae and its adhesive ability. The above results provide important information in designing bio-mimic setae and bio-gecko robots.     

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.     

Genetic variability of the tokay gecko based on microsatellite analysis

The black-spotted tokay gecko and red-spotted tokay gecko have different distribution areas and are significantly different in appearance but are classified into the same species Gekko gecko. Twelve microsatellite loci were isolated, characterized and evaluated from wild black-spotted tokay geckos for the first time. Of them, nine loci were successfully amplified in red-spotted tokay geckos using multiplex polymerase chain reactions (PCRs). A total of 208 different alleles were observed in the 70 wild black-spotted and red-spotted tokays, and the average number of alleles per locus was 17.3. The average values for observed heterozygosity, expected heterozygosity and polymorphism information content were 0.762, 0.891 and 0.871, respectively, which showed that the wild G. gecko population had a high level of genetic variability. Both black-spotted tokays and red-spotted tokays showed a significant (P < 0.001) deficit of heterozygotes. The red-spotted tokay (H_E = 0.881, A = 16.4) had a higher level of genetic variability than black-spotted tokay (H_E = 0.804, A = 10.7). The pairwise F_ST (P < 0.001) estimates of the two types of tokay were 0.143, which indicated that there was a significant level of genetic differentiation between the two.     

Ultrahydrophobicity indicates a non-adhesive default state in gecko setae

Geckos may represent the world’s most demanding adhesives application. The adhesive setae on the toes of climbing geckos must adhere strongly yet avoid fouling or attachment at inappropriate times. We tested the hypothesis that gecko setae are non-adhesive in their unloaded default state by comparing the water droplet contact angle (θ) of isolated setal arrays to the smooth surface of eye spectacle scales of tokay geckos (Gekko gecko). At equilibrium, θ was 98.3 ± 3.4° in spectacle scales of live geckos and 93.3 ± 3.5° in isolated spectacles. Isolated setal arrays were ultrahydrophobic, with θ of 160.6 ± 1.3° (means ± SD). The difference in θ of setal arrays and smooth spectacles indicates a very low contact fraction. Using Cassie’s law of surface wettability, we infer that less than 6.6% of the surface of unloaded setae is solid and at least 93.4% is air space. We calculated that the contact fraction must increase from 6.6% in the unloaded state to 46% in the loaded state to account for previously measured values of adhesion. Thus gecko setae may be non-sticky by default because only a very small contact fraction is possible without mechanically deforming the setal array.     

Total lactate dehydrogenase activity of tail muscle is not cold-adapted in nocturnal lizards from cool-temperate habitats

The dependence of metabolic processes on temperature constrains the behavior, physiology and ecology of many ectothermic animals. The evolution of nocturnality in lizards, especially in temperate regions, requires adaptations for activity at low temperatures when optimal body temperatures are unlikely to be obtained. We examined whether nocturnal lizards have cold-adapted lactate dehydrogenase (LDH). LDH was chosen as a representative metabolic enzyme. We measured LDH activity of tail muscle in six lizard species (n = 123: three nocturnal, two diurnal and one crepuscular) between 5 and 35 °C and found no differences in LDH-specific activity or thermal sensitivity among the species. Similarly, the specific activity and thermal sensitivity of LDH were similar between skinks and geckos. Similar enzyme activities among nocturnal and diurnal lizards indicate that there is no selection of temperature specific LDH enzyme activity at any temperature. As many nocturnal lizards actively thermoregulate during the day, LDH may be adapted for a broad range of temperatures rather than adapted specifically for the low temperatures encountered when the animals are active. The total activity of LDH in tropical and temperate lizards is not cold-adapted. More data are required on biochemical adaptations and whole animal thermal preferences before trends can be established.     

Comparative myology of the forelimb of Liolaemus sand lizards (Liolaemidae)

The lizard genus Liolaemus includes numerous constituent clusters of putatively related taxa, one of which is the Liolaemus boulengeri group, which in turn includes the sand lizards (of the Liolaemus wiegmannii subgroup). Members of the sand lizard group exhibit three different modes of burying into sand. The general morphology of the forelimb muscles of those Liolaemus species is analysed. Herein, we present a study of the forelimb musculature of all species considered by Halloy et al. (1998). This study has three principal goals. First, we are seeking myological characters that will be useful in formulating phylogenetic hypothesis about the species of Liolaemus. With these characters, we also wish to compile morphological data that represent the morphological space implied in the diverse locomotor behaviours of these animals. Second, we are looking for derived features that reflect functional changes in the use of forelimb. Third, we wish to provide a cladistic analysis that can be used to test phylogenetic hypothesis derived from other sources of data. We present 48 characters in a data set and analyse it cladistically. We obtained a hypothesis of relationships of the Liolaemus species and compared this with previous hypotheses based on other characters. The trees obtained are not congruent with previously proposed phylogenies. We were unable to identify in our trees nodes that are based on structures reflecting functional changes in the use of the forelimb. The morphological similarities in the forelimb musculature of all species analysed seems to conform a very conservative general anatomical pattern with which Liolaemus sand lizards perform most of their locomotor behaviours.