Temperature effects on oxygen consumption of two nocturnal geckos,Ptyodactylus hasselquistii (Donndorff) andBunopus tuberculatus (Blanford) (Reptilia: Gekkonidae) in Saudi Arabia

Summary Oxygen consumption rates of the lizardsPtyodactylus hasselquistii (adult and subadults) andBunopus tuberculatus (adult) were determined in relation to ambient temperatures ranging from 10 to 35°C using a double-chamber, volumetric closed system. The metabolic rate-temperature curves for both species were triphasic and similar in shape, but O₂ consumption differed between species.The low thermal dependence at temperatures between 15 and 25°C, common to both species, was correlated with the lizards' dual mode of thermoregulatory activity and ecology.     

Development of the subdigital adhesive pads of Ptyodactylus guttatus (Reptilia: Gekkonidae)

Subdigital adhesive pads play an important role in the locomotion of many species of gekkonid lizards. These pads consist of integrated components derived from the epidermis, dermis, vascular system, subcuticular tendons, and phalanges. These components become intimately associated with each other during the developmental differentiation of the digits and the sequence of this integration is outlined herein in Ptyodactylus guttatus. The pads initially appear as paired swellings at the distal tips of the digits. Subsequently, a fan-like array of naked scansors develops on the ventral surface of each digit, at about the same time that scales differentiate over the surface of the foot as a whole. At the time of appearance of the naked scansors, the vascular sinus system of the pad also differentiates, along with subcuticular connective tissue specializations. At this stage the digits, along with the rest of the body, are clad in an embryonic periderm. Only after hatching and as the periderm is shed, do the epidermal setae and spines appear. The developmental sequence described here is consistent with predictions previously advanced about the evolutionary origin and elaboration of subdigital pads in gekkonid lizards. The paucity of available staged embryonic material leaves many questions unresolved.     

A new endemic gecko (Reptilia: Gekkonidae) from Mauritius

A previously undescribed gecko, Nactus coindemirensis sp. nov. is reported from Gunner's Quoin, a small island off Mauritius. Nactus coindemirensis is not especially closely related to the other Mauritian member of the genus, N. serpensinsula; thus, it is likely that the precursors of these two species reached Mauritius separately, rather than both being descended from a single colonizer. Unlike other Mauritian reptiles now known only from small off-shore islands, N. coindemirensis coexists with rats, perhaps because it can evade them by taking refuge in small holes and crevices of the basalt it inhabits. This raises the possibility that it may still survive on other islands with rats, including Mauritius itself, but has escaped notice because of its size and cryptic behaviour.     

The phylogeography of the gecko Cyrtopodion kotschyi (Reptilia: Gekkonidae) in the Aegean archipelago

Cyrtopodion kotschyi is a small gecko, widely distributed on the islands of the Aegean archipelago and the adjacent mainland. We unveiled the phylogeography of the species by using a portion of the cytochrome oxidase I mitochondrial DNA gene from 35 insular and mainland populations. The distinct geographic distribution of the major clades of the phylogenetic tree and its topology suggest a spatial and temporal sequence of phylogenetic separations that coincide with some major paleogeographical separations during the geological history of the Aegean and support a mainly vicariant pattern of differentiation. The separation times and 95% confidence limits among the different clades were estimated according to two different paleogeographical scenarios. The very high interpopulation genetic divergence (up to 20% uncorrected pairwise distances) and the better concordance between paleogeographical and phylogenetic separations for one of the scenarios suggest that species differentiation started during Miocene (about 10 Mya) due to the fragmentation of the united landmass of "Agais" that was Aegean at that time.     

Isospora ptyodactyli n. sp. (Apicomplexa: Eimeriidae), a new coccidian parasite of the fan-footed gecko Ptyodactylus puiseuxi Boutan, 1893 (Reptilia: Gekkonidae) from Jordan

Faecal samples from 17 fan-footed geckoes Ptyodactylus puiseuxi Boutan were examined for coccidian parasites. Five geckoes (29%) were found to be passing oöcysts of the genus Isospora Schneider. Comparison with other members of the genus Isospora indicates that the coccidian found represents a new species. Sporulated oöcysts of I. ptyodactyli n. sp. are spherical or subspherical, 22.1 (19.0–24.0) × 21.2 (18.0–23.0) µm, with a shape-index (length/width) of 1.04; and a smooth and bilayered oöcyst wall, 1.0–1.5 µm thick. A micropyle, oöcyst residuum and polar granule are absent. The sporocysts are ellipsoidal, 12.2 (11.0–14.0) × 8.0 (7.5–9.0) µm, with a shape index of 1.5 (1.4–1.9). Stieda and substieda bodies are present, the Stieda body being knob-like and the substieda body spherical to subspherical. A sporocyst residuum is present and composed of numerous granules of different size scattered among the sporozoites. The sporozoites are vermiform, with a slightly granulated surface appearance, and are arranged head to tail within the sporocyst. Most oöcysts have still to sporulate when excreted; sporulation was completed within 12 h at 25 °C. Endogenous development occurs inside the nuclei of enterocytes in the small intestine.     

Sexual characteristics and spermatogenesis in males of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia, Gekkonidae)

Obligately parthenogenetic lizards usually are all-female populations of hybrids producing diploid oocytes by premeiotic endomitosis and quasi-normal meiosis. In an all-female strain of the gekkonid lizard Lepidodactylus lugubris several phenotypic males arose spontaneously. The sexual characteristics of these males were studied using light and electron microscopy and compared with normal males of the bisexual genus Lygodactylus. Emphasis was layed on morphology of seminiferous tubules, occurrence of spermatogenic stages and ultrastructure of spermatozoa. The phenotypic males possessed preanal pores filled with secretions and a sexual nephric segment which were exactly the same as in normal, reproductively active males. In the testes, density and morphology of non-spermatogenic cell types, the Leydig and Sertoli cells, indicate a normal production of testicular testosterone and a normal function of the blood-testis barrier, respectively. Both in the normal and the phenotypic males, all meiotic cell types of spermatogenesis can be recognised in the seminiferous tubules and are apparently identical, indicating a normal meiosis without impairment in the phenotypic males. In contrast, the differentiation process of spermatids is markedly disturbed in the phenotypic males of L. lugubris. In the normal male, spermiogenesis results in mature spermatids and spermatozoa with small elongated nuclei, an acrosomal complex, and a flagellar tail possessing one axoneme. Spermatozoa fill both the lumen of most seminiferous tubules and the lumina of ductus epididymidis and ductus deferens. In the phenotypic male, spermiogenesis results in seemingly normal spermatids and in spermatozoa with large, non-elongated, deformed nuclei and/or irregular tails possessing more than one axoneme. Both the lumen of most seminiferous tubules and the lumina of the ductus epididymidis and the ductus deferens contain relatively few spermatozoa. We suggest that the phenotypic males inherited the ability for a premeiotic endomitosis from their all-female ancestral lineage. While in females this leads to quasi-normal meiosis and diploid oocytes capable of development, the small nuclei of the spermatozoa are unable to contain a diploid set of chromosomes. Because of the high amount of deformed spermatozoa and possibly uncontrolled loss of genetic material in structurally normal, but aneuploid spermatozoa we conclude that these otherwise perfect males are infertile, thus constituting another example of gametic sterility.     

Complete mitochondrial genome of the red-spotted tokay gecko (Gekko gecko, Reptilia: Gekkonidae): comparison of red- and black-spotted tokay geckos

Here, we sequenced the complete mitochondrial genome of the red-spotted tokay gecko (Squamata: Gekkonidae). The genome is 16,590 bp in size. Its gene arrangement pattern was identical with that of black-spotted tokay gecko. We compared the mitochondrial genome of red-spotted tokay gecko with that of the black-spotted tokay gecko. Nucleotide sequence of the two whole mitochondrial genomes was 97.99% similar, and the relatively high similarity seems to indicate that they may be separated at the subspecies level. The information of mitochondrial genome comparison of the two morphological types of tokay gecko is discussed in detail.     

Conditioning reduces metabolic rate and time to steady-state in the lizard Naultinus manukanus (Reptilia: Gekkonidae)

The rate of oxygen consumption (VO2) is commonly used as a measure of whole organism metabolic rate, but requires the animal to be motionless and at rest. Few studies have measured whether animals that appear motionless are truly at rest, or whether being in a novel environment elevates metabolic rate. We investigated whether conditioning of the gecko Naultinus manukanus to experimental procedures influenced the VO2 and probability of achieving a constant rate of oxygen consumption. Metabolic rate was measured at 24 degrees C in 22 individuals until a steady-state was achieved, or for 80 min if no steady-state was reached, once a day on 5 consecutive days (five trials). Geckos in the first trial, when compared with subsequent trials, had a significantly higher mass-adjusted VO2 (0.89+/-0.06 vs. 0.67+/-0.05 ml O2 h(-1), respectively), and time to reach a steady-state VO2 (66+/-8 vs. 47+/-3 min, respectively), as well as a significantly lower probability of reaching a steady-state VO2 (24% vs. 74%, respectively). We conclude that there may be hidden inaccuracies in studies that do not condition animals and that at least one conditioning trial should be used to obtain a metabolic rate at rest for small lizards.     

Gas exchange morphometry of the lungs of the tokay,Gekko gecko L. (Reptilia: Squamata: Gekkonidae)

The tokay lizard (Gekko gecko) possesses singlechambered lungs, eacch of which is a mirror image of the other reflected in the midsagittal body plane. When standard techniques are employed for instilling 2% phosphate-buffered glutaraldehyde to three-quarters of the total lung capacity, neither the left nor the right lung is consistently larger. Internally, the lungs are characterized by a row of 11 dorsomedial niches and by honeycomb-like (faveolar) gas exchange tissue, which is deeper cranially than caudally. Based upon mean values for all experimental animals, a 100-g tokay would have an overall anatomical diffusion factor (respiratory surface area divided by the appropriate _ht) of 203 cm²·m^-1·100 g^-1, 61% of which is located on the interfaveolar septa. Of the total septal anatomical diffusion factor, 94% is evenly divided between the anterior and middle thirds of the lung, with 6% in the posterior third. The 39% of the anatomical diffusion factor located on the inner lung wall is predominantly (76%) in the middle and posterior lung thirds, with only 24% in the anterior region. These tendencies toward heterogeneous distribution of anatomical diffusion factor were most pronounced in a 55 g juvenile animal. In this animal the total anatomical diffusion faxtor/body mass was 3.6 times that of a 197 g adult. This difference was attributable to a greater body massspecific lung volume and respiratory surface area as well as to a greater surface-to-volume ratio in the parenchyma and to a thinner air-blood diffusion barrier in the juvenile animal.Abbreviations ADF anatomical diffusion factor - %AR percentage of potential respiratory surface area which makes up S_AR - DtO₂ diffusing capacity for air-blood tissue barrier - IUR isotropic uniform randomly distributed - bm body mass - %P percentage of lung volume devoted to parenchyma - S _A potential respiratory surface area (S _L minus the surface area of the trabeculae) - S _ANR non-respiratory surface area - S _AR respiratory surface area - S _L total internal surface area of the lung - S _v surface area-to-volume ratio in parenchyma - _ht harmonic mean thickness of the air-blood tissue barrier - V _L morphometrically determined volume of both lungs, fixed at 0.75· V _Lm - V _Lm maximal lung volume, similar to total lung capacity in mammals - V _Lr resting lung volume, similar to functional residual capacity in mammals - VP morphometrically determined volume of parenchyma of both lungs, fixed at three-quarters of V_Lm     

Seasonal variation of chiasma frequency in Phyllodactylus marmoratus (Gray) (Gekkonidae — Reptilia)

A study of the male meiotic system in two populations of the gekko Phyllodactylus marmoratus (Gray) has shown that both total and interstitial chiasma frequencies vary cyclically throughout the year. This variation is consistent in each population and was observed over a number of years. The total chiasma frequency (an index of the number of terminal chiasmata) has a different form of cyclic variation than does the interstitial chiasma frequency, and it is argued that they are under independent genetic controls. Reproductive studies suggest that only the sperm with the lowest total chiasma frequencies and greatest range of interstitial frequencies are used for fertilization. An experimental approach has shown that prolonged exposure to low temperature produces a significant increase in total chiasma frequency. It is believed that this environmental cue is responsible for the cyclic nature of total chiasma frequency.     

A new large species of gecko of the genus Hemidactylus Oken, 1817 (Reptilia: Sauria: Gekkonidae) from the Eastern Ghats,India

A new large species of gecko superficially resembling Hemidactylus maculatus Duméril & Bibron and its allied large Hemidactylus is described from Eastern Ghats. The new species, Hemidactylus kangerensis sp. nov. can be easily distinguished from members of the H. maculatus complex based on the number of femoral pores, i.e. 18–21 on each side, separated medially by 4 non-pored scales. A phylogenetic analysis based on partial sequence of mitochondrial gene cytochrome b shows that the gecko is a member of the “H. prashadi” clade and is sister to H. maculatus, from which it differs in an uncorrected pairwise sequence divergence of 10%. The discovery of a new large gecko from Eastern Ghats advocates the need for biodiversity assessment across the neglected Eastern Ghats.     

Temperature-Dependent Sex Determination in Gekko japonicus (Gekkonidae, Reptilia)

The effects of temperature on sexual differentiation in early development of the gekkonid lizard, Gekko japonicus were studied. The eggs were collected within 24 hr after the oviposition and were incubated at 20, 24, 28 and 32°C. The number of eggs hatched was 14 at 24°C, 20 at 28°C and 21 at 32°C. Hatching never occurred at 20°C. The hatched lizards without Müllerian ducts were judged as males. The sex of all lizards with Müllerian ducts were identified histologically. The sex ratios, male/(male+female), were 0.07 at 24°C, 0.75 at 28°C and 0.24 at 32°C. The disparities of the sex ratio from 1/2 were statistically significant and differences in the sex ratio with various incubation temperatures were also significant. These sex ratios can probably be best interpreted by a temperature-dependent sex determination. The different sex ratios do not seem to be related to a predetermination of sex with a differential mortality.     

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.     

Lungs of the gecko Rhacodactylus leachianus (Reptilia: Gekkonidae): a correlative gross anatomical and light and electron microscopic study

The lungs of the New Caldeonian gecko Rhacodactylus leachianus were examined by means of gross dissection and light and electron microscopy. This tropical species, which is the largest living gecko, possesses two simple, single-chambered lungs. Right and left lungs are of similar size and shape. The lung volume (27.2 ml.100 g-1) is similar to that of the tokay (Gekko gecko) but differs in that the gas exchange tissue is approximately homogeneously distributed, and the parenchymal units (ediculae) are very large, approximately 2 mm in diameter. The parenchymal depth varies according to the location in the lung, being deepest near the middle of the lung and shallowest caudally. Scanning and transmission electron microscopy reveal an unusual distribution of ciliated cells in patches on the edicular walls as well as on the trabeculae. Secretory cells are very numerous, particularly in the bronchial epithelium, where they greatly outnumber the ciliated cells. The secretory cells form a morphological continuum characterized by small secretory droplets apically and large vacuoles basally. This continuum includes cells resembling type II pneumocytes but which are devoid of lamellar bodies. Type I pneumocytes similar to those of other reptiles cover the respiratory capillaries, where they form a thin, air-blood barrier together with the capillary endothelial cells and the fused basement laminae. The innervation, musculature, and vascular distribution in R. leachianus are also characterized. Apparent simplification of the lungs in this taxon may be related to features of its sluggish habits, whereas peculiarities of cell and tissue composition may reflect demands of its mesic habitat.     

Ultrastructural autoradiographic and immunocytochemical analysis of setae formation and keratinization in the digital pads of the gecko Hemidactylus turcicus (Gekkonidae,Reptilia)

The modified subdigital scales of some lizards allow them to climb vertical surfaces. This is due to the action of millions of tiny setae present in the digital pads. Setae are mainly composed of beta-keratin which may have some modality of aggregation similar to that of barbs and barbules of feathers. Keratins and associated proteins are involved in the organization of setae. The formation of setae in the climbing pad lamellae of the gecko Hemidactylus turcicus has been analyzed under the electron microscope after injection of tritiated histidine and immunocytochemistry for a chick scale beta-keratin. Setae are made up of dense and pale filaments, both oriented along the longer axis of setae. Beta-keratin is present in the oberhautchen layer and in the growing setae which are highly modified oberhautchen cells. Most of the immunolabeling concentrated in the central part of setae. This cross-reactivity suggests that some epitopes in chick beta-keratin are also present in gecko setae. Four hours after injection of tritiated histidine, the labeling is localized over setae, in particular in the dense filaments and less in the pale filaments. Some labeling is also seen in the keratinaceous material present in the cytoplasm of clear cells, which are believed to mold setae. The present observations suggest that both beta-keratin and denser matrix proteins, possibly incorporating histidine, are packed into growing setae. These proteins may be mixed to form pale and dense filaments oriented along the longer axis of setae, a pattern resembling that of barb and barbule cells of feathers. The role of matrix material in the orientation of the deposited beta-keratin during setal outgrowth is discussed with the problem of barb and barbule differentiation in avian feathers.     

The genus Paragehyra (Reptilia: Sauria: Gekkonidae) in southern Madagascar

Paragehyra Angel is a gekkonine genus endemic to Madagascar. From 1929 until the present, the genus was represented only by the holotype of the single known species. Paragehyra petiti. The type locality of P. petiti is in the driest part of Madagascar (south-west) where rainless periods may exceed 11 months and the original vegetation consists of thorn scrub or dry deciduous forest. No new individuals of P. petiti were observed. However, a second, undescribed species of the genus was discovered in October 1990 on the opposite side of the island (south-east) in primary-low montane rainforest. The new form was observed at four localities at the southernmost extremity of rainforest in Madagascar.     

Karyotypic variation in the Australian Gekko Phyllodactylus marmoratus (Gray) (Gekkonidae: Reptilia)

The gekko Phyllodactylus marmoratus has at least three distinct chromosome races; 2n=36, 2n=36 ZZ/ZW and 2n=34. Specimens from these races are morphologically distinguishable, have a degree of habitat specialization and occur in a defined distribution. The 2n=36 race found in Eastern Australia is the presumed primordial type. The 2n=34 race occurs in Western Australia and is regarded as a fusion derivative. The 2n=36 ZZ/ZW race, which is only found on the Murray River system in Eastern Australia has a heteromorphic sex chromosome system present in the female. Giemsa banding suggests that this heteromorphism is the result of a pericentric inversion.     

The origin of parachuting locomotion in gekkonid lizards (Reptilia: Gekkonidae)

Several recent studies have focused on the ability of the gekkonid Ptychozoon lionatum to parachute, utilizing its enlarged lateral body folds. Little attention has been paid, however, to the evolution of such behavious and here several aspects pertaining to the origin of parachuting are integrated. Behavioural shifts and morphological modifications are considered together and evaluated in the light of ecological information. It is apparent that certain behavioural shifts were the precursors of subsequent morphological changes. The structural design of the body folds is also considered in relation to parachuting behaviour and both the gross morphology and histology are shown to be significantly modified to permit effective parachuting. The absene of musculature in the lateral body flaps of geckos is confirmed and a model for the integration of the various factors involved in effective parachuting is presented. Here the importance of the "structure-function" and "habitat-behaviour" sets are emphasized together with their new interrelationships when a protoadaptation becomes functional.