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Hemidactylus
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Hemidactylus
Top: Flat-tailed house gecko
Bottom: Asian house gecko
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Gekkota
Family: Gekkonidae
Subfamily: Gekkoninae
Genus: Hemidactylus
Oken, 1817[1]
Type species
Gecko tuberculosus
Raddi, 1823
Diversity
194 species, see text
Synonyms
List (in alphabetical order)

Hemidactylus, from Ancient Greek ἡμι- (hēmi-), meaning "half", and δάκτυλος (dáktulos), meaning "finger", is a genus of the common gecko family, Gekkonidae.[3][4] It has 194[5] described species, newfound ones being described every few years. These geckos are found in all the tropical regions of the world, extending into the subtropical parts of Africa and Europe. They excel in colonizing oceanic islands by rafting on flotsam, and are for example found across most of Polynesia. In some archipelagoes, cryptic species complexes are found.[2] Geckos like to live in and out of houses. They have been introduced to many areas around the world.[citation needed]

This species is closely related to the genus Gehyra, which belongs to the same family in Gekkonidae.

The species are typically known as house geckos, due to their readiness to adapt to and coexist with humans, and can be easily encountered in human habitations.

Taxonomy

[edit]

This genus was originally established by Lorenz Oken in 1817 for the species at that time known as Hemidactylus tuberculosus, and now described as the tropical house gecko (Hemidactylus mabouia).[2] The species name in turn comes from the Greek words ἡμι hemi "half" and δάκτυλος dáktylos "fingers" because its toes has split or "half" lamella underneath them.[6]

Evolution

[edit]

The origin of the genus Hemidactylus is still unclear as the higher level phylogeny is not well resolved. Moreover, much of the diversity in this group still remains to be discovered.

Feces

[edit]

A house gecko will usually confine its excretions to one area of a house. This is sometimes considered a nuisance by home owners, and may stain certain surfaces.[7] The feces are approximately five (5) millimeters in length, two (2) millimeters wide, and dark brown (almost black) in color.

Description

[edit]
Foot upperside (left) and underside of the Oriental leaf-toed gecko (H. bowringii).

The dorsal scale pattern is either uniform or heterogeneous. The pupil of the eye is vertical. Males have pre-anal or femoral pores. Each finger or toe has a slender distal clawed joint, angularly bent and rising from within the extremity of the dilated portion.[8]

The fingers and toes are free, or more or less webbed, and dilated; underneath they bear a straight line running down their lamellae, which is in a pattern resembling a paripinnate compound leaf.[8] This leads to their other and more ambiguous common name, "leaf-toed geckos", used mainly for species from South Asia and its surroundings to prevent confusion with the many "leaf-toed" Gekkota not in Hemidactylus.

Some members of the genus, such as H. platyurus, are able to run quadrupedally across water by a partially surface tension-dependent mechanism distinct from the bipedal gait of basilisks.[9]

Communication

[edit]

Like many other gecko species, species in the genus Hemidactylus are able to communicate with distinct vocalizations. Depending on the species, their vocalizations range from quiet clicks to short squeaks and chirps. For example, the Asian common house gecko (Hemidactylus frenatus) is notable for its distinctive chirping.

Species

[edit]
H. brookii
H. flaviviridus
Adult common house gecko (H. frenatus) in Chennai, India
H. garnotii
Adult giant leaf-toed gecko (H. giganteus) from Dindigul (Tamil Nadu, India)
H. graniticolus
H. maculatus
H. prashadi
Mediterranean house gecko (H. turcicus)
H. varadgirii

Phylogeny

[edit]

The following phylogeny is from Pyron, et al. (2013),[14] and includes 47 Hemidactylus species. Hemidactylus is a sister group of Cyrtodactylus.[14]

Hemidactylus

References

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Hemidactylus

View on Grokipedia
from Grokipedia
Hemidactylus is a genus of geckos in the family Gekkonidae, comprising 198 species of small to medium-sized lizards that are primarily nocturnal, insectivorous, and equipped with specialized adhesive toe pads for climbing. The generic name derives from the Ancient Greek words hemi- (half) and daktylos (finger), referring to the divided subdigital lamellae on their toes that enable adhesion. These geckos typically measure 28–75 mm in snout-vent length, often featuring dorsal tubercles that vary in size, keeling, and arrangement, and exhibit cryptic color patterns such as spots or bands for camouflage. Native to tropical and subtropical regions worldwide, particularly with high diversity in , the , , and , the genus has been shaped by vicariance events like the formation of the and human-mediated dispersal, leading to introduced populations on islands and continents. Many species, such as H. frenatus and H. mabouia, are synanthropic, thriving in human-modified habitats like buildings and urban areas, where they prey on insects attracted to lights. Ecologically diverse, they occupy varied niches from rocky arid zones to humid forests, often showing in size and scalation, and some exhibit vocalizations unique among geckos. The genus is notable for its rapid , with molecular studies revealing cryptic diversity and ongoing taxonomic revisions; for instance, the Arabian and African clades highlight hotspots of , while pose ecological challenges by outcompeting native in introduced ranges.

Taxonomy and Phylogeny

Taxonomic History

The Hemidactylus was established by in 1817 in the journal Isis von Oken, with the name derived from words hemi (half) and daktylos (), alluding to the divided subdigital lamellae characteristic of the toes in these geckos. The is Hemidactylus mabouia (Moreau de Jonnès, 1818), originally described as Lacerta mabouia from the , though some authorities attribute the genus establishment to Goldfuss (1820) due to Oken's names being considered nomina nuda. Early taxonomic treatments included a broad assemblage of species within Hemidactylus, with over 100 taxa assigned to the genus by the late , encompassing a wide range of geckos from tropical regions. George Albert Boulenger's 1885 catalogue of in the provided the first comprehensive revision, recognizing 55 and subspecies while synonymizing several others based on morphological characters such as scale patterns and lamellae counts; this work became a foundational for subsequent classifications. In the 20th century, Arthur Loveridge's 1947 revision focused on African , cataloging 48 taxa and introducing keys for identification while resolving several synonyms, though it retained a lumping approach that later proved overly conservative given emerging cryptic diversity. Major splits occurred during this period, including the separation of subgenera like Hemitheconyx (now often treated as a distinct ) for with distinct morphological traits such as enlarged dorsal tubercles and specific cloacal arrangements. Post-2000 revisions, driven by molecular data, have dramatically reshaped the through synonymies and elevations of cryptic , particularly in complexes like H. brookii and H. flaviviridis. Taxonomists such as Rajesh Vyas and Aaron M. Bauer have played key roles; Vyas contributed to descriptions like H. gujaratensis (Giri et al., 2009), highlighting regional in , while Bauer's phylogenetic analyses (e.g., Bauer et al., 2006, 2010) supported the recognition of over 50 new via mitochondrial and nuclear markers, reducing the genus's perceived but clarifying its diversification across .

Phylogenetic Relationships

Hemidactylus belongs to the family Gekkonidae, within the subfamily Gekkoninae, a diverse group of tropical and subtropical geckos characterized by adhesive toe pads and vocalizations. Phylogenetic analyses utilizing mitochondrial DNA markers, including the 16S rRNA and ND2 genes, position Hemidactylus closely alongside genera such as Gehyra and elements of the Cyrtodactylus radiation, forming a core component of the Gekkoninae clade that diverged from other gekkonid subfamilies around 60-70 million years ago. Internally, the exhibits a complex phylogeny divided into major that highlight extensive diversification, including the mabouia (encompassing tropical African species like H. mabouia), the frenatus (Southeast Asian house geckos such as H. frenatus), and the brookii (South and Southeast Asian forms like H. brookii). These groupings reflect rapid radiations, particularly in tropical and during the , driven by ecological opportunities in fragmented habitats and anthropogenic dispersal, with divergence times estimated between 10-30 million years ago based on calibrations. Evidence from multi-locus datasets supports polytomous branching indicative of explosive events, resolving into nearly 200 recognized (as of 2025) with ongoing discoveries of cryptic lineages. Early morphological phylogenies, such as Underwood's 1954 classification, established foundational groupings within based on scalation and , placing Hemidactylus among "true geckos" with scansorial adaptations. Subsequent molecular studies have refined these, with Gamble et al. (2008) providing a broad gekkotan framework that integrates Hemidactylus into radiations, and Bauer et al. (2010) elucidating South Asian endemic diversity through concatenated mtDNA and nDNA analyses, identifying undescribed and resolving longstanding polytomies in Asian clades. These works underscore the genus's evolutionary dynamism, with genetic data revealing hidden diversity exceeding 20% uncorrected pairwise distances in some lineages. Higher-level relationships within continue to be debated, with varying support for the of subfamilies like Gekkoninae amid ongoing genomic reassessments. An African origin for Hemidactylus has been hypothesized based on the antiquity of its tropical African clades, but recent biogeographic models incorporating fossil calibrations suggest an alternative cradle around 58 million years ago, followed by dispersals to and beyond, with a 2024 comprehensive phylogeny of 132 supporting this Indian origin; the precise ancestral range remains under study.

Description

Morphology

Hemidactylus species are small to medium-sized , with snout-vent lengths typically ranging from 30 to 100 mm, though some reach up to 150 mm or more in larger forms. They possess a slender body form with a cylindrical, often regenerable , and exhibit typical gekkonid features such as the absence of movable eyelids and vertical slit-like pupils adapted for low-light vision. The scalation of Hemidactylus is diverse but characteristically includes small, granular dorsal scales that may be uniform or intermixed with larger, keeled tubercles in some species, creating a heterogeneous . Ventral scales are larger, flat, and imbricate, forming overlapping rows that provide a smoother underbody surface. These scale arrangements vary across the but contribute to the overall cryptic appearance. Sexual dimorphism in Hemidactylus is prominent in the presence of preanal and , which are well-developed in males, typically numbering 10 to 40 in total and used for scent marking. Females generally lack these secretory pores or possess far fewer non-functional ones, while other differences such as slight variations in body size or head proportions may occur but are less consistent across species. The digits of Hemidactylus are equipped with expanded adhesive pads bearing lamellae, numbering 4 to 8 under the first toe and up to 10 or more under the fourth, enabling climbing on vertical surfaces. In many species, particularly those in the median group such as H. frenatus, the lamellae are divided medially, with proximal and distal portions separated by a shallow notch, a derived trait unique to the . Coloration is typically cryptic, featuring gray to brown backgrounds with irregular spots, bands, or mottling that enhances nocturnal against bark or walls.

Adaptations

Hemidactylus exhibit remarkable capabilities through microscopic hair-like structures known as , which cover the lamellae on their toes. These , terminating in spatulate tips, generate adhesion primarily via van der Waals forces, allowing the geckos to climb smooth vertical and inverted surfaces with ease. This mechanism has been demonstrated in geckos, including Hemidactylus, where the intermolecular attractions between the tips and substrates provide strong yet reversible attachment, independent of surface chemistry. A key survival adaptation in Hemidactylus is caudal autotomy, the ability to voluntarily fracture the at predetermined fracture planes within the vertebrae to escape predators. The detached continues to wriggle, distracting the threat, while the gecko regenerates a new from a of undifferentiated cells at the wound site. In species like Hemidactylus frenatus and Hemidactylus flaviviridis, this regeneration process restores functionality, though the replacement often lacks skeletal elements and is shorter. Certain Hemidactylus species possess modifications in the and associated musculature that enable vocalization, producing chirping or clicking sounds for territorial defense and communication. In Hemidactylus turcicus, for instance, the laryngeal skeleton and tracheal structure support the generation of short, high-frequency calls, with males using these vocalizations more frequently than females during agonistic encounters. These adaptations are particularly useful in nocturnal environments where visual cues are limited. The skin of Hemidactylus geckos displays hydrophobic properties due to micro- and nanostructures, such as tiny spines and scales, which create a superhydrophobic surface with high angles. This allows like Hemidactylus platyurus to run across wet surfaces or even without sinking, as the beads off and reduces drag during rapid movement. Studies on this show they achieve speeds of up to 1 m/s on , comparable to , by combining skin repellency with foot-slapping and body undulation. Nocturnal vision in Hemidactylus is enhanced by enlarged eyes and the presence of a , a reflective layer behind the that amplifies low-light sensitivity by redirecting photons to photoreceptors. This enables effective hunting and in dim conditions, with cone-dominated s allowing color discrimination at levels in related nocturnal geckos, a trait applicable to Hemidactylus frenatus.

Distribution and Habitat

Native Range

The genus Hemidactylus is natively distributed across the tropical and subtropical regions of the , with its core range encompassing tropical and subtropical as the primary origin hotspot, the , , , and parts of the including the . This distribution reflects a historical rooted in an Indian origin approximately 58 million years ago, followed by major dispersal events into and subsequent radiations shaped by vicariance and overland or oceanic dispersal across the region. Pre-human ranges were largely confined to these tropics, with limited natural extension into subtropical zones of and northern . Africa hosts the highest species diversity within the genus, with numerous endemic taxa resulting from independent radiations, particularly in eastern and southern regions; for instance, the arid clade alone includes multiple radiations confined to African highlands and valleys. The , including areas in , , and , exhibits notable cryptic diversity and endemism, underscoring its role as a key evolutionary hotspot for montane and semi-arid lineages. In , the stands out for parallel diversification, with high endemism in the biodiversity hotspot, where more than 20 species are known, many restricted to rocky habitats and forests. and the represent secondary centers, with the latter facilitating dispersal corridors and additional events influenced by climatic shifts. Madagascar supports a smaller but distinct native assemblage, with two native species (H. mercatorius and H. platycephalus) occurring naturally, likely resulting from overwater dispersal across the Mozambique Channel. As of 2025, the genus comprises 198 recognized species, the majority endemic to Africa and southern Asia, highlighting the continent's dominance in overall diversity.

Introduced Populations

Several species within the genus Hemidactylus have been introduced to regions far beyond their native African and Asian ranges through human activities, establishing viable populations in the , Pacific islands, , and the . For instance, H. mabouia () was transported to the Neotropics via the Atlantic slave trade and associated shipping routes, with the earliest records dating to the mid-17th century in locations such as St. Kitts (around 1640) and (1637–1654). Similarly, H. frenatus (Asian house gecko) has achieved a pantropical distribution, appearing in , numerous Pacific islands, (prior to 1840), and parts of the , often displacing native s through aggressive interactions. H. turcicus () has spread to southern and , , and the , while H. brookii occurs in northern and the . These introductions highlight the genus's propensity for global dispersal. The primary vectors for these introductions include maritime trade ships, cargo shipments, and ornamental plants, which facilitate unintentional transport as stowaways. H. frenatus, for example, arrived in the via imported ornamental plants, enabling rapid establishment in urban and peri-urban environments. In , H. frenatus was likely introduced through before 1840, and subsequent spread has been linked to increased international shipping since the mid-20th century. These vectors exploit the geckos' adaptability to human-modified habitats, such as ports and settlements, allowing quick colonization of new areas upon arrival. Ornamental plant trade has been particularly implicated in Pacific and introductions, where eggs or juveniles adhere to foliage during transit. Establishment success is notably high for these introduced Hemidactylus species, attributed to their opportunistic diets, ability to store for extended periods (facilitating in low-density populations), and tolerance for urban disturbances. In competitive scenarios, H. frenatus often outcompetes native geckos on Pacific islands through mechanisms like sexual interference, leading to local extirpations. While occurs in some related geckos (e.g., , formerly classified under Hemidactylus), it is not a primary factor in core Hemidactylus invasions; instead, high and broad thermal tolerances drive persistence. These traits enable rapid , with introduced groups reaching densities comparable to natives within years. Key case studies illustrate these patterns: H. turcicus was first documented in the United States in , , in 1915 (though possibly present earlier), spreading via ships to establish populations across the southeastern U.S. by the mid-, including by 1933. In , H. mabouia has expanded since the late 19th or early , marginalizing earlier invasives like H. turcicus through superior competitive ability. Climate modeling predicts further range expansions for five invasive Hemidactylus species (H. frenatus, H. mabouia, H. turcicus, H. brookii, and H. garnotii) under future warming scenarios, potentially covering additional tropical and subtropical areas in the and Pacific by 2050, with H. frenatus showing the broadest potential increase.

Behavior and Ecology

Activity Patterns and Communication

Hemidactylus species are predominantly nocturnal, emerging at to and interact while retreating to sheltered crevices, bark, or walls during daylight hours to avoid predation and . In tropical and subtropical native ranges, their activity peaks shortly after sunset and continues through the night, influenced by temperature thresholds above 25°C for optimal movement. Some species, such as Hemidactylus mabouia, exhibit crepuscular tendencies in cooler climates or during seasonal transitions, showing limited activity in early morning or late afternoon when temperatures moderate. Locomotion in Hemidactylus involves rapid scanning movements across surfaces, facilitated by their specialized toe pads that enable on vertical and inverted substrates without slipping. These geckos achieve speeds of approximately 0.3–0.8 m/s on smooth vertical surfaces, with stride frequencies averaging 12–13 Hz, allowing efficient traversal of walls and ceilings in both natural and built environments. The system, composed of setae on expanded pads, permits dynamic attachment and detachment during high-speed runs, supporting their arboreal and saxicolous lifestyles. Communication in Hemidactylus relies on both acoustic and visual signals, primarily for territorial defense and alarm responses, as they maintain limited social structures with minimal group cohesion. Vocalizations include short chirps, clicks, and barks produced by and inflated throat sacs, serving to deter intruders or signal distress; for instance, Hemidactylus frenatus emits a series of "tchk-tchk-tchk" calls with dominant frequencies around 1.5–2.5 kHz and harmonics extending to 5–12 kHz. These sounds vary by and context, with Hemidactylus turcicus producing harmonious chirps in the 1.4–4.9 kHz range during aggressive encounters. Visual signals complement acoustics, featuring waving, body arching, or posturing during conspecific interactions; aggressive displays often begin with undulation followed by rapid wagging to assert dominance without physical contact. Such behaviors are more frequent in males defending perches, though females may use similar posturing in territorial disputes. In urban settings, artificial light pollution disrupts natural circadian rhythms in Hemidactylus, drawing individuals to illuminated areas and extending nocturnal activity periods or inducing sporadic daytime near streetlights and building exteriors. This alteration enhances to predators but provides access to concentrated prey, leading to increased overall activity levels compared to dimly lit rural habitats. Recent studies (as of 2025) indicate that human-dominated environments reduce tail rates in Hemidactylus species, suggesting decreased predation pressure or behavioral shifts in urban settings. Species like Hemidactylus frenatus show heightened responsiveness to urban , potentially shifting peak activity toward and in high-pollution zones.

Diet and Predation

Hemidactylus are primarily insectivorous, feeding on a variety of small arthropods including moths (), ants and other , beetles (Coleoptera), flies (Diptera such as mosquitoes), and spiders (Araneae), which can constitute the majority of their diet depending on local availability. In urban environments, they opportunistically consume light-attracted near artificial sources. Some exhibit opportunistic omnivory, supplementing their diet with , fruits, and sap, particularly larger individuals. These geckos employ a sit-and-wait strategy, often ambushing prey from elevated perches such as walls or ceilings, using adhesive toe pads for positioning and a prehensile to project and capture items at a distance. Nocturnal activity enhances their hunting efficiency by targeting active prey in low-light conditions. Hemidactylus individuals face predation from a range of vertebrates and , including birds, snakes, mammals such as cats and rats, larger lizards, dogs, large spiders, and praying mantids. In introduced populations, heightened exposure to non-native predators like cats and rats can increase mortality rates, potentially contributing to ecological disruptions by altering native prey dynamics. As both predators and prey, Hemidactylus species play a key trophic role in food webs, particularly in urban settings where they help control insect pests like mosquitoes and , reducing potential vectors. They serve as important prey for larger reptiles and birds, supporting higher trophic levels. Feeding activity shows seasonal variation, with reduced consumption during dry seasons due to lower availability, though certain prey like and Diptera increase in the rainy period; reproductive periods may demand higher protein intake from arthropods to support egg production.

Reproduction

Hemidactylus species are oviparous, with females typically laying clutches of one to two eggs in concealed locations such as under bark, in rock crevices, or within building structures to protect them from predators and environmental extremes. These eggs are small, , and leathery-shelled, adhering firmly to substrates upon deposition. Incubation periods generally last 40–60 days, influenced by environmental temperatures ranging from 25–31°C; higher temperatures accelerate but may affect offspring viability. Eggs are highly susceptible to due to the lack of , leaving hatchlings independent upon emergence. Mating behaviors in Hemidactylus involve brief rituals, where males approach females by touching them with the , sometimes grasping the or lightly to position for copulation. Males may exhibit visual displays such as head-bobbing or arching to signal interest, while rivals engage in aggressive combat through , pivoting, and thrashing to establish dominance. In tropical populations, breeding can occur year-round, enabling females to produce multiple clutches (2–4 per year), with intervals of approximately 15 days between layings; in temperate regions, reproduction is seasonal. The life cycle of Hemidactylus begins with hatchlings measuring 40–60 mm in total length, reaching in 6–12 months based on rather than age, with females maturing at snout-vent lengths around 50 mm. Lifespans in the wild typically range from 5–7 years, though some individuals may live up to 10 years under optimal conditions. Females can store sperm for up to a year, facilitating asynchronous production without repeated matings. Parthenogenesis is rare within the genus but occurs in introduced populations of Hemidactylus garnotii, which consist entirely of females producing viable from unfertilized eggs without male involvement. This mode, involving diploid eggs, contributes to the species' rapid establishment in non-native ranges but is not observed in most sexual Hemidactylus congeners.

Human Interactions

Invasiveness and Impacts

Introduced populations of Hemidactylus species, particularly H. frenatus and H. mabouia, pose significant ecological threats through competitive displacement of native geckos. In , H. frenatus excludes endemic Nactus species from preferred refugia such as rock crevices, increasing their exposure to predation and environmental stressors, which has contributed to local extinctions. Similarly, in the tropical Pacific, H. frenatus competitively displaces native in urban and suburban habitats by outperforming it in sprint speed and resource acquisition near artificial lights. H. mabouia exhibits comparable aggression, displacing native Phyllodactylus martini and other invasive geckos like H. turcicus in the Neotropics through predation and interference competition. These interactions often favor Hemidactylus in anthropogenically modified environments with clumped insect resources. As voracious nocturnal insectivores, invasive Hemidactylus alter communities by reducing populations of native and spiders, which can disrupt food webs and indirectly affect higher trophic levels. This consumption provides some benefits by curbing household , potentially lowering reliance on chemical pesticides in urban areas. However, the broader economic toll of invasive s, including Hemidactylus, contributes to the economic costs of biological invasions in the United States, which exceeded $1.2 trillion from 1960 to 2020 (as of 2022), with annual costs averaging around $21 billion across all , encompassing and expenses. Hemidactylus may act as vectors for exotic parasites such as nematodes, potentially introducing novel pathogens to endemic populations and exacerbating threats in ecosystems. As of 2025, new populations of the Asian house gecko (H. frenatus) have been reported in , illustrating continued expansion via human transport. Management efforts focus on surveillance and targeted removal to mitigate impacts in vulnerable habitats. In , cost-effective monitoring protocols using info-gap decision theory guide detection on Barrow Island, emphasizing early intervention to prevent establishment. Eradication attempts include glue traps and experimental baits combined with toxicants, tested on small invasive including Hemidactylus species, though success varies due to their cryptic and high reproductive rates. Ongoing monitoring in biodiversity hotspots like prioritizes containment over widespread eradication, given their established presence. Climate change is projected to exacerbate invasiveness by expanding suitable ranges for Hemidactylus species into temperate zones. modeling from 2017 indicates that H. brookii and H. turcicus could see range increases of 8–95% by 2050 under warming scenarios, potentially intensifying competition with natives in newly invaded areas. These projections underscore the need for strategies to address shifting distributions.

Feces and Urban Nuisance

The droppings of Hemidactylus species, commonly known as house geckos, are small, cylindrical pellets typically measuring 3-6 mm in length and about 2 mm in width, with a dark brown to black fecal portion topped by a white urate cap. This urate cap consists primarily of , a nitrogenous product excreted in a semisolid form that aids in by minimizing liquid loss during elimination, an adaptation common to reptiles. The high uric acid content allows these geckos to thrive in arid or urban environments where water is scarce. In urban settings, Hemidactylus geckos often deposit their feces in communal latrines, favoring sheltered, elevated spots such as light fixtures, window sills, or ceiling corners near artificial lights that attract insect prey. These repeated defecation sites can accumulate, and the droppings' adhesive quality—due to residual moisture and urates—leaves persistent sticky residues that stain walls, fabrics, and other surfaces, complicating routine cleaning in homes. Identification of these droppings aids pest control efforts, as the distinctive white urate cap differentiates them from similar-looking bat guano or rodent feces, which lack this feature and may indicate different infestation issues. While allergic reactions to Hemidactylus droppings are rare, the primary nuisances stem from concerns and the effort required for thorough cleaning, particularly in high-traffic areas like kitchens or bedrooms. Health risks are generally minimal, with low pathogen transmission rates, though geckos can carry bacteria in their feces, potentially leading to gastrointestinal illness if ingested through contaminated surfaces. In densely populated urban habitats, where gecko numbers can be higher due to abundant from outdoor , the volume of droppings increases, exacerbating cleanup demands. Mitigation focuses on preventing access rather than chemical controls, as non-toxic repellents like essential oils or garlic sprays prove largely ineffective against persistent infestations. Sealing entry points—such as cracks around doors, windows, and vents—with or is the most reliable strategy to reduce presence and subsequent fecal deposition in living spaces.

Species Diversity

Number and Distribution of Species

As of 2025, the genus Hemidactylus includes 198 recognized , reflecting ongoing taxonomic revisions and new discoveries documented in the Reptile Database. This count has grown substantially from approximately 122 reported in , with an average of about 6-7 new described each year since then, predominantly from biodiversity hotspots in and . The distribution of Hemidactylus species is centered in tropical and subtropical regions, with the majority occurring in the (including ), followed by the Indomalayan region (South and ); approximately 4 species are endemic to . Human activities have facilitated cosmopolitan spread via introductions to the , , and beyond. Levels of endemism are elevated on isolated islands, such as where multiple species like H. forbesii and H. pumilio are restricted to the archipelago, and the where at least two species occur. Cryptic species complexes further complicate patterns, as seen in the H. brookii group, which encompasses about 7 distinct clades differentiated primarily through molecular analyses rather than morphology. Conservation assessments indicate that the majority of Hemidactylus species are categorized as Least Concern due to their adaptability and wide-ranging habits, but a small number face threats from habitat degradation; for instance, H. hajarensis from Oman's is endemic to rocky habitats that are undergoing loss. Recent trends show accelerated species discoveries, particularly through efforts that have uncovered hidden cryptic diversity, elevating counts from around 85 species prior to 2010; continued findings in regions like the of and contribute to this growth.

Notable Species

Hemidactylus frenatus, commonly known as the common house gecko, exemplifies the genus's invasive potential, originating from South and Southeast Asia but achieving a pantropical distribution through human-mediated introductions dating back to the 19th century. This small lizard typically measures 7.5–15 cm in total length, with males slightly larger than females, and features a slender body adapted for climbing vertical surfaces. It is notorious for its vocalizations, producing a series of soft chirping or chapping calls used in territorial defense and courtship, which are among the loudest sounds emitted by any lizard species. As a synanthropic species, H. frenatus thrives in urban environments worldwide, from Asia to the Americas and Oceania, often outcompeting native geckos by monopolizing artificial light sources that attract insect prey. The , Hemidactylus mabouia, serves as the of the Hemidactylus and highlights African origins with extensive invasive spread. Native to , this relatively large reaches up to 15 cm in total length, with females often exceeding 6.5 cm in snout-vent length, and displays a robust body with mottled gray to brown coloration for camouflage. Introduced to the since the via shipping routes, it has established populations across Central and , where it competes aggressively with native reptiles for resources in urban and forested habitats. Its adaptability to disturbed environments underscores the genus's success as global colonizers, though it poses ecological threats by preying on and hybridizing with local species. Hemidactylus turcicus, the , represents a classic case of invasion into the New World, first documented in the United States in in 1910. This pale, ghostly , typically 10–13 cm long, exhibits a light gray to white morph with warty tubercles covering its body, aiding nocturnal on urban walls. Unlike its chirping relatives, H. turcicus is relatively silent, relying on stealthy hunting tactics to capture without vocal alerts, though it may emit occasional squeaks during territorial disputes. Now widespread across the southeastern U.S. and beyond, it exploits human structures for shelter and foraging, demonstrating resilience in temperate to subtropical climates. Hemidactylus platycephalus, known as the flat-headed gecko, illustrates regional endemism with unique morphological adaptations in arid environments. Native to eastern Africa, including baobab-rich habitats, this species features a distinctly flattened head and keeled dorsal scales that enhance traction on rough bark and rock surfaces. Though not Australian endemic as sometimes misattributed, its body form supports agile climbing, potentially aiding in accessing water sources or evading predators in dry landscapes; however, direct water-running observations are more characteristic of related species like H. platyurus. Among regional endemics, Hemidactylus sinaitus stands out as a specialist, occurring in desert regions including parts of the where its spiny, keeled scales provide camouflage against sandy substrates. This small , under 10 cm long, inhabits rocky outcrops and wadis across , adapting to extreme aridity through nocturnal activity and minimal water needs. In contrast, Hemidactylus rishivalleyensis, a recently described dweller from Andhra Pradesh's granite hills, exemplifies micro-endemism in South Asia's scrublands. Restricted to Rishi Valley's boulder-strewn landscapes, it measures about 6–8 cm with cryptic patterning suited to rocky crevices, highlighting the genus's diversity in isolated rupicolous niches.

References

  1. https://www.frontiersin.org/journals/ecology-and-evolution/articles/10.3389/fevo.2022.791762/full
  2. https://amphibian-reptile-conservation.org/pdfs/Volume/Vol_13_no_2/ARC_13_2_%5BGeneral_Section%5D_239-258_e209.pdf
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