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Natural parthenogenesis in the gekkonid lizardLepidodactylus lugubris

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jez.1401600203openalex-snapshot

Cytophotometric evidence for triploidy in hybrids of the gynogenetic fish, Poecilia formosa

inferredcites →https://doi.org/10.1002/jez.1401660114openalex-snapshot

Skin grafting in the bisexual teiid lizard Cnemidophorus sexlineatus and in the unisexual C. tesselatus

inferredcites →https://doi.org/10.1002/jmor.1051250307openalex-snapshot

The reproductive morphology of Cnemidophorus neomexicanus X Cnemidophorus inornatus hybrid males

inferredcites →https://doi.org/10.1002/jmor.1051330203openalex-snapshot

Reproduction and the mechanism of meiotic restitution in the parthenogenetic lizard Cnemidophorus uniparens

inferredcites →https://doi.org/10.1007/bf01898012openalex-snapshot

Three probable cases of parthenogenesis in lizards (Agamidae, Chamaeleontidae, Gekkonidae)

inferredcites →https://doi.org/10.1007/bf02982453openalex-snapshot

Investigations concerning the reproductive behaviour ofMollienisia “formos 4”

inferredcites →https://doi.org/10.1007/bf02986114openalex-snapshot

Gynogenesis in the teleost,Mollienesia formosa (Girard), with a discussion of the detection of parthenogenesis in vertebrates by tissue transplantation

inferredcites →https://doi.org/10.1038/219280a0openalex-snapshot

Triploid Hybrids between the All-female Teleost Poecilia formosa and Poecilia sphenops

inferredcites →https://doi.org/10.1093/genetics/50.4.583openalex-snapshot

AN ESTIMATE OF THE NUMBER OF HISTOCOMPATIBILITY LOCI IN THE TELEOST XIPHOPHORUS MACULATUS

inferredcites →https://doi.org/10.1093/icb/11.2.351openalex-snapshot

Special Adaptive Problems Associated with Unisexual Fishes

inferredcites →https://doi.org/10.1111/j.1558-5646.1960.tb03114.xopenalex-snapshot

PSEUDOGAMY AS AN EVOLUTIONARY FACTOR IN THE POECILIID FISHMOLLIENISIA FORMOSA

inferredcites →https://doi.org/10.1111/j.1558-5646.1962.tb03239.xopenalex-snapshot

POPULATION GENETICS OF THE GYNOGENETIC TELEOST, MOLLIENESIA FORMOSA (GIRARD)

inferredcites →https://doi.org/10.1111/j.1558-5646.1967.tb00140.xopenalex-snapshot

MATROCLINOUS INHERITANCE AND CLONAL STRUCTURE OF A MEXICAN POPULATION OF THE GYNOGENETIC FISH,POECILIA FORMOSA

inferredcites →https://doi.org/10.1111/j.1749-6632.1962.tb45354.xopenalex-snapshot

A SKIN‐GRAFTING ANALYSIS OF FOWL PARTHENOGENS: EVIDENCE FOR A NEW TYPE OF GENETIC HISTOCOMPATIBILITY*

inferredcites →https://doi.org/10.1126/science.135.3499.212openalex-snapshot

All-Female Species of the Lizard Genus Cnemidophorus , Teiidae

inferredcites →https://doi.org/10.1126/science.139.3550.113openalex-snapshot

Natural Triploidy in Salamanders Related to Ambystoma jeffersonianum

inferredcites →https://doi.org/10.1126/science.149.3683.539openalex-snapshot

Triploidy in Parthenogenetic Species of the Teiid Lizard, Genus Cnemidophorus

inferredcites →https://doi.org/10.1126/science.153.3732.212openalex-snapshot

Myeloma Cells and Immunoglobulin Formation

inferredcites →https://doi.org/10.1126/science.157.3796.1564openalex-snapshot

Gynogenesis and Triploidy in the Viviparous Fish Poeciliopsis

inferredcites →https://doi.org/10.1126/science.76.1983.628openalex-snapshot

Apparent Parthenogenesis in Nature, in a Form of Fish of Hybrid Origin

inferredcites →https://doi.org/10.1126/science.77.1999.389-aopenalex-snapshot

THE INVOLVED GENETICS OF FISH

inferredcites →https://doi.org/10.1146/annurev.ge.03.120169.000531openalex-snapshot

EXPERIMENTAL POLYPLOIDY IN ANIMALS

inferredcites →https://doi.org/10.11606/0031-1049.1970.23.p63-68openalex-snapshot

Unisexual Cnemidophorus lemniscatus in the Amazonas valley: a preliminary note (Sauria, Teiidae)

inferredcites →https://doi.org/10.1508/cytologia.15.96openalex-snapshot

An Idiogram Study of the Chromosomes in Some Species of Reptiles

inferredcites →https://doi.org/10.2307/1441023openalex-snapshot

Relations of the Diploid and Triploid Species of the Ambystoma jeffersonianum Complex (Amphibia, Caudata)

inferredcites →https://doi.org/10.2307/1441559openalex-snapshot

Weeds, Polyploids, Parthenogenesis, and the Geographical and Ecological Distribution of All-Female Species of Cnemidophorus

inferredcites →https://doi.org/10.2307/1441611openalex-snapshot

Skin Homografts in the All-Female Gekkonid Lizard Hemidactylus garnotii

inferredcites →https://doi.org/10.2307/1441613openalex-snapshot

Conclusive Evidence of Parthenogenesis in Three Species of Cnemidophorus (Teiidae)

inferredcites →https://doi.org/10.2307/1441670openalex-snapshot

Ecological Observations on an All Female Population of the Lizard Lepidophyma flavimaculatum (Xantusiidae) in Panamá

inferredcites →https://doi.org/10.2307/1441764openalex-snapshot

Distribution of the Gynogenetic Fish, Poecilia formosa, with Remarks on the Evolution of the Species

inferredcites →https://doi.org/10.2307/1441789openalex-snapshot

Hemidactylus garnotii Duméril and Bibron, a Triploid All-Female Species of Gekkonid Lizard

inferredcites →https://doi.org/10.2307/1441883openalex-snapshot

Males of Three Normally Parthenogenetic Species of Teiid Lizards (Genus Cnemidophorus)

inferredcites →https://doi.org/10.2307/1441932openalex-snapshot

The Systematics of the Parthenogenetic Lizards of the Cnemidophorus cozumela Complex

inferredcites →https://doi.org/10.2307/1562588openalex-snapshot

Natural Parthenogenesis in a Polymorphic Group of Caucasian Rock Lizards Related to Lacerta saxicola Eversmann

inferredcites →https://doi.org/10.2307/1562592openalex-snapshot

Lepidodactylus lugubris Dumeril and Bibron in Western South America

inferredcites →https://doi.org/10.2307/2423092openalex-snapshot

The Sex of Hatchlings of Five Apparently Unisexual Species of Whiptail Lizards (Cnemidophorus, Teiidae)

inferredcites →https://doi.org/10.2307/40022362openalex-snapshot

Species of the Cnemidophorus exsanguis Subgroup of Whiptail Lizards

inferredcites →https://doi.org/10.2307/40022405openalex-snapshot

A New Uniparental Whiptail Lizard (Genus Cnemidophorus) from Sonora, Mexico

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/zootaxa.4999.1.6zenodo-depositor-declared

Who’s your daddy? On the identity and distribution of the paternal hybrid ancestor of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia: Squamata: Gekkonidae)

inferred← citeshttps://doi.org/10.1002/9781119389934.ch14openalex-snapshot

Geckos

inferred← citeshttps://doi.org/10.1002/dvdy.72openalex-snapshot

Embryonic development of a parthenogenetic vertebrate, the mourning gecko (Lepidodactylus lugubris)

inferred← citeshttps://doi.org/10.1002/jez.1401960308openalex-snapshot

Natural hybridization between parthenogenetic and bisexual lizards: Detection of uniparental source by skin grafting

inferred← citeshttps://doi.org/10.1002/jez.1402190313openalex-snapshot

Low water vapor conductance of hard‐shelled eggs of the gecko lizards Hemidactylus and Lepidodactylus

inferred← citeshttps://doi.org/10.1002/jmor.1052120106openalex-snapshot

Histology of the reproductive tract of hybrids between gonochoristic males and parthenogenetic females of Lepidodactylus lugubris in French Polynesia (Reptilia, Gekkonidae)

inferred← citeshttps://doi.org/10.1007/978-3-642-66069-6_32openalex-snapshot

Evolution of Parthenogenetic Species of Reptiles

inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_21openalex-snapshot

Lost Sex in the Reptiles: Constraints and Correlations

inferred← citeshttps://doi.org/10.1007/978-94-009-2605-9_7openalex-snapshot

Alternative life-history styles in reptiles

inferred← citeshttps://doi.org/10.1007/978-94-009-8629-9_60openalex-snapshot

Cape York Peninsula: Major region of faunal interchange

inferred← citeshttps://doi.org/10.1007/bf00048090openalex-snapshot

Der Artbegriff and seine Bedeutung fur die Klassifikation der Echsen (Reptilia: Sauria)

inferred← citeshttps://doi.org/10.1007/bf00056034openalex-snapshot

Polyclony and low relative heterozygosity in a widespread unisexual vertebrate, Lepidodactylus lugubris (Sauria)

inferred← citeshttps://doi.org/10.1007/bf00317861openalex-snapshot

Divergent ecology of sympatric clones of the asexual gecko, Lepidodactylus lugubris

inferred← citeshttps://doi.org/10.1007/bf02002783openalex-snapshot

Parthenogenetic reptiles: New subjects for laboratory research

inferred← citeshttps://doi.org/10.1007/s10530-010-9870-0openalex-snapshot

Ecological aspects of biosecurity surveillance design for the detection of multiple invasive animal species

inferred← citeshttps://doi.org/10.1016/0016-6480(78)90169-7openalex-snapshot

Quantitative analysis of the ovarian cycle of the lizard Lepidodactylus lugubris

inferred← citeshttps://doi.org/10.1016/0306-4565(90)90014-9openalex-snapshot

Habitat-dependent thermal regimes of two hawaiian geckos (Reptilla: gekkonidae)

inferred← citeshttps://doi.org/10.1016/b978-0-12-503365-7.50007-9openalex-snapshot

The Evolution of Parthenogenesis: A Historical Perspective11This chapter is dedicated to Åke Gustafsson.

inferred← citeshttps://doi.org/10.1016/j.fooweb.2025.e00415openalex-snapshot

First record of nectar feeding by the exotic lizard Lepidodactylus lugubris (Duméril & Bibron, 1836) in urban environments in Brazil with notes on unusual feeding behaviors

inferred← citeshttps://doi.org/10.1016/s0145-305x(79)80060-9openalex-snapshot

The effect of a laboratory environment on graft rejection in Lacerta viridis, the European green lizard

inferred← citeshttps://doi.org/10.1038/hdy.1988.65openalex-snapshot

Presumptive sex chromosomes of a unisexual homomorphic species of lizards, Lepidodactylus lugubris

inferred← citeshttps://doi.org/10.1038/s41467-021-26321-9openalex-snapshot

Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells

inferred← citeshttps://doi.org/10.1038/s41467-023-40206-zopenalex-snapshot

Single-cell analysis of lizard blastema fibroblasts reveals phagocyte-dependent activation of Hedgehog-responsive chondrogenesis

inferred← citeshttps://doi.org/10.1080/03946975.1991.10539489openalex-snapshot

A unisexual species ofTeiusMerrem 1820 (Sauria Teiidae) from central Argentina

inferred← citeshttps://doi.org/10.1093/cz/zoac036openalex-snapshot

Evolution of parthenogenetic reproduction in Caucasian rock lizards: A review

inferred← citeshttps://doi.org/10.1098/rspb.1995.0022openalex-snapshot

When species collide: the origin and spread of an asexual species of gecko

inferred← citeshttps://doi.org/10.1111/j.1095-8312.1993.tb00882.xopenalex-snapshot

Genetic diversity and the history of pacific island house geckos (Hemidactylus and Lepidodactylus)

inferred← citeshttps://doi.org/10.1111/j.1439-0310.1980.tb01068.xopenalex-snapshot

Apparent Homosexual Behaviour in an All‐female Population of a Lizard, Lepidodactylus lugubris and its Probable Interpretation

inferred← citeshttps://doi.org/10.1111/j.1439-0310.1982.tb00329.xopenalex-snapshot

Social Behaviour of the Parthenogenetic Indo-Pacific Gecko, Hemidactylus garnotii

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1977.tb00978.xopenalex-snapshot

GENETIC HOMOGENEITY AND SPECIATION IN THE PARTHENOGENETIC LIZARDSCNEMIDOPHORUS VELOXANDC. NEOMEXICANUS:EVIDENCE FROM INTRASPECIFIC HISTOCOMPATIBILITY

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1979.tb04659.xopenalex-snapshot

CLONAL DIVERSITY IN THE UNISEXUAL FISH POECILIOPSIS MONACHA‐LUCIDA : A TISSUE GRAFT ANALYSIS

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1979.tb04710.xopenalex-snapshot

THE POPULATION STRUCTURE OF AN ASEXUAL VERTEBRATE, POECILIOPSIS 2 MONACHA‐LUCIDA (PISCES: POECILIIDAE)

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1984.tb00270.xopenalex-snapshot

HISTOCOMPATIBILITY IN HAWAIIAN AND POLYNESIAN POPULATIONS OF THE PARTHENOGENETIC GECKOLEPIDODACTYLUS LUGUBRIS

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1987.tb02464.xopenalex-snapshot

PARTHENOGENESIS IN THE TROPICAL GEKKONID LIZARD,NACTUS ARNOUXII(SAURIA: GEKKONIDAE)

inferred← citeshttps://doi.org/10.1111/jbi.12645openalex-snapshot

Deep divergence and structure in the Tropical Oceanic Pacific: a multilocus phylogeography of a widespread gekkonid lizard (Squamata: Gekkonidae:Gehyra oceanica)

inferred← citeshttps://doi.org/10.1126/science.779030openalex-snapshot

Intraclonal Histocompatibility in a Parthenogenetic Lizard: Evidence of Genetic Homogeneity

inferred← citeshttps://doi.org/10.1126/science.887925openalex-snapshot

Animal Parthenogenesis

inferred← citeshttps://doi.org/10.1134/s1062359025700566openalex-snapshot

Studies on the Unisexual Reptiles by and since I.S. Darevsky

inferred← citeshttps://doi.org/10.1196/annals.1336.022openalex-snapshot

Male Gamete Contributions to the Embryo

inferred← citeshttps://doi.org/10.1371/journal.pone.0132380openalex-snapshot

Comparative Chromosome Painting and NOR Distribution Suggest a Complex Hybrid Origin of Triploid Lepidodactylus lugubris (Gekkonidae)

inferred← citeshttps://doi.org/10.1371/journal.pone.0143630openalex-snapshot

Experimental Crossing of Two Distinct Species of Leopard Geckos, Eublepharis angramainyu and E. macularius: Viability, Fertility and Phenotypic Variation of the Hybrids

inferred← citeshttps://doi.org/10.1371/journal.pone.0183143openalex-snapshot

Pet snakes illegally marketed in Brazil: Climatic viability and establishment risk

inferred← citeshttps://doi.org/10.15560/13.2.2082openalex-snapshot

Second record of the invasive gecko Lepidodactylus lugubris (Duméril & Bibron, 1836) (Squamata: Gekkonidae) from Venezuela

inferred← citeshttps://doi.org/10.17161/randa.v25i3.14297openalex-snapshot

High abundance of the introduced Mourning Gecko (Lepidodactylus lugubris) in southwestern Grande Terre, Guadeloupe, French West Indies

inferred← citeshttps://doi.org/10.17161/randa.v30i1.18399openalex-snapshot

First record of the Mourning Gecko, Lepidodactylus lugubris (Duméril and Bibron), in Martinique, French Antilles

inferred← citeshttps://doi.org/10.2307/1939550openalex-snapshot

Invasions and Competitive Displacement among House Geckos in the Tropical Pacific

inferred← citeshttps://doi.org/10.2307/2409091openalex-snapshot

Parthenogenesis in the Tropical Gekkonid Lizard, Nactus arnouxii (Sauria: gekkonidae)

inferred← citeshttps://doi.org/10.2307/2844923openalex-snapshot

The Biogeography of the Lizards of the Seychelles Islands

inferred← citeshttps://doi.org/10.2307/3558386openalex-snapshot

Evidence for a switch in the reproductive biology of Rubus alceifolius (Rosaceae) towards apomixis, between its native range and its area of introduction

inferred← citeshttps://doi.org/10.2994/sajh-d-20-00036.1openalex-snapshot

Invasive Amphibians and Reptiles Living in Brazil

inferred← citeshttps://doi.org/10.31390/gradschool_theses.5309openalex-snapshot

Determining the Effects of Exogenous Human Chorionic Gonadotropin and Pregnant Mare Serum Gonadotropin on Plasma Testosterone, Testicular Volume, and Semen Production in Leopard Geckos (Eublepharis macularius)

inferred← citeshttps://doi.org/10.3390/ani13030471openalex-snapshot

Genome Evolution and the Future of Phylogenomics of Non-Avian Reptiles

inferred← citeshttps://doi.org/10.3853/j.1031-8062.7.1992.72openalex-snapshot

The herpetofauna of the Weipa region, Cape York Peninsula

inferred← citeshttps://doi.org/10.3897/herpetozoa.33.e53625openalex-snapshot

First record of the invasive gecko, Lepidodactylus lugubris Duméril & Bibron, 1836 in mainland Chile (Squamata, Gekkonidae)

inferred← citeshttps://doi.org/10.3897/herpetozoa.35.e84045openalex-snapshot

First record of Lepidodactylus lugubris (Duméril & Bibron, 1836) (Squamata, Gekkonidae) from Hainan Island, China

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