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Destabilizing Hybridization, General-Purpose Genotypes and Geographic Parthenogenesis
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.1401710205openalex-snapshot
Adenosine deaminase phenotypes among sexual and parthenogenetic lizards in the genus Cnemidophorus (teiidae)
inferredcites →https://doi.org/10.1007/978-1-4613-3069-1_16openalex-snapshot
Polyploidy in Insect Evolution
inferredcites →https://doi.org/10.1007/978-1-4615-6950-3_5openalex-snapshot
Evolution of Parthenogenetic Insects
inferredcites →https://doi.org/10.1007/978-1-4615-6953-4_6openalex-snapshot
Evolution and Ecology of Unisexual Fishes
inferredcites →https://doi.org/10.1007/978-1-4615-6959-6_3openalex-snapshot
Hybrid Release of Mutator Activity and the Genetic Structure of Natural Populations
inferredcites →https://doi.org/10.1007/978-1-4684-6270-8openalex-snapshot
Evolution and Genetics of Life Histories
inferredcites →https://doi.org/10.1007/978-1-4684-6270-8_6openalex-snapshot
The Prophecies of Parthenogenesis
inferredcites →https://doi.org/10.1007/978-3-642-66069-6_32openalex-snapshot
Evolution of Parthenogenetic Species of Reptiles
inferredcites →https://doi.org/10.1007/bf00284775openalex-snapshot
Cytogenetics of ticks (Acari: Ixodoidea)
inferredcites →https://doi.org/10.1007/bf00284841openalex-snapshot
Oogenesis and chromosomal heterozygosity in the thelytokous midge, Lundstroemia parthenogenetica (Diptera, Chironomidae)
inferredcites →https://doi.org/10.1007/bf00285964openalex-snapshot
Cytogenetics of the parthenogenetic grasshopper Warramaba (formerly Moraba) virgo and its bisexual relatives
inferredcites →https://doi.org/10.1007/bf00321153openalex-snapshot
Cytogenetic studies of Poecilia (Pisces)
inferredcites →https://doi.org/10.1007/bf00326365openalex-snapshot
Structural heterozygosity in parthenogenetic populations of Cnemidophorus lemniscatus (Sauria, Teiidae) from the Amazonas valley
inferredcites →https://doi.org/10.1007/bf00327397openalex-snapshot
Cytogenetics of the parthenogenetic grasshopper Warramaba (formerly Moraba) virgo and its bisexual relatives
inferredcites →https://doi.org/10.1007/bf01922547openalex-snapshot
Selection in parthenogenetic lines ofAsplanchna sieboldi (Leydig) 1854 (Rotatoria)
inferredcites →https://doi.org/10.1007/bf02371647openalex-snapshot
The biosystematic relations between a thelytokous and an arrhenotokous form ofAphytis mytilaspidis (Le Baron) [Hymenoptera: aphelinidae] I. The Reproductive relations
inferredcites →https://doi.org/10.1016/0027-5107(64)90047-8openalex-snapshot
The relation of recombination to mutational advance
inferredcites →https://doi.org/10.1016/0040-5809(81)90026-5openalex-snapshot
Population dynamics of species with gynogenetic sibling species
inferredcites →https://doi.org/10.1016/0047-2484(80)90077-9openalex-snapshot
Animal cytology and evolution
inferredcites →https://doi.org/10.1016/b978-1-4831-9953-5.50010-xopenalex-snapshot
Experimental Alterations of the Developmental Cytogenetic Mechanisms in Mulberry Silkworms: Artificial Parthenogenesis, Polyploidy, Gynogenesis, and Androgenesis
inferredcites →https://doi.org/10.1016/b978-1-4832-2776-4.50015-0openalex-snapshot
Parthenogenesis in Vertebrates
inferredcites →https://doi.org/10.1016/s0065-2660(08)60086-3openalex-snapshot
Parthenogenesis in Animals
inferredcites →https://doi.org/10.1017/s0080455x00000801openalex-snapshot
XIII.—The Cytology of a Diploid Bisexual Spider Beetle, Ptinus clavipes Panzer and its Triploid Gynogenetic form mobilis Moore
inferredcites →https://doi.org/10.1017/s0080456800009534openalex-snapshot
XVI.—Cytological Studies of Melaniidæ (Mollusca) with Special Reference to Parthenogenesis and Polyploidy. I. Oögenesis of the Parthenogenetic Species ofMelanoides(Prosobranchia-Gastropoda)
inferredcites →https://doi.org/10.1038/274317a0openalex-snapshot
Mutator genes—pacemakers of evolution
inferredcites →https://doi.org/10.1038/293437a0openalex-snapshot
Palaeontological documentation of speciation in Cenozoic molluscs from Turkana Basin
inferredcites →https://doi.org/10.1038/302495a0openalex-snapshot
Frequency of fixation of adaptive mutations is higher in evolving diploid than haploid yeast populations
inferredcites →https://doi.org/10.1038/hdy.1952.4openalex-snapshot
The chromosomes of the earthworms: I. The evolution of polyploidy
inferredcites →https://doi.org/10.1071/zo9590007openalex-snapshot
Observations on the biology of Haemaphysalis bispinosa Neumann (Acarina: Ixodidae) with particular reference to its mode of reproduction by parthenogenesis.
inferredcites →https://doi.org/10.1071/zo9680647openalex-snapshot
Origin and evolution of Parthenogenetic reproduction in the grasshopper Maraba virgo (Eumastacidae: Morabinae)
inferredcites →https://doi.org/10.1073/pnas.42.4.194openalex-snapshot
A CASE OF POLYPLOIDY IN DIPTERA
inferredcites →https://doi.org/10.1073/pnas.74.3.1130openalex-snapshot
Evolutionary consequences of parthogenesis: evidence from the Warramaba virgo complex.
inferredcites →https://doi.org/10.1080/00087114.1952.10797539openalex-snapshot
Cariologia deiLumbricidae
inferredcites →https://doi.org/10.1080/11250006209440615openalex-snapshot
La partenogenesi negli Afidi
inferredcites →https://doi.org/10.1086/280047openalex-snapshot
Why Polyploidy is Rarer in Animals Than in Plants
inferredcites →https://doi.org/10.1086/282095openalex-snapshot
Parthenogenesis in Drosophila mangabeirai Malog.
inferredcites →https://doi.org/10.1086/282389openalex-snapshot
Evolution in Sexual and Asexual Populations
inferredcites →https://doi.org/10.1086/282412openalex-snapshot
Sexual Isolation in a Parthenogenetic Strain of Drosophila mercatorum
inferredcites →https://doi.org/10.1086/282629openalex-snapshot
Hybridization, Unisexuality, and Polyploidy in the Teleost Poeciliopsis (Poeciliidae) and Other Vertebrates
inferredcites →https://doi.org/10.1086/282678openalex-snapshot
Meiotic Mechanisms of Naturally Occurring Unisexual Vertebrates
inferredcites →https://doi.org/10.1086/282809openalex-snapshot
Intragenic Recombination as a Source of Population Genetic Variability
inferredcites →https://doi.org/10.1086/282940openalex-snapshot
On the Origin of Parthenogenesis in Vertebrates: The Cytogenetic Factors
inferredcites →https://doi.org/10.1086/283012openalex-snapshot
Pest Pressure and Recombination Systems in Plants
inferredcites →https://doi.org/10.1086/283071openalex-snapshot
What Determines the Rate of Evolution?
inferredcites →https://doi.org/10.1086/283098openalex-snapshot
Animal Population Structure Under Close Inbreeding: The Land Snail Rumina in Southern France
inferredcites →https://doi.org/10.1086/283251openalex-snapshot
Variation and Clonal Structure in a Unisexual Fish
inferredcites →https://doi.org/10.1086/283293openalex-snapshot
Parental Investment: Comparative Reproductive Energetics in Bisexual and Unisexual Lizards, Genus Cnemidophorus
inferredcites →https://doi.org/10.1086/283308openalex-snapshot
Sexuality and the Components of Environmental Uncertainty: Clues from Geographic Parthenogenesis in Terrestrial Animals
inferredcites →https://doi.org/10.1086/283622openalex-snapshot
Clonal Niche Structure in the Parthenogenetic Earthworm Octolasion tyrtaeum
inferredcites →https://doi.org/10.1086/284050openalex-snapshot
Parent-Offspring Pathogen Transmission: A Selective Agent Promoting Sexual Reproduction
inferredcites →https://doi.org/10.1086/284169openalex-snapshot
Phenotypic Evolution and Parthenogenesis
inferredcites →https://doi.org/10.1093/aesa/49.3.195openalex-snapshot
Parthenogenesis in Cockroaches1
inferredcites →https://doi.org/10.1093/aesa/54.1.12openalex-snapshot
A Study of Bisexual and Parthenogenetic Strains of Pycnoscelus surinamensis (Blattaria : Epilamprinae)
inferredcites →https://doi.org/10.1093/aesa/60.4.774openalex-snapshot
Sexual Isolation in Parthenogenetic Pycnoscelus surinamensis and Application of the Name Pycnoscelus indicus to Its Bisexual Relative (Dictyoptera: Blattaria: Blaberidae: Pycnoscelinae)
inferredcites →https://doi.org/10.1093/aesa/67.2.215openalex-snapshot
Reproductive Potential of Bisexual Pycnoscelus indicus and Clones of Its Parthenogenetic Relative, Pycnoscelus surinamensis1
inferredcites →https://doi.org/10.1093/genetics/39.1.4openalex-snapshot
PARTHENOGENESIS IN DROSOPHILA
inferredcites →https://doi.org/10.1093/genetics/55.1.157openalex-snapshot
SELECTION FOR PARTHENOGENESIS IN DROSOPHILA MERCATORUM
inferredcites →https://doi.org/10.1093/genetics/78.2.737openalex-snapshot
THE EVOLUTIONARY ADVANTAGE OF RECOMBINATION
inferredcites →https://doi.org/10.1093/genetics/82.2.349openalex-snapshot
THE UNIT OF SELECTION IN DROSOPHILA MERCATORUM I. THE INTERACTION OF SELECTION AND MEIOSIS IN PARTHENOGENETIC STRAINS
inferredcites →https://doi.org/10.1093/genetics/84.4.791openalex-snapshot
THE ORGANIZATION OF GENETIC DIVERSITY IN THE PARTHENOGENETIC LIZARD CNEMIDOPHORUS TESSELATUS
inferredcites →https://doi.org/10.1093/genetics/92.4.1265openalex-snapshot
THE UNIT OF SELECTION IN DROSOPHILA MERCATORUM. II. GENETIC REVOLUTION AND THE ORIGIN OF COADAPTED GENOMES IN PARTHENOGENETIC STRAINS
inferredcites →https://doi.org/10.1093/icb/11.2.273openalex-snapshot
Systematic and Evolutionary Implications of Parthenogenesis in the Hymenoptera
inferredcites →https://doi.org/10.1093/icb/11.2.301openalex-snapshot
Parthenogenesis in Coccids (Homoptera)
inferredcites →https://doi.org/10.1093/icb/11.2.341openalex-snapshot
Parthenogenesis and Polyploidy in Beetles
inferredcites →https://doi.org/10.1093/icb/19.3.729openalex-snapshot
Evolution and Ecology of Parthenogenesis in Earthworms
inferredcites →https://doi.org/10.1093/icb/19.3.773openalex-snapshot
On the Ecology of Coexistence in Parthenogenetic and Bisexual Lizards of the GenusCnemidophorus
inferredcites →https://doi.org/10.1093/icb/19.3.787openalex-snapshot
Factors Affecting Clonal Diversity and Coexistence
inferredcites →https://doi.org/10.1111/j.1095-8312.1979.tb00038.xopenalex-snapshot
Stability and variation in aphid clonal lineages
inferredcites →https://doi.org/10.1111/j.1365-2311.1981.tb00975.xopenalex-snapshot
The adaptive and evolutionary significance of wing polymorphism and parthenogenesis in Ptinella Motschulsky (Coleoptera: Ptiliidae)
inferredcites →https://doi.org/10.1111/j.1365-3032.1974.tb00046.xopenalex-snapshot
Inherited changes in enzyme patterns within parthenogenetic clones of Aphis fabae
inferredcites →https://doi.org/10.1111/j.1439-0418.1941.tb01027.xopenalex-snapshot
Über Parthenogenese bei forstschädlichen Otior‐rhynchusarten in den während der Eiszeit vergletscherten Gebieten der Ostalpen
inferredcites →https://doi.org/10.1111/j.1558-5646.1948.tb02733.xopenalex-snapshot
THE CHROMOSOMES OF THE PARTHENOGENETIC MANTID BRUNNERIA BOREALIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1956.tb02862.xopenalex-snapshot
ON THE EVOLUTION OF PARTHENOGENESIS IN LONCHOPTERA (DIPTERA)
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.1558-5646.1971.tb01869.xopenalex-snapshot
THE ECOLOGICAL RELATIONSHIP OF THE SALAMANDER AMBYSTOMA LATERALE TO ITS ALL‐FEMALE, GYNOGENETIC ASSOCIATE
inferredcites →https://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
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb01070.xopenalex-snapshot
BIOLOGICAL VARIABILITY IN THE PARTHENOGENETIC GRASSHOPPER WARRAMABA VIRGO (KEY) AND ITS SEXUAL RELATIVES. 1. THE EASTERN AUSTRALIAN POPULATIONS
inferredcites →https://doi.org/10.1111/j.1558-5646.1977.tb01076.xopenalex-snapshot
GENETIC DIVERSITY IN COLONIZING PARTHENOGENETIC COCKROACHES
inferredcites →https://doi.org/10.1111/j.1558-5646.1978.tb00653.xopenalex-snapshot
BIOLOGICAL VARIABILITY IN THE PARTHENOGENETIC GRASSHOPPER WARRAMABA VIRGO (KEY) AND ITS SEXUAL RELATIVES. II. THE WESTERN AUSTRALIAN TAXA
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04659.xopenalex-snapshot
CLONAL DIVERSITY IN THE UNISEXUAL FISH POECILIOPSIS MONACHA‐LUCIDA : A TISSUE GRAFT ANALYSIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04664.xopenalex-snapshot
CYTOGENETICS OF THE PARTHENOGENETIC GRASSHOPPER WARRAMABA (FORMERLY MORABA) VIRGO AND ITS BISEXUAL RELATIVES. V. INTERACTION OF W. VIRGO AND A BISEXUAL SPECIES IN GEOGRAPHIC CONTACT
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04731.xopenalex-snapshot
ARE PARTHENOGENETIC AND RELATED BISEXUAL INSECTS EQUAL IN FERTILITY?
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04733.xopenalex-snapshot
GENETIC VARIATION AND HOST PLANT RELATIONS IN A PARTHENOGENETIC MOTH
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04739.xopenalex-snapshot
HETEROSIS AND INTERCLONAL VARIATION IN THERMAL TOLERANCE IN UNISEXUAL FISHES
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04765.xopenalex-snapshot
HYBRIDIZATION IN MILKWEED BUGS OF THE GENUS ONCOPELTUS (HEMIPTERA: LYGAEIDAE)
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04769.xopenalex-snapshot
PHENOTYPIC CONSEQUENCES OF PARTHENOGENESIS INCNEMIDOPHORUSLIZARDS. I. VARIABILITY IN PARTHENOGENETIC AND SEXUAL POPULATIONS
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04043.xopenalex-snapshot
THEORY OF POPULATION GENETICS AND EVOLUTIONARY ECOLOGY: AN INTRODUCTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04051.xopenalex-snapshot
CONSIDERATION OF MULLER'S RATCHET MECHANISM THROUGH STUDIES OF GENETIC LINKAGE AND GENOMIC COMPATIBILITIES IN CLONALLY REPRODUCING POECILIOPSIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04813.xopenalex-snapshot
EVOLUTIONARY GENETICS OF A GYNOGENETIC FISH, POECILIA FORMOSA , THE AMAZON MOLLY
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb05545.xopenalex-snapshot
ECOLOGICAL GENETICS OF DAPHNIA PULEX
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb05571.xopenalex-snapshot
THE ACCUMULATION OF GENETIC VARIATION IN A PARTHENOGENETIC SNAIL
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb05601.xopenalex-snapshot
CLONAL DIVERSITY AND EVOLUTIONARY DYNAMICS IN A DIPLOID‐TRIPLOID BREEDING COMPLEX OF UNISEXUAL FISHES ( POECILIA )
inferredcites →https://doi.org/10.1111/j.1601-5223.1961.tb01777.xopenalex-snapshot
ON MORPHOLOGICAL DIFFERENCES AND EVOLUTION OF DIFFERENT POLYPLOID PARTHENOGENETIC WEEVIL POPULATIONS
inferredcites →https://doi.org/10.1111/j.1601-5223.1976.tb01570.xopenalex-snapshot
Genetic polymorphism and evolution in parthenogenetic animals
inferredcites →https://doi.org/10.1111/j.1601-5223.1976.tb01571.xopenalex-snapshot
Genetic polymorphism and evolution in parthenogenetic animals
inferredcites →https://doi.org/10.1111/j.1601-5223.1979.tb01660.xopenalex-snapshot
Differential distribution of genetic variants in triploid parthenogenetic Trichoniscus pusillus (Isopoda, Crustacea) in a heterogeneous environment
inferredcites →https://doi.org/10.1126/science.199.4328.549openalex-snapshot
Coexistence of Clones in a Heterogeneous Environment
inferredcites →https://doi.org/10.1126/science.207.4437.1363openalex-snapshot
Clonal Coexistence in Daphnia pulex (Leydig): Another Planktonic Paradox
inferredcites →https://doi.org/10.1126/science.218.4567.68openalex-snapshot
Decay of female sexual behavior under parthenogenesis.
inferredcites →https://doi.org/10.1126/science.779030openalex-snapshot
Intraclonal Histocompatibility in a Parthenogenetic Lizard: Evidence of Genetic Homogeneity
inferredcites →https://doi.org/10.1139/g66-085openalex-snapshot
THE CHROMOSOMES OF BISEXUAL AND PARTHENOGENETIC SPECIES OFCALLIGRAPHA(COLEOPTERA: CHRYSOMELIDAE) WITH NOTES ON SEX RATIO, ABUNDANCE AND EGG NUMBER
inferredcites →https://doi.org/10.1139/z59-060openalex-snapshot
TRIPLOIDY IN NATURAL POPULATIONS OF THE BLACK FLY CNEPHIA MUTATA (MALLOCH)
inferredcites →https://doi.org/10.1139/z78-094openalex-snapshot
Comparative observations on the ecology of four species of ostracods living in a temporary freshwater puddle
inferredcites →https://doi.org/10.1146/annurev.es.07.110176.002225openalex-snapshot
Evolution and Ecological Value of Duplicate Genes
inferredcites →https://doi.org/10.1146/annurev.ge.03.120169.000531openalex-snapshot
EXPERIMENTAL POLYPLOIDY IN ANIMALS
inferredcites →https://doi.org/10.1242/jcs.34.1.247openalex-snapshot
Nuclear volume control by nucleoskeletal DNA, selection for cell volume and cell growth rate, and the solution of the DNA C-value paradox
inferredcites →https://doi.org/10.2183/pjab1945.52.126openalex-snapshot
On the Chromosomes of Parthenogenetic Curculionid Weevils in Japan
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/10.2307/1441764openalex-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/10.2307/1442879openalex-snapshot
Biochemical Evidence for the Hybrid Origin of the Parthenogenetic Species of the Lacerta saxicola Complex (Sauria: Lacertidae), with a Discussion of Some Ecological and Evolutionary Implications
inferredcites →https://doi.org/10.2307/1540952openalex-snapshot
ARTEMIAHEMOGLOBINS: GENETIC VARIATION IN PARTHENOGENETIC AND ZYGOGENETIC POPULATIONS
inferredcites →https://doi.org/10.2307/1936026openalex-snapshot
Coexistence in Unisexual‐Bisexual Species Complexes of Poeciliopsis (Pisces: Poeciliidae)
inferredcites →https://doi.org/10.2307/1936839openalex-snapshot
An Experimental Model: Bacterial Specialists and Generalists Competing in Chemostats
inferredcites →https://doi.org/10.2307/1937409openalex-snapshot
Competition Experiments Between Parthenogenetic and Sexual Strains of the Brine Shrimp, Artemia Salina
inferredcites →https://doi.org/10.2307/2424935openalex-snapshot
The Systematics, and Geographical and Ecological Distribution of Ptiliopycna, a Nearctic Genus of Parthenogenetic Featherwing Beetles (Coleoptera: Ptiliidae)
inferredcites →https://doi.org/10.2307/2529912openalex-snapshot
Introduction to Quantitative Genetics.
inferredcites →https://doi.org/10.2307/3279161openalex-snapshot
Differential Variation of Parthenogenetic and Bisexual Haemaphysalis longicornis (Acari : Ixodidae)
inferredcites →https://doi.org/10.2307/3543500openalex-snapshot
Vertical Distribution of Lumbricids in Southern Sweden
inferredcites →https://doi.org/10.2307/j.ctvx5wbbhopenalex-snapshot
Evolution in Changing Environments
inferredcites →https://doi.org/10.4039/ent87131-3openalex-snapshot
Cytogenetics of Obligatory Parthenogenesis
inferredcites →https://doi.org/10.4319/lo.1984.29.2.0225openalex-snapshot
Spatial heterogeneity of Daphnia genotypes: Vertical migration and habitat partitioning1
inferredcites →https://doi.org/10.5962/bhl.part.14767openalex-snapshot
Leposoma percarinatum, a unisexual species related to L. guianense; and Leposoma ioanna, a new species from Pacific Coastal Colombia (Sauria, Teiidae)
inferredcites →https://doi.org/10.5962/bhl.part.75584openalex-snapshot
Le croisement des espèces parthénogénétique et bisexuée chez Luffia (Lépidoptère Psychide). Les élevages et leurs résultats
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1080/00222933.2021.1936678zenodo-depositor-declared
Amblypygi parthenogenesis, embryonic and post-embryonic development: a case study with the Amazonian species Charinus guto Giupponi and Miranda, 2016 (Amblypygi: Charinidae)
inferred← citeshttps://doi.org/10.5324/cjcr.v0i33.3478zenodo-depositor-declared
Evidence of parthenogenetic populations from the Paratanytarsus laccophilus species group (Diptera: Chironomidae) in the Alaskan Arctic
inferred← citeshttps://doi.org/10.1002/9780470015902.a0028485openalex-snapshot
The Queen of Problems in Evolutionary Biology
inferred← citeshttps://doi.org/10.1002/9781119072799.ch1openalex-snapshot
FOUNDATIONS OF INVASION GENETICS
inferred← citeshttps://doi.org/10.1002/ajb2.16149openalex-snapshot
Dispersal and establishment traits provide a colonization advantage for a polyploid apomictic plant
inferred← citeshttps://doi.org/10.1002/ajb2.1653openalex-snapshot
Patterns of population genomic diversity in the invasive Japanese knotweed species complex
inferred← citeshttps://doi.org/10.1002/ajb2.1771openalex-snapshot
Genetic structure in patchy populations of a candidate foundation plant: a case study of Leymus chinensis using genetic and clonal diversity
inferred← citeshttps://doi.org/10.1002/ece3.3895openalex-snapshot
The fitness effects of delayed switching to sex in a facultatively asexual insect
inferred← citeshttps://doi.org/10.1002/ece3.471openalex-snapshot
Adaptive responses and invasion: the role of plasticity and evolution in snail shell morphology
inferred← citeshttps://doi.org/10.1002/ece3.4992openalex-snapshot
Difference in reproductive mode rather than ploidy explains niche differentiation in sympatric sexual and apomictic populations ofPotentilla puberula
inferred← citeshttps://doi.org/10.1002/ece3.58openalex-snapshot
Improbable but true: the invasive inbreeding ambrosia beetle Xylosandrus morigerus has generalist genotypes
inferred← citeshttps://doi.org/10.1002/ece3.70145openalex-snapshot
Does ecology shape geographical parthenogenesis? Evidence from the facultatively parthenogenetic stick insect Megacrania batesii
inferred← citeshttps://doi.org/10.1002/ece3.7047openalex-snapshot
Repeated convergent evolution of parthenogenesis in Acariformes (Acari)
inferred← citeshttps://doi.org/10.1002/ece3.71046openalex-snapshot
Older Lineages of Oribatid Mites in Mountain Ranges Have Broader Geographic Ranges and Exhibit More Generalistic Traits
inferred← citeshttps://doi.org/10.1002/ece3.72316openalex-snapshot
Polyembryonic or Apomictic Seeds Enable Fig Trees to Establish New Populations Without Their Pollinating Wasps, a Case Observation in Ficus gasparriniana
inferred← citeshttps://doi.org/10.1002/ece3.9036openalex-snapshot
“Jack‐of‐all‐trades” is parthenogenetic
inferred← citeshttps://doi.org/10.1002/etc.5620160925openalex-snapshot
Effects of triphenyltin and pH on the growth and development ofRana lessonaeandRana esculentatadpoles
inferred← citeshttps://doi.org/10.1002/etc.5620210229openalex-snapshot
Comparing the acute response to cadmium toxicity of nauplii from different populations of Artemia
inferred← citeshttps://doi.org/10.1002/evl3.2017.1.issue-6openalex-snapshot
Evolution and comparative ecology of parthenogenesis in haplodiploid arthropods
inferred← citeshttps://doi.org/10.1002/evl3.30openalex-snapshot
Evolution and comparative ecology of parthenogenesis in haplodiploid arthropods
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1987.tb08586.xopenalex-snapshot
PATTERNS OF GENOTYPIC DIVERSITY IN CLONAL PLANT SPECIES
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1991.tb12596.xopenalex-snapshot
LIFE HISTORY VARIATION WITHIN POPULATIONS OF AN ASEXUAL PLANT, ERIGERON ANNUUS (ASTERACEAE)
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1995.tb11587.xopenalex-snapshot
A llozyme diversity in the apomictic vine B ryonia alba ( cucurbitaceae ): potential consequences of multiple introductions
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1996.tb12724.xopenalex-snapshot
Low Levels of Intraspecific Genetic Variation at a Rapidly Evolving Chloroplast DNA Locus in North American Duckweeds (Lemnaceae)
inferred← citeshttps://doi.org/10.1002/mmnz.20010770106openalex-snapshot
The future of the selfish hemiclone: A Neodarwinian approach to water frog evolution
inferred← citeshttps://doi.org/10.1002/mmnz.4850770106openalex-snapshot
The future of the selfish hemiclone: A Neodarwinian approach to water frog evolution
inferred← citeshttps://doi.org/10.1002/njz2.70019openalex-snapshot
Potential Drivers of Successful Biocontrol: A Perspective on Parasitoids
inferred← citeshttps://doi.org/10.1002/njz2.70044openalex-snapshot
Investigating the Possibility of Wolbachia ‐ and Cardinium ‐Induced Parthenogenesis in Two Mite Species
inferred← citeshttps://doi.org/10.1002/ps.3643openalex-snapshot
Global genetic variation in the Asian citrus psyllid, Diaphorina citri (Hemiptera: Liviidae) and the endosymbiont Wolbachia: links between Iran and the USA detected
inferred← citeshttps://doi.org/10.1002/tax.602009openalex-snapshot
Evolution and biogeography of alpine apomictic plants
inferred← citeshttps://doi.org/10.1007/978-1-4615-2389-5_11openalex-snapshot
Cytogenetics of Holokinetic Chromosomes and Inverted Meiosis: Keys to the Evolutionary Success of Mites, with Generalizations on Eukaryotes
inferred← citeshttps://doi.org/10.1007/978-1-4615-2389-5_5openalex-snapshot
Evolutionary Aspects of Oribatid Mite Life Histories and Consequences for the Origin of the Astigmata
inferred← citeshttps://doi.org/10.1007/978-1-4684-1402-8_2openalex-snapshot
Phylogenetic Perspectives on Genetic Systems and Reproductive Modes of Mites
inferred← citeshttps://doi.org/10.1007/978-3-0348-6273-8_9openalex-snapshot
Patterns in plant parthenogenesis
inferred← citeshttps://doi.org/10.1007/978-3-0348-6426-8_4openalex-snapshot
Population Extinction by Mutational Load and Demographic Stochasticity
inferred← citeshttps://doi.org/10.1007/978-3-0348-7527-1_28openalex-snapshot
The evolutionary ecology of Daphnia
inferred← citeshttps://doi.org/10.1007/978-3-0348-8880-6openalex-snapshot
Evolutionary Ecology of Freshwater Animals
inferred← citeshttps://doi.org/10.1007/978-3-0348-8880-6_10openalex-snapshot
Evolution and ecological correlates of uniparental and biparental reproduction in freshwater snails
inferred← citeshttps://doi.org/10.1007/978-3-0348-8880-6_9openalex-snapshot
Population biology, genetic structure, and mating system parameters in freshwater snails
inferred← citeshttps://doi.org/10.1007/978-3-319-19932-0_16openalex-snapshot
Apomixis as a Facilitator of Range Expansion and Diversification in Plants
inferred← citeshttps://doi.org/10.1007/978-3-540-36832-8_6openalex-snapshot
Population Genetics: Evolutionary Features of Asexual Species
inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_1openalex-snapshot
Asex and Evolution: A Very Large-Scale Overview
inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_12openalex-snapshot
Parthenogenesis in Oribatid Mites (Acari, Oribatida): Evolution Without Sex
inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_15openalex-snapshot
Cyclical Parthenogenesis in Daphnia: Sexual Versus Asexual Reproduction
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/10.1007/978-90-481-2770-2_6openalex-snapshot
Geographical Parthenogenesis: General Purpose Genotypes and Frozen Niche Variation
inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_8openalex-snapshot
Geographical Parthenogenesis: Opportunities for Asexuality
inferred← citeshttps://doi.org/10.1007/978-94-009-1541-1_7openalex-snapshot
Environmental stress and the distribution of traits within populations
inferred← citeshttps://doi.org/10.1007/978-94-009-4059-8_17openalex-snapshot
Ecology of bdelloids: how to be successful
inferred← citeshttps://doi.org/10.1007/978-94-011-3102-5_7openalex-snapshot
The distribution, mechanisms and evolutionary significance of parthenogenesis in oribatid mites
inferred← citeshttps://doi.org/10.1007/bf00025734openalex-snapshot
Ecology of bdelloids: how to be successful
inferred← citeshttps://doi.org/10.1007/bf00048262openalex-snapshot
The distributions of parthenogenetic ascid mites (Acari: Parasitiformes) do not support the biotic uncertainty hypothesis
inferred← citeshttps://doi.org/10.1007/bf00168589openalex-snapshot
Feeding behavior in sexual and clonal strains of Poeciliopsis
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/bf00317885openalex-snapshot
Tests for host-associated fitness trade-offs in the milkweed-oleander aphid
inferred← citeshttps://doi.org/10.1007/bf00333948openalex-snapshot
Variability in grape phylloxera preference and performance on canyon grape (Vitis arizonica)
inferred← citeshttps://doi.org/10.1007/bf00377515openalex-snapshot
Life history variation among low-arctic clones of obligately parthenogenetic Daphnia pulex: a diploid-polyploid complex
inferred← citeshttps://doi.org/10.1007/bf01138462openalex-snapshot
Natural hybridization in freshwater animals Ecological implications and molecular approaches
inferred← citeshttps://doi.org/10.1007/bf01194176openalex-snapshot
Further experimental proof of thelytokous parthenogenesis in oribatid mites (Acari: Oribatida: Desmonomata)
inferred← citeshttps://doi.org/10.1007/bf01204401openalex-snapshot
Taxonomic, geographic and seasonal distribution of thelytokous parthenogenesis in the Desmonomata (Acari: Oribatida)
inferred← citeshttps://doi.org/10.1007/bf01237772openalex-snapshot
Comparisons of life-history traits between clonal and sexual fish (Poeciliopsis:Poeciliidae) raised in monoculture and mixed treatments
inferred← citeshttps://doi.org/10.1007/bf01238194openalex-snapshot
Comparative ecology of sexual and asexual gecko species (Lepidodactylus) in French Polynesia
inferred← citeshttps://doi.org/10.1007/bf01435044openalex-snapshot
The origin and evolution of parthenogenesis in theHeteronotia binoei complex: Synthesis
inferred← citeshttps://doi.org/10.1007/bf01923444openalex-snapshot
Bdelloid rotifers in Dominican amber: Evidence for parthenogenetic continuity
inferred← citeshttps://doi.org/10.1007/bf02067393openalex-snapshot
Anisogamy, sexual selection, and the evolution and maintenance of sex
inferred← citeshttps://doi.org/10.1007/bf02143200openalex-snapshot
Population genetic structure and mating system evolution in freshwater pulmonates
inferred← citeshttps://doi.org/10.1007/bf02143201openalex-snapshot
Evolution and ecological correlates of uniparental reproduction in freshwater snails
inferred← citeshttps://doi.org/10.1007/bf02143202openalex-snapshot
Population biology of bryozoans: correlates of sessile, colonial life histories in freshwater habitats
inferred← citeshttps://doi.org/10.1007/bf02329054openalex-snapshot
Competitive trade-off strategies in Arctic Daphnia linked to melanism and UV-B stress
inferred← citeshttps://doi.org/10.1007/s000360050020openalex-snapshot
Clonal diversity in high arctic ostracodes
inferred← citeshttps://doi.org/10.1007/s000360050117openalex-snapshot
Evolutionary genetics and ecology of sperm-dependent parthenogenesis
inferred← citeshttps://doi.org/10.1007/s000400050126openalex-snapshot
Colony structure and reproduction in the thelytokous parthenogenetic ant Platythyrea punctata (F. Smith) (Hymenoptera, Formicidae)
inferred← citeshttps://doi.org/10.1007/s001289900828openalex-snapshot
Acute Lethal Toxicity of the Organophosphorus Pesticide Chlorpyrifos to Different Species and Strains of Artemia
inferred← citeshttps://doi.org/10.1007/s00227-006-0406-1openalex-snapshot
Physiological ecology of the clonal corallimorpharian Corynactis californica
inferred← citeshttps://doi.org/10.1007/s00300-025-03423-4openalex-snapshot
The distribution of Smittia brevipennis (Diptera, Chironomidae, Orthocladiinae) in the Russian high-Arctic assessed using molecular analyses
inferred← citeshttps://doi.org/10.1007/s00425-014-2053-yopenalex-snapshot
Genetic structure of duckweed population of Spirodela, Landoltia and Lemna from Lake Tai, China
inferred← citeshttps://doi.org/10.1007/s00442-002-0939-zopenalex-snapshot
A general purpose genotype in an ancient asexual
inferred← citeshttps://doi.org/10.1007/s00442-011-2113-yopenalex-snapshot
Two parthenogenetic populations of Chara canescens differ in their capacity to acclimate to irradiance and salinity
inferred← citeshttps://doi.org/10.1007/s004420050959openalex-snapshot
Performance of native grape phylloxera on host plants within and among terrestrial islands in Arizona, USA
inferred← citeshttps://doi.org/10.1007/s004420100674openalex-snapshot
Coexistence in space and time of sexual and asexual populations of the cereal aphid Sitobion avenae
inferred← citeshttps://doi.org/10.1007/s00606-020-01692-6openalex-snapshot
Negative effect of inbreeding on fitness of an arctic–alpine Hieracium alpinum (Asteraceae), a species with a geographical parthenogenesis distribution pattern
inferred← citeshttps://doi.org/10.1007/s10340-012-0458-6openalex-snapshot
First evidence of deuterotokous parthenogenesis in the tomato leafminer, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae)
inferred← citeshttps://doi.org/10.1007/s10340-016-0752-9openalex-snapshot
Life cycle and population genetics of bird cherry-oat aphids Rhopalosiphum padi in China: an important pest on wheat crops
inferred← citeshttps://doi.org/10.1007/s10452-012-9396-xopenalex-snapshot
Salinity adaptation of the invasive New Zealand mud snail (Potamopyrgus antipodarum) in the Columbia River estuary (Pacific Northwest, USA): physiological and molecular studies
inferred← citeshttps://doi.org/10.1007/s10493-005-3360-6openalex-snapshot
Adaptation in the Asexual False Spider Mite Brevipalpus phoenicis: Evidence for Frozen Niche Variation
inferred← citeshttps://doi.org/10.1007/s10493-006-9016-3openalex-snapshot
The ecological distribution of reproductive mode in oribatid mites, as related to biological complexity
inferred← citeshttps://doi.org/10.1007/s10493-008-9140-3openalex-snapshot
Ecological and morphological attributes of parthenogenetic Japanese Schwiebea species (Acari: Acaridae)
inferred← citeshttps://doi.org/10.1007/s10493-014-9801-3openalex-snapshot
Positive correlation of trophic level and proportion of sexual taxa of oribatid mites (Acari: Oribatida) in alpine soil systems
inferred← citeshttps://doi.org/10.1007/s10528-011-9442-8openalex-snapshot
Genetic Structure of Marchalina hellenica (Hemiptera: Margarodidae) Populations from Turkey: Preliminary mtDNA Sequencing Data
inferred← citeshttps://doi.org/10.1007/s10530-020-02270-0openalex-snapshot
Genetic evidence of multiple introductions and mixed reproductive strategy in the peregrine earthworm Pontoscolex corethrurus
inferred← citeshttps://doi.org/10.1007/s10658-015-0624-9openalex-snapshot
No evidence of superclones in leaf-feeding forms of austrian grape phylloxera (Daktulosphaira vitifoliae)
inferred← citeshttps://doi.org/10.1007/s10682-005-5631-4openalex-snapshot
Variation in Sex Ratio and Evolutionary Rate of Hemiclonal Rana esculenta Populations
inferred← citeshttps://doi.org/10.1007/s10682-009-9314-4openalex-snapshot
Differential survival among genotypes of Daphnia pulex differing in reproductive mode, ploidy level, and geographic origin
inferred← citeshttps://doi.org/10.1007/s10682-012-9564-4openalex-snapshot
Colonization ability of two invasive weevils with different reproductive modes
inferred← citeshttps://doi.org/10.1007/s10682-014-9730-yopenalex-snapshot
Do ecological niches differ between sexual and asexual lineages of an aphid species?
inferred← citeshttps://doi.org/10.1007/s10682-018-9942-7openalex-snapshot
Evidence for plasticity, but not local adaptation, in invasive Japanese knotweed (Reynoutria japonica) in North America
inferred← citeshttps://doi.org/10.1007/s10709-006-9130-5openalex-snapshot
The gynogenetic reproduction of diploid and triploid hybrid spined loaches (Cobitis: Teleostei), and their ability to establish successful clonal lineages—on the evolution of polyploidy in asexual vertebrates
inferred← citeshttps://doi.org/10.1007/s10709-015-9858-xopenalex-snapshot
Rare diploid females coexist with rare males: a novel finding in triploid parthenogenetic populations in the psyllid Cacopsylla myrtilli (W. Wagner, 1947) (Hemiptera, Psylloidea) in northern Europe
inferred← citeshttps://doi.org/10.1007/s10750-007-9085-2openalex-snapshot
Models of ontogenetic allometry in cladoceran morphology studies
inferred← citeshttps://doi.org/10.1007/s10886-004-7947-xopenalex-snapshot
EFFECT OF HOST DEFENSE CHEMICALS ON CLONAL DISTRIBUTION AND PERFORMANCE OF DIFFERENT GENOTYPES OF THE CEREAL APHID Sitobion avenae
inferred← citeshttps://doi.org/10.1007/s11104-009-0068-0openalex-snapshot
OCBIL theory: towards an integrated understanding of the evolution, ecology and conservation of biodiversity on old, climatically buffered, infertile landscapes
inferred← citeshttps://doi.org/10.1007/s11538-006-9112-xopenalex-snapshot
Behavioural Interactions Selecting for Symmetry and Asymmetry in Sexual Reproductive Systems of Eusocial Species
inferred← citeshttps://doi.org/10.1007/s11692-012-9219-yopenalex-snapshot
Adaptive Significance and Long-Term Survival of Asexual Lineages
inferred← citeshttps://doi.org/10.1007/s13592-017-0509-3openalex-snapshot
Genetic diversity of Varroa destructor parasitizing Apis mellifera unicolor in Madagascar
inferred← citeshttps://doi.org/10.1016/0006-3207(93)90667-popenalex-snapshot
Population extinction by mutational load and demographic stochasticity
inferred← citeshttps://doi.org/10.1016/0022-0981(88)90201-8openalex-snapshot
Effects of temperature and relative fitness of sexual and asexual brine shrimp Artemia
inferred← citeshttps://doi.org/10.1016/0022-0981(95)00137-9openalex-snapshot
Competition between sexual and parthenogenetic Artemia: temperature and strain effects
inferred← citeshttps://doi.org/10.1016/0045-6535(96)00188-9openalex-snapshot
Asexual reproductive adaptation to simulated cretaceous climatic variables by Norway spruce cells in vitro
inferred← citeshttps://doi.org/10.1016/0168-9525(86)90271-4openalex-snapshot
Some evolutionary consequences of the molecular recombination process
inferred← citeshttps://doi.org/10.1016/0169-5347(92)90051-copenalex-snapshot
Population genetics and ecology of Artemia: Insights into parthenogenetic reproduction
inferred← citeshttps://doi.org/10.1016/0169-5347(94)90124-4openalex-snapshot
Origin and evolution of animal hybrid species
inferred← citeshttps://doi.org/10.1016/0304-3770(93)90068-8openalex-snapshot
Evolutionary processes in aquatic plant populations
inferred← citeshttps://doi.org/10.1016/0304-3800(92)90092-sopenalex-snapshot
Assessing the response of demographic parameters to density in a rotifer population
inferred← citeshttps://doi.org/10.1016/0305-1978(92)90056-jopenalex-snapshot
Genetic diversity in thelytokous oribatid mites (Acari; Acariformes: Desmonomata)
inferred← citeshttps://doi.org/10.1016/b978-0-12-092860-6.50017-xopenalex-snapshot
The Selective Advantage of Outcrossing
inferred← citeshttps://doi.org/10.1016/b978-0-12-372568-4.00013-6openalex-snapshot
Unusual gametic and genetic systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-398760-0.50037-7openalex-snapshot
THE SELECTION OPERATING ON THE EVOLUTION EQUILIBRIUM OF THE FREQUENCY OF SEXUAL REPRODUCTION IN PREDOMINANTLY ASEXUAL POPULATIONS
inferred← citeshttps://doi.org/10.1016/b978-0-12-402960-6.50022-6openalex-snapshot
The Demographic Consequences of Sexuality and Apomixis in Antennaria
inferred← citeshttps://doi.org/10.1016/b978-0-12-503365-7.50006-7openalex-snapshot
Genetic Transmission and the Evolution of Reproduction: The Significance of Parent–Offspring Relatedness to the “Cost of Meiosis”
inferred← citeshttps://doi.org/10.1016/j.anbehav.2005.10.009openalex-snapshot
Behavioural mechanisms of invasion and displacement in Pacific island geckos (Hemidactylus)
inferred← citeshttps://doi.org/10.1016/j.apsoil.2017.09.013openalex-snapshot
Badger (Meles meles) disturbances affect oribatid mite (Acari: Oribatida) communities in European temperate forests
inferred← citeshttps://doi.org/10.1016/j.apsoil.2023.104912openalex-snapshot
Changes in oribatid mite community structure along two altitudinal gradients in Asia and Europe as related to environmental factors
inferred← citeshttps://doi.org/10.1016/j.aquabot.2016.03.006openalex-snapshot
Ecological and evolutionary consequences of sexual and clonal reproduction in aquatic plants
inferred← citeshttps://doi.org/10.1016/j.aquatox.2016.03.015openalex-snapshot
Induction of multixenobiotic defense mechanisms in resistant Daphnia magna clones as a general cellular response to stress
inferred← citeshttps://doi.org/10.1016/j.cois.2018.01.004openalex-snapshot
Biological and genetic features of introduced aphid populations in agroecosystems
inferred← citeshttps://doi.org/10.1016/j.cub.2011.05.026openalex-snapshot
Molecular Evidence for Ancient Asexuality in Timema Stick Insects
inferred← citeshttps://doi.org/10.1016/j.envpol.2005.08.009openalex-snapshot
Has long-term metal exposure induced changes in life history traits and genetic diversity of the enchytraeid worm Cognettia sphagnetorum (Vejd.)?
inferred← citeshttps://doi.org/10.1016/j.isci.2019.10.039openalex-snapshot
Signatures of the Evolution of Parthenogenesis and Cryptobiosis in the Genomes of Panagrolaimid Nematodes
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2025.104812openalex-snapshot
Parthenogenesis in the neotropical katydid Conocephalus ictus
inferred← citeshttps://doi.org/10.1016/j.jtbi.2009.08.012openalex-snapshot
Sperm-dependent parthenogens delay the spatial expansion of their sexual hosts
inferred← citeshttps://doi.org/10.1016/j.pedobi.2006.08.004openalex-snapshot
Little effect of forest age on oribatid mites on the bark of trees
inferred← citeshttps://doi.org/10.1016/j.pedobi.2006.11.001openalex-snapshot
Resources and sex: Soil re-colonization by sexual and parthenogenetic oribatid mites
inferred← citeshttps://doi.org/10.1016/j.pedobi.2013.07.001openalex-snapshot
More sex at higher altitudes: Changes in the frequency of parthenogenesis in oribatid mites in tropical montane rain forests
inferred← citeshttps://doi.org/10.1016/j.pedobi.2020.150625openalex-snapshot
Move or change, an eco-evolutionary dilemma: The case of Collembola
inferred← citeshttps://doi.org/10.1016/j.ppees.2014.01.001openalex-snapshot
Sexual Hieracium pilosella plants are better inter-specific, while apomictic plants are better intra-specific competitors
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.140046openalex-snapshot
Breaking ecological barriers: Anthropogenic disturbance leads to habitat transitions, hybridization, and high genetic diversity
inferred← citeshttps://doi.org/10.1016/j.soilbio.2022.108890openalex-snapshot
New perspectives on soil animal trophic ecology through the lens of C and N stable isotope ratios of oribatid mites
inferred← citeshttps://doi.org/10.1016/j.tree.2003.09.021openalex-snapshot
Why is sex so unpopular in the Australian desert?
inferred← citeshttps://doi.org/10.1016/j.tree.2005.06.005openalex-snapshot
Hybridization, glaciation and geographical parthenogenesis
inferred← citeshttps://doi.org/10.1016/j.tree.2017.06.002openalex-snapshot
Sexual Conflict, Facultative Asexuality, and the True Paradox of Sex
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.04.013openalex-snapshot
Phylogenetic relationships of coexisting Heterocypris (Crustacea, Ostracoda) lineages with different reproductive modes from Lampedusa Island (Italy)
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.11.029openalex-snapshot
Is polyploidy a persevering accident or an adaptive evolutionary pattern? The case of the brine shrimp Artemia
inferred← citeshttps://doi.org/10.1016/s0016-6995(86)80103-6openalex-snapshot
Kovalevskiella (Ostracoda, Timiriaseviinae), genre à mode de vie benthique depuis l'Oligocène, son adaptation à la vie interstitielle
inferred← citeshttps://doi.org/10.1016/s0022-0981(01)00363-xopenalex-snapshot
Estimating genetic and environmental components of variance using sexual and clonal Artemia
inferred← citeshttps://doi.org/10.1016/s0022-0981(99)00125-2openalex-snapshot
Combined effects of salinity and temperature on survival and reproduction of five species of Artemia
inferred← citeshttps://doi.org/10.1016/s0022-5193(05)80688-5openalex-snapshot
Males and the two-fold disadvantage of dioecy
inferred← citeshttps://doi.org/10.1016/s0022-5193(88)80158-9openalex-snapshot
Reproductive wastage and the evolution of genetic systems
inferred← citeshttps://doi.org/10.1016/s0065-2660(08)60012-7openalex-snapshot
The Molecular Basis of the Evolution of Sex
inferred← citeshttps://doi.org/10.1016/s0254-6299(15)30771-7openalex-snapshot
Genetic diversity of an exploited species, Flagellaria guineensis
inferred← citeshttps://doi.org/10.1016/s1095-6433(98)10060-0openalex-snapshot
The effects of temperature and oxygen tension (PO2) on the oxygen consumption rates of adults of different Artemia strains
inferred← citeshttps://doi.org/10.1017/s0007485307004907openalex-snapshot
Distribution of common genotypes of Myzus persicae (Hemiptera: Aphididae) in Greece, in relation to life cycle and host plant
inferred← citeshttps://doi.org/10.1017/s0007485307005585openalex-snapshot
Genotypic diversity of the cotton-melon aphidAphis gossypii(Glover) in Tunisia is structured by host plants
inferred← citeshttps://doi.org/10.1017/s0007485309990447openalex-snapshot
Reproductive performance of asexual clones of the peach-potato aphid, (Myzus persicae, Homoptera: Aphididae), colonising Scotland in relation to host plant and field ecology
inferred← citeshttps://doi.org/10.1017/s0007485316000754openalex-snapshot
Evidence of plastic probing behavior in a ‘superclone’ of the grain aphidSitobion avenae
inferred← citeshttps://doi.org/10.1017/s0016672300026938openalex-snapshot
Accumulation of mutations in sexual and asexual populations
inferred← citeshttps://doi.org/10.1017/s0031182000062156openalex-snapshot
Interactions between population growth and sexual reproduction in the viviparous monogenean Gyrodactylus turnbulli Harris, 1986 from the guppy, Poecilia reticulata Peters
inferred← citeshttps://doi.org/10.1017/s0269-915x(04)00415-xopenalex-snapshot
A futile act? Thoughts on the reproductive biology of Candida albicans
inferred← citeshttps://doi.org/10.1017/s0269915x0400415xopenalex-snapshot
A futile act? Thoughts on the reproductive biology of Candida albicans
inferred← citeshttps://doi.org/10.1021/acs.est.0c01438openalex-snapshot
Multigenerational Mitigating Effects of Ocean Acidification on In Vivo Endpoints, Antioxidant Defense, DNA Damage Response, and Epigenetic Modification in an Asexual Monogonont Rotifer
inferred← citeshttps://doi.org/10.1023/a:1003508210166openalex-snapshot
Geographical parthenogenesis in European non-marine ostracods: post-glacial invasion or Holocene stability?
inferred← citeshttps://doi.org/10.1023/a:1003519418925openalex-snapshot
Spatial and ecological overlap between coexisting sexual and parthenogenetic Schmidtea polychroa (Tricladida; Platyhelminthes)
inferred← citeshttps://doi.org/10.1023/a:1023346824722openalex-snapshot
A genetic mechanism of species replacement in European waterfrogs?
inferred← citeshttps://doi.org/10.1023/a:1025833814356openalex-snapshot
Radiation in sexual and parthenogenetic oribatid mites (Oribatida, Acari) as indicated by genetic divergence of closely related species
inferred← citeshttps://doi.org/10.1023/a:1026557901479openalex-snapshot
To the importance of genetic diversity of Phragmites australisin the development of reed stands
inferred← citeshttps://doi.org/10.1023/b:hydr.0000033124.49676.5copenalex-snapshot
Salinity Effects on Survival, Growth and Morphometry of Four Egyptian Artemia Populations (International Study on Artemia. LXVII)
inferred← citeshttps://doi.org/10.1034/j.1601-5223.2002.1360302.xopenalex-snapshot
Genetic diversity and the phylogeography of parthenogenesis: comparing bisexual and thelytokous populations of Nemasoma varicorne (Diplopoda: Nemasomatidae) in Denmark
inferred← citeshttps://doi.org/10.1038/36099openalex-snapshot
Explaining the geographic distributions of sexual and asexual populations
inferred← citeshttps://doi.org/10.1038/hdy.1986.134openalex-snapshot
Genotypic diversity and variation in mode of reproduction among populations in the Daphnia pulex group
inferred← citeshttps://doi.org/10.1038/hdy.1993.134openalex-snapshot
The local displacement of a sexually reproducing ostracod by a conspecific parthenogen
inferred← citeshttps://doi.org/10.1038/hdy.1993.143openalex-snapshot
Ecological genetics of Norwegian Daphnia. III. Clonal richness in an Arctic apomictic complex
inferred← citeshttps://doi.org/10.1038/hdy.1993.24openalex-snapshot
Macrogeographic patterns of breeding system diversity in the Daphnia pulex group. I. Breeding systems of Canadian populations
inferred← citeshttps://doi.org/10.1038/hdy.1994.154openalex-snapshot
Abundant asexuality in tropical freshwater ostracodes
inferred← citeshttps://doi.org/10.1038/hdy.1995.175openalex-snapshot
Genetic characterization of breeding systems, ploidy levels and species boundaries in Cypricercus (Ostracoda)
inferred← citeshttps://doi.org/10.1038/hdy.2009.65openalex-snapshot
Thelytokous parthenogenesis in the damselfly Ischnura hastata (Odonata, Coenagrionidae): genetic mechanisms and lack of bacterial infection
inferred← citeshttps://doi.org/10.1038/hdy.2011.84openalex-snapshot
Population genetic structure of sexual and parthenogenetic damselflies inferred from mitochondrial and nuclear markers
inferred← citeshttps://doi.org/10.1038/hdy.2012.57openalex-snapshot
The genetics of obligate parthenogenesis in an aphid species and its consequences for the maintenance of alternative reproductive modes
inferred← citeshttps://doi.org/10.1038/hdy.2012.78openalex-snapshot
Can resource costs of polyploidy provide an advantage to sex?
inferred← citeshttps://doi.org/10.1038/hdy.2013.1openalex-snapshot
Geographical parthenogenesis and population genetic structure in the alpine species Ranunculus kuepferi (Ranunculaceae)
inferred← citeshttps://doi.org/10.1038/s41559-024-02439-zopenalex-snapshot
A somatic genetic clock for clonal species
inferred← citeshttps://doi.org/10.1038/s41598-019-50907-5openalex-snapshot
Plant apomixis is rare in Himalayan high-alpine flora
inferred← citeshttps://doi.org/10.1038/s41598-020-64367-9openalex-snapshot
Dynamics of apomictic and sexual reproduction during primary succession on a glacier forefield in the Swiss Alps
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800028openalex-snapshot
Clonal reproduction and population genetic structure of grape phylloxera, Daktulosphaira vitifoliae, in Australia
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800245openalex-snapshot
Gene flow between arrhenotokous and thelytokous populations of Venturia canescens (Hymenoptera)
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800262openalex-snapshot
Predominance of sexual reproduction in Romanian populations of the aphid Sitobion avenae inferred from phenotypic and genetic structure
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800393openalex-snapshot
Fine-scale genetic structure of grape phylloxera from the roots and leaves of Vitis
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800486openalex-snapshot
Clonal diversity in the ancient asexual ostracod Darwinula stevensoni assessed by RAPD-PCR
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800662openalex-snapshot
Genetic structure and clonal diversity of an introduced pest in Chile, the cereal aphid Sitobion avenae
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800772openalex-snapshot
The conversion of variance and the evolutionary potential of restricted recombination
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800794openalex-snapshot
Genetic variability and adaptive evolution in parthenogenetic root-knot nematodes
inferred← citeshttps://doi.org/10.1038/sj.hdy.6883590openalex-snapshot
Allozyme variability in sexual and parthenogenetic freshwater planarians: evidence for polyphyletic origin of parthenogenetic lineages through hybridization with coexisting sexuals
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00175.xopenalex-snapshot
Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00181.xopenalex-snapshot
Genetic variation in sexual and clonal lineages of a freshwater snail
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00186.xopenalex-snapshot
Evolution in the slow lane: molecular rates of evolution in sexual and asexual ostracods (Crustacea: Ostracoda)
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00189.xopenalex-snapshot
The dynamic clonal genome and its adaptive potential
inferred← citeshttps://doi.org/10.1046/j.1365-2427.2000.00599.xopenalex-snapshot
Neritid and thiarid gastropods from French Polynesian streams: how reproduction (sexual, parthenogenetic) and dispersal (active, passive) affect population structure
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