On the public citation graph

Wolbachia and host intrinsic reproductive barriers contribute additively to post-mating isolation in spider mites

https://doi.org/10.1101/2020.06.29.178699

0 signed · 124 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/ece3.1535openalex-snapshot

Tetracycline‐exposed Drosophila melanogaster males produce fewer offspring but a relative excess of sons

inferredcites →https://doi.org/10.1002/ece3.2724openalex-snapshot

Adaptation of acaricide stress facilitates Tetranychus urticae expanding against Tetranychus cinnabarinus in China

inferredcites →https://doi.org/10.1002/ece3.6015openalex-snapshot

Population‐specific effect of Wolbachia on the cost of fungal infection in spider mites

inferredcites →https://doi.org/10.1002/tax.595004openalex-snapshot

Polymorphism of postmating reproductive isolation within plant species

inferredcites →https://doi.org/10.1007/bf00051553openalex-snapshot

Genetic distinctness between two forms of Tetranychus urticae Koch (Acari: Tetranychidae) detected by electrophoresis

inferredcites →https://doi.org/10.1007/bf00053306openalex-snapshot

Wolbachia: intracellular manipulators of mite reproduction

inferredcites →https://doi.org/10.1007/bf00055999openalex-snapshot

Partial hybrid sterility between strains of the arrhenotokous spider mite, Tetranychus urticae complex (Acari, Tetranychidae)

inferredcites →https://doi.org/10.1007/bf00286052openalex-snapshot

Heterochromatinization, chromatin elimination and haploidization in the parahaploid mite Metaseiulus occidentalis (Nesbitt) (Acarina: Phytoseiidae)

inferredcites →https://doi.org/10.1007/bf01196192openalex-snapshot

Evolution of pseudo-arrhenotoky

inferredcites →https://doi.org/10.1007/bf01507446openalex-snapshot

Karyotypes and sex-determination in spider mites (Tetranychidae)

inferredcites →https://doi.org/10.1007/bf02515473openalex-snapshot

Reproductive compatibility between populations of the citrus red mite, Panonychus citri ( McGregor ) (Acarina: Tetranychidae)

inferredcites →https://doi.org/10.1007/s00248-013-0198-zopenalex-snapshot

Diversity of Wolbachia in Natural Populations of Spider Mites (genus Tetranychus): Evidence for Complex Infection History and Disequilibrium Distribution

inferredcites →https://doi.org/10.1007/s00265-016-2124-0openalex-snapshot

Incomplete species recognition entails few costs in spider mites, despite first-male precedence

inferredcites →https://doi.org/10.1007/s10144-012-0313-xopenalex-snapshot

The presence of heterospecific males causes an Allee effect

inferredcites →https://doi.org/10.1007/s10493-007-9072-3openalex-snapshot

Wolbachia-induced cytoplasmic incompatibility in Japanese populations of Tetranychus urticae (Acari: Tetranychidae)

inferredcites →https://doi.org/10.1007/s10493-014-9846-3openalex-snapshot

Inter-population variation for Wolbachia induced reproductive incompatibility in the haplodiploid mite Tetranychus urticae

inferredcites →https://doi.org/10.1007/s10493-015-9878-3openalex-snapshot

Incomplete premating and postmating reproductive barriers between two parapatric populations of a social spider mite

inferredcites →https://doi.org/10.1007/s10493-018-0224-4openalex-snapshot

Identification of spider-mite species and their endosymbionts using multiplex PCR

inferredcites →https://doi.org/10.1007/s13355-010-0014-xopenalex-snapshot

Variable fitness and reproductive effects of Wolbachia infection in populations of the two-spotted spider mite Tetranychus urticae Koch in China

inferredcites →https://doi.org/10.1016/j.cois.2019.08.006openalex-snapshot

Rapid host-plant adaptation in the herbivorous spider mite Tetranychus urticae occurs at low cost

inferredcites →https://doi.org/10.1016/j.cub.2011.03.063openalex-snapshot

Reproductive interference

inferredcites →https://doi.org/10.1016/j.tree.2006.03.003openalex-snapshot

Disruptive selection and then what?

inferredcites →https://doi.org/10.1016/j.tree.2008.10.008openalex-snapshot

Generalized linear mixed models: a practical guide for ecology and evolution

inferredcites →https://doi.org/10.1016/j.tree.2008.10.011openalex-snapshot

Ecological explanations for (incomplete) speciation

inferredcites →https://doi.org/10.1016/s0169-5347(01)02177-2openalex-snapshot

Theory and speciation

inferredcites →https://doi.org/10.1016/s0169-5347(01)02198-xopenalex-snapshot

Ecology and the origin of species

inferredcites →https://doi.org/10.1016/s0169-5347(02)02480-1openalex-snapshot

Wolbachia dynamics and host effects: what has (and has not) been demonstrated?

inferredcites →https://doi.org/10.1023/a:1006432604611openalex-snapshot

Genetic Differentiation in Tetranychus Urticae (Acari: Tetranychidae): polymorphism, host races or sibling species?

inferredcites →https://doi.org/10.1023/a:1010133721121openalex-snapshot

Questioning species realities

inferredcites →https://doi.org/10.1038/346558a0openalex-snapshot

Microorganisms associated with chromosome destruction and reproductive isolation between two insect species

inferredcites →https://doi.org/10.1038/35055543openalex-snapshot

Wolbachia-induced incompatibility precedes other hybrid incompatibilities in Nasonia

inferredcites →https://doi.org/10.1038/hdy.1997.121openalex-snapshot

Wolbachia and cytoplasmic incompatibility in the spider mites Tetranychus urticae and T. turkestani

inferredcites →https://doi.org/10.1038/hdy.2008.75openalex-snapshot

Wolbachia plays no role in the one-way reproductive incompatibility between the hybridizing field crickets Gryllus firmus and G. pennsylvanicus

inferredcites →https://doi.org/10.1038/hdy.2009.53openalex-snapshot

Cytoplasmic incompatibility and host population structure

inferredcites →https://doi.org/10.1038/hdy.2014.53openalex-snapshot

Testing for reproductive interference in the population dynamics of two congeneric species of herbivorous mites

inferredcites →https://doi.org/10.1038/hdy.2016.103openalex-snapshot

Detection of genetic incompatibilities in non-model systems using simple genetic markers: hybrid breakdown in the haplodiploid spider mite Tetranychus evansi

inferredcites →https://doi.org/10.1038/hdy.2017.56openalex-snapshot

Reproductive interference and fecundity affect competitive interactions of sibling species with low mating barriers: experimental and theoretical evidence

inferredcites →https://doi.org/10.1038/nature12678openalex-snapshot

Genetic incompatibilities are widespread within species

inferredcites →https://doi.org/10.1038/nrmicro1969openalex-snapshot

Wolbachia: master manipulators of invertebrate biology

inferredcites →https://doi.org/10.1038/s41437-020-0297-9openalex-snapshot

Endosymbiont diversity in natural populations of Tetranychus mites is rapidly lost under laboratory conditions

inferredcites →https://doi.org/10.1038/sj.hdy.6800063openalex-snapshot

Infection polymorphism and cytoplasmic incompatibility in Hymenoptera-Wolbachia associations

inferredcites →https://doi.org/10.1038/sj.hdy.6800329openalex-snapshot

Wolbachia distribution and cytoplasmic incompatibility based on a survey of 42 spider mite species (Acari: Tetranychidae) in Japan

inferredcites →https://doi.org/10.1038/sj.hdy.6800552openalex-snapshot

Intergenomic interactions affect female reproduction: evidence from introgression and inbreeding depression in a haplodiploid mite

inferredcites →https://doi.org/10.1038/sj.hdy.6800605openalex-snapshot

Wolbachia and nuclear–nuclear interactions contribute to reproductive incompatibility in the spider mite Panonychus mori (Acari: Tetranychidae)

inferredcites →https://doi.org/10.1038/sj.hdy.6883370openalex-snapshot

Selfish genetic elements and speciation

inferredcites →https://doi.org/10.1038/srep00375openalex-snapshot

From father to son: transgenerational effect of tetracycline on sperm viability

inferredcites →https://doi.org/10.1038/srep27900openalex-snapshot

Screening of spider mites (Acari: Tetranychidae) for reproductive endosymbionts reveals links between co-infection and evolutionary history

inferredcites →https://doi.org/10.1046/j.1365-2540.1998.00349.xopenalex-snapshot

Species-wide homogeneity of nuclear ribosomal ITS2 sequences in the spider mite Tetranychus urticae contrasts with extensive mitochondrial COI polymorphism

inferredcites →https://doi.org/10.1046/j.1420-9101.2002.00446.xopenalex-snapshot

Contrasting effects of Wolbachia on cytoplasmic incompatibility and fecundity in the haplodiploid mite Tetranychus urticae

inferredcites →https://doi.org/10.1046/j.1420-9101.2003.00679.xopenalex-snapshot

Wolbachia affects oviposition and mating behaviour of its spider mite host

inferredcites →https://doi.org/10.1051/acarologia/20132102openalex-snapshot

Evidence for synonymy between Tetranychus urticae and Tetranychus cinnabarinus (Acari, Prostigmata, Tetranychidae): Review and new data

inferredcites →https://doi.org/10.1086/590510openalex-snapshot

Reproductive Interference Between Animal Species

inferredcites →https://doi.org/10.1086/684583openalex-snapshot

Hybrid Incompatibilities, Local Adaptation, and the Genomic Distribution of Natural Introgression between Species

inferredcites →https://doi.org/10.1093/acprof:osobl/9780199587100.001.0001openalex-snapshot

Ecological Speciation

inferredcites →https://doi.org/10.1093/aesa/49.1.43openalex-snapshot

Revision of the Two-Spotted Spider Mite (Acarina, Tetranychidae) Complex, Tetranychus Telarius (Linnaeus)1

inferredcites →https://doi.org/10.1093/aesa/71.6.862openalex-snapshot

Interspecific Competition and Hybridization between Twospotted and Carmine Spider Mites1

inferredcites →https://doi.org/10.1093/aesa/84.1.37openalex-snapshot

Variation in Reproductive Compatibility in Trichogramma and Its Taxonomic Significance (Hymenoptera: Trichogrammatidae)

inferredcites →https://doi.org/10.1093/beheco/arx161openalex-snapshot

Despite reproductive interference, the net outcome of reproductive interactions among spider mite species is not necessarily costly

inferredcites →https://doi.org/10.1093/ee/4.4.588openalex-snapshot

Spider Mites:1 Population Suppression by Interspecific Hybridization23

inferredcites →https://doi.org/10.1093/femsec/fiy015openalex-snapshot

Endosymbiont diversity and prevalence in herbivorous spider mite populations in South-Western Europe

inferredcites →https://doi.org/10.1093/genetics/143.1.609openalex-snapshot

Maternal Effect as a Cause of Exceptions for H aldane's Rule

inferredcites →https://doi.org/10.1093/genetics/154.4.1663openalex-snapshot

Dominance, Epistasis and the Genetics of Postzygotic Isolation

inferredcites →https://doi.org/10.1093/jee/45.2.308openalex-snapshot

Mating Experiments with the Two-spotted Spider Mite Complex1

inferredcites →https://doi.org/10.1093/jhered/esu033openalex-snapshot

Hybridization, Introgression, and the Nature of Species Boundaries

inferredcites →https://doi.org/10.1098/rspb.1997.0010openalex-snapshot

The evolution of polyandry II: post–copulatory defenses against genetic incompatibility

inferredcites →https://doi.org/10.1098/rspb.2000.1232openalex-snapshot

Wolbachia–induced ‘hybrid breakdown’ in the two–fspotted spider miteTetranychus urticaeKoch

inferredcites →https://doi.org/10.1098/rspb.2015.0249openalex-snapshot

The incidence of bacterial endosymbionts in terrestrial arthropods

inferredcites →https://doi.org/10.1098/rstb.2008.0022openalex-snapshot

Lifelong commitment to the wrong partner: hybridization in ants

inferredcites →https://doi.org/10.1098/rstb.2008.0081openalex-snapshot

Hybridization, ecological races and the nature of species: empirical evidence for the ease of speciation

inferredcites →https://doi.org/10.1101/395301openalex-snapshot

Environments with a high probability of incompatible crosses do not select for mate avoidance in spider mites

inferredcites →https://doi.org/10.1101/gr.196485.115openalex-snapshot

Linked selection and recombination rate variation drive the evolution of the genomic landscape of differentiation across the speciation continuum of Ficedula flycatchers

inferredcites →https://doi.org/10.1101/sqb.1959.024.01.017openalex-snapshot

SPECIATION IN MOSQUITOES: Speciation by Cytoplasmic Isolation in the Culex Pipiens-Complex

inferredcites →https://doi.org/10.1111/1365-2664.13101openalex-snapshot

Back and forth Wolbachia transfers reveal efficient strains to control spotted wing drosophila populations

inferredcites →https://doi.org/10.1111/ele.13525openalex-snapshot

Co‐occurrence is not evidence of ecological interactions

inferredcites →https://doi.org/10.1111/evo.12209openalex-snapshot

GENETIC DIVERGENCE ALONG THE SPECIATION CONTINUUM: THE TRANSITION FROM HOST RACE TO SPECIES INRHAGOLETIS(DIPTERA: TEPHRITIDAE)

inferredcites →https://doi.org/10.1111/evo.13037openalex-snapshot

“Darwin's corollary” and cytoplasmic incompatibility induced by Cardinium may contribute to speciation in Encarsia wasps (Hymenoptera: Aphelinidae)

inferredcites →https://doi.org/10.1111/evo.13880openalex-snapshot

The evolution of partial reproductive isolation as an adaptive optimum

inferredcites →https://doi.org/10.1111/imb.12620openalex-snapshot

Transcriptome of Tetranychus urticae embryos reveals insights into Wolbachia ‐induced cytoplasmic incompatibility

inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00019.xopenalex-snapshot

EVIDENCE FOR FEMALE MORTALITY IN WOLBACHIA-MEDIATED CYTOPLASMIC INCOMPATIBILITY IN HAPLODIPLOID INSECTS: EPIDEMIOLOGIC AND EVOLUTIONARY CONSEQUENCES

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00691.xopenalex-snapshot

WITHIN-SPECIES DIVERSITY OF WOLBACHIA-INDUCED CYTOPLASMIC INCOMPATIBILITY IN HAPLODIPLOID INSECTS

inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01447.xopenalex-snapshot

WITHIN- AND BETWEEN-POPULATION VARIATION FOR WOLBACHIA-INDUCED REPRODUCTIVE INCOMPATIBILITY IN A HAPLODIPLOID MITE

inferredcites →https://doi.org/10.1111/j.1095-8649.2009.02419.xopenalex-snapshot

Along the speciation continuum in sticklebacks

inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00760.xopenalex-snapshot

Tetracycline treatment influences mitochondrial metabolism and mtDNA density two generations after treatment in Drosophila

inferredcites →https://doi.org/10.1111/j.1365-2583.2010.01066.xopenalex-snapshot

Effects of Wolbachia on mtDNA variation and evolution in natural populations of Tetranychus urticae Koch

inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02213.xopenalex-snapshot

Reproductive effects and geographical distributions of twoWolbachiastrains infecting the Neotropical beetle,Chelymorpha alternansBoh. (Chrysomelidae, Cassidinae)

inferredcites →https://doi.org/10.1111/j.1439-0418.1975.tb02361.xopenalex-snapshot

An analysis of the Tetranychid complexes in the Mediterranean area

inferredcites →https://doi.org/10.1111/j.1461-0248.2011.01606.xopenalex-snapshot

Ecology, sexual selection and speciation

inferredcites →https://doi.org/10.1111/j.1558-5646.1982.tb05076.xopenalex-snapshot

LABORATORY HYBRIDIZATION BETWEEN SEMI-INCOMPATIBLE RACES OF THE ARRHENOTOKOUS SPIDER MITE TETRANYCHUS URTICAE KOCH (ACARI: TETRANYCHIDAE)

inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb02307.xopenalex-snapshot

HYBRID BREAKDOWN BETWEEN TWO HAPLODIPLOID SPECIES: THE ROLE OF NUCLEAR AND CYTOPLASMIC GENES

inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb04529.xopenalex-snapshot

WOLBACHIAAND THE EVOLUTION OF REPRODUCTIVE ISOLATION BETWEENDROSOPHILA RECENSANDDROSOPHILA SUBQUINARIA

inferredcites →https://doi.org/10.1111/j.1570-7458.1960.tb02121.xopenalex-snapshot

INVESTIGATIONS ON THE TETRANYCHUS URTICAE COMPLEX IN NORTH WEST EUROPE (ACARI: TETRANYCHIDAE)

inferredcites →https://doi.org/10.1111/j.1570-7458.1962.tb00578.xopenalex-snapshot

CROSSBREEDING EXPERIMENTS WITH SOME SPECIES OF THE TETRANYCHUS URTICAE GROUP

inferredcites →https://doi.org/10.1111/j.1570-7458.1965.tb00866.xopenalex-snapshot

GENETIC AFFINITIES BETWEEN ADJACENT POPULATIONS OF SPIDER MITES (TETRANYCHUS URTICAE KOCH)

inferredcites →https://doi.org/10.1111/j.1570-7458.1976.tb02639.xopenalex-snapshot

PARTIAL REPRODUCTIVE INCOMPATIBILITY BETWEEN POPULATIONS OF SPIDER MITES (ACARINA: TETRANYCHIDAE)

inferredcites →https://doi.org/10.1111/j.1570-7458.1979.tb02882.xopenalex-snapshot

ON GENE FLOW BETWEEN TETRANYCHUS URTICAE KOCH, 1836 AND TETRANYCHUS CINNABARINUS (BOISDUVAL) BOUDREAUX, 1956 (ACARI: TETRANYCHIDAE): SYNONOMY BETWEEN THE TWO SPECIES

inferredcites →https://doi.org/10.1111/j.1570-7458.1989.tb02320.xopenalex-snapshot

Nuclear‐nuclear and nuclear‐cytoplasmic interactions contribute to the reproductive incompatibility between two strains of the twospotted spider mite

inferredcites →https://doi.org/10.1111/j.1570-7458.1993.tb01700.xopenalex-snapshot

Host race formation in Tetranychus urticae: genetic differentiation, host plant preference, and mate choice in a tomato and a cucumber strain

inferredcites →https://doi.org/10.1111/jeb.12533openalex-snapshot

How much can history constrain adaptive evolution? A real‐time evolutionary approach of inversion polymorphisms in Drosophila subobscura

inferredcites →https://doi.org/10.1111/jeb.13270openalex-snapshot

Patterns of reproductive isolation in a haplodiploid – strong post‐mating, prezygotic barriers among three forms of a social spider mite

inferredcites →https://doi.org/10.1111/mec.12006openalex-snapshot

A disproportionate role for mt DNA in D obzhansky– M uller incompatibilities?

inferredcites →https://doi.org/10.1111/mec.12901openalex-snapshot

Wolbachiado not live by reproductive manipulation alone: infection polymorphism inDrosophila suzukiiandD. subpulchrella

inferredcites →https://doi.org/10.1126/science.1160006openalex-snapshot

Evidence for Ecological Speciation and Its Alternative

inferredcites →https://doi.org/10.1146/annurev-ecolsys-102209-144644openalex-snapshot

Divergence with Gene Flow: Models and Data

inferredcites →https://doi.org/10.1146/annurev.ecolsys.110308.120206openalex-snapshot

The Ecology and Evolution of Microbes that Manipulate Host Reproduction

inferredcites →https://doi.org/10.1146/annurev.ecolsys.38.091206.095804openalex-snapshot

Sympatric Speciation: Models and Empirical Evidence

inferredcites →https://doi.org/10.1186/1471-2148-11-68openalex-snapshot

Sexual and postmating reproductive isolation between allopatric Drosophila montana populations suggest speciation potential

inferredcites →https://doi.org/10.1186/1741-7007-6-27openalex-snapshot

The diversity of reproductive parasites among arthropods: Wolbachiado not walk alone

inferredcites →https://doi.org/10.1186/s12862-015-0486-yopenalex-snapshot

Divergence with gene flow across a speciation continuum of Heliconius butterflies

inferredcites →https://doi.org/10.1201/9780203009918-22openalex-snapshot

Symbiosis and the Origin of Species

inferredcites →https://doi.org/10.1201/9780203009918.ch17openalex-snapshot

Symbiosis And The Origin Of Species

inferredcites →https://doi.org/10.1242/jcs.03095openalex-snapshot

Paternal chromosome segregation during the first mitotic division determinesWolbachia-induced cytoplasmic incompatibility phenotype

inferredcites →https://doi.org/10.1303/aez.2002.127openalex-snapshot

Hybrid affinities between the green and the red forms of the two-spotted spider mite Tetranychus urticae(Acari: Tetranychidae) under laboratory and seminatural conditions.

inferredcites →https://doi.org/10.1371/journal.pbio.0040325openalex-snapshot

Asymmetrical Reinforcement and Wolbachia Infection in Drosophila

inferredcites →https://doi.org/10.1371/journal.pone.0110625openalex-snapshot

The Complete Mitochondrial Genomes of Six Species of Tetranychus Provide Insights into the Phylogeny and Evolution of Spider Mites

inferredcites →https://doi.org/10.1371/journal.pone.0203136openalex-snapshot

Phylogeny of the spider mite sub-family Tetranychinae (Acari: Tetranychidae) inferred from RNA-Seq data

inferredcites →https://doi.org/10.1534/genetics.106.065979openalex-snapshot

Asymmetric Postmating Isolation: Darwin's Corollary to Haldane's Rule

inferredcites →https://doi.org/10.1534/genetics.116.196238openalex-snapshot

Wolbachia in the Drosophila yakuba Complex: Pervasive Frequency Variation and Weak Cytoplasmic Incompatibility, but No Apparent Effect on Reproductive Isolation

inferredcites →https://doi.org/10.1554/05-034.1openalex-snapshot

THE EFFECT OF WOLBACHIA VERSUS GENETIC INCOMPATIBILITIES ON REINFORCEMENT AND SPECIATION

inferredcites →https://doi.org/10.1603/0022-2585-41.5.894openalex-snapshot

Characterization ofWolbachiaInfections and Interspecific Crosses ofAedes(Stegomyia)polynesiensisandAe.(Stegomyia)riversi(Diptera: Culicidae)

inferredcites →https://doi.org/10.2307/2640819openalex-snapshot

Wolbachia and the Evolution of Reproductive Isolation between Drosophila recens and Drosophila subquinaria

inferredcites →https://doi.org/10.2307/4615733openalex-snapshot

A Simple Sequentially Rejective Multiple Test Procedure

inferredcites →https://doi.org/10.32614/rj-2017-066openalex-snapshot

glmmTMB Balances Speed and Flexibility Among Packages for Zero-inflated Generalized Linear Mixed Modeling

inferredcites →https://doi.org/10.4238/vol8-3gmr595openalex-snapshot

Effect of intracellular Wolbachia on interspecific crosses between Drosophila melanogaster and Drosophila simulans

What points at this work

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

inferred← citeshttps://doi.org/10.24072/pci.evolbiol.100116openalex-snapshot

Speciation in spider mites: disentangling the roles of Wolbachia-induced vs. nuclear mating incompatibilities

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.