On the public citation graph

The Transmission Patterns of the Endosymbiont Wolbachia within the Hawaiian Drosophilidae Adaptive Radiation

0 signed · 77 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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.

inferreduses_data →https://doi.org/10.5281/zenodo.10723540zenodo-depositor-declared

inferredcites →https://doi.org/10.1002/ece3.4844openalex-snapshot

Hawaiian picture‐winged Drosophila exhibit adaptive population divergence along a narrow climatic gradient on Hawaii Island

inferredcites →https://doi.org/10.1007/s00248-006-9036-xopenalex-snapshot

Closely Related Wolbachia Strains within the Pumpkin Arthropod Community and the Potential for Horizontal Transmission via the Plant

inferredcites →https://doi.org/10.1007/s00284-007-0055-8openalex-snapshot

Revisiting Wolbachia Supergroup Typing Based on WSP: Spurious Lineages and Discordance with MLST

inferredcites →https://doi.org/10.1007/s10530-020-02217-5openalex-snapshot

Population genomic and phenotype diversity of invasive Drosophila suzukii in Hawai‘i

inferredcites →https://doi.org/10.1016/j.chom.2021.03.006openalex-snapshot

Living in the endosymbiotic world of Wolbachia: A centennial review

inferredcites →https://doi.org/10.1016/j.cub.2005.06.069openalex-snapshot

Evidence for a Global Wolbachia Replacement in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.cub.2018.02.015openalex-snapshot

Rapid Global Spread of wRi-like Wolbachia across Multiple Drosophila

inferredcites →https://doi.org/10.1016/j.ympev.2015.04.025openalex-snapshot

Pattern of association between endemic Hawaiian fruit flies (Diptera, Tephritidae) and their symbiotic bacteria: Evidence of cospeciation events and proposal of “Candidatus Stammerula trupaneae”

inferredcites →https://doi.org/10.1016/j.ympev.2015.06.014openalex-snapshot

Rapid adaptive radiation and host plant conservation in the Hawaiian picture wing Drosophila (Diptera: Drosophilidae)

inferredcites →https://doi.org/10.1016/j.ympev.2016.12.034openalex-snapshot

Molecular diversity of Wolbachia in Lepidoptera: Prevalent allelic content and high recombination of MLST genes

inferredcites →https://doi.org/10.1016/s0960-9822(95)00229-6openalex-snapshot

Pattern of ecological shifts in the diversification of Hawaiian Drosophila inferred from a molecular phylogeny

inferredcites →https://doi.org/10.1016/s0965-1748(98)00119-2openalex-snapshot

Wolbachia infections are distributed throughout insect somatic and germ line tissues

inferredcites →https://doi.org/10.1017/s0031182000007149openalex-snapshot

A phylogenetic analysis of filarial nematodes: comparison with the phylogeny of Wolbachia endosymbionts

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

Wolbachia-induced incompatibility precedes other hybrid incompatibilities in Nasonia

inferredcites →https://doi.org/10.1038/ismej.2016.164openalex-snapshot

Plant–mediated horizontal transmission of Wolbachia between whiteflies

inferredcites →https://doi.org/10.1038/ncomms6117openalex-snapshot

Phylogenomic analyses uncover origin and spread of the Wolbachia pandemic

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

Wolbachia: master manipulators of invertebrate biology

inferredcites →https://doi.org/10.1046/j.1365-2583.2000.00203.xopenalex-snapshot

Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty‐three arthropod species

inferredcites →https://doi.org/10.1073/pnas.1409284111openalex-snapshot

Evolutionary origin of insect– Wolbachia nutritional mutualism

inferredcites →https://doi.org/10.1080/01621459.1995.10476572openalex-snapshot

Bayes Factors

inferredcites →https://doi.org/10.1080/10635150390192780openalex-snapshot

Stochastic Mapping of Morphological Characters

inferredcites →https://doi.org/10.1080/10635150490522629openalex-snapshot

Frequentist Properties of Bayesian Posterior Probabilities of Phylogenetic Trees Under Simple and Complex Substitution Models

inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot

MRBAYES: Bayesian inference of phylogenetic trees

inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot

MrBayes 3: Bayesian phylogenetic inference under mixed models

inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot

RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies

inferredcites →https://doi.org/10.1093/conphys/cou062openalex-snapshot

Physiological effects of heat stress on Hawaiian picture-wingDrosophila: genome-wide expression patterns and stress-related traits

inferredcites →https://doi.org/10.1093/gbe/evaa219openalex-snapshot

Phylogenomic Analysis of Wolbachia Strains Reveals Patterns of Genome Evolution and Recombination

inferredcites →https://doi.org/10.1093/gbe/evt034openalex-snapshot

Linking Genomics and Ecology to Investigate the Complex Evolution of an Invasive Drosophila Pest

inferredcites →https://doi.org/10.1093/gigascience/gix135openalex-snapshot

Analysis of the Aedes albopictus C6/36 genome provides insight into cell line utility for viral propagation

inferredcites →https://doi.org/10.1093/icb/42.2.340openalex-snapshot

Effects of Wolbachia on Genetic Divergence Between Populations: Mainland-Island Model

inferredcites →https://doi.org/10.1093/molbev/msj049openalex-snapshot

Widespread Recombination Throughout Wolbachia Genomes

inferredcites →https://doi.org/10.1093/molbev/msn133openalex-snapshot

Genome Evolution of Wolbachia Strain wPip from the Culex pipiens Group

inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot

MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets

inferredcites →https://doi.org/10.1093/nar/gku1099openalex-snapshot

FlyBase: introduction of the Drosophila melanogaster Release 6 reference genome assembly and large-scale migration of genome annotations

inferredcites →https://doi.org/10.1093/sysbio/syq085openalex-snapshot

Improving Marginal Likelihood Estimation for Bayesian Phylogenetic Model Selection

inferredcites →https://doi.org/10.1098/rspb.1995.0196openalex-snapshot

Distribution ofWolbachiaamong neotropical arthropods

inferredcites →https://doi.org/10.1098/rstb.1995.0093openalex-snapshot

Molecular phylogenies and host-parasite cospeciation: gophers and lice as a model system

inferredcites →https://doi.org/10.1101/gr.141689.112openalex-snapshot

A second-generation assembly of the Drosophila simulans genome provides new insights into patterns of lineage-specific divergence

inferredcites →https://doi.org/10.1111/brv.12663openalex-snapshot

Wolbachiahost shifts: routes, mechanisms, constraints and evolutionary consequences

inferredcites →https://doi.org/10.1111/j.1574-6968.2008.01110.xopenalex-snapshot

How many species are infected with Wolbachia? – a statistical analysis of current data

inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot

phytools: an R package for phylogenetic comparative biology (and other things)

inferredcites →https://doi.org/10.1126/science.1191864openalex-snapshot

Sequencing of Culex quinquefasciatus Establishes a Platform for Mosquito Comparative Genomics

inferredcites →https://doi.org/10.1128/aem.00731-06openalex-snapshot

Multilocus Sequence Typing System for the Endosymbiont Wolbachia pipientis

inferredcites →https://doi.org/10.1128/genomea.00032-13openalex-snapshot

Draft Genome Sequence of the Wolbachia Endosymbiont of Drosophila suzukii

inferredcites →https://doi.org/10.1128/jb.01731-08openalex-snapshot

Genome Sequence of the Wolbachia Endosymbiont of Culex quinquefasciatus JHB

inferredcites →https://doi.org/10.1128/mbio.01768-20openalex-snapshot

Pervasive Effects of Wolbachia on Host Temperature Preference

inferredcites →https://doi.org/10.1146/annurev.ento.42.1.587openalex-snapshot

BIOLOGY OF WOLBACHIA

inferredcites →https://doi.org/10.1146/annurev.ento.54.110807.090529openalex-snapshot

Bayesian Phylogenetics and Its Influence on Insect Systematics

inferredcites →https://doi.org/10.1146/annurev.micro.53.1.71openalex-snapshot

Wolbachia Pipientis: Microbial Manipulator of Arthropod Reproduction

inferredcites →https://doi.org/10.1155/2012/280169openalex-snapshot

The Role of Parasitism in Adaptive Radiations—When Might Parasites Promote and When Might They Constrain Ecological Speciation?

inferredcites →https://doi.org/10.11646/zootaxa.1728.1.1openalex-snapshot

A review of the endemic Hawaiian Drosophilidae and their host plants

inferredcites →https://doi.org/10.1186/1748-7188-5-16openalex-snapshot

Jane: a new tool for the cophylogeny reconstruction problem

inferredcites →https://doi.org/10.1186/gb-2005-6-3-r23openalex-snapshot

Serendipitous discovery of Wolbachia genomes in multiple Drosophilaspecies

inferredcites →https://doi.org/10.1186/gb-2005-6-9-231openalex-snapshot

Canonical Wnt signaling: high-throughput RNAi widens the path.

inferredcites →https://doi.org/10.1371/journal.pbio.0020069openalex-snapshot

Phylogenomics of the Reproductive Parasite Wolbachia pipientis wMel: A Streamlined Genome Overrun by Mobile Genetic Elements

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

Asymmetrical Reinforcement and Wolbachia Infection in Drosophila

inferredcites →https://doi.org/10.1371/journal.pgen.1003381openalex-snapshot

Comparative Genomics of Wolbachia and the Bacterial Species Concept

inferredcites →https://doi.org/10.1371/journal.pone.0038544openalex-snapshot

Still a Host of Hosts for Wolbachia: Analysis of Recent Data Suggests That 40% of Terrestrial Arthropod Species Are Infected

inferredcites →https://doi.org/10.1371/journal.ppat.1003607openalex-snapshot

Rapid Sequential Spread of Two Wolbachia Variants in Drosophila simulans

inferredcites →https://doi.org/10.1371/journal.ppat.1004672openalex-snapshot

The Intracellular Bacterium Wolbachia Uses Parasitoid Wasps as Phoretic Vectors for Efficient Horizontal Transmission

inferredcites →https://doi.org/10.1534/genetics.117.300583openalex-snapshot

Phylogeny of the Genus Drosophila

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/10.2307/1310849openalex-snapshot

Speciation in the Hawaiian "Drosophila": Sexual Selection Appears to Play an Important Role

inferredcites →https://doi.org/10.2307/1313355openalex-snapshot

"Wolbachia" Infections and Arthropod Reproduction

inferredcites →https://doi.org/10.3389/fmicb.2017.02237openalex-snapshot

Horizontal Transmission of Intracellular Insect Symbionts via Plants

inferredcites →https://doi.org/10.3389/fmicb.2021.706321openalex-snapshot

Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance

inferredcites →https://doi.org/10.3390/ijms21218064openalex-snapshot

An Earliest Endosymbiont, Wolbachia massiliensis sp. nov., Strain PL13 from the Bed Bug (Cimex hemipterus), Type Strain of a New Supergroup T

inferredcites →https://doi.org/10.3390/insects12090788openalex-snapshot

High Incidence of Related Wolbachia across Unrelated Leaf-Mining Diptera

inferredcites →https://doi.org/10.4161/fly.21161openalex-snapshot

Diversity and phylogenetic relationships of Wolbachia in Drosophila and other native Hawaiian insects

inferredcites →https://doi.org/10.7717/peerj.1840openalex-snapshot

Breakdown of coevolution between symbiotic bacteria Wolbachia and their filarial hosts

inferredcites →https://doi.org/10.7717/peerj.529openalex-snapshot

Recent genome reduction of Wolbachia in Drosophila recens targets phage WO and narrows candidates for reproductive parasitism

What points at this work

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

inferred← citeshttps://doi.org/10.1093/sysbio/syae025openalex-snapshot

Stochastic Character Mapping, Bayesian Model Selection, and Biosynthetic Pathways Shed New Light on the Evolution of Habitat Preference in Cyanobacteria

inferred← citeshttps://doi.org/10.1101/2025.05.06.652154openalex-snapshot

Abiotic factors are the primary determinants of endemic Hawaiian Drosophila microbiome assembly

inferred← citeshttps://doi.org/10.1111/mec.70417openalex-snapshot

Microbiome Structure of Endemic Hawaiian Drosophila Is Shaped More by Habitat Than Host Identity

inferred← citeshttps://doi.org/10.1242/jeb.250973openalex-snapshot

Microbiome composition shapes temperature tolerance in a Hawaiian picture-winged Drosophila

inferred← citeshttps://doi.org/10.3390/genes15081000openalex-snapshot

Editorial for the “Genetics, Phylogeny, and Evolution of Insects” Special Issue

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.