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On the phylogeny of the Drosophila hydei subgroup: New insights from combined analyses of nuclear and mitochondrial data

https://doi.org/10.1016/j.ympev.2006.12.021

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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/10.1002/0471650129.dob0534openalex-snapshot

PHYLIP (Phylogeny Inference Package)

inferredcites →https://doi.org/10.1006/mpev.2000.0824openalex-snapshot

Phylogenetic Analysis of the repleta Species Group of the Genus Drosophila Using Multiple Sources of Characters

inferredcites →https://doi.org/10.1006/mpev.2000.0893openalex-snapshot

Phylogenetic Utility of Mitochondrial COI and Nuclear Gpdh Genes in Drosophila

inferredcites →https://doi.org/10.1006/mpev.2001.1002openalex-snapshot

Phylogenetic Relationships among Species Groups of the virilis–repleta Radiation of Drosophila

inferredcites →https://doi.org/10.1007/978-1-4615-6977-0_3openalex-snapshot

Interspecific Hybridization in the Genus Drosophila

inferredcites →https://doi.org/10.1007/978-1-4757-0432-7openalex-snapshot

Ecological Genetics and Evolution

inferredcites →https://doi.org/10.1007/bf00173155openalex-snapshot

Phylogenetic utility of the mitochondrial cytochrome oxidase gene: Molecular evolution of the Drosophila buzzatii species complex

inferredcites →https://doi.org/10.1007/bf01734359openalex-snapshot

Evolutionary trees from DNA sequences: A maximum likelihood approach

inferredcites →https://doi.org/10.1007/bf02338836openalex-snapshot

Molecular systematics of theDrosophila hydei subgroup as inferred from mitochondrial DNA sequences

inferredcites →https://doi.org/10.1007/bf02352289openalex-snapshot

Maximum-likelihood models for combined analyses of multiple sequence data

inferredcites →https://doi.org/10.1016/j.ympev.2005.04.009openalex-snapshot

Phylogeny and molecular evolution of the Drosophila hydei subgroup (Drosophila repleta group) inferred from the Xanthine dehydrogenase gene

inferredcites →https://doi.org/10.1016/j.ympev.2005.05.005openalex-snapshot

Molecular phylogeny of the subgenus Drosophila (Diptera, Drosophilidae) with an emphasis on Neotropical species and groups: A nuclear versus mitochondrial gene approach

inferredcites →https://doi.org/10.1016/s1055-7903(02)00445-1openalex-snapshot

Using AFLP to resolve phylogenetic relationships in a morphologically diversified plant species complex when nuclear and chloroplast sequences fail to reveal variability

inferredcites →https://doi.org/10.1016/s1055-7903(03)00139-8openalex-snapshot

Phylogeny reconstruction in the gap between too little and too much divergence: the closest relatives of Senecio jacobaea (Asteraceae) according to DNA sequences and AFLPs

inferredcites →https://doi.org/10.1073/pnas.090541597openalex-snapshot

The phylogeny of closely related species as revealed by the genealogy of a speciation gene, Odysseus

inferredcites →https://doi.org/10.1093/aibsbulletin/3.1.14-dopenalex-snapshot

Evolution in the Genus Drosophila

inferredcites →https://doi.org/10.1093/bioinformatics/13.5.555openalex-snapshot

PAML: a program package for phylogenetic analysis by maximum likelihood

inferredcites →https://doi.org/10.1093/genetics/23.1.28openalex-snapshot

INVERSIONS IN THE CHROMOSOMES OF DROSOPHILA PSEUDOOBSCURA

inferredcites →https://doi.org/10.1093/molbev/msg136openalex-snapshot

Assessing the Phylogenetic Utility of Four Mitochondrial Genes and a Nuclear Intron in the Asian Pit Viper Genus, Trimeresurus: Separate, Simultaneous, and Conditional Data Combination Analyses

inferredcites →https://doi.org/10.1093/nar/16.6.2736openalex-snapshot

Rapid isolation ofDrosophilahigh molecular weight DNA to obtain genomic libraries

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025664openalex-snapshot

Quartet Puzzling: A Quartet Maximum-Likelihood Method for Reconstructing Tree Topologies

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026392openalex-snapshot

Molecular Evolution and Phylogeny of the buzzatii Complex (Drosophila repleta Group): A Maximum-Likelihood Approach

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040182openalex-snapshot

Tests of applicability of several substitution models for DNA sequence data.

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040214openalex-snapshot

Molecular phylogeny and divergence times of drosophilid species.

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040517openalex-snapshot

Relationships between gene trees and species trees.

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040763openalex-snapshot

The rate and pattern of nucleotide substitution in Drosophila mitochondrial DNA.

inferredcites →https://doi.org/10.1093/sysbio/44.1.64openalex-snapshot

Testing Species Phylogenies and Phylogenetic Methods with Congruence

inferredcites →https://doi.org/10.1093/sysbio/44.4.570openalex-snapshot

Constructing a Significance Test for Incongruence

inferredcites →https://doi.org/10.1093/sysbio/46.4.654openalex-snapshot

Multiple Sources of Character Information and the Phylogeny of Hawaiian Drosophilids

inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00179.xopenalex-snapshot

BRANCH SUPPORT AND TREE STABILITY

inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot

TESTING SIGNIFICANCE OF INCONGRUENCE

inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb02497.xopenalex-snapshot

THE LIMITS OF AMINO ACID SEQUENCE DATA IN ANGIOSPERM PHYLOGENETIC RECONSTRUCTION

inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb01827.xopenalex-snapshot

BEST‐FIT MAXIMUM‐LIKELIHOOD MODELS FOR PHYLOGENETIC INFERENCE: EMPIRICAL TESTS WITH KNOWN PHYLOGENIES

inferredcites →https://doi.org/10.1146/annurev.ecolsys.28.1.437openalex-snapshot

Phylogeny Estimation and Hypothesis Testing Using Maximum Likelihood

inferredcites →https://doi.org/10.1186/1471-2148-1-6openalex-snapshot

Polytene chromosomes as indicators of phylogeny in several species groups of Drosophila

inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot

BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT

inferredcites →https://doi.org/10.2307/3215openalex-snapshot

Ecological Genetics and Evolution

inferredcites →https://doi.org/10.2307/3558364openalex-snapshot

Species relationships in Lactuca s.l. (Lactuceae, Asteraceae) inferred from AFLP fingerprints

inferredcites →https://doi.org/10.5281/zenodo.10764026openalex-snapshot

Drosophila guayllabambae n.sp., un nuevo miembro del grupo repleta, subgrupo hydei (Diptera, Drosophilidae).

inferredcites →https://doi.org/10.5281/zenodo.10764027openalex-snapshot

Subgrupo inca, un nuevo subgrupo del grupo repleta, con descripcion de Drosophila huancavilcae n.sp. (Diptera, Drosophilidae).

inferredcites →https://doi.org/10.5281/zenodo.10771994openalex-snapshot

A revision of the Drosophila repleta species group (Diptera, Drosophilidae).

inferredcites →https://doi.org/10.5281/zenodo.10772516openalex-snapshot

Cytological studies of the repleta group of the genus Drosophila: IV. The hydei subgroup.

inferredcites →https://doi.org/10.5281/zenodo.10772889openalex-snapshot

Interspecific hybridization in the repleta group.

inferredcites →https://doi.org/10.5281/zenodo.10772936openalex-snapshot

Taxonomic studies on the Drosophilidae.

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.012openalex-snapshot

Monophyly, divergence times, and evolution of host plant use inferred from a revised phylogeny of the Drosophila repleta species group

inferred← citeshttps://doi.org/10.1163/187631208788784237openalex-snapshot

A supertree analysis and literature review of the genus Drosophila and closely related genera (Diptera, Drosophilidae)

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