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Species boundaries in Zausodes-complex species (Copepoda : Harpacticoida : Harpacticidae) from the north-eastern Gulf of Mexico

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What this work says

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

inferredcites →https://doi.org/10.1007/978-1-4612-1694-0_15openalex-snapshot

Information Theory and an Extension of the Maximum Likelihood Principle

inferredcites →https://doi.org/10.1007/978-1-4615-2381-9openalex-snapshot

Molecular Markers, Natural History and Evolution

inferredcites →https://doi.org/10.1007/978-94-017-2184-4_8openalex-snapshot

Molecular genetic analyses of species boundaries in the sea

inferredcites →https://doi.org/10.1007/bf00349126openalex-snapshot

Genetic differentiation and reproductive incompatibility among Baja California populations of the copepod Tigriopus californicus

inferredcites →https://doi.org/10.1007/bf00394527openalex-snapshot

Short-term temporal variation in population structure of two harpacticoid copepods, Zausodes arenicolus and Paradactylopodia brevicornis

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

Evolutionary trees from DNA sequences: A maximum likelihood approach

inferredcites →https://doi.org/10.1007/s00227-001-0728-yopenalex-snapshot

Sympatry of distinct mitochondrial DNA lineages in a copepod inhabiting estuarine creeks in the southeastern USA

inferredcites →https://doi.org/10.1007/s002270050640openalex-snapshot

Molecular population structure of the marine benthic copepod Microarthridion littorale along the southeastern and Gulf coasts of the USA

inferredcites →https://doi.org/10.1016/0022-0981(88)90076-7openalex-snapshot

Response of a harpacticoid copepod to a small-scale natural disturbance

inferredcites →https://doi.org/10.1016/b978-1-4832-3211-9.50009-7openalex-snapshot

Evolution of Protein Molecules

inferredcites →https://doi.org/10.1016/j.gene.2004.09.001openalex-snapshot

Unusual structure of ribosomal DNA in the copepod Tigriopus californicus: intergenic spacer sequences lack internal subrepeats

inferredcites →https://doi.org/10.1016/j.ympev.2006.03.014openalex-snapshot

Relationship between morphological taxonomy and molecular divergence within Crustacea: Proposal of a molecular threshold to help species delimitation

inferredcites →https://doi.org/10.1016/s0065-2881(05)48001-3openalex-snapshot

Systematics and Phylogeny

inferredcites →https://doi.org/10.1023/a:1003933603879openalex-snapshot

Molecular genetic analyses of species boundaries in the sea

inferredcites →https://doi.org/10.1073/pnas.91.11.5197openalex-snapshot

Nuclear and mitochondrial gene genealogies and allozyme polymorphism across a major phylogeographic break in the copepod Tigriopus californicus.

inferredcites →https://doi.org/10.1080/10635150701701083openalex-snapshot

Species Concepts and Species Delimitation

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

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

MrBayes 3: Bayesian phylogenetic inference under mixed models

inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003880openalex-snapshot

Decoupling of Molecular and Morphological Evolution in Deep Lineages of a Meiobenthic Harpacticoid Copepod

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026241openalex-snapshot

Mitochondrial Genomes of Galathealinum, Helobdella, and Platynereis: Sequence and Gene Arrangement Comparisons Indicate that Pogonophora Is Not a Phylum and Annelida and Arthropoda Are Not Sister Taxa

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot

The neighbor-joining method: a new method for reconstructing phylogenetic trees.

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot

CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://doi.org/10.1126/science.2448875openalex-snapshot

Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase

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

Phylogeny Estimation and Hypothesis Testing Using Maximum Likelihood

inferredcites →https://doi.org/10.1146/annurev.es.24.110193.001201openalex-snapshot

Sibling Species in the Sea

inferredcites →https://doi.org/10.1163/193724094x00614openalex-snapshot

PHYLOGENETICSTUDY OF CIRRIPEDES AND SELECTED RELATIVES (THECOSTRACA) BASED ON 18S RDNA SEQUENCE ANALYSIS

inferredcites →https://doi.org/10.1371/journal.pbio.0020312openalex-snapshot

Identification of Birds through DNA Barcodes

inferredcites →https://doi.org/10.1651/c-2600.1openalex-snapshot

Genetic Isolation Discovered among Previously Described Sympatric Morphs of a Meiobenthic Copepod

inferredcites →https://doi.org/10.2144/04362bm02openalex-snapshot

Sodium boric acid: a Tris-free, cooler conductive medium for DNA electrophoresis

inferredcites →https://doi.org/10.2307/1548858openalex-snapshot

Phylogenetic Study of Cirripedes and Selected Relatives (Thecostraca) Based on 18S rDNA Sequence Analysis

inferredcites →https://doi.org/10.3354/meps035059openalex-snapshot

Habitat utilization by harpacticoid copepods: a morphometric approach

inferredcites →https://doi.org/10.3354/meps214161openalex-snapshot

An improved protocol for separating meiofauna from sediments using colloidal silica sols

inferredcites →https://doi.org/10.5281/zenodo.16269141openalex-snapshot

Systematics and phylogeny of Zausodes C.B. Wilson, 1932 (Copepoda, Harpacticoida, Harpacticidae), including three new species from the northern Gulf of Mexico

inferredcites →https://doi.org/10.5281/zenodo.16438593openalex-snapshot

A Unified Concept of Species and Its Consequences for the Future of Taxonomy

inferredcites →https://doi.org/10.5479/si.03629236.158.iopenalex-snapshot

The copepods of the Woods Hole region, Massachusetts

What points at this work

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

inferred← citeshttps://doi.org/10.5852/ejt.2018.439zenodo-depositor-declared

Laophontodes typicus T. Scott (Copepoda, Harpacticoida, Laophontodinae) – discovering a species complex by morphology

inferred← citeshttps://doi.org/10.1002/ece3.11471openalex-snapshot

Cryptic diversity and speciation in an endemic copepod crustacean Harpacticella inopinata within Lake Baikal

inferred← citeshttps://doi.org/10.1007/s00300-017-2229-6openalex-snapshot

Composition of Harpacticoida (Crustacea, Copepoda) of the Laptev Sea in comparison with faunas of adjacent Arctic seas

inferred← citeshttps://doi.org/10.1007/s12526-025-01583-4openalex-snapshot

Revealing high genetic divergence masked by low morphological variability in harpacticoid genus Leptastacus Scott T., 1906 (Copepoda, Harpacticoida, Leptastacidae) including the description of five new species

inferred← citeshttps://doi.org/10.1016/j.dsr.2011.05.008openalex-snapshot

Submarine ridges do not prevent large-scale dispersal of abyssal fauna: A case study of Mesocletodes (Crustacea, Copepoda, Harpacticoida)

inferred← citeshttps://doi.org/10.1016/j.dsr.2012.12.010openalex-snapshot

Assemblages gradually change from bathyal to hadal depth: A case study on harpacticoid copepods around the Kuril Trench (north-west Pacific Ocean)

inferred← citeshttps://doi.org/10.1016/j.gene.2013.12.053openalex-snapshot

The mitochondrial genomes of Amphiascoides atopus and Schizopera knabeni (Harpacticoida: Miraciidae) reveal similarities between the copepod orders Harpacticoida and Poecilostomatoida

inferred← citeshttps://doi.org/10.1016/j.jembe.2014.06.016openalex-snapshot

An effective procedure for DNA isolation and voucher recovery from millimeter-scale copepods and new primers for the 18S rRNA and cytb genes

inferred← citeshttps://doi.org/10.1016/j.parint.2024.102964openalex-snapshot

Caligus minimus Otto, 1821 (Copepoda: Caligidae): A commercially important but poorly described parasite of cultured European Sea Bass, Dicentrarchus labrax (Linnaeus, 1758)

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.10.004openalex-snapshot

Unraveling the intricate biodiversity of the benthic harpacticoid genus Nannopus (Copepoda, Harpacticoida, Nannopodidae) in Korean waters

inferred← citeshttps://doi.org/10.1038/s41598-019-45718-7openalex-snapshot

Revealing higher than expected diversity of Harpacticoida (Crustacea:Copepoda) in the North Sea using MALDI-TOF MS and molecular barcoding

inferred← citeshttps://doi.org/10.1111/mec.12016openalex-snapshot

Cryptic diversity of the ‘cosmopolitan’ harpacticoid copepod N annopus palustris: genetic and morphological evidence

inferred← citeshttps://doi.org/10.1111/mec.13744openalex-snapshot

Do some deep‐sea, sediment‐dwelling species of harpacticoid copepods have 1000‐km‐scale range sizes?

inferred← citeshttps://doi.org/10.1134/s1995082918020086openalex-snapshot

Morphological and Molecular-Genetic Polymorphism of Canthocamptus staphylinus Jurine (Harpacticoida, Copepoda, Crustacea)

inferred← citeshttps://doi.org/10.1186/s40064-016-3724-xopenalex-snapshot

A simple and efficient total genomic DNA extraction method for individual zooplankton

inferred← citeshttps://doi.org/10.3160/3732.1openalex-snapshot

Phylogenetic Study of Dioecious and Parthenogenetic Populations ofCanthocamptus staphylinus(Crustacea, Copepoda, Harpacticoida)

inferred← citeshttps://doi.org/10.3390/d13090448openalex-snapshot

Patterns of Cryptic Diversity and Phylogeography in Four Freshwater Copepod Crustaceans in European Lakes

inferred← citeshttps://doi.org/10.3897/zookeys.378.6695openalex-snapshot

A new subspecies of Nitokra affinis Gurney, 1927 (Copepoda, Harpacticoida) from the Caribbean coast of Colombia

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