On the public citation graph
Molecular data delineate crypticNassariusspecies and characterize spatial genetic structure ofN. nitidus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/ecss.2002.1037openalex-snapshot
Dispersal, Genetic Differentiation and Speciation in Estuarine Organisms
inferredcites →https://doi.org/10.1007/978-1-4615-2381-9openalex-snapshot
Molecular Markers, Natural History and Evolution
inferredcites →https://doi.org/10.1007/bf00354622openalex-snapshot
The genetic effects of larval dispersal depend on spatial scale and habitat characteristics
inferredcites →https://doi.org/10.1007/bf01059068openalex-snapshot
Recent taxonomic discoveries concerning the musselMytilus: Implications for biomonitoring
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/s00227-005-0139-6openalex-snapshot
Population genetic structure of the prosobranch Nassarius reticulatus (L.) in a ria seascape (NW Iberian Peninsula) as revealed by RAPD analysis
inferredcites →https://doi.org/10.1007/s10592-007-9320-4openalex-snapshot
Foot mucus is a good source for non-destructive genetic sampling in Polyplacophora
inferredcites →https://doi.org/10.1016/j.tree.2006.11.004openalex-snapshot
Cryptic species as a window on diversity and conservation
inferredcites →https://doi.org/10.1017/s0025315400016234openalex-snapshot
Differences revealed by paper partition chromatography between the gastropod Nassarius reticulatus (L.) and specimens believed to be N. nitida (Jeffreys)
inferredcites →https://doi.org/10.1017/s0025315400036183openalex-snapshot
Allozyme Evidence for Cryptic Speciation in Sympatric Populations ofNassariusspp. (Mollusca: Gastropoda)
inferredcites →https://doi.org/10.1017/s0025315400051985openalex-snapshot
The Larval Stages of Nassarius reticulatus and Nassarius incrassatus
inferredcites →https://doi.org/10.1038/hdy.1991.81openalex-snapshot
Genetic subdivision of the intertidal snail Bembicium vittatum (Gastropoda: Littorinidae) varies with habitat in the Houtman Abrolhos Islands, Western Australia
inferredcites →https://doi.org/10.1046/j.1095-8312.2002.00018.xopenalex-snapshot
Allozyme, mitochondrial-DNA, and morphometric variability indicate cryptic species of anchovy (Engraulis encrasicolus)
inferredcites →https://doi.org/10.1046/j.1365-294x.1997.00256.xopenalex-snapshot
Cryptic invasions of the crab Carcinus detected by molecular phylogeography
inferredcites →https://doi.org/10.1071/mf04051openalex-snapshot
Estuaries, lagoons and enclosed embayments: habitats that enhance population subdivision of inshore fishes
inferredcites →https://doi.org/10.1073/pnas.0406166101openalex-snapshot
Ten species in one: DNA barcoding reveals cryptic species in the neotropical skipper butterfly Astraptes fulgerator
inferredcites →https://doi.org/10.1093/bioinformatics/btg359openalex-snapshot
DnaSP, DNA polymorphism analyses by the coalescent and other methods
inferredcites →https://doi.org/10.1093/genetics/131.2.479openalex-snapshot
Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data.
inferredcites →https://doi.org/10.1093/jhered/esm067openalex-snapshot
Genetic Isolation by Distance among Populations of the Netted Dog Whelk Nassarius reticulatus (L.) along the European Atlantic Coastline
inferredcites →https://doi.org/10.1093/molbev/msm092openalex-snapshot
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0
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.a026036openalex-snapshot
Median-joining networks for inferring intraspecific phylogenies
inferredcites →https://doi.org/10.1098/rsbl.2003.0025openalex-snapshot
Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species
inferredcites →https://doi.org/10.1098/rspb.2002.2218openalex-snapshot
Biological identifications through DNA barcodes
inferredcites →https://doi.org/10.1098/rspb.2008.0216openalex-snapshot
Global patterns in marine dispersal estimates: the influence of geography, taxonomic category and life history
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03385.xopenalex-snapshot
Contrasting phylogeography in three endemic Hawaiian limpets (Cellana spp.) with similar life histories
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03477.xopenalex-snapshot
Pillars of Hercules: is the Atlantic–Mediterranean transition a phylogeographical break?
inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.011802.132421openalex-snapshot
Species-Level Paraphyly and Polyphyly: Frequency, Causes, and Consequences, with Insights from Animal Mitochondrial DNA
inferredcites →https://doi.org/10.1146/annurev.es.24.110193.001201openalex-snapshot
Sibling Species in the Sea
inferredcites →https://doi.org/10.1146/annurev.marine.010908.163757openalex-snapshot
Larval Dispersal and Marine Population Connectivity
inferredcites →https://doi.org/10.1177/117693430500100003openalex-snapshot
Arlequin (version 3.0): An integrated software package for population genetics data analysis
inferredcites →https://doi.org/10.1371/journal.pbio.0020354openalex-snapshot
DNA Barcoding: Promise and Pitfalls
inferredcites →https://doi.org/10.1371/journal.pbio.0030001openalex-snapshot
Biology by Numbers—Introducing Quantitation into Life Science Education
inferredcites →https://doi.org/10.1371/journal.pbio.0030422openalex-snapshot
DNA Barcoding: Error Rates Based on Comprehensive Sampling
inferredcites →https://doi.org/10.1890/08-0257.1openalex-snapshot
EVALUATING SIGNATURES OF GLACIAL REFUGIA FOR NORTH ATLANTIC BENTHIC MARINE TAXA
inferredcites →https://doi.org/10.1890/1051-0761(2003)013[0146:pgdcat]2.0.co;2openalex-snapshot
POPULATION GENETICS, DEMOGRAPHIC CONNECTIVITY, AND THE DESIGN OF MARINE RESERVES
inferredcites →https://doi.org/10.2307/3809697openalex-snapshot
Molecular Markers, Natural History and Evolution
inferredcites →https://doi.org/10.3354/meps003051openalex-snapshot
Population Dynamics of Nassarius reticulatus (Gastropoda, Prosobranchia) in Gullmar Fjord, Sweden
inferredcites →https://doi.org/10.3354/meps218203openalex-snapshot
Imposex, organotin bioaccumulation and sterility of female Nassarius reticulatus in polluted areas of NW Spain
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
inferredcites →https://doi.org/10.5281/zenodo.16487746openalex-snapshot
An example of the application of geometric morphometric tools to the morphological diagnosis of two sibling species in Nassarius (Mollusca, Prosobranchia)
inferredcites →https://doi.org/10.5281/zenodo.4641409openalex-snapshot
Nassarius reticulatus (Linnaeus, 1758) y Nassarius nitidus (Jeffreys, 1867) (Gastropoda, Nassariidae), dos especies válidas de los mares de Europa
inferredcites →https://doi.org/10.5962/bhl.title.16342openalex-snapshot
British conchology : or, an account of the Mollusca which now inhabit the British Isles and the surrounding seas
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.2017.275zenodo-depositor-declared
Review of the Nassarius pauperus (Gould, 1850) complex (Nassariidae): Part 3, reinstatement of the genus Reticunassa, with the description of six new species
inferred← citeshttps://doi.org/10.1002/ece3.10360openalex-snapshot
How we study cryptic species and their biological implications: A case study from marine shelled gastropods
inferred← citeshttps://doi.org/10.1007/978-3-030-18616-6_11openalex-snapshot
Selected Wildlife Trematodes
inferred← citeshttps://doi.org/10.1007/978-3-031-60121-7_11openalex-snapshot
Selected Wildlife Trematodes
inferred← citeshttps://doi.org/10.1007/s00227-012-1975-9openalex-snapshot
Recent history of the European Nassarius nitidus (Gastropoda): phylogeographic evidence of glacial refugia and colonization pathways
inferred← citeshttps://doi.org/10.1007/s00227-021-03861-8openalex-snapshot
Looking for diversity in all the right places? Genetic diversity is highest in peripheral populations of the reef-building polychaete Sabellaria alveolata
inferred← citeshttps://doi.org/10.1016/j.quaint.2015.05.042openalex-snapshot
Nassarius shells: Preferred beads of the Palaeolithic
inferred← citeshttps://doi.org/10.1111/zsc.12489openalex-snapshot
Mitogenomic phylogeny of mud snails of the mostly Atlantic/Mediterranean genusTritia(Gastropoda: Nassariidae)
inferred← citeshttps://doi.org/10.3389/fmars.2021.661389openalex-snapshot
Field Monitoring of Tritia mutabilis (Linnaeus, 1758) Egg Capsule Deposition and Intracapsular Embryonic Patterns Using Artificial Substrates and Machine Learning-Based Approaches
inferred← citeshttps://doi.org/10.3390/ijms19102931openalex-snapshot
Advances in DNA Barcoding of Toxic Marine Organisms
inferred← citeshttps://doi.org/10.4003/006.032.0202openalex-snapshot
Description and Molecular Characterization of Six New Species of Nassarius (Gastropoda, Nassariidae) from the Western Pacific Ocean
inferred← citeshttps://doi.org/10.7287/peerj.5684v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5684v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5684v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5684v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.5684v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.5684openalex-snapshot
Meta-analysis of northeast Atlantic marine taxa shows contrasting phylogeographic patterns following post-LGM expansions
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