On the public citation graph

Population structure and gene flow in the Sheepnose mussel (Plethobasus cyphyus) and their implications for conservation

https://doi.org/10.1002/ece3.8630
0 signed · 82 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/ece3.3470openalex-snapshot
Detection of barriers to dispersal is masked by long lifespans and large population sizes
inferredcites →https://doi.org/10.1002/ece3.8630openalex-snapshot
Population structure and gene flow in the Sheepnose mussel (Plethobasus cyphyus) and their implications for conservation
inferredcites →https://doi.org/10.1007/s10592-006-9175-0openalex-snapshot
Population genetics of the freshwater mussel, Amblema plicata (Say 1817) (Bivalvia: Unionidae): Evidence of high dispersal and post-glacial colonization
inferredcites →https://doi.org/10.1007/s10592-007-9290-6openalex-snapshot
Range-wide population genetic analysis of the endangered northern riffleshell mussel, Epioblasma torulosa rangiana (Bivalvia: Unionoida)
inferredcites →https://doi.org/10.1007/s10592-017-1015-xopenalex-snapshot
A comparison of genetic diversity and population structure of the endangered scaleshell mussel (Leptodea leptodon), the fragile papershell (Leptodea fragilis) and their host-fish the freshwater drum (Aplodinotus grunniens)
inferredcites →https://doi.org/10.1007/s10750-007-9011-7openalex-snapshot
Global diversity of freshwater mussels (Mollusca, Bivalvia) in freshwater
inferredcites →https://doi.org/10.1007/s10750-010-0190-2openalex-snapshot
Strategies for the conservation of endangered freshwater pearl mussels (Margaritifera margaritifera L.): a synthesis of Conservation Genetics and Ecology
inferredcites →https://doi.org/10.1007/s10750-013-1524-7openalex-snapshot
Biodiversity on the brink: an assessment of conservation strategies for North American freshwater mussels
inferredcites →https://doi.org/10.1007/s10750-016-3076-0openalex-snapshot
Signature of postglacial colonization on contemporary genetic structure and diversity of Quadrula quadrula (Bivalvia: Unionidae)
inferredcites →https://doi.org/10.1007/s10750-017-3139-xopenalex-snapshot
Ecosystem services provided by freshwater mussels
inferredcites →https://doi.org/10.1016/0006-3207(94)00091-4openalex-snapshot
Translocation as a tool for conserving imperiled fishes: Experiences in western United States
inferredcites →https://doi.org/10.1016/0006-3207(95)00034-8openalex-snapshot
Small dams as barriers to freshwater mussels (Bivalvia, Unionoida) and their hosts
inferredcites →https://doi.org/10.1016/s0169-5347(01)02338-2openalex-snapshot
Cryptic northern refugia and the origins of the modern biota
inferredcites →https://doi.org/10.1016/s1055-7903(03)00026-5openalex-snapshot
Molecular systematics of the North American freshwater bivalve genus Quadrula (Unionidae: Ambleminae) based on mitochondrial ND1 sequences
inferredcites →https://doi.org/10.1017/cbo9780511623400.007openalex-snapshot
Effective population size, genetic variation, and their use in population management
inferredcites →https://doi.org/10.1017/cbo9781139048217openalex-snapshot
North American Freshwater Mussels
inferredcites →https://doi.org/10.1017/s1464793105006950openalex-snapshot
Freshwater biodiversity: importance, threats, status and conservation challenges
inferredcites →https://doi.org/10.1029/1999wr900016openalex-snapshot
Dam nation: A geographic census of American dams and their large‐scale hydrologic impacts
inferredcites →https://doi.org/10.1038/35016000openalex-snapshot
The genetic legacy of the Quaternary ice ages
inferredcites →https://doi.org/10.1038/72708openalex-snapshot
An economic method for the fluorescent labeling of PCR fragments
inferredcites →https://doi.org/10.1038/hdy.2013.104openalex-snapshot
Phylogeographic and population genetic analyses reveal Pleistocene isolation followed by high gene flow in a wide ranging, but endangered, freshwater mussel
inferredcites →https://doi.org/10.1038/hdy.2016.111openalex-snapshot
Landscape genetics informs mesohabitat preference and conservation priorities for a surrogate indicator species in a highly fragmented river system
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00784.xopenalex-snapshot
Intraspecific phylogeography ofLasmigona subviridis(Bivalvia: Unionidae): conservation implications of range discontinuity
inferredcites →https://doi.org/10.1080/00222933.2015.1083059openalex-snapshot
Early life history of the sheepnose (Plethobasus cyphyus) (Mollusca: Bivalvia: Unionoida)
inferredcites →https://doi.org/10.1086/204195openalex-snapshot
The Genetic Structure of Ancient Human Populations
inferredcites →https://doi.org/10.1093/bioinformatics/btp187openalex-snapshot
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/bts460openalex-snapshot
GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research—an update
inferredcites →https://doi.org/10.1093/genetics/129.2.555openalex-snapshot
Pairwise comparisons of mitochondrial DNA sequences in stable and exponentially growing populations.
inferredcites →https://doi.org/10.1093/genetics/144.4.2001openalex-snapshot
Description and Power Analysis of Two Tests for Detecting Recent Population Bottlenecks From Allele Frequency Data
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/genetics/163.3.1177openalex-snapshot
Bayesian Inference of Recent Migration Rates Using Multilocus Genotypes
inferredcites →https://doi.org/10.1093/jhered/89.3.238openalex-snapshot
Distortion of allele frequency distributions provides a test for recent population bottlenecks
inferredcites →https://doi.org/10.1093/jhered/90.4.502openalex-snapshot
Computer note. BOTTLENECK: a computer program for detecting recent reductions in the effective size using allele frequency data
inferredcites →https://doi.org/10.1093/mollus/eym029openalex-snapshot
Review of the systematics and global diversity of freshwater mussel species (Bivalvia: Unionoida)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026036openalex-snapshot
Median-joining networks for inferring intraspecific phylogenies
inferredcites →https://doi.org/10.1093/sysbio/syy032openalex-snapshot
Posterior Summarization in Bayesian Phylogenetics Using Tracer 1.7
inferredcites →https://doi.org/10.1098/rspb.2004.2720openalex-snapshot
Habitat fragmentation causes bottlenecks and inbreeding in the European tree frog (Hyla arborea)
inferredcites →https://doi.org/10.1111/1467-9868.00353openalex-snapshot
Bayesian Measures of Model Complexity and Fit
inferredcites →https://doi.org/10.1111/1755-0998.12509openalex-snapshot
pophelper : an R package and web app to analyse and visualize population structure
inferredcites →https://doi.org/10.1111/2041-210x.12410openalex-snapshot
popart : full‐feature software for haplotype network construction
inferredcites →https://doi.org/10.1111/bij.12437openalex-snapshot
Historical demography of freshwater mussels (Bivalvia: Unionidae): genetic evidence for population expansion and contraction during the late Pleistocene and Holocene
inferredcites →https://doi.org/10.1111/brv.12028openalex-snapshot
The role of fecundity and reproductive effort in defining life‐history strategies of N orth A merican freshwater mussels
inferredcites →https://doi.org/10.1111/ele.12388openalex-snapshot
Locally adapted traits maintained in the face of high gene flow
inferredcites →https://doi.org/10.1111/faf.12312openalex-snapshot
Fish dispersal in flowing waters: A synthesis of movement‐ and genetic‐based studies
inferredcites →https://doi.org/10.1111/gcb.13369openalex-snapshot
Predicting the effects of climate change on population connectivity and genetic diversity of an imperiled freshwater mussel, Cumberlandia monodonta (Bivalvia: Margaritiferidae), in riverine systems
inferredcites →https://doi.org/10.1111/j.0014-3820.2005.tb01814.xopenalex-snapshot
A STANDARDIZED GENETIC DIFFERENTIATION MEASURE
inferredcites →https://doi.org/10.1111/j.1095-8312.1996.tb01434.xopenalex-snapshot
Some genetic consequences of ice ages, and their role in divergence and speciation
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00936.xopenalex-snapshot
The phylogeographical and management implications of genetic population structure in the imperiled snuffbox mussel, Epioblasma triquetra (Bivalvia: Unionidae)
inferredcites →https://doi.org/10.1111/j.1095-8312.2010.01596.xopenalex-snapshot
Testing congruency of geographic and genetic population structure for a freshwater mussel (Bivalvia: Unionoida) and its host fish
inferredcites →https://doi.org/10.1111/j.1095-8649.2010.02769.xopenalex-snapshot
Post‐glacial expansion into the Paleozoic Plateau: evidence of an Ozarkian refugium for the Ozark minnow Notropis nubilus (Teleostei: Cypriniformes)
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02420.xopenalex-snapshot
Genetic diversity and differentiation of central European freshwater pearl mussel (Margaritifera margaritifera L.) populations: implications for conservation and management
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03887.xopenalex-snapshot
G ST and its relatives do not measure differentiation
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04784.xopenalex-snapshot
Calculations of population differentiation based on GST and D: forget GST but not all of statistics!
inferredcites →https://doi.org/10.1111/j.1471-8286.2004.00684.xopenalex-snapshot
micro ‐ checker : software for identifying and correcting genotyping errors in microsatellite data
inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02847.xopenalex-snapshot
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
inferredcites →https://doi.org/10.1111/jbi.12535openalex-snapshot
Contrasting population‐level responses to Pleistocene climatic oscillations in an alpine bat revealed by complete mitochondrial genomes and evolutionary history inference
inferredcites →https://doi.org/10.1139/z83-109openalex-snapshot
Environmental determinants of unionid clam distribution in the Middle Thames River, Ontario
inferredcites →https://doi.org/10.1577/1548-8446(1989)014<0002:fonaet>2.0.co;2openalex-snapshot
Fishes of North America Endangered, Threatened, or of Special Concern: 1989
inferredcites →https://doi.org/10.1577/1548-8446(1993)018<0006:csofmo>2.0.co;2openalex-snapshot
Conservation Status of Freshwater Mussels of the United States and Canada
inferredcites →https://doi.org/10.1890/04-0491openalex-snapshot
RARITY, FRAGMENTATION, AND THE SCALE DEPENDENCE OF EXTINCTION RISK IN DESERT FISHES
inferredcites →https://doi.org/10.1899/07-058.1openalex-snapshot
Community and foodweb ecology of freshwater mussels
inferredcites →https://doi.org/10.1899/08-171.1openalex-snapshot
Freshwater biodiversity conservation: recent progress and future challenges
inferredcites →https://doi.org/10.1899/12-028.1openalex-snapshot
Population structure, multiple paternity, and long-distance transport of spermatozoa in the freshwater musselLampsilis cardium(Bivalvia:Unionidae)
inferredcites →https://doi.org/10.2307/1467542openalex-snapshot
Mantle Biopsy: A Technique for Nondestructive Tissue-Sampling of Freshwater Mussels
inferredcites →https://doi.org/10.2307/2408065openalex-snapshot
CONSERVATION AND EVOLUTION
inferredcites →https://doi.org/10.2307/2422648openalex-snapshot
The Impact of Impoundment on the Mussel Fauna of Kentucky Reservoir, Tennessee River
inferredcites →https://doi.org/10.2307/2489openalex-snapshot
A Quantitative Study of Growth and Production of Unionid Mussels in the River Thames at Reading
inferredcites →https://doi.org/10.2983/0730-8000(2006)25[527:gmgfcp]2.0.co;2openalex-snapshot
GENETIC MANAGEMENT GUIDELINES FOR CAPTIVE PROPAGATION OF FRESHWATER MUSSELS (UNIONOIDEA)
inferredcites →https://doi.org/10.2983/0730-8000(2006)25[975:nmtodf]2.0.co;2openalex-snapshot
NON-INVASIVE METHOD TO OBTAIN DNA FROM FRESHWATER MUSSELS (BIVALVIA: UNIONIDAE)
inferredcites →https://doi.org/10.31931/fmbc.v23i2.2020.124-133openalex-snapshot
Population Genetics of a Common Freshwater Mussel, Amblema plicata, in a Southern U.S. River
inferredcites →https://doi.org/10.3390/d12030118openalex-snapshot
Evidence for Plio-Pleistocene Duck Mussel Refugia in the Azov Sea River Basins
inferredcites →https://doi.org/10.5860/choice.29-0315openalex-snapshot
After the Ice Age: the return of life to glaciated North America
inferredcites →https://doi.org/10.5860/choice.36-5685openalex-snapshot
The freshwater mussels of Tennessee
inferredcites →https://doi.org/10.5962/bhl.title.49774openalex-snapshot
Notes on the natural hosts of fresh-water mussels
inferredcites →https://doi.org/10.7717/peerj.281openalex-snapshot
Poppr : an R package for genetic analysis of populations with clonal, partially clonal, and/or sexual reproduction

What points at this work

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

inferred← citeshttps://doi.org/10.37828/em.2024.73.20zenodo-depositor-declared
Identification of microsatellite markers for the invasive freshwater mussel Sinanodonta lauta (E. von Martens, 1877) (Bivalvia: Unionida)
inferred← citeshttps://doi.org/10.1007/s10592-025-01732-zopenalex-snapshot
Saving what’s left: conservation genomics of Plethobasus, a critically endangered genus of freshwater mussel
inferred← citeshttps://doi.org/10.1111/fwb.14317openalex-snapshot
Riverscape genomics of the endangered freshwater mussel Lampsilis rafinesqueana
inferred← citeshttps://doi.org/10.31931/fmbc-d-23-00005openalex-snapshot
Impacts of Propagation on Population Genetics of the Threeridge Mussel Amblema plicata (Say, 1817)
showing the first 4 of 5 · page through all 5
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.