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Localization of quantitative trait loci for diapause and other photoperiodically regulated life history traits important in adaptation to seasonally varying environments

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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/ece3.14openalex-snapshot
Adaptation to a seasonally varying environment: a strong latitudinal cline in reproductive diapause combined with high gene flow in Drosophila montana
inferredcites →https://doi.org/10.1007/978-0-387-92125-9openalex-snapshot
A Guide to QTL Mapping with R/qtl
inferredcites →https://doi.org/10.1007/978-1-4615-6941-1_7openalex-snapshot
Phenology and Photoperiodic Diapause in Northern Populations of Drosophila
inferredcites →https://doi.org/10.1007/978-1-4757-0190-6_8openalex-snapshot
Relationship between Cold Hardiness and Diapause
inferredcites →https://doi.org/10.1007/bf00352399openalex-snapshot
A combined molecular and cytogenetic approach to genome evolution in Drosophila using large-fragment DNA cloning
inferredcites →https://doi.org/10.1007/bf00378041openalex-snapshot
The impact of diapause on the evolution of other life history traits in flesh flies
inferredcites →https://doi.org/10.1007/s00018-010-0311-0openalex-snapshot
Gene expression, metabolic regulation and stress tolerance during diapause
inferredcites →https://doi.org/10.1007/s00122-010-1372-zopenalex-snapshot
Effects of missing marker and segregation distortion on QTL mapping in F2 populations
inferredcites →https://doi.org/10.1007/s00412-006-0075-3openalex-snapshot
Comparative polytene chromosome maps of D. montana and D. virilis
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.03.018openalex-snapshot
Meeting the energetic demands of insect diapause: Nutrient storage and utilization
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.09.007openalex-snapshot
Effects of photoperiodically induced reproductive diapause and cold hardening on the cold tolerance of Drosophila montana
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.02.004openalex-snapshot
Photoperiodic regulation of cold tolerance and expression levels of regucalcin gene in Drosophila montana
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.09.007openalex-snapshot
Photoperiodic regulation of life-history traits before and after eclosion: Egg-to-adult development time, juvenile body mass and reproductive diapause in Drosophila montana
inferredcites →https://doi.org/10.1016/j.jinsphys.2013.05.006openalex-snapshot
Northern Drosophila montana flies show variation both within and between cline populations in the critical day length evoking reproductive diapause
inferredcites →https://doi.org/10.1017/s0016672399004176openalex-snapshot
Testing the correspondence between map positions of quantitative trait loci
inferredcites →https://doi.org/10.1038/nprot.2006.79openalex-snapshot
Analysis of locomotor activity rhythms in Drosophila
inferredcites →https://doi.org/10.1038/sj.hdy.6800786openalex-snapshot
Quantitative trait loci for thermotolerance phenotypes in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.0604592103openalex-snapshot
Natural variation in Drosophila melanogaster diapause due to the insulin-regulated PI3-kinase
inferredcites →https://doi.org/10.1093/aesa/33.4.768aopenalex-snapshot
Studies in the Genetics of Drosophila
inferredcites →https://doi.org/10.1093/bioinformatics/btg112openalex-snapshot
R/qtl: QTL mapping in experimental crosses
inferredcites →https://doi.org/10.1093/bioinformatics/bti610openalex-snapshot
Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research
inferredcites →https://doi.org/10.1093/icb/44.6.413openalex-snapshot
Bergmann and Converse Bergmann Latitudinal Clines in Arthropods: Two Ends of a Continuum?
inferredcites →https://doi.org/10.1098/rspb.2012.1917openalex-snapshot
Footprints in time: comparative quantitative trait loci mapping of the pitcher-plant mosquito,Wyeomyia smithii
inferredcites →https://doi.org/10.1098/rstb.2010.0111openalex-snapshot
Phenology, seasonal timing and circannual rhythms: towards a unified framework
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00623.xopenalex-snapshot
CHILL-COMA TOLERANCE, A MAJOR CLIMATIC ADAPTATION AMONG DROSOPHILA SPECIES
inferredcites →https://doi.org/10.1111/j.1365-2052.2011.02183.xopenalex-snapshot
G enotypechecker : an interactive tool for checking the inheritance consistency of genotyped pedigrees
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00746.xopenalex-snapshot
Genetic basis for reproductive diapause is correlated with life history traits within the Culex pipiens complex
inferredcites →https://doi.org/10.1111/j.1365-2583.2011.01119.xopenalex-snapshot
Cold tolerance and cold‐induced modulation of gene expression in two Drosophila virilis group species with different distributions
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03335.xopenalex-snapshot
Knockdown resistance to heat stress and slow recovery from chill coma are genetically associated in a quantitative trait locus region of chromosome 2 in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03945.xopenalex-snapshot
QTL for the thermotolerance effect of heat hardening, knockdown resistance to heat and chill‐coma recovery in an intercontinental set of recombinant inbred lines of Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04951.xopenalex-snapshot
Identification of X-linked quantitative trait loci affecting cold tolerance in Drosophila melanogaster and fine mapping by selective sweep analysis
inferredcites →https://doi.org/10.1111/j.1420-9101.2009.01916.xopenalex-snapshot
A microsatellite linkage map for Drosophila montana shows large variation in recombination rates, and a courtship song trait maps to an area of low recombination
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00351.xopenalex-snapshot
REPRODUCTIVE DIAPAUSE AND LIFE-HISTORY CLINES IN NORTH AMERICAN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1601-5223.1978.tb01282.xopenalex-snapshot
Photoperiodic diapause in Drosophila lummei Hackman is controlled by an X-chromosomal factor
inferredcites →https://doi.org/10.1111/j.1601-5223.1981.tb01759.xopenalex-snapshot
Localization of the genetic unit controlling the photoperiodic adult diapause in Drosophila littoralis
inferredcites →https://doi.org/10.1146/annurev.ecolsys.37.091305.110115openalex-snapshot
Evolution of Animal Photoperiodism
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.63openalex-snapshot
Plasticity in Life-History Traits
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145137openalex-snapshot
Regulation of Diapause
inferredcites →https://doi.org/10.1177/0748730410365656openalex-snapshot
What Season Is It Anyway? Circadian Tracking vs. Photoperiodic Anticipation in Insects
inferredcites →https://doi.org/10.1186/1471-213x-14-19openalex-snapshot
Interaction of light regimes and circadian clocks modulate timing of pre-adult developmental events in Drosophila
inferredcites →https://doi.org/10.1186/1471-2164-11-218openalex-snapshot
A comparison of SNPs and microsatellites as linkage mapping markers: lessons from the zebra finch (Taeniopygia guttata)
inferredcites →https://doi.org/10.1534/genetics.105.047985openalex-snapshot
Chromosome Inversions, Local Adaptation and Speciation
inferredcites →https://doi.org/10.1534/genetics.106.068726openalex-snapshot
Quantitative Trait Loci Associated with Photoperiodic Response and Stage of Diapause in the Pitcher-Plant Mosquito, Wyeomyia smithii
inferredcites →https://doi.org/10.1534/genetics.112.139899openalex-snapshot
Where's the Money? Inversions, Genes, and the Hunt for Genomic Targets of Selection
inferredcites →https://doi.org/10.1554/0014-3820(2001)055[1063:cctamc]2.0.co;2openalex-snapshot
CHILL-COMA TOLERANCE, A MAJOR CLIMATIC ADAPTATION AMONG DROSOPHILA SPECIES
inferredcites →https://doi.org/10.2307/4831openalex-snapshot
Seasonal Adaptations of Insects
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.4161/psb.3.8.6340openalex-snapshot
Interactions between the circadian clock and cold-response in Arabidopsis
inferredcites →https://doi.org/10.5281/zenodo.10741286openalex-snapshot
Photoperiodism and seasonal development of insects.
inferredcites →https://doi.org/10.5281/zenodo.10754122openalex-snapshot
Malt as a culture medium for Drosophila species.

What points at this work

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

inferred← citeshttps://doi.org/10.1002/evl3.301openalex-snapshot
Divergence and introgression among the virilis group of Drosophila
inferred← citeshttps://doi.org/10.1016/b978-0-443-29068-8.00133-1openalex-snapshot
Studying the genetics of behavior in the genomics era
inferred← citeshttps://doi.org/10.1017/9781108609364openalex-snapshot
Insect Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.001openalex-snapshot
Preface
inferred← citeshttps://doi.org/10.1017/9781108609364.002openalex-snapshot
Confronting the Challenges of a Seasonal Environment
inferred← citeshttps://doi.org/10.1017/9781108609364.003openalex-snapshot
Which Seasons Are Being Avoided?
inferred← citeshttps://doi.org/10.1017/9781108609364.004openalex-snapshot
Variation in the Diapause Response
inferred← citeshttps://doi.org/10.1017/9781108609364.005openalex-snapshot
The Cost of Diapause and Some Diapause Alternatives
inferred← citeshttps://doi.org/10.1017/9781108609364.006openalex-snapshot
Interpreting Seasonal Cues to Program Diapause Entry
inferred← citeshttps://doi.org/10.1017/9781108609364.007openalex-snapshot
Preparing for Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.008openalex-snapshot
The Diapause State
inferred← citeshttps://doi.org/10.1017/9781108609364.009openalex-snapshot
Ending Diapause and Reinitiating Development
inferred← citeshttps://doi.org/10.1017/9781108609364.010openalex-snapshot
Molecular Signaling Pathways that Regulate Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.011openalex-snapshot
Genetic Control of Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.012openalex-snapshot
Evolution of Diapause
inferred← citeshttps://doi.org/10.1017/9781108609364.013openalex-snapshot
Wider Implications
inferred← citeshttps://doi.org/10.1017/9781108609364.014openalex-snapshot
References
inferred← citeshttps://doi.org/10.1017/9781108609364.015openalex-snapshot
Species Index
inferred← citeshttps://doi.org/10.1017/9781108609364.016openalex-snapshot
Subject Index
inferred← citeshttps://doi.org/10.1017/9781108609364.017openalex-snapshot
Plate Section (PDF Only)
inferred← citeshttps://doi.org/10.1080/19336934.2021.2016327openalex-snapshot
Adaptation and ecological speciation in seasonally varying environments at high latitudes: Drosophila virilis group
inferred← citeshttps://doi.org/10.1093/gbe/evy147openalex-snapshot
Inter and Intraspecific Genomic Divergence in Drosophila montana Shows Evidence for Cold Adaptation
inferred← citeshttps://doi.org/10.1101/075960openalex-snapshot
Correlations of genotype with climate parameters suggest Caenorhabditis elegans niche preferences
inferred← citeshttps://doi.org/10.1111/eea.12753openalex-snapshot
Diapause research in insects: historical review and recent work perspectives
inferred← citeshttps://doi.org/10.1111/nyas.13256openalex-snapshot
Pleiotropy, constraint, and modularity in the evolution of life histories: insights from genomic analyses
inferred← citeshttps://doi.org/10.1111/phen.12194openalex-snapshot
Sex‐linked inheritance of diapause induction in the butterfly P ieris napi
inferred← citeshttps://doi.org/10.1134/s1062360424700231openalex-snapshot
“Genes of Speciation”: History and Present: A Brief Review
inferred← citeshttps://doi.org/10.1534/g3.116.035162openalex-snapshot
Correlations of Genotype with Climate Parameters Suggest Caenorhabditis elegans Niche Adaptations
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