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Broad geographic sampling reveals predictable, pervasive, and strong seasonal adaptation in Drosophila

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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/tpbi.1996.0022openalex-snapshot
Patterns of Genetic Polymorphism Maintained by Fluctuating Selection with Overlapping Generations
inferredcites →https://doi.org/10.1007/bf02458284openalex-snapshot
Environmental fluctuations and the maintenance of genetic diversity in age or stage-structured populations
inferredcites →https://doi.org/10.1016/j.cub.2006.11.035openalex-snapshot
Global Warming: Fly Populations Are Responding Rapidly to Climate Change
inferredcites →https://doi.org/10.1016/j.cub.2015.11.069openalex-snapshot
Divergence and Functional Degradation of a Sex Chromosome-like Supergene
inferredcites →https://doi.org/10.1016/j.jinsphys.2005.09.008openalex-snapshot
Eco-physiological phases of insect diapause
inferredcites →https://doi.org/10.1016/s0169-5347(98)01378-0openalex-snapshot
Rapid evolution as an ecological process
inferredcites →https://doi.org/10.1038/nature01767openalex-snapshot
Rapid evolution drives ecological dynamics in a predator–prey system
inferredcites →https://doi.org/10.1038/nature10811openalex-snapshot
The Drosophila melanogaster Genetic Reference Panel
inferredcites →https://doi.org/10.1038/nature10944openalex-snapshot
The genomic basis of adaptive evolution in threespine sticklebacks
inferredcites →https://doi.org/10.1038/nrg3803openalex-snapshot
Sequencing pools of individuals — mining genome-wide polymorphism data without big funding
inferredcites →https://doi.org/10.1038/s41559-017-0385-2openalex-snapshot
What genomic data can reveal about eco-evolutionary dynamics
inferredcites →https://doi.org/10.1038/s41559-020-01305-yopenalex-snapshot
Ecology shapes epistasis in a genotype–phenotype–fitness map for stick insect colour
inferredcites →https://doi.org/10.1038/s41598-017-13901-3openalex-snapshot
Population genomics of Wolbachia and mtDNA in Drosophila simulans from California
inferredcites →https://doi.org/10.1073/pnas.1207553109openalex-snapshot
Upper thermal limits of Drosophila are linked to species distributions and strongly constrained phylogenetically
inferredcites →https://doi.org/10.1073/pnas.1408589111openalex-snapshot
Evolutionary tipping points in the capacity to adapt to environmental change
inferredcites →https://doi.org/10.1073/pnas.1410372111openalex-snapshot
Divergence of Drosophila melanogaster repeatomes in response to a sharp microclimate contrast in Evolution Canyon, Israel
inferredcites →https://doi.org/10.1073/pnas.1423275112openalex-snapshot
Causes of natural variation in fitness: Evidence from studies of Drosophila populations
inferredcites →https://doi.org/10.1073/pnas.1702994114openalex-snapshot
Seasonally fluctuating selection can maintain polymorphism at many loci via segregation lift
inferredcites →https://doi.org/10.1073/pnas.1907787116openalex-snapshot
Microbiome composition shapes rapid genomic adaptation of Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.1919039117openalex-snapshot
Estimating the genome-wide contribution of selection to temporal allele frequency change
inferredcites →https://doi.org/10.1086/283468openalex-snapshot
Genetic Variation in a Heterogeneous Environment VII. Temporal and Spatial Heterogeneity in Infinite Populations
inferredcites →https://doi.org/10.1086/284698openalex-snapshot
Long-Distance Migration of Drosophila. 3. Dispersal of D. melanogaster Alleles from a Maryland Orchard
inferredcites →https://doi.org/10.1086/285610openalex-snapshot
Role of Overlapping Generations in Maintaining Genetic Variation in a Fluctuating Environment
inferredcites →https://doi.org/10.1086/285671openalex-snapshot
Antagonistic Pleiotropy, Reversal of Dominance, and Genetic Polymorphism
inferredcites →https://doi.org/10.1086/661780openalex-snapshot
Thermal Tolerance in Widespread and Tropical Drosophila Species: Does Phenotypic Plasticity Increase with Latitude?
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/gbe/evaa056openalex-snapshot
The Limits to Estimating Population-Genetic Parameters with Temporal Data
inferredcites →https://doi.org/10.1093/genetics/152.2.807openalex-snapshot
Genetic Variation Maintained in Multilocus Models of Additive Quantitative Traits Under Stabilizing Selection
inferredcites →https://doi.org/10.1093/genetics/28.2.162openalex-snapshot
GENETICS OF NATURAL POPULATIONS IX. TEMPORAL CHANGES IN THE COMPOSITION OF POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/33.2.158openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XVI. ALTITUDINAL AND SEASONAL CHANGES PRODUCED BY NATURAL SELECTION IN CERTAIN POPULATIONS OF DROSOPHILA PSEUDOOBSCURA AND DROSOPHILA PERSIMILIS
inferredcites →https://doi.org/10.1093/genetics/82.2.323openalex-snapshot
CHROMOSOME STUDIES IN WILD POPULATIONS OF D. MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/84.1.145openalex-snapshot
GENETIC VARIATION IN A HETEROGENEOUS ENVIRONMENT. II. TEMPORAL HETEROGENEITY AND DIRECTIONAL SELECTION
inferredcites →https://doi.org/10.1093/genetics/95.1.211openalex-snapshot
CHROMOSOME STUDIES IN WILD POPULATIONS OF DROSOPHILA MELANOGASTER. II. RELATIONSHIP OF INVERSION FREQUENCIES TO LATITUDE, SEASON, WING-LOADING AND FLIGHT ACTIVITY
inferredcites →https://doi.org/10.1093/molbev/msaa120openalex-snapshot
Genomic Analysis of European Drosophila melanogaster Populations Reveals Longitudinal Structure, Continent-Wide Selection, and Previously Unknown DNA Viruses
inferredcites →https://doi.org/10.1093/molbev/mst205openalex-snapshot
Massive Habitat-Specific Genomic Response in D. melanogaster Populations during Experimental Evolution in Hot and Cold Environments
inferredcites →https://doi.org/10.1093/molbev/msw016openalex-snapshot
Genomic Evidence for Adaptive Inversion Clines inDrosophila melanogaster
inferredcites →https://doi.org/10.1093/molbev/msw195openalex-snapshot
A Thousand Fly Genomes: An Expanded Drosophila Genome Nexus
inferredcites →https://doi.org/10.1098/rsbl.2013.0228openalex-snapshot
Genome-wide evolutionary response to a heat wave in Drosophila
inferredcites →https://doi.org/10.1098/rspb.2014.2688openalex-snapshot
Variation inDrosophila melanogastercentral metabolic genes appears driven by natural selection both within and between populations
inferredcites →https://doi.org/10.1098/rspb.2017.2599openalex-snapshot
Rapid seasonal evolution in innate immunity of wild Drosophila melanogaster
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.129684.111openalex-snapshot
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
inferredcites →https://doi.org/10.1111/evo.12291openalex-snapshot
THE INTENSITY OF SELECTION ACTING ON THE COUCH POTATO GENE-SPATIAL-TEMPORAL VARIATION IN A DIAPAUSE CLINE
inferredcites →https://doi.org/10.1111/evo.12546openalex-snapshot
A highly pleiotropic amino acid polymorphism in the Drosophila insulin receptor contributes to life-history adaptation
inferredcites →https://doi.org/10.1111/evo.12813openalex-snapshot
Variability in thermal and phototactic preferences inDrosophilamay reflect an adaptive bet‐hedging strategy
inferredcites →https://doi.org/10.1111/evo.13719openalex-snapshot
Different mechanisms drive the maintenance of polymorphism at loci subject to strong versus weak fluctuating selection
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00505.xopenalex-snapshot
ENVIRONMENTAL HETEROGENEITY AND THE MAINTENANCE OF GENETIC VARIATION FOR REPRODUCTIVE DIAPAUSE IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.0269-8463.2004.00904.xopenalex-snapshot
Cold adaptation in geographical populations of Drosophila melanogaster : phenotypic plasticity is more important than genetic variability
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05731.xopenalex-snapshot
Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica
inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01533.xopenalex-snapshot
Adaptive topography of fluctuating selection in a Mendelian population
inferredcites →https://doi.org/10.1111/j.1461-0248.2009.01381.xopenalex-snapshot
It’s about time: the temporal dynamics of phenotypic selection in the wild
inferredcites →https://doi.org/10.1111/j.1558-5646.1970.tb01785.xopenalex-snapshot
FURTHER GENETIC STUDIES OF THE SOUTH AMHERST POPULATION OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00391.xopenalex-snapshot
GENOTYPE-ENVIRONMENT INTERACTION AND THE EVOLUTION OF PHENOTYPIC PLASTICITY
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03917.xopenalex-snapshot
CYCLICAL ENVIRONMENTAL CHANGES AS A FACTOR MAINTAINING GENETIC POLYMORPHISM. 2. DIPLOID SELECTION FOR AN ADDITIVE TRAIT
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00891.xopenalex-snapshot
A STRUCTURED COALESCENT PROCESS FOR SEASONALLY FLUCTUATING POPULATIONS
inferredcites →https://doi.org/10.1111/jeb.12690openalex-snapshot
Seasonal variation in life history traits in two Drosophila species
inferredcites →https://doi.org/10.1111/jeb.12988openalex-snapshot
Adaptive dynamics of cuticular hydrocarbons in Drosophila
inferredcites →https://doi.org/10.1111/mec.12468openalex-snapshot
Whole‐genome sequencing of two N orth A merican D rosophila melanogaster populations reveals genetic differentiation and positive selection
inferredcites →https://doi.org/10.1111/mec.13137openalex-snapshot
Population genomic analysis uncovers African and European admixture in Drosophila melanogaster populations from the south‐eastern United States and Caribbean Islands
inferredcites →https://doi.org/10.1111/mec.13446openalex-snapshot
Comparative population genomics of latitudinal variation in Drosophila simulans and Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.14226openalex-snapshot
Gene flow and selection interact to promote adaptive divergence in regions of low recombination
inferredcites →https://doi.org/10.1111/mec.14814openalex-snapshot
Spatiotemporal dynamics and genome‐wide association analysis of desiccation tolerance in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.14871openalex-snapshot
The adaptive significance of chromosomal inversion polymorphisms inDrosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.15783openalex-snapshot
Temperature, rainfall and wind variables underlie environmental adaptation in natural populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.1070315openalex-snapshot
Unpredictable Evolution in a 30-Year Study of Darwin's Finches
inferredcites →https://doi.org/10.1126/science.1193954openalex-snapshot
The Newest Synthesis: Understanding the Interplay of Evolutionary and Ecological Dynamics
inferredcites →https://doi.org/10.1126/science.abg0718openalex-snapshot
A chromosomal inversion contributes to divergence in multiple traits between deer mouse ecotypes
inferredcites →https://doi.org/10.1146/annurev-physiol-022516-034142openalex-snapshot
The Integrative Physiology of Insect Chill Tolerance
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145137openalex-snapshot
Regulation of Diapause
inferredcites →https://doi.org/10.1146/annurev.es.24.110193.000343openalex-snapshot
Genetics and Evolution of Phenotypic Plasticity
inferredcites →https://doi.org/10.1175/jtech-d-11-00103.1openalex-snapshot
An Overview of the Global Historical Climatology Network-Daily Database
inferredcites →https://doi.org/10.1186/s13059-018-1503-4openalex-snapshot
A simple genetic basis of adaptation to a novel thermal environment results in complex metabolic rewiring in Drosophila
inferredcites →https://doi.org/10.1242/jeb.037630openalex-snapshot
Physiological climatic limits inDrosophila: patterns and implications
inferredcites →https://doi.org/10.1242/jeb.115790openalex-snapshot
Parallel ionoregulatory adjustments underlie phenotypic plasticity and evolution ofDrosophilacold tolerance
inferredcites →https://doi.org/10.1371/journal.pbio.3000128openalex-snapshot
Genetic redundancy fuels polygenic adaptation in Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1000924openalex-snapshot
Evidence that Adaptation in Drosophila Is Not Limited by Mutation at Single Sites
inferredcites →https://doi.org/10.1371/journal.pgen.1002905openalex-snapshot
The Many Landscapes of Recombination in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1003056openalex-snapshot
Population Genomics of Inversion Polymorphisms in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1003080openalex-snapshot
Population Genomics of Sub-Saharan Drosophila melanogaster: African Diversity and Non-African Admixture
inferredcites →https://doi.org/10.1371/journal.pgen.1004775openalex-snapshot
Genomic Evidence of Rapid and Stable Adaptive Oscillations over Seasonal Time Scales in Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1005869openalex-snapshot
The Adaptive Significance of Natural Genetic Variation in the DNA Damage Response of Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1007016openalex-snapshot
Genomics of parallel adaptation at two timescales in Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1009110openalex-snapshot
Unique genetic signatures of local adaptation over space and time for diapause, an ecologically relevant complex trait, in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0041901openalex-snapshot
Empirical Validation of Pooled Whole Genome Population Re-Sequencing in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0048588openalex-snapshot
LDx: Estimation of Linkage Disequilibrium from High-Throughput Pooled Resequencing Data
inferredcites →https://doi.org/10.1371/journal.pone.0106909openalex-snapshot
Integrating Temperature-Dependent Life Table Data into a Matrix Projection Model for Drosophila suzukii Population Estimation
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.1534/g3.114.015883openalex-snapshot
Global Diversity Lines–A Five-Continent Reference Panel of SequencedDrosophila melanogasterStrains
inferredcites →https://doi.org/10.1534/genetics.108.088906openalex-snapshot
Quantitative Trait Loci Affecting Phenotypic Plasticity and the Allometric Relationship of Ovariole Number and Thorax Length in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.110.114819openalex-snapshot
Using Environmental Correlations to Identify Loci Underlying Local Adaptation
inferredcites →https://doi.org/10.1534/genetics.110.123059openalex-snapshot
Genomic Differentiation Between Temperate and Tropical Australian Populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.113.152462openalex-snapshot
Robust Identification of Local Adaptation from Allele Frequencies
inferredcites →https://doi.org/10.1534/genetics.114.161463openalex-snapshot
Parallel Geographic Variation in Drosophila melanogaster

What points at this work

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

inferred← citeshttps://doi.org/10.1002/ece3.5887openalex-snapshot
Phenotypic plasticity, but not adaptive tracking, underlies seasonal variation in post‐cold hardening freeze tolerance of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/978-1-0716-0199-0_15openalex-snapshot
Population Genomics on the Fly: Recent Advances in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cois.2018.11.002openalex-snapshot
Evolutionary insights from large scale resequencing datasets in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/s41598-020-79720-1openalex-snapshot
Demographic analyses of a new sample of haploid genomes from a Swedish population of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1073/pnas.1907787116openalex-snapshot
Microbiome composition shapes rapid genomic adaptation of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1073/pnas.1919039117openalex-snapshot
Estimating the genome-wide contribution of selection to temporal allele frequency change
inferred← citeshttps://doi.org/10.1093/gbe/evaa190openalex-snapshot
Reconstructing the Invasion Route of the P-Element inDrosophila melanogasterUsing Extant Population Samples
inferred← citeshttps://doi.org/10.1093/molbev/msaa227openalex-snapshot
Ecological Load and Balancing Selection in Circumboreal Barnacles
inferred← citeshttps://doi.org/10.1093/molbev/msab173openalex-snapshot
Fluctuating Environments Maintain Genetic Diversity through Neutral Fitness Effects and Balancing Selection
inferred← citeshttps://doi.org/10.1093/ve/veab031openalex-snapshot
The discovery, distribution, and diversity of DNA viruses associated withDrosophila melanogasterin Europe
inferred← citeshttps://doi.org/10.1098/rspb.2021.1812openalex-snapshot
The promise and deceit of genomic selection component analyses
inferred← citeshttps://doi.org/10.1101/2021.07.30.454552openalex-snapshot
Unique signals of clinal and seasonal allele frequency change at eQTLs in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/288696openalex-snapshot
Rapid evolution of learning and reproduction in natural populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/313759openalex-snapshot
Genomic analysis of European Drosophila melanogaster populations reveals longitudinal structure, continent-wide selection, and previously unknown DNA viruses
inferred← citeshttps://doi.org/10.1101/321133openalex-snapshot
A map of climate change-driven natural selection in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/691741openalex-snapshot
Phenotypic plasticity, but not genetic adaptation, underlies seasonal variation in the cold hardening response of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/729889openalex-snapshot
Reconstructing the invasion route of DNA transposons using extant population samples
inferred← citeshttps://doi.org/10.1111/1758-2229.12826openalex-snapshot
Common structuring principles of the Drosophila melanogaster microbiome on a continental scale and between host and substrate
inferred← citeshttps://doi.org/10.1111/evo.13719openalex-snapshot
Different mechanisms drive the maintenance of polymorphism at loci subject to strong versus weak fluctuating selection
inferred← citeshttps://doi.org/10.1111/evo.13759openalex-snapshot
A clinal polymorphism in the insulin signaling transcription factor foxo contributes to life‐history adaptation in Drosophila *
inferred← citeshttps://doi.org/10.1111/evo.14300openalex-snapshot
Clinal and seasonal changes are correlated in Drosophila melanogaster natural populations
inferred← citeshttps://doi.org/10.1111/mec.14871openalex-snapshot
The adaptive significance of chromosomal inversion polymorphisms inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1111/mec.14963openalex-snapshot
Population‐specific dynamics and selection patterns of transposable element insertions in European natural populations
inferred← citeshttps://doi.org/10.1111/mec.15939openalex-snapshot
Allelic polymorphism at foxo contributes to local adaptation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/mec.15949openalex-snapshot
From tides to nucleotides: Genomic signatures of adaptation to environmental heterogeneity in barnacles
inferred← citeshttps://doi.org/10.1186/s12864-025-12111-wopenalex-snapshot
Long-read sequencing-based analyses of the adult Drosophila brain transcriptome in physiological and pathological settings
inferred← citeshttps://doi.org/10.1186/s13100-020-00213-zopenalex-snapshot
Transposable elements in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008945openalex-snapshot
Predicting evolutionary change at the DNA level in a natural Mimulus population
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009110openalex-snapshot
Unique genetic signatures of local adaptation over space and time for diapause, an ecologically relevant complex trait, in Drosophila melanogaster
inferred← citeshttps://doi.org/10.3389/fgene.2021.676218openalex-snapshot
Genomic Responses to Climate Change: Making the Most of the Drosophila Model
inferred← citeshttps://doi.org/10.70675/00dbd2ffz4271z4c8bz8b6azd41857860271openalex-snapshot
Dynamique des éléments transposables chez Drosophila suzukii
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