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Disparate patterns of thermal adaptation between life stages in temperate vs. tropical Drosophila melanogaster

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

inferredcites →https://doi.org/10.1002/dvg.1020110405openalex-snapshot
Heat shock causes the collapse of the intermediate filament cytoskeleton in Drosophila embryos
inferredcites →https://doi.org/10.1002/jez.1402140203openalex-snapshot
Variability of response of early Drosophila embryos to heat shock
inferredcites →https://doi.org/10.1002/joc.1276openalex-snapshot
Very high resolution interpolated climate surfaces for global land areas
inferredcites →https://doi.org/10.1007/bf00139728openalex-snapshot
Extreme events in a changing climate: Variability is more important than averages
inferredcites →https://doi.org/10.1007/bf01937401openalex-snapshot
The circadian rhythm of oviposition inDrosophila melanogaster: A genetic latitudinal cline in wild populations
inferredcites →https://doi.org/10.1007/s00442-016-3561-1openalex-snapshot
Geographic divergence in upper thermal limits across insect life stages: does behavior matter?
inferredcites →https://doi.org/10.1007/s10709-006-9010-zopenalex-snapshot
Climatic selection on genes and traits after a 100 year-old invasion: a critical look at the temperate-tropical clines in Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1016/0960-9822(93)90218-dopenalex-snapshot
A new method for manipulating transgenes: engineering heat tolerance in a complex, multicellular organism
inferredcites →https://doi.org/10.1016/bs.ctdb.2015.06.002openalex-snapshot
Coordinating Cell Cycle Remodeling with Transcriptional Activation at the Drosophila MBT
inferredcites →https://doi.org/10.1016/j.jembe.2011.02.006openalex-snapshot
Spreading the risk: Small-scale body temperature variation among intertidal organisms and its implications for species persistence
inferredcites →https://doi.org/10.1016/j.jtherbio.2008.11.007openalex-snapshot
Thermal preference in Drosophila
inferredcites →https://doi.org/10.1016/j.tig.2015.05.006openalex-snapshot
Revisiting classic clines in Drosophila melanogaster in the age of genomics
inferredcites →https://doi.org/10.1038/nclimate1539openalex-snapshot
Thermal tolerance and the global redistribution of animals
inferredcites →https://doi.org/10.1038/nclimate2100openalex-snapshot
Increasing frequency of extreme El Niño events due to greenhouse warming
inferredcites →https://doi.org/10.1038/sj.hdy.6800786openalex-snapshot
Quantitative trait loci for thermotolerance phenotypes in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/sj.hdy.6885330openalex-snapshot
The direct response of Drosophila melanogaster to selection on knockdown temperature
inferredcites →https://doi.org/10.1038/srep16717openalex-snapshot
Molecular basis of canalization in an ascidian species complex adapted to different thermal conditions
inferredcites →https://doi.org/10.1046/j.1365-2435.1997.00060.xopenalex-snapshot
Natural thermal stress and heat‐shock protein expression in Drosophila larvae and pupae
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00367.xopenalex-snapshot
Opposing clines for high and low temperature resistance in Drosophila melanogaster
inferredcites →https://doi.org/10.1071/bi9560463openalex-snapshot
Concept of General and Specific Combining Ability in Relation to Diallel Crossing Systems
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.210066997openalex-snapshot
Quantitative transcript imaging in normal and heat-shocked Drosophila embryos by using high-density oligonucleotide arrays
inferredcites →https://doi.org/10.1074/jbc.m110.103374openalex-snapshot
Evolution of Escherichia coli for Growth at High Temperatures
inferredcites →https://doi.org/10.1086/284150openalex-snapshot
Geographic Variation of Tolerance to Environmental Stress in Drosophila pseudoobscura
inferredcites →https://doi.org/10.1086/285522openalex-snapshot
Evolutionary Response of Escherichia coli to Thermal Stress
inferredcites →https://doi.org/10.1086/316738openalex-snapshot
A Comparative Analysis of the Upper Thermal Tolerance Limits of Eastern Pacific Porcelain Crabs, Genus Petrolisthes : Influences of Latitude, Vertical Zonation, Acclimation, and Phylogeny
inferredcites →https://doi.org/10.1086/515853openalex-snapshot
Thermal Sensitivity ofDrosophila melanogaster:Evolutionary Responses of Adults and Eggs to Laboratory Natural Selection at Different Temperatures
inferredcites →https://doi.org/10.1086/663633openalex-snapshot
Neural Thermal Performance in Porcelain Crabs, GenusPetrolisthes
inferredcites →https://doi.org/10.1093/conphys/cot018openalex-snapshot
Heat tolerance during embryonic development has not diverged among populations of a widespread species (Sceloporus undulatus)
inferredcites →https://doi.org/10.1093/icb/42.4.780openalex-snapshot
Thermal Physiology and Vertical Zonation of Intertidal Animals: Optima, Limits, and Costs of Living
inferredcites →https://doi.org/10.1093/icb/icw004openalex-snapshot
How Extreme Temperatures Impact Organisms and the Evolution of their Thermal Tolerance
inferredcites →https://doi.org/10.1093/molbev/mss111openalex-snapshot
Functional Determinants of Temperature Adaptation in Enzymes of Cold- versus Warm-Adapted Mussels (Genus Mytilus)
inferredcites →https://doi.org/10.1093/molbev/msv120openalex-snapshot
Temperature-Related Reaction Norms of Gene Expression: Regulatory Architecture and Functional Implications
inferredcites →https://doi.org/10.1098/rspb.2010.1295openalex-snapshot
Global analysis of thermal tolerance and latitude in ectotherms
inferredcites →https://doi.org/10.1098/rspb.2011.0542openalex-snapshot
Limited potential for adaptation to climate change in a broadly distributed marine crustacean
inferredcites →https://doi.org/10.1098/rspb.2016.2104openalex-snapshot
Rates of change in climatic niches in plant and animal populations are much slower than projected climate change
inferredcites →https://doi.org/10.1111/1365-2435.12145openalex-snapshot
Heat stress and the fitness consequences of climate change for terrestrial ectotherms
inferredcites →https://doi.org/10.1111/1365-2435.12264openalex-snapshot
Thermal adaptation of cellular membranes in natural populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1111/1365-2435.12406openalex-snapshot
Thermoregulatory behaviour limits local adaptation of thermal niches and confers sensitivity to climate change
inferredcites →https://doi.org/10.1111/1365-2435.12499openalex-snapshot
Evolutionary potential of multiple measures of upper thermal tolerance in D rosophila melanogaster
inferredcites →https://doi.org/10.1111/1365-2435.12687openalex-snapshot
Limited scope for plasticity to increase upper thermal limits
inferredcites →https://doi.org/10.1111/evo.12254openalex-snapshot
ECOLOGICAL NOVELTY BY HYBRIDIZATION: EXPERIMENTAL EVIDENCE FOR INCREASED THERMAL TOLERANCE BY TRANSGRESSIVE SEGREGATION INTIGRIOPUS CALIFORNICUS
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.12617openalex-snapshot
Low evolutionary potential for egg-to-adult viability inDrosophila melanogasterat high temperatures
inferredcites →https://doi.org/10.1111/evo.13064openalex-snapshot
Basking behavior predicts the evolution of heat tolerance in Australian rainforest lizards
inferredcites →https://doi.org/10.1111/gcb.12521openalex-snapshot
Sensitivity to thermal extremes in Australian Drosophila implies similar impacts of climate change on the distribution of widespread and tropical species
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00151.xopenalex-snapshot
ALLELE FREQUENCY SHIFTS IN RESPONSE TO CLIMATE CHANGE AND PHYSIOLOGICAL CONSEQUENCES OF ALLOZYME VARIATION IN A MONTANE INSECT
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00193.xopenalex-snapshot
RESPONSE TO NATURAL AND LABORATORY SELECTION AT THE DROSOPHILA HSP70 GENES
inferredcites →https://doi.org/10.1111/j.1365-2435.2008.01481.xopenalex-snapshot
Phenotypic variance, plasticity and heritability estimates of critical thermal limits depend on methodological context
inferredcites →https://doi.org/10.1111/j.1365-2435.2009.01666.xopenalex-snapshot
Thermal ramping rate influences evolutionary potential and species differences for upper thermal limits in Drosophila
inferredcites →https://doi.org/10.1111/j.1365-2435.2012.01987.xopenalex-snapshot
Geographic variation in vulnerability to climate warming in a tropical Caribbean lizard
inferredcites →https://doi.org/10.1111/j.1365-2435.2012.02036.xopenalex-snapshot
Upper thermal limits in terrestrial ectotherms: how constrained are they?
inferredcites →https://doi.org/10.1111/j.1365-2699.2009.02218.xopenalex-snapshot
Historical changes in the distributions of invasive and endemic marine invertebrates are contrary to global warming predictions: the effects of decadal climate oscillations
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.1420-9101.2010.02110.xopenalex-snapshot
A comprehensive assessment of geographic variation in heat tolerance and hardening capacity in populations of Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1111/j.1558-5646.1991.tb04343.xopenalex-snapshot
THERMAL SENSITIVITY OF DROSOPHILA MELANOGASTER RESPONDS RAPIDLY TO LABORATORY NATURAL SELECTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1992.tb01981.xopenalex-snapshot
EVOLUTIONARY ADAPTATION TO TEMPERATURE. I. FITNESS RESPONSES OF ESCHERICHIA COLI TO CHANGES IN ITS THERMAL ENVIRONMENT
inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb03774.xopenalex-snapshot
EVOLUTIONARY ADAPTATION TO TEMPERATURE. VII. EXTENSION OF THE UPPER THERMAL LIMIT OF ESCHERICHIA COLI
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01566.xopenalex-snapshot
IN A VARIABLE THERMAL ENVIRONMENT SELECTION FAVORS GREATER PLASTICITY OF CELL MEMBRANES IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/jeb.12436openalex-snapshot
A D rosophila laboratory evolution experiment points to low evolutionary potential under increased temperatures likely to be experienced in the future
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.13455openalex-snapshot
Secondary contact and local adaptation contribute to genome‐wide patterns of clinal variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/oik.03933openalex-snapshot
Thermoregulatory behaviour explains countergradient variation in the upper thermal limit of a rainforest skink
inferredcites →https://doi.org/10.1126/science.1076814openalex-snapshot
Climate Change and Latitudinal Patterns of Intertidal Thermal Stress
inferredcites →https://doi.org/10.1126/science.1210288openalex-snapshot
The Pace of Shifting Climate in Marine and Terrestrial Ecosystems
inferredcites →https://doi.org/10.1126/science.1224836openalex-snapshot
A Global Pattern of Thermal Adaptation in Marine Phytoplankton
inferredcites →https://doi.org/10.1126/science.aai7825openalex-snapshot
Cell-wide analysis of protein thermal unfolding reveals determinants of thermostability
inferredcites →https://doi.org/10.1175/1520-0477(2000)081<0427:tiewac>2.3.co;2openalex-snapshot
Trends in Extreme Weather and Climate Events: Issues Related to Modeling Extremes in Projections of Future Climate Change*
inferredcites →https://doi.org/10.1242/dev.033183openalex-snapshot
The maternal-to-zygotic transition: a play in two acts
inferredcites →https://doi.org/10.1242/jeb.02258openalex-snapshot
Thermal stress on intertidal limpets: long-term hindcasts and lethal limits
inferredcites →https://doi.org/10.1242/jeb.02259openalex-snapshot
Following the heart: temperature and salinity effects on heart rate in native and invasive species of blue mussels (genus Mytilus )
inferredcites →https://doi.org/10.1242/jeb.037630openalex-snapshot
Physiological climatic limits inDrosophila: patterns and implications
inferredcites →https://doi.org/10.1242/jeb.041228openalex-snapshot
The proteomic response of the mussel congeners Mytilus galloprovincialis and M. trossulus to acute heat stress: implications for thermal tolerance limits and metabolic costs of thermal stress
inferredcites →https://doi.org/10.1242/jeb.046094openalex-snapshot
Transcriptomic responses to heat stress in invasive and native blue mussels (genusMytilus): molecular correlates of invasive success
inferredcites →https://doi.org/10.1242/jeb.061283openalex-snapshot
Ecologically relevant measures of tolerance to potentially lethal temperatures
inferredcites →https://doi.org/10.1242/jeb.073577openalex-snapshot
The impact of acute temperature stress on hemocytes of invasive and native mussels ( Mytilus galloprovincialis and M. californianus ): DNA damage, membrane integrity, apoptosis and signalling pathways
inferredcites →https://doi.org/10.1242/jeb.076620openalex-snapshot
Behavior and survival ofMytiluscongeners following episodes of elevated body temperature in air and seawater
inferredcites →https://doi.org/10.1242/jeb.079830openalex-snapshot
Heat stress survival in the pre-adult stage of the life cycle in an intercontinental set of recombinant inbred lines ofDrosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.114298openalex-snapshot
Adaptations of protein structure and function to temperature: there is more than one way to ‘skin a cat’
inferredcites →https://doi.org/10.1242/jeb.114926openalex-snapshot
Thermal variation, thermal extremes and the physiological performance of individuals
inferredcites →https://doi.org/10.1242/jeb.132696openalex-snapshot
Proteomic data reveals a physiological basis for costs and benefits associated with thermal acclimation
inferredcites →https://doi.org/10.1242/jeb.185.1.151openalex-snapshot
Effects of Temperature on Mitochondria From Abalone (Genus Haliotis): Adaptive Plasticity and its Limits
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.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/10.1554/0014-3820(2001)055[0738:bdioai]2.0.co;2openalex-snapshot
BEHAVIORAL DIFFERENTIATION IN OVIPOSITION ACTIVITY IN DROSOPHILA BUZZATII FROM HIGHLAND AND LOWLAND POPULATIONS IN ARGENTINA: PLASTICITY OR THERMAL ADAPTATION?
inferredcites →https://doi.org/10.1890/09-0097.1openalex-snapshot
Partial thermoregulatory compensation by a rapidly evolving invasive species along a latitudinal cline
inferredcites →https://doi.org/10.2307/2409801openalex-snapshot
Evolutionary Adaptation to Temperature. I. Fitness Responses of Escherichia coli to Changes in its Thermal Environment
inferredcites →https://doi.org/10.2307/2640775openalex-snapshot
Evolutionary Adaptation to Temperature. VII. Extension of the Upper Thermal Limit of Escherichia coli
inferredcites →https://doi.org/10.2307/3593122openalex-snapshot
Evolutionary and Acclimation-Induced Variation in the Thermal Limits of Heart Function in Congeneric Marine Snails (GenusTegula): Implications for Vertical Zonation
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
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