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Energy metabolites mediated cross-protection to heat, drought and starvation induced plastic responses in tropical D.ananassae of wet-dry seasons
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00360-007-0172-5openalex-snapshot
Shifts in the carbohydrate, polyol, and amino acid pools during rapid cold-hardening and diapause-associated cold-hardening in flesh flies (Sarcophaga crassipalpis): a metabolomic comparison
inferredcites →https://doi.org/10.1007/s00726-008-0061-6openalex-snapshot
Proline accumulation in plants: a review
inferredcites →https://doi.org/10.1016/j.cbpa.2005.11.012openalex-snapshot
Changes in free amino acids in Alphitobius diaperinus (Coleoptera: Tenebrionidae) during thermal and food stress
inferredcites →https://doi.org/10.1016/j.cbpa.2008.12.009openalex-snapshot
Dehydration-induced cross tolerance of Belgica antarctica larvae to cold and heat is facilitated by trehalose accumulation
inferredcites →https://doi.org/10.1016/j.cbpa.2013.12.007openalex-snapshot
Seasonal changes in humidity impact drought resistance in tropical Drosophila leontia: Testing developmental effects of thermal versus humidity changes
inferredcites →https://doi.org/10.1016/j.cbpa.2016.10.011openalex-snapshot
Cold and desiccation stress induced changes in the accumulation and utilization of proline and trehalose in seasonal populations of Drosophila immigrans
inferredcites →https://doi.org/10.1016/j.cbpa.2017.04.014openalex-snapshot
Cross-tolerance effects due to adult heat hardening, desiccation and starvation acclimation of tropical drosophilid- Zaprionus indianus
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.06.012openalex-snapshot
Metabolomic profiling of rapid cold hardening and cold shock in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.01.003openalex-snapshot
Metabolomics reveals unique and shared metabolic changes in response to heat shock, freezing and desiccation in the Antarctic midge, Belgica antarctica
inferredcites →https://doi.org/10.1016/j.jinsphys.2009.01.008openalex-snapshot
Seasonal changes in humidity level in the tropics impact body color polymorphism and desiccation resistance in Drosophila jambulina—Evidence for melanism-desiccation hypothesis
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.05.004openalex-snapshot
Water loss in insects: An environmental change perspective
inferredcites →https://doi.org/10.1016/j.jtherbio.2014.07.007openalex-snapshot
Linking energetics and overwintering in temperate insects
inferredcites →https://doi.org/10.1016/j.tplants.2009.11.009openalex-snapshot
Proline: a multifunctional amino acid
inferredcites →https://doi.org/10.1016/s0022-1910(00)00141-4openalex-snapshot
Cold tolerance and proline metabolic gene expression in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0022-1910(98)00055-9openalex-snapshot
The effect of cold acclimation and deacclimation on cold tolerance, trehalose and free amino acid levels in Sitophilus granarius and Cryptolestes ferrugineus (Coleoptera)
inferredcites →https://doi.org/10.1017/cbo9780511675997openalex-snapshot
Low Temperature Biology of Insects
inferredcites →https://doi.org/10.1017/cbo9780511675997.002openalex-snapshot
A primer on insect cold-tolerance
inferredcites →https://doi.org/10.1021/ac60289a036openalex-snapshot
New spectrophotometric method for the determination of proline in tissue hydrolyzates
inferredcites →https://doi.org/10.1042/bj0580046openalex-snapshot
Liberation of amino acids in perennial rye grass during wilting
inferredcites →https://doi.org/10.1046/j.1365-2311.2000.00272.xopenalex-snapshot
Humidity‐terminated diapause in the tropical braconid parasitoid Microplitis demolitor
inferredcites →https://doi.org/10.1073/pnas.1107060108openalex-snapshot
Hyperprolinemic larvae of the drosophilid fly, Chymomyza costata , survive cryopreservation in liquid nitrogen
inferredcites →https://doi.org/10.1074/jbc.m300815200openalex-snapshot
Why Is Trehalose an Exceptional Protein Stabilizer?
inferredcites →https://doi.org/10.1089/ars.2012.5074openalex-snapshot
Proline Mechanisms of Stress Survival
inferredcites →https://doi.org/10.1093/acprof:oso/9780198570875.001.1openalex-snapshot
Thermal Adaptation
inferredcites →https://doi.org/10.1093/ee/27.3.523openalex-snapshot
Moisture, a Vital but Neglected Factor in the Seasonal Ecology of Insects: Hypotheses and Tests of Mechanisms
inferredcites →https://doi.org/10.1093/icb/ict004openalex-snapshot
Cross-tolerance and Cross-talk in the Cold: Relating Low Temperatures to Desiccation and Immune Stress in Insects
inferredcites →https://doi.org/10.1093/jxb/erm284openalex-snapshot
Compatible solute accumulation and stress-mitigating effects in barley genotypes contrasting in their salt tolerance
inferredcites →https://doi.org/10.1111/evo.12541openalex-snapshot
Cold adaptation shapes the robustness of metabolic networks inDrosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2435.2005.00959.xopenalex-snapshot
Relative importance of plastic vs genetic factors in adaptive differentiation: geographical variation for stress resistance in Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1111/j.1365-2435.2005.01025.xopenalex-snapshot
Hardening capacity in the Drosophila melanogaster species group is constrained by basal thermotolerance
inferredcites →https://doi.org/10.1111/j.1365-2435.2012.01985.xopenalex-snapshot
Exploring the plastic response to cold acclimation through metabolomics
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.1420-9101.2012.02536.xopenalex-snapshot
A multivariate test of evolutionary constraints for thermal tolerance in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1439-0469.1999.tb00983.xopenalex-snapshot
Climatic selection of starvation and desiccation resistance in populations of some tropical drosophilids
inferredcites →https://doi.org/10.1126/science.1175443openalex-snapshot
Fundamental Evolutionary Limits in Ecological Traits Drive Drosophila Species Distributions
inferredcites →https://doi.org/10.1126/science.7112124openalex-snapshot
Living with Water Stress: Evolution of Osmolyte Systems
inferredcites →https://doi.org/10.1146/annurev.mi.45.100191.003033openalex-snapshot
PROKARYOTIC OSMOREGULATION: Genetics and Physiology
inferredcites →https://doi.org/10.1186/1471-2180-12-207openalex-snapshot
Role of trehalose in heat and desiccation tolerance in the soil bacterium Rhizobium etli
inferredcites →https://doi.org/10.1242/jeb.01737openalex-snapshot
Metabolic responses to cold in subterranean crustaceans
inferredcites →https://doi.org/10.1242/jeb.037630openalex-snapshot
Physiological climatic limits inDrosophila: patterns and implications
inferredcites →https://doi.org/10.1242/jeb.092502openalex-snapshot
Stress-induced plastic responses inDrosophila simulansfollowing exposure to combinations of temperature and humidity levels
inferredcites →https://doi.org/10.1371/journal.pone.0016163openalex-snapshot
E2F1 Regulates Cellular Growth by mTORC1 Signaling
inferredcites →https://doi.org/10.1603/0046-225x-29.4.714openalex-snapshot
Dry-Season Embryonic Dormancy inDeois flavopicta(Homoptera: Cercopidae): Roles of Temperature and Moisture in Nature
inferredcites →https://doi.org/10.2307/2410321openalex-snapshot
Chromosomal Analysis of Heat-Shock Tolerance in Drosophila melanogaster Evolving at Different Temperatures in the Laboratory
inferredcites →https://doi.org/10.5281/zenodo.10767142openalex-snapshot
Cold-induced freezing tolerance in diapausing and non-diapausing larvae of Chymomyza costata (Diptera: Drosophilidae) with accumulation of trehalose and proline.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41598-020-80277-2openalex-snapshot
RNA interference of trehalose-6-phosphate synthase and trehalase genes regulates chitin metabolism in two color morphs of Acyrthosiphon pisum Harris
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