Adaptive peak shifts in a heterogenous environment. |
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Annual climatic fluctuations and short-term genetic variation in the eastern spadefoot toad |
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Antibiotic cross-resistance in the lab and resistance co-occurrence in the clinic: Discrepancies and implications in E.coli |
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Antibiotic Restriction Might Facilitate the Emergence of Multi-drug Resistance |
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Bimodal regulation of ICR1 levels generates self-organizing auxin distribution |
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Classification of plants acoustic emissions, 2017: |
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Condition-dependent sex: who does it, when and why? |
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Dispersing away from bad genotypes: the evolution of Fitness-Associated Dispersal (FAD) in homogeneous environments |
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Does stress induce (para)sex? Implications for Candida albicans evolution |
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Drug induced superinfection in HIV and the evolution of drug resistance |
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The effect of habitat and climatic on microsatellite diversity and allele length variation |
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The evolution of condition-dependent sex in the face of high costs |
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The evolution of paternal care: a role for microbes? |
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The evolution of plastic recombination |
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The evolution of stress-induced hypermutation in asexual populations |
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Floral complexity can help maintain plant diversity by inducing pollinator specialization |
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Flowers respond to pollinator sound within minutes by increasing nectar sugar concentration.: Supplementary Data |
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Food selectivity and diet switch can explain the slow feeding of herbivorous coral-reef fishes during the morning |
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Gamblers: An Antibiotic-Induced Evolvable Cell Subpopulation Differentiated by Reactive-Oxygen-Induced General Stress Response |
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Home and away- the evolutionary dynamics of homing endonucleases |
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Host-microbiome coevolution can promote cooperation in a rock-paper-scissors dynamics |
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Implications of stress-induced genetic variation for minimizing multidrug resistance in bacteria |
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Increased sugar concentration in response to a wide range of pollinator sounds can be adaptive for the plant: answer to Raguso et al |
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Key issues review: evolution on rugged adaptive landscapes |
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Less fit Lamium amplexicaule plants produce more dispersible seeds |
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Microbes can help explain the evolution of host altruism |
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Plant-pollinator population dynamics. |
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Plants' ability to sense and respond to airborne sound is likely to be adaptive: reply to comment by Pyke et al |
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Pollinator-mediated selection on floral size and tube color in Linum pubescens: Can differential behavior and preference in different times of the day maintain dimorphism? |
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Pollinators' mating rendezvous and the evolution of floral advertisement |
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Potential contribution of fish restocking to the recovery of deteriorated coral reefs: an alternative restoration method? |
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Predicting antibiotic resistance in hospitalized patients by applying machine learning to electronic medical records |
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Predicting microbial relative growth in a mixed culture from growth curve data |
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The probability of improvement in Fisher's geometric model: a probabilistic approach. |
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Random search with resetting as a strategy for optimal pollination |
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Regulated superinfection may help HIV adaptation on rugged landscape |
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Reply to Balsa-Canto et al.: Growth models are applicable to growth data, not to stationary-phase data |
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Resistance profiles of coagulase-negative staphylococci contaminating blood cultures predict pathogen resistance and patient mortality |
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Restocking Herbivorous Fish Populations As a Social-Ecological Restoration Tool in Coral Reefs |
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Sexual selection and the evolution of obligatory sex |
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Some topics in theoretical population genetics: Editorial commentaries on a selection of Marc Feldman's TPB papers |
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Sounds emitted by plants under stress are airborne and informative |
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Spontaneous Changes in Ploidy Are Common in Yeast. |
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Stress-induced mutagenesis and complex adaptation. |
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Transgenerational inheritance of sexual attractiveness via small RNAs enhances evolvability in C. elegans |
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Why are sex and recombination so common? |
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Why is stress so deadly? An evolutionary perspective |
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ストレス下にある植物が発する音は空中に伝わり、多くの情報を得られる |
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