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Principles of experimental design for ecology and evolution.
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- Ecology Letters, 2024, v. 27, n. 4, p. 1, doi. 10.1111/ele.14400
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The hidden costs of resistance: Contrasting the energetics of successfully and unsuccessfully fighting infection.
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- Functional Ecology, 2024, v. 38, n. 4, p. 714, doi. 10.1111/1365-2435.14523
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Copepod life history evolution under high‐ and low‐food regimes.
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- Evolutionary Applications, 2023, v. 16, n. 7, p. 1274, doi. 10.1111/eva.13563
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Life history optimisation drives latitudinal gradients and responses to global change in marine fishes.
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- PLoS Biology, 2023, v. 21, n. 5, p. 1, doi. 10.1371/journal.pbio.3002114
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Mapping the correlations and gaps in studies of complex life histories.
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- Ecology & Evolution (20457758), 2023, v. 13, n. 2, p. 1, doi. 10.1002/ece3.9809
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Carry‐over effects and fitness trade‐offs in marine life histories: The costs of complexity for adaptation.
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- Evolutionary Applications, 2023, v. 16, n. 2, p. 474, doi. 10.1111/eva.13477
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Macroevolutionary patterns in marine hermaphroditism.
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- Evolution, 2022, v. 76, n. 12, p. 3014, doi. 10.1111/evo.14639
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Avoiding growing pains in reproductive trait databases: the curse of dimensionality.
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- Global Ecology & Biogeography, 2022, v. 31, n. 12, p. 2384, doi. 10.1111/geb.13589
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A comparative analysis testing Werner's theory of complex life cycles.
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- Functional Ecology, 2022, v. 36, n. 8, p. 1986, doi. 10.1111/1365-2435.14086
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How does spawning frequency scale with body size in marine fishes?
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- Fish & Fisheries, 2022, v. 23, n. 2, p. 316, doi. 10.1111/faf.12617
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Phytoplankton diversity affects biomass and energy production differently during community development.
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- Functional Ecology, 2022, v. 36, n. 2, p. 446, doi. 10.1111/1365-2435.13955
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Predicting the response of disease vectors to global change: The importance of allometric scaling.
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- Global Change Biology, 2022, v. 28, n. 2, p. 390, doi. 10.1111/gcb.15950
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Metabolic phenotype mediates the outcome of competitive interactions in a response‐surface field experiment.
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- Ecology & Evolution (20457758), 2021, v. 11, n. 24, p. 17952, doi. 10.1002/ece3.8388
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Larger cells have relatively smaller nuclei across the Tree of Life.
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- Evolution Letters, 2021, v. 5, n. 4, p. 306, doi. 10.1002/evl3.243
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Geographical bias in physiological data limits predictions of global change impacts.
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- Functional Ecology, 2021, v. 35, n. 7, p. 1572, doi. 10.1111/1365-2435.13807
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Plastic but not adaptive: habitat‐driven differences in metabolic rate despite no differences in selection between habitats.
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- Oikos, 2021, v. 130, n. 6, p. 931, doi. 10.1111/oik.08305
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Cell size influences inorganic carbon acquisition in artificially selected phytoplankton.
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- New Phytologist, 2021, v. 229, n. 5, p. 2647, doi. 10.1111/nph.17068
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Metabolic rate, context‐dependent selection, and the competition‐colonization trade‐off.
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- Evolution Letters, 2020, v. 4, n. 4, p. 333, doi. 10.1002/evl3.174
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Metabolic rate, context‐dependent selection, and the competition‐colonization trade‐off.
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- Evolution Letters, 2020, v. 4, n. 4, p. 333, doi. 10.1002/evl3.174
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Metabolic rate, context‐dependent selection, and the competition‐colonization trade‐off.
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- Evolution Letters, 2020, v. 4, n. 4, p. 333, doi. 10.1002/evl3.174
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Community efficiency during succession: a test of MacArthur's minimization principle in phytoplankton communities.
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- Ecology, 2020, v. 101, n. 6, p. 1, doi. 10.1002/ecy.3015
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Physical and physiological impacts of ocean warming alter phenotypic selection on sperm morphology.
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- Functional Ecology, 2020, v. 34, n. 3, p. 646, doi. 10.1111/1365-2435.13483
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Testing the drivers of the temperature–size covariance using artificial selection.
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- Evolution, 2020, v. 74, n. 1, p. 169, doi. 10.1111/evo.13896
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Size and density mediate transitions between competition and facilitation.
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- Ecology Letters, 2019, v. 22, n. 11, p. 1879, doi. 10.1111/ele.13381
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Size‐abundance rules? Evolution changes scaling relationships between size, metabolism and demography.
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- Ecology Letters, 2019, v. 22, n. 9, p. 1407, doi. 10.1111/ele.13326
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The outsized trophic footprint of marine urbanization.
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- Frontiers in Ecology & the Environment, 2019, v. 17, n. 7, p. 400, doi. 10.1002/fee.2074
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Underestimating the benefits of marine protected areas for the replenishment of fished populations.
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- Frontiers in Ecology & the Environment, 2019, v. 17, n. 7, p. 407, doi. 10.1002/fee.2075
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Can competitive asymmetries maintain offspring size variation? A manipulative field test.
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- Evolution, 2019, v. 73, n. 8, p. 1663, doi. 10.1111/evo.13790
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Linking life‐history theory and metabolic theory explains the offspring size‐temperature relationship.
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- Ecology Letters, 2019, v. 22, n. 3, p. 518, doi. 10.1111/ele.13213
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Influence of food, body size, and fragmentation on metabolic rate in a sessile marine invertebrate.
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- Invertebrate Biology, 2019, v. 138, n. 1, p. 55, doi. 10.1111/ivb.12241
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Releasing small ejaculates slowly increases per‐gamete fertilization success in an external fertilizer: Galeolaria caespitosa (Polychaeta: Serpulidae).
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- Journal of Evolutionary Biology, 2019, v. 32, n. 2, p. 177, doi. 10.1111/jeb.13403
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Resources mediate selection on module longevity in the field.
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- Journal of Evolutionary Biology, 2018, v. 31, n. 11, p. 1666, doi. 10.1111/jeb.13362
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Biochemical evolution in response to intensive harvesting in algae: Evolution of quality and quantity.
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- Evolutionary Applications, 2018, v. 11, n. 8, p. 1389, doi. 10.1111/eva.12632
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Testing MacArthur's minimisation principle: do communities minimise energy wastage during succession?
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- Ecology Letters, 2018, v. 21, n. 8, p. 1182, doi. 10.1111/ele.13087
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Global environmental drivers of marine fish egg size.
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- Global Ecology & Biogeography, 2018, v. 27, n. 8, p. 890, doi. 10.1111/geb.12748
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Cell size, photosynthesis and the package effect: an artificial selection approach.
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- New Phytologist, 2018, v. 219, n. 1, p. 449, doi. 10.1111/nph.15163
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A global synthesis of offspring size variation, its eco‐evolutionary causes and consequences.
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- Functional Ecology, 2018, v. 32, n. 6, p. 1436, doi. 10.1111/1365-2435.13099
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Metabolic scaling across succession: Do individual rates predict community‐level energy use?
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- Functional Ecology, 2018, v. 32, n. 6, p. 1447, doi. 10.1111/1365-2435.13103
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Does the cost of development scale allometrically with offspring size?
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- Functional Ecology, 2018, v. 32, n. 3, p. 762, doi. 10.1111/1365-2435.13015
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Genotypic covariance between the performance of a resident species and community assembly in the field.
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- Functional Ecology, 2018, v. 32, n. 2, p. 533, doi. 10.1111/1365-2435.13005
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Beneficial Mutations from Evolution Experiments Increase Rates of Growth and Fermentation.
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- Journal of Molecular Evolution, 2018, v. 86, n. 2, p. 111, doi. 10.1007/s00239-018-9829-9
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Eco-energetic consequences of evolutionary shifts in body size.
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- Ecology Letters, 2018, v. 21, n. 1, p. 54, doi. 10.1111/ele.12870
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Phytoplankton size-scaling of net-energy flux across light and biomass gradients.
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- Ecology, 2017, v. 98, n. 12, p. 3106, doi. 10.1002/ecy.2032
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Does energy flux predict density-dependence? An empirical field test.
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- Ecology, 2017, v. 98, n. 12, p. 3116, doi. 10.1002/ecy.2033
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Do invasive species live faster? Mass-specific metabolic rate depends on growth form and invasion status.
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- Functional Ecology, 2017, v. 31, n. 11, p. 2080, doi. 10.1111/1365-2435.12913
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Should mothers provision their offspring equally? A manipulative field test.
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- Ecology Letters, 2017, v. 20, n. 8, p. 1025, doi. 10.1111/ele.12800
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Do low oxygen environments facilitate marine invasions? Relative tolerance of native and invasive species to low oxygen conditions.
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- Global Change Biology, 2017, v. 23, n. 6, p. 2321, doi. 10.1111/gcb.13668
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Field manipulations of resources mediate the transition from intraspecific competition to facilitation.
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- Journal of Animal Ecology, 2017, v. 86, n. 3, p. 654, doi. 10.1111/1365-2656.12644
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Dispersal duration mediates selection on offspring size.
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- Oikos, 2017, v. 126, n. 4, p. 480, doi. 10.1111/oik.03604
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The other 96%: Can neglected sources of fitness variation offer new insights into adaptation to global change?
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- Evolutionary Applications, 2017, v. 10, n. 3, p. 267, doi. 10.1111/eva.12447
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