| scholarly article | Q13442814 |
| P50 | author | Pablo A. Marquet | Q42693104 |
| P2093 | author name string | J H Brown | |
| M L Taper | |||
| P433 | issue | 4 | |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 573-584 | |
| P577 | publication date | 1993-10-01 | |
| P1433 | published in | The American Naturalist | Q3085258 |
| P1476 | title | Evolution of body size: consequences of an energetic definition of fitness | |
| P478 | volume | 142 |
| Q35663696 | A Multi Size-Level Assessment of Benthic Marine Communities in a Coastal Environment: Are They Different Sides of the Same Coin? |
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| Q30668952 | A macrophysiological analysis of energetic constraints on geographic range size in mammals |
| Q47172900 | A statistical test of unbiased evolution of body size in birds |
| Q51686217 | A test of reproductive power in snakes. |
| Q21245377 | A universal scaling relationship between body mass and proximal limb bone dimensions in quadrupedal terrestrial tetrapods |
| Q36601798 | Accounting for size-specific predation improves our ability to predict the strength of a trophic cascade |
| Q33408531 | Adaptation and diversification on islands |
| Q54289676 | An analysis and review of models of the sociobiology of the Mustelidae |
| Q36091688 | An empirical test of 'universal' biomass scaling relationships in kelps: evidence of convergence with seed plants. |
| Q36054145 | An example of phenotypic adherence to the island rule? - Anticosti gray jays are heavier but not structurally larger than mainland conspecifics |
| Q57059782 | Are smaller subspecies of common brushtail possums more omnivorous than larger ones? |
| Q47363437 | Area, isolation and body size evolution in insular carnivores. |
| Q55952041 | Atlantic salmon Salmo salar L., brown trout Salmo trutta L. and Arctic charr Salvelinus alpinus (L.): a review of aspects of their life histories |
| Q38557935 | Benefits of the destinations, not costs of the journeys, shape partial migration patterns. |
| Q55870963 | Body mass estimation in non-avian bipeds using a theoretical conversion to quadruped stylopodial proportions |
| Q47275208 | Body size and human energy requirements: reduced mass-specific resting energy expenditure in tall adults |
| Q51115389 | Body size and mortality rates in coral reef fishes: a three-phase relationship. |
| Q28710268 | Body size distribution of the dinosaurs |
| Q28656065 | Body size diversity and frequency distributions of Neotropical cichlid fishes (Cichliformes: Cichlidae: Cichlinae) |
| Q57006967 | Body size does not predict species richness among the metazoan phyla |
| Q33538029 | Body size evolution in insular speckled rattlesnakes (Viperidae: Crotalus mitchellii) |
| Q29543084 | Body size evolution in insular vertebrates: generality of the island rule |
| Q56488035 | Body size evolution of palaeo-insular mammals: temporal variations and interspecific interactions |
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| Q34611673 | Body size is a significant predictor of congruency in species richness patterns: a meta-analysis of aquatic studies |
| Q57053528 | Body sizes and diversification rates of lizards, snakes, amphisbaenians and the tuatara |
| Q28610504 | Body-size trends of the extinct giant shark Carcharocles megalodon: a deep-time perspective on marine apex predators |
| Q46825259 | Changes in body size, abundance, and energy allocation in rockfish assemblages of the northeast Pacific |
| Q58691837 | Coloration of Anuran Tadpoles (Amphibia): Development, Dynamics, Function, and Hypotheses |
| Q57193774 | Community functional trait composition at the continental scale: the effects of non-ecological processes |
| Q57014641 | Connecting landscape structure and patterns in body size distributions |
| Q51555658 | Connecting species richness, abundance and body size in deep-sea gastropods |
| Q56609014 | Conservation status, rarity, and geographic priorities for conservation of Chilean mammals: an assessment |
| Q37115196 | Contrasting size evolution in marine and freshwater diatoms |
| Q43033305 | Convergent evolution of reduced energy demands in extremophile fish |
| Q39412451 | Costs and benefits of group living in primates: an energetic perspective |
| Q46321246 | Cranial size and shape variation in isolated populations of the Olkhon mountain vole (Alticola olchonensis Litvinov, 1960). |
| Q38209952 | Discontinuities, cross-scale patterns, and the organization of ecosystems. |
| Q50964497 | Distribution pattern and number of ticks on lizards. |
| Q55092569 | Does energy availability predict gastropod reproductive strategies? |
| Q31091079 | Dwarfism in insular sloths: biogeography, selection, and evolutionary rate |
| Q49305552 | Dynamics of starvation and recovery predict extinction risk and both Damuth's law and Cope's rule |
| Q46433261 | Economic thermoregulatory response explains mismatch between thermal physiology and behaviour in newts |
| Q57039802 | Effects of increasing nutrient supply and omnivorous feeding on the size spectrum slope: a size-based nutrient-phytoplankton-zooplankton model |
| Q34189261 | Empirical evidence for an optimal body size in snakes |
| Q52655986 | Endothiodon cf. bathystoma (Synapsida: Dicynodontia) bony labyrinth anatomy, variation and body mass estimates. |
| Q33734520 | Energetic basis of colonial living in social insects |
| Q52704993 | Energetic cost of calling: general constraints and species-specific differences. |
| Q60264382 | Energy efficiency drives the global seasonal distribution of birds |
| Q56425176 | Energy expenditure and body size are targets of natural selection across a wide geographic range, in a terrestrial invertebrate |
| Q91297601 | Energy requirements, length of digestive tract compartments and body mass in six gerbilline rodents of the Negev Desert |
| Q28652205 | Entrapment bias of arthropods in Miocene amber revealed by trapping experiments in a tropical forest in Chiapas, Mexico |
| Q36284656 | Environments and evolution: interactions between stress, resource inadequacy and energetic efficiency |
| Q46301722 | Evidence of developmental niche construction in dung beetles: effects on growth, scaling and reproductive success |
| Q101632947 | Evidence of predation risk increases with body size in a diminutive snake |
| Q47322501 | Evolution of body size in food webs: does the energetic equivalence rule hold? |
| Q34007751 | Evolution of extreme body size disparity in monitor lizards (Varanus). |
| Q29998999 | Evolution on a desert island: body size divergence between the reptiles of Nevada's Anaho Island and the mainland around Pyramid Lake |
| Q52598002 | Evolutionary optimality applied to Drosophila experiments: hypothesis of constrained reproductive efficiency. |
| Q55923307 | Exceptionally preserved Cambrian loriciferans and the early animal invasion of the meiobenthos |
| Q28608341 | Exploring the Relationship between Skeletal Mass and Total Body Mass in Birds |
| Q36230037 | Extensions of Island Biogeography Theory predict the scaling of functional trait composition with habitat area and isolation |
| Q57263542 | Extreme polygyny in the previously unstudied subtropical ant Temnothorax tuscaloosae with implications for the biogeographic study of the evolution of polygyny |
| Q58827529 | Factors explaining increased body size in common shrews (Sorex araneus) on Scottish islands |
| Q57443155 | Genetic Diversity and the Survival of Populations |
| Q39237566 | Geographic and temporal correlations of mammalian size reconsidered: a resource rule |
| Q33935831 | Global energy gradients and size in colonial organisms: worker mass and worker number in ant colonies |
| Q34776196 | Growth trajectory influences temperature preference in fish through an effect on metabolic rate. |
| Q28742886 | How big should a mammal be? A macroecological look at mammalian body size over space and time |
| Q45928337 | How large are the extinct giant insular rodents? New body mass estimations from teeth and bones. |
| Q34232242 | Hypothalamic neuropeptide mechanisms for regulating energy balance: from rodent models to human obesity |
| Q46158747 | Increased energy differentially increases richness and abundance of optimal body sizes in deep-sea wood falls |
| Q47300191 | Increased energy promotes size-based niche availability in marine mollusks |
| Q51416949 | Inferring species roles in metacommunity structure from species co-occurrence networks. |
| Q55842533 | Insularity and adaptation in coupled victim-enemy associations |
| Q28776365 | Invariant size-frequency distributions along a latitudinal gradient in marine bivalves |
| Q57053562 | Is the island rule general? Turtles disagree |
| Q33455853 | Larger than life: humans' nonverbal status cues alter perceived size |
| Q47423477 | Latitudinal variation in the shape of the species body size distribution: an analysis using freshwater fishes |
| Q48384996 | Life history traits to predict biogeographic species distributions in bivalves |
| Q28764823 | Life-history evolution under a production constraint |
| Q38693268 | Measuring Selection on Physiology in the Wild and Manipulating Phenotypes (in Terrestrial Nonhuman Vertebrates). |
| Q52924854 | Mechanical sensitivity and the dynamics of evolutionary rate shifts in biomechanical systems. |
| Q35155717 | Metabolic efficiency in response to environmental agents predicts hormesis and invalidates the linear no-threshold premise: ionizing radiation as a case study |
| Q38201389 | Metabolic scaling in animals: methods, empirical results, and theoretical explanations |
| Q46254053 | Metabolism drives distribution and abundance in extremophile fish |
| Q56158545 | Minimizing energy expenditure facilitates vertebrate persistence on oceanic islands |
| Q35566726 | Morphological shifts in island-dwelling birds: the roles of generalist foraging and niche expansion |
| Q21089998 | New horned dinosaurs from Utah provide evidence for intracontinental dinosaur endemism |
| Q51535467 | New macroecological insights into functional constraints on mammalian geographical range size. |
| Q33346431 | On being the right size: food-limited feedback on optimal body size |
| Q57014794 | On size and area: Patterns of mammalian body size extremes across landmasses |
| Q47303733 | Parasite body size distributions: interpreting patterns of skewness |
| Q37947340 | Patterns and processes in abundance-body size relationships for marine benthic invertebrates |
| Q40330260 | Patterns in body mass distributions: sifting among alternative hypotheses. |
| Q24630919 | Phylogenetic signal in primate behaviour, ecology and life history |
| Q24655910 | Physiological and life history strategies of a fossil large mammal in a resource-limited environment |
| Q34581764 | Physiological variation in insects: large-scale patterns and their implications |
| Q34191480 | Predicted correspondence between species abundances and dendrograms of niche similarities |
| Q34110435 | Quantitative genetics of body size and timing of maturation in two nine-spined stickleback (Pungitius pungitius) populations |
| Q34498527 | Red Wolf (Canis rufus) Recovery: A Review with Suggestions for Future Research |
| Q28710087 | Resonance-induced multimodal body-size distributions in ecosystems |
| Q56770803 | Review of impacts of the introduced house mouse on islands in the Southern Ocean: are mice equivalent to rats? |
| Q50045807 | Rule reversal: Ecogeographical patterns of body size variation in the common treeshrew (Mammalia, Scandentia). |
| Q92057976 | Scaling the risk landscape drives optimal life-history strategies and the evolution of grazing |
| Q57898436 | Scaling up the curvature of mammalian metabolism |
| Q58849794 | Seasonal behavioural patterns of free-living rock hyrax (Procavia capensis) |
| Q81757861 | Seasonal thermoregulatory responses in mammals |
| Q35944644 | Sibling Competition & Growth Tradeoffs. Biological vs. Statistical Significance |
| Q57053682 | Size evolution in island lizards |
| Q52206957 | Spatial scaling laws yield a synthetic theory of biodiversity. |
| Q24677074 | Species-range size distributions: products of speciation, extinction and transformation |
| Q60503828 | Stability and endemicity of benthic diatom assemblages from different substrates in a maritime stream on Byers Peninsula, Livingston Island, Antarctica: the role of climate variability |
| Q97092532 | Survival of the cheapest: how proteome cost minimization drives evolution |
| Q56806449 | THE ISLAND RULE IN LARGE MAMMALS: PALEONTOLOGY MEETS ECOLOGY |
| Q39190824 | The allometry of rodent intestines |
| Q30769943 | The animal species-body size distribution of Marion Island |
| Q57068499 | The body-size structure of macrobenthos changes predictably along gradients of hydrodynamic stress and organic enrichment |
| Q39186533 | The energetics of a Malagasy rodent, Macrotarsomys ingens (Nesomyinae): a test of island and zoogeographical effects on metabolism |
| Q47203501 | The evolution of body armor in mammals: plantigrade constraints of large body size |
| Q30626626 | The evolution of mammal body sizes: responses to Cenozoic climate change in North American mammals. |
| Q47371699 | The evolution of placental mammal body sizes: evolutionary history, form, and function |
| Q37785859 | The evolutionary consequences of oxygenic photosynthesis: a body size perspective |
| Q60354346 | The fast life of a dwarfed giant |
| Q91943372 | The genetic and cultural evolution of unsustainability |
| Q43754043 | The genetic architecture of growth rate in juvenile Takifugu species |
| Q90745804 | The geographical diversification in varanid lizards: the role of mainland versus island in driving species evolution |
| Q56446947 | The imbalance of nature: revisiting a Darwinian framework for invasion biology |
| Q39190833 | The influence of climate on the basal metabolic rate of small mammals: a slow-fast metabolic continuum |
| Q47383438 | The inverse relationship between species diversity and body mass: do primates play by the "rules"? |
| Q58039107 | The island rule and the evolution of body size in the deep sea |
| Q57053504 | The island rule is not valid in terrestrial isopods (Crustacea: Oniscidea) |
| Q56924094 | The island rule: An assessment of biases and research trends |
| Q28756364 | The island rule: made to be broken? |
| Q29041195 | The mammal fauna in the Early Cretaceous Jehol Biota: implications for diversity and biology of Mesozoic mammals |
| Q46708909 | The natural selection of metabolism and mass selects lifeforms from viruses to multicellular animals |
| Q24557547 | The rate of DNA evolution: effects of body size and temperature on the molecular clock |
| Q35762118 | The role of body size and shape in understanding competitive interactions within a community of Neotropical dung beetles. |
| Q58067854 | The role of landscape texture in conservation biogeography: a case study on birds in south-eastern Australia |
| Q38733860 | The role of local versus biogeographical processes in influencing diversity and body-size variation in mammal assemblages |
| Q44945010 | The tempo and mode of evolution: body sizes of island mammals |
| Q40939720 | Thermodynamics predicts density-dependent energy use in organisms and ecological communities |
| Q55871166 | Trophic strategies, animal diversity and body size |
| Q58832861 | Which community indicators can measure the impact of fishing? A review and proposals |
| Q33874848 | Why are there so many explanations for primate brain evolution? |
| Q57399719 | Within- and among-genus components of size evolution during mass extinction, recovery, and background intervals: a case study of Late Permian through Late Triassic foraminifera |
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