Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 52 checked references that resolve
resolves10.1093/treephys/14.7-8-9.833Genotypic and phenotypic variation as stress adaptations in temperate tree species: a review of several case studies
resolves10.2307/1939389Relating Wet and Dry Year Ecophysiology to Leaf Structure in Contrasting Temperate Tree Species
resolves10.1006/anbo.2000.1175The McCree–de Wit–Penning de Vries–Thornley Respiration Paradigms: 30 Years Later
resolves10.1111/j.1365-2745.2009.01494.xPhysiological responses and statistical models of the environmental niche: a comparative study of two co‐occurring <i>Eucalyptus</i> species
resolves10.1111/j.1469-8137.2011.03673.xImpacts of drought on leaf respiration in darkness and light in <i>Eucalyptus saligna</i> exposed to industrial‐age atmospheric CO<sub>2</sub> and growth temperature
resolves10.1093/jxb/46.9.1185The respiratory energy requirements involved in nocturnal carbohydrate export from starch-storing mature source leaves and their contribution to leaf dark respiration
resolves10.1007/s00442-002-0931-7Root respiration in North American forests: effects of nitrogen concentration and temperature across biomes
resolves10.1111/j.1365-3040.2009.02089.xWarmer and drier conditions stimulate respiration more than photosynthesis in a boreal peatland ecosystem: Analysis of automatic chambers and eddy covariance measurements
resolves10.1093/treephys/tpp076Plasticity in the Huber value contributes to homeostasis in leaf water relations of a mallee Eucalypt with variation to groundwater depth
resolves10.1111/j.1469-8137.1989.tb02405.xAnalysis of specific leaf area and photosynthesis of two inbred lines of <i>Plantago major</i> differing in relative growth rate
resolves10.1007/BF00377192Photosynthesis and nitrogen relationships in leaves of C3 plants
resolves10.1046/j.1365-3040.2002.00923.xStomatal responses of Douglas‐fir seedlings to elevated carbon dioxide and temperature during the third and fourth years of exposure
resolves10.1046/j.0016-8025.2001.00815.xEffects of age and ontogeny on photosynthetic responses of a determinate annual plant to elevated CO<sub>2</sub> concentrations
resolves10.1007/s00442-006-0367-6Nutrient and water addition effects on day- and night-time conductance and transpiration in a C3 desert annual
resolves10.1038/191974a0Photoperiodic Effects on Stomatal Behaviour in Xanthium Pennsylvanicum
resolves10.1071/FP02007<i>Research note</i>
: Can decreased transpiration limit plant nitrogen acquisition in elevated CO
<i>2</i>
?
resolves10.1111/j.1365-3040.2006.01577.xCyclitols and carbohydrates in leaves and roots of 13 <i>Eucalyptus</i> species suggest contrasting physiological responses to water deficit
resolves10.1093/aob/mcm234Contrasting Physiological Responses of Six Eucalyptus Species to Water Deficit
resolves10.1007/s00442-008-1152-5Using multiple trait associations to define hydraulic functional types in plant communities of south-western Australia
resolves10.1093/treephys/19.6.337Sap-flux-scaled transpiration responses to light, vapor pressure deficit, and leaf area reduction in a flooded Taxodium distichum forest
resolves10.1007/s004420050471Relationships of leaf dark respiration to leaf nitrogen, specific leaf area and leaf life-span: a test across biomes and functional groups
resolves10.1093/treephys/27.4.551Removal of nutrient limitations by long-term fertilization decreases nocturnal water loss in savanna trees
resolves10.1111/j.1469-8137.2004.01046.xResponse of <i>Xanthium strumarium</i> leaf respiration in the light to elevated CO<sub>2</sub> concentration, nitrogen availability and temperature
resolves10.1093/jxb/erg082Night-time conductance in C3 and C4 species: do plants lose water at night?
resolves10.2307/2390018Effect of Seasonal Water Availability on Phenology and the Annual Shoot Carbohydrate Cycle of Tropical Forest Shrubs
resolves10.1093/treephys/22.15-16.1157Leaf respiration at different canopy positions in sweetgum (Liquidambar styraciflua) grown in ambient and elevated concentrations of carbon dioxide in the field
resolves10.1111/j.1365-2486.2008.01548.xCoupling of respiration, nitrogen, and sugars underlies convergent temperature acclimation in <i>Pinus banksiana</i> across wide‐ranging sites and populations
resolves10.1111/j.1365-2435.2006.01198.xEcotype adaptation and acclimation of leaf traits to rainfall in 29 species of 16‐year‐old <i>Eucalyptus</i> at two common gardens
resolves10.2307/1937336Primary Production and Abiotic Controls in Forests, Grasslands, and Desert Ecosystems in the United States
resolves10.1111/j.1529-8817.2003.00739.xResponse of total night‐time respiration to differences in total daily photosynthesis for leaves in a <i>Quercus rubra</i> L. canopy: implications for modelling canopy CO<sub>2</sub> exchange
resolves10.1111/j.1469-8137.2005.01590.xIrradiance, temperature and rainfall influence leaf dark respiration in woody plants: evidence from comparisons across 20 sites
resolves10.1093/treephys/tpq053Rates of nocturnal transpiration in two evergreen temperate woodland species with differing water-use strategies
resolves10.1093/treephys/tpr024Interactive effects of elevated CO2 and drought on nocturnal water fluxes in Eucalyptus saligna
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