Works by Phillips, Richard P.
Results: 91
An integrated assessment of the potential impacts of climate change on Indiana forests.
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- Climatic Change, 2020, v. 163, n. 4, p. 1917, doi. 10.1007/s10584-018-2326-8
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- Article
Drought Response of Eastern US Oaks in the Context of Their Declining Abundance.
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- BioScience, 2022, v. 72, n. 4, p. 333, doi. 10.1093/biosci/biab135
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- Article
Why Coordinated Distributed Experiments Should Go Global.
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- BioScience, 2021, v. 71, n. 9, p. 918, doi. 10.1093/biosci/biab033
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- Article
Modeling the carbon cost of plant nitrogen acquisition: Mycorrhizal trade-offs and multipath resistance uptake improve predictions of retranslocation.
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- Journal of Geophysical Research. Biogeosciences, 2014, v. 119, n. 8, p. 1684, doi. 10.1002/2014JG002660
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- Article
Effects of changing precipitation regimes on dryland soil respiration and C pool dynamics at rainfall event, seasonal and interannual scales.
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- Journal of Geophysical Research. Biogeosciences, 2008, v. 113, n. G3, p. n/a, doi. 10.1029/2008JG000685
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- Article
Leaf litter decay rates differ between mycorrhizal groups in temperate, but not tropical, forests.
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- New Phytologist, 2019, v. 222, n. 1, p. 556, doi. 10.1111/nph.15524
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Linking variation in intrinsic water‐use efficiency to isohydricity: a comparison at multiple spatiotemporal scales.
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- New Phytologist, 2019, v. 221, n. 1, p. 195, doi. 10.1111/nph.15384
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Ecosystem responses to elevated CO<sub>2</sub> governed by plant-soil interactions and the cost of nitrogen acquisition.
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- New Phytologist, 2018, v. 217, n. 2, p. 507, doi. 10.1111/nph.14872
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Dominant mycorrhizal association of trees alters carbon and nutrient cycling by selecting for microbial groups with distinct enzyme function.
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- New Phytologist, 2017, v. 214, n. 1, p. 432, doi. 10.1111/nph.14343
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Phosphorus cycling in deciduous forest soil differs between stands dominated by ecto- and arbuscular mycorrhizal trees.
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- New Phytologist, 2016, v. 209, n. 3, p. 1184, doi. 10.1111/nph.13720
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Redefining fine roots improves understanding of below-ground contributions to terrestrial biosphere processes.
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- New Phytologist, 2015, v. 207, n. 3, p. 505, doi. 10.1111/nph.13363
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Mycorrhizal type determines the magnitude and direction of root-induced changes in decomposition in a temperate forest.
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- New Phytologist, 2015, v. 206, n. 4, p. 1274, doi. 10.1111/nph.13303
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The rhizosphere and hyphosphere differ in their impacts on carbon and nitrogen cycling in forests exposed to elevated CO<sub>2</sub>.
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- New Phytologist, 2015, v. 205, n. 3, p. 1164, doi. 10.1111/nph.13122
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The mycorrhizal-associated nutrient economy: a new framework for predicting carbon-nutrient couplings in temperate forests.
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- New Phytologist, 2013, v. 199, n. 1, p. 41, doi. 10.1111/nph.12221
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Fertilization effects on fineroot biomass, rhizosphere microbes and respiratory fluxes in hardwood forest soils.
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- New Phytologist, 2007, v. 176, n. 3, p. 655, doi. 10.1111/j.1469-8137.2007.02204.x
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- Article
Towards a rhizo-centric view of plant-microbial feedbacks under elevated atmospheric CO<sub>2</sub>.
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- New Phytologist, 2007, v. 173, n. 4, p. 664, doi. 10.1111/j.1469-8137.2007.02006.x
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- Article
Asymmetric effects of hydroclimate extremes on eastern US tree growth: Implications on current demographic shifts and climate variability.
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- Global Change Biology, 2024, v. 30, n. 8, p. 1, doi. 10.1111/gcb.17474
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- Article
Nitrogen cycling microbiomes are structured by plant mycorrhizal associations with consequences for nitrogen oxide fluxes in forests.
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- Global Change Biology, 2021, v. 27, n. 5, p. 1068, doi. 10.1111/gcb.15439
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Linking drought legacy effects across scales: From leaves to tree rings to ecosystems.
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- Global Change Biology, 2019, v. 25, n. 9, p. 2978, doi. 10.1111/gcb.14710
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Tree mycorrhizal type predicts within‐site variability in the storage and distribution of soil organic matter.
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- Global Change Biology, 2018, v. 24, n. 8, p. 3317, doi. 10.1111/gcb.14132
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Soil carbon cycling proxies: Understanding their critical role in predicting climate change feedbacks.
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- Global Change Biology, 2018, v. 24, n. 3, p. 895, doi. 10.1111/gcb.13926
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Faster turnover of new soil carbon inputs under increased atmospheric CO<sub>2</sub>.
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- Global Change Biology, 2017, v. 23, n. 10, p. 4420, doi. 10.1111/gcb.13752
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Pushing precipitation to the extremes in distributed experiments: recommendations for simulating wet and dry years.
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- Global Change Biology, 2017, v. 23, n. 5, p. 1774, doi. 10.1111/gcb.13504
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Forest biogeochemistry in response to drought.
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- Global Change Biology, 2016, v. 22, n. 7, p. 2318, doi. 10.1111/gcb.13105
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Tree-mycorrhizal associations detected remotely from canopy spectral properties.
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- Global Change Biology, 2016, v. 22, n. 7, p. 2596, doi. 10.1111/gcb.13264
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Carbon cost of plant nitrogen acquisition: global carbon cycle impact from an improved plant nitrogen cycle in the Community Land Model.
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- Global Change Biology, 2016, v. 22, n. 3, p. 1299, doi. 10.1111/gcb.13131
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Greenness indices from digital cameras predict the timing and seasonal dynamics of canopy-scale photosynthesis.
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- Ecological Applications, 2015, v. 25, n. 1, p. 99, doi. 10.1890/14-0005.1
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- Article
TREE SPECIES AND MYCORRHIZAL ASSOCIATIONS INFLUENCE THE MAGNITUDE OF RHIZOSPHERE EFFECTS.
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- Ecology, 2006, v. 87, n. 5, p. 1302, doi. 10.1890/0012-9658(2006)87[1302:TSAMAI]2.0.CO;2
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Guidelines and considerations for designing field experiments simulating precipitation extremes in forest ecosystems.
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- Methods in Ecology & Evolution, 2018, v. 9, n. 12, p. 2310, doi. 10.1111/2041-210X.13094
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- Article
Elevated CO2 increases root exudation from loblolly pine (Pinus taeda) seedlings as an N-mediated response.
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- Tree Physiology, 2009, v. 29, n. 12, p. 1513, doi. 10.1093/treephys/tpp083
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Fast-decaying plant litter enhances soil carbon in temperate forests but not through microbial physiological traits.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28715-9
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- Article
Mycorrhizal feedbacks influence global forest structure and diversity.
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- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-05410-z
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- Article
Rhizosphere processes are quantitatively important components of terrestrial carbon and nutrient cycles.
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- Global Change Biology, 2015, v. 21, n. 5, p. 2082, doi. 10.1111/gcb.12816
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- Article
An improved approach for remotely sensing water stress impacts on forest C uptake.
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- Global Change Biology, 2014, v. 20, n. 9, p. 2856, doi. 10.1111/gcb.12537
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- Article
Chronic water stress reduces tree growth and the carbon sink of deciduous hardwood forests.
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- Global Change Biology, 2014, v. 20, n. 8, p. 2531, doi. 10.1111/gcb.12528
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- Article
Patterns of rhizosphere carbon flux in sugar maple (Acer saccharum) and yellow birch (Betula allegheniensis) saplings.
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- Global Change Biology, 2005, v. 11, n. 6, p. 983, doi. 10.1111/j.1365-2486.2005.00959.x
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- Article
Root‐derived inputs are major contributors to soil carbon in temperate forests, but vary by mycorrhizal type.
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- Ecology Letters, 2021, v. 24, n. 4, p. 626, doi. 10.1111/ele.13651
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Drought legacies are dependent on water table depth, wood anatomy and drought timing across the eastern US.
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- Ecology Letters, 2019, v. 22, n. 1, p. 119, doi. 10.1111/ele.13173
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- Article
Feedbacks between plant N demand and rhizosphere priming depend on type of mycorrhizal association.
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- Ecology Letters, 2017, v. 20, n. 8, p. 1043, doi. 10.1111/ele.12802
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Roots and fungi accelerate carbon and nitrogen cycling in forests exposed to elevated CO<sub>2</sub>.
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- Ecology Letters, 2012, v. 15, n. 9, p. 1042, doi. 10.1111/j.1461-0248.2012.01827.x
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Increases in the flux of carbon belowground stimulate nitrogen uptake and sustain the long-term enhancement of forest productivity under elevated CO.
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- Ecology Letters, 2011, v. 14, n. 4, p. 349, doi. 10.1111/j.1461-0248.2011.01593.x
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Enhanced root exudation induces microbial feedbacks to N cycling in a pine forest under long-term CO.
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- Ecology Letters, 2011, v. 14, n. 2, p. 187, doi. 10.1111/j.1461-0248.2010.01570.x
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Global pattern of soil priming effect intensity and its environmental drivers.
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- Ecology, 2022, v. 103, n. 11, p. 1, doi. 10.1002/ecy.3790
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Variation in hyphal production rather than turnover regulates standing fungal biomass in temperate hardwood forests.
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- Ecology, 2021, v. 102, n. 3, p. 1, doi. 10.1002/ecy.3260
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Resource stoichiometry and the biogeochemical consequences of nitrogen deposition in a mixed deciduous forest.
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- Ecology, 2016, v. 97, n. 12, p. 3369, doi. 10.1002/ecy.1595
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Beneficial effects of climate warming on boreal tree growth may be transitory.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05705-4
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Understanding the ecological versatility of Tetracladium species in temperate forest soils.
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- Environmental Microbiology, 2024, v. 26, n. 11, p. 1, doi. 10.1111/1462-2920.70001
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Plant-microbe Symbioses Reveal Underestimation of Modeled Climate Impacts.
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- Biogeosciences Discussions, 2018, p. 1, doi. 10.5194/bg-2018-293
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Younger trees in the upper canopy are more sensitive but also more resilient to drought.
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- Nature Climate Change, 2022, v. 12, n. 12, p. 1168, doi. 10.1038/s41558-022-01528-w
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The increasing importance of atmospheric demand for ecosystem water and carbon fluxes.
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- Nature Climate Change, 2016, v. 6, n. 11, p. 1023, doi. 10.1038/nclimate3114
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