Tree density reduction mitigates the decline of Larix principis-rupprechtii plantations: Evidence from a combination of dendroclimatic and physiological measurements
暂无分享,去创建一个
[1] M. Sánchez-González,et al. Forest disturbances and climate constrain carbon allocation dynamics in trees , 2022, Global change biology.
[2] Wenfa Xiao,et al. Climate, soil nutrients, and stand characteristics jointly determine large-scale patterns of biomass growth rates and allocation in Pinus massoniana plantations , 2022, Forest Ecology and Management.
[3] Qiushi Ning,et al. Differences in growth pattern and response to climate warming between Larix olgensis and Pinus koraiensis in Northeast China are related to their distinctions in xylem hydraulics , 2022, Agricultural and Forest Meteorology.
[4] Beibei Zhang,et al. Effects of understory removal and thinning on water uptake patterns in Pinus massoniana Lamb. plantations: Evidence from stable isotope analysis , 2022, Forest Ecology and Management.
[5] N. Pederson,et al. Higher plasticity of water uptake in spruce than larch in an alpine habitat of North-Central China , 2021, Agricultural and Forest Meteorology.
[6] F. Ripullone,et al. Declines in canopy greenness and tree growth are caused by combined climate extremes during drought-induced dieback. , 2021, The Science of the total environment.
[7] D. Bell,et al. Tree mortality response to drought‐density interactions suggests opportunities to enhance drought resistance , 2021, Journal of Applied Ecology.
[8] Q. Ye,et al. Greater hydraulic safety contributes to higher growth resilience to drought across seven pine species in a semi-arid environment. , 2021, Tree physiology.
[9] Zongshan Li,et al. Elevation-dependent growth trends of forests as affected by climate warming in the southeastern Tibetan Plateau , 2021 .
[10] Guang‐You Hao,et al. Contrasting patterns of radial growth rate between Larix principis-rupprechtii and Pinus sylvestris var. mongolica along an elevational gradient are mediated by differences in xylem hydraulics , 2021 .
[11] G. Nabuurs,et al. Optimizing stand density for climate-smart forestry: a way forward towards resilient forests with enhanced carbon storage under extreme climate events , 2021, Soil Biology and Biochemistry.
[12] T. Quine,et al. High forest stand density exacerbates growth decline of conifers driven by warming but not broad-leaved trees in temperate mixed forest in northeast Asia. , 2021, The Science of the total environment.
[13] T. C. Hennessey,et al. Long-term effects of stand density management and genotype on wood properties of loblolly pine (Pinus taeda L.) in the mid-South USA , 2021, Forest Ecology and Management.
[14] I. Cañellas,et al. Sensitivity to water stress drives differential decline and mortality dynamics of three co-occurring conifers with different drought tolerance , 2021 .
[15] R. Plichta,et al. Low resistance but high resilience to drought of flushing Norway spruce seedlings. , 2021, Tree physiology.
[16] Jianguo Huang,et al. Radial growth responses of two dominant conifers to climate in the Altai Mountains, Central Asia , 2021 .
[17] H. Pretzsch,et al. Growth–density relationship in mixed stands – Results from long-term experimental plots , 2021, Forest Ecology and Management.
[18] J. HilleRisLambers,et al. Increasing climate sensitivity of subtropical conifers along an aridity gradient , 2021 .
[19] M. Hirota,et al. Linking plant hydraulics and the fast-slow continuum to understand resilience to drought in tropical ecosystems. , 2021, The New phytologist.
[20] Quan-fa Zhang,et al. Prioritized carbon allocation to storage of different functional types of species at the upper range limits is driven by different environmental drivers. , 2021, The Science of the total environment.
[21] B. Choat,et al. Coordination of stem and leaf traits define different strategies to regulate water loss and tolerance ranges to aridity. , 2021, The New phytologist.
[22] W. Anderegg,et al. Rapid and surprising dieback of Utah juniper in the southwestern USA due to acute drought stress , 2021 .
[23] Xiaojun Xu,et al. Thinning effects on forest evolution in Masson pine (Pinus massoniana Lamb.) conversion from pure plantations into mixed forests , 2020 .
[24] Jiaojun Zhu,et al. Hydraulic limitation underlies the dieback of Populus pseudo-simonii trees in water-limited areas of northern China , 2020 .
[25] G. Battipaglia,et al. Effects of thinning intensity on productivity and water use efficiency of Quercus robur L , 2020 .
[26] W. Anderegg,et al. Divergent forest sensitivity to repeated extreme droughts , 2020, Nature Climate Change.
[27] P. Zhao,et al. Whole-plant water hydraulic integrity to predict drought-induced Eucalyptus urophylla mortality under drought stress , 2020 .
[28] S. Fraver,et al. Low stand density moderates growth declines during hot droughts in semi‐arid forests , 2020 .
[29] R. Sánchez‐Salguero,et al. Growth and resilience responses of Scots pine to extreme droughts across Europe depend on predrought growth conditions , 2020, Global change biology.
[30] Hong Yin,et al. Greater risk of hydraulic failure due to increased drought threatens pine plantations in Horqin Sandy Land of northern China , 2020 .
[31] P. Balandier,et al. Competition and water stress indices as predictors of Pinus halepensis Mill. radial growth under drought , 2020, Forest Ecology and Management.
[32] G. Goldstein,et al. Contrasts in xylem hydraulics and water use underlie the sorting of different sand-fixing shrub species to early and late stages of dune stabilization , 2020 .
[33] J. Linares,et al. Low growth resilience to drought is related to future mortality risk in trees , 2020, Nature Communications.
[34] Wenfa Xiao,et al. Combined Effects of Drought and Shading on Growth and Non-Structural Carbohydrates in Pinus massoniana Lamb. Seedlings , 2019, Forests.
[35] E. Rotenberg,et al. Stand density effects on carbon and water fluxes in a semi-arid forest, from leaf to stand-scale , 2019 .
[36] Amilcare Porporato,et al. Reduced resilience as an early warning signal of forest mortality , 2019, Nature Climate Change.
[37] A. Rubtsov,et al. Canopy transpiration of a Larix sibirica and Pinus sylvestris forest in Central Siberia , 2019, Agricultural and Forest Meteorology.
[38] J. Ogée,et al. Mortality versus survival in drought‐affected Aleppo pine forest depends on the extent of rock cover and soil stoniness , 2019, Functional Ecology.
[39] R. Ruess,et al. Stand basal area and solar radiation amplify white spruce climate sensitivity in interior Alaska: Evidence from carbon isotopes and tree rings , 2018, Global change biology.
[40] Miao Wang,et al. The interaction between nonstructural carbohydrate reserves and xylem hydraulics in Korean pine trees across an altitudinal gradient , 2018, Tree physiology.
[41] S. Pacala,et al. Tree carbon allocation explains forest drought-kill and recovery patterns. , 2018, Ecology letters.
[42] J. Kane,et al. Thinning, tree-growth, and resistance to multi-year drought in a mixed-conifer forest of northern California , 2018, Forest Ecology and Management.
[43] S. Mayr,et al. Water stress limits transpiration and growth of European larch up to the lower subalpine belt in an inner‐alpine dry valley , 2018, The New phytologist.
[44] F. Meinzer,et al. Hydraulics play an important role in causing low growth rate and dieback of aging Pinus sylvestris var. mongolica trees in plantations of Northeast China. , 2018, Plant, cell & environment.
[45] J. Linares,et al. Reprint of “Managing drought-sensitive forests under global change. Low competition enhances long-term growth and water uptake in Abies pinsapo “ , 2018, Forest Ecology and Management.
[46] B. Choat,et al. Triggers of tree mortality under drought , 2018, Nature.
[47] Richard P Phillips,et al. Coarse roots prevent declines in whole-tree non-structural carbohydrate pools during drought in an isohydric and an anisohydric species , 2018, Tree physiology.
[48] B. Schuldt,et al. Hydraulic traits and tree-ring width in Larix sibirica Ledeb. as affected by summer drought and forest fragmentation in the Mongolian forest steppe , 2018, Annals of Forest Science.
[49] Ximeng Li,et al. Tree hydraulic traits are coordinated and strongly linked to climate-of-origin across a rainfall gradient. , 2018, Plant, cell & environment.
[50] A. Bräuning,et al. Tree-ring record in Ethiopian church forests reveals successive generation differences in growth rates and disturbance events , 2018 .
[51] A. Rigling,et al. Competition for water in a xeric forest ecosystem – Effects of understory removal on soil micro-climate, growth and physiology of dominant Scots pine trees , 2018 .
[52] F. Mouillot,et al. Thinning increases tree growth by delaying drought-induced growth cessation in a Mediterranean evergreen oak coppice , 2018 .
[53] Juan A. Blanco,et al. Tree‐to‐tree competition in mixed European beech–Scots pine forests has different impacts on growth and water‐use efficiency depending on site conditions , 2018 .
[54] Qiong Zhao,et al. The influence of a five-year nitrogen fertilization treatment on hydraulic architecture of Pinus sylvestris var. mongolica in a water-limited plantation of NE China , 2017, Forest Ecology and Management.
[55] J. Bauhus,et al. Silver fir and Douglas fir are more tolerant to extreme droughts than Norway spruce in south‐western Germany , 2017, Global change biology.
[56] M. Battaglia,et al. Density‐dependent vulnerability of forest ecosystems to drought , 2017 .
[57] Jordi Martínez-Vilalta,et al. A multi-species synthesis of physiological mechanisms in drought-induced tree mortality , 2017, Nature Ecology & Evolution.
[58] D. Bell,et al. A window of opportunity for climate-change adaptation: easing tree mortality by reducing forest basal area , 2017 .
[59] J. Bauhus,et al. Potential of forest thinning to mitigate drought stress: A meta-analysis , 2016 .
[60] F. Hartig,et al. Heavy and frequent thinning promotes drought adaptation in Pinus sylvestris forests. , 2016, Ecological applications : a publication of the Ecological Society of America.
[61] Cara R. Nelson,et al. The effect of competition on responses to drought and interannual climate variability of a dominant conifer tree of western North America , 2016 .
[62] Marco Carrer,et al. Wood anatomy and carbon‐isotope discrimination support long‐term hydraulic deterioration as a major cause of drought‐induced dieback , 2016, Global change biology.
[63] C. W. Chase,et al. The response of light, water, and nutrient availability to pre-commercial thinning in dry inland Douglas-fir forests , 2016 .
[64] Y. Malhi,et al. Death from drought in tropical forests is triggered by hydraulics not carbon starvation , 2015, Nature.
[65] N. McDowell,et al. Darcy's law predicts widespread forest mortality under climate warming , 2015 .
[66] Sergio M. Vicente-Serrano,et al. To die or not to die: early warnings of tree dieback in response to a severe drought , 2015 .
[67] Pieter A. Zuidema,et al. Time-dependent effects of climate and drought on tree growth in a Neotropical dry forest: Short-term tolerance vs. long-term sensitivity , 2014 .
[68] P. Jones,et al. Updated high‐resolution grids of monthly climatic observations – the CRU TS3.10 Dataset , 2014 .
[69] Sylvain Delzon,et al. Limited genetic variability and phenotypic plasticity detected for cavitation resistance in a Mediterranean pine. , 2014, The New phytologist.
[70] Harald Bugmann,et al. Reduction of stand density increases drought resistance in xeric Scots pine forests , 2013 .
[71] C. Ammer,et al. Mitigation of drought by thinning: Short-term and long-term effects on growth and physiological performance of Norway spruce (Picea abies) , 2013 .
[72] C. Leuschner,et al. Increased Summer Temperatures Reduce the Growth and Regeneration of Larix sibirica in Southern Boreal Forests of Eastern Kazakhstan , 2013, Ecosystems.
[73] Dali Guo,et al. Rapid warming accelerates tree growth decline in semi‐arid forests of Inner Asia , 2013, Global change biology.
[74] N. McDowell,et al. How do trees die? A test of the hydraulic failure and carbon starvation hypotheses , 2013, Plant, cell & environment.
[75] Hervé Cochard,et al. Embolism resistance as a key mechanism to understand adaptive plant strategies. , 2013, Current opinion in plant biology.
[76] S. Trumbore,et al. Lethal drought leads to reduction in nonstructural carbohydrates in Norway spruce tree roots but not in the canopy , 2013 .
[77] R. B. Jackson,et al. Hydraulic limits on maximum plant transpiration and the emergence of the safety-efficiency trade-off. , 2013, The New phytologist.
[78] W. Oberhuber,et al. Drought sensitivity of three co-occurring conifers within a dry inner Alpine environment , 2013, Trees.
[79] A. Nardini,et al. Global convergence in the vulnerability of forests to drought , 2012, Nature.
[80] D. Woodruff,et al. Carbon dynamics in trees: feast or famine? , 2012, Tree physiology.
[81] F. Lloret,et al. Stand- and tree-level determinants of the drought response of Scots pine radial growth , 2012, Oecologia.
[82] F. Lloret,et al. Components of tree resilience: effects of successive low‐growth episodes in old ponderosa pine forests , 2011 .
[83] F. Lloret,et al. Carbon reserves and canopy defoliation determine the recovery of Scots pine 4 yr after a drought episode. , 2011, The New phytologist.
[84] C. Leuschner,et al. Climate response of tree-ring width in Larix sibirica growing in the drought-stressed forest-steppe ecotone of northern Mongolia , 2011, Annals of Forest Science.
[85] D. Peterson,et al. Forest responses to climate change in the northwestern United States: Ecophysiological foundations for adaptive management , 2011 .
[86] N. McDowell,et al. A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests , 2010 .
[87] Christoph Leuschner,et al. The different strategies of Pinus sylvestris and Larix sibirica to deal with summer drought in a northern Mongolian forest-steppe ecotone suggest a future superiority of pine in a warming climate , 2009 .
[88] Daniel M. Johnson,et al. Xylem hydraulic safety margins in woody plants: coordination of stomatal control of xylem tension with hydraulic capacitance , 2009 .
[89] Z. Fan,et al. Growth–climate responses of high-elevation conifers in the central Hengduan Mountains, southwestern China , 2009 .
[90] N. McDowell,et al. Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought? , 2008, The New phytologist.
[91] N. McDowell,et al. Homeostatic maintenance of ponderosa pine gas exchange in response to stand density changes. , 2006, Ecological applications : a publication of the Ecological Society of America.
[92] Christof Bigler,et al. Drought as an Inciting Mortality Factor in Scots Pine Stands of the Valais, Switzerland , 2006, Ecosystems.
[93] P. Villagra,et al. Water stress effects on the seedling growth of Prosopis argentina and Prosopis alpataco , 2006 .
[94] P. Zuidema,et al. Relating tree growth to rainfall in Bolivian rain forests: a test for six species using tree ring analysis , 2005, Oecologia.
[95] N. Cobb,et al. TREE-RING VARIATION IN PINYON PREDICTS LIKELIHOOD OF DEATH FOLLOWING SEVERE DROUGHT , 2000 .
[96] M. Linder,et al. Developing adaptive forest management strategies to cope with climate change. , 2000, Tree physiology.
[97] G. Aussenac. Interactions between forest stands and microclimate: Ecophysiological aspects and consequences for silviculture , 2000 .
[98] M. G. Ryan,et al. Hydraulic Limits to Tree Height and Tree Growth , 1997 .
[99] William T. Pockman,et al. Use of centrifugal force in the study of xylem cavitation , 1997 .
[100] J. Sperry,et al. Mechanism of water stress-induced xylem embolism. , 1988, Plant physiology.
[101] T. Wigley,et al. On the Average Value of Correlated Time Series, with Applications in Dendroclimatology and Hydrometeorology , 1984 .
[102] D. Smith,et al. Starch estimation in leaf tissue--a comparison of results using six methods. , 1974, Journal of the science of food and agriculture.
[103] Yuhong Dong,et al. Effects of stand density on soil microbial community composition and enzyme activities in subtropical Cunninghamia lanceolate (Lamb.) Hook plantations , 2021 .
[104] J. Camarero,et al. High resilience, but low viability, of pine plantations in the face of a shift towards a drier climate , 2021 .
[105] P. Reich,et al. Biomass allocation to leaves, stems and roots: meta-analyses of interspecific variation and environmental control. , 2012, The New phytologist.
[106] J. Kane,et al. Sensitivity of ring growth and carbon allocation to climatic variation vary within ponderosa pine trees. , 2012, Tree physiology.
[107] L. Poorter,et al. The importance of wood traits and hydraulic conductance for the performance and life history strategies of 42 rainforest tree species. , 2010, The New phytologist.
[108] Zhai Hongbo. Discussion on Rational Density of Larix principis-rupprechtii Plantation in Semi-arid Region , 2006 .
[109] M. Dobbertin. Tree growth as indicator of tree vitality and of tree reaction to environmental stress: a review , 2005, European Journal of Forest Research.
[110] A. Tyree,et al. Vulnerability of Xylem to Cavitation and Embolism , 1989 .
[111] R. Phipps,et al. Decline in long-term growth trends of white oak , 1988 .
[112] Melvin T. Tyree,et al. A method for measuring hydraulic conductivity and embolism in xylem , 1988 .
[113] S. Seifter,et al. The estimation of glycogen with the anthrone reagent. , 1950, Archives of biochemistry.