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1. Warming and provenance limit tree recruitment across and beyond the elevation range of subalpine forest

2. Disturbance legacies and climate jointly drive tree growth and mortality in an intensively studied boreal forest

3. Growing‐season frost is a better predictor of tree growth than mean annual temperature in boreal mixedwood forest plantations.

4. Applying space‐for‐time substitution to infer the growth response to climate may lead to overestimation of tree maladaptation: Evidence from the North American White Spruce Network

5. Current and future drought vulnerability for three dominant boreal tree species.

6. No xylem phenotypic plasticity in mature Picea abies and Fagus sylvatica trees after 5 years of throughfall precipitation exclusion

7. Tree ring evidence of rapid development of drunken forest induced by permafrost warming

8. How tree species, tree size, and topographical location influenced tree transpiration in northern boreal forests during the historic 2018 drought

9. Warming induces divergent stomatal dynamics in co‐occurring boreal trees

10. Extraradical hyphae exhibit more plastic nutrient-acquisition strategies than roots under nitrogen enrichment in ectomycorrhiza-dominated forests.

11. Direct response of tree growth to soil water and its implications for terrestrial carbon cycle modelling

12. Spruce beetle outbreak was not driven by drought stress: Evidence from a tree‐ring iso‐demographic approach indicates temperatures were more important

13. Moisture‐driven shift in the climate sensitivity of white spruce xylem anatomical traits is coupled to large‐scale oscillation patterns across northern treeline in northwest North America

14. The climatic drivers of primary Picea forest growth along the Carpathian arc are changing under rising temperatures

15. Carbon flux from decomposing wood and its dependency on temperature, wood N 2 fixation rate, moisture and fungal composition in a Norway spruce forest

16. Dynamics of initial carbon allocation after drought release in mature Norway spruce-Increased belowground allocation of current photoassimilates covers only half of the carbon used for fine-root growth.

17. Cross‐scale controls on carbon emissions from boreal forest megafires

18. Drought response of five conifer species under contrasting water availability suggests high vulnerability of Norway spruce and European larch.

19. No xylem phenotypic plasticity in mature Picea abies and Fagus sylvatica trees after 5 years of throughfall precipitation exclusion.

20. Tree ring evidence of rapid development of drunken forest induced by permafrost warming.

21. Warming drives a front of white spruce establishment near western treeline, Alaska

22. Risk of genetic maladaptation due to climate change in three major European tree species

23. Carbon isotope discrimination indicates improving water-use efficiency of trees in northern Eurasia over the last 100 years.

24. Divergent long-term trends and interannual variation in ecosystem resource use efficiencies of a southern boreal old black spruce forest 1999-2017

25. High resilience of carbon transport in long-term drought-stressed mature Norway spruce trees within 2 weeks after drought release.

26. Trends in climatically driven extreme growth reductions of Picea abies and Pinus sylvestris in Central Europe.

27. Taxonomy, together with ontogeny and growing conditions, drives needleleaf species' sensitivity to climate in boreal North America

28. Stand basal area and solar radiation amplify white spruce climate sensitivity in interior Alaska: Evidence from carbon isotopes and tree rings

29. Disentangling the effects of acidic air pollution, atmospheric CO

30. Limited prospects for future alpine treeline advance in the Canadian Rocky Mountains

31. Stable carbon isotope analysis reveals widespread drought stress in boreal black spruce forests

32. How tree species, tree size, and topographical location influenced tree transpiration in northern boreal forests during the historic 2018 drought.

33. Warming induces divergent stomatal dynamics in co-occurring boreal trees.

34. Improved performance of the eastern spruce budworm on black spruce as warming temperatures disrupt phenological defences.

35. Large-scale disturbance legacies and the climate sensitivity of primary Picea abies forests

36. Quantitative losses vs. qualitative stability of ectomycorrhizal community responses to 3 years of experimental summer drought in a beech-spruce forest

37. Recent climatic drying leads to age-independent growth reductions of white spruce stands in western Canada

38. Silver fir and Douglas fir are more tolerant to extreme droughts than Norway spruce in south-western Germany

39. Deep peat warming increases surface methane and carbon dioxide emissions in a black spruce-dominated ombrotrophic bog

40. Survival of Norway spruce remains higher in mixed stands under a dryer and warmer climate

41. Interactive effects of elevated <scp>CO</scp> 2 and nitrogen deposition on fatty acid molecular and isotope composition of above‐ and belowground tree biomass and forest soil fractions

42. Autumn warming reduces the CO2sink of a black spruce forest in interior Alaska based on a nine-year eddy covariance measurement

43. Divergent species-specific impacts of whole ecosystem warming and elevated CO 2 on vegetation water relations in an ombrotrophic peatland.

44. Direct response of tree growth to soil water and its implications for terrestrial carbon cycle modelling.

45. Anthropogenic nitrogen deposition in boreal forests has a minor impact on the global carbon cycle

46. Warming and provenance limit tree recruitment across and beyond the elevation range of subalpine forest

47. Bud break responds more strongly to daytime than night-time temperature under asymmetric experimental warming

48. Climate-diameter growth relationships of black spruce and jack pine trees in boreal Ontario, Canada

49. Spruce beetle outbreak was not driven by drought stress: Evidence from a tree-ring iso-demographic approach indicates temperatures were more important.

50. Contrasting acclimation responses to elevated CO 2 and warming between an evergreen and a deciduous boreal conifer.

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