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1. Intraspecific diversity mitigates the negative soil‐legacy impacts of an invasive plant.

2. Negative plant–soil feedback influences a dominant seeded species, Western yarrow (Achillea millefolium), in grassland restoration.

3. No home-field advantage in upper Andean tropical forests despite strong differences in site environmental characteristics.

4. Prolonged drought legacies influence the performance of foliar herbivores on legumes through shifts in plant–soil biotic interactions.

5. A common ericoid shrub modulates the diversity and structure of fungal communities across an arbuscular to ectomycorrhizal tree dominance gradient.

6. Why are graminoid species more dominant? Trait‐mediated plant–soil feedbacks shape community composition.

9. Genotype diversity enhances invasion resistance of native plants via soil biotic feedbacks.

10. Distinct effects of phyllosphere and rhizosphere microbes on invader Ageratina adenophora during its early life stages

12. Plant–soil feedbacks among boreal forest species.

13. Field to Greenhouse: How Stable Is the Soil Microbiome after Removal from the Field?

14. The role of plant-fungus and plant-insect interactions in the dynamics of secondary and mature tropical rainforests

16. Removal of N‐fixing vs. non‐N‐fixing herbs in postfire chaparral: Competition and contributions to soil N and C cycling.

17. Synergistic effects of canopy chemistry and autogenic soil biota on a global invader.

18. Do plant–soil feedbacks promote coexistence in a sagebrush steppe?

19. Development of negative soil feedback by an invasive plant near the northern limit of its invaded range.

20. Fire modifies plant–soil feedbacks.

21. Light availability and plant shade tolerance modify plant–microbial interactions and feedbacks in subtropical trees.

22. Plant-soil interactions in response to grazing intensity in a semi-arid ecosystem from NE Spain.

23. Using root economics traits to predict biotic plant soil-feedbacks.

24. Local and non‐local soil microbiota impede germination of the endangered Acacia whibleyana.

25. The temporal and spatial dimensions of plant–soil feedbacks.

26. Removal of N‐fixing vs. non‐N‐fixing herbs in postfire chaparral: Competition and contributions to soil N and C cycling

27. Field to Greenhouse: How Stable Is the Soil Microbiome after Removal from the Field?

28. Spatial Structure within Root Systems Moderates Stability of Arbuscular Mycorrhizal Mutualism and Plant-Soil Feedbacks.

29. Global pine tree invasions are linked to invasive root symbionts.

30. Microbial drivers of plant richness and productivity in a grassland restoration experiment along a gradient of land‐use intensity.

31. Elevated P availability slows N recycling in northern hardwood forests.

34. Plant landscape abundance and soil fungi modulate drought effects on plant–soil feedbacks.

35. Bracken-induced increase in soil P availability, along with its high P acquisition efficiency, enables it to invade P-deficient meadows.

36. No robust multispecies coexistence in a canonical model of plant–soil feedbacks.

37. The functional form of specialised predation affects whether Janzen–Connell effects can prevent competitive exclusion.

38. A quantitative synthesis of soil microbial effects on plant species coexistence.

39. Direct and legacy‐mediated drought effects on plant performance are species‐specific and depend on soil community composition.

40. Of mutualism and migration: will interactions with novel ericoid mycorrhizal communities help or hinder northward Rhododendron range shifts?

41. Aboveground competition influences density‐dependent effects of cordgrass on sediment biogeochemistry.

42. Globally, plant‐soil feedbacks are weak predictors of plant abundance

43. Effects of three coniferous plantation species on plant‐soil feedbacks and soil physical and chemical properties in semi‐arid mountain ecosystems

45. Drought legacy in rhizosphere bacterial communities alters subsequent plant performance.

46. Positive heterospecific interactions can increase long‐term diversity of plant communities more than negative conspecific interactions alone.

47. Growth responses of ectomycorrhizal and arbuscular mycorrhizal seedlings to low soil nitrogen availability in a tropical montane forest.

48. Metapopulations with habitat modification.

49. Conspecific and heterospecific plant–soil biota interactions of Lonicera japonica in its native and introduced range: implications for invasion success.

50. Escape from natural enemies depends on the enemies, the invader, and competition

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