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1. Macrofossil evidence for Quaternary plant extinction and vegetation change in western Tasmania

3. Burning giants in the tropics

17. The evolutionary history of Nothofagus (Nothofagaceae)

18. The AusTraits plant dictionary.

19. Arsenic and mercury exposure in different insect trophic guilds from mercury mining areas in Mexico.

20. Distinctive Arbutin-Containing Markers: Chemotaxonomic Significance and Insights into the Evolution of Proteaceae Phytochemistry.

21. No cell is an island: characterising the leaf epidermis using epidermalmorph, a new R package.

22. Convergent tip-to-base widening of water-conducting conduits in the tallest bryophytes.

23. Natural products isolation studies of the paleoendemic plant species Nothofagus gunnii and Nothofagus cunninghamii.

24. An agent based force vector model of social influence that predicts strong polarization in a connected world.

25. Diversity and abundance of soil microbial communities decline, and community compositions change with severity of post-logging fire.

26. Elimination communication contributes to a reduction in unexplained infant crying.

27. A Permeable Cuticle, Not Open Stomata, Is the Primary Source of Water Loss From Expanding Leaves.

28. A PEROXO-Tag Enables Rapid Isolation of Peroxisomes from Human Cells.

29. Leaf hydraulic conductance is linked to leaf symmetry in bifacial, amphistomatic leaves of sunflower.

30. Accuracy of ancestral state reconstruction for non-neutral traits.

31. Links between environment and stomatal size through evolutionary time in Proteaceae.

32. Distinct Drimane Chemotypes in Tasmanian Mountain Pepper ( Tasmannia lanceolata ): Differences in the Profiles of Pungent Leaf Phytochemicals Associated with Altitudinal Cline.

33. TRY plant trait database - enhanced coverage and open access.

34. Extended differentiation of veins and stomata is essential for the expansion of large leaves in Rheum rhabarbarum.

35. Wheat leaves embolized by water stress do not recover function upon rewatering.

36. The dimensionality of niche space allows bounded and unbounded processes to jointly influence diversification.

37. Similar geometric rules govern the distribution of veins and stomata in petals, sepals and leaves.

38. Development of 15 nuclear EST microsatellite markers for the paleoendemic conifer Pherosphaera hookeriana (Podocarpaceae).

39. Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera.

40. 2017 HIV Medicine Association of Infectious Diseases Society of America Clinical Practice Guideline for the Management of Chronic Pain in Patients Living With Human Immunodeficiency Virus.

41. 2017 HIVMA of IDSA Clinical Practice Guideline for the Management of Chronic Pain in Patients Living With HIV.

42. Habitat type and dispersal mode underlie the capacity for plant migration across an intermittent seaway.

43. Ferns are less dependent on passive dilution by cell expansion to coordinate leaf vein and stomatal spacing than angiosperms.

44. Amphistomatic leaf surfaces independently regulate gas exchange in response to variations in evaporative demand.

45. Two fossil species of Metrosideros (Myrtaceae) from the Oligo-Miocene Golden Fleece locality in Tasmania, Australia.

46. Vein density is independent of epidermal cell size in Arabidopsis mutants.

47. Cell expansion not cell differentiation predominantly co-ordinates veins and stomata within and among herbs and woody angiosperms grown under sun and shade.

48. Gondwanan conifer clones imperilled by bushfire.

49. Pliocene reversal of late Neogene aridification.

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