Tree diseases and landscape processes: The challenge of landscape pathology

Trends in Ecology and Evolution

Volumn 19, Issue 8, 2004, Pages 446-452

  Holdenrieder, Ottmar ^a   Pautasso, Marco ^a,b   Weisberg, Peter J ^c   Lonsdale, David ^d  

^a ETH ZURICH   (Switzerland)

^b UNIVERSITY OF SHEFFIELD   (United Kingdom)

^c UNIVERSITY OF NEVADA   (United States)

^d 33 Kings Road   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE; FOREST; HABITAT FRAGMENTATION; LANDSCAPE; PATHOLOGY;

EID: 3342927091     PISSN: 01695347     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tree.2004.06.003     Document Type: Review

References (79)

1. Hansen E.M. Disease and diversity in forest ecosystems. Aust. Plant Pathol. 28:1999;313-319
2. Johnson A.C., Wilcock P. Association between cedar decline and hillslope stability in mountainous regions of southeast Alaska. Geomorphology. 46:2002;129-142
3. Castello J.D., et al. Pathogens, patterns, and processes in forest ecosystems. Bioscience. 45:1995;16-24
4. Manion P.D., Griffin D.H. Large landscape scale analysis of tree death in the Adirondack Park, New York. For. Sci. 47:2001;542-549
5. Hansen E.M., Goheen E.M. Phellinus weirii and other native root pathogens as determinants of forest structure and process in western North America. Annu. Rev. Phytopathol. 38:2000;515-539
6. Kelly M., Meentemeyer R.K. Landscape dynamics of the spread of sudden oak death. Photog. Eng. Rem. Sens. 68:2002;1001-1009
7. Griffin J.M., et al. The distribution and severity of beech bark disease in the Catskill Mountains, NY. Can. J. For. Res. 33:2003;1754-1760
8. Yoshiko A., Dieter M.D. A landscape perspective of the Hawaiian rain-forest dieback. J. Veg. Sci. 6:1995;449-464
9. O'Neill R.V., et al. Epidemiology theory and disturbance spread on landscapes. Landsc. Ecol. 7:1992;19-26
10. Gilligan C.A. An epidemiological framework for disease management. Adv. Bot. Res. 38:2002;2-65
11. Park A.W., et al. Extinction times for closed epidemics: the effects of host spatial structure. Ecol. Lett. 5:2002;747-755
12. Vanderplank J.E. Plant Disease Epidemics and Control. 1963;Academic Press
13. Jeger M.J. Spatial Components of Plant Disease Epidemics. 1989;Prentice-Hall
14. Kranz J. Comparative Epidemiology of Plant Diseases. 2003;Springer
15. Coulston J.W., Riitters K.H. Geographic analysis of forest health indicators using spatial scan statistics. Environ. Manage. 31:2003;764-773
16. van Staden V., et al. Modelling the spatial distribution of two important South African plantation forestry pathogens. For. Ecol. Manage. 187:2004;61-73
17. Turner M.G. Landscape ecology - the effect of pattern on process. Annu. Rev. Ecol. Syst. 20:1989;171-197
18. Wilcove D.S. From fragmentation to extinction. Nat. Areas J. 7:1987;23-29
19. Hess G.R. Conservation corridors and contagious disease - a cautionary note. Conserv. Biol. 8:1994;256-262
20. Ledig F.T. Human impacts on genetic diversity in forest ecosystems. Oikos. 63:1992;87-109
21. Orwig D.A. Ecosystem to regional impacts of introduced pests and pathogens: historical context, questions and issues. J. Biogeogr. 29:2002;1471-1474
22. McCallum H., Dobson A. Disease, habitat fragmentation and conservation. Proc. R. Soc. Lond. Ser. B. 269:2002;2041-2049
23. Perkins T.E., Matlack G.R. Human-generated pattern in commercial forests of southern Mississippi and consequences for the spread of pests and pathogens. For. Ecol. Manage. 157:2002;143-154
24. Jules E.S., et al. Spread of an invasive pathogen over a variable landscape: a nonnative root rot on Port Orford cedar. Ecology. 83:2002;3167-3181
25. Hamelin R.C., et al. Barrier to gene flow between eastern and western populations of Cronartium ribicola in North America. Phytopathology. 90:2000;1073-1078
26. Manter D.K., et al. Assessment of Swiss needle cast disease: temporal and spatial investigations of fungal colonization and symptom severity. J. Phytopathol. 151:2003;344-351
27. Wilson B.A., et al. Spatial model for predicting the presence of cinnamom fungus (Phytophthora cinnamomi) in sclerophyll vegetation communities in south-eastern Australia. Aust. Ecol. 28:2003;108-115
28. McDougall K.L., et al. Distribution of Phytophthora cinnamomi in the northern jarrah (Eucalyptus marginata) forest of Western Australia in relation to dieback age and topography. Aust. J. Bot. 50:2002;107-114
29. Venier L.A., et al. A spatial, climate-determined risk rating for scleroderris disease of pines in Ontario. Can. J. For. Res. 28:1998;1398-1404
30. Pryce J., et al. Distribution of Phytophthora cinnamomi at different spatial scales: when can a negative result be considered positively? Aust. Ecol. 27:2002;459-462
31. Nevalainen S. The incidence of Gremmeniella abietina in relation to topography in southern Finland. Silva Fenn. 36:2002;459-473
32. Bernier D., Lewis K.J. Site and soil characteristics related to the incidence of Inonotus tomentosus. For. Ecol. Manage. 120:1999;131-142
33. Kallas M.A., et al. Modeling the probability of observing Armillaria root disease in the Black Hills. For. Pathol. 33:2003;241-252
34. Termorshuizen A.J., Arnolds E.J.M. Geographical distribution of the Armillaria species in The Netherlands in relation to soil type and hosts. Eur. J. For. Pathol. 24:1994;129-136
35. Camy C., et al. Soil factors associated with infection by Collybia fusipes and decline of oaks. For. Pathol. 33:2003;253-266
36. Hessburg, P.F. et al. (1999) Modeling change in potential landscape vulnerability to forest insect and pathogen disturbances: Methods for forested subwatersheds sampled in the midscale interior Columbia River basin assessment. USDA Forest Service, General Technical Report, PNW-GTR-454, 1-56.
37. Piou D., et al. Hosts and distribution of Collybia fusipes in France and factors related to the disease's severity. For. Pathol. 32:2002;29-41
38. Campbell E.M., Antos J.A. Distribution and severity of white pine blister rust and mountain pine beetle on whitebark pine in British Columbia. Can. J. For. Res. 30:2000;1051-1059
39. White M.A., et al. Landscape analysis of risk factors for white pine blister rust in the Mixed Forest Province of Minnesota, USA. Can. J. For. Res. 32:2002;1639-1650
40. Walchhuetter T., et al. Regeneration after dieback due to Phytophthora cinnamomi - are suppressive soils involved? Hansen E., Sutton W. Phytophthora Diseases of Forest Trees. 2000;40-43 IUFRO Working Party
41. Swinton J., Gilligan C.A. Dutch elm disease and the future of the elm in the UK: a quantitative analysis. Philos. Trans. R. Soc. Lond. Ser. B. 351:1996;605-615
42. Perry D.A. Landscape pattern and forest pests. Northw. Environ. 4:1988;213-228
43. Pautasso, M. et al. Susceptibility to fungal pathogens of forests differing in tree diversity. In The Functional Significance of Tree Species Diversity (Scherer-Lorenzen, M. et al., eds), Springer (in press).
44. Witzell J., Karlman M. Importance of site type and tree species on disease incidence of Gremmeniella abietina in areas with a harsh climate in Northern Sweden. Scand. J. For. Res. 15:2000;202-209
45. Le Guerrier C., et al. A modelling approach to assess the long-term impact of beech bark disease in northern hardwood forest. Can. J. For. Res. 33:2003;2416-2425
46. Hennon P.E., Shaw C.G. III. Did climatic warming trigger the onset and development of yellow-cedar decline in southeast Alaska? Eur. J. For. Pathol. 24:1994;399-418
47. Ayres M.P., Lombardero M.J. Assessing the consequences of global change for forest disturbance from herbivores and pathogens. Sci. Total Environ. 262:2000;263-286
48. Guillaumin J.-J., et al. Geographical distribution and ecology of the Armillaria species in western Europe. Eur. J. For. Pathol. 23:1993;321-341
49. Ristaino J.B., Gumpertz M.L. New frontiers in the study of dispersal and spatial analysis of epidemics caused by species in the genus Phytophthora. Ann. Rev. Phytopathol. 38:2000;541-576
50. Brandt J.P., et al. Factors affecting trembling aspen (Populus tremuloides Michx.) health in the boreal forest of Alberta, Saskatchewan, and Manitoba, Canada. For. Ecol. Manage. 178:2003;287-300
51. Ferguson B.A., et al. Coarse-scale population structure of pathogenic Armillaria species in a mixed-conifer forest in the Blue Mountains of northeast Oregon. Can. J. For. Res. 33:2003;612-623
52. McLaughlin J.A. Distribution, hosts, and site relationships of Armillaria spp. in central and southern Ontario. Can. J. For. Res. 31:2001;1481-1490
53. Hubbes M. Impact of molecular biology on forest pathology: a literature review. Eur. J. For. Pathol. 23:1993;201-217
54. Lundquist J.E., Klopfenstein N.B. Integrating concepts of landscape ecology with the molecular biology of forest pathogens. For. Ecol. Manage. 150:2001;213-222
55. Jackson R.B., et al. Linking molecular insight and ecological research. Trends Ecol. Evol. 17:2002;409-414
56. Manel S., et al. Landscape genetics: combining landscape ecology and population genetics. Trends Ecol. Evol. 18:2003;189-197
57. Malanson G.P., Cairns D.M. Effects of dispersal, population delays, and forest fragmentation on tree migration rates. Plant Ecol. 131:1997;67-79
58. Sork V.L., et al. Landscape approaches to historical and contemporary gene flow in plants. Trends Ecol. Evol. 14:1999;219-224
59. Dobson A.P., Crawley M. Pathogens and the structure of plant communities. Trends Ecol. Evol. 9:1994;393-398
60. Gilbert G.S. Evolutionary ecology of plant diseases in natural ecosystems. Annu. Rev. Phytopathol. 40:2002;13-43
61. Coops N., et al. Assessment of Dothistroma needle blight of Pinus radiata using airborne hyperspectral imagery. Phytopathology. 93:2003;1524-1532
62. Leckie D.G., et al. Detection and assessment of trees with Phellinus weirii (laminated root rot) using high resolution multi-spectral imagery. Int. J. Remote Sens. 25:2004;793-818
63. Clark D.B., et al. Quantifying mortality of tropical rain forest trees using high-spatial-resolution satellite data. Ecol. Lett. 7:2004;52-59
64. Francl, L.J. (2001) The disease triangle: a plant pathological paradigm revisited. Plant Health Instructor DOI: 10.1094/PHI-T-2001-0517-01 (http://www.apsnet.org).
65. Rizzo D.M., et al. Phytophthora ramorum as the cause of extensive mortality of Quercus spp. and Lithocarpus densiflorus in California. Plant Dis. 86:2002;205-214
66. Davidson J.M., et al. Phytophthora ramorum and Sudden Oak Death in California: II. Transmission and survival. USDA Forest Service, General Technical Report. PSW-GTR-184:2002;741-750
67. Stokstad E. Nurseries may have shipped Sudden Oak Death pathogen nationwide. Science. 303:2004;1959
68. Kelly N.M. Monitoring Sudden Oak Death in California using high-resolution imagery. USDA Forest Service, General Technical Report. PSW-GTR-184:2002;799-811
69. Kelly N.M., Tuxen K. WebGIS for monitoring 'Sudden Oak Death' in coastal California. Comp., Environ. Urb. Syst. 27:2003;527-547
70. Erwin D.C., Ribeiro O.K. Phytophthora Diseases Worldwide. 1996;APS Press
71. Gilbert M., et al. Long-distance dispersal and human population density allow the prediction of invasive patterns in the horse chestnut leafminer Cameraria ohridella. J. Anim. Ecol. 73:2004;459-468
72. Bennett A.F. Linkages in the Landscape. The Role of Corridors and Connectivity in Wildlife Conservation. 1999;IUCN
73. Thomas F.M., et al. Abiotic and biotic factors and their interactions as causes of oak decline in Central Europe. For. Pathol. 32:2002;277-307
74. Lewis K.J., Lindgren B.S. A conceptual model of biotic disturbance ecology in the central interior of BC: how forest management can turn Dr. Jekyll into Mr. Hyde. For. Chron. 76:2000;433-443
75. Gibbs J.N., et al. The impact of Phytophthora disease on riparian populations of common alder (Alnus glutinosa) in southern Britain. Eur. J. For. Pathol. 29:1999;39-50
76. Jung T., Blaschke M. Phytophthora root and collar root of alders in Bavaria: distribution, modes of spread and possible management strategies. Plant Pathol. 53:2004;197-208
77. Bicout D.J., Sache I. Dispersal of spores following a persistent random walk. Phys. Rev. E. 67:2003;031913
78. Caraco T., et al. Host spatial heterogeneity and the spread of vector-borne infection. Theor. Popul. Biol. 59:2001;185-206
79. Sherratt J.A., et al. The effects of the size and shape of landscape features on the formation of traveling waves in cyclic populations. Am. Nat. 162:2003;504-515