바로가기메뉴

본문 바로가기 주메뉴 바로가기

logo

  • KOREAN
  • P-ISSN2287-8327
  • E-ISSN2288-1220
  • SCOPUS, KCI

Examining the factors influencing leaf disease intensity of Kalopanax septemlobus (Thunb. ex Murray) Koidzumi (Araliaceae) over multiple spatial scales: from the individual, forest stand, to the regions in the Japanese Archipelago

Journal of Ecology and Environment / Journal of Ecology and Environment, (P)2287-8327; (E)2288-1220
2012, v.35 no.4, pp.359-365
Shota Sakaguchi (Kyoto University)
Michimasa Yamasaki (Kyoto University)
Chihiro Tanaka (Kyoto University)
Yuji Isagi (Kyoto University)

Abstract

We investigated leaf disease intensity of Kalopanax septemlobus (prickly castor oil tree) caused by the parasitic fungus Mycosphaerella acanthopanacis, in thirty natural host populations in the Japanese Archipelago. The disease intensity observed for individual trees were analyzed using a generalized additive model as a function of tree size, tree density,climatic terms and spatial trend surface. Individual tree size and conspecific tree density were shown to have significant negative and positive effects on disease intensity, respectively. The findings suggest that the probability of disease infection is partly determined by dispersal of infection agents (ascospores) from the fallen leaves on the ground, which can be enhanced by aggregation of host trees in a forest stand. Regional-scale spatial bias was also present in disease intensity;the populations in northern Japan and southern Kyushu were more severely infected by the fungus than those in southwestern Honshu and Shikoku. Regional variation of disease intensity was explained by both climatic factors and a trend surface term, with a latitudinal cline detected, which increases towards the north. Further research should be conducted in order to understand all of the factors generating the latitudinal cline detected in this study.

keywords
castor aralia, host density, interspecific interaction, leaf disease, tree size

Reference

1.

Burdon JJ, Chilvers GA. 1982. Host density as a factor in plant disease ecology. Annu Rev Phytopathol 20: 143-166.

2.

Burdon JJ, Thrall PH. 2000. Coevolution at multiple spatial scales: Linum marginale—Melampsora lini—from the individual to the species. Evol Ecol 14: 261-281.

3.

Caicedo AL. 2008. Geographic diversity cline of R gene homologs in wild populations of Solanum pimpinellifolium (Solanaceae). Am J Bot 95: 393-398.

4.

El Chartouni L, Tisserant B, Siah A, Duyme F, Leducq JB, Deweer C, Fichter-Roisin C, Sanssené J, Durand R, Halama P, Reignault P. 2011. Genetic diversity and population structure in French populations of Mycosphaerella graminicola. Mycologia 103: 764-774.

5.

Fujimori N. 2007. Mechanisms of population maintenance in sparsely distributed species, Kalopanax pictus. PhD Dissertation. Kyoto University, Kyoto, Japan.

6.

Fujimori N, Samejima H, Kenta T, Ichie T, Shibata M, Iida S, Nakashizuka T. 2006. Reproductive success and distance to conspecific adults in the sparsely distributed tree Kalopanax pictus. J Plant Res 119: 195-203.

7.

Gilbert GS. 2002. Evolutionary ecology of plant diseases in natural ecosystems. Annu Rev Phytopathol 40: 13-43.

8.

Gilbert GS, Hubbell SP, Foster RB. 1994. Density and distance-to-adult effects of a canker disease of trees in a moist tropical forest. Oecologia 98: 100-108.

9.

Hayden HL, Carlier J, Aitken EAB. 2003. Genetic structure of Mycosphaerella fijiensis populations from Australia, Papua New Guinea and the Pacific Islands. Plant Pathol 52: 703-712.

10.

Hayden HL, Carlier J, Aitken EAB. 2005. The genetic structure of Australian populations of Mycosphaerella musicola suggests restricted gene flow at the continental scale. Phytopathology 95: 489-498.

11.

Holdenrieder O, Pautasso M, Weisberg PJ, Lonsdale D. 2004. Tree diseases and landscape processes: the challenge of landscape pathology. Trends Ecol Evol 19: 446-452.

12.

Ito K. 1973. Jubyo-gaku Taikei II. Norin-syuppan, Tokyo. (in Japanese)

13.

Manel S, Schwartz MK, Luikart G, Taberlet P. 2003. Landscape genetics: combining landscape ecology and population genetics. Trends Ecol Evol 18: 189-197.

14.

McLaughlin JA. 2001. Distribution, hosts, and site relationships of Armillaria spp. in central and southern Ontario. Can J For Res 31: 1481-1490.

15.

Moore SM, Borer ET. 2012. The influence of host diversity and composition on epidemiological patterns at multiple spatial scales. Ecology 93: 1095-1105.

16.

Nossov DR, Hollingsworth TN, Ruess RW, Kielland K. 2011. Development of Alnus tenuifolia stands on an Alaskan floodplain: patterns of recruitment, disease and succession. J Ecol 99: 621-633.

17.

Ohashi H 1994. Nomenclature of Kalopanax septemlobus (Thunb. ex Murray) Koidzumi and classification of its infraspecific taxa (Araliaceae). J Jpn Bot 69: 28-31.

18.

Ohba H. 1999. Family Araliacecae. In: Flora of Japan, IIc (Iwatsuki K, Boufford DE, Ohba H, eds). Kodan-sha, Tokyo, pp 259-267.

19.

Osono T, Mori A, Koide K. 2004. Defoliation of giant dogwood (Swida controversa) caused by zonate leaf blight. Appl For Sci 13: 161-164.

20.

R Development Core Team. 2010. R version 2.12.0: A Language and Environment for Statistical Computing. R Development Core Team, Vienna.

21.

Sakaguchi S, Qiu YX, Liu YH, Qi XS, Kim SH, Han J, Takeuchi Y, Worth JRP, Yamasaki M, Sakurai S, Isagi Y. 2012. Climate oscillation during the Quaternary associated with landscape heterogeneity promoted allopatric lineage divergence of a temperate tree Kalopanax septemlobus (Araliaceae) in East Asia. Mol Ecol 21: 3823-3838.

22.

Sakaguchi S, Sakurai S, Yamasaki M, Isagi Y. 2010. How did the exposed seafloor function in postglacial northward range expansion of Kalopanax septemlobus? Evidence from ecological niche modelling. Ecol Res 25: 1183-1195.

23.

Sakaguchi S, Takeuchi Y, Yamasaki M, Sakurai S, Isagi Y. 2011. Lineage admixture during postglacial range expansion is responsible for the increased gene diversity of Kalopanax septemlobus in a recently colonised territory. Heredity (Ednib) 107: 338-348.

24.

Sakamoto Y. 1994. Life history of Mycosphaerella acanthopanacis causing the brown leaf spot of Kalopanax pictus. Trans Mtg Hokkaido Br Jpn For Soc 42: 123-125.

25.

Springer YP. 2007. Clinal resistance structure and pathogen local adaptation in a serpentine flax-flax rust interaction. Evolution 61: 1812-1822.

26.

Thompson J. 2005. The Geographic Mosaic of Coevolution. The University of Chicago Press, Chicago and London.

27.

Wood S. 2010. GAMs with GCV/AIC/REML smoothness estimation and GAMMs by PQL. http://cran.r-project.org/package=mgcv. Accessed 2012 Mar 1.

28.

Xiang Q, Lowry PP. 2007. Flora of China. Vol. 13. Science Press, Beijing and Missouri Botanical Garden Press, St. Louis, p 441.

29.

Yamazaki M, Iwamoto S, Seiwa K. 2009. Distance- and density-dependent seedling mortality caused by several diseases in eight tree species co-occurring in a temperate forest. Plant Ecol 201: 181-196.

Journal of Ecology and Environment