A unified measure of the number, volume and diversity of dead trees and the response of fungal communities

Summary 1.  Much of ecological research focuses on the responses of species and species communities to variation in the amount and quality of resources that are required for survival and reproduction. In such research, it is critical to measure the availability of resources in a manner that is relevant in relation to the ecological requirements of the species. 2.  We have developed a measure for resource availability that integrates the contributions of the number, volume and diversity of resource units to quantify the amount of habitat that is available for a species community. We apply this measure to data on the occurrence of 116 species of wood-decaying polyporous fungi in 47 study plots of boreal forest within an area of 150 × 150 km. 3.  We show that species richness and pooled abundance of common species is explained well by the number of downed logs, whereas the occurrence of 41 red-listed species is best explained by the total volume of logs and by the abundance of large logs in particular. The occurrence of common species is explained by the local availability of dead wood, whereas the occurrence of red-listed species is additionally affected by the spatial connectivity of the focal forest stand to the surrounding larger expanses of old-growth forest. 4.  Our results elicit the contrasting ecologies of common and red-listed species in relation to how the number of logs, their size distribution and diversity, and forest connectivity affect species occurrences. The results suggest that the most cost-effective means of preventing further declines of threatened species is to increase the amount of large downed logs through restoration and biodiversity-oriented management in the vicinity of existing areas of natural-like forests. 5.  Synthesis. Our results illustrate that the most relevant way of measuring resource availability can differ greatly even within a taxonomically coherent community seemingly sharing the same resources. Our approach for modelling resource availability applies to the resources that occur as discrete objects with variation in the size and quality of individual resource units.

[1]  J. Siitonen,et al.  Significance of woodland key habitats for polypore diversity and red-listed species in boreal forests , 2008, Biodiversity and Conservation.

[2]  Lena Gustafsson,et al.  Dying and dead trees. A review of their importance for biodiversity , 1994 .

[3]  Otso Ovaskainen,et al.  The metapopulation capacity of a fragmented landscape , 2000, Nature.

[4]  G. Ståhl,et al.  Wood-inhabiting cryptogams on dead Norway spruce (Picea abies) trees in managed Swedish boreal forests , 1999 .

[5]  M. Villard,et al.  Foraging patterns of pileated woodpeckers in a managed Acadian forest: a resource selection function , 2005 .

[6]  L. Boddy,et al.  Interactions between saprotrophic fungi , 2008 .

[7]  J. Kouki,et al.  Are woodland key habitats in Finland hotspots for polypores (Basidiomycota)? , 2006 .

[8]  William N. Venables,et al.  Modern Applied Statistics with S , 2010 .

[9]  Lynne Boddy,et al.  Fungal decomposition of wood. Its biology and ecology. , 1988 .

[10]  Walter Krämer,et al.  Review of Modern applied statistics with S, 4th ed. by W.N. Venables and B.D. Ripley. Springer-Verlag 2002 , 2003 .

[11]  I. Hanski,et al.  Consequences of forest fragmentation for polyporous fungi at two spatial scales , 2006 .

[12]  B. Nordén,et al.  Conceptual problems of Ecological Continuity and its bioindicators , 2001, Biodiversity & Conservation.

[13]  J. Siitonen,et al.  Polypore diversity in managed and old-growth boreal Picea abies forests in southern Finland , 2004 .

[14]  Mike Rees,et al.  5. Statistics for Spatial Data , 1993 .

[15]  B. Nordén,et al.  Partial cutting reduces species richness of fungi on woody debris in oak-rich forests , 2008 .

[16]  Juha Siitonen,et al.  Forest management, coarse woody debris and saproxylic organisms: Fennoscandian boreal forests as an example , 2001 .

[17]  B. Jonsson,et al.  Colonization and extinction patterns of wood‐decaying fungi in a boreal old‐growth Picea abies forest , 2008 .

[18]  A. Cajander,et al.  Theory of forest types , 1926 .

[19]  J. Rolstad,et al.  Wood-decaying fungi in boreal forest: are species richness and abundances influenced by small-scale spatiotemporal distribution of dead wood? , 2004 .

[20]  Lynne Boddy,et al.  Ecology of Saprotrophic Basidiomycetes , 2008 .

[21]  L. Boddy,et al.  Interspecific combative interactions between wood-decaying basidiomycetes. , 2000, FEMS microbiology ecology.

[22]  P. Renvall Community structure and dynamics of wood-rotting Basidiomycetes on decomposing conifer trunks in northern Finland , 1995 .

[23]  Bengt Gunnar Jonsson,et al.  Ecology of Species Living on Dead Wood - Lessons for Dead Wood Management , 2005 .

[24]  Bengt Gunnar Jonsson,et al.  Fine woody debris is important for species richness on logs in managed boreal spruce forests of northern Sweden , 1999 .

[25]  Olli-Pekka Tikkanen,et al.  Red-listed boreal forest species of Finland : associations with forest structure, tree species, and decaying wood , 2006 .

[26]  I. Hanski The shrinking world : ecological consequences of habitat loss , 2005 .

[27]  J. Siitonen,et al.  Coarse woody debris, polyporous fungi and saproxylic insects in an old-growth spruce forest in Vodlozero National Park, Russian Karelia , 2001 .

[28]  L. Boddy,et al.  Chapter 7 Interactions between saprotrophic fungi , 2008 .

[29]  B. Nordén,et al.  Relative importance of coarse and fine woody debris for the diversity of wood-inhabiting fungi in temperate broadleaf forests , 2004 .

[30]  B. Jonsson,et al.  Verifying an Extinction Debt among Lichens and Fungi in Northern Swedish Boreal Forests , 2005 .

[31]  T. Ahti,et al.  Vegetation zones and their sections in northwestern Europe , 1968 .

[32]  J. Kouki,et al.  Assemblages of wood‐inhabiting fungi along the gradients of succession and naturalness in boreal pine‐dominated forests in Fennoscandia , 2006 .

[33]  B. Jonsson,et al.  Wood-inhabiting fungi and substratum decline in selectively logged boreal spruce forests , 1995 .

[34]  G. Gilbert,et al.  Polypore fungal diversity and host density in a moist tropical forest , 2002, Biodiversity & Conservation.

[35]  T. Niemelä,et al.  Interactions of fungi at late stages of wood decomposition. , 1995 .

[36]  Noel A. C. Cressie,et al.  Statistics for Spatial Data: Cressie/Statistics , 1993 .

[37]  I. Lindblad Wood-inhabiting fungi on fallen logs of Norway spruce: relations to forest management and substrate quality , 1998 .

[38]  Ilkka Hanski,et al.  Estimating the consequences of habitat fragmentation on extinction risk in dynamic landscapes , 2002, Landscape Ecology.

[39]  M. Keller,et al.  Coarse woody debris in undisturbed and logged forests in the eastern Brazilian Amazon , 2004 .

[40]  J. Rolstad,et al.  Using forest stand reconstructions to assess the role of structural continuity for late-successional species , 2002 .

[41]  L. Boddy,et al.  Chapter 5 Fruit bodies: Their production and development in relation to environment , 2008 .