The occurrence of entomopathogenic fungi in soils from mid-field woodlots and adjacent small-scale arable fields

The aim of this study was to compare the species composition and the intensity of entomopathogenic fungi occurrence in the soil from mid-field woodlots and adjacent small farmlands. The study material consisted of soil samples taken from a mid-field woodlot and an adjacent small-scale arable field in three different localities in the vicinity of Siedlce. Entomopathogenic fungi were isolated from soil using two methods: the insect bait method and the selective medium. The comparative study showed that the soil from mid-field woodlots was characterized by a richer species composition of entomopathogenic fungi than of adjacent arable fields. A total of six fungal species representing the anamorphs of Hypocreales (Ascomycota) were isolated from the soil collected from mid-field woodlots: B. bassiana, B. brongniartii, M. anisopliae, M. flavoviride, I. farinosa and I. fumosorosea . The presence of only three species was reported in the farmland soil: B. bassiana, M. anisopliae and I. fumosorosea . This fact confirms the important role of semi-natural habitats as a source of biodiversity of entomopathogenic fungi in agricultural landscape. It was found that entomopathogenic fungi together formed more colony-forming units in the soil from arable fields than that of neighbouring mid-field woodlots. B. bassiana was the species of fungus which infected more bait insect larvae and formed significantly more colony-forming units (CFU) in the soil from mid-field woodlots than that of farmland in the localities studied, whereas the trend was the opposite in the case of I. fumosorosea and M. anisopliae . Given the presence of entomopathogenic fungi in the farmland soil in the three test places together, it was found that I. fumosorosea was dominant in the soil from the two arable fields, where this fungus infected more G. mellenella larvae and formed significantly more CFUs than the other species of fungi. M. anisopliae was the second most frequently isolated farmland species.

[1]  A. S. Silva,et al.  Natural Occurrence of Beauveria bassiana (Balsamo) Vuillemin (Hyphomycetes: Moniliales) on Anticarsia gemmatalis Hübner (Lepidoptera: Noctuidae) in the State of Mato Grosso do Sul , 2013 .

[2]  J. Karg,et al.  Effect of landscape structure on the occurrence of agrophagous pests and their antagonists. , 2009 .

[3]  J. Karg,et al.  Wpływ struktury krajobrazu na występowanie agrofagów i ich antagonistów w uprawach rolniczych , 2009 .

[4]  C. Tkaczuk Wystepowanie i potencjal infekcyjny grzybow owadobojczych w glebach agrocenoz i srodowisk seminaturalnych w krajobrazie rolniczym , 2008 .

[5]  N. Meyling Ecology of entomopathogenic fungi in agroecosystems , 2008 .

[6]  J. Spatafora,et al.  Phylogenetic classification of Cordyceps and the clavicipitaceous fungi , 2007, Studies in mycology.

[7]  Jørgen Eilenberg,et al.  Occurrence and distribution of soil borne entomopathogenic fungi within a single organic agroecosystem , 2006 .

[8]  C. Schweizer,et al.  Distribution of insect pathogenic soil fungi in Switzerland with special reference to Beauveria brongniartii and Metharhizium anisopliae , 2003, BioControl.

[9]  L. Ryszkowski,et al.  Impact of young shelterbelts on organic matter content and development of microbial and faunal communities of adjacent fields , 2003 .

[10]  J. Eilenberg,et al.  Effects of farming system, field margins and bait insect on the occurrence of insect pathogenic fungi in soils , 2002 .

[11]  M. Nowakowski,et al.  The effect of arable field margin composition on invertebrate biodiversity , 2002 .

[12]  S. Anna Field margins in northern Europe: their functions and interactions with agriculture , 2002 .

[13]  M. Altieri The ecological role of biodiversity in agroecosystems , 1999 .

[14]  M. Bidochka,et al.  Occurrence of the entomopathogenic fungi Metarhizium anisopliae and Beauveria bassiana in soils from temperate and near-northern habitats , 1998 .

[15]  D. Chandler,et al.  Sampling and occurrence of entomopathogenic fungi and nematodes in UK soils , 1997 .

[16]  C. Tkaczuk,et al.  Occurence of entomopathogenic fungi in different kinds of soil , 1996 .

[17]  I. Vänninen Distribution and occurrence of four entomopathogenic fungi in Finland: effect of geographical location, habitat type and soil type , 1996 .

[18]  P. Ewald,et al.  The evolution of virulence: a unifying link between parasitology and ecology. , 1995, The Journal of parasitology.

[19]  B. Głowacka,et al.  Wystepowanie grzybow owadobojczych w sciolce i glebie borow sosnowych w gradiencie skazenia srodowiska lesnego , 1995 .

[20]  M. Zurek,et al.  Temperature requirements of four entomopathogenic fungi , 1994 .

[21]  G. Storey,et al.  Penetration and Persistence of Commercially Formulated Beauveria bassiana Conidia in Soil of Two Tillage Systems , 1989 .

[22]  R. Gaugler Ecological considerations in the biological control of soil-inhabiting insects with entomopathogenic nematodes , 1988 .

[23]  R. A. Daoust,et al.  Survival of Beauveria bassiana (Deuteromycetes: Moniliales) Conidia on Cadavers of Cowpea Pests Stored Outdoors and in Laboratory in Brazil , 1986 .

[24]  G. Zimmermann The ‘Galleria bait method’ for detection of entomopathogenic fungi in soil , 1986 .

[25]  P. Ewald,et al.  Host-Parasite Relations, Vectors, and the Evolution of Disease Severity , 1983 .

[26]  W. Otieno Microbial Control of Pest and Plant Diseases 1970–1980 , 1982 .

[27]  P. Ferron,et al.  Pest control by the fungi Beauveria and Metarhizium , 1981 .

[28]  D. L. Hostetter,et al.  Stability of Conidia of an Entomopathogenic Fungus, Nomuraea rileyi , in and on Soil , 1978 .