Aphyllophorales del Bosco della Mesola (Ferrara)

Abstract

Aphyllophorales from Mesola Forest (Ferrara) Italy—The present check-list is the first contribution to the knowledge of Aphyllophorales growing in the area of the Mesola Forest. The paper deals with 72 species of Aphyllophorales collected during the years 1980-1983. A further contribution will complete the picture of the Aphyllophorales flora which is particularly interesting and abundant in the forest.

Some of the species listed in the present paper are quite interesting since they are uncommon: Meruliopsis hirtellus and Oxyporus latemarginatus are new to Italy; Flaviporus semisupiniformis is the first European finding and the second world collection.     

Soil organic matter,nutrient distribution,fungal and microbial biomass and enzyme activities in a forest beech stand on the Apennines of southern Italy

The aim of this study was to analyse the amount and qualitative characteristics of organic matter (OM) in the litter horizon (considering leaf litter at different decomposition stages) and underlying soil to a 30-cm depth in a beech stand on the Apennines in southern Italy. Distribution of major nutrients as well as fungal and microbial biomass were also evaluated, in addition to beech leaf nutrient content monitor from full expansion to abscission in order to estimate annual nutrient input to soil from litterfall and nutrient retranslocation before abscission. OM was significantly higher in leaf litter. C/N ratio and the Na, Mn, Fe levels also decreased along the decomposition continuum, whereas N and S contents slowly decreased with soil depth. Generally, leaf nutrient content was also significantly lower in dead leaves, indicating efficient retranslocation to persistent organs. Fungal biomass was the highest in leaf layers, with no significant changes between spring and autumn samplings. Enzyme activities did not differ significantly along the decomposition continuum but marked decreases were found in the upper soil layer; these remained relatively constant, with the exception of laccase, at deeper soil depths. No seasonal effect on enzyme activities and OM content was found.     

Synthesis of cyclobutane nucleoside analogues 3: Preparation of carbocyclic derivatives of oxetanocin

Abstract

A synthesis of cyclobutene nucleoside analogs in which the nucleobase is tethered by a methylene group is described. The coupling of 6-chloropurine with 3-hydroxymethyl-cyclobutanone proceeds via its triflate to give both N-7 and N-9 regioisomers with relative yields corresponding to the calculated charge distribution of the 6-chloropurinyl anion. The stereoselective reduction of the N-alkylated ketones yielded quantitatively one stereoisomer in each case. The structural assignments were based on spectroscopic data and single crystal X-ray diffraction. Attempts to photoexcite the N-7 and N-9 ketones in order to promote ring-expansion did not ensue. Preliminary evidence suggests a photodecarbonylation to cyclopropanes took place.     

Assessment of trends in predation pressure on insects across temperate forest microhabitats

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