The amounts of harvestable logging residues and stump and root wood were examined in the area where 100,000 solid m3 of stemwood was cut in 1975. The cutting amounts of stemwood from work sites suitable for harvesting of logging residues was 35,000 m3, and suitable for harvesting of stump and root wood 38,000 m3. The increase in the yield of wood (without bark) from logging residues compared with the unbarked stemwood was 2.4%. The same percentage of wood from stump and root wood was 5.0–5.8% depending on the harvesting loss.
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The utilization of stump and root wood is analysed in this paper on the basis of literature from middle of 19th century to the present date. According to the information available, the utilization of pine stumps in tar production was small compared to that of peeled Scots pine stemwood in the 19th century. During the 1st and 2nd World War the utilization of stumps for tar production reached its highest levels. Other industrial utilization of stumps has been small up to the present time but now stumps are beginning to be used in the pulp industry.
The greatest amounts of stumps have been utilized by the rural population. Stumps were used as fuel. In the thirties, the yearly amount used was over 200,000 m3 (solid measure), and even in the sixties over 100,00 m3. No industrial utilization method has yet reached these levels.
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The study was carried out in a Norway spruce (Picea abies (L.) H. Karst.) stand in Southern Finland which was to be clear-cut due to decay. The species composition and incidence of decay fungi were investigated from the cut surfaces of the stumps. In addition, the colour and size of the decayed spot was observed.
About 28% of the total number of trees were decayed. Fomes annosus (Heterobasidion annosum) was the most common decay fungus. It was identified from 75% of the decayed trees, and was the sole agent in 43% of these trees. Armillaria mellea was the second commonest decay fungus. It decayed trees mostly in combination with Fomes annosus. The most common colours of the decay produced by F. annosus were reddish or yellowish brown. The decay caused by A. mellea was blackish brown. The causative agent cannot be reliably identified on the basis of the colour of the decayed part.
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The aim of this investigation was to clarify aerial infection of Fomes annosus (now Heterbasision annosum) in the cross-sections of stumps of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) in Southern Finland. In addition, an attempt was made to study possibilities to reduce an eventual aerial infection by means of spreading various protecting substances on the cross-section of the stumps immediately after cutting. The stumps were treated withs creosote, ceruse (lead white) and a product named ”Ventti”, which active constituent is copper. The effect of prescribed burning of the site on the aerial spreading of the fungus was studied.
Five sample plots were located in spruce stands and one in a pine stand. One of the spruce stands was prescribed burned. Samples were taken from the stumps 14–17 and 24–29 months after cutting. To identify the fungi, the samples were cultivated on a nutrient substrate in laboratory conditions. The results show that Heterobasidion annosum had spread by air to cross-sections of stumps of spruce. 11.5% of the samples taken from the spruce stumps 14–17 months and 17% of samples taken 24–29 months after cutting were infected. Burning of the site reduced strongly the aerial infection of stumps by the fungus. The stumps of Scots pine were not infected by Heterobasidion annosum in this study. The infection could be limited by treating the cross-sections with substances that are used to prevent growth of mould.
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The aim of the study was to identify the microbes which reach the cut surface of Norway spruce (Picea abies (L.) Karst.) stumps during the first year after felling by means of air born spores, determine their occurrence frequency and the combinations in which they occur, investigate the colour changes in the wood caused by microbes and identify the microbial species isolated from the sap- and heart-wood.
The material consisted of 360 spruce stumps. 300 of the stumps were innoculated with five different fungi (Phlebia gigantea, Botrytis cinerea, Gliocladium deliquescens, Trichoderma viride, Verticicladiella procera) in order to inhibit air-born attack by Heterobasidion annosum. 60 stumps were left untreated as controls.
The cultural characteristics of the following fungi isolated from the stumps have been described e.g.: Ceraceomerulius serpens, Chondrostereum purpureum, Cylindrobasidium evolvens, Peniophora pithya, Phlebia gigantea (Phlebiopsis gigantea) , P. subserialis, Sistotrema brinhmannii, Bjerkandera adusta, Coriolellus serialis, Trametes zonata, Armillariella mellea, Panellus mitis, Nectria fucheliana (microconidial-stage), Ascocoryne cylichnium (conidial-stage), Leptographium lundbergii, Acremonium butyri, Gliocladium deliquescens, Verticicladiella procera.
The proportion of Basidiomycotina fungi out of the whole material was 53 %, Ascomycotina and Deuteromycotina fungi 37,6 % and bacteria 7,3 %.
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The incidence of the conidiophores of Fomes annosus (Heterobasision annosum) was investigated in Helsinki in 1967–71 in a Norway spruce (Picea abies (L.) H. Karst.) stand growing on a site of Oxalis-Myrtillus type. The investigation comprised stump surfaces of spruce and pieces of wood, decayed by F. annosus, placed on the ground.
Conidiophores and conidia were seen during a few weeks in May-June on the surfaces of stumps covered by spruce branches. Conidiophores were sometimes seen on the stump surfaces even later in the summer and autumn, but by that time they were only very few. Their occurrence on the stumps that had not been covered was extremely rare, and the conidiophores were always very few in number. Surfaces of trees felled the year before showed no conidiophores. Conidiophores were also found below the pieces of decayed wood lying on the ground.
When spruce trees decayed by F. Annosus were felled in the summer and autumn, the surfaces of stumps covered with spruce branches showed the first conidiophores one week after the felling. The occurrence continued almost uninterruptedly until the winter.
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An attempt was made to restrict the aerial distribution of Fomes annosus (now Heterobasidion annosum) through the cut surfaces of spruce stumps by inoculating the surfaces, immediately after felling, with mycelial suspension, grown in the laboratory on malt agar, of Fomes pinicola, Lenzites sepiaria, Peniophora gigantea (now Phlebiopsis gigantea), Polyporus abietinus and Trichoderma viride. Trees were felled once a month for a year. Samples were taken from the cut surfaces of the stumps approximately one year after the felling and the inoculation.
P. gigantea inhibited the infection of cut stump surfaces by airborne F. annosus. P. gigantea cut down both the total number and the number of the species of fungi infecting the stump through aerial distribution. T. viride had a parallel but less marked effect. F. pinicola, L. sepiaria and P. abietinus proved to be weak colonizers of spruce stumps. When they were used to inoculate the stumps, the number of fungi infecting the cut surfaces was larger than that infecting the stumps treated with P. gigantea and T. Viride. A year after the inoculation some stumps were excavated with their roots. Fungi from the discoloured spots of wood in the stumps were cultured for identification. It was found that many different fungal species from the soil and the points of root grafting had infected the roots of the stump in the course of the year. The majority of the identified microbes were non-Basidiomycetes fungi, and bacteria.
A year after the felling and inoculation, a white mycelial sheet was seen between the wood and bark of many stumps. Several fungi, including Armillaria mellea, Trichoderma viride, Penicillium species, and Peniophora gigantea were isolated from this sheet.
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In Finland the increasing use of biofuel in transport presupposes a search for new raw material sources for biorefining. The aim of this study was, at the regional level, to compare the procurement costs of logging residues, stumps, delimbed stems and cereal straw for biorefining. The accumulation and procurement costs of forest chips and cereal straw were estimated within a 100-kilometre transporting distance via existing road network from an end-use-facility located in Kouvola in South-East Finland. The analyses were performed as simulated treatments in thinnings of young stands, cereal fields and regeneration fellings using existing productivity and cost functions and yield calculations based on crop statistics, the forest industry stand data and the sample plots data of the National Forest Inventory of Finland. Accumulation of raw material assortments and costs of production stages were defined per dry tonnes. Subsidies and raw material prices were excluded from consideration in the study. The results indicate that recovering logging residues requires lower costs than utilization of stumps, delimbed stems or cereal straw. Cereal straw represents an important source of biomass in Kouvola but the cost competiveness is poor compared the procurement costs of forest chips. When the annual procurement volume of biomass was 50 000 dry tonnes the cost at the plant was 49 € dry tonne –1 and biomass was comprised totally of logging residues. Procurement cost grew to 59 € dry tonne –1 when the annual procurement volume of biomass was doubled to 100 000 dry tonnes. Of that amount, the proportion of logging residues was 58.4%, stumps 24.3% and delimbed stems 17.3%. First cereal straw dry tonnes were delivered to end-use-facility, when procurement cost grew to 60 € dry tonne –1 and annual procurement volume of biomass was 110 000 dry tonnes.
The density of Picea abies [L.] Karst. regeneration on different microsites, the quantity and quality of woody microsites, and seedling occurrence probability on stumps and fallen deadwood were studied in a subalpine forest that has been under protection for approximately 30–40 years (Gorce Mountains in the western Carpathians). Thirty percent of seedlings and 29% of saplings grew on stumps and fallen deadwood, while the remaining regeneration occurred on soil surface and mounds created by uprooted trees. The occurrence probability of Picea seedlings on fallen deadwood increased with deadwood diameter and decay stage and with the volume of living trees, and decreased with increased density of living trees, sapling density, and land slope. Furthermore, seedlings were more likely to grow on stumps with a greater diameter and in plots with higher sapling density, but less likely to grow on higher stumps. Stumps and fallen deadwood covered about 4% of the forest floor, but the material that is most important for promoting regeneration (strongly decomposed logs and those of a diameter exceeding 30 cm) took up only about 22 m2 ha-1. We have concluded that in a subalpine forest that has been protected for 30–40 years regeneration processes take place mostly on soil surface and stumps. The role of fallen deadwood increases over time as a greater number of suitable logs (in terms of size and decay stage) become available.