Articles containing the keyword 'shoots'

Damage on Scots pine (Pinus sylvestris L.) caused by Gremmeniella abietina (Lagerb.) Morelet was assessed in the summer of 1992 in 67 stands in eastern Lapland. The area and severity of damage were smaller and lighter than had earlier been estimated and occurred especially in stands in the first-thinning stage or in middle-age. Significant new infection of 1991 occurred in stands previously heavily infected by G. abietina near Kemihaara river, lake Naruska, the Naruska river, the Tuntsa river and lake Vilma. Fresh damage occurred mainly in the lower or middle parts of the Scots pine canopies.

• Kaitera, E-mail: jk@mm.unknown
• Jalkanen, E-mail: rj@mm.unknown

Shoot losses due to maturation feeding by pine shoot beetles (Tomicus piniperda (L.) and T. minor (Hart.), Col., Scolytidae) and subsequent growth losses were studied in Scots pine (Pinus sylvestris L.) stands growing at different distances from a timber yard, where pine timber was stored during the years 1982–84. In autumn 1985, pine trees were felled at 20, 40, 80, 500 and 1,500 m distance from the timber yard, five trees in each distance class. Trees were analysed for beetle attack, needle biomass and growth. In autumn 1988, increment cores were taken from 20 trees in each distance class.

In 1985, different damage estimates showed that beetle damage was more than 10-fold in the crowns of pine trees growing close to the timber yard as compared to less damaged trees in greater distance. Crude needle biomass estimates indicated that the trees attacked most had lost more than half of the total foliage. Following three years of attack, basal area growth decreased for 2–3 years and recovered during the subsequent 3 years, the total period of loss thus being 5–6 years. The loss in volume growth during 1983–85 was ca. 70, 40, 20 and 10% at 20, 40, 80 and 500 m distance from the beetle source, respectively, compared to the stand at 1,500. Growth losses did not occur until the number of beetle-attacks, ”pegs”, exceeded ca. 200 per tree. The highest observed growth losses occurred in trees with more than 1,000 pegs per tree.

The PDF includes an abstract in Finnish

• Långström, E-mail: bl@mm.unknown
• Hellqvist, E-mail: ch@mm.unknown

A study based on four young Scots pines (Pinus sylvestris L.) showed that the number of needle-covered shoots per crown volume unit was independent on tree position representing a constant value of 600–700 shoots/m³. This was true, even though the total shoot number decreased with deteriorating tree position. In tree crown there were fourth-order shoots in good light conditions but only first- and second-order-shoots, when light conditions were poor. The length of shoots decreased in accordance with increasing order of the shoot.

The share of the needle biomass and growth increased, when the shoot order increased. Similarly, the share of needles increased with deteriorating tree position. This was especially true in the upper crown. On the other hand, the share of the crown from the total biomass and growth increased with improving tree position. The percentage of crown system of a dominant tree in a sparse stand was 64% of that of biomass and 83% of that of growth. The corresponding values for a suppressed tree in a dense stand were 36% and 35%. The growth of wood, bark and needles in crown systems was linearly correlated with prevailing light conditions around the branch. It is evident that the tree position and light condition within the stand control the wood, bark and needle growth in the crown system and their interrelationships.

The PDF includes a summary in English.

• Viherä, E-mail: av@mm.unknown
• Kellomäki, E-mail: sk@mm.unknown

Downy birch (Betula pubescens Ehrh.) trees growing on a drained peatland were cut during dormancy. The properties of the one-year old shoots produced by the stumps were measured in the autumn after one growing season. The one-year old willow shoots (a mixture of Salix phylicifolia L., S. pentandra L. and S. caprea L.) were collected from an abandoned field.

The basic density of unbarked shoots was 443 kg/m³ for birch and 346 kg/m³ for willow. The basic density of the bark was much higher than that of the wood. The effect of shoot length on the properties was small with the exception of cellular proportions. The fibre percentage increased and vessel percentage decreased with increasing shoot length.

The PDF includes a summary in Finnish.

• Bhat, E-mail: kb@mm.unknown
• Ferm, E-mail: af@mm.unknown
• Kärkkäinen, E-mail: mk@mm.unknown

In the eastern parts of South-Finland the growing season of 1967 was highly favourable, which resulted in good height growth during the following year. During the summer 1968, temperature conditions were unfavourable, while the middle of summer was cold and the later part of the growing season unusually hot. The following winter had exceptionally cold spells from January to March, which caused Norway spruce (Picea abies (L.) H. Karst.) abundant winter frost damages such as dead shoots and buds, and destroyed needles.

These damages occurred particularly in stands with height of 0.5–3 m, and the occurrence of damages seemed to concentrate to the parts of saplings that had been immediately above the snow cover. Detailed observations on spruce plantations growing under a dense nurse stand of alder (Alnus sp.) indicated that explicitly the top shoots suffered from damages and not so much the laterals. When the needles of the leader suffered from minor damages, the shoot continued to grow normally. Still, sometimes a branch took over and became a new leader. If only the leader bud was killed, further stem development became dependent on one of the topmost lateral buds. When the upper part of the leaded died, one of the lateral shoots at its base usually became the new leader.

The PDF includes a summary in English.

• Yli-Vakkuri, E-mail: py@mm.unknown

The article deals with outer characters of a pine from Patsjoki-river, in Finnish Lapland (Pinus silvestris L. var. lapponica (Fr.) Hn.). The tables describe the length of the needles, length of the shoots, branching and inflorescence. The statistical calculations of the data are based on W. Johannsen’s  (Elemente der exakten Erblichkeitslehre, Jena 1909)  (Elements of exact genetics) methods. The results cannot be generalized because of the insufficient amount of data. 

• Renvall, E-mail: ar@mm.unknown