Articles containing the keyword 'dormancy'

Studies of phenotypic as well as mixed population plasticities are urgently needed in a world that supposedly experiences a gradual change of its environment. It is important to understand that man creates his environment and silviculture. This is one of the reasons why for breeding it cannot be expected to find optimal phenotypes in nature. Other reasons are the phylogenetic constraints and migration of pollen and seeds.

Forest genetics up to now is characterized by the study of one trait at a time. There is an urgent need for simultaneous analysis of several traits by the aid of genetic correlations or multivariate analysis. Generally there is a need for inclusion of larger numbers of genetic entries in forest genetic investigations.

For the long-rotation-time species there is a need to determine the curves for degree of dormancy and hardiness during the annual cycle. Information of plasticity in two-dimensional environments like water availability and temperature is needed. Studies on nutrient utilization and acquisition will tell us whether or not we must have different breeding populations for different soil fertilities. An understanding of the phase changes between juvenile and adult opens up possible applications such as faster generation turn-over in the breeding population via early flowering and early testing as well as better plants for frost-prone and weedy sites.

• Eriksson, E-mail: ge@mm.unknown

The effect of photon flux density on bud dormancy release in two-year-old seedlings of Norway spruce (Picea abies (L.) H. Karst.) was examined. The seedlings were first chilled for 0–21 weeks under natural conditions and then forced in a warm greenhouse either in low (15 μEm^-2s^-1) or in high (300 μEm^-2s^-1) photon flux density. Occurrence of bud burst was observed in the forcing conditions, and the observations were used for estimating the cumulative frequency distribution of the chilling requirement for growth competence. The estimated distribution had greater variance in the low photon flux density than in the high photon flux density forcing. This finding suggests that unnaturally low photon flux densities during forcing may yield overestimates of the genetic within-population variation in the chilling requirement for growth competence.

The PDF includes an abstract in Finnish.

• Höyhtyä, E-mail: rh@mm.unknown
• Hänninen, E-mail: hh@mm.unknown

The relationships between bud dormancy and frost hardiness were examined using two-year-old Pinus sylvestris L. seedlings. The chilling temperatures used were +4 and -2°C. To examine the dormancy release of the seedlings, a forcing technique was used. Frost hardiness was determined by artificial freezing treatments and measurements of electrical impedance. At the start of the experiment, the frost hardiness of the seedlings was about -25°C. After the rest break, the seedlings kept at +4°C dehardened until after eight weeks their frost hardiness reached -5°C. At the lower chilling temperature (-2°C) the frost hardiness remained at the original level. When moved from +4 to -2°C, seedlings were able to reharden only after the time required for bud burst in the forcing conditions had reached the minimum.

The PDF includes an abstract in Finnish

• Valkonen, E-mail: mv@mm.unknown
• Hänninen, E-mail: hh@mm.unknown
• Pelkonen, E-mail: pp@mm.unknown
• Repo, E-mail: tr@mm.unknown

Models concerning the effects of temperature on dormancy release in woody plants were tested using two-year old seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.). Chilling experiments suggest that the rest period has a distinct end point. Before the attainment of this end point high temperatures do not promote bud development towards dormancy release, and after it further chilling does not affect the subsequent bud development. A new hypothesis of dormancy release is suggested on the basis of a comparison between present and earlier findings. No difference in the proportion of growth commencing seedlings were detected between the forcing temperatures of 17°C and 22°C. The rest break of 50% of Norway spruce and Scots pine seedlings required six and eight weeks of chilling, respectively. Great variation in the chilling requirement was found, especially for Scots pine.

The PDF includes an abstract in Finnish.

• Hänninen, E-mail: hh@mm.unknown
• Pelkonen, E-mail: pp@mm.unknown

Seasonal changed in total nitrogen, protein, amino acid, ammonia, nitrate and nitrite concentrations, and nitrate reductase and γ-glutamyltransferase activities in the needles, buds and shoots of young Scots pine (Pinus sylvestris L.) were studied. A relationship between the variation in the nitrogen metabolism and both winter dormancy and its breaking was proposed. Pine tissues stored soluble nitrogen over the winter largely in the form of arginine which, in addition to a high nitrogen content, can neutralize acidic cytoplasmic constituents such as nitrates and nitrites. Specific nitrate reductase and γ-glutamyltransferase activities were highest in late summer or autumn, and is apparently connected to the mobilization of nitrogen reserves for the winter.

The PDF includes an abstract in Finnish.

• Lähdesmäki, E-mail: pl@mm.unknown
• Pietiläinen, E-mail: pp@mm.unknown

This issue of Silva Fennica consists of eight articles, which are based on a co-nordic conference ”Frost hardiness and over-wintering in forest tree seedlings”, held in Joensuu, Finland, during December 1–3, 1986. The whole annual cycle of the trees is considered. Emphasis is given on methods for the study of frost hardiness, genetic variation in frost hardiness, nitrogen metabolism, bud dormancy release, and joint effect of natural and anthropogenic stress factors in the winter damage of forest trees. Practical implications for tree breeding and nursery management are discussed.

The PDF includes an abstract in Finnish.

• Hänninen, E-mail: –
• Pelkonen, E-mail: –

The occurrence of Caleopsis bifida on clear-cut and burned forest soil and its disappearance in 4–6 years after disturbance is attributed to its germination ecology. Initially the seeds are dormant 96–100% and remain dormant in nylon gaze bags in different types of forest humus layers at least 10 years. Dormancy is released in laboratory (1) by treatment of 100 ppm aqueous solution of GA₃, (2) by heating the dormant seeds to 40–55°C for 1–5 h, and (3) by 1% KNO₃ solution. It is concluded that conditions in clear-cut and burned areas favour germination of seeds in regard to temperature and content of nitrates in contrast to humus of closed vegetation where the seeds remain dormant.

The PDF includes an abstract in Finnish.

• Hintikka, E-mail: vh@mm.unknown

Logical structure of three simulation models and one conceptual model concerning effects of temperature on dormancy release in woody plants was examined. The three basic types of simulation models differed in their underlying assumptions. Contrasting implications of the models were inferred by deduction. With the aid of these implications, the model types can be tested using experiments with continuous and interrupted chilling. Similarly, implications of the conceptual model of rest phases were inferred, by which the model can be tested using experiments with continuous chilling and forcing in multiple temperatures. The possibilities to synthetize the conceptual model with any of the three simulation model types, as well as the biological interpretation of the model variables, were discussed.

The PDF includes an abstract in Finnish.

• Hänninen, E-mail: hh@mm.unknown

Six seed collections were made in September–December 1984 in a natural Scots pine (Pinus sylvestris L.) stand in Southern Finland. The seeds were germinated immediately after the cone collection and three photoperiods (0.8 and 24 hours) were used in germination tests.

The seeds collected in September and October possessed relative dormancy, i.e. they did not germinate in darkness and at 10°C. Later in November and December the seeds were capable to germinate in darkness and at low temperature also. The gradual change in germination capacity is attributed to chilling temperatures in natural environments or in cone storage.

The PDF includes a summary in English.

• Nygren, E-mail: mn@mm.unknown

Different approaches to the study of the annual rhythm of forest trees are described and compared by analysing the concepts and theories presented in the literature. The seasonality varying morphological and physiological state of forest trees is referred to as the annual rhythm s. lat., from which the annual ontogenetic rhythm is separated as a distinct type. The dormancy phenomena of the trees are grouped into four categories. Theories concerning the regulation of the annual rhythm are divided into two main types, the most common examples of which are the photoperiod theory and the temperature sum theory. Recent efforts towards a synthetic theory are described.

The PDF includes a summary in English.

• Hänninen, E-mail: hh@mm.unknown

The activation of CO₂ exchange was monitored in two Scots pine (Pinus sylvestris L.) seedlings transferred from the field to the laboratory in December. Gas exchange was monitored by an URAS I infrared gas analyser in a so-called open IRGA-system with trap type chambers. Transpiration was also measured at the same time by weighing the potted seedlings twice a day. The measuring period lasted eleven days. During the period, the level of both transpiration and net photosynthesis increased about ten times. Furthermore, it was found that the level of photosynthesis at high temperatures was relatively lower at the beginning than at the end of the measuring period.

The PDF includes a summary in English.

• Pelkonen, E-mail: pp@mm.unknown
• Smolander, E-mail: hs@mm.unknown

The premises of several models obtained from literature on bud dormancy release in trees from cool and temperate regions differs from each other with respect to responses to air temperature during the rest period of the buds. The predicted timing of bud burst in natural conditions varied among the models, as did the prediction of the models for the outcome of a chilling experiment.

Experimental results with two-year old seedlings of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) did not agree with any of the models. The experimental results also deviated from abundand earlier findings, which also disagreed with any of the models. This finding suggests that Finnish provenances of Scots pine and Norway spruce differ from more southern provenances with respect to temperature regulation of bud dormancy release.

A synthesis model for the effects of air temperature on bud dormancy release in trees was developed on the basis of the previous models and the experimental results of both the present and previous studies. The synthesis model contains part of the original models as special cases. The parameters of the synthesis model represent several aspects of the bud dormancy release of trees that should be addressed separately with each species and provenance in experimental studies. Further aspects of dormancy release were discussed, in order to facilitate further development of the models.

The PDF includes a summary in Finnish.

• Hänninen, E-mail: hh@mm.unknown

Germination tests in varying photoperiod- and temperature-regimes showed that for early autumn collections, germination of Scots pine (Pinus sylvestris L.) seeds is delayed, especially at low incubation temperature (+10°C) and in darkness. The presence of light during germination (8- or 24-hour photoperiod) or high incubation temperature (+20°C) enhanced germination. As autumn proceeded, a greater proportion of seed were able of germinate in darkness and also in low temperature regime. This result was consistent in both populations studied – in seeds from natural stand (Hyytiälä, Southern Finland) and in seeds from the Hyytiälä clone archive trees, growing in the same site.

An attempt was made to relate the development of germinability during autumn to previously accumulated chilling unit (optimum temperature +3.5°C) sum. Germination percent variation in subsequent cone-collection could not, however, be explained with accumulated chilling.

The PDF includes a summary in Finnish.

• Nygren, E-mail: mn@mm.unknown

• Kaunisto, Finnish Forest Research Institute, Parkano Research Station, Kaironiementie 54, FIN-39700 Parkano, Finland E-mail: seppo.kaunisto@metla.fi
• Sarjala, Finnish Forest Research Institute, Parkano Research Station, Kaironiementie 54, FIN-39700 Parkano, Finland E-mail: ts@nn.fi

• Hänninen, Plant Ecophysiology and Climate Change Group (PECC), Department of Biological and Environmental Sciences, Box 65, FI-00014 University of Helsinki, Finland E-mail: heikki.hanninen@helsinki.fi
• Kramer, Alterra, P.O. Box 47, 6700 AA Wageningen, The Netherlands E-mail: kk@nn.nl

The effect of cutting the root connection by detaching the shoot from the root system on dormancy release and vegetative bud burst was examined in 2-year-old seedlings of Norway spruce (Picea abies [L.] Karst.). Seedlings were transferred at 1–4 week intervals between October and January from outdoor conditions to experimental forcing in a heated greenhouse. Before forcing, half of the seedlings were cut above ground line, and the detached shoots were forced with their cut ends placed in water. The intact seedlings were forced with their root system remaining intact in the pots. Vegetative bud burst was observed visually. Cutting the root connection slightly increased days to bud burst in the forcing conditions, however, no consistent effect on bud burst percentage was found. Our preliminary seedling data suggest that using detached tree material in dormancy release experiments may have a small effect on bud burst date but it will evidently not lead to drastically erroneous conclusions. Further studies, using different seed lots, are needed to assess the effect of detaching on the dormancy release and bud burst, especially in adult trees.

• Partanen, Natural Resources Institute Finland (Luke), Management and Production of Renewable Resources, Juntintie 154, FI-77600 Suonenjoki, Finland E-mail: jouni.partanen@luke.fi
• Häkkinen, Natural Resources Institute Finland (Luke), Management and Production of Renewable Resources, P.O. Box 18, FI-01301 Vantaa, Finland E-mail: risto.hakkinen@luke.fi
• Hänninen, University of Helsinki, Department of Biosciences, Viikki Plant Science Centre (ViPS), P.O. Box 65, FI-00014 University of Helsinki, Finland E-mail: heikki.hanninen@helsinki.fi