Articles containing the keyword 'xylem'

In this study the width and height of 1,588 uniseriate and 454 fusiform rays were measured from tangential sections of four Scots pine (Pinus sylvestris L.) trunks. The samples represented various height levels and distances from the pith. The average width of the uniseriate rays was 19.7 μm and that of the fusiform rays, 51.9 μm. The average height of the uniseriate rays was 215.7 μm and that of the fusiform rays 406.2 μm. Due to this difference in height, it may be possible to develop an automatic system for distinguishing between uniseriate end fusiform rays on the basis of their height.

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• Kärkkäinen, E-mail: mk@mm.unknown

The influence of various environmental factors on the diameter growth of trees has been studied based on data collected by following daily increment of trees and various environmental factors during the growing season in 1964–1967. The field work was carried out in two experimental stands, a Scots pine (Pinus sylvestris L.) stand and a mixed stands growing birch (Betula sp.), Norway spruce (Picea abies (L.) H. Karst.) and Scots pine, in Southern Finland.

The results show that the temperature sums preceding the beginning of diameter growth were of the same magnitude in the years studied, which indicates dependence in the relationship. Formation of new xylem cells took place in the pine stem ca. every third day when the diameter growth was most active. No summer growth inhibition was detected in diameter growth.

None of the cumulative temperature sums tried determined the time of cessation of diameter growth. In several cases, positive correlation was found between the length of the growing season and the width of the annual ring formed. When studying the relationships between the diameter increment and the environmental factors, it was found that diameter increment was totally masked in the records by the hydrostatic changes in the stem. Relationships between the diameter increment and the environmental factors of the second day preceding growth were found to be poor. In studying the deviations of the recorded daily increments from the regression surface, no clear general trend was seen for pine and spruce, but clear diminishing trend toward the end og the growing season could be seen for birch in 1967.

• Leikola, E-mail: ml@mm.unknown

It is commonly accepted that the period of early-spring xylem sap exudation marks a stage during which a positive pressure builds inside the tree trunks. This state changes when leaves appear, initiating water transport within the trunk. It is unknown, however, how the wood anatomical structure and its mechanical resistance influences the sap. We present the results of research on the relationship between exudation of sap from Betula pendula Roth trees from the interior of a forest stand and from its edge, and the anatomical structure of the trunk wood and its bending strength. During the period between March 21 and April 18, we performed five sets of measurements of sap exudation from trees at the edge of the stand and from the forest interior. The resulting radial wood samples were tested for bending strength using a fractometer. We tested the sap for electrolytic conductivity and sugars content. For the anatomical analysis of the wood, we determined the number of vessels per 1 mm², average vessel lumen area and potential conductivity index. We found that the trees along the edge of the stand exude more sap, but it is less concentrated than the sap from the trees from the interior. Bending strength perpendicular to wood fibres is higher in the trees from the stand edge and in the western side of the trunk, where the number of vessels per 1 mm² and conductivity index are smaller. Seemingly, this is the result of western winds, which are dominant in Poland.

• Zajączkowska, Department of Forest Botany, Faculty of Forestry, Warsaw University of Life Sciences, 159 Nowoursynowska St., 02-776 Warsaw, Poland E-mail: urszula.zajaczkowska@wl.sggw.pl
• Kaczmarczyk, Department of Forest Botany, Faculty of Forestry, Warsaw University of Life Sciences, 159 Nowoursynowska St., 02-776 Warsaw, Poland E-mail: karina.kaczmarczyk@wl.sggw.pl
• Liana, Department of Forest Botany, Faculty of Forestry, Warsaw University of Life Sciences, 159 Nowoursynowska St., 02-776 Warsaw, Poland E-mail: janusz.liana@wl.sggw.pl

In trees, xylem must fulfil three important tasks: conducting water to leaves, storing nutrients and water, and supporting the trunk. The origin of the trunk, i.e., seed or basal bud that forms sprouts, and the growth site may affect xylem anatomy, differences of which can affect successful growth of trees. Both seedlings and sprouts of downy birch (Betula pubescens Ehrh.) from four different growth sites with two different soil media, peat and mineral soil, were studied. The diameter of fibres and vessels and the thickness of the double fibre wall were measured, and the number of vessels, rays and axial parenchyma cells was counted. The fibre wall:lumen ratio, vessel percentage area and vessel size:number ratio were calculated. Xylem from sprouts showed only occasionally more mature characteristics than that of seedlings. The number of rays was similar at all four sites, but differences were observed in all other studied characteristics between sites, particularly if soil type was different. The vessel size and number correlated with the number of axial parenchyma cells in juvenile wood, which emphasises the importance of their connections with storage cells particularly at this stage of growth. Good water conductivity was connected with weaker wood, particularly in maturing wood.

• Luostarinen, School of Forest Sciences, University of Eastern Finland, P.O. Box 111, FI-80101 Joensuu, Finland E-mail: katri.luostarinen@uef.fi
• Hakkarainen, Natural Resources Institute of Finland (Luke), Yliopistokatu 6, FI-80100 Joensuu, Finland E-mail: katjahak@gmail.com
• Kaksonen, School of Forest Sciences, University of Eastern Finland, P.O. Box 111, FI-80101 Joensuu, Finland E-mail: hkaksone@gmail.com

• Luostarinen, University of Eastern Finland, School of Forest Sciences, P.O. Box 111, FI-80101 Joensuu, Finland E-mail: katri.luostarinen@uef.fi

• Susiluoto, University of Helsinki, Department of Forest Ecology, PL 27, 00014 University of Helsinki, Finland E-mail: sannamaija.susiluoto@helsinki.fi
• Berninger, Departement des Sciences biologiques, Université du Québec à Montréal, CP 8888 Succ Centre Ville, Montreal, Canada E-mail: fb@nn.ca

Trees are particularly susceptible to climate change due to their long lives and slow dispersal. However, trees can adjust the timing of their growing season in response to weather conditions without evolutionary change or long-distance migration. This makes understanding phenological cueing mechanisms a critical task to forecast climate change impacts on forests. Because of slow data accumulation, unconventional and repurposed information is valuable in the study of phenology. Here, I develop and use a framework to interpret what phenological patterns among provenances of a species in a common garden reveal about their leafing cues, and potential climate change responses. Species whose high elevation/latitude provenances leaf first likely have little chilling requirement, or for latitude gradients only, a critical photoperiod cue met relatively early in the season. Species with low latitude/elevation origins leafing first have stronger controls against premature leafing; I argue that these species are likely less phenologically flexible in responding to climate change. Among published studies, the low to high order is predominant among frost-sensitive ring-porous species. Narrow-xylemed species show nearly all possible patterns, sometimes with strong contrasts even within genera for both conifers and angiosperms. Some also show complex patterns, indicating multiple mechanisms at work, and a few are largely undifferentiated across broad latitude gradients, suggesting phenotypic plasticity to a warmer climate. These results provide valuable evidence on which temperate and boreal tree species are most likely to adjust in place to climate change, and provide a framework for interpreting historic or newly-planted common garden studies of phenology.

• Salk, Southern Swedish Forest Research Centre, Swedish University of Agricultural Sciences, P.O. Box 49, SE- 230 53 Alnarp, Sweden; Faculty of International Studies, Utsunomiya University, 350 Minemachi, Utsunomiya-shi, Tochigi 321-8505 Japan; Institute for Globally Distributed Open Research and Education (IGDORE) E-mail: carl.salk@slu.se

Physiological studies of long-lived trees are particularly important at this time, especially in light of the need for trees to adapt to global climate change. The results of the present studies were obtained on an approximately 700-year-old Quercus robur L. – the ‘Bartek’ oak. The tree has to adapt to changing climatic conditions, starting from the transition between the Medieval Warm Period and the Little Ice Age, up to the present time of rapid global climate change. Tomograph imaging showed decay of the tree trunk interior and revealed that undamaged wood forms a thin layer around the trunk perimeter. Two series of experiments were carried out to assess the physiological state of the tree. The first concerned measurements related to photosynthetic capacity: chlorophyll a fluorescence, gas exchange (CO₂ assimilation, transpiration), stomatal conductance and leaf water potential. The second series concerned xylem sap flow velocity and anatomical studies of stem wood. Photosynthetic capacity was within the limits reported for young healthy trees. The diurnal pattern of velocity of xylem sap flow was also typical for young vigorous trees and flow velocity correlated positively with solar radiation and negatively with air relative humidity. Anatomical observations of the outermost wood showed relatively narrow annuals rings with large diameter earlywood vessels. The results indicate that the veteran tree does not show signs of water stress probably due to a good balance of water flow and that leaf area of the canopy needs only the current ring of wood to feed transpiration of the canopy.

• Zajączkowska, Department of Forest Botany, Warsaw University of Life Sciences - SGGW, 159 Nowoursynowska Street, 02-776 Warsaw, Poland https://orcid.org/0000-0002-7119-7547 E-mail: urszula_zajaczkowska@sggw.edu.pl
• Dąbrowski, Department of Environmental Development Warsaw University of Life Sciences - SGGW, Warsaw, Poland https://orcid.org/0000-0002-2867-8839 E-mail: piotr_dabrowski@sggw.edu.pl
• Kowalczuk, Ekosystem Waldemar Kowalczuk Tomasz Kowalczuk, Otwock, Poland E-mail: ekosystem@ekosystem.waw.pl
• Tarwacki, Forest Protection Department, Forest Research Institute, Sękocin Las, Poland https://orcid.org/0000-0001-5979-7788 E-mail: G.Tarwacki@ibles.waw.pl