Effects of increasing saturation vapour pressure deficit on growth and ABA levels in black spruce and jack pine

Trees ◽  
1997 ◽  
Vol 11 (4) ◽  
pp. 223 ◽  
Author(s):  
Alan B. Darlington ◽  
Anna Halinska ◽  
James F. Dat ◽  
T. J. Blake
1986 ◽  
Vol 22 (4) ◽  
pp. 329-338 ◽  
Author(s):  
J. L. Monteith

SUMMARYIn monsoon climates, the mean daytime saturation vapour pressure deficit (D), measured at screen height, decreases from a maximum of 3–4 kPa attained several months before rain arrives to a minimum of 0.5–1 kPa in the month of highest rainfall. Climatic records from India and West Africa were analysed to give the relation between D and precipitation (P mm month−1) as:where n ranged from 0.5 to 0.9 between stations.The dependence of dry matter production on D and therefore on P is evaluated when growth is restricted by rain and when this restriction is removed by irrigation. In the first case, the decrease in demand for water associated with a decrease in D is comparable in importance with the increase of water supply (P). The analysis has implications for the marginal response of crops to supplemental irrigation and for the interpretation of experiments with a line-source or rain-shelter.


Forests ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 59
Author(s):  
Olivier Fradette ◽  
Charles Marty ◽  
Pascal Tremblay ◽  
Daniel Lord ◽  
Jean-François Boucher

Allometric equations use easily measurable biometric variables to determine the aboveground and belowground biomasses of trees. Equations produced for estimating the biomass within Canadian forests at a large scale have not yet been validated for eastern Canadian boreal open woodlands (OWs), where trees experience particular environmental conditions. In this study, we harvested 167 trees from seven boreal OWs in Quebec, Canada for biomass and allometric measurements. These data show that Canadian national equations accurately predict the whole aboveground biomass for both black spruce and jack pine trees, but underestimated branches biomass, possibly owing to a particular tree morphology in OWs relative to closed-canopy stands. We therefore developed ad hoc allometric equations based on three power models including diameter at breast height (DBH) alone or in combination with tree height (H) as allometric variables. Our results show that although the inclusion of H in the model yields better fits for most tree compartments in both species, the difference is minor and does not markedly affect biomass C stocks at the stand level. Using these newly developed equations, we found that carbon stocks in afforested OWs varied markedly among sites owing to differences in tree growth and species. Nine years after afforestation, jack pine plantations had accumulated about five times more carbon than black spruce plantations (0.14 vs. 0.80 t C·ha−1), highlighting the much larger potential of jack pine for OW afforestation projects in this environment.


1983 ◽  
Vol 13 (6) ◽  
pp. 1030-1036 ◽  
Author(s):  
G. F. Weetman ◽  
D. Algar

An old, merchantable, low-site class black spruce (Piceamariana (Mill.) B.S.P.) stand growing on a Lithic Humo-Ferric Podzol overlying a granite bedrock, and a younger but merchantable low-site class jack pine (Pinusbanksiana Lamb.) stand growing on a Ferro-Humic Podzol overlying a deep coarse sand near Baie Comeau, P.Q., were analysed for stand biomass and macronutrient contents of both stand and soil. The magnitude of the depletions of macronutrients from the site, in full-tree and tree-length methods of logging, are compared with their available and total quantities in the soil. The range of values from the literature for nutrient inputs are presented and discussed in relation to logging losses. The results suggest that full-tree logging in the dry jack pine stand could cause a severe loss of potentially mineralizable N supply; P, K, and Mg deficiency problems owing to export are not apparent, but a Ca balance problem is apparent. The implication is that full-tree logging should be avoided on such sites.


1998 ◽  
Vol 25 (3) ◽  
pp. 287 ◽  
Author(s):  
Saman P. Seneweera ◽  
Oula Ghannoum ◽  
Jann Conroy

The hypothesis that shoot growth responses of C4 grasses to elevated CO2 are dependent on shoot water relations was tested using a C4 grass, Panicum coloratum (NAD-ME subtype). Plants were grown for 35 days at CO2 concentrations of 350 or 1000 µL CO2 L-1. Shoot water relations were altered by growing plants in soil which was brought daily to 65, 80 or 100% field capacity (FC) and by maintaining the vapour pressure deficit (VPD) at 0.9 or 2.1 kPa. At 350 µL CO2 L-1, high VPD and lower soil water content depressed shoot dry mass, which declined in parallel at each VPD with decreasing soil water content. The growth depression at high VPD was associated with increased shoot transpiration, whereas at low soil water, leaf water potential was reduced. Elevated CO2 ameliorated the impact of both stresses by decreasing transpiration rates and raising leaf water potential. Consequently, high CO2 approximately doubled shoot mass and leaf length at a VPD of 2.1 kPa and soil water contents of 65 and 80% FC but had no effect on unstressed plants. Water use efficiency was enhanced by elevated CO2 under conditions of stress but this was primarily due to increases in shoot mass. High CO2 had a greater effect on leaf growth parameters than on stem mass. Elevated CO2 increased specific leaf area and leaf area ratio, the latter at high VPD only. We conclude that high CO2 increases shoot growth of C4 grasses by ameliorating the effects of stress induced by either high VPD or low soil moisture. Since these factors limit growth of field-grown C4 grasses, it is likely that their biomass will be enhanced by rising atmospheric CO2 concentrations.


1987 ◽  
Vol 63 (6) ◽  
pp. 446-450 ◽  
Author(s):  
James E. Wood ◽  
Richard Raper

In the alternate strip clearcutting system, first-cut strips are regenerated by seed produced by black spruce (Picea mariana [Mill.] B.S.P.) in the forested leave strips. However, after the second cut, such a seed source is not available for regenerating the leave strips. Therefore, the forest manager must consider a number of alternative regeneration options. The selection of the most appropriate regeneration option is dependent upon several economic and biological criteria. These include future costs of delivered wood, site productivity, post-harvest site condition, future alternative sources of supply, and future demand for industrial wood. Regeneration options such as preservation of advance growth and direct seeding are recommended for sites on which the manager is concerned primarily with regenerating first cut strips and is willing to accept a lower level of stocking in leave strips. Planting, the most intensive option discussed, should be reserved for sites offering the highest potential return or greatest future cost savings. Direct seeding of jack pine (Pinus banksiana Lamb.) should be considered on the upland portions of this patterned site type. Mixing jack pine and black spruce is a suggested regeneration option if the site contains both upland and lowland topographic positions. Other seeding options include the use of semi-transparent plastic seed shelters. The manager might consider combining two or more of these options to meet management objectives.


2017 ◽  
Vol 47 (8) ◽  
pp. 1116-1122 ◽  
Author(s):  
Rongzhou Man ◽  
Pengxin Lu ◽  
Qing-Lai Dang

Conifer winter damage results primarily from loss of cold hardiness during unseasonably warm days in late winter and early spring, and such damage may increase in frequency and severity under a warming climate. In this study, the dehardening dynamics of lodgepole pine (Pinus contorta Dougl. ex. Loud), jack pine (Pinus banksiana Lamb.), white spruce (Picea glauca (Moench) Voss), and black spruce (Picea mariana (Mill.) B.S.P.) were examined in relation to thermal accumulation during artificial dehardening in winter (December) and spring (March) using relative electrolyte leakage and visual assessment of pine needles and spruce shoots. Results indicated that all four species dehardened at a similar rate and to a similar extent, despite considerably different thermal accumulation requirements. Spring dehardening was comparatively faster, with black spruce slightly hardier than the other conifers at the late stage of spring dehardening. The difference, however, was relatively small and did not afford black spruce significant protection during seedling freezing tests prior to budbreak in late March and early May. The dehardening curves and models developed in this study may serve as a tool to predict cold hardiness by temperature and to understand the potential risks of conifer cold injury during warming–freezing events prior to budbreak.


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