Many researchers are using sap flux to estimate tree-level transpiration, and to scale to standand catchment-level transpiration; yet studies evaluating the comparability of sap flux-based estimates of transpiration (Et) with alternative methods for estimating Et at this spatial scale are rare. Our ability to accurately scale from the probe to the tree to the watershed has not yet been demonstr...

[1] Assumed representative center-of-stand measurements are typical inputs to models that scale forest transpiration to stand and regional extents. These inputs do not consider gradients in transpiration at stand boundaries or along moisture gradients and therefore potentially bias the large-scale estimates. We measured half-hourly sap flux (JS) for 173 trees in a spatially explicit cyclic samp...

This study is focused on twoand three-dimensional incompressible flow past a circular cylinder for Reynolds number Re 6 1000. To gain insight into the mechanisms underlying the suppression of unsteadiness for this flow we determine the nonlinear optimal open-loop control driven by surface-normal wall transpiration. The spanwise-constant wall transpiration is allowed to oscillate in time, althou...

Variation in the sources of water used by tree species has important ramifications for forest water balances. The fraction of tree transpiration water derived from the unsaturated soil zone and groundwater in a riparian forest was quantified for Populus fremontii, Salix gooddingii, and Prosopis velutina across a gradient of groundwater depth and streamflow regime on the San Pedro River in south...

Rapid changes in the transpiration rate from a leaf or leafy shoot as a result of excision of that leaf or shoot have been observed in many plants bv many investigators (1, 2, 5, 7, 10, 11, 12, 13, 16). In banana plants, both photosynthesis and transpiration have been found to change rapidly following excision of the leaf (7). The mechanism underlying such rapid changes in transpiration has bee...

Stand transpiration was measured during the 2003 and 2004 growing seasons using heat dissipation sap flow sensors in a Scots pine (Pinus sylvestris L.) and a pubescent oak (Quercus pubescens Willd.) forests located in a montane area of the Eastern Pyrenees (NE Spain). The first aim of the study was to assess the differences in quantitative estimates of transpiration (Ec) and the response to eva...

We examined the extent of osmotic adjustment and the changes in relative water content (RWC) and transpiration rate (i.e., relative stomatal function) that occur in water-deficit-conditioned 6-year-old Thuja occidentalis L. (eastern white cedar) trees in response to a severe drought. Trees conditioned by successive cycles of mild or moderate nonlethal water stress (conditioning) and nonconditio...

Cottonwood (Populus spp.) forests are conspicuous and functionally important elements of riparian vegetation throughout much of the western U.S. Understanding how transpiration by this vegetation type responds to environmental forcing is important for determining the water balance dynamics of riparian ecosystems threatened by groundwater depletion. Transpiration was measured in semiarid riparia...

To quantify the relationship between temporal and spatial variation in tree transpiration, we measured sap flow in 129 trees with constant-heat sap flow sensors in a subalpine forest in southern Wyoming, USA. The forest stand was located along a soil water gradient from a stream side to near the top of a ridge. The stand was dominated by Pinus contorta Dougl. ex Loud. with Picea engelmannii Par...

Water conservation is a significant physiological problem for many insects, particularly as temperature increases. Early experimental work supported the concept of a transition temperature, above which water-loss rates increase rapidly as temperature increases. The transition phenomenon was hypothesized to result from melting of epicuticular lipids, the main barrier to cuticular transpiration. ...