Corrigendum to “High water vapour pressure deficit influence on Quercus ilex and Pinus pinea field monoterpene emission in the central Iberian Peninsula (Spain)”

2003 ◽  
Vol 37 (4) ◽  
pp. 587
Author(s):  
L. Núñez ◽  
J. Plaza ◽  
R. Pérez-Pastor ◽  
M. Pujadas ◽  
B.S. Gimeno ◽  
...  
2017 ◽  
Vol 284 (1867) ◽  
pp. 20171478 ◽  
Author(s):  
E. C. Eto ◽  
P. C. Withers ◽  
C. E. Cooper

Birds have many physiological characteristics that are convergent with mammals. In the light of recent evidence that mammals can maintain a constant insensible evaporative water loss (EWL) over a range of perturbing environmental conditions, we hypothesized that birds might also regulate insensible EWL, reflecting this convergence. We found that budgerigars ( Melopsittacus undulatus ) maintain EWL constant over a range of relative humidities at three ambient temperatures. EWL, expressed as a function of water vapour pressure deficit, differed from a physical model where the water vapour pressure deficit between the animal and the ambient air is the driver of evaporation, indicating physiological control of EWL. Regulating EWL avoids thermoregulatory impacts of varied evaporative heat loss; changes in relative humidity had no effect on body temperature, metabolic rate or thermal conductance. Our findings that a small bird can regulate EWL are evidence that this is a common feature of convergently endothermic birds and mammals, and may therefore be a fundamental characteristic of endothermy.


Food Research ◽  
2021 ◽  
Vol 5 (6) ◽  
pp. 109-118
Author(s):  
D. Lentzou ◽  
G. Xanthopoulos ◽  
C. Templalexis ◽  
A. Kaltsa

Transpiration and respiration are two mechanisms of water loss in fresh agricultural products, resulting in visual and texture degradation. Neglecting respiration as a mechanism of water loss may lead to erroneous results at saturation where water vapour pressure deficit is zero and thus water loss is expected to be zero, however, the existence of a finite water loss is noted. In this context, an analysis of the associated with transpiration and respiration water loss in figs (Ficus carica L.) was carried out at 0oC, 10oC and 20oC and 45.64%, 80.22% and 98.65% relative humidity as well as the air conditions of walk-in cold storage rooms. The estimated transpiration rate ranged between 0.11-1.416 mg cm-2 h -1 for a water vapour pressure deficit of 0.0-0.98 kPa. The water vapour pressure deficit estimation was based on the difference between cold air temperature and figs’ surface temperature. The respiration rate was calculated at 0oC, 10oC and 20oC as 0.47±0.08, 0.94±0.11 and 2.69±0.17 mLCO2100g-1 h -1 . Quantification of the water loss showed that at 20oC and saturation, the water loss due to respiration accounts for 3.9% of the respective water loss due to water vapour pressure deficit while on average, the water loss due to respiration accounts for 1.5%, 2.1% and 2.6% of the water loss due to water vapour pressure deficit at 0oC, 10oC and 20oC.


1981 ◽  
Vol 105 ◽  
pp. 41-44
Author(s):  
C.R.L Friend ◽  
D.J Hughes

Windley et al. (1973) have postulated that the Fiskenæsset anorthosite complex crystalIised under conditions of high water vapour pressure. This hypothesis readily explains several of the distinct characteristics of the complex. In particular, the late precipitation of chromitite layers towards the top of the complex in the anorthosite sensu stricto (Ghisler & Windley, 1967) is not normally expected in large layered intrusions (Wager & Brown, 1968), and is explained because the early precipitation of chromite is suppressed under such conditions (Shiraki, 1966). AIso, Windley et al. (1973) have suggested that chromium amphibole, rather than pyroxene, was precipitated in association with the chromite as a direct consequence of the enrichment of volatiles in the upper parts of the intrusion.


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