We suggest a way to estimate phytoplankton respiration separately from heterotrophic respiration. The analysis is based on three previous observations: (1) that carbon loss in the plankton overnight is phytoplankton respiration; (2) that phytoplankton respiration occurs during the day at the same rate as at night; and (3) that uptake of C estimates net primary production. Based on these three f...

The respiration of Escherichia coli is severely inhibited, during hyperosmotic stress period, as a consequence of plasmolysis; deplasmolysis allows the cell to recover respiration. A mutant lacking all K+ transport systems can neither deplasmolyze nor recover respiration unless betaine is present in the medium. Betaine, in these conditions, increases both cytoplasmic volume and respiration; thi...

Oral respiration associated with an obstructed nasal airway is common in orthodontic patients. For several years chronic oral respiration has been implicated as a prime causative factor in the development of "adenoid facies or the "long-face syndrome. The animal experiment reported here begins a series designed to study, as separate variables, the 2 components of chronic oral respiration: (1) c...

BACKGROUND AND AIMS Accounting for the acclimation of respiration of plants to temperature remains a major problem in analysis of carbon balances of plants and ecosystems. Translocation of carbohydrates out of leaves in the dark requires energy from respiration. In this study relationships between the responses of leaf respiration and translocation to temperature are examined. METHODS Direct ...

[1] Changes in soil respiration, one of the major fluxes of global carbon cycling, could significantly slow down or accelerate the increase in atmospheric CO2, with consequent feedbacks to climate change. It is critical to understand how substrate availability regulates soil respiration in projecting the response of carbon cycling to changed climate. We conducted a clipping and shading experime...

Although snags and coarse woody debris are a small component of ecosystem respiration, disturbances can significantly increase the mass and respiration from these carbon (C) pools. The objectives of this study were to (1) measure respiration rates of snags and coarse woody debris throughout the year in a forest previously defoliated by gypsy moths, (2) develop models for dead stem respiration r...

Respiration rate has been used as an indicator of metabolic rate and associated cost of transport (COT) of free-ranging cetaceans, discounting potential respiration-by-respiration variation in O2 uptake. To investigate the influence of respiration timing on O2 uptake, we developed a dynamic model of O2 exchange and storage. Individual respiration events were revealed from kinematic data from 10...

Respiration has a profound influence on crop yield because dry matter accumulation by a crop is closely related to assimilation of CO and respiratory activity. This paper describes the development of a 2 simulation model for respiration in wheat. While the growth respiration can be assumed to be proportional to the assimilation of CO , the model concentrated on the effects of biotic and environ...

Foliar respiration is a major component of ecosystem respiration, yet extrapolations are often uncertain in tropical forests because of indirect estimates of leaf area index (LAI). A portable tower was used to directly measure LAI and night-time foliar respiration from 52 vertical transects throughout an old-growth tropical rain forest in Costa Rica. In this study, we (1) explored the effects o...

Gametangia of the aquatic phycomycete Allomyces macrogynus have a cyanide- and antimycin A-insensitive respiration, which is sensitive to salicylhydroxamic acid (alternative respiration). Propyl gallate is also an inhibitor of this alternative pathway, and propyl gallate is more efficient than hydroxamic acid. Gametangial respiration is insensitive to propyl gallate, but propyl gallate sensitiv...