Patterns of dark respiration in aquatic systems

2020 ◽  
Vol 71 (4) ◽  
pp. 432
Author(s):  
Mustafa Mantikci ◽  
Peter A. Staehr ◽  
Jørgen L. S. Hansen ◽  
Stiig Markager

We used continuous measurements of dissolved oxygen (DO) in dark bottles to characterise patterns of the dark respiration rate (Rdark) for three marine phytoplankton monocultures and in natural-water samples from two marine coastal systems. Furthermore, patterns of ecosystem community respiration rate were determined from open-water changes in DO in a fjord and in a lake. We considered two models of Rdark to describe temporal changes in DO: constant Rdark and decreasing Rdark; increasing Rdark. In addition, the effect of incubation time on Rdark was investigated in bottle incubations. Constant Rdark was observed in short-term (12-h) bottle incubations in natural-water samples from two marine coastal systems. Declining Rdark was observed in marine phytoplankton cultures and open-water measurements in a lake. Increasing Rdark was observed in open-water measurements in a fjord, particularly during summer. Long-term (120-h) bottle incubations in natural-water samples showed an increase in Rdark after 48 and 72h. We show that the conventional expectation of constant rates of respiration in darkness is far from typical, because non-linear changes are common under both controlled experimental conditions, as well as for open-water measurements of ecosystem respiration.

1990 ◽  
Vol 47 (5) ◽  
pp. 888-893 ◽  
Author(s):  
William J. Cooper ◽  
Richard G. Zepp

Hydrogen peroxide decay studies have been conducted in suspensions of several well-characterized soils and in natural water samples. Kinetic and product studies indicated that the decay was biologically-mediated, and could be described by pseudo first-order rate expressions. At an initial H2O2 concentration of 0.5 μM, the hydrogen peroxide half-life varied from 1 to 8 h. The decay was inhibited by thermal and chemical sterilization of the soils. Peroxidase activity was inferred in several natural water samples, where the suspended particles catalyzed the oxidation of p-anisidine by hydrogen peroxide. The mass spectrum of the major reaction product indicated that it was the dimer, possibly benzoquinone-4-methoxyanil, a product that also was observed from the horseradish peroxidase-catalyzed oxidation of p-anisidine by hydrogen peroxide.


Sign in / Sign up

Export Citation Format

Share Document