INTERACTION OF PHOTOCHEMICAL AND MICROBIAL PROCESSES IN THE DEGRADATION OF REFRACTORY DISSOLVED ORGANIC-MATTER FROM A COASTAL MARINE-ENVIRONMENT

Citation
Wl. Miller et Ma. Moran, INTERACTION OF PHOTOCHEMICAL AND MICROBIAL PROCESSES IN THE DEGRADATION OF REFRACTORY DISSOLVED ORGANIC-MATTER FROM A COASTAL MARINE-ENVIRONMENT, Limnology and oceanography, 42(6), 1997, pp. 1317-1324
Citations number
40
Categorie Soggetti
Oceanografhy,Limnology
Journal title
ISSN journal
00243590
Volume
42
Issue
6
Year of publication
1997
Pages
1317 - 1324
Database
ISI
SICI code
0024-3590(1997)42:6<1317:IOPAMP>2.0.ZU;2-R
Abstract
The interaction between photochemical and biological processes in the degradation of marine dissolved organic matter (DOM) was investigated with seawater from a coastal southeastern U.S. salt marsh. Seawater su pplemented with humic substances was exposed to alternating cycles of sunlight (equivalent to 8 h of midday sun) and dark incubations with n atural bacterial populations (1-2 weeks in length). Photochemical degr adation of the DOM was monitored during sunlight exposure by direct me asurements of dissolved inorganic carbon (DIC) and carbon monoxide (CO ) formation in 0.2-mu m filtered seawater. Bacterial degradation was m onitored during dark incubations by tritiated leucine uptake and chang es in bacterial numbers in bacterivore-free incubations and by direct measurements of DOM loss. The alternating cycles of sunlight and micro bial activity resulted in more complete degradation of bulk DOM and ma rine humic substances than was found for nonirradiated controls (i.e. with microbial activity alone) by a factor of up to 3-fold. Increased decomposition was due both to direct losses of carbon gas photoproduct s (DIC and CO in a 15:1 ratio) and to enhanced microbial degradation o f photodegraded DOM, with approximately equal contributions from each pathway. Mass balance calculations indicated that low-molecular-weight carbon photoproducts, currently considered to be the compounds respon sible for stimulating bacterial activity following photodegradation of DOM, were insufficient to account for the enhanced bacterial producti on observed. Thus, higher molecular weight, chemically uncharacterized fractions of DOM may also be modified to more biologically available forms during exposure to natural sunlight.