Bromoform production from seawater treated with bromoperoxidase

Bromoform (CHBr₃; 11–486 fmol L−1 h−1), dibromomethane (CH₂Br₂; 0–9.4 fmol L−1 h−1), and low amounts of chloride-substituted chlorobromomethanes were produced from southern California coastal surface seawater upon the addition of algal bromoperoxidase (BrPO) and hydrogen peroxide. Production was gre...

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Published inLimnology and oceanography Vol. 57; no. 6; pp. 1857 - 1866
Main Authors Lin, Chia Yu, Manley, Steven L.
Format Journal Article
LanguageEnglish
Published Waco, TX John Wiley and Sons, Inc 01.11.2012
American Society of Limnology and Oceanography
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Abstract Bromoform (CHBr₃; 11–486 fmol L−1 h−1), dibromomethane (CH₂Br₂; 0–9.4 fmol L−1 h−1), and low amounts of chloride-substituted chlorobromomethanes were produced from southern California coastal surface seawater upon the addition of algal bromoperoxidase (BrPO) and hydrogen peroxide. Production was greater from water collected near shore than 16 km offshore, presumably reflecting the difference in the reactive dissolved organic matter (DOMreact) concentrations. In the spring, there was an increase in phytoplankton abundance, and CHBr₃ production from BrPO incubations was greater, presumably due to increased DOMreact. In the winter, CH₂Br₂ production was enhanced, although still lower than CHBr₃, suggesting a qualitative change in DOM composition due to terrestrial runoff. During the month of the highest precipitation, CHBr₃ and CH2Br₂ production was enhanced in samples obtained from the mouth of an urban river, suggesting a higher concentration of DOMreact of terrestrial origins. DOM was fractionated by ultrafiltration and subject to the BrPO incubation. The higher molecular weight fractions contained a higher concentration of DOM that was susceptible to BrPO bromination, yielding polybromomethanes. Polybromomethane and iodomethane production associated with phytoplankton blooms results from the reaction between the surrounding DOM, and hypobromous acid (HOBr) and hypoiodous acid released from extracellular (apoplastic) BrPO. The reaction of HOBr and DOM (biological bleaching) could represent a significant DOM degradation pathway. Cell-free BrPO, derived from dead cells, could remain catalytically active in seawater and produce low amounts of polyhalomethanes prior to biological degradation.
AbstractList Bromoform (CHBr 3 ; 11–486 fmol L −1 h −1 ), dibromomethane (CH 2 Br 2 ; 0–9.4 fmol L −1 h −1 ), and low amounts of chloride‐substituted chlorobromomethanes were produced from southern California coastal surface seawater upon the addition of algal bromoperoxidase (BrPO) and hydrogen peroxide. Production was greater from water collected near shore than 16 km offshore, presumably reflecting the difference in the reactive dissolved organic matter (DOM react ) concentrations. In the spring, there was an increase in phytoplankton abundance, and CHBr 3 production from BrPO incubations was greater, presumably due to increased DOM react . In the winter, CH 2 Br 2 production was enhanced, although still lower than CHBr 3 , suggesting a qualitative change in DOM composition due to terrestrial runoff. During the month of the highest precipitation, CHBr 3 and CH 2 Br 2 production was enhanced in samples obtained from the mouth of an urban river, suggesting a higher concentration of DOM react of terrestrial origins. DOM was fractionated by ultrafiltration and subject to the BrPO incubation. The higher molecular weight fractions contained a higher concentration of DOM that was susceptible to BrPO bromination, yielding polybromomethanes. Polybromomethane and iodomethane production associated with phytoplankton blooms results from the reaction between the surrounding DOM, and hypobromous acid (HOBr) and hypoiodous acid released from extracellular (apoplastic) BrPO. The reaction of HOBr and DOM (biological bleaching) could represent a significant DOM degradation pathway. Cell‐free BrPO, derived from dead cells, could remain catalytically active in seawater and produce low amounts of polyhalomethanes prior to biological degradation.
Bromoform (CHBr3; 11–486 fmol L−1 h−1), dibromomethane (CH2Br2; 0–9.4 fmol L−1 h−1), and low amounts of chloride‐substituted chlorobromomethanes were produced from southern California coastal surface seawater upon the addition of algal bromoperoxidase (BrPO) and hydrogen peroxide. Production was greater from water collected near shore than 16 km offshore, presumably reflecting the difference in the reactive dissolved organic matter (DOMreact) concentrations. In the spring, there was an increase in phytoplankton abundance, and CHBr3 production from BrPO incubations was greater, presumably due to increased DOMreact. In the winter, CH2Br2 production was enhanced, although still lower than CHBr3, suggesting a qualitative change in DOM composition due to terrestrial runoff. During the month of the highest precipitation, CHBr3 and CH2Br2 production was enhanced in samples obtained from the mouth of an urban river, suggesting a higher concentration of DOMreact of terrestrial origins. DOM was fractionated by ultrafiltration and subject to the BrPO incubation. The higher molecular weight fractions contained a higher concentration of DOM that was susceptible to BrPO bromination, yielding polybromomethanes. Polybromomethane and iodomethane production associated with phytoplankton blooms results from the reaction between the surrounding DOM, and hypobromous acid (HOBr) and hypoiodous acid released from extracellular (apoplastic) BrPO. The reaction of HOBr and DOM (biological bleaching) could represent a significant DOM degradation pathway. Cell‐free BrPO, derived from dead cells, could remain catalytically active in seawater and produce low amounts of polyhalomethanes prior to biological degradation.
Bromoform (CHBr₃; 11–486 fmol L−1 h−1), dibromomethane (CH₂Br₂; 0–9.4 fmol L−1 h−1), and low amounts of chloride-substituted chlorobromomethanes were produced from southern California coastal surface seawater upon the addition of algal bromoperoxidase (BrPO) and hydrogen peroxide. Production was greater from water collected near shore than 16 km offshore, presumably reflecting the difference in the reactive dissolved organic matter (DOMreact) concentrations. In the spring, there was an increase in phytoplankton abundance, and CHBr₃ production from BrPO incubations was greater, presumably due to increased DOMreact. In the winter, CH₂Br₂ production was enhanced, although still lower than CHBr₃, suggesting a qualitative change in DOM composition due to terrestrial runoff. During the month of the highest precipitation, CHBr₃ and CH2Br₂ production was enhanced in samples obtained from the mouth of an urban river, suggesting a higher concentration of DOMreact of terrestrial origins. DOM was fractionated by ultrafiltration and subject to the BrPO incubation. The higher molecular weight fractions contained a higher concentration of DOM that was susceptible to BrPO bromination, yielding polybromomethanes. Polybromomethane and iodomethane production associated with phytoplankton blooms results from the reaction between the surrounding DOM, and hypobromous acid (HOBr) and hypoiodous acid released from extracellular (apoplastic) BrPO. The reaction of HOBr and DOM (biological bleaching) could represent a significant DOM degradation pathway. Cell-free BrPO, derived from dead cells, could remain catalytically active in seawater and produce low amounts of polyhalomethanes prior to biological degradation.
Author Lin, Chia Yu
Manley, Steven L.
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Issue 6
Keywords chlorides
sea water
rivers
gas chromatograms
hydrogen peroxide
bromine
runoff
concentration
degradation
North America
halides
offshore
hydrochemistry
organic materials
phytoplankton
plankton
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Snippet Bromoform (CHBr₃; 11–486 fmol L−1 h−1), dibromomethane (CH₂Br₂; 0–9.4 fmol L−1 h−1), and low amounts of chloride-substituted chlorobromomethanes were produced...
Bromoform (CHBr3; 11–486 fmol L−1 h−1), dibromomethane (CH2Br2; 0–9.4 fmol L−1 h−1), and low amounts of chloride‐substituted chlorobromomethanes were produced...
Bromoform (CHBr 3 ; 11–486 fmol L −1 h −1 ), dibromomethane (CH 2 Br 2 ; 0–9.4 fmol L −1 h −1 ), and low amounts of chloride‐substituted chlorobromomethanes...
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SubjectTerms Animal and plant ecology
Animal, plant and microbial ecology
Biological and medical sciences
Earth sciences
Earth, ocean, space
Exact sciences and technology
External geophysics
Fundamental and applied biological sciences. Psychology
Geochemistry
Mineralogy
Physical and chemical properties of sea water
Physics of the oceans
Sea water ecosystems
Silicates
Synecology
Water geochemistry
Title Bromoform production from seawater treated with bromoperoxidase
URI https://www.jstor.org/stable/26955262
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