三丁基锡的命运

R. Lee
{"title":"三丁基锡的命运","authors":"R. Lee","doi":"10.1109/OCEANS.1989.586791","DOIUrl":null,"url":null,"abstract":"The degradation of TBT in natural waters is primarily due to biological processes resulting in TBT half-lives ranging from 4 to 14 days. In upper waters with high nutrient levels, microalgae or bottom plants can be important in TBT degradation. Biological TBT degradation in sunlight resulted in the production of various hydroxybutyldibutyltins. TBT half-life in sunlit estuarine water supplemented with nutrients was 1 day. Fine-grained sediments can catalyze the non-biological dealkylation of TBT to form monobutyltin and inorganic tin. The half-lives of TBT added to fine-grained sediments ranged from 2 to 4 days. Biological, i.e. microbial, degradation of TBT added to sandy sediments resulted in longer half-lives, e.g. 13 days for one sandy area. Further work is required to assess the fate of TBT in anaerobic sediments and the TBT associated with paint chips in the sediments. INTRODUCTION The fate of tributyltin, like other toxic organics, is determined by various physical, chemical and biological processes. Photolysis and biological degradation act to modify TBT in coastal waters. Some of the TBT adsorbs to suspended particulates and these particulates can be carried to the bottom by sedimentation. Chemical and biological degradation can degrade TBT in sediment to various metabolic products. Since the fate of TBT has recently been reviewed (Maguire, 1987; Seligman et al., 1989), this article briefly discusses processes affecting the fate of TBT and describes in more detail the latest work on TBT degradation in both sediment and water. Fate of TBT in Water At TBT concentrations of 1 pg/liter or less, there was biological degradation resulting in TBT half-lives of 414 days (Francois et al., 1989; Hattori et al., 1987; Hinga et a1.,1987; Olson and Brinckman, 1986; Seligman et al., 1989; Thain et al., 1987). At high TBT concentrations (= 1 mgfliter) degradation was very slow, presumably due to inhibition of TBT-degrading microorganisms (Seligman et al., 1986). In the dark bacteria and fungi are important in TBT degradation. Recent studies have shown that photosynthetic organisms in natural waters play an important role in TBT degradation (Francois et al., 1989; Lee et al., 1989; Olson and Brinkman, 1986). These studies demonstrated higher TBT degradation in sunlit estuarine water compared with dark degradation rates (Table l), production of hydroxybutyldibutyltins in the light but not in the dark (Table 2), and metabolism of TBT to dibutyltin and hydroxylated metabolites by cultures of diatoms and dinoflagellates (Table 3). Maguire et al. (1984) found that the freshwater green algae, Ankistrodesmus falcatus, degraded TBT to dibutyltin, a small amount of butyltin and inorganic tin. The marine green algae (Dunaliella tertiolecta) and chrysophytes (Isochrysis galbana and Cricosphuera ricoco) showed a very limited ability to degrade TBT (Table 2). Both diatom cultures and sunlit natural waters with added TBT produced hydroxybutyldibutyltin compounds, which included delta-hydroxybutyldibutyltin, gammahydroxybutyldibutyltin, and beta-hydroxybutyldibutyltin (Table 2). There was a significant increase in TBT when nitrate was added to estuarine water before light exposure. The TBT half-life was 1 day in nitrate supplemented water. There was no increase in TBT degradation when nitrate was added to water kept in the dark. Eel grass (Zostera marina) found in intertidal areas can degrade TBT to diand monobutyltin (Francois et al., 1989). The half-lives of TBT in eelgrass under light and dark were 6.7 days and 13.8 days, respectively. Sunlight photolysis of TBT was relatively slow (half-life = 90 days, Maguire et al., 1983), since TBT absorbs in the ultra-violet region. Sterilization of estuarine water before adding TBT followed by incubation under sunlight resulted in no significant degradation of TBT after 6 days (Lee et al., 1989). Possibly, TBT found in the surface microlayer (Maguire and Tkacz, 1987) could be more rapidly degraded by direct photolysis. Fate of TBT in Sediment TBT adsorbed to suspended particulates in the water can enter the bottom by sedimentation processes. The TBT can gradually desorb from these particles (Unger et al., 1988). In areas Table 1 Degradation of Radiolabeled and Nonlabeled Tributyltin (TBT) Added to Estuarine Water from Skidaway River (Savannah, GA) (Data from Lee et al., 1989) Initial TBT Month/ TBT Concentration Treatment Temperature Half-life (Witer) (days) 0.5 (unlabeled) Light Sept./28-29\"C 6 0.91 (unlabeled) Dark SeptJ28-29OC 9 1.5 (labeled) Light AugJ29\"C 6 1.5 (labeled) Dark Aug.129\"C 10 1.30 (unlabeled) Light Feb./lZ\"C 7 1.60 (unlabeled) Dark Feb.ll2OC 11 1.5 (labeled) Light Jan./l 1°C 8 1.5 (labeled) Dark Jan./l 1 \"C 13 0.4 (labeled) Light July/28 \"C 3 0.4 (labeled) Dark July128 \"C 7 512","PeriodicalId":331017,"journal":{"name":"Proceedings OCEANS","volume":"53 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1989-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Fate Of Tributyltin\",\"authors\":\"R. Lee\",\"doi\":\"10.1109/OCEANS.1989.586791\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The degradation of TBT in natural waters is primarily due to biological processes resulting in TBT half-lives ranging from 4 to 14 days. In upper waters with high nutrient levels, microalgae or bottom plants can be important in TBT degradation. Biological TBT degradation in sunlight resulted in the production of various hydroxybutyldibutyltins. TBT half-life in sunlit estuarine water supplemented with nutrients was 1 day. Fine-grained sediments can catalyze the non-biological dealkylation of TBT to form monobutyltin and inorganic tin. The half-lives of TBT added to fine-grained sediments ranged from 2 to 4 days. Biological, i.e. microbial, degradation of TBT added to sandy sediments resulted in longer half-lives, e.g. 13 days for one sandy area. Further work is required to assess the fate of TBT in anaerobic sediments and the TBT associated with paint chips in the sediments. INTRODUCTION The fate of tributyltin, like other toxic organics, is determined by various physical, chemical and biological processes. Photolysis and biological degradation act to modify TBT in coastal waters. Some of the TBT adsorbs to suspended particulates and these particulates can be carried to the bottom by sedimentation. Chemical and biological degradation can degrade TBT in sediment to various metabolic products. Since the fate of TBT has recently been reviewed (Maguire, 1987; Seligman et al., 1989), this article briefly discusses processes affecting the fate of TBT and describes in more detail the latest work on TBT degradation in both sediment and water. Fate of TBT in Water At TBT concentrations of 1 pg/liter or less, there was biological degradation resulting in TBT half-lives of 414 days (Francois et al., 1989; Hattori et al., 1987; Hinga et a1.,1987; Olson and Brinckman, 1986; Seligman et al., 1989; Thain et al., 1987). At high TBT concentrations (= 1 mgfliter) degradation was very slow, presumably due to inhibition of TBT-degrading microorganisms (Seligman et al., 1986). In the dark bacteria and fungi are important in TBT degradation. Recent studies have shown that photosynthetic organisms in natural waters play an important role in TBT degradation (Francois et al., 1989; Lee et al., 1989; Olson and Brinkman, 1986). These studies demonstrated higher TBT degradation in sunlit estuarine water compared with dark degradation rates (Table l), production of hydroxybutyldibutyltins in the light but not in the dark (Table 2), and metabolism of TBT to dibutyltin and hydroxylated metabolites by cultures of diatoms and dinoflagellates (Table 3). Maguire et al. (1984) found that the freshwater green algae, Ankistrodesmus falcatus, degraded TBT to dibutyltin, a small amount of butyltin and inorganic tin. The marine green algae (Dunaliella tertiolecta) and chrysophytes (Isochrysis galbana and Cricosphuera ricoco) showed a very limited ability to degrade TBT (Table 2). Both diatom cultures and sunlit natural waters with added TBT produced hydroxybutyldibutyltin compounds, which included delta-hydroxybutyldibutyltin, gammahydroxybutyldibutyltin, and beta-hydroxybutyldibutyltin (Table 2). There was a significant increase in TBT when nitrate was added to estuarine water before light exposure. The TBT half-life was 1 day in nitrate supplemented water. There was no increase in TBT degradation when nitrate was added to water kept in the dark. Eel grass (Zostera marina) found in intertidal areas can degrade TBT to diand monobutyltin (Francois et al., 1989). The half-lives of TBT in eelgrass under light and dark were 6.7 days and 13.8 days, respectively. Sunlight photolysis of TBT was relatively slow (half-life = 90 days, Maguire et al., 1983), since TBT absorbs in the ultra-violet region. Sterilization of estuarine water before adding TBT followed by incubation under sunlight resulted in no significant degradation of TBT after 6 days (Lee et al., 1989). Possibly, TBT found in the surface microlayer (Maguire and Tkacz, 1987) could be more rapidly degraded by direct photolysis. Fate of TBT in Sediment TBT adsorbed to suspended particulates in the water can enter the bottom by sedimentation processes. The TBT can gradually desorb from these particles (Unger et al., 1988). In areas Table 1 Degradation of Radiolabeled and Nonlabeled Tributyltin (TBT) Added to Estuarine Water from Skidaway River (Savannah, GA) (Data from Lee et al., 1989) Initial TBT Month/ TBT Concentration Treatment Temperature Half-life (Witer) (days) 0.5 (unlabeled) Light Sept./28-29\\\"C 6 0.91 (unlabeled) Dark SeptJ28-29OC 9 1.5 (labeled) Light AugJ29\\\"C 6 1.5 (labeled) Dark Aug.129\\\"C 10 1.30 (unlabeled) Light Feb./lZ\\\"C 7 1.60 (unlabeled) Dark Feb.ll2OC 11 1.5 (labeled) Light Jan./l 1°C 8 1.5 (labeled) Dark Jan./l 1 \\\"C 13 0.4 (labeled) Light July/28 \\\"C 3 0.4 (labeled) Dark July128 \\\"C 7 512\",\"PeriodicalId\":331017,\"journal\":{\"name\":\"Proceedings OCEANS\",\"volume\":\"53 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings OCEANS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/OCEANS.1989.586791\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings OCEANS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/OCEANS.1989.586791","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

摘要

天然水体中TBT的降解主要是由于生物过程导致TBT的半衰期为4至14天。在高营养水平的上层水域,微藻或底生植物对TBT的降解可能很重要。TBT在阳光下的生物降解导致了各种羟基丁基二丁丁酯的产生。TBT在添加营养物质的阳光照射的河口水中的半衰期为1 d。细粒沉淀物可以催化TBT的非生物脱烷基反应生成单丁基锡和无机锡。细粒沉积物中添加TBT的半衰期为2 ~ 4天。添加到沙质沉积物中的TBT的生物(即微生物)降解导致半衰期延长,例如一个沙质区域的半衰期为13天。需要进一步的工作来评估厌氧沉积物中TBT的命运以及沉积物中与油漆屑相关的TBT。与其他有毒有机物一样,三丁基锡的命运是由各种物理、化学和生物过程决定的。光解和生物降解作用改变了沿海水域的TBT。一些TBT吸附在悬浮颗粒上,这些颗粒可以通过沉降作用被带到底部。化学和生物降解可将沉积物中的TBT降解为各种代谢产物。由于最近对TBT的命运进行了审查(Maguire, 1987;Seligman et al., 1989),本文简要讨论了影响TBT命运的过程,并更详细地介绍了TBT在沉积物和水中降解的最新工作。当TBT浓度为1 pg/l或更低时,生物降解导致TBT的半衰期为414天(Francois et al., 1989;Hattori等人,1987;Hinga等,1987;奥尔森和布林克曼,1986;Seligman et al., 1989;Thain et al., 1987)。在高TBT浓度(= 1 mgflter)下,降解非常缓慢,可能是由于TBT降解微生物受到抑制(Seligman et al., 1986)。在黑暗中,细菌和真菌对TBT的降解很重要。最近的研究表明,天然水体中的光合生物在TBT降解中起着重要作用(Francois et al., 1989;Lee et al., 1989;奥尔森和布林克曼,1986)。这些研究表明更高的TBT退化阳光河口水与黑暗的降解率(表l)相比,生产的hydroxybutyldibutyltins光而不是在黑暗中(表2),和新陈代谢的TBT dibutyltin和羟化代谢产物硅藻和甲藻的文化(表3)。马奎尔et al。(1984)发现,淡水绿藻,纤维藻属falcatus,退化的TBT dibutyltin,少量的butyltin和无机锡。海洋绿藻(Dunaliella terolecta)和绿藻(Isochrysis galbana和Cricosphuera ricoco)对TBT的降解能力非常有限(表2)。添加了TBT的硅藻培养物和阳光照射下的自然水体都产生了羟基丁基二丁基锡化合物,包括δ -羟基丁基二丁基锡、γ -羟基丁基二丁基锡和β -羟基丁基二丁基锡(表2)。在光照前向河口水中添加硝酸盐,TBT显著增加。在添加硝酸盐的水中,TBT的半衰期为1天。在暗处的水中添加硝酸盐后,TBT的降解没有增加。潮间带发现的鳗鱼草(Zostera marina)可将TBT降解为二丁基锡和一丁基锡(Francois et al., 1989)。大叶藻中TBT在光照和黑暗条件下的半衰期分别为6.7 d和13.8 d。由于TBT在紫外线区吸收,因此TBT的阳光光解相对较慢(半衰期= 90天,Maguire et al., 1983)。在加入TBT之前对河口水进行灭菌,然后在阳光下孵育,6天后TBT没有明显降解(Lee et al., 1989)。可能,在表面微层中发现的TBT (Maguire和Tkacz, 1987)可以通过直接光解更快地降解。TBT吸附在水中的悬浮颗粒上,通过沉降过程进入水底。TBT可以逐渐从这些颗粒中解吸(Unger et al., 1988)。表1添加到Skidaway河(Savannah, GA)河口水中的放射性标记和非标记三丁基锡(TBT)的降解情况(数据来自Lee等人,1989)初始TBT月份/ TBT浓度处理温度半衰期(Witer)(天)0.5(未标记)Light Sept. 28-29"C 6 0.91(未标记)Dark Sept. 28- 29oc 9 1.5(已标记)Light AugJ29"C 6 1.5(已标记)Dark Aug.129"C 10 1.30(未标记)Light february /lZ"C 7 1.60(未标记)Dark february . ll2oc 11 1.5(已标记)Light january /l 1°C 8 1.5(已标记)Dark Jan. 1 /l 1°C 13 0.4(已标记)Light July/28 "C 3 0.4(已标记)Dark July/ 128 "C 7 512
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fate Of Tributyltin
The degradation of TBT in natural waters is primarily due to biological processes resulting in TBT half-lives ranging from 4 to 14 days. In upper waters with high nutrient levels, microalgae or bottom plants can be important in TBT degradation. Biological TBT degradation in sunlight resulted in the production of various hydroxybutyldibutyltins. TBT half-life in sunlit estuarine water supplemented with nutrients was 1 day. Fine-grained sediments can catalyze the non-biological dealkylation of TBT to form monobutyltin and inorganic tin. The half-lives of TBT added to fine-grained sediments ranged from 2 to 4 days. Biological, i.e. microbial, degradation of TBT added to sandy sediments resulted in longer half-lives, e.g. 13 days for one sandy area. Further work is required to assess the fate of TBT in anaerobic sediments and the TBT associated with paint chips in the sediments. INTRODUCTION The fate of tributyltin, like other toxic organics, is determined by various physical, chemical and biological processes. Photolysis and biological degradation act to modify TBT in coastal waters. Some of the TBT adsorbs to suspended particulates and these particulates can be carried to the bottom by sedimentation. Chemical and biological degradation can degrade TBT in sediment to various metabolic products. Since the fate of TBT has recently been reviewed (Maguire, 1987; Seligman et al., 1989), this article briefly discusses processes affecting the fate of TBT and describes in more detail the latest work on TBT degradation in both sediment and water. Fate of TBT in Water At TBT concentrations of 1 pg/liter or less, there was biological degradation resulting in TBT half-lives of 414 days (Francois et al., 1989; Hattori et al., 1987; Hinga et a1.,1987; Olson and Brinckman, 1986; Seligman et al., 1989; Thain et al., 1987). At high TBT concentrations (= 1 mgfliter) degradation was very slow, presumably due to inhibition of TBT-degrading microorganisms (Seligman et al., 1986). In the dark bacteria and fungi are important in TBT degradation. Recent studies have shown that photosynthetic organisms in natural waters play an important role in TBT degradation (Francois et al., 1989; Lee et al., 1989; Olson and Brinkman, 1986). These studies demonstrated higher TBT degradation in sunlit estuarine water compared with dark degradation rates (Table l), production of hydroxybutyldibutyltins in the light but not in the dark (Table 2), and metabolism of TBT to dibutyltin and hydroxylated metabolites by cultures of diatoms and dinoflagellates (Table 3). Maguire et al. (1984) found that the freshwater green algae, Ankistrodesmus falcatus, degraded TBT to dibutyltin, a small amount of butyltin and inorganic tin. The marine green algae (Dunaliella tertiolecta) and chrysophytes (Isochrysis galbana and Cricosphuera ricoco) showed a very limited ability to degrade TBT (Table 2). Both diatom cultures and sunlit natural waters with added TBT produced hydroxybutyldibutyltin compounds, which included delta-hydroxybutyldibutyltin, gammahydroxybutyldibutyltin, and beta-hydroxybutyldibutyltin (Table 2). There was a significant increase in TBT when nitrate was added to estuarine water before light exposure. The TBT half-life was 1 day in nitrate supplemented water. There was no increase in TBT degradation when nitrate was added to water kept in the dark. Eel grass (Zostera marina) found in intertidal areas can degrade TBT to diand monobutyltin (Francois et al., 1989). The half-lives of TBT in eelgrass under light and dark were 6.7 days and 13.8 days, respectively. Sunlight photolysis of TBT was relatively slow (half-life = 90 days, Maguire et al., 1983), since TBT absorbs in the ultra-violet region. Sterilization of estuarine water before adding TBT followed by incubation under sunlight resulted in no significant degradation of TBT after 6 days (Lee et al., 1989). Possibly, TBT found in the surface microlayer (Maguire and Tkacz, 1987) could be more rapidly degraded by direct photolysis. Fate of TBT in Sediment TBT adsorbed to suspended particulates in the water can enter the bottom by sedimentation processes. The TBT can gradually desorb from these particles (Unger et al., 1988). In areas Table 1 Degradation of Radiolabeled and Nonlabeled Tributyltin (TBT) Added to Estuarine Water from Skidaway River (Savannah, GA) (Data from Lee et al., 1989) Initial TBT Month/ TBT Concentration Treatment Temperature Half-life (Witer) (days) 0.5 (unlabeled) Light Sept./28-29"C 6 0.91 (unlabeled) Dark SeptJ28-29OC 9 1.5 (labeled) Light AugJ29"C 6 1.5 (labeled) Dark Aug.129"C 10 1.30 (unlabeled) Light Feb./lZ"C 7 1.60 (unlabeled) Dark Feb.ll2OC 11 1.5 (labeled) Light Jan./l 1°C 8 1.5 (labeled) Dark Jan./l 1 "C 13 0.4 (labeled) Light July/28 "C 3 0.4 (labeled) Dark July128 "C 7 512
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