Environmental Change and Rising DOC Trends: Implications for Public Health

环境变化和 DOC 上升趋势：对公共卫生的影响

• 批准号: NE/G00286X/1
• 负责人: Christopher Freeman
• 金额: $ 55.03万
• 依托单位: Bangor University
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2009
• 资助国家: 英国
• 起止时间: 2009 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=NE%2FG00286X%2F1
• 关键词: Environmental; Change; Rising; DOC; Trends

This highly integrated multidisciplinary project engages the skills of environmental scientists, mathematical modellers, analytical chemists, toxicologists and public health scientists to address health vulnerability issues resulting from future environmental change impacts on soil-water ecosystems at a regional scale. It will address the health implications of a recently observed alarming trend for rising Dissolved Organic Carbon (DOC) concentrations in aquatic ecosystems used for potable water abstraction. Over the past two decades the concentration of dissolved organic carbon (DOC) in many source waters of these source waters has more than doubled and continues to rise (Freeman et al., 2001). There is increasing evidence to suggest that the process is being driven by environmental changes such as a decline in acid deposition (Evans et al., 2006; Monteith et al. 2007), combined with rising temperatures, increased frequency of drought and changes in the seasonal distribution of rainfall. We aim to analyse data from monitoring programmes and various other studies to allow us to predict the likely impact of future changes in climate and air pollution on DOC concentrations in water entering reservoirs and water treatment works. The increase in the level of DOC reaching water treatment works has major implications for human health. Organic matter in raw water is only partially removed by conventional treatment using inorganic coagulants; what remains may react with disinfectants. During chlorination of water supplies the chlorine reacts not only with the microorganisms but also with most of the other organic material present in the water, either dissolved or in suspension. This produces a range of organic compounds known as disinfection by-products (DPBs) including a group of chemicals called trihalomethanes (THMs), plus haloacetic acids, halonitriles, haloaldehydes and chlorophenols. We will carry out laboratory experiments to test the likely implications of the future changes in DOC we have predicted for the generation of these compounds within the water treatment system. Furthermore, a wide variety of other chemical contaminants, derived from air pollutants from industry, fertilizer application and urban waste water may bind (by sorption) to natural organic matter and be transported into reservoirs and water treatment works in association with DOC. Their fate within the treatment system, i.e. whether they are removed or remain within solution, depends heavily on the type of contaminant, the nature (or quality) of the DOC, the chemistry (e.g. pH and ionic strength) of the aqueous solution and the type of treatment process. We will carry out laboratory experiments to determine the extent to which these contaminants are bound to DOC at the point they enter the water treatment process and what is likely to happen as a result of the process, e.g. the extent to which contaminants are likely to be removed or remain in solution. Living organisms respond in various ways and on a spectrum of timescales when exposed to chemical contaminants. Some effects in organisms are immediate while others effects may be delayed and not show up for 10 or 20 years or more; for example, cancer in humans. We will draw on existing risk assessment approaches from national and international (EU) governmental agencies to evaluate the potential human health impacts of changes in levels of a range of contaminants under environmental change scenarios. Finally, we will bring together the findings of our research in the form of a Decision Support System (DSS) that will provide information to the water industry, the environmental agencies and other stake holders. The DSS will provide predictions of likely DOC trends under future climate change scenarios and the likely importance of predicted changes for wider water quality and human health.

这个高度综合的多学科项目吸引了环境科学家，数学建模者，分析化学家，毒理学家和公共卫生科学家的技能，以解决未来环境变化对土壤水域生态系统的影响，以区域规模对土壤水域生态系统产生影响。它将解决最近观察到的溶解有机碳（DOC）浓度在用于饮用水抽象的水生生态系统中溶解有机碳（DOC）浓度上升的趋势。在过去的二十年中，这些来源水域的许多来源水域中溶解有机碳（DOC）的浓度增加了一倍以上，并继续上升（Freeman等，2001）。越来越多的证据表明，这一过程是由环境变化所驱动的，例如酸沉积的下降（Evans等，2006； Monteith等人，2007年），加上温度上升，干旱频率的增加以及降雨量季节性分布的变化。我们旨在分析监测计划和其他各种研究的数据，以使我们能够预测气候和空气污染未来变化对进入水库和水处理厂水中DOC浓度的可能影响。到达水处理工作水平的增加对人类健康具有重大影响。原始水中的有机物仅通过使用无机凝血剂的常规处理来部分去除。剩下的可能与消毒剂反应。在氯化期间，氯不仅与微生物反应，而且还与水中存在的大多数有机材料（溶解或悬浮液中）反应。这会产生一系列称为消毒副产品（DPB）的有机化合物，包括一组称为三甲米甲烷（THMS）的化学物质，加上卤乙酸，氟硝基甲硝基酯，卤代醛和氯苯酚。我们将进行实验室实验，以测试我们预测在水处理系统中产生这些化合物的DOC的未来变化的可能含义。此外，来自工业，施肥和城市废水的空气污染物衍生而来的多种其他化学污染物可能与自然有机物结合（通过吸附）结合，并将其运输到储层中，水处理与DOC相关。它们在治疗系统中的命运，即是将其去除还是在解决方案中，在很大程度上取决于污染物的类型，DOC的性质（或质量），水溶液的化学（例如pH和离子强度）和处理过程的类型。我们将进行实验室实验，以确定这些污染物在进入水处理过程的程度以及由于过程中可能发生的情况，例如污染物可能被去除或留在溶液中的程度。暴露于化学污染物时，活生物体以各种方式和一系列时间尺度做出反应。生物体的某些影响是直接的，而其他影响可能会延迟，并且不会出现10或20年或更长时间；例如，人类的癌症。我们将利用来自国家和国际（欧盟）政府机构的现有风险评估方法，以评估环境变化情景下一系列污染物水平变化的潜在人类健康影响。最后，我们将以决策支持系统（DSS）的形式汇集我们的研究结果，该发现将为水产行业，环境机构和其他利益持有人提供信息。 DSS将在未来的气候变化情景下对可能的DOC趋势进行预测，以及预测变化对更广泛的水质和人类健康的重要性。

项目成果

Dissolved organic carbon and trihalomethane precursor removal at a UK upland water treatment works.

• DOI: 10.1016/j.scitotenv.2013.08.048
• 发表时间: 2014-01
• 期刊: The Science of the total environment
• 作者: R. Gough;P. Holliman;N. Willis;C. Freeman

A decision support system for drinking water production integrating health risks assessment.

• DOI: 10.3390/ijerph110707354
• 发表时间: 2014-07-18
• 期刊: International journal of environmental research and public health
• 作者: Delpla I;Monteith DT;Freeman C;Haftka J;Hermens J;Jones TG;Baurès E;Jung AV;Thomas O
• 通讯作者: Thomas O

The drinking water contaminant dibromoacetonitrile delays G1-S transition and suppresses Chk1 activation at broken replication forks.

• DOI: 10.1038/s41598-017-13033-8
• 发表时间: 2017-10-06
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Caspari T;Dyer J;Fenner N;Dunn C;Freeman C
• 通讯作者: Freeman C

Carbon preservation in humic lakes; a hierarchical regulatory pathway.

腐殖质湖泊的碳保存；

• DOI: 10.1111/gcb.12066
• 发表时间: 2013
• 期刊: Global change biology
• 影响因子: 11.6
• 作者: Fenner N