Investigating pesticide transport in the León-Chinandega aquifer, Nicaragua

Nicaragua’s León-Chinandega aquifer has seen extensive contamination by persistent organochlorine pesticides applied over decades of intensive agricultural activity. Models of flow and transport of a 330 km² sub-region of the aquifer were developed to test conceptual models of contaminant transport, to constrain the value of certain key transport parameters, and to investigate contamination-related concerns raised in past studies. To support these models, a variety of hydrogeologic and geochemical data were collected. It was concluded that the organochlorine pesticides seen in groundwater originate in soils, and are transported to the water table through widespread preferential flow, through shortcutting around wells, or through wind-blown particles delivered to poorly protected hand-dug wells. The distribution coefficient (K _d) of these pesticides is estimated to be between 0.1 and 100 ml/g and the concentration of pesticides being delivered to the water table is estimated to be between 10² and 10⁵ ng/L. It was found that the distribution and concentration of pesticides in the aquifer would be affected by an increase in groundwater abstraction within the region.

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Résumé L’aquifère du León-Chinandega au Nicaragua a été soumis à des contaminations étendues par des pesticides organochlorés persistants qui ont été répandus pendant des dizaines d’années d’agriculture intensive. Des modèles d’écoulement et de transport d’une sous-région de 330 km² de l’aquifère ont été construits pour tester des modèles conceptuels du transport de contaminants, pour contraindre la valeur de certains paramètres de transport clefs, et pour étudier les problèmes liés au transport de contaminations qui avaient été rencontrés lors d’études précédentes. Différents types de données hydrogéologiques et géochimiques ont été collectés pour réaliser ces modèles. La conclusion montre que les pesticides organochlorés rencontrés dans les eaux souterraines proviennent des sols et qu’ils sont transportés jusqu’à l’aquifère via de grandes zones d’écoulement préférentiel, via des raccourcis hydrauliques autour des puits, ou encore via des particules emportées par le vent et tombées dans des puits creusés à la main et mal protégés. Le coefficient de distribution (K _d) de ces pesticides est estimé entre 0.1 et 100 ml/g et la concentration de pesticides arrivant dans la nappe est estimée entre 10² et 10⁵ ng/L. L’étude a montré qu’une augmentation des prélèvements d’eau souterraine dans la région aurait un impact sur la distribution et la concentration des pesticides dans l’aquifère.

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Resumen El acuifero León-Chinandega (Nicaragua) presenta una contaminación extensiva por la aplicación de plaguicidas organoclorados en la agricultura intensiva durante décadas. Se han desarrollado modelos de flujo y transporte de una subregión del acuífero de 330 km² para comprobar los modelos conceptuales del transporte de contaminantes, estimar los valores de ciertos parámetros clave de transporte e investigar los temas relacionados con la contaminación en estudios anteriores. Para elaborar estos modelos, se recogió una variedad de datos hidrogeológicos y geoquímicos. Se ha concluido que los plaguicidas organoclorados presentes en el agua subterránea se originan en el suelo y son transportados hacia el nivel freático a través de flujos preferentes generalizados, a través de cortes alrededor de los pozos o a través de partículas transportadas por el viento depositadas en pozos excavados a mano con poca protección. El coeficiente de distribución (K _d) de estos plaguicidas se ha estimado entre 0.1 y 100 ml/g y la concentración de plaguicidas que sale hacia el nivel freático se estima que puede estar entre 10² y 10⁵ ng/L. Se ha concluido que el incremento de la extracción de aguas subterráneas dentro de la región afectaría la distribución y concentración de plaguicidas en el acuífero.

     

有机磷农药对扁藻的联合毒性研究

采用水生毒理联合效应相加指数法，比较了久效磷、辛硫磷、敌敌畏以及对硫磷的单剂和混合剂对扁藻的急性毒性和联合毒性。结果表明：久效磷和辛硫磷的联合毒性为协同作用；久效磷和敌敌畏的联合毒性为拮抗作用；久效磷和敌敌畏和对硫磷的48h联合毒性为协同作用，72h、96h则为拮抗作用。     

Enrichment of organochlorine contaminants in the sea surface microlayer: An organic carbon-driven process

Over 50 seawater samples from two different sites—Barcelona (Spain) and Banyuls-sur-Mer (France)—were analyzed in order to study the extent and postulate the processes driving the enrichment of hydrophobic organic pollutants in the sea surface microlayer (SML). A number of individual polychlorinated biphenyl (PCB) congeners (41) were measured to study their partitioning between the particulate (fraction > 0.7 μm) and the dissolved + colloidal phases (fraction < 0.7 μm), with the latter being differentiated into estimated dissolved and colloidal phases. In addition, several organochlorine pesticides were also measured, namely, HCB, α-HCH, γ-HCH, 4,4′-DDE, 4,4′-DDD and 4,4′-DDT. The presence of PCB congener profiles found in the SML suggests a dynamic coupling with the atmosphere in Banyuls sampling site, whereas offshore Barcelona the presence of highly chlorinated congeners was due to persistent sediment resuspension. The average PCB concentration in the SML dissolved + colloidal phase were higher in Banyuls (7.8 ng L^{− 1}) than in Barcelona (3.6 ng L^{− 1}) samples, but in the particulate phase concentrations were higher in Barcelona (3.2 ng L^{− 1}) to that of Banyuls (1.4 ng L^{− 1}). However, PCB concentrations in the SML generally also showed large variability. Enrichment factors of PCBs and other organochlorine compounds in the SML with respect to the underlying water column ranged from 0.2 to 7.4. This may be explained for both the dissolved + colloidal and particulate phases by the enrichment in the SML of organic carbon (OC) as discerned from particle–water and colloid–water partitioning.     

生物样品母乳中有机氯农药类化合物近二十年研究进展

有机氯农药(OCPs)至今是人体内残留浓度和检出率最高的有机污染物,母乳作为一种生物介质,被广泛用于人体中OCPs蓄积量、母乳中OCPs浓度的影响因素、婴幼儿母乳喂养期OCPs摄入量、人体中OCPs排泄动力学等研究领域。近二十年的研究表明:母乳中残留的OCPs主要有六氯苯(HCB)、滴滴涕(DDTs)和六六六(HCHs),浓度持续下降,总体上发展中国家高于发达国家,沿海地区高于内陆地区,热带地区高于其他地区;母乳中OCPs浓度主要受饮食习惯、年龄和分娩次数等因素的影响,在哺乳期浓度并不是持续下降,其排泄速度呈波动性变化趋势;不同国家和地区婴幼儿母乳喂养时OCPs日摄入量普遍低于WHO/FAO建议值,但在一些仍然使用OCPs的热带地区,婴幼儿OCPs日摄入量比WHO/FAO建议值高出几十倍。未来有关母乳中OCPs的研究将主要集中于:继续开展母乳中OCPs方法学研究,推进分析方法的标准化,提高评价方法和统计学方法的应用范围和可靠性;研究高暴露区和污染区OCPs对婴幼儿早期发育和未来生长健康的影响;研究OCPs在人体内的蓄积和排泄规律;结合统计学方法,开展母乳中OCPs与新生儿或成年人各种疾病相关性的统计流行病学研究。     

Distribution and Fate of Organochlorine Pollutants in the Pearl River Estuary

Samples of surface sediment and suspended particulate matter (SPM) were collected from the Pearl River estuary, China, and the distribution and concentration of hexachlorocyclohexanes (HCHs), DDTs and polychlorinated biphenyls (PCBs) were extensively studied. The concentration ranges of HCHs, DDTs and PCBs in the sediments were 0.28–1.23 ng g⁻¹, 1.36–8.99 ng g⁻¹ and 0.18–1.82 ng g⁻¹, respectively. The concentrations of HCHs, DDTs and PCBs in the SPM varied both with the sampling locations and the season of collection. Higher concentrations were recorded in the SPM as compared with sediments. The distribution pattern of such organochlorine compounds (OCs), in the Pearl River estuary, showed that sources were some major river mouths and input from Shenzhen Bay. The concentrations of OCs were, however, low as compared with other estuaries and seas. The environmental fate of the OCs during estuarine mixing was determined, in part, by physicochemical and biochemical properties. The absorption and sedimentation of SPM were also considered important factors. Marine sediments may, therefore, be regarded as an important reservoir of hydrophobic and persistent OCs.     

Distribution of organochlorine compounds in water, porewater and sediments in Xiamen Harbour

I~IOXAmong a large number of man-made chemicals, organochlorines such as DDTs, HCHs (hexachlorobenzene) are of great concern due to their highly bioaccumulative nature and toxic biological effects. These chemicals are persistent in nature, can biomagnify in the food web and imalvarious toxic effects in marine mammals. They can cause abnormal thyroid function in Herringgull, feminising in western gull, and can impair Avian reproduction, among other deleterious effects (Carmichael, 1988).Th…     

Fate and Behavior of Organochlorine Pesticides in the Indonesian Tropical Climate: A Study in the Segara Anakan Estuarine Ecosystem

The fate and behavior of organochlorine pesticides (OCPs) in the Segara Anakan Estuarine ecosystem was studied in the Indonesian tropical climate, which is characterized by heavy rainfall in the rainy season and low rainfall in the dry season. Since OCPs have high affinity for soil, a field study on the dissipation and degradation pattern of soil‐applied 1,1,1‐trichloro‐2,2‐bis (4‐chlorophenyl) ethane (p,p′‐DDT) and 1,1‐dichloro‐2,2‐bis (4‐chlorophenyl) ethylene (p,p′‐DDE) as model OCPs was carried out. They occurred at a faster rate in the biphasic mode in wet conditions and at a slower rate in dry conditions. In wet conditions, the conversion from p,p′‐DDT to p,p′‐DDE and p,p′‐DDD (1,1‐dichloro‐2,2‐bis (4‐chlorophenyl) ethane) was governed by a parallel reaction. In dry conditions, only p,p′‐DDE was formed. The fate and behavior of OCPs in sediment estuary are similar to those in soil under wet conditions, except that their sorption‐desorption constants are influenced by estuarine surface water salinity. In the dry season, due to high salinity, the sediment acts as an OCP sink and a secondary source for the ecosystem, causes higher OCP concentration of local bio‐monitors, i. e., Geloina spp. and Mugil spp. In the rainy season, high water inflow washed the desorbed OCP pesticides out of the estuarine ecosystem, and caused lower concentrations of bio‐monitors. A risk evaluation for the uptake of OCP pesticides during the dry season suggests that adult fish meal consumers are safe, but risk management is required for pregnant woman.     

Baseline survey of sediments and marine organisms in Liaohe Estuary: Heavy metals,polychlorinated biphenyls and organochlorine pesticides

A geographically extensive investigation was carried out to analyze the concentrations of heavy metals, PCBs and OCPs in the sediments and marine organisms collected from the Liaohe Estuary. In order to determine the spatial distribution and potential ecological risk of heavy metals, the surface sediments were collected from 44 sites in the Liaohe Estuary. The results showed that the heavy metal contents in the sediments were observed in the following order: Cr (11.2–84.8 mg/kg) > Cu (1.7–47.9 mg/kg) > Pb (4.3–28.3 mg/kg) > As (1.61–12.77 mg/kg) > Cd (0.06–0.47 mg/kg) > Hg (0.005–0.113 mg/kg). In comparison with the concentrations of heavy metals and POPs in other regions, the concentrations of As, Pb and DDTs in the Liaohe Estuary were generally low, and other pollutant concentrations were inconsistent with those reported in other regions. The contamination factor (CF), the pollution load index (PLI), the geoaccumulation index and the potential ecological risk index were used to analyze the pollution situation, which showed that the heavy metal pollution in Liaohe Estuary is mainly dominated by Cd and Hg. The concentrations of the four heavy metals varied significantly in the three kinds of tested organisms (fish, mollusk and crustacean), indicating the different accumulative abilities of the species. The results obtained in this study provide useful information background information for further ecology investigation and management in this region.     

Antioxidant responses to polycyclic aromatic hydrocarbons and organochlorine pesticides in green-lipped mussels (Perna viridis): Do mussels “integrate” biomarker responses?

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCs) are generally present in the marine environment in complex mixtures. The ecotoxicological nature of contaminant interactions, however, is poorly understood, with most scientific observations derived from single contaminant exposure experiments. The objective of this experiment was to examine dose-response relationships between antioxidant parameters and body contaminant levels in mussels exposed to different exposure regimes under laboratory conditions. Accordingly, the green-lipped mussel, Perna viridis, was challenged with a mixture of PAHs (anthracene, fluoranthene, pyrene, benzo[a]pyrene) and OC pesticides (α-HCH, aldrin, dieldrin, p,p′-DDT) over a 4 week period. Contaminants were delivered under four different dosing regimes, with all treatments receiving the same total contaminant load by the end of the exposure period. Antioxidant biomarkers were measured after 1, 2, 3 and 4 weeks, including glutathione (GSH), gluathione-S-transferase (GST), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR) and lipid peroxidase (LPO). GST and CAT were induced in hepatic tissues in most of the exposure regimes, with the majority of significant induction occurring in a constant exposure regime and a two-step alternate exposure regime. Significant differences among exposure regimes were detected in the body burden of contaminants after 28 days. Hepatic CAT and GSH are proposed as potentially useful biomarkers as they showed good correlation with target contaminants and were not readily affected by different dosing patterns.     

大连湾和杭州湾表层沉积物中多氯联苯和有机氯农药及风险评价

对大连湾与杭州湾沉积物样品中多氯联苯(Polychlorinated Biphenyls,PCBs)和有机氯农药(Organochlorine Pesticides,OCPs)进行了分析测定。结果表明,大连湾和杭州湾沉积物中PCBs的含量为0.72~14.87 ng/g和0.76~3.86 ng/g,其中3、4、5氯联苯比例较高,其和超过总含量的70%;OCPs的含量为2.98~32.23 ng/g和1.61~4.71 ng/g,其中主要成分为六六六(Hexachlorocyclohexanes,HCHs)和滴滴涕(Dichlorodiphenyldichloroethylenes,DDTs)。大连湾和杭州湾表层沉积物中HCHs主要来自农业使用,而且大连湾有新的DDTs输入,杭州湾表层沉积物中的DDTs则主要来自历史残留。生态风险评价的结果表明,PCBs几乎不会对研究区域产生生态风险,OCPs对杭州湾也不会造成潜在的生态风险,但大连湾的OCPs处于中等风险水平,应当引起关注。