Instituto Español de Oceanografía, Centro Oceanográfico de Murcia, Apdo. 22, C/ Varadero 1, 30740 San Pedro del Pinatar, Murcia, Spain.
Instituto Español de Oceanografía, Centro Oceanográfico de Murcia, Apdo. 22, C/ Varadero 1, 30740 San Pedro del Pinatar, Murcia, Spain.
Sci Total Environ. 2019 Jun 20;670:672-684. doi: 10.1016/j.scitotenv.2019.03.216. Epub 2019 Mar 15.
In this study the role of plastic debris as a pollution vector has been evaluated by determining the concentrations of hydrophobic organic contaminants in polymers from three Western Mediterranean coastal areas as well as their potential transfer to seawater. Plastic debris was sampled at three Iberian Peninsula Southeastern beaches, each affected by different predominant anthropogenic activities (tourism, agriculture, urban activities, transport and industry). Plastic debris was characterized by attenuated total reflection Fourier-transform infrared spectrometry. The organic contaminants were extracted from plastics by ultrasonic extraction with methanol and quantified by stir bar sorptive extraction coupled to gas chromatography-mass spectrometry (GC-MS). In two areas, the desorption of these contaminants from plastic debris to seawater during 24 h was also evaluated. The contaminant groups considered in this study (polycyclic aromatic hydrocarbons (PAHs), personal care products (PCPs), current use pesticides (CUPs), organochlorinated compounds (OCPs, including polychlorinated biphenyls and organochlorinated pesticides) and plastic additives were found in polymers from the three areas. The most abundant contaminants were plastic additives and PCPs, underlining the relevance of the leaching of plastic components, and urban and tourism activities as typical pollution sources in the coastal areas. In general, large piece-to-piece variability was found for all polymers and areas mainly as a consequence of their different origin, exposition time, use and surface-to-volume ratio. This fact difficulted the visualization of significant differences between polymers or areas, but for CUPs, whose concentrations were significantly higher in Cape Cope than in the other areas due to the influence of close agricultural activities. PCPs and CUPs were desorbed partially in seawater for 24 h, particularly the most hydrophilic compounds such as triazines and other CUPs. However, a significant fraction of other contaminants (mainly PAHs) was retained, which suggests they can be transported far away from their origin.
在这项研究中,通过测定来自三个西地中海沿海地区的聚合物中疏水性有机污染物的浓度及其向海水的潜在转移,评估了塑料碎片作为污染载体的作用。在伊比利亚半岛东南部的三个海滩上采集了塑料碎片,每个海滩都受到不同的主要人为活动(旅游、农业、城市活动、运输和工业)的影响。使用衰减全反射傅里叶变换红外光谱法对塑料碎片进行了特征描述。使用甲醇通过超声波萃取从塑料中提取有机污染物,并通过搅拌棒吸附萃取与气相色谱-质谱联用(GC-MS)进行定量。在两个地区,还评估了这些污染物在 24 小时内从塑料碎片解吸到海水中的情况。本研究中考虑的污染物组(多环芳烃(PAHs)、个人护理产品(PCPs)、当前使用的农药(CUPs)、有机氯化合物(OCPs,包括多氯联苯和有机氯农药)和塑料添加剂)存在于三个地区的聚合物中。最丰富的污染物是塑料添加剂和 PCPs,这强调了塑料成分浸出的重要性,以及城市和旅游活动是沿海地区典型的污染源。一般来说,所有聚合物和地区的片到片的变异性都很大,主要是由于它们的不同来源、暴露时间、用途和表面积与体积比。这一事实使得很难在聚合物或地区之间观察到显著差异,但对于 CUPs 来说,由于附近农业活动的影响,其浓度在 Cape Cope 显著高于其他地区。PCPs 和 CUPs 在海水中 24 小时内部分解吸,特别是最亲水的化合物,如三嗪类和其他 CUPs。然而,其他污染物(主要是 PAHs)的很大一部分被保留下来,这表明它们可以从其来源处被运输到很远的地方。