China's marginal seas (CMSs, including the Bohai Sea, Yellow Sea, East China Sea) are a significant sink for both terrestrial organic matter (OM) and marine OM, and they play an important role in the global biogeochemical carbon cycle. The spatial distribution and origin of organic matter based on n-alkanes in the surface sediments of CMSs and the implications of carbon sinks were comparatively analyzed. The n-alkane content in surface sediment from the Bohai Sea was higher than that of the Yellow Sea and the East China Sea. The spatial distribution trends of marine and terrestrial organic matter are obviously different in the surface sediments of China's marginal seas. The n-alkanes in the sediments of the Yellow Sea and the East China Sea were mainly derived from terrestrial higher plants, and land-based influence gradually decreased from the near shore to the open sea. Higher concentration of terrigenous OM are concentrated nearshore, especially near estuaries, such as the Yellow River Estuary, the Old Yellow River Estuary and the Yangtze River Estuary. The input of n-alkanes from woody plants in the Bohai Sea area was slightly higher than that of herbaceous plants, and the input of herbaceous plants in the Yellow Sea and East China Sea was slightly dominant. The distribution of marine organic matter is controlled by marine productivity and the sedimentary environment. Due to climate change, the decomposition and enrichment of organic matter also show the climate effect of carbon molecular combinations. As a semiclosed sea area, the Bohai Sea was beneficial to the growth and reproduction of marine phytoplankton. From the perspective of petroleum pollution, the Bohai Sea was the most serious, followed by the Yellow Sea, and the East China Sea was the lightest. The carbon burial amount of terrestrial organic matter accounts for approximately 7% of the terrestrial organic matter burial amount of global marginal sea sediments, indicating that China's marginal sea plays an important role in the global carbon cycle. The result provide a basis for further understanding the source pattern and burial preservation of sedimentary organic matter in this sea area.

Marine debris is an environmental issue of increasing importance worldwide, with 80% of marine plastics estimated to originate from land-based sources. While much work has been conducted to quantify plastics in coastal environments, many of these approaches are site-specific and not amenable to rapid surveys. We surveyed beaches around Nova Scotia, Canada for plastic and other anthropogenic debris to: 1) quantify debris density on the high tide line; and 2) test a rapid survey technique using digital photos, with applications for community science and remote regions. Most (72%) beaches in Nova Scotia contained debris, but plastic densities along the daily high tide line were relatively low (mean 0.2 debris/m²) with little interannual variation. Despite small differences in plastic densities between observers, this rapid assessment technique appears viable for relative quantification and monitoring of plastic debris on beaches across large geographic scales to assess trends and sources.

Agricultural development is inevitable to meet the growing need for food. But along with this development, there are unintended and undesirable consequences for human life and the environment that need, found a solution and corrected. One of the most important adverse consequences of agricultural development is the pollution of surface and groundwater resources, which results from various factors such as soil erosion and improper use of different pesticides. This study aimed to conduct an environmental monitoring program in Naseri wetland to determine the concentrations of organophosphorus pesticides (OPPₛ) in water samples and also to evaluate the potential risks (ecological and health risk assessment) of these pesticides. The salting-out assisted liquid-liquid extraction method was used to extract pesticides. The residual concentrations of OPPₛ evaluated by gas chromatography/mass spectrometry (GC/MS). In this study, the ecological risk of OPPₛ calculated for wetland ecosystem, based on the acute risk quotient (RQᵢ) formula with maximum (RQₘₐₓ), mean (RQₘₑₐₙ), and mixture (RQₘᵢₓ) concentrations of organophosphorus pesticides in the wetland water. Also, to assess the health risk of consuming contaminated fish with organophosphate pesticides, the potential non-carcinogenic and carcinogenic risks were determined by the hazard quotient (Index) (HQ, HI) and incremental lifetime cancer risk (ILCR) indices, respectively. The mean ± SD concentration of OPPₛ (Chlorpyrifos, Malathion, Ethion, Dichlorvos, Trifluralin and Diazinon) in samples of wetland water ranged from 0.14 ± 0.08 to 0.35 ± 0.12 and 0.054 ± 0.06 to 0.2 ± 0.1 (μg/L) in summer and autumn, respectively. The mean ± SD of OPPₛ in fish varied from 0.68 ± 0.86 to 3.94 ± 2.7 (μg/kg). Overall, the concentrations of pesticides in all water and fish samples were below the maximum residue limit (30 μg/kg) during the study period, according to the Environmental Protection Agency (EPA) and the World Health Organization (WHO). The results of acute risk quotient were in summer (RQₘₐₓ = 3.49E-4 to 0.067, RQₘₑₐₙ = 5.8E-5 to 0.029, RQₘᵢₓ = 0.139-0.026, 0.018-3.42E-3) and autumn (RQₘₐₓ = 8E-4 to 0.051, RQₘₑₐₙ = 7.74E-6 to 0.018 RQₘᵢₓ = 0.1–0.013, 6E-3- 1.5E-3). The non-carcinogenic and carcinogenic risk indexes due to fish consumption for adults and children were (HQ = 0.026-4.68E-4, HI = 0.041, ILCR = 1.7E-7) and (HQ = 1.85E-3-1.3E-5, HI = 0.041, ILCR = 5.55E-8), respectively. The risk of OPPₛ was generally low. But cumulative risk (pesticide mixtures), should not be ignored.

From 2006 to 2020, groundwater investigations were conducted in the Korba coastal aquifer in northern Tunisia along two flow paths (transects S1 and S2), perpendicular to the shoreline. Groundwater sampling, hydrodynamic monitoring, and electrical tomography imaging were performed in situ. Geochemical analysis (Ionic ratios, ionic deltas, conventional diagrams, and stable isotopes) and modelling using PHREEQC, and multivariate statistical analysis were applied. The objective was to identify the potential origin of groundwater salinization (i.e., high TDS and NO₃) and to study associated processes. The groundwater flow inversion was corroborated by the piezometric survey in transect S1, where a piezometric depression of 5 m was detected at 4000 m from the seashore. Seawater intrusion and agricultural contamination, mainly through N-fertilizers, both contribute to groundwater mineralization and consequently salinization, according to PCA analysis. The impacted geochemical area of seawater intrusion was estimated to be 4000 and 1500 m, respectively, along transect S1 and transect S2. Inversely, agricultural contamination acts in internal areas beginning at 2000 m and 1500 m from the shoreline for S1 and S2, respectively. Results of different scenarios of inverse geochemical modelling along flow paths indicated that mixing, ion exchange, dissolution of gypsum, and precipitation of dolomite and calcite are the main processes controlling the groundwater composition in the coastal study area.

In this study, surface seawater was collected from 82 stations in the Drake Passage and Antarctic Peninsula sea area, and the distribution characteristics and correlations of 11 trace elements (i.e., V, Cr, Mn, Co, Cu, Zn, As, Mo, Cd, Pb, and U) in the seawater were analyzed. Results showed remarkable differences in the concentration of different elements, among which those of Mn (53.15%), Mo (22.77%), Zn (9.81%), and U (6.23%) were relatively high. The concentration of trace elements in Drake Passage water was relatively low, likely because a westerly drift that enhances large circulating currents exists in the sea area, thereby affecting the distribution of substances in the water. Mn, Co, Cu, Zn, Cd, and Pb showed relatively high concentrations at more stations than the other elements, and the high concentrations of Mn, Co, and Cd were mainly found in shallow water areas. UV, MoV, AsV, AsMo, AsU, and MoU demonstrated good linear correlations with correlation coefficients in the range of 0.878–0.961. These results could provide support for further explorations of the environmental behavior of trace elements in Antarctica.

Sustainable management of groundwater needs comprehensive study on water quality in present scenario. Hence, an understanding on the hydro geochemistry, saltwater intrusion, spatiotemporal-seasonal variations and irrigational suitability of groundwater becomes a must, especially in coastal regions. Our study area is one such place where all the parameters play a major role against sustainable management. The study pointed out that majority of the samples is brackish with two notable geochemical facies for pre monsoon and post monsoon. Factor and cluster analyses revealed that EC, TDS, Na⁺, Cl⁻, Mg²⁺ and Ca²⁺ are the major contributors. Gibb's diagram supported the dominance of rock weathering and evaporation in controlling the groundwater chemistry. Sea water intrusion was mapped using HFE diagrams and the Irrigational suitability is studied using USSL, SAR, %Na, etc. The data and results from this study might provide crucial information to water management authorities in dealing groundwater scarcity and pollution problems.

The agrochemicals and nutrient losses from farming areas such as paddy farming significantly dictate quality and eutrophication of the freshwater resource. However, how farming and land use pattern affect water qualities and eutrophication remain poorly understood in most African agro-ecosystems. The present study characterized how paddy farming influences water qualities and eutrophication in 10 irrigation schemes in Usangu agro-ecosystem (UA). About 42 water samples were sampled from intakes, channels, paddy fields, and drainages and analyzed for EC, Cl, P, NH₄-N, NO₃-N, TN, Zn, Cu, Ca, and Mg. We observed water pH ranging from 4.89 to 6.76, which was generally below the acceptable range (6.5–8.4) for irrigation water. NH₄-N concentration was in a range of 10.6–70.0 mg/L, NO₃-N (8.4–33.9 mg/L), and TN (19.1–21,104 mg/L). NH₄-N increased along sampling transect (sampling points) from intakes (5.7–29.1 mg/L), channels (19–20 mg/L), fields (12.9–35.8 mg/L), and outflow (10.6–70.0 mg/L), the same trend were found for NO₃-N and TN. The TP determined in water samples were in the range of 0.01 to 1.65 mg/L; where some sites had P > 0.1 mg/L exceeding the allowable P concentration in freshwater resource, thus indicating P enrichment and eutrophication status. The P concentration was observed to increase from intake through paddy fields to drainages, where high P was determined in drainages (0.02–1.65 mg/L) and fields (0.0–0.54 mg/L) compared to channels (0.01–0.13 mg/L) and intakes (0.01–0.04 mg/L). Furthermore, we determined appreciable amount of potentially toxic elements (PTEs) such as Cu, Pb, Cd and Cr in studied water samples. The high N, P, and PTEs in drainages indicate enrichment from agricultural fields leading to water quality degradation and contaminations (eutrophication). The study demonstrates that water quality in UA is degrading potentially due to paddy rice farming and other associated activities in the landscape. Thus, the current study recommends starting initiatives to monitor irrigation water quality in UA for better crop productivity, and improved quality of drainage re-entering downstream through the introduction of mandatory riparian buffer, revising irrigation practices, to include good agronomic practices (GAP) to ensure water quality and sustainability.

Sedimentary organic pollution in the urban reaches of the Thames estuary is changing from fossil fuel hydrocarbons to emerging synthetic chemicals. De-industrialisation of London was assessed in three cores from Chiswick (Ait/Eyot) mud island using pharmaceuticals, faecal sterols, hydrocarbons (TPH, PAH), Black Carbon (BC) and organotins (TBT). These ranked in the order; BC 7590-30219 mg/kg, mean 16,000 mg/kg > TPH 770–4301, mean 1316 mg/kg > Σ¹⁶PAH 6.93–107.64, mean 36.46 mg/kg > coprostanol 0.0091–0.42 mg/kg, mean of 0.146 mg/kg > pharmaceuticals 2.4–84.8 μg/kg, mean 25 μg/kg. Hydrocarbons co-varied down-profile revealing rise (1940s), peak (1950s -1960s) and fall (1980s) and an overall 3 to 25-fold decrease. In contrast, antibiotics, anti-inflammatory (ibuprofen, paracetamol) and hormone (17β-estradiol) increased 3 to 50-fold toward surface paralleling increasing use (1970s-2018). The anti-epileptics, carbamazepine and epoxcarbamazepine showed appreciable down-core mobility. Faecal sterols confirmed non-systematic incorporation of treated sewage. Comparison to UK sediment quality guidelines indicate exceedance of AL2 for PAH whereas TBT was below AL1.

In this study, we provide a baseline assessment of introduced marine species along the extensive (~600 km) Brazilian semiarid coast. We reported 27 introduced and 26 cryptogenic species. Moreover, the main vectors of introduction were ballast water, shipping lines, oil and gas activities, biofouling, and rafting on plastic debris. The taxa were Ascidiacea (17 species) and Bryozoa (17), followed by Crustacea (6), Mollusca (6), Cnidaria (3), Echinodermata (3), and Porifera (1). Among these invertebrates, some species are recognized as drivers of impacts such as the invasive corals (Tubastraea tagusensis and Tubastraea coccinea), the bivalves Isognomom bicolor and Perna viridis, the crab Charybdis hellerii, the brittle star Ophiothela mirabilis, and, finally, the bryozoan Membraniporopsis tubigera. These species threaten the biodiversity of unique ecosystems such as intertidal sandstone reefs, shallow-water coral reefs, and mesophotic ecosystems. Moreover, the up-to-date results highlight that this region is a hotspot of bioinvasion in the tropical South Atlantic.

Marine plastic pollution is one of the most talked about environmental issues of our time. While marine plastic pollution generally originates from mismanaged waste from land, waste from ships and fishing gear produce a unique threat to the global seas. Using a choice experiment, we explore preference for a marine debris removal and prevention programme focusing on derelict fishing gear. Additionally, we explore preferences for increasing removal efforts of debris in the North Western Hawaiian Islands. We find overwhelming support for these interventions; however, we find evidence that change, and therefore subsequent action, is strongest for individuals who believe that governments hold the majority of the responsibility for reducing and cleaning plastic pollution in marine environments.