Promotive effects of marine-derived dimethyl sulfoxide on the photodegradation of phenanthrene in the atmosphere.

Dimethyl sulfoxide (DMSO), a versatile medium, is a particular component in the marine atmosphere that possibly causes polycyclic aromatic hydrocarbons (PAHs) to degrade differently than they do in the continental atmosphere. In this study, phenanthrene (Phe) was used as a model PAH in batch photochemical experiments to investigate the chemical actions of DMSO and the underlying mechanisms. The photodegradation of Phe in aqueous solutions with DMSO volume fractions from 0 % to 100 % was initiated by ultraviolet (UV) radiation and promoted by singlet oxygen, which was consistent with pseudo-first-order kinetics. Phe photodegraded faster in a mixture of DMSO and water than in water or DMSO alone, and the rate constant showed a unimodal distribution over the DMSO fraction range, peaking at 33 % DMSO (0.0333 ± 0.0009 min-1) and 40 % DMSO (0.0199 ± 0.0005 min-1) under 254 nm and 302 nm UV radiation, respectively. This interesting phenomenon was attributed to the competition of DMSO for UV radiation and singlet oxygen and changes in dissolved oxygen and free water contents caused by the interaction between DMSO and water molecules. In addition, 9,10-phenanthrenequinone (9,10-PhQ) with high cytotoxicity was the main photodegradation product of Phe under various conditions. The photodegradation rate of Phe in the mixtures of DMSO and water was comparable to its reaction rate with OH radicals, suggesting that 9,10-PhQ can be rapidly generated in the marine atmosphere, driven by a mechanism different from that in the continental or urban atmosphere. Under the presented experimental conditions, UV intensity and DMSO fraction were the primary factors that affected the photodegradation rate of Phe and 9,10-PhQ and altered their integrated toxicity. The findings of this study support the conclusion that the marine atmosphere is an essential field in the atmospheric transport of PAHs, in which DMSO is an important component that affects their photodegradation.

Unique transport paths of 137Cs from the Indian to Southern Oceans.

To assess ocean-scale transport systems, we examined the latitudinal cross-sectional distribution of 137Cs activity concentrations in the Indian and Southern Oceans between December 2019 and January 2020 using low-background γ-spectrometry. At 0°-20°S, 137Cs concentrations exhibited a gradual decrease below the mixing layer (1-0.1 mBq/L). However, the concentrations steeply decreased toward the Southern Ocean along a transect of 30°-60°S (from 0.8 to 0.02 mBq/L) with minor vertical variation at each site. For the 137Cs inventories (0-800 m depth) from 15 to 600 Bq/m2, a maximum value was recorded at 30°S, indicating the downwelling of 137Cs as a reservoir for the Subantarctic Mode Water. The significantly low concentrations (0.02 mBq/L) at 60°S suggest minimal transport of 137Cs to the Southern Ocean. These findings assist in understanding 137Cs circulation patterns and provide valuable insights into the transport pathways of soluble contaminants.

Autumn and spring observations of PM2.5-bound polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons in China and Japan.

The transboundary transport of polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) aggravated by the East Asian winter monsoon is a major atmospheric environmental issue in East Asia. To thoroughly elucidate the role of the East Asian monsoon on regional PAH and NPAH pollution in East Asia, PM2.5-bound PAHs and NPAHs were investigated concurrently at five sites in Beijing and Shenyang in China and Tsukuba, Kanazawa, and Wajima in Japan in autumn (November 2018) and spring (March 2019). During both autumn and spring sampling periods, the concentrations of PM2.5, PAHs, and NPAHs at sites in China were 1-2 orders of magnitude higher than those at sites in Japan, and showed an opposite temporal variation, with higher concentrations during the autumn sampling period due to intensive emissions and unfavourable weather conditions. During the sampling periods, PAHs at the Beijing and Shenyang sites had mixed sources of traffic emissions and coal and biomass combustion, while those at the Tsukuba, Kanazawa, and Wajima sites were mainly characterized by domestic traffic emissions. In addition, NPAHs at the five sites were jointly affected by primary combustion sources and atmospheric generation, with a greater contribution of atmospheric generation to the Beijing and Shenyang sites. Based on backwards trajectory clustering and concentration-weighted trajectory analysis, external contributions to PM2.5, PAHs, and NPAHs at each site were relatively stable during the two sampling periods, and potential source areas were mainly distributed in domestic cities and nearby sea areas. Therefore, the apparent temporal differences in the characteristics and sources of pollutants between sites in the two countries indicate that transboundary pollution dominated by the East Asian winter monsoon was unobvious in autumn and spring. The results of the study provide a time-specific solution for the effective management of regional air pollution during the East Asian winter monsoon.

Subarctic-scale transport of 134Cs to ocean surface off northeastern Japan in 2020.

We studied the spatiotemporal variations in 134Cs, 137Cs, and 228Ra concentrations at the sea surface off southeastern Hokkaido, Japan (off-Doto region) from 2018 to 2022 using low-background γ-spectrometry. The 134Cs concentrations in the off-Doto region, decay-corrected to the date of the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, exhibited wide lateral variation each year (e.g., 0.7-1.1 mBq/L in 2020). By studying the 228Ra concentrations and salinity, this variation was explained based on the current mixing patterns. Furthermore, the 134Cs concentrations in the waters highly affected by the Oyashio Current (OYC) gradually increased from 2018 to 2020, and subsequently decreased in 2022. This implies that the water mass maximally contaminated with 134Cs was transported back to the side of the Japanese islands 10 years after the FDNPP accident along with counter-clockwise currents (e.g., the OYC) in the northern North Pacific Ocean. The 134Cs concentrations in the OYC-affected waters in the off-Doto region in 2020 were ~ 1/6 times those in the 134Cs-enriched core of waters off the western American Coast in 2015, which can be ascribed to dilution via spatial dispersion during subarctic current circulation. Overall, we elucidated the ocean-scale subarctic current systems in the northwestern North Pacific Ocean, including water circulation timespans.

140 years-long sedimentary records of PAHs and CN stable isotopes from Ninomiya River, Japan.

Anthropogenic activities' impacts over 140 years were studied at West Nanao Bay using a variety of geochemical techniques on sedimentary records. The bay is influenced by the Ninomiya River which is fed by a small watershed at which Tatzuruhama Town is located. Sedimentation rate was calculated using 210Pb-excess and 137Cs activities. C/N decreased after 1975, indicating a decrease in lignin-rich organic matter. From δ13C, δ15N and biogenic silica it was indicated that the population increased sewage-discharges until the construction of waste-water treatment plant in 1986. Several recorded changes in the landuse matched with the variation of the particle size. Total PAHs concentration was 1.17-62.78 µg g-1, being highest during Japan's fastest economic growth period (1946-1975). Using diagnostic ratios and PCA analysis, PAHs' sources were identified as pyrogenic for all depths, varying from coal combustion (90.7 %) before 1946 to a mixture of biomass and vehicle combustion after 1961.

Spatiotemporal variation in microplastics derived from polymer-coated fertilizer in an agricultural small river in Ishikawa Prefecture, Japan.

Marine plastic pollution has highlighted the need to address the disposal of plastic materials used in agricultural fields and prevent their runoff. To assess the status of microplastics derived from polymer-coated fertilizers (microcapsules), we investigated their seasonal and daily variations in a small agricultural river in Ishikawa Prefecture, Japan, throughout the irrigation period of April to October 2021 and 2022. We also investigated the relationship between microcapsule concentration and water quality. The mean microcapsule concentration over the study period ranged from 0.0 to 783.2 mg/m3 (median 18.8 mg/m3) and was positively correlated with total litter weight, but it was not correlated with common water quality parameters such as total nitrogen or suspended solids. Concentrations of microcapsules in river water showed distinct seasonal variations, being particularly high in late April and late May (median 55.5 mg/m3 in 2021, 62.6 mg/m3 in 2022) and almost undetectable thereafter. The timing of the increase in concentration coincided with the timing of the outflow from paddy fields, suggesting that microcapsules that flowed out of the paddy fields would reach the sea relatively quickly. The results of a tracer experiment supported this conclusion. Intensive observations revealed that microcapsule concentrations varied widely over time, with differences reaching a maximum of 110-fold (range 7.3-783.2 mg/m3) over a 3-day period. Daytime concentrations were higher than those at night, reflecting the fact that microcapsules are discharged from paddies by daytime operations such as puddling and surface drainage. Microcapsule concentrations in the river were not correlated with river discharge, making estimating their loading a future research challenge.

Origin of surface water in the Southern Ocean: Implications of soluble radionuclide distributions.

Concentration data of soluble radionuclides in the southern South Indian Ocean and Southern Ocean transition zone are rare or insufficient for the study of its current system. We examined the lateral surface variations in soluble natural (226Ra and 228Ra) and anthropogenic (134Cs and 137Cs) radionuclide activity concentrations in the surface waters in this area from November 2021 to March 2022. The surface distributions of 226Ra and 137Cs concentrations were classified into Subantarctic Mode Water-, Antarctic Intermediate Water-, and Upper Circumpolar Deep Water (UCDW)-dominated areas along latitudinal band (40°S-65°S, 110°E-120°E). Notably, the highest 226Ra concentrations occurred along the longitudinal band (60°S-65°S, 40°E-120°E). Significantly lower 137Cs concentrations in the Southern Ocean than those in surface waters in other global oceans were observed along with depletion of 228Ra. Additionally, 226Ra and 137Cs concentrations appeared to show small variations between eastern and western areas (2.5-3.0 mBq/L and 0.06-0.03 mBq/L, respectively). Lateral profiles in the Southern Ocean are governed by a large contribution from deep/old waters (e.g., UCDW), with a small effect from southward transport of Subantarctic Mode Water.

Environmental processes and fate of PAHs at a shallow and enclosed bay: West Nanao Bay, Noto Peninsula, Japan.

From August 2019 to August 2020, particulate and dissolved polycyclic aromatic hydrocarbons concentrations (PAHs) were analyzed in the water body of West Nanao Bay, Japan, to determinate their levels, environmental pathways, and ecological risks at this remote but shallow and semi-enclosed bay. The 14 targeted PAHs were analyzed by high performance liquid chromatography-fluorescence detector. Even when water column stratifies, the summatory of 14 targeted dissolved PAHs did not follow significantly change with depth. Results agreed with our previous findings in the surface distribution at the bay and can be attributed to long retention time of the water mass of the semi-enclosed bay. Suspended solids start precipitating according to their size; with biggest particles rapidly settling in the proximities of river mouths. Partition coefficients (Kp) varied from 103 to 107, according to molecular weights. In general, highest Kp were found in the nepheloid layer. The risk quotients, RQ∑14 PAHs (NCs) (1.04-174.08), indicated that PAHs represented a very low to low environmental risks.

DISTRIBUTIONS OF 210PB, 137CS AND PHYSICAL PROPERTIES IN BOTTOM SEDIMENTS OF WEST NANAO BAY, JAPAN.

This study revealed sedimentation processes based on 137Cs and 210Pb distribution, grain size and magnetic susceptibility of bottom sediments in West Nanao Bay, Japan. Surface sediment concentrations and inventories of these radionuclides were relatively low in the middle and eastern areas of the bay and high in the western area, which has several major river mouths, suggesting that the contribution of riverine input affected only the western area. In the middle and eastern areas, the level of 137Cs inventory was much lower than that of the soils, and the excess 210Pb inventory was at the same level or lower. These results indicate that removal effects are stronger than accumulation effects (riverine input) in these areas. The patterns of radionuclides were consistent with the results, that grain size was relatively large in the middle and eastern areas, implying strong current conditions, and that fine sediment accumulated less in these areas.

TEMPORAL VARIATION IN RADIOCESIUM CONCENTRATIONS IN WATERS OF THE NATSUI AND SAME RIVERS, SOUTH FUKUSHIMA PREFECTURE, JAPAN FROM 2011 TO 2020.

In order to determine the long-term impacts of radiocesium contamination on ecosystems in watersheds and coastal areas following the Fukushima Daiichi Nuclear Power Plant accident in March 2011, it was important to monitor the transport behavior of radiocesium from an early stage. In this study, conducted from July 2011 to October 2020, we carried out field research along the Natsui and Same rivers running through watersheds in the south of Fukushima Prefecture, Japan, in which there had been a relatively low accumulation of radiocesium. We found that under normal flow conditions, the total (dissolved + particulate phase) activity of 137Cs decreased with increasing time following the accident. However, the water samples collected after rain events showed higher activity of up to 895 mBq l-1 with a higher percentage (>92% of total) of the particulate phase. These findings indicate that radiocesium deposited on the ground surface is predominantly transported in the particulate phase from watersheds to rivers via precipitation. The decontamination process, which was performed in the farmland during December 2014 to March 2015 and in forest during February 2013 to April 2014, was small effects of the transport of 137Cs. Under normal flow conditions, total 137Cs activity was largely determined by the suspended solids (SS) concentration and/or 137Cs concentration in the SS.

Addition of polyvinyl pyrrolidone during density separation with sodium iodide solution improves recovery rate of small microplastics (20-150 µm) from soils and sediments.

The purpose of this study was to identify a method to accurately separate small microplastics (<100 µm) from soil and sediment. We initially conducted spike-and-recovery tests using polyethylene microbeads and density separation and found that the recovery rate of microplastic particles smaller than 100 µm was less than 60%. This result suggested that previous reports have underestimated the concentrations of microplastics smaller than 100 µm in soil. When polyvinyl pyrrolidone was added and dispersed in a heavy liquid, the recovery rate exceeded 90%, regardless of the microplastic particle size. This improved recovery rate was independent of the type of polymer (polyethylene, polypropylene, polystyrene, polyethylene terephthalate, or nylon 6) and the physicochemical properties of the soil (Andisols, Entisols, or Ultisols), and the method was also effective for marine and lake sediments. Using this method, we measured microplastic concentrations in paddy soil. The results showed that the most common particle size, 20-100 µm, accounted for 64% of all microplastics. Accurate separation from the soil of fractions smaller than 100 µm, which account for the majority of microplastics in soil, will enable an accurate assessment of the impact of microplastics on the soil ecosystem. The method identified in this study can serve as the basic technique for achieving that goal.

Sustainable Plant Growth Promotion and Chemical Composition of Pyroligneous Acid When Applied with Biochar as a Soil Amendment.

The pyrolysis of biomass material results in pyroligneous acid (PA) and biochar, among other by-products. In agriculture, PA is recognized as an antimicrobial agent, bio-insecticide, and bio-herbicide due to antioxidant activity provided by a variety of constituent materials. Application of PA to crop plants and soil can result in growth promotion, improved soil health, and reduced reliance on polluting chemical crop inputs. More detailed information regarding chemical compound content within PA and identification of optimal chemical profiles for growth promotion in different crop species is essential for application to yield effective results. Additionally, biochar and PA are often applied in tandem for increased agricultural benefits, but little is known regarding the optimal proportion of each crop input. This work reports on the effect of combined applications of different proportions of PA (200- and 800-fold dilutions) and chemical fertilizer rates (100%, 75%, 50%, and 0%) in the presence or absence of biochar on Komatsuna (Brassica rapa var. perviridis, Japanese mustard spinach) plant growth. To elucidate the chemical composition of the applied PA, four different spectroscopic measurements of fluorescence excitation were utilized for analysis-excitation-emission matrix, ion chromatography, high-performance liquid chromatography, and gas chromatography-mass spectrometry. It was determined that PA originating from pyrolysis of Japanese pine wood contained different classes of biostimulants (e.g., tryptophan, humic acid, and fulvic acid), and application to Komatsuna plants resulted in increased growth when applied alone, and in different combinations with the other two inputs. Additionally, application of biochar and PA at the higher dilution rate increased leaf accumulation of nutrients, calcium, and phosphorus. These effects reveal that PA and biochar are promising materials for sustainable crop production.

Variations in traffic-related polycyclic aromatic hydrocarbons in PM2.5 in Kanazawa, Japan, after the implementation of a new vehicle emission regulation.

A three-year sampling campaign was conducted at a roadside air pollution monitoring station in the urban area of Kanazawa, Japan. Due to a new emission regulation, PAHs levels decreased over the sampling campaign, exhibiting values of 706 ± 413 pg/m3 in 2017, 559 ± 384 pg/m3 in 2018, and 473 ± 234 pg/m3 in 2019. In each year, similar seasonal variations in PAHs levels were observed, with higher levels observed in winter and lower levels in summer. Among the PAHs isomer ratios, we observed that the ratio of benzo[b]fluoranthene (BbF) and benzo[k]fluoranthene (BkF), [BbF]/([BbF] + [BkF]), and the ratio of indeno[1,2,3-cd]pyrene (IDP) and benzo[ghi]perylene (BgPe), [IDP]/([BgPe] + [IDP]), showed stability over the sampling campaign and were less affected by the new emission regulation, seasonal variations, and regional characteristics. When using the combined ratio ranges of 0.66 - 0.80 ([BbF]/([BbF] + [BkF]) and 0.26-0.49 ([IDP]/([BgPe] + [IDP]), traffic emissions were clearly distinguished from other PAHs emission sources. Principal component analysis (PCA) and positive matrix factorization (PMF) were also performed to further analyse the characteristics of traffic-related PAHs. Overall, this study affirmed the effectiveness of the new emission regulation in the reduction of PAHs emissions and provided a combined range for identifying PAHs traffic emission sources.

Transport paths of radiocesium and radium isotopes in the intermediate layer of the southwestern Sea of Okhotsk.

The spatial distributions of 134Cs, 137Cs, 226Ra, and 228Ra in/around the southwestern Sea of Okhotsk were examined in July 2019 and July 2021. Wide variations in the concentrations of these radionuclides were detected at the surface, including 0.2-0.7 mBq/L of 134Cs (decay-corrected to the date of the Fukushima Dai-ichi Nuclear Power Plant accident), which indicated a large mixing ratio between the Soya Warm Current and East Sakhalin Current/Okhotsk Sea Surface Water. The Intermediate Cold Water at depths of approximately 30-300 m was subjected to the effects of 226Ra-rich and 228Ra-poor intermediate (or deeper) seawater. Moreover, the 134Cs concentrations were maximum in 2021 (approximately 0.6 mBq/L), which most probably resulted from the increase in 134Cs concentrations in the southward dense shelf water along the eastern Sakhalin Island along with the effect in the Okhotsk Sea Intermediate Water originating from the western subarctic water (e.g., the East Kamchatka Current) in the Pacific Ocean.

Seasonal variations in marine polycyclic aromatic hydrocarbons off Oki Island, Sea of Japan, during 2015-2019.

Concentrations of 13 phase-partitioned polycyclic aromatic hydrocarbons (PAHs) in seawater were monitored monthly off Oki Island, Japan, during 2015-2019 to elucidate seasonal variations, main source, and transport pathways of PAHs in the southwestern Sea of Japan. Total PAH (dissolved plus particulate) concentrations in surface seawater at 36°09.0'N, 133°17.3'E (site OK) were in the range 0.49-9.36 ng L-1 (mean 2.77, SD 2.05 ng L-1) with higher levels in summer-autumn, an order of magnitude lower than those in the East China Sea during 2005 and 2009-2011 and about one-third of those recorded in the Sea of Japan in 2008 and 2010. The main sources of dissolved and particulate PAHs were combustion products. Increasing dissolved PAH levels during July-October indicate that the area around southern Oki Island is impacted by PAH-rich summer continental-shelf water transported by the Tsushima Warm Current flowing from the East China Sea.

PM-Bound Polycyclic Aromatic Hydrocarbons and Nitro-Polycyclic Aromatic Hydrocarbons in the Ambient Air of Vladivostok: Seasonal Variation, Sources, Health Risk Assessment and Long-Term Variability.

Total suspended particles (TSP) were collected in Vladivostok, Russia, which is a typical port city. This study investigated the concentration, potential sources, and long-term variation in particle PAHs and NPAHs in the atmosphere of Vladivostok. The PAH and NPAH concentrations were higher in winter than in summer (PAHs: winter: 18.6 ± 9.80 ng/m3 summer: 0.54 ± 0.21 ng/m3; NPAHs: winter: 143 ± 81.5 pg/m3 summer: 143 ± 81.5 pg/m3). The diagnostic ratios showed that PAHs and NPAHs mainly came from vehicle emissions in both seasons, while heating systems were the main source of air pollution in winter. The TEQ assessment values were 2.90 ng/m3 and 0.06 ng/m3 in winter and summer, respectively, suggesting a significant excess cancer risk in the general population in winter. The ILCR values conveyed a potential carcinogenic risk because the value was between 1 × 10-5 and 1 × 10-7 and ingestion was a main contributor in Vladivostok. However, it is worth noting that the concentrations of PAHs and NPAHs showed an overall downward trend from 1999 to 2020. An important reason for this is the cogenerations project implemented by the Far Eastern Center for Strategic Research on Fuel and Energy Complex Development in 2010. This research clarified the latest variations in PAHs and NPAHs to provide continuous observation data for future chemical reaction or model prediction research.

Unique current connecting Southern and Indian Oceans identified from radium distributions.

We examined the spatial variations in 226Ra and 228Ra (activities) concentrations from the surface to a depth of 830 m in the Indian and Southern Oceans from December 2019 to January 2020. 226Ra concentrations at the surface increased sharply from 30° S to 60° S along a ~ 55° E transect (1.4-2.9 mBq/L), exhibiting small vertical variations, while 228Ra decreased southward and became depleted in the Southern Ocean. These distributions indicated the ocean-scale northward lateral transport of 226Ra-rich and 228Ra-depleted currents originating from the Antarctic Circumpolar Current (ACC). 226Ra concentrations indicated that the fractions of the ACC at depths of 0-800 m decreased from 0.95 to 0.14 between 60° S and 30° S. The ACC fractions in the subantarctic western Indian Ocean were higher than those previously reported in the eastern Indian region, indicating preferential transport of the ACC. The fractions obtained were approximately equivalent to those in the western Indian Ocean in the 1970s. This could be attributed to the minimal southward shift of the polar front due to global warming over the last 50 years.

Geochemical Control of PAHs by Inflowing River Water to West Nanao Bay, Japan, and Its Influences on Ecological Risk: Small-Scale Changes Observed under Near-Background Conditions at an Enclosed Bay.

Polycyclic aromatic hydrocarbons (PAHs), even at low concentrations, have been shown to trigger changes in life cycles and provoke abnormal behaviors in numerous marine organisms. From May 2019 to September 2020, particulate and dissolved PAH concentrations were analyzed on the surface water of West Nanao Bay, Japan, to determinate their levels, emission sources, environmental pathways, and ecological risks at this remote but semi-enclosed bay. The 14 targeted PAHs were analyzed by HPLC-fluorescence detector. Mean total PAH concentrations were lower than 20.0 ng L-1 for most samples. Based on fluoranthene (Flu) to pyrene (Pyr) ([Flu]/[Flu + Pyr]) and benzo[a]anthracene (BaA) to chrysene (Chr) ([BaA]/[BaA + Chr]) isomeric ratios and a varimax rotated PCA, it was established that biomass combustion was the principal source in the particulate phase and that liquid fossil fuel combustion was the principal source in the dissolved phase. From salinity and turbidity distribution, riverine discharges were determined to be the major and continuous transportation pathway of particulate PAHs. It was observed that rain events had a role in the transport of dissolved PAHs. The risk quotients (RQ∑14 PAHs (NCs): 0-84.53) indicated that PAHs represented a very low to low acute environmental risk. The results of this study will contribute to filling the paradigm gap of ecotoxicological studies in remote areas, working as a booster for future in-lab studies of non-lethal implications of endocrine disruptors such as PAHs.

Development of a gel-in-oil emulsion as a transdermal drug delivery system for successful delivery of growth factors.

Growth factors (GFs) are indispensable in regenerative medicine because of their high effectiveness. However, as GFs degenerate easily, the development of a suitable carrier with improved stability for GFs is necessary. In this study, we developed a gel-in-oil (G/O) emulsion technology for the transdermal delivery of growth factors. Nanogel particles prepared with heparin-immobilized gelatin that can bind growth factors were dispersed in isopropyl myristate. The particle size of the G/O emulsion could be controlled by changing the surfactant concentration, volume ratio of the water phase to the oil phase, and gelatin concentration. In vitro skin penetration studies showed better penetration through the stratum corneum of fluorescent proteins containing G/O emulsions than of the aqueous solution of GF. Similarly, an in vivo study showed an angiogenesis-inducing effect after transdermal application of GF-immobilized G/O emulsion. Angiogenesis in mice was confirmed owing to both an increased blood vessel network and higher hemoglobin content in the blood. Therefore, the G/O emulsion could be a promising carrier for GFs with better stability and can effectively deliver GFs at the target site.

The input-output balance of microplastics derived from coated fertilizer in paddy fields and the timing of their discharge during the irrigation season.

Polymer-based microcapsules derived from coated fertilizers are not recovered after use. Therefore, they are a source of microplastics to the agricultural lands and coastal areas of Japan. In this study, we investigated the input-output balance of microcapsules in three paddy fields and the timing of microcapsule discharge from the fields with the aim of developing effective techniques to reduce microcapsule discharge. Microcapsules were discharged from the paddy fields primarily during puddling, when the weir plate was overflowed, and when surface drainage was implemented. About 50% of the total discharge during the irrigation period occurred during puddling, which is a process for leveling paddy fields. Therefore, contamination of the surrounding environment by microcapsules from paddy fields can be effectively reduced by preventing the release of microplastics from paddy fields during puddling. We also showed that the total microcapsule discharge cannot be controlled solely by irrigation water management, such as by adjusting the height of the weir plate. We found that about 0.067-0.076% of the total number of microcapsules accumulated in the soil of the paddy fields was discharged during the irrigation season in 2020. Furthermore, 70% of the microcapsules discharged from one field in 2020 had resided in the soil for at least two years. The use as fertilizer coatings of biodegradable polymers that would degrade completely in the soil within a few years could therefore substantially reduce the amount of microplastics released into the ocean from agricultural fields, and their development is thus urgently needed.