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Identifying the sources and transformations of riverine nitrate plays a critical role in mitigating nitrogen enrichment of river networks. Several previous studies have used δ18O-NO3− to quantitatively assess riverine nitrate contributed by atmospheric nitrate and terrestrial sources, but their results have great uncertainty due to the wide range of δ18O-NO3− values and isotopic fractionation during nitrogen-cycling processes in terrestrial environment. The nitrate 17O anomaly (△17O-NO3−), as an unambiguous tracer of atmospheric nitrate, is a promising tool to effectively separate atmospheric nitrate from microbially produced nitrate. However, to our knowledge, △17O-NO3− approach has not been previously applied to identify nitrate pollution sources in plain river networks of eastern China. In this study, we used a multiple isotope approach (δD/δ18O-H2O and δ15N/δ18O/△17O-NO3−) for the first time to quantitatively identify sources and transformations of riverine nitrate in a hypereutrophic coastal plain river network namely Wen-Rui Tang River located in eastern China, which is a region receiving high inputs of atmospheric nitrogen deposition. The △17O-NO3− values in precipitation and river water during the study period (April–June of 2021) varied from 14.83‰ to 31.39‰ and from − 2.82‰ to 9.66‰, respectively. The δD/δ18O-H2O values revealed that river water mainly originated from recent precipitation with little evaporation. Moreover, the δ15N/δ18O-NO3− values indicated that microbial nitrification, not denitrification, was the predominant nitrogen-cycling process in the watershed. Based on a Bayesian mixing model (Stable Isotope Analysis in R, SIAR) using δ15N/△17O-NO3−, municipal sewage was identified as the dominant nitrate source (50.5 ± 11.7%), followed by soil nitrogen (23.8 ± 13.7%), atmospheric nitrate deposition (14.3 ± 2.9%), and nitrogen fertilizer (11.4 ± 8.7%). Finally, an uncertainty analysis for nitrate source apportionment demonstrated that the greatest uncertainty was associated with soil nitrogen, followed by municipal sewage, nitrogen fertilizer, and atmospheric nitrate deposition. This study provides important scientific information on riverine nitrate source apportionment to guide pollution control/remediation strategies and highlights the benefits of utilizing △17O-NO3− to enhance nitrate source apportionment.

The stomatal index of the leaf is the ratio of the number of stomata to the total number of stomata and epidermal cells. Comparing with the stomatal density, the stomatal index is relatively constant in environmental conditions and the age of the leaf and, therefore, of diagnostic characteristics for a given genotype or species. Traditional assessment methods involve manual counting of the number of stomata and epidermal cells in microphotographs, which is labor-intensive and time-consuming. Although several automatic measurement algorithms of stomatal density have been proposed, no stomatal index pipelines are currently available. The main aim of this research is to develop an automated stomatal index measurement pipeline. The proposed method employed Faster regions with convolutional neural networks (R-CNN) and U-Net and image-processing techniques to count stomata and epidermal cells, and subsequently calculate the stomatal index. To improve the labeling speed, a semi-automatic strategy was employed for epidermal cell annotation in each micrograph. Benchmarking the pipeline on 1,000 microscopic images of leaf epidermis in the wheat dataset (Triticum aestivum L.), the average counting accuracies of 98.03 and 95.03% for stomata and epidermal cells, respectively, and the final measurement accuracy of the stomatal index of 95.35% was achieved. R 2 values between automatic and manual measurement of stomata, epidermal cells, and stomatal index were 0.995, 0.983, and 0.895, respectively. The average running time (ART) for the entire pipeline could be as short as 0.32 s per microphotograph. The proposed pipeline also achieved a good transferability on the other families of the plant using transfer learning, with the mean counting accuracies of 94.36 and 91.13% for stomata and epidermal cells and the stomatal index accuracy of 89.38% in seven families of the plant. The pipeline is an automatic, rapid, and accurate tool for the stomatal index measurement, enabling high-throughput phenotyping, and facilitating further understanding of the stomatal and epidermal development for the plant physiology community. To the best of our knowledge, this is the first deep learning-based microphotograph analysis pipeline for stomatal index assessment. [ABSTRACT FROM AUTHOR]