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This paper presents a comprehensive approach to predicting short-term (for the upcoming 2 weeks) changes in estuarine dissolved oxygen concentrations via machine learning models that integrate historical water sampling, historical and upcoming 2-week meteorological data, and river discharge and discharge metrics. Dissolved oxygen is a critical indicator of ecosystem health, and this approach is implemented for the Neuse River Estuary, North Carolina, U.S.A., which has a long history of hypoxia-related habitat degradation. Through meticulous data preprocessing and feature selection, this research evaluates the predictions of dissolved oxygen concentrations by comparing a recurrent neural network with four other models, including a Multilayer Perceptron, Long Short-Term Memory, Gradient Boosting, and AutoKeras, through sensitivity experiments. The input predictors to our prediction models include water temperature, turbidity, chlorophyll-a, aggregated river discharge, and aggregated wind based on eight directions. By emphasizing the most impactful predictors, we streamlined the model-building processes and built a hindcast system from 2015 to 2019. We found that the recurrent neural network model was most effective in predicting the dissolved oxygen concentrations, with an R2 value of 0.99 at multiple stations. Different from our machine learning hindcast models that used observed upcoming meteorological and discharge data, an actual forecast system would use forecasted meteorological and discharge data. Therefore, an actual operational forecast may have lower accuracy than the hindcast, as determined by the accuracy of the predicted meteorological and discharge data. Nevertheless, our studies enhance our understanding of the factors influencing dissolved oxygen variability and set the basis for the implementation of a predictive tool for environmental monitoring and management. We also emphasized the importance of building station-specific models to improve the prediction results. 

The accurate forecast of algal blooms can provide helpful information for water resource management. However, the complex relationship between environmental variables and blooms makes the forecast challenging. In this study, we build a pipeline incorporating four commonly used machine learning models, Support Vector Regression (SVR), Random Forest Regression (RFR), Wavelet Analysis (WA)-Back Propagation Neural Network (BPNN) and WA-Long Short-Term Memory (LSTM), to predict chlorophyll-a in coastal waters. Two areas with distinct environmental features, the Neuse River Estuary, NC, USA—where machine learning models are applied for short-term algal bloom forecast at single stations for the first time—and the Scripps Pier, CA, USA, are selected. Applying the pipeline, we can easily switch from the NRE forecast to the Scripps Pier forecast with minimum model tuning. The pipeline successfully predicts the occurrence of algal blooms in both regions, with more robustness using WA-LSTM and WA-BPNN than SVR and RFR. The pipeline allows us to find the best results by trying different numbers of neuron hidden layers. The pipeline is easily adaptable to other coastal areas. Experience with the two study regions demonstrated that enrichment of the dataset by including dominant physical processes is necessary to improve chlorophyll prediction when applying it to other aquatic systems. 

We investigate how matrix stiffness regulates chromatin reorganization and cell reprogramming and find that matrix stiffness acts as a biphasic regulator of epigenetic state and fibroblast-to-neuron conversion efficiency, maximized at an intermediate stiffness of 20 kPa. ATAC sequencing analysis shows the same trend of chromatin accessibility to neuronal genes at these stiffness levels. Concurrently, we observe peak levels of histone acetylation and histone acetyltransferase (HAT) activity in the nucleus on 20 kPa matrices, and inhibiting HAT activity abolishes matrix stiffness effects. G-actin and cofilin, the cotransporters shuttling HAT into the nucleus, rises with decreasing matrix stiffness; however, reduced importin-9 on soft matrices limits nuclear transport. These two factors result in a biphasic regulation of HAT transport into nucleus, which is directly demonstrated on matrices with dynamically tunable stiffness. Our findings unravel a mechanism of the mechano-epigenetic regulation that is valuable for cell engineering in disease modeling and regenerative medicine applications. 

Rapid and ultrasensitive point-of-care RNA detection plays a critical role in the diagnosis and management of various infectious diseases. The gold-standard detection method of reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is ultrasensitive and accurate yet limited by the lengthy turnaround time (1-2 days). On the other hand, antigen test offers rapid at-home detection (15-20 min) but suffers from low sensitivity and high false-negative rates. An ideal point-of-care diagnostic device would combine the merits of PCR-level sensitivity and rapid sample-to-result workflow comparable to antigen testing. However, the existing RNA detection platform typically possesses superior sensitivity or rapid sample-to-result time, but not both. This paper reports a point-of-care microfluidic device that offers ultrasensitive yet rapid detection of viral RNA from clinical samples. The device consists of a microfluidic chip for precisely manipulating small volumes of samples, a miniaturized heater for viral lysis and ribonuclease (RNase) inactivation, a CRISPR Cas13a- electrochemical sensor for target preamplification-free and ultrasensitive RNA detection, and a smartphone-compatible potentiostat for data acquisition. As demonstrations, the devices achieve the detection of heat-inactivated SARS-CoV-2 samples with a limit of detection (LOD) down to 10 aM within 25 minutes, which is comparable to the sensitivity of RT-PCR and rapidness of antigen test. The platform also successfully distinguishes all nine positive unprocessed clinical SARS-CoV-2 nasopharyngeal swab samples from four negative samples within 25 minutes of sample-to-result time. Together, this device provides a point-of-care solution that can be deployed in diverse settings beyond laboratory environments for rapid and accurate detection of RNA from clinical samples. The device can potentially be expandable to detect other viral targets, such as human immunodeficiency virus (HIV) self-testing and Zika virus, where rapid and ultrasensitive point-of-care detection is required. 

Abstract A photochemical model of photosynthetic electron transport (PET) is needed to integrate photophysics, photochemistry, and biochemistry to determine redox conditions of electron carriers and enzymes for plant stress assessment and mechanistically link sun‐induced chlorophyll fluorescence to carbon assimilation for remotely sensing photosynthesis. Towards this goal, we derived photochemical equations governing the states and redox reactions of complexes and electron carriers along the PET chain. These equations allow the redox conditions of the mobile plastoquinone pool and the cytochrome b₆f complex (Cyt) to be inferred with typical fluorometry. The equations agreed well with fluorometry measurements from diverse C₃/C₄species across environments in the relationship between the PET rate and fraction of open photosystem II reaction centres. We found the oxidation of plastoquinol by Cyt is the bottleneck of PET, and genetically improving the oxidation of plastoquinol by Cyt may enhance the efficiency of PET and photosynthesis across species. Redox reactions and photochemical and biochemical interactions are highly redundant in their complex controls of PET. Although individual reaction rate constants cannot be resolved, they appear in parameter groups which can be collectively inferred with fluorometry measurements for broad applications. The new photochemical model developed enables advances in different fronts of photosynthesis research. 

Annual U.S. production of bioethanol, primarily produced from corn starch in the U.S. Midwest, rose to 57 billion liters in 2021, which fulfilled the required conventional biofuel target set forth by the Energy Independence and Security Act (EISA) of 2007. At the same time, the U.S. fell short of the cellulosic or advanced biofuel target of 79 billion liters. The growth of bioenergy grasses (e.g., Miscanthus and switchgrass) across the Central and Eastern U.S. has the potential to feed enhanced cellulosic bioethanol production and, if successful, increase renewable fuel volumes. However, water consumption and climate change and its extremes are critical concerns in corn and bioenergy grass productivity. These concerns are compounded by the demands on potentially productive land areas and water devoted to producing biofuels. This is a fundamental Food-Energy-Water System (FEWS) nexus challenge. We apply a computational framework to estimate potential bioenergy yield and conversion to bioethanol yield across the U.S., based on crop field studies and conversion technology analysis for three crops—corn, Miscanthus, and two cultivars of switchgrass (Cave-in-Rock and Alamo). The current study identifies regions where each crop has its highest yield across the Center and Eastern U.S. While growing bioenergy grasses requires more water than corn, one advantage they have as a source of bioethanol is that they control nitrogen leaching relative to corn. Bioenergy grasses also maintain steadily high productivity under extreme climate conditions, such as drought and heatwaves in the year 2012 over the U.S. Midwest, because the perennial growing season and the deeper and denser roots can ameliorate the soil water stress. While the potential ethanol yield could be enhanced using energy grasses, their practical success in becoming a potential source of ethanol yield remains limited by socio-economic and operational constraints and concerns regarding competition with food production.