Phytotoxicity of petroleum hydrocarbons: Sources, impacts and remediation strategies.

Extraction and exploration of petroleum hydrocarbons (PHs) to satisfy the rising world population's fossil fuel demand is playing havoc with human beings and other life forms by contaminating the ecosystem, particularly the soil. In the current review, we highlighted the sources of PHs contamination, factors affecting the PHs accumulation in soil, mechanisms of uptake, translocation and potential toxic effects of PHs on plants. In plants, PHs reduce the seed germination andnutrients translocation, and induce oxidative stress, disturb the plant metabolic activity and inhibit the plant physiology and morphology that ultimately reduce plant yield. Moreover, the defense strategy in plants to mitigate the PHs toxicity and other potential remediation techniques, including the use of organic manure, compost, plant hormones, and biochar, and application of microbe-assisted remediation, and phytoremediation are also discussed in the current review. These remediation strategies not only help to remediate PHs pollutionin the soil rhizosphere but also enhance the morphological and physiological attributes of plant and results to improve crop yield under PHs contaminated soils. This review aims to provide significant information on ecological importance of PHs stress in various interdisciplinary investigations and critical remediation techniques to mitigate the contamination of PHs in agricultural soils.

Near-Earth space balloon-based multi-band airglow imager optic design.

As a common tracer in the atmosphere, airglow can be used as an important means to study the interaction between the lower atmosphere, near space, and ionosphere. In the near-Earth space, the high-altitude balloon can realize long time flight, which makes the airglow detection realize both high range resolution and time resolution. In this paper, a balloon-based multi-band airglow imager is designed, which can observe OI (557.7 nm), Na (589.3 nm), OI (630.0 nm), and OH (720-910 nm) with annular field of view (30° inner ring and 80° outer ring), and its resolution is 500 m at 250 km. The multi-band airglow imager designed in this paper is equipped in the payload cabin and raised to above 30 km for flat flying for more than 6 h. The experimental results show that the imager worked normally, and airglow images were photographed and stored; the optical system can stand the harsh environment in the near space. The multi-band airglow imager designed in this paper will take part in other near-space exploration tasks in the future and obtain corresponding results.

High-Altitude Balloon-Based Sensor System Design and Implementation.

As a kind of large-scale unmanned aerial vehicle, a high-altitude balloon can carry a large load up to tens of kilometers in the near space for a long time, which brings a new way for the stratosphere atmospheric detection. In order to provide a suitable working environment for the near-space detection load, it is necessary to design a sensor system based on a high-altitude balloon, which is used to provide environmental temperature, height position, and attitude information, current working, and video surveillance. The high-altitude balloon-based sensor system designed in this paper had participated in the near-space flight experiment, whose total flight time was 30 h and 53 min, and the horizontal flight time was 28 h and 58 min crossing the day and night. The high-altitude balloon-based sensor system had withstood the severe environment of the near-space during the day and night, providing accurate temperature measurement, real-time altitude position and attitude data acquisition, reliable current monitoring, and comprehensive video surveillance. In the next three years, the high-altitude balloon-based sensor system developed in this paper will continue to participate in the experiment and provide support for more detection loads.

Simultaneous adsorption and reduction of hexavalent chromium on biochar-supported nanoscale zero-valent iron (nZVI) in aqueous solution.

Flax straw biochar (FSBC)-supported nanoscale zero-valent iron (nZVI) composite (nZVI-FSBC) combining the advantages of nZVI and biochar was synthesized and tested for Cr(VI) removal efficiency from aqueous solution. Surface morphology and structure of FSBC and nZVI-FSBC were characterized by scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller techniques, which help to clarify the mechanism of Cr(VI) removal from aqueous solution. The adsorption of Cr(VI) onto FSBC and nZVI-FSBC was best described by the pseudo-second-order and the Sips model. Compared with FSBC, nZVI-FSBC remarkably improved the performance in removing Cr(VI) under identical experimental conditions. Due to the collaborative effect of adsorption and reduction of nZVI-FSBC, the adsorption capacity of nZVI-FSBC for Cr(VI) is up to 186.99 mg/g. The results obtained by XPS, XRD, and FTIR confirmed that adsorption and reduction dominated the processes of Cr(VI) removal by nZVI-FSBC. As a supporter, FSBC not only improved the dispersion of nZVI, but also undertook the adsorption task of Cr(VI) removal. The surface oxygen-containing functional groups of nZVI-FSBC mainly participated in the adsorption part, and the nZVI promoted the Cr(VI) removal through the redox reactions. These observations indicated that the nZVI-FSBC can be considered as potential adsorbents to remove Cr(VI) for environment remediation.

5-Substituted-N-pyridazinylbenzamides as potent and selective LRRK2 inhibitors: Improved brain unbound fraction enables efficacy.

We describe the discovery and optimization of 5-substituted-N-pyridazinylbenzamide derivatives as potent and selective LRRK2 inhibitors. Extensive SAR studies led to the identification of compounds 18 and 23, which demonstrated good in vitro pharmacokinetic profile and excellent selectivity over 140 other kinases. Both compounds demonstrated high unbound fractions in both blood and brain. Compound 18 proved to be brain penetrant, and the high unbound fraction of compound 18 in brain enabled its in vivo efficacy in CNS, wherein a significant inhibition of LRRK2 Ser935 phosphorylation was observed in rat brain following intravenous infusion at 5 mg/kg/h.

Synthesis of magnetic biochar derived from cotton stalks for the removal of Cr(VI) from aqueous solution.

A magnetic cotton stalk biochar (MCSBC) was synthesized through chemical co-precipitation, based on cotton stalk biochar (CSBC). The MCSBC and CSBC were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy and vibrating sample magnetometry. The characterization analyses showed that the magnetization process endowed the CSBC with excellent magnetic properties with a superparamagnetic magnetization of 27.59 emu/g. Batch adsorption experiment results indicated that the Cr(VI) maximum adsorption capacity of MCSBC was 20.05 mg/g, which was higher than that of CSBC (18.77 mg/g). The adsorption kinetic data were well fitted by the pseudo-second-order model and the adsorption isotherms were well represented by the Sips isotherm model. The thermodynamic studies indicated that the adsorption process was spontaneous and endothermic, and the entropy increased. The potential adsorption mechanism was the electrostatic adsorption of anionic Cr(VI) to the positively charged MCSBC surface, the reduction of Cr(VI) into Cr(III) and the complexation of Cr(III) by oxygen-containing functional groups of MCSBC. The regeneration studies showed that MCSBC kept 80% of its initial Cr(VI) adsorption capacity in the cycle. All the findings suggest that this novel magnetic biochar could be used in the field of Cr(VI)-containing wastewater treatment.

Discovery of 4-ethoxy-7H-pyrrolo[2,3-d]pyrimidin-2-amines as potent, selective and orally bioavailable LRRK2 inhibitors.

Inhibition of LRRK2 kinase activity with small molecules has emerged as a potential novel therapeutic treatment for Parkinson's disease. Herein we disclose the discovery of a 4-ethoxy-7H-pyrrolo[2,3-d]pyrimidin-2-amine series as potent LRRK2 inhibitors identified through a kinase-focused set screening. Optimization of the physicochemical properties and kinase selectivity led to the discovery of compound 7, which exhibited potent in vitro inhibition of LRRK2 kinase activity, good physicochemical properties and kinase selectivity across the kinome. Moreover, compound 7 was able to penetrate into the CNS, and in vivo pharmacology studies revealed significant inhibition of Ser935 phosphorylation in the brain of both rats (30 and 100 mg/kg) and mice (45 mg/kg) following oral administration.

Sulfate sorption on rape (Brassica campestris L.) straw biochar, loess soil and a biochar-soil mixture.

The effects of biochar amendment on sulfur behavior in soils are unknown. In this paper, sulfate (SO42-) sorption on rape (Brassica campestris L.) straw biochar produced at 600 °C (BC), loess soil (soil) and a 1:9 (w/w) biochar-soil mixture (BC-soil) was investigated by batch experiments. The effects of contact time, initial SO42- concentration, temperature and solution pH value on sorption were tested. Kinetics, isotherms and thermodynamics for sorption were investigated. Pre- and post-sorption characterizations of BC and soil were respectively studied using Fourier transform infrared (FTIR) and X-ray diffraction (XRD) spectroscopy, respectively. It has been shown that SO42- sorption on three sorbents was well described by pseudo-second-order kinetic model. The sorption isotherms could be fitted using Langmuir and Freundlich models. BC amendment did not increase the sorption capacity of soil for SO42-. The values of ΔG0, ΔH0 and ΔS0 indicated that the nature of sorption was spontaneous, endothermic and feasible. Increasing solution pH value led to a slight reduction in the sorption amount of SO42-. Sulfate was mainly sorbed onto BC through electrostatic interaction, whereas onto the soil via electrostatic interaction and formation of poorly soluble CaSO4.

Effects of biochars derived from chicken manure and rape straw on speciation and phytoavailability of Cd to maize in artificially contaminated loess soil.

While biochar can reduce the bioavailability of heavy metals in acidic soils and reduce their risk of entering the food chain, conditions for alkaline soils such as loess soils with high pH values, high carbonate content and low organic matter content remain unclear. Pot experiments were conducted to assess the effects of four rates (1%, 5%, 10%, and 15% w/w) of biochars prepared at 600 °C from chicken manure and rape straw (CBC and RBC) on soil properties, Cd speciation and phytoavailability, and plant growth in Cd contaminated (20 mg kg-1) light sierozem using maize (Zea mays L.) as an indicator plant. Biochar additions significantly (P < 0.05) increased soil pH values, cation exchange capacity (CEC) and soil organic matter (OM). The results showed that Cd speciation turned somewhat into stable state as biochar application increased. When CBC and RBC was applied at the rate of 15%, the content of acid-extractable Cd decreased only by 16.3% and 11.64%, respectively. The uptake of Cd by maize shoots scarcely decreased with CBC and RBC amendment at the rate of 1% and 5%, respectively. Although it seemed that additions of more than 5% CBC or RBC significantly (P < 0.05) reduced Cd contents in maize shoots, maize growth was largely inhibited due to the high value of soil pH. These results could provide different implications for immobilization remediation of loess soils (e.g., light sierozem) contaminated with Cd.

Adsorption of cadmium by biochar produced from pyrolysis of corn stalk in aqueous solution.

The purpose of this work is to investigate adsorption characteristic of corn stalk (CS) biochar for removal of cadmium ions (Cd2+) from aqueous solution. Batch adsorption experiments were carried out to evaluate the effects of pH value of solution, adsorbent particle size, adsorbent dosage, and ionic strength of solution on the adsorption of Cd2+ onto biochar that was pyrolytically produced from CS at 300 °C. The results showed that the initial pH value of solution played an important role in adsorption. The adsorptive amount of Cd2+ onto the biochar decreased with increasing the adsorbent dosage, adsorbent particle size, and ionic strength, while it increased with increasing the initial pH value of solution and temperature. Cd2+ was removed efficiently and quickly from aqueous solutions by the biochar with a maximum capacity of 33.94 mg/g. The adsorption process was well described by the pseudo-second-order kinetic model with the correlation coefficients greater than 0.986. The adsorption isotherm could be well fitted by the Langmuir model. The thermodynamic studies showed that the adsorption of Cd2+ onto the biochar was a spontaneous and exothermic process. The results indicate that CS biochar can be considered as an efficient adsorbent.

[Fourier Transform Spectrometer Based on Rotating Parallel-Mirror-Pair].

In the temporally-modulated Fourier transform spectroscopy, the translational moving mirror is difficult to drive accurately, causing tilt and shear problems. While, a rotational moving mirror can solve these problems. A rotary Fourier transform spectrometer is recommanded in this paper. Its principle is analyzed and the optical path difference is deduced. Also, the constrains for engineering realization are presented. This spectrometer consists of one beamsplitter, two fixed mirrors, one rotating parallel mirror pair, a collimating lens, a collecting lens, and one detector. From it's principle, this spectrometer show a simple structure, and it is assembled and adjustmented easily because the two split light are interfered with each other after reflected through the same plane mirror; By calculating the expression of it's optical path difference, the spectrometer is easy to realize large optical path difference, meaning high spectral resolution; Through analyzing it's engineering design constraints and computer simulation, it is known that the spectrometer should get the high resolution sample by high-speed spinning motor, so it is easy to achieve precise motion control, good stability, fast measurement speed.

[Multi-DSP parallel processing technique of hyperspectral RX anomaly detection].

To satisfy the requirement of high speed, real-time and mass data storage etc. for RX anomaly detection of hyperspectral image data, the present paper proposes a solution of multi-DSP parallel processing system for hyperspectral image based on CPCI Express standard bus architecture. Hardware topological architecture of the system combines the tight coupling of four DSPs sharing data bus and memory unit with the interconnection of Link ports. On this hardware platform, by assigning parallel processing task for each DSP in consideration of the spectrum RX anomaly detection algorithm and the feature of 3D data in the spectral image, a 4DSP parallel processing technique which computes and solves the mean matrix and covariance matrix of the whole image by spatially partitioning the image is proposed. The experiment result shows that, in the case of equivalent detective effect, it can reach the time efficiency 4 times higher than single DSP process with the 4-DSP parallel processing technique of RX anomaly detection algorithm proposed by this paper, which makes a breakthrough in the constraints to the huge data image processing of DSP's internal storage capacity, meanwhile well meeting the demands of the spectral data in real-time processing.

Characteristics of Fe/C catalysts based on pyrolysis of ferric citrate and its peroxymonosulfate activation performance to degrade sulfadiazine in water.

Advanced oxidation techniques based on peroxysulfate activation have been paid much attention owing to their excellent performance in degrading stubborn pollutants in water. In response to the current situation that requires more raw materials and higher costs and involves more complicated processes for the preparation of Fe/C catalysts to activate persulfates, novel catalysts (Fe/C-700, Fe/C-800, Fe/C-900 and Fe/C-1000) were prepared by a high-temperature carbonization method at different pyrolysis temperatures (700, 800, 900 and 1000 °C) using inexpensive and environmentally friendly ferric citrate as raw material. Fe/C catalysts were characterized using SEM, EDS, XRD, XPS, and VSM and were screened for the activation of peroxymonosulfate (PMS) to degrade sulfadiazine (SDZ) in water, where Fe/C-900 exhibited higher efficiency. Thus, its activation performance for PMS to degrade SDZ was comprehensively investigated and the mechanisms of activation degradation were analyzed. The results showed that the degradation rate of 98.7% can be achieved to 10 mg L-1 SDZ by 0.1 g L-1 Fe/C-900 and 0.5 mmol L-1 PMS within 60 min. A wide range of solution pH, low catalyst dosage and good recycling performance were found in the Fe/C-900 application and the amount of iron ions dissolved at the end of the reaction was low (0.350 mg L-1). It was shown that both free radical and non-free radical pathways existed in the reaction system, where 1O2, SO4-˙ and O2-˙ played dominant roles in the degradation process of SDZ. The results could provide new ideas for the preparation of Fe/C catalysts and their heterogeneous activation for PMS to degrade stubborn organic pollutants in water.

Effects of microplastics and cadmium co-contamination on soil properties, maize (Zea mays L.) growth characteristics, and cadmium accumulation in maize in loessial soil-maize systems.

Microplastics (MPs) are pervasive pollutants found in agricultural soils, yet research on the combined impacts of MPs and heavy metals on soil-plant systems remains limited. This study investigates the combined impact of low-density polyethylene (LDPE) microplastics (L: 1 mm, S: 100 µm, 0.1%, 1%) and Cd on soil properties, available Cd content, maize growth, and Cd accumulation by mazie through pot experiments. The findings unveiled notable impacts of the treatment groups, namely MP-L0.1%, MP-S0.1%, MP-L1%, and MP-S1%, on soil organic carbon (SOC), maize height, and catalase (CAT) activity (P < 0.05). The dosage of MPs significantly influenced maize height, MP-S0.1% treatment resulted in a 5.6% reduction, while the other groups had insignificant effects. Particle size and dosage significantly affected SOC and CAT (P < 0.01). The MP-L1% and MP-S1% groups resulted in increases of SOC by 121.5% and 281.0%, respectively. CAT reductions were 32.6%, 62.8%, 41.9%, and 34.9% in MP-L0.1%, MP-S0.1%, MP-L1%, and MP-S1% groups, individually. The Cd treatment induced a significant decrease in soil cation exchange capacity (CEC), maize stem diameter, and root length, accompanied by significant increases in maize plant height, malondialdehyde (MDA), CAT, and superoxide dismutase (SOD) activities. Combined LDPE and Cd contamination had significant effects on maize height and Cd content in leaves. Specifically, MP-L0.1%+Cd, MP-S0.1%+Cd, MP-L1%+Cd, and MP-S1%+Cd reduced maize height by 4.1%, 4.5%, 8.7%, and 13.8%, respectively. The co-presence of LDPE and Cd increased available Cd content in soil while elevating Cd concentration in maize shoots and roots, with a notable 25.5% increase in Cd concentration in maize leaves in the MP-L1%+Cd group compared to the Cd group. Furthermore, LDPE effects on soil-plant systems varied depending on particle size and dosage. This research provides important perspectives on evaluating the concurrent contamination and potential dangers of MPs and toxic metals in soil-plant environments.

Novel complex crystal structure of prolyl hydroxylase domain-containing protein 2 (PHD2): 2,8-Diazaspiro[4.5]decan-1-ones as potent, orally bioavailable PHD2 inhibitors.

We have discovered a novel complex crystal structure of the PHD2 enzyme with its inhibitor, the 2,8-diazaspiro[4.5]decan-1-one analogue 4b. The widely reported salt bridge between Arg383 of the enzyme and its inhibitors in all complex structures published thus far was not observed in our case. In our complex structure compound 4b forms several novel interactions with the enzyme, which include a hydrogen bond with Arg322, a π-cation interaction with Arg322, a π-π stacking with Trp389, and a π-π stacking with His313. Guided by the structural information, SAR studies were performed on the 2,8-diazaspiro[4.5]decan-1-one series leading to the discovery of compound 9p with high potency and good oral pharmacokinetic profile in mice.

Micellar-enhanced ultrafiltration of copper ions using sodium dodecyl sulfate and its mixture with Brij 35, Tween 80 and Triton X-100.

The performance of copper ion removal using sodium dodecyl sulfate (SDS) and its mixtures with Brij 35, Tween 80 (TW80) and Triton X-100 (TX100) by micellar-enhanced ultrafiltration (MEUF) was investigated. The effects of the molar ratio of nonionic surfactant to SDS on the critical micelle concentration (CMC) of SDS/Brij 35, SDS/TW80 and SDS/TX100, the removal efficiency of Cu(2+), the residual concentration of SDS in the permeate solution and the permeate flux were tested. The results showed that the CMCs of the mixed surfactants were sharply less than that of pure SDS. The removal efficiencies of Cu(2+) were up to the maximum values 98.3 and 95.8% when the molar ratios of Brij 35 and TW80 to SDS were 0.3, and it was 93.5% given 0.7 molar ratio of TX100 to SDS. The concentration of SDS in the permeate decreased dramatically with the addition of nonionic surfactant, and the permeate flux decreased slightly as the molar ratio increased. Compared with the performance by single SDS, the mixed SDS/Brij 35, SDS/TW80 and SDS/TX100 at an optimum composition could result in not only higher rejection of Cu(2+) but also much less dosage of surfactant and concentration of SDS in the permeate.

[Impact and improvement of the mechanical shutter on large-array filter-type multispectral imaging system].

The present paper analyzes the impact of mechanical shutter on the spectral image acquisition and processing of large-array filter-type multispectral imaging system. The final image quality relies highly on the mechanical shutter due to the fluctuation at exposure time. The conventional mechanical shutter's structure and driving method was analyzed to find out the key fact for its poor stability. An improved method of mechanical transmission and circuit driving was proposed. Laboratory experiments showed that with the improved design strategy, the maximum rate of change between adjacent exposures was reduced from 15.05% to 0.96%, which is a great improvement of the exposure time stability. Field test was also carried out and the results show that the combined color images are closer to the realistic targets and no abrupt color change iwas found. It's of great significance for practical application in multispectral image process, interpretation and target identification.

Indole-propionic acid derivatives as potent, S1P3-sparing and EAE efficacious sphingosine-1-phosphate 1 (S1P1) receptor agonists.

Novel indole-propionic acid derivatives were developed as sphingosine-1-phosphate (S1P) receptor agonists through a systematic SAR study. The optimized and S1P(3) selective S1P(1) agonist 9f induced peripheral blood lymphocyte reduction in vivo and has an excellent efficacy in mouse experimental autoimmune encephalomyelitis (EAE).

Influence of Intrinsic Physicochemical Properties of Agroforestry Waste on Its Pyrolysis Characteristics and Behavior.

To obtain a comprehensive understanding of the qualitative and quantitative effects of the intrinsic properties of biomass on its pyrolysis characteristics and assess the behavior of agroforestry waste, thermogravimetric analyses of three representative agroforestry wastes, namely rape (Brassica campestris L.) straw (RS), apple (Malus domestica) tree branches (ATB), and pine (Pinus sp.) sawdust (PS), were carried out by pyrolysis under dynamic conditions (30 to 900 °C) at different heating rates of 5, 10, and 15 °C·min-1. Correlation analysis showed that intrinsic physicochemical properties play distinct roles in different stages of pyrolysis. The ash content was negatively correlated with the temperature range (R2) of the second stage (190-380 °C) of pyrolysis. The lignin content and the amount of pyrolysis residues (RSS) were positively correlated. Kinetic triplets, including the activation energy (Ea), pre-exponential factor (A), and reaction model [f(α)], were obtained using different methods, including the Flynn-Wall-Ozawa (FWO), Freidman, Kissinger-Akahira-Sunose (KAS), and Starink methods. The mean activation energy (Ea[mean]) for RS, ATB, and PS calculated by the different methods ranged from 167.15 to 195.58 kJ·mol-1, 195.37 to 234.95 kJ·mol-1, and 191.27-236.45 kJ·mol-1, respectively. Correlation analysis of the intrinsic physicochemical characteristics and kinetic factors of agroforestry waste showed that the minimum Ea (Ea[min]) was significantly positively correlated with heat capacity (C0) and negatively correlated with thermal diffusivity (D). The Ea[mean] and the maximum value of Ea (Ea[max]) significantly positively correlated with the sum content of cellulose and lignin, indicating that the contents of cellulose and lignin determines the energy required for the pyrolysis process of agroforestry waste. The mechanism of degradation involves the diffusion model (D1, D2, and D3), the growth model (A4), and the geometrical contraction model (R3). These results indicate that the pyrolysis of agroforestry waste is a complex process due to the heterogeneity of its intrinsic physicochemical properties.

Investigating Biochar-Derived Dissolved Organic Carbon (DOC) Components Extracted Using a Sequential Extraction Protocol.

Biochar-derived dissolved organic carbon (DOC), as the most important component of biochar, can be released on farmland, improving fertility and playing a role in soil amendment and remediation. The complexity of molecular structures and diversity of DOC compounds have influenced these functions to some extent. A sequential extract protocol consisting of water (25 °C), hot water (80 °C), and NaOH solution (0.05 M) was used to fully extract DOC compounds and gain a thorough understanding of the possible DOC components released from biochar. Rape straw (RS), apple tree branches (ATB), and pine sawdust (PS) were pyrolyzed at 300, 500, and 700 °C, respectively, to make nine distinct biochars. A TOC analyser, ultraviolet-visible spectroscopy (UV-vis), and excitation-emission fluorescence (EEM) spectrophotometer were used in conjunction with parallel factor analysis (PARAFAC) to determine the distribution of DOC content, the diversity of aromaticity, molecular weight characteristics and components of biochar-derived DOC. The results show that the relative distribution of water-extractable fractions ranged from 3.21 to 35.57%, with a low-aromaticity and extremely hydrophilic fulvic-acid-like compounds being found in the highest amounts (C2 and C3). The smallest amount of hot water-extractable components was produced from the release of small-molecule aliphatic compounds adsorbed on biochar and susceptible to migration loss once in a soil solution. More than half of the biochar-derived DOC was released in a NaOH solution, which primarily consisted of humic-acid-like compounds (C1), with higher molecular weights, more aromaticity, and lower bioavailability, according to the distribution of DOC in various extractants. In addition, the pyrolysis temperature and biomass type had a significant impact on the DOC properties released by biochar. As a result, the findings of this study showed that using a sequential extract protocol of water, hot water, and NaOH solution in combination with spectroscopic methods could successfully reveal the diversity of biochar-derived components, which could lead to new insights for the accurate assessment of potential environmental impacts and new directions for biochar applications.