Yield Variation Characteristics of Red Paddy Soil under Long-Term Green Manure Cultivation and Its Influencing Factors.

Rice is an important food crop in China, fertilization measures significantly affect soil properties and ultimately change rice yield. Thus, examining the effects of long-term green manure cultivation on the rice yield and the driving factors on rice yield, plays a crucial role in maintaining food security. Based on the long-term green manure cultivation, the treatments included no fertilizer (CK), chemical fertilizer (NPK), chemical fertilizer + Chinese milk vetch (NPK + GM), chemical fertilizer + Chinese milk vetch + rice straws (NPK + GM + S), and chemical fertilizer + Chinese milk vetch + pig manure (NPK + GM + M) treatments. One-way repeated ANOVA was used to determine the effects of diverse fertilizer modes on temporal variations in rice yields. The redundancy analysis (RDA) was used to calculate the magnitudes of the effects of soil properties on rice yield. Compared with the CK treatment, four fertilizer treatments led to significantly increased double-season rice yields (116.40−124.49%), with no significant difference between four fertilizer treatments (p> 0.05). There were five soil properties accounting for 66.3% variation in rice yield (p< 0.05), with available potassium (AK) being the most influential factor (32.2% variation), whereas potential of hydrogen (pH), total nitrogen (TN), total phosphorus (TP), and soil organic carbon (SOC) accounted for 15.3%, 10.5%, 5.1%, and 3.2% variation in rice yield (p< 0.05), respectively. Thus, SOC, TN, TP, AK, and pH were major factors affecting the double-season rice yield of red paddy soil under long-term green manure cultivation. However, the results suggested that the effect of green manure on soil fertility is limited by the relatively large amount of chemical fertilizer. The results reported herein can not only increase soil fertility and improve the soil ecological environment, but also enhance and stabilize the yields of double-season rice grown in the red paddy soil of southern China.

The Controlled Synthesis of Birnessite Nanoflowers via H2O2 Reducing KMnO4 For Efficient Adsorption and Photooxidation Activity.

Birnessite nanoflowers composed of layers have been proven to be the strongest adsorbent and oxidant in the surface environment. However, the current synthesis methods of birnessite nanoflowers are suffering from long reaction time and high reaction temperature. Based on these, this paper explores a new method for the rapid and controlled synthesis of layered manganese oxides. The method relies on the molar ratios of KMnO4 and H2O2 redox reacting species to drive the production of birnessite nanoflowers under acidic conditions. The molar ratios of KMnO4 and H2O2 are the key to the crystal structure of the as-prepared. It was found that when the molar ratios of KMnO4 and H2O2 is from 1:1.25 to 1:1.90, the sample is birnessite nanoflowers, and when the ratio is increased to 1:2.0, the sample is a mixture of birnessite nanoflowers and feitknechtite nanoplates. Among the as-prepared samples, BF-1.85 (molar ratios of KMnO4 and H2O2 is 1:1.85) shows the highest capacity for Pb2+ adsorption (2,955 mmol/kg) and greatest degradation efficiency of phenol and TOC. The method proposed herein is economical and controllable, and it yields products with high efficiency for the elimination of inorganic and organic pollutants.

Characterisation of hexagonal birnessite with a new and rapid synthesis method-comparison with traditional synthesis.

Birnessite is one of the most important manganese oxides that can control the geochemical behaviors of pollutants or can be applied to form industrial products. Many studies have been conducted on the synthesis of hexagonal birnessite because different synthesis methods can affect the structural, morphological, and physicochemical properties of hexagonal birnessite. However, there are still some defects in these synthesis methods. Therefore, a new synthesis method that is rapid, simple, and low-cost was proposed in this study involving the reduction of KMnO4 by H2O2 in a H2SO4 solution without controlling the pH, temperature and pressure. Using a series of XRD, chemical composition, AOS, SSA, SEM, FTIR, and TGA analyses, Bir-H2O2 was found to have lower crystallinity than Bir-HCl. However, the AOS and SSA of Bir-H2O2 were 3.87 and 103 m2 g-1 higher than those of Bir-HCl, i.e., 3.70 and 22 m2 g-1, respectively. Moreover, both Bir-H2O2 and Bir-HCl had similar particle morphology and thermal stability; in addition, the maximum adsorption content of Pb2+ on Bir-H2O2 (∼3006 mmol kg-1) was ∼30% greater than that on Bir-HCl (∼2285 mmol kg-1) at pH 5.5; this indicated that the adsorption of Pb2+ on Bir-H2O2 was better and belonged to a pseudo-second-order model. All the abovementioned results indicate that Bir-H2O2 synthesized herein using the proposed synthesis method can have large application value.

What is crop heterosis: new insights into an old topic.

Heterosis (or hybrid vigor) refers to a natural phenomenon whereby hybrid offspring of genetically diverse individuals out-perform their parents in multiple traits including yield, adaptability and resistances to biotic and abiotic stressors. Innovations in technology and research continue to clarify the mechanisms underlying crop heterosis, however the intrinsic relationship between the biological basis of heterosis remain unclear. In this review, we aim to provide insight into the molecular genetic basis of heterosis by presenting recent advances in the 'omics' of heterosis and the role of non-coding regions, particularly in relation to energy-use efficiency. We propose that future research should focus on integrating the expanding datasets from different species and hybrid combinations, to mine key heterotic genes and unravel interactive 'omics' networks associated with heterosis. Improved understanding of heterosis and the biological basis for its manipulation in agriculture should help to streamline its use in enhancing crop productivity.

Mechanism of lead immobilization by oxalic acid-activated phosphate rocks.

Lead (Pb) chemical fixation is an important environmental aspect for human health. Phosphate rocks (PRs) were utilized as an adsorbent to remove Pb from aqueous solution. Raw PRs and oxalic acid-activated PRs (APRs) were used to investigate the effect of chemical modification on the Pb-binding capacity in the pH range 2.0-5.0. The Pb adsorption rate of all treatments above pH 3.0 reached 90%. The Pb binding on PRs and APRs was pH-independent, except at pH 2.0 in activated treatments. The X-ray diffraction analysis confirmed that the raw PRs formed cerussite after reacting with the Pb solution, whereas the APRs formed pyromorphite. The Fourier Transform Infrared spectroscopy analysis indicated that carbonate (CO3(2-)) in raw PRs and phosphate (PO4(3)) groups in APRs played an important role in the Pb-binding process. After adsorption, anomalous block-shaped particles were observed by scanning electron microscopy with energy dispersive spectroscopy. The X-ray photoelectron spectroscopy data further indicated that both chemical and physical reactions occurred during the adsorption process according to the binding energy. Because of lower solubility of pyromorphite compared to cerussite, the APRs are more effective in immobilizing Pb than that of PRs.