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The partial replacement of chemical fertilizer with straw return is considered an effective method for improving the accumulation of organic matter and soil fertility, but the characteristics of soil nitrogen fixation and mineralization in a double-cropped rice paddy system are unclear. Based on a 12-year field experiment, we conducted a waterlogged incubation experiment for 49 days to determine the effect of long-term straw return combined with reducing chemical fertilizer application on the dynamic changes of mineralized soil nitrogen (N) content and mineralized N rate under the treatments, including NPK (chemical fertilizers application with straw removal), SBR (straw burned return), and SR (straw return). Results showed that, compared with SBR and NPK, SR significantly increased available nitrogen by 7.4% and 16.5%, respectively, due to the higher ammonium nitrogen and nitrate nitrogen, as well as the total carbon, available phosphorus, and slowly available potassium, suggesting that it could stock a sufficient nitrogen source. During the incubation period, the amount of N mineralization was relatively higher under SR than under SBR and NPK treatments, especially during the later mineralization time, whereas there was no difference in the N mineralization rate. In addition, SR significantly increased soil cumulative N mineralization and N mineralization potential. However, SBR significantly decreased the soil mineralizable N ratio compared with SR and NPK, which may result in a worsening of the N mineralization potential. The results indicated that long-term straw return combined with reducing chemical fertilizer application could significantly improve the N supply capacity of paddy rice field soil to better coordinate the soil N supply and immobilization. [ABSTRACT FROM AUTHOR]

Maize is one of the most successful crops with regard to the utilization of heterosis. The haploid induction technique is one of the fastest methods to obtain pure maize material at the present stage. However, the molecular mechanism of haploid doubling is rarely reported. In this study, we treated B73 and ZNC442 haploid young shoots with colchicine for 0 h, 6.2 h, and 10 h, and analyzed the differentially expressed genes (DEGs). We found that colchicine treatment for 6.2 h and 10 h compared to 0 h resulted in a total of 4868 co-DEGs. GO enrichment analysis and KEGG metabolic pathway analysis found significantly enriched 282 GO terms and 31 significantly pathways, respectively. Additionally, The GO term and KEGG pathway genes of spindle, cytoskeleton, microtubules and nuclear division were selected for analysis, and three candidate genes were screened by taking intersections. Zm00001d033112, Zm00001d010525, and Zm00001d043386 were annotated as kinesin-associated protein 13, kinesin-like protein KIN-10C, and kinesin light-chain LC6, respectively. The real-time fluorescence quantification (RT-PCR) results revealed that Zm00001d033112, Zm00001d010525, and Zm00001d043386 had the same trends as RNA-seq. Interestingly, Zm00001d033112 is homologous gene AT3G20150 in Arabidopsis, which was involved in the regulation of chromosome movement and mitotic spindle assembly. Our study suggests that kinesin genes may play an important role in doubling chromosomes, thus providing valuable information for future studies on the molecular mechanisms of chromosome doubling in maize. [ABSTRACT FROM AUTHOR]