To extract the sensitive bands for estimating the winter wheat growth status and yields, field experiments were conducted. The crop variables including aboveground biomass (AGB), soil and plant analyzer development (SPAD) value, yield, and canopy spectra were determined. Statistical methods of correlation analysis, partial least squares (PLS), and stepwise multiple linear regression (SMLR) were used to extract sensitive bands and estimate the crop variables with calibration set. The predictive model based on the selected bands was tested with validation set. The results showed that the crop variables were significantly correlated with spectral reflectance. The major spectral regions were selected with the B-coefficient and variable importance on projection (VIP) parameter derived from the PLS analysis. The calibrated SMLR model based on the selected wavelengths demonstrated an excellent performance as the R2, TC, and RMSE were 0.634, 0.055, and 843.392 for yield; 0.671, 0.017, and 1.798 for SPAD; and 0.760, 0.081, and 1.164 for AGB. These models also performed accurately and robustly by using the field validation data set. It indicated that these wavelengths retained in models were important. The determined wavelengths for yield, SPAD, and AGB were 350, 410, 730, 1015, 1185 and 1245 nm; 355, 400, 515, 705, 935, 1090, and 1365 nm; and 470, 570, 895, 1170, 1285, and 1355 nm, respectively. This study illustrated that it was feasible to predict the crop variables by using the multivariate method. The step-by-step procedure to select the significant bands and optimize the prediction model of crop variables may serve as a valuable approach. The findings of this study may provide a theoretical and practical reference for rapidly and accurately monitoring the crop growth status and predicting the yield of winter wheat.

Based on qualitative and quantitative melissopalynological analyses, 19 Chinese honeys were classified by botanical origin to determine their floral sources. The honey samples were collected during 2010–2011 from the central region of Shanxi Province, North China. A diverse spectrum of 61 pollen types from 37 families was identified. Fourteen samples were classified as unifloral, whereas the remaining samples were multifloral. Bee-favoured families (occurring in more than 50% of the samples) included Caprifoliaceae (found in 10 samples), Laminaceae (10), Brassicaceae (12), Rosaceae (12), Moraceae (13), Rhamnaceae (15), Asteraceae (17), and Fabaceae (19). In the unifloral honeys, the predominant pollen types were Ziziphus jujuba (in 5 samples), Robinia pseudoacacia (3), Vitex negundo var. heterophylla (2), Sophora japonica (1), Ailanthus altissima (1), Asteraceae type (1), and Fabaceae type (1). The absolute pollen count (i.e., the number of pollen grains per 10 g honey sample) suggested that 13 samples belonged to Group I (<20,000 pollen grains), 4 to Group II (20,000–100,000), and 2 to Group III (100,000–500,000). The dominance of unifloral honeys without toxic pollen grains and the low value of the HDE/P ratio (i.e., honey dew elements/pollen grains from nectariferous plants) indicated that the honey samples are of good quality and suitable for human consumption.

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Rapid and non-destructive estimation of plant water status is essential for adjusting field practices and irrigation schemes of winter wheat. The objective of this study was to find new combination spectral indices based on canopy reflectance for the estimation of plant water status. Two experiments with different irrigation regimes were conducted in 2015–2016 and 2016–2017. The canopy spectra were collected at different growth stages of winter wheat. The raw and derivative reflectance of canopy spectra showed obvious responses to the change of plant water status. Except for equivalent water thickness (EWT), other water metrics had good relationships with new combination spectral indices (R 2 >0.7). An acceptable model of canopy water content (CWC) was established with the best spectral index (RVI (1605, 1712)). Models of leaf water content (LWC) and plant water content (PWC) had better performances. Optimal spectral index of LWC was FDRVI (687, 531), having R 2 , RMSE and RPD of 0.77, 2.181 and 2.09; R 2 , RMSE and RPD of 0.87, 2.652 and 2.34 for calibration and validation, respectively. And PWC could be well estimated with FDDVI (688, 532) (R 2 , RMSE and RPD of 0.79, 3.136 and 2.21; R 2 , RMSE and RPD of 0.83, 3.702 and 2.18 for calibration and validation, respectively). Comparing the performances of estimation models, the new combination spectral indices FDRVI (687, 531) based on canopy reflectance improved the accuracy of estimation of plant water status. Besides, based on FDRVI (687, 531), LWC was the optimal water metrics for plant water status estimation.

Determining the influence of soil environmental factors on degradation of Cry1Ac protein from Bt cotton residues is vital for assessing the ecological risks of this commercialized transgenic crop. In this study, the degradation of Cry1Ac protein in leaves and in buds of Bt cotton in soil was evaluated under different soil water content and temperature settings in the laboratory. An exponential model and a shift-log model were used to fit the degradation dynamics of Cry1Ac protein and estimate the DT50 and DT90 values. The results showed that Cry1Ac protein in the leaves and buds underwent rapid degradation in the early stage (before day 48), followed by a slow decline in the later stage under different soil water content and temperature. Cry1Ac protein degraded the most rapidly in the early stage at 35°C with 70% soil water holding capacity. The DT50 values were 12.29 d and 10.17 d and the DT90 values were 41.06 d and 33.96 d in the leaves and buds, respectively. Our findings indicated that the soil temperature was a major factor influencing the degradation of Cry1Ac protein from Bt cotton residues. Additionally, the relative higher temperature (25°C and 35°C) was found to be more conducive to degradation of Cry1Ac protein in the soil and the greater water content (100%WHC) retarded the process. These findings suggested that under appropriate soil temperature and water content, Cry1Ac protein from Bt cotton residues will not persist and accumulate in soil.