不同施氮量下覆膜滴灌玉米相对根长密度模型研究

为探明施氮量对宁夏引黄灌区覆膜滴灌玉米根长密度(RLD)的影响,设置5个施氮水平和1个对照(CK,不施氮与不覆膜)进行试验,测定玉米RLD,建立不同施氮量下相对根长密度(NRLD)模型,并加以检验。结果表明:不同施氮处理的玉米RLD分布区域均随土层深度的增加而减小,且大部分集中在0～20 cm土层;随着施氮量的增加,RLD分布区域明显扩大; NRLD分布满足三阶多项式函数模型,模拟曲线的决定系数R2为0.951,模型检验结果R2为0.845,均方根误差(RMSE)为0.248,拟合效果好,但该多项式模型不能保证NRLD在相对取样深度Zr为1时达到0,故对玉米NRLD分布多项式模型进行优化。优化模型验证结果显示,各施氮处理RMSE不大于0.308,CK、N0、N1、N2、N3和N4处理的标准化均方根误差分别为0.242、0.193、0.184、0.226、0.208和0.273,R2分别为0.903、0.953、0.920、0.944、0.962和0.898,具有较高的拟合度,解决了NRLD在Zr=1时达到0的问题。本研究可为宁夏引黄灌区膜下滴灌玉米NRLD分布拟合、根系养分吸收和施肥管理提供理论参考。     

Boundary-fitted grid in landscape modeling

Landscape modeling requires the delineation of system boundaries and interior features. Quite often, these components are complex and difficult to accurately represent. A rectangular grid is used to represent the study and adjacent non-study areas in most cases. When the non-study area occupies a large portion of the grid, computer memory is wasted, and computational time increases. An elliptical grid generator for non-orthogonal curvilinear coordinates is used to generate a boundary-fitted grid for a landscape model. In a boundary-fitted grid coordinate system, one coordinate axis follows the landscape domain boundary and is non-orthogonal to the second axis. The boundary-fitted grid uses elliptic partial differential equations to distribute grid points inside the landscape domain. Although the boundary-fitted grid follows the domain boundary, the grid pattern and point allocation remain structured. Thus, a landscape model can use a boundary-fitted grid without changing the model’s data structure or the computational scheme. In this study, a boundary-fitted grid and a raster-based grid were applied to the Everglades Landscape Fire Model. Use of the boundary-fitted grid decreased model simulation time by about one fifth and computer storage by 58% relative to the raster-based grid. Also, the linear characteristics of interior geographical features such as rivers and airboat trails were preserved by the boundary-fitted grid, but not by the raster-based grid. This preservation provided a more reasonable base map for simulating ecological processes, such as fire across heterogenous landscapes.     

电导法测定林木种子活力的研究

本文研究了林木种子电导法测定条件和测定电导率或相对电导率,通过回归分析建立电导率或相对电导率与种子活力指数的相关方程,找出了电导法测定林木种子活力的方法。     

三阶时滞泛函微分方程解的渐近性

本文讨论一类三阶时滞泛函微分方程解的渐近性质,给出了若干解的有界性及解趋于零的判定准则.     

二阶拟线性椭圓型Euler方程组解的Pohozaev型恒等式及其应用

本文对于二阶椭圆型Euler方程组 -∑D_αF_(q_α~i)(x,u,Du)+F_(ui)(x,u,Du)=0得到了一些积分恒等式,利用这些恒等式证明了某些方程组非平凡解的不存在性。     

河南省杨树材种出材率表的研编

用削度方程和单株带皮—去皮胸径的转换关系式两个模型对河南省杨树进行计算机理论造材．经精度检验，满足要求，方法可行，依此编制了河南省杨树材种出材率表。     

某类高阶非线性偏微分方程组弱解的正则性

本文研究一类2k阶非线性偏微分方程组之解的正则性,没有假定通常的椭圆性条件而只假定所谓"无穷远处"的椭圆性条件,证明了解的k-1阶导数为李普希兹连续的.     

以电导法配合Log istic方程确定茶梅‘小玫瑰’的抗寒性

 摘　要: 以不同处理时间、不同低温处理下茶梅‘小玫瑰’叶片的电解质外渗率(REC) 变化作曲线,并结合Logistic方程分别计算茶梅的半致死温度(LT50 ) , 结果发现在低温处理6 h以上, 茶梅叶片的REC均随着处理温度的降低而呈“S”形上升, 由此计算出“S”形拐点对应的温度即为茶梅叶片的LT50 , 其温度值在- 1215℃至- 14℃之间, 这可认为是茶梅抗寒能力的重要指标。关键词:     

Sporulation of Pyrenopeziza brassicae (light leaf spot) on oilseed rape (Brassica napus) leaves inoculated with ascospores or conidia at different temperatures and wetness durations

In controlled environment experiments, sporulation of Pyrenopeziza brassicae was observed on leaves of oilseed rape inoculated with ascospores or conidia at temperatures from 8 to 20°C at all leaf wetness durations from 6 to 72 h, except after 6 h leaf wetness duration at 8°C. The shortest times from inoculation to first observed sporulation ( l ₀), for both ascospore and conidial inoculum, were 11–12 days at 16°C after 48 h wetness duration. For both ascospore and conidial inoculum (48 h wetness duration), the number of conidia produced per cm² leaf area with sporulation was seven to eight times less at 20°C than at 8, 12 or 16°C. Values of Gompertz parameters c (maximum percentage leaf area with sporulation), r (maximum rate of increase in percentage leaf area with sporulation) and l ₃₇ (days from inoculation to 37% of maximum sporulation), estimated by fitting the equation to the observed data, were linearly related to values predicted by inserting temperature and wetness duration treatment values into existing equations. The observed data were fitted better by logistic equations than by Gompertz equations (which overestimated at low temperatures). For both ascospore and conidial inoculum, the latent period derived from the logistic equation (days from inoculation to 50% of maximum sporulation, l ₅₀) of P. brassicae was generally shortest at 16°C, and increased as temperature increased to 20°C or decreased to 8°C. Minimum numbers of spores needed to produce sporulation on leaves were ≈25 ascospores per leaf and ≈700 conidia per leaf, at 16°C after 48 h leaf wetness duration.