642 research outputs found
Characteristics of the grain-filling process and starch accumulation of high-yield common buckwheat âcv. Fengtian 1â and tartary buckwheat âcv. Jingqiao 2â
High-yield common buckwheat âcv. Fengtian 1â (FT1) and tartary buckwheat âcv. Jingqiao 2â (JQ2) were selected to investigate the characteristics of the grain-filling process and starch accumulation of high-yield buckwheat. FT1 had an average yield that was 43.0% higher than that of the control âcv. Tongliaobendixiaoliâ (TLBDXL) in two growing seasons, while JQ2 had an average yield that was 27.3% higher than that of the control âcv. Chuanqiao 2â (CQ2). The Richards equation was utilized to evaluate the grain-filling process of buckwheat. Both FT1 and JQ2 showed higher values of initial growth power and final grain weight and longer linear increase phase, compared with respective control. These values suggest that the higher initial increasing rate and the longer active growth period during grain filling play important roles to increase buckwheat yield. Similar patterns of starch, amylose and amylopectin accumulation were detected in common buckwheat, leading to similar concentration of each constituent at maturity in FT1 and TLBDXL. Tartary buckwheat showed an increasing accumulation pattern of amylose in developing seeds, which differed from that of starch and amylopectin. This pattern led to a significant difference of the concentrations of amylose and amylopectin at maturity between JQ2 and CQ2, the mechanisms of which remained unclear. Nevertheless, both FT1 and JQ2 showed increased starch, amylose, and amylopectin accumulation during the physiological maturity of grains. The results suggest that prolonging the active grain-filling period to increase carbohydrate partitioning from source to seed sink can be an effective strategy to improve buckwheat yield
Risk factors for Lyme disease : A scale-dependent effect of host species diversity and a consistent negative effect of host phylogenetic diversity
Biodiversity can influence disease risk. One example of a diversity-disease relationship is the dilution effect, which suggests higher host species diversity (often indexed by species richness) reduces disease risk. While numerous studies support the dilution effect, its generality remains controversial. Most studies of diversity-disease relationships have overlooked the potential importance of phylogenetic diversity. Furthermore, most studies have tested diversity-disease relationships at one spatial scale, even though such relationships are likely scale dependent. Using Lyme disease as a model system, we investigated the effects of host species richness and phylogenetic relatedness on the number of reported Lyme disease cases in humans in the U.S.A. at two spatial scales (the county level and the state level) using piecewise structural equation modelling. We also accounted for relevant climatic and habitat-related factors and tested their correlations with the number of Lyme disease cases. We found that species assemblages with more related species (i.e., host species in the order Rodentia) were associated with more Lyme disease cases in humans. Host species richness correlated negatively with the number of Lyme disease cases at the state level (i.e., a dilution effect), a pattern that might be explained by the higher number of reservoir-incompetent species at high levels of species richness at this larger spatial scale. In contrast, a positive correlation was found between species richness and the number of Lyme disease cases at the county level, where a higher proportion of rodent species was associated with higher levels of species richness, potentially amplifying the disease risk. Our results highlight that analyse at a single spatial scale can miss some impacts of biodiversity on human health. Thus, multi-scale analyses with consideration of host phylogenetic diversity are critical for improving our understanding of diversity-disease relationships.Peer reviewe
Photosynthetic characteristics of summer maize under different planting patterns and the responses to nitrogen application of previous crop
Maize (Zea mays L.) is one of the most important grain crops in the North China Plain. Management practices affect the photosynthetic characteristics and the production of summer maize. This two-year (2014-2015) study examined the effects of different planting patterns and the application of nitrogen to previous winter wheat (Triticum aestivum L.) on the photosynthetic characteristics, yield and radiation use efficiency (RUE) of summer maize. Field experiments used a two-factor split-plot design with three replicates at Taian, Shandong Province, China (36°09âČ N, 117°09âČ E). The experiments involved two planting patterns (ridge planting, RP; and uniform row planting, UR) and two nitrogen application levels of previous winter wheat (N1, 112.50 kg ha-1; N2, 225.00 kg ha-1). The results indicated that the application of nitrogen on previous crop and ridge planting of the following crop had significant effects on the photosynthetic characteristics and yields of summer maize. Compared with UR, this study found that RP increased the chlorophyll content index (CCI), leaf area index (LAI), net photosynthetic rate (Pn), dry matter (DM), yield and grain RUE by 4.1%, 6.3%, 5.2%, 6.4%, 8.9% and 9.4%, respectively. The CCI, LAI, Pn, yield, and grain RUE of N2 were 9.7%, 3.3%, 3.7%, 10.0% and 10.1% higher than those of N1, respectively. RP combined with the application of nitrogen on previous crop of winter wheat could increase the CCI, LAI, Pn, DM, ultimately increasing the grain yield and RUE of the following summerâs maize. It was concluded that previous crop nitrogen application and RP pattern treatment resulted in optimal cropping conditions for the North China plain
Computing the first eigenpair of the p-Laplacian via inverse iteration of sublinear supersolutions
We introduce an iterative method for computing the first eigenpair
for the -Laplacian operator with homogeneous Dirichlet
data as the limit of as , where
is the positive solution of the sublinear Lane-Emden equation
with same boundary data. The method is
shown to work for any smooth, bounded domain. Solutions to the Lane-Emden
problem are obtained through inverse iteration of a super-solution which is
derived from the solution to the torsional creep problem. Convergence of
to is in the -norm and the rate of convergence of
to is at least . Numerical evidence is
presented.Comment: Section 5 was rewritten. Jed Brown was added as autho
The evolution of microstructure and electrical performance in doped Mn-Co and Cu-Mn oxide layers with the extended oxidation time
Mn-Co and Cu-Mn based alloy coatings are deposited on 430 SS by high energy micro-arc alloying process, and then alloy coatings are oxidized at 750 â in air to form the spinel oxides. Some composite oxides, such as Co3O4, Mn2O3 and (Mn,Co)3O4, are formed at the initial stage of oxidation. The single-phase spinel (pure MnCo2O4) without impurity phases is only found on the surface of Co-33Mn-17Cu oxide layer with the extended oxidation time, its area-specific resistance values at 500 â to 800 â are low and close to that of Mn-35Cu oxide layer which mainly composed of Cu1.2Mn1.8O4 spinel
Measurements of the observed cross sections for exclusive light hadrons containing at , 3.650 and 3.6648 GeV
By analyzing the data sets of 17.3, 6.5 and 1.0 pb taken,
respectively, at , 3.650 and 3.6648 GeV with the BES-II
detector at the BEPC collider, we measure the observed cross sections for
, , ,
and at the three energy
points. Based on these cross sections we set the upper limits on the observed
cross sections and the branching fractions for decay into these
final states at 90% C.L..Comment: 7 pages, 2 figure
Partial wave analysis of J/\psi \to \gamma \phi \phi
Using events collected in the BESII detector, the
radiative decay is
studied. The invariant mass distribution exhibits a near-threshold
enhancement that peaks around 2.24 GeV/.
A partial wave analysis shows that the structure is dominated by a
state () with a mass of
GeV/ and a width of GeV/. The
product branching fraction is: .Comment: 11 pages, 4 figures. corrected proof for journa
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