【目的】探究在不同尿素类型与施用深度下,冬小麦开花后旗叶光合性能和光系统Ⅱ(PSⅡ)性能及氮素利用的差异,以期为协同提高氮素利用效率与籽粒产量,简化小麦生产过程提供理论依据。【方法】于2015—2016年与2016—2017年冬小麦生长季进行试验,以‘济麦22’为供试材料,采用二因素裂区试验设计,尿素类型处理(T)为主区,施用深度处理(D)为裂区。尿素类型包括普通尿素处理(T1,基追比为4∶6)与普通和控释尿素配施处理(T2,普通尿素、硫包膜尿素、树脂包膜尿素以4∶3∶3混合一次性基施),施用深度为地下5 cm (D1)与10 cm (D2)。测定了开花后旗叶气体交换参数和叶绿素荧光诱导动力学曲线(OJIP),及不同生育时期地上植株氮素积累量。【结果】2年试验结果表明,相较于普通尿素处理,普通和控释尿素配施处理可显著提高冬小麦有效穗数和千粒重,对穗粒数影响不显著;施用深度对2016—2017年千粒重影响显著,对2年单位面积有效穗数和穗粒数影响不显著;普通和控释尿素配合深施处理(T2D2)产量显著高于其它处理。尿素类型和施用深度对气体交换参数影响显著,普通和控释尿素配合深施处理可显著提高花后旗叶净光合速率(Pn)和气孔导度(Gs),显著降低胞间CO2浓度(Ci),相对延长了高光合持续期。普通和控释尿素配合处理较普通尿素处理显著提高了旗叶光系统Ⅱ(PSⅡ)反应中心对光能的吸收(φPo)、转化(φEo)以及电子在电子传递链中转移的效率(ψo);显著改善了电子传递链供体侧(Wk)和受体侧(Vj)性能,有效提高了产量形成期光合性能的稳定性。同一尿素类型下,深施处理对光系统Ⅱ(PSⅡ)性能的改善大于浅施处理。相较于普通尿素处理,普通和控释尿素配施处理可显著提高冬小麦生育中后期植株氮素积累量;相较于浅施处理,深施处理对冬小麦不同生育期氮素积累均有不同程度的提高。除对2016—2017年氮素生理利用率(NPE)影响不显著外,普通和控释尿素配合深施处理显著提高了2年冬小麦氮肥农学利用效率(NAE)、氮肥偏肥生产力(PEPN)、成熟期氮肥表观回收率(NRE)和2015—2016年氮素利用效率。【结论】普通尿素与控释尿素配合深施可显著提高冬小麦花期旗叶光合性能,促进氮素利用,增加产量,有利于冬小麦产量与氮肥利用之间的协同提高,省时增效效果明显,是本试验中最佳组合模式。 相似文献
Comparative functional responses (FRs) can predict impacts of invasive species, including piscivorous fishes, via quantifying their depletion of native food resources as a function of prey density. The utility of FRs for predicting impacts on prey populations by invasive fishes of different trophic guilds was tested here by comparing the FRs of the invaders Cyprinus carpio and Carassius auratus, with three native, trophically analogous fishes, Barbus barbus, Squalius cephalus and Tinca tinca. Chironomid larvae and Gammarus pulex were used as prey items. Predictions, developed from studies on the foraging of C. carpio and C. auratus in the literature, were that the invaders would have significantly higher consumption rates for chironomids than the native fishes, but not for G. pulex. Mean consumption rates for chironomids were significantly lower for both invaders than B. barbus and S. cephalus, but were similar to T. tinca. Barbus barbus had a significantly lower consumption rate of G. pulex than both invaders, but there were no significant differences between S. cephalus, T. tinca and the invaders. All FRs were type II, with FR curves for the invaders preying upon chironomids never being significantly higher than the native fishes, contrary to predictions. For G. pulex, some significant differences were apparent between the invaders and native fishes, but again were contrary to predictions. These results indicated that when predation impacts of invasive fishes could also be a function of their population density and body sizes, these parameters should be incorporated into FR models to improve impact predictions. 相似文献
1. The purpose of this study was to investigate the distribution of Toll-like receptor-4 (TLR4) and major histocompatibility complex (MHC) class II molecules of the spleen in chicks treated with lipopolysaccharide (LPS) during the first 2 weeks of their life.
2. A total of 225 Ross-308 commercial broiler chicks were used. Within the 2-week experimental period, chicks were divided into 5 main groups according to the days of decapitation which were 1, 4, 7, 10 and 14 d after hatch. Each main group had 45 chicks. The main groups were further divided into three subgroups (15 chicks each), which included control chicks (no injection), and phosphate-buffered saline (PBS) and LPS-injected chicks. Spleen samples were collected 1-, 3-, 6-, 12- and 24-h after the PBS or LPS administrations. Tissue sections were stained using streptavidin–biotin–peroxidase complex staining method.
3. From 1 d of age, TLR4 positivity was found in the spleen in diffuse granular form. The cells showing intense TLR4 positivity were observed in periellipsoidal lymphoid tissue in 4-d-old chicks. The same cells were determined in the germinal centre of the spleen in 7-d-old chicks. LPS stimulation led to an increase in the intensity of TLR4 positivity in 14-d-old chicks.
4. From 1 d of age, MHC class II positivity was found in both white pulp and red pulp. This was higher in 14-d-old chicks injected with LPS than in the controls and the chicks injected with PBS.
5. The findings indicate that, from 1 d of age in chicks, the spleen has both non-specific defence elements and the molecules having the information to induce adaptive immunity. In addition, at the end of the 2-week experimental period, it was determined that the spleen had the capacity to recognise antigens. 相似文献
AIM: To study the effect of p65 gene silencing by adeno-associated virus type 9 (AAV9)-mediated RNA interference on angiotensin Ⅱ (Ang Ⅱ; 10-6 mol/L for 24 h)-induced apoptosis of rat ventricular H9c2 myocytes, and to elucidate the possible mechanism. METHODS: The H9c2 cells were transfected with rAAV9-eGFP and rAAV9-eGFP-NF-κB p65-siRNA at multiplicity of infection (MOI)=4×106 vg/cell. eGFP expression in the cells was observed under an inverted fluorescence microscope, and the percentage of eGFP positive cells was determined by flow cytometry. The expression of p65 was determined by Western blot. CCK-8 assay was used to measured the viability of transfected H9c2 cells. The apoptosis of the cells transfected with the virus and with Ang Ⅱ stimulation was analyzed by flow cytometry. RESULTS: The cells began to exhibit eGFP expression on the 2nd day after transfection. The fluorescence intensity was increased over the time of transfection. eGFP expression reached the maximum on the 5th day, and the transfection efficiency was (52.7±1.9)% at this time point. Compared with blank control group, no significant effect of AAV9 on the viability of H9c2 cells was observed. In resting state, p65 in the H9c2 cells had a certain activity. After Ang Ⅱ stimulation, the activity of p65 was obviously increased, while transfection of rAAV9-eGFP-NF-κB p65-siRNA effectively inhibited the expression of p65. The apoptosis of H9c2 cells in Ang Ⅱ stimulation group was significantly higher than that in blank control group, while transfection of rAAV9-eGFP-NF-κB p65-siRNA effectively inhibited apoptosis of H9c2 cells. CONCLUSION: Transfection of rAAV9-eGFP-NF-κB p65-siRNA effectively inhibits the expression of p65 gene of NF-κB pathway in the H9c2 cells without causing cell growth inhibition, and reduces the apoptosis induced by Ang Ⅱ. 相似文献
A boron-containing pectic polysaccharide was isolated from Driselase digests of akamatsu (Pinus densiflora) cell wall. The boron-containing polysaccharide was purified by successive column chromatography of Cosmosil C18 OPN, DEAE Sepharose FF, and Superdex 75. The complex had 0.12% (w/w) boron (B) and11B-NMR spectroscopy showed the complex to be the tetrahedral diester form of boron. The sugar composition and glycosyl linkage analyses showed that the sugar portion of the complex was rhamnogalacturonan-II (RG-11). The boron-attached glycosyl residue was identified to be 2-O-Me-xylose-containing apiosyl side chain in RG-II. These results established that the location of borate in the cell wall is conserved among dicots, gramineous monocots, and coniferous gymnosperm.Part of this study was presented at the 8th Cell Wall Symposium, Norwich, September 3, 1998 相似文献