施氮处理对不同筋型小麦产量和品质的影响

为探究施氮处理对不同筋型小麦的植株性状、籽粒产量和品质的影响,采用盆栽试验,选用强筋小麦品种中麦578（A1）和中麦5051（A2）、弱筋小麦品种扬麦15（A3）和扬麦24（A4）为供试品种,在施氮量相同的条件下进行底施（B1）和追施（B2）处理。结果表明：在其他栽培措施相同条件下,强筋小麦穗长、总小穗数、千粒重和籽粒产量均优于弱筋小麦,其中A1籽粒产量分别比A2、A3和A4高0.44%、49.81%和15.27%;施氮处理中B2的株高、穗长、穗粒数、总小穗数和籽粒产量均高于B1;不同处理组合中,强筋小麦品种A1B2的植株和产量性状优于其他处理;强筋小麦品种的籽粒蛋白质含量和蛋白质产量均高于弱筋小麦品种,且具有极显著差异（P<0.01)。本试验中强筋小麦品种中麦5051在氮肥追施处理中可以兼顾籽粒产量、蛋白质含量和蛋白质产量。     

光氮互作对芹菜幼苗生长及生理特性的影响

光质和施氮量是影响芹菜生长发育的关键因素,适宜的光氮组合能有效提升芹菜幼苗质量。为优化芹菜工厂化育苗,本试验设置2种光质(白光,W;蓝光,B)和2种施氮量(8mmol/L KNO_3,高氮,H;4mmol/L KNO_3,低氮,L),以WH为对照,研究光氮互作对芹菜幼苗生长、生理代谢和元素积累的影响。结果表明:与WH相比,WL和BH处理的芹菜全株干重分别显著减少43.18%和55.07%,WL处理的叶片和叶柄中硝酸盐、可溶性蛋白质和总游离氨基酸质量分数均显著降低,BH处理的叶片和叶柄中硝酸盐、可溶性蛋白质和矿质元素质量分数显著增加,而叶片中可溶性糖、丙氨酸族和丝氨酸族氨基酸质量分数均显著降低。然而BL处理的芹菜全株干重比WH显著增加32.18%,叶片可溶性蛋白质、叶柄组氨酸(His)和脯氨酸(Pro)质量分数均显著增加。利用隶属函数分析对芹菜幼苗生长发育进行综合评价发现,BL处理表现最优。综上所述,蓝光和低氮组合能促进芹菜干物质积累,提高可溶性蛋白质和游离氨基酸质量分数,进而促进芹菜幼苗生长发育。     

减氮控水对日光温室番茄-小型西瓜产量、品质及氮素利用的影响

研究日光温室滴灌施肥条件下,不同水肥组合对作物产量、品质和氮素利用的影响,综合评价优化水肥和常规水肥管理的调控效应。田间试验设置4个水氮处理,包括不施氮+常规灌溉(N_0+FI)、常规施氮+常规灌溉(FT+FI)、优化施氮+常规灌溉(OPT+FI)、优化施氮+优化灌溉(OPT+OI)。测定不同处理下秋冬茬番茄-春茬小型西瓜的产量、品质以及根、茎、叶、果实氮素吸收量。结果表明:优化水氮处理(OPT+OI)番茄产量和果实可溶性糖、可滴定酸和Vc含量与农户常规水氮处理(FT+FI)无显著差异,但番茄果实的硝酸盐含量降低了66.3%(P0.05);灌溉量相同时,减氮40%处理(OPT+FI)的小型西瓜产量相比常规施氮处理(FT+FI)提高了13.1%;OPT+OI处理果实的可溶性糖、可滴定酸和Vc含量较对照处理(N_0+FI)均显著提高。不同水肥处理下,两季作物氮在各器官的累积量均表现为果实叶茎根。随着番茄的生长,果实和茎的氮素携出量占总携出量的比例分别由62.4%和5.9%增加至67.1%和6.3%,而根和叶中氮素携出量降低,OPT+OI处理果实氮素携出所占比例增量最大,促进了营养器官中的氮素向果实中转运。在当前日光温室栽培条件下,适当优化施氮量和灌溉量既可以保证作物产量和氮素吸收,同时提高果实的品质。     

不同保水剂对土壤特性及烤烟生长的影响

为提高秦巴山区黄棕壤烟田的土壤性能,减少季节性干旱对烤烟生长的影响,以不施保水剂为对照,在烟田整地起垄前分别施入聚丙烯酸钾(K-PAM)、聚丙烯酰胺(PAM)和腐殖酸钾(KHm)3种保水剂,测定施用不同保水剂后的土壤容重、土壤水分和烤烟生长状况、常规化学成分及经济性状。结果表明,聚丙烯酸钾和聚丙烯酰胺保水剂均降低0～40cm土层土壤容重,在烤烟旺长期提高0～40cm土层土壤水分。不同保水剂均可提高烤烟常规化学成分含量,其中腐殖酸钾保水剂显著降低烤烟的糖碱比和氮碱比。聚丙烯酸钾保水剂提高烤烟的产量、产值、上等烟比例及净增产值,而聚丙烯酰胺和腐殖酸钾保水剂处理组则降低烤烟的净增产值。因此,建议秦巴山区黄棕壤烟田选用聚丙烯酸钾类保水剂。     

不同贮藏温度和保鲜处理对黄秋葵贮藏品质及生理的影响

为探讨采后不同贮藏温度对黄秋葵贮藏品质的影响以及不同保鲜剂对黄秋葵抗氧化酶活性的影响，以台湾“五福”黄秋葵为试材，分别置于低温（（4±1）℃、（9±1）℃、（14±1）℃）和常温（（20±1）℃）条件下贮藏，研究温度对其贮藏品质的影响；采用1.0%壳聚糖、5.0 mmol/L水杨酸、0.5片安喜布、5%O2+8%CO2处理黄秋葵，研究保鲜处理对其抗氧化酶活力的影响。结果表明：（9±1）℃贮藏组的保鲜效果最好，显著改善了贮藏期间黄秋葵的失重率、硬度、叶绿素含量、VC含量、L值、呼吸强度、乙烯释放量、MDA含量、细胞膜相对电导率；4种保鲜处理均能显著提高黄秋葵的SOD、POD、CAT活性，并维持其活性在相对较高的水平；同时，显著抑制黄秋葵果实MDA含量的升高。通过研究发现，壳聚糖涂膜液处理组的效果最佳，水杨酸处理组次之并优于1-MCP处理组，气调处理组的效果相对较差。     

鲜枣片组合干燥技术研究

分别采用真空微波干燥、变温压差干燥和二者组合方式对鲜枣片进行干燥处理。研究不同功率、不同真空度下真空微波干燥的特性,确定鲜枣片真空微波干燥的适宜干燥参数为:功率4 kW,真空度0.05 MPa。研究不同温度、不同真空度和不同物料含水量下变温压差干燥的特性,确定鲜枣片变温压差干燥的适宜参数为:温度60℃,真空度0.05 MPa,含水量16%。以产品色泽、复水比、收缩比、硬度、脆度等品质特性为评价指标,比较真空微波干燥、变温压差干燥和组合干燥3种干燥方式对鲜枣片品质的影响,结果表明组合干燥相比单一干燥可明显提高枣片品质。     

中药对肉仔鸡脂质代谢及肉品质的影响

将120只1周龄肉仔鸡随机分成4组,每组30只,前3组(试验Ⅰ、Ⅱ、Ⅲ组)分别喂以含1%的3种不同中药组方的饲粮,第Ⅳ组为对照组,只喂基础日粮.试验期6周.结果(1)与对照组相比,Ⅰ组血清TC、LDL-C极显著下降(P＜0.01);Ⅱ组血清TC、LDL-C极显著下降(P＜0.01),TG也下降(P＜0.05),HDL-C显著升高(P＜0.01);Ⅲ组血清LDL-C极显著下降(P＜0.01),HDL-C则显著升高(P＜0.01);试验Ⅰ～Ⅲ组血清总脂都极显著下降(P＜0.01);与Ⅱ组相比,Ⅰ组血清LDL-C、Ⅲ组TC存在显著差异(P＜0.01).(2)与对照组相比,胸肌组织中,各试验组TG极显著下降(P＜0.01),Ⅱ组TC显著下降(P＜0.05);腿肌中,各组TC显著下降(P＜0.05),TG下降极显著(P＜0.01);肝脏中各组TC、TG均极显著下降(P＜0.01);与Ⅱ组相比,Ⅰ组肝TG差异极显著(P＜0.01);Ⅲ组胸肌TG、肝TG有显著差异性(P＜0.05).(3)7周龄末鸡体重与对照组相比,Ⅱ组差异极显著(P＜0.01),Ⅲ组差异显著(P＜0.05);Ⅱ组料肉比比对照组极显著下降(P＜0.01).(4)肌肉中的营养成分,Ⅰ、Ⅱ组腿肌中粗脂肪比对照组极显著下降(P＜0.01),Ⅱ组腿肌中粗蛋白含量显著升高(P＜0.01).结论中药组方能不同程度地调整鸡脂质代谢,提高生产性能和改善鸡肉品质.在3个不同中药组方中,综合效果Ⅱ方最优.     

Genotypic Variability in Biomass Protein and Nucleic Acids in Four Linum Species to Sodicity Stress

Differences in gas exchange parameters i.e. carbon exchange rate (CER), transpiration (Tr), water vapor conductance (g) were investigated, under a controlled environment, in a semi-dwarf (SD) Triticum aestivum line, its tall (TL) near isoline and the Payne (PA) variety characterized by small leaves. The plants were maintained in: (a) optimal substrate moisture condition (CTR); (b) salinized by watering with a 0.12 m NaCl solution (SLT); (c) water stressed by withholding waterings during a period of six days (STR); (d) stressed and salinized during the same period and with the same saline solution (S + S). CER and Tr were negatively affected by the stresses; SLT and S + S treatments had a higher WUE compared to their respective controls CTR and STR.
SD line had a better performance in terms of CER and WUE, particularly when water and salt stresses interacted. Leaf anatomy and assimilation/internal CO₂ concentration curves contributed to explaining the SD performance.     

Impact of postovulatory food deprivation on the ova transport, hormonal profiles and metabolic changes in sows.

The effect of food deprivation on ova transport, hormonal profiles and metabolic changes was studied in 20 crossbred multiparous sows during their second oestrus after weaning. To determine the time of ovulation, transrectal ultrasonographic examination was performed. The sows were divided into 2 groups, one control group (C-group), which was fed according to Swedish standards, and one experimental group (E-group). The E-group sows were deprived of food from the first morning meal after ovulation until slaughter. Blood samples were collected every second hour from about 12 h before expected ovulation in the second oestrus after weaning until slaughter and were analysed for progesterone, prostaglandin F2 alpha-metabolite, insulin, glucose, free fatty acids and triglycerides. All sows were slaughtered approximately 48 h after ovulation and the genital tract was recovered. The isthmic part of the oviduct was divided into 3 equally long segments and flushed separately with phosphate buffered saline (PBS). Uterine horns were also flushed with PBS. A significantly greater number of ova were found in the first and second part of the isthmus in the E-group (p = 0.05) while in the C-group most of the ova were found in the third part of the isthmus or the uterus (p = 0.01). The level of prostaglandin F2 alpha-metabolite was significantly higher in the E-group compared with the C-group. The concentration of progesterone increased in both groups after ovulation but there were no significant differences between the groups. The other blood parameters showed that the food-deprived sows were in a catabolic state. The 48 h period of fasting results, directly or indirectly in an delayed ova transport, which may be due to a delayed relaxation in the smooth circular muscle layer of the isthmus.