光谱判断田间鲜烟叶成熟度的影响因子研究

利用便携式地物波谱仪Field Spec 3测量烤烟成熟期烟叶的反射光谱,针对采收成熟度M2、M3,分析比较同一时间不同测量位点、及同一位点不同测量时间的反射光谱差异。结果表明:反射光谱的差异在不同测量位点主要体现在350~780 nm可见光波段和780~1300 nm近红外波段,在不同测量时间主要体现在780~1300 nm近红外波段。因此,利用光谱仪判断鲜烟叶成熟度,受测量位点的影响较大,而受测量时间的影响较小,但若测量烟叶生理生化组分、厚度和水分等内在指标,时间及天气状况是必须考虑的重要因素。     

基于相对熵排序的建筑工程项目投标决策

投标决策是施工企业面对的重要问题．在建筑工程项目投标问题上，先建立风险指标体系，再结合层次分析法和信息熵法求得风险指标的综合权重，然后借助相对熵排序法，对各个方案进行综合评价，得到有效反映各方案差异的评价模型，通过对比可知此法可行有效，且灵敏度高．     

铜仁烤烟单叶重现状与提升烟叶质量对策

根据铜仁烤烟单叶重的调查数据，认真梳理了铜仁烤烟单叶重的现状，分析了铜仁烤烟单叶重存在的问题，从烟叶收购政策和烟叶生产技术两个方面有针对性的提出提升铜仁烟叶质量的对策，为铜仁烤烟产业的持续健康发展提供理论指导。     

茶树小分子量热激蛋白基因CsHSP17.2的克隆与表达分析

[目的]进一步了解茶树小分子量热激蛋白基因CsHSP17.2在逆境胁迫条件下的分子生物学功能.[方法]利用RT-PCR技术从茶树‘迎霜’中克隆得到CsHSP1 7.2基因,运用生物信息学软件分析其核苷酸和编码蛋白,通过Real-timePCR分析其表达模式.[结果]该基因开放阅读框长度为453 bp,编码150个氨基酸,蛋白质相对分子质量为17.2×10a,理论等电点5.56;无信号肽位点,属于非分泌型蛋白;被定位于细胞质中.系统发育树分析表明,茶树CsHSP1 7.2与水稻(GenBank登录号:P27777)和花生(ABC41131)的进化关系较近,属于小分子量热激蛋白基因家族第Ⅰ亚族.qRT-PCR分析发现,茶树CsHSP17.2属于组成型基因;高温(38℃)处理1h能显著提高CsHSP17.2 mRNA的相对表达量(P＜0.05);干旱(100 g·L-1 PEG 6000)、高盐(200 mmol· L-1 NaCl)和外源脱落酸(200 mg· L-1 ABA)处理条件下,该基因的转录水平均出现不同程度的上调.[结论]克隆得到茶树‘迎霜’小分子量热激蛋白基因CsHSP17.2,其在花中表达量最高,且响应高温、干旱、高盐和外源脱落酸胁迫.     

水稻粒宽突变体gw87的基因定位及候选基因分析

【目的】对水稻粒宽突变体gw87（grain width 87）进行表型鉴定、遗传分析、基因定位及候选基因分析,为探明该基因调控水稻籽粒大小的分子机制及应用潜力奠定基础。【方法】利用甲基磺酸乙酯诱变籼稻恢复系材料676R,获得一份籽粒宽度和千粒重显著增加的突变体gw87。对该突变体进行表型观察、农艺性状调查及外源油菜素内酯（BL）敏感性、叶绿素含量、光合参数测定,了解其表型特征及生理特性。调查gw87与676R杂交F₁的表型和F₂群体的分离情况,分析其遗传行为;选取该群体中的突变植株进行高通量测序,并利用gw87与粳稻品种日本晴杂交的F₂代作为定位群体,通过MutMap分析和分子标记定位,遴选候选基因并进行DNA和cDNA测序验证。利用qRT-PCR分析gw87和676R中BR合成途径基因OsDWARF4、D11和D2的表达差异。【结果】与野生型亲本676R相比,gw87突变体的株高降低,节间缩短,其中,倒一节间长度缩短最大,并呈现出扭曲的形态;叶片长度减少,宽度增加;单株有效穗数、主穗穗长和结实率显著降低,但籽粒宽度和千粒重显著增大。BL敏感性试验显示,gw87突变体幼苗对外源BL的敏感性降低。光合色素和光合参数测定表明,gw87光合色素含量增加,光合速率也有所增加。遗传分析表明gw87的突变性状是由1对隐性核基因控制。MutMap分析显示gw87突变基因位于第5染色体中部,在该染色体区域仅有1个碱基突变引起编码氨基酸变化;分子标记连锁分析表明该突变基因位于InDel标记X2和X3之间约101 kb的染色体区域;综合这两方面分析结果,最后遴选出gw87候选基因是编码一个含有AP2/EREBP DNA绑定结构域的转录因子基因LOC_Os05g32270。对该候选基因进行DNA和cDNA测序验证,发现gw87突变体中该基因DNA的第1 041位的碱基由G突变为A,导致与该位点相邻的76 bp内含子序列被剪接为外显子,引起阅读框移码,蛋白翻译提前终止。qRT-PCR分析显示gw87突变体中BR合成途径基因的表达量显著上调,表明gw87突变体中BR信号减弱。【结论】gw87是smos1、shb、rla1、ngr5的新等位突变体,但与这些突变体表型不同,gw87籽粒的宽度和千粒重显著增加,可能是LOC_Os05g32270的突变位点不同,导致其编码蛋白的功能活性不同所造成。     

从一本六年产量收入日记帐分析茶叶增产增收途径

2012年,我们在实施全国农业示范推广补助项目,对湖北省宜昌市夷陵区茶叶科技示范户周先明进行调查,发现该户从2009年起每天采茶都记了日记帐,我们分析了他4年采茶产量收入,春茶产量占全年29%,其收入占全年60%,亩产鲜叶量为1256.3公斤,亩现金收入为6054元。2013年实施该项目后,我们一是通过他多年每日记载数据分析绘制成图;二是实地茶园土壤肥力性状,树体结构和管理措施调查分析,提出其水田茶园不同于过去旱坡茶园的综合高效管理增产增收途径,在2013-2014年早春干旱情况下,茶叶产量收入得到较大提高,对全区茶叶生产具有重要指导作用。     

Controlling sprouting in potato tubers using ultraviolet-C irradiance

Legislation limiting the use of chlorpropham (CIPC), the major potato sprout suppressant, has led to a need for new technologies to extend storage life of tubers. Ultra violet C (UV-C) has been used postharvest to reduce disease incidence on many crops, yet its use and efficacy as a sprout suppressant has not been investigated. The aim of this project was to identify the optimum dose and treatment timing of UV-C treatment on potato tubers as an alternative method of sprout suppression to reduce the dependence on chemical sprout suppressants. Up to six potato cultivars over two seasons were treated with varying doses of UV-C ranging from 0 to 30 kJ m⁻² either at harvest or at first indication of dormancy break. The tubers were stored at 9 °C and sprout growth and incidence assessed. Treatment with moderate UV-C doses (5–20 kJ m⁻²) suppressed sprout length and sprout incidence in a range of cultivars. Periderm DNA damage and programmed cell death were not detected in response to any of the UV-C doses. The inactive ABA metabolite, ABA-GE, increased in response to 10 or 20 kJ m⁻² within 72 h of treatment. Multivariate analysis showed a negative relationship between ABA metabolites and sprout growth/incidence during storage. This study found that UV-C reduced sprout growth in potato with no deleterious effects on tuber quality. This suggests potential for further development as an alternative or supplement to conventional sprout suppressant technologies.     

鸡脚重性状的全基因组关联分析

鸡(Gallus gallus)脚重性状为鸡产业中的重要经济性状.为了揭示鸡脚重性状的遗传基础,寻找可用于鸡脚改良的分子标记,本研究以核心群京海黄鸡为实验动物,测定其脚重,利用简化基因组测序技术在整个基因组范围内检测与脚重相关的SNPs.共检测到16个与脚重相关的SNPs位点,其中13个集中分布在4号染色体上72.8～77.9 Mb区域;2个SNP位点rs475641139和rs475548810达到5％ Bonferroni全基因组显著水平(P＜5.5E-07),其余位点达到全基因组潜在显著水平(P＜1.1E-05).筛选每个SNP周围1 Mb区域内的基因,共找到9个可能的候选基因,并使用基因本体论(Gene Ontology,GO)数据库对9个候选基因的细胞组分、分子功能和参与的生物学进程进行了分析.结果表明二氢蝶啶还原酶(dihydropteridine deductase,QDPR)基因、LIM域结合蛋白2(LIM domain-binding protein 2,LDB2)基因、类184B家族(family with sequence similarity 184 memberB,FAM184B)基因、复合信号免疫球蛋白J结合蛋白(recombination signal binding protein for immunoglobulin kappa J region,RBPJ)基因、纤维母细胞生长因子结合蛋白2(fibroblast growth factor-binding protein 2,FGFBP2)基因、富亮氨酸重复蛋白5(F-box and leucine-rich repeat protein 5,FBXL5)基因、胆囊收缩素受体A(cholecystokinin receptor type A,CCK1R)基因、肌动蛋白互作蛋白1 (WD repeat containing protein 1,WDR1)基因和类桶状蛋白4(tubby like protein 4,TULP4)9个基因和4号染色体72.8～77.9 Mb区域可能为影响鸡脚重性状的重要候选基因和潜在功能区域.本研究为鸡脚重性状的标记辅助选择提供了理论依据.     

不同生态环境下甘蔗组合的生长表现和适应性

以2017—2018年组配的119个甘蔗组合为材料,分别在广西的南宁、崇左、来宾同时开展组合评价试验,基于锤重性状进行联合方差分析和遗传参数估计,并采用回归分析和AMMI模型对组合进行稳定性分析。结果表明:不同的组合、环境及组合与环境互作在锤重间的差异均达到了极显著水平(P0.01);3个试验点锤重的广义遗传率均属于中等偏低水平;崇左、来宾试验点的锤重变异系数较大,南宁试验点的锤重变异系数较小;643、404、575、972、636、144、YC95、1470、755、409、701、832、YC37、579等组合表现出高产、稳产和适应性广的特性;结合锤重和组合入选率综合分析,组合449、YC127、796、YC44、533、570、YC123、391、546、403、YC90、252在南宁试验点的表现为锤重和组合入选率较高;组合643、212、YC61、432、903、YC95、YC44、368、YC83、YC127、YC112、701、411、YC90、YC123在崇左试验点的表现为锤重和组合入选率较高;组合643、404、449、144、403、YC48在来宾试验点的表现为锤重和组合入选率较高。     

Effect of feeding different sources of selenium on growth performance and antioxidant status of broilers

ABSTRACT

1. This study was conducted to determine the effect of different sources of selenium (Se) on breast and liver tissue deposition, apparent metabolisable energy (AME), growth performance and antioxidant status of broilers, measured as Se content in liver and breast tissues and glutathione peroxidase (GSH-Px) in blood, when used in 0–35 d broiler chicken diets.

2. A total of 200 male Ross 308 broilers were used in the feeding trial, which comprised two dietary phases, a starter from 0 to 21 d and finisher from 21 to 35 d of age. Four treatments with 10 replications each were used. A control diet (C) was formulated that was sufficient in protein and energy (230 and 215 g/kg of crude protein and 12.67 and 13.11 MJ/kg of metabolisable energy, respectively), for both phases, but contained background Se only from the feed ingredients. Diet 2 (IS) was supplemented with 10.35 g/t inorganic, elemental source of Se. Diet 3 (SY) was supplemented with 136.36 g/t selenised yeast, an organic source derived from Saccharomyces cerevisiae. Diet 4 (SS) was supplemented with 0.666 g/t sodium selenite, an inorganic source.

3. Birds fed the SY diet consumed less and weighed less than those fed IS or C (P < 0.05; 0–35 d of age), but there was no difference compared to birds fed SS diets. There were no differences in FCR or dietary AME between broilers fed different Se sources. All diets containing supplementary Se increased concentrations in the liver and breast muscle, and for GSH-Px levels in blood compared to birds fed the C diet (P < 0.001). Birds fed SY diets had greater Se levels in liver and breast tissues compared to birds fed any of the other diets (P < 0.001).

4. Diets supplemented with Se had variable effects on broiler growth performances and antioxidant status. Feeding Se from a yeast source has higher transfer into breast tissues. Feeding different sources and levels of Se to birds in a more challenging situation to induce oxidative stress may bring more conclusive results.