青藏高原青稞品质评价体系构建及生态区划分析

为探究青藏高原地区青稞(Hordeum vulgare L.var.nudum Hook.f.)品种品质间的差异,建立青稞品质评价指标体系,对青稞品质生态适应性进行区划。该研究以15个青藏高原主栽青稞品种为试验材料,连续两年种植于青藏高原具有代表性的8个生态区,测定了籽粒总淀粉、粗蛋白、粗脂肪、β-葡聚糖等13个品质指标,并利用单因素方差分析、相关性分析、主成分分析和聚类分析方法对被测指标进行分析排序。结果表明:(1)13个品质指标中有11个指标在15个参试品种间存在显著差异,有12个指标在8个种植区间存在显著差异;品质指标总黄酮含量与总多酚含量具有显著正相关关系,与β-葡聚糖含量存在极显著正相关关系;结合不同品种在不同生态区的表现,确定支链淀粉、直链淀粉、总黄酮、β-葡聚糖和总多酚含量为对青稞综合品质影响最大的指标。(2)聚类分析将15个参试品种分成4类,将8个种植地区聚类成3个生态区,各生态区品质表现较好的品种为‘昆仑18号’、‘昆仑19号’、‘昆仑15号’、‘甘青8号’和‘甘青4号’。(3)对所测品质指标在品种水平和地区水平上进行主成分分析发现,将13个品质指标均划分为5个主成分,累计方差贡献率分别为85.16%和94.40%;籽粒品质综合评价得分最高的品种为‘昆仑18号’,品质最优生态地区为青海省贵南县。     

国家大豆核心种质在黄淮夏播生态区的农艺性状及适应性初探

本研究对国家大豆核心种质在黄淮夏播生态区的农艺性状和适应性进行初步评价和研究,结果认为国家大豆核心种质在黄淮夏播生态区种植农艺性状变异丰富:主要农艺性状的变异系数在11 39%～54 12%之间,结荚高度、有效分枝和单株总荚数的变异系数分别达54 12%、52 50%和51 70%;50%以上的品种有1个或1个以上主要农艺性状与黄淮夏播生态区审定品种近似,部分品种单株荚数超过200个,在育种工作中具有实用价值.各生态类型大豆品种在黄淮夏播生态区的农艺性状与原生态区相比有所改变:除长江春大豆外,东北春大豆、北方春大豆、南方春大豆和南方夏大豆的生育期变异均变小;东北春大豆和北方春大豆的适应性不同,这验证了东北春大豆和北方春大豆是不同生态类型的观点;不同生态类型品种的生育期、株高、百粒重均有一定的改变,株高随着生长坏境的变化较易改变,生育期次之,百粒重表现较稳定.本研究为国家大豆核心种质在该地区的利用提供了参考.     

花生主要品质性状的主成分分析与综合评价

【目的】综合评价花生品种的主要品质性状,为花生品质育种和生产利用提供依据。【方法】利用DPSS软件对花生含油量、蛋白质、油酸、亚油酸、油亚比（O∕L）等主要品质性状进行主成分分析和聚类分析。【结果】主成分分析表明,将10个品质性状综合成为4个主成分因子,可以代表花生品质80.73﹪的原始数据信息量;聚类分析将51个花生品种划分为6类,各类别间品质和遗传距离有较大差距。【结论】利用主成分分析和聚类分析进行花生品质的综合评价,可以避免单一指标的片面性和不稳定性,对花生亲本的利用和品质育种提供重要的科学依据。     

不同抗旱性花生品种结荚期叶片生理特性

以12个花生品种为试验材料,在人工控水条件下,于结荚期设置0~80 cm土层相对含水量为70%和50% 2个处理,研究与花生抗旱性相关的叶片生理生化性状及不同品种抗旱的叶片机制.结果表明： 利用产量抗旱系数可将12个花生品种的抗旱性分为强、中、弱3级,抗旱性强的品种有A596、山花11号、如皋西洋生,中度抗旱品种有花育20、农大818、海花1号、山花9号和79266,抗旱性弱的品种有ICG6848、白沙1016、花17和蓬莱一窝猴.A596、山花11号、如皋西洋生的抗旱机制是具有较强的叶片抗氧化保护能力、较高的PSⅡ活性及光合速率(P_n).海花1号的叶片抗氧化保护能力较强,山花9号的PSⅡ活性有显著优势.相关分析表明,叶片P_n、气孔限制值(L_s)、最大光化学效率(F_v/F_m)、光化学猝灭系数(q_P)、丙二醛(MDA)含量、相对电导率和超氧化物歧化酶(SOD)活性与花生品种的抗旱系数有显著的相关性,是花生结荚期的重要抗旱性状.SOD活性的抗旱级别需在干旱胁迫下鉴定,其他性状可在正常灌水条件下鉴定.山花11号和79266可分别作为花生强、弱抗旱性鉴定的标准品种,山花11号可作为花生叶片优异抗旱性状鉴定的标准品种.     

干旱胁迫对花生根系生长发育和生理特性的影响

以花育17号和唐科8号两个花生品种为试验材料,在防雨棚栽培池内进行土柱栽培试验,研究了中度干旱胁迫和正常供水处理下花生生育后期根系形态发育特征和生理特性.结果表明: 唐科8号具有较发达的根系及较高的产量和抗旱系数,花育17号根系对干旱胁迫的适应性小于唐科8号.两品种根长密度、根系生物量均主要分布于0～40 cm土层中,但同一土层内两品种根系性状存在差异.与正常供水处理相比,干旱胁迫处理使花育17号各生育期总根长、根系总表面积和总体积均降低,而唐科8号除花针期显著降低外,其余生育期均明显升高;干旱胁迫增加了两品种20～40 cm土层内根系生物量、根系表面积和体积,而降低了40 cm以下土层内各根系性状;干旱胁迫处理使两品种饱果期40 cm以下土层内根系活力降低,且花育17号降低幅度高于唐科8号.干旱胁迫下两品种生育后期根系发育和生理特性的差异表明其根系在干旱胁迫下对水分吸收和利用存在差异.     

不同抗旱性花生品种的根系形态发育及其对干旱胁迫的响应

为明确不同抗旱性花生品种的根系形态发育特征,探讨其根系形态发育特征对不同土壤水分状况的响应机制,在防雨棚旱池内进行土柱栽培试验,研究抗旱型品种“花育22号”、“唐科8号”和干旱敏感型品种“花育23号”3个不同抗旱性花生品种根系形态发育特征及其对干旱胁迫的响应.结果表明:抗旱型品种根系较发达,具有较大的根系生物量、总根长、总根系表面积.干旱胁迫使抗旱型品种根系总表面积和体积增加,而干旱敏感型品种则相反.干旱胁迫显著增加抗旱型品种“花育22号”20 cm以下土层内根长密度分布比例及根系表面积和体积,但“唐科8号”相应根系性状仅在20-40 cm土层内增加;干旱胁迫使干旱敏感型品种“花育23号”40 cm以下土层内各根系性状升高,但未达显著水平且其深层土壤内各根系性状增加幅度小于“花育22号”.花生根系总长、总表面积及0-20 cm土层内根系性状与产量间呈显著或极显著正相关.土壤水分亏缺条件下,花生主要通过增加深层土壤内根长、根系表面积和体积等形态特性,优化空间分布构型,以调节植株对水分的利用.     

26份黄麻种质资源产量性状的主成分聚类分析及其评价

为了解所收集黄麻种质资源的产量性状及遗传多样性,为黄麻育种和生产利用提供科学依据。本研究对26份黄麻品种(系)的8个产量性状进行主成分估算,并以前3个主成分为基础,分别作聚类分析和二维排序图。结果表明:参试材料产量相关性状的变异系数为2.54%~14.70%,其中,皮厚、单株鲜皮重、单株鲜骨重、鲜皮晒干率、单株干皮产量5个产量性状的变异系数超过10%,说明产量性状的变异潜力较高。主成分分析表明,单株鲜皮重因子、鲜皮晒干率因子、分枝高因子这3个主因子提供了原始性状88.247%的信息;在欧氏距离聚类图中,当取值D=2.15时,可把26个黄麻育成品种(系)分成4类,第Ⅰ类群包含18份材料,占69.23%,第Ⅱ类群包含5份材料,占19.23%,第Ⅲ类群只有1个品种(系),第Ⅳ类群包括黄麻179和宽叶长果2份材料,各个类群具有不同的特点,在黄麻杂交育种上可根据不同类别的特点加以利用;二维排序表明9(09品-11)、11(89m5-83)、12(09繁-7)、19(福黄麻1号)、21(黄麻831)、25(Y007-10)等6个高产品种(系)的3个主成分构成因子协调最好。将聚类分析和二维排序分析结合起来的分析方法,能较好地为黄麻品种改良以及亲本利用提供科学依据。     

辽宁花生品种系谱分析及农艺性状的演变

分析了辽宁省1949-2012年育成的95个花生品种系谱及农艺性状的演变。结果表明:辽宁花生育成品种共涉及100个亲本,其中,来自辽宁的有45个,49个是育种单位的中间材料,鲁花12号、白沙1016、伏花生、豫花11号等是辽宁花生育成品种的骨干亲本。进入21世纪以来,辽宁省育成的花生品种株高、侧枝长逐渐增加,从变异区间来看,百仁重、出米率呈增加趋势,而粗蛋白与粗脂肪含量变化较小。在分析辽宁省花生育种背景的基础上,提出辽宁省花生育种上宜重视回交手段的利用,发展食用型品种,把抗旱、抗寒、抗病、抗虫、耐连作作为重要的育种目标,利用生物技术手段和野生资源加速育种进程,进一步拓宽辽宁花生品种的遗传基础。     

基于小麦种子发芽逆境抗逆指数的种子活力评价

以16个小麦品种的种子为材料,通过标准发芽、逆境发芽和田间出苗试验,测定不同基因型小麦品种的种子活力,以不同发芽条件下种子活力指数的抗逆指数和田间出苗率作为衡量抗逆性的指标,利用主成分分析、聚类分析对种子活力进行综合评价.结果表明: 干旱胁迫、人工老化和冷浸胁迫3种逆境对种子活力都有一定的影响.人工老化抗逆指数和冷浸胁迫抗逆指数与田间出苗率呈显著正相关,干旱胁迫抗逆指数与田间出苗率的相关性不显著.通过主成分分析和聚类分析将16个小麦品种划分为3类、豫农949、豫麦49-198、鲁原502、郑育麦9987、石麦21、山农23号、石新828为高活力品种;许农5号、豫农982、唐麦8号、济麦20、济麦22、济南17号、山农20为中活力品种;长4738和轮选061属低活力品种.     

AMMI模型在旱地春小麦稳定性分析中的应用

基因型与环境的互作(GEI)决定了作物在多变环境下性状的稳定性。AMMI模型是一种将方差分析和主成分分析结合于一体,能更有效分析GEI、进而评价基因型稳定性和环境对基因型差异分辨力的有力工具。利用AMMI模型对10个品种(系)、13个试点组成的全国旱地春小麦区域试验产量资料分析表明,试点间平均产量变幅为396.6~4050.2 kg.hm-2,现代品种间的平均产量变幅为1318.6~2315.6 kg.hm-2;基因型间、环境间和GEI引起的产量变异达到极显著水平,三者的变异平方和分别占总处理平方和的6.2%、70.3%、23.5%,表明环境和GEI对产量变化的影响远大于基因型。用前3个代表了90.8%GEI信息的显著主成分计算基因型稳定性参(Di)和试点分辨力(Dj),基因型间Di最大相差达3倍、而试点间Dj最大相差19倍;属于高产、稳产的品种有:定西35、西旱1号、定丰889,而在这两方面均表现最差的品种为蒙麦35号。有些品种对某些试点有特殊适应性,局部推广价值也大。     

花生抗旱性鉴定指标的筛选与评价

为确定鉴定花生(Arachis hypogaea)品种(系)抗旱性指标体系, 综合评价花生品种(系)的抗旱性, 在人工控水条件下, 通过盆栽试验, 测定了29个花生品种(系)苗期和花针期的株高、分枝数、生物累积量、叶片含水量和光合色素含量等与抗旱性有关的13个表观形态性状和生理性状的指标, 采用抗旱系数法和隶属函数值法, 对各指标性状进行了水分胁迫下的抗性评价和鉴定。结果表明, 29个花生品种(系)可划分为抗旱性较强、中等、较弱和不抗旱4类, 其中‘唐科8号’、‘冀花2号’、‘大唐油’、‘花育25号’、‘花育17号’、‘鲁花14号’、‘丰花1号’ 7个品种(系)具有较强的抗旱能力; 苗期同一品种(系)的主茎高、分枝数和生物累积量等形态指标和光合色素等生理指标的隶属函数值均有较大差别, 苗期各指标隶属函数值与品种(系)抗旱性无显著相关关系, 苗期单一形态指标不能作为鉴定品种(系)抗旱性的指标; 但苗期抗旱性综合评价值(D)与抗旱系数间存在显著相关关系, D的大小可作为抗旱性的鉴定指标。花针期形态指标和生理指标D值间, 以及各类指标D值与抗旱系数间均存在显著或极显著的相关关系, 此期植株形态指标、生理指标隶属函数值以及综合D值均可作为鉴定品种(系)抗旱性的指标。     

钙对镉胁迫下花生生理特性、产量和品质的影响

通过盆栽试验,选用高油品种豫花15和高蛋白品种XB023,研究了不同浓度钙对镉胁迫下不同类型花生品种营养生长、叶片叶绿素含量、光合速率、保护酶活性等生理特性及产量和品质的影响.结果表明： 施钙可以缓解镉胁迫对花生植株主茎高和侧枝长的抑制作用,增加花生植株干物质量,提高叶片叶绿素含量和光合速率,提高叶片超氧化物歧化酶（SOD）、过氧化氢酶（CAT）、过氧化物酶（POD）活性和可溶性蛋白质含量,降低丙二醛（MDA）的积累量,减轻镉胁迫对花生叶片的伤害;施钙可以缓解镉胁迫对花生的减产作用,增加花生荚果和籽仁产量,其增产的主要原因是增加了单株结荚数和出仁率;施钙可以促使籽仁中可溶性糖向粗脂肪和蛋白质转化,增加籽仁中脂肪和蛋白质含量,改善镉胁迫下花生籽仁品质.施钙可以降低两花生品种籽仁中镉含量,对豫花15的降低效果好于XB023.     

小麦磷素利用效率的品种差异

通过土培盆栽试验,研究了小麦不同品种在低磷水平下生物量、磷浓度、磷素干物质生产效率及磷素籽粒生产效率的差异,以筛选磷高效利用小麦品种.结果表明：分蘖期、拔节期、扬花期和成熟期,供试小麦品种单株生物量的变幅分别为0.46～1.09、0.85～2.10、3.00～7.00和3.85～12.88 g,磷浓度变幅分别为2.21～4.26、2.38～4.42、2.44～4.96和1.30～5.09 mg·g^-1.随生育时期的推进,小麦磷素累积量、磷素干物质生产效率对生物量形成的影响程度呈减小趋势.分蘖期（CV=16.3%）、拔节期（CV=15.0%）、扬花期磷素干物质生产效率（CV=13.3%）和成熟期磷素籽粒生产效率（CV=20.5%）的品种差异较大.CD1158-7和省A3宜03-4具有较高的磷素干物质生产效率和磷素籽粒生产效率,而渝02321较低;不同生育时期高效品种磷浓度极显著低于低效品种,而高效品种CD1158-7和省A3宜03-4的籽粒产量分别是低效品种渝02321的1.98和1.78倍.     

钙对镉胁迫下花生生理特性、产量和品质的影响水

通过盆栽试验,选用高油品种豫花15和高蛋白品种XB023,研究了不同浓度钙对镉胁迫下不同类型花生品种营养生长、叶片叶绿素含量、光合速率、保护酶活性等生理特性及产量和品质的影响.结果表明:施钙可以缓解镉胁迫对花生植株主茎高和侧枝长的抑制作用,增加花生植株干物质量,提高叶片叶绿素含量和光合速率,提高叶片超氧化物歧化酶( SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)活性和可溶性蛋白质含量,降低丙二醛(MDA)的积累量,减轻镉胁迫对花生叶片的伤害;施钙可以缓解镉胁迫对花生的减产作用,增加花生荚果和籽仁产量,其增产的主要原因是增加了单株结荚数和出仁率;施钙可以促使籽仁中可溶性糖向粗脂肪和蛋白质转化,增加籽仁中脂肪和蛋白质含量,改善镉胁迫下花生籽仁品质.施钙可以降低两花生品种籽仁中镉含量,对豫花15的降低效果好于XB023.     

二倍体、四倍体和六倍体小麦产量及水分利用效率

试验选用了6个不同染色体倍性的小麦进化材料（3个二倍体、2个四倍体和1个六倍体）,分别在不同水肥条件下研究其根系、地上生物量、产量、蒸腾耗水量和水分利用效率等指标,旨在阐明小麦进化材料产量及水分利用效率的差异及水肥条件对这些特性的影响。试验表明：不同倍性小麦进化材料的生物量、产量和水分利用存在显著的差异,而且水肥条件对其有显著影响。在染色体倍性由2n→4n→6n的进化过程中,小麦根系及地上生物量均先增加后降低,而产量却显著增加,这与收获指数的增加有关。小麦产量的大小顺序为：T.aestivum〉T.dicoccum〉T.dicoccoides〉Ae.squarrosa〉Ae.speltoides〉T.boeoticum。水分亏缺显著降低小麦的生物量、产量和收获指数;在不同水分条件下,增加施肥量有利于这些指标的增加。但是水分亏缺下,增加施肥却降低各小麦材料的根系生物量。随小麦的进化,蒸腾耗水量显著降低,这与其生育期缩短有关;而生物量水分利用效率和产量水分利用效率却显著升高,且后者的差异要大于前者。各小麦产量水分利用效率的大小排序与产量的完全一致。水分亏缺处理显著减少各小麦进化材料的蒸腾耗水量47％～52％,而显著增加生物量水分利用效率3％～40％;但水分亏缺对产量水分利用效率的促进作用却随染色体倍性的增加而降低,甚至降低六倍体小麦T.aestivum的产量水分利用效率19％。不同水分条件下,高肥处理均有利于蒸腾耗水量、生物量水分利用效率和产量水分利用效率的增加。     

Comparative photosynthesis,growth, productivity,and nutrient use efficiency among tall- and short-stemmed rain-fed cassava cultivars

Field trials under rain-fed conditions at the International Center for Tropical Agriculture (CIAT) in Colombia were conducted to study the comparative leaf photosynthesis, growth, yield, and nutrient use efficiency in two groups of cassava cultivars representing tall (large leaf canopy and shoot biomass) and short (small leaf canopy and shoot biomass) plant types. Using the standard plant density (10,000 plants ha⁻¹), tall cultivars produced higher shoot biomass, larger seasonal leaf area indices (LAIs) and greater final storage root yields than the short cultivars. At six months after planting, yields were similar in both plant types with the short ones tending to form and fill storage roots at a much earlier time in their growth stage. Root yield, shoot and total biomass in all cultivars were significantly correlated with seasonal average LAI. Short cultivars maintained lower than optimal LAI for yield. Seasonal P _N, across cultivars, was 12% greater in short types, with maximum values obtained in Brazilian genotypes. This difference in P _N was attributed to nonstomatal factors (i.e., anatomical/biochemical mesophyll characteristics). Compared with tall cultivars, short ones had 14 to 24 % greater nutrient use efficiency (NUE) in terms of storage root production. The lesser NUE in tall plants was attributed mainly to more total nutrient uptake than in short cultivars. It was concluded that short-stemmed cultivars are superior in producing dry matter in their storage roots per unit nutrient absorbed, making them advantageous for soil fertility conservation while their yields approach those in tall types. It was recommended that breeding programs should focus on selection for more efficient short- to medium-stemmed genotypes since resource-limited cassava farmers rarely apply agrochemicals nor recycle residual parts of the crop back to the soil. Such improved short types were expected to surpass tall types in yields when grown at higher than standard plant population densities (>10,000 plants ha⁻¹) in order to maximize irradiance interception. Below a certain population density (<10,000 plants ha⁻¹), tall cultivars should be planted. Findings were discussed in relation to cultivation and cropping systems strategies for water and nutrient conservation and use efficiencies under stressful environments as well as under predicted water deficits in the tropics caused by trends in global climate change. Cassava is expected to play a major role in food and biofuel production due to its high photosynthetic capacity and its ability to conserve water as compared to major cereal grain crops. The interdisciplinary/interinstitutions research reported here, including an associated release of a drought-tolerant, short-stem cultivar that was eagerly accepted by cassava farmers, reflects well on the productivity of the CIAT international research in Cali, Colombia.     

Diversity and compatibility of peanut (Arachis hypogaea L.) bradyrhizobia and their host plants

A high degree of genetic diversity among 125 peanut bradyrhizobial strains and among 32 peanut cultivars collected from different regions of China was revealed by using the amplified fragment length polymorphism (AFLP) technique. Eighteen different peanut bradyrhizobial genotypes and six peanut cultivars were selected for symbiotic cross-inoculation experiments. The genomic diversity was reflected in the symbiotic diversity. The peanut cultivars varied in their ability to nodulate with the strains used. Some cultivars had a more restricted host range than the others. Also the strains displayed a range of nodulation patterns. In yield formation there were clear differences between the plant cultivar/bradyrhizobium combinations. There was good compatibility between some peanut bradyrhizobial strains and selected cultivars, with inoculation resulting in well-nodulated, high-yielding symbiotic combinations, but no plant cultivar was compatible with all strains used. The strains displayed a varying degree of effectiveness, with some strains being fairly effective with all cultivars and others with selected ones. The AFLP genotypes of the strains did not explain the symbiotic behavior, whereas the yield formation of the plant cultivars was more related to the genotype. It is concluded that to obtain optimal nitrogen fixation efficiency of peanut in the field, compatible plant cultivar-bradyrhizobium combinations should be selected either by finding inoculant strains compatible with the plant cultivars used, or plant cultivars compatible with the indigenous bradyrhizobia.     

Water and Nutrient Use Efficiency in Diploid, Tetraploid and Hexaploid Wheats

Three diploid (Triticum boeoticum, AA; Aegilops speltoides, BB and Ae. tauschii, DD), two tetraplold (T. dlcoccoides,AABB and T. dicoccon, AABB) and one hexaploid (T. vulgare, AABBDD) varieties of wheat, which are very important in the evolution of wheat were chosen in this study. A pot experiment was carried out on the wheat under different water and nutrient conditions (i) to understand the differences in biomass, yield, water use efficiency (WUE), and nutrient (N, P and K) use efficiency (uptake and utilization efficiency) among ploldles in the evolution of wheat; (ii) to clarify the effect of water and nutrient conditions on water and nutrient use efficiency; and (iii) to assess the relationship of water and nutrient use efficiency in the evolution of wheat. Our results showed that from diploid to tetraploid then to hexaploid during the evolution of wheat, both root biomass and above-ground biomass increased initially and then decreased. Water consumption for transpiration decreased remarkably, correlating with the decline of the growth period, while grain yield, harvest index, WUE, N, P and K uptake efficiency, and N, P and K utilization efficiency increased significantly. Grain yield, harvest index and WUE decreased in the same order: T.vulgare ＞ T. dicoccon ＞ T. dicoccoides ＞ Ae. tauschii ＞ Ae. speltoides ＞ T. boeoticum. Water stress significantly decreased root biomass, above-ground biomass, yield, and water consumption for transpiration by 47-52%, butremarkably increased WUE. Increasing the nutrient supply increased wheat above-ground biomass, grain yield,harvest index, water consumption for transpiration and WUE under different water levels, but reduced root biomass under drought conditions. Generally, water stress and low nutrient supply resulted in the lower nutrientuptake efficiency of wheat. However, water and nutrient application had no significant effects on nutrient utilization efficiency, suggesting that wheat nutrient utilization efficiency is mainly controlled by genotypes. Compared to theother two diploid wheats, Ae. squarrosa (DD) had significant higher WUE and nutrient utilization efficiency, Indicating that the D genome may carry genes controlling high efficient utilization of water and nutrient. Significant relationships were found between WUE and N, P and K utilization efficiency.