B_9对花生某些生理过程的影响

B_9促进花生叶片加厚,其中以同化组织加厚为主。B_9能显著地提高叶片的叶绿素含量,加快叶片光合速度,每株干物质积累较多。B_9促使嫩叶气孔的分化,增加气孔数目,加强蒸腾作用。 B_9抑制花生主茎和侧枝的生长,处理后半个月内不显著伸长,植株矮壮,株型紧凑,抗倒伏。 B_9改变花生植株光合产物的分配比例,减少地上部(叶和茎)的干重,增加地下部(荚果和根)的干重,加强荚果发育。     

不同时期喷施多效唑对花生生理特性、产量和品质的影响

为确定高产条件下不同花生品种的最佳化控时期,以小花生品种‘花育20’(HY20)和大花生品种‘花育25’(HY25)为试验材料,研究了多效唑(PBZ)不同喷施时期对花生根系活力、叶绿素含量、叶片保护酶和碳、氮代谢酶活性,以及荚果产量和籽仁品质的影响.结果表明:不同时期喷施PBZ均提高了2个品种花生在结荚期的叶绿素含量、根系活力,以及叶片超氧化物歧化酶、过氧化物酶、过氧化氢酶、蔗糖合成酶、蔗糖磷酸合成酶和磷酸烯醇式丙酮酸羧化酶活性,降低了丙二醛(MDA)含量以及硝酸还原酶、谷氨酰胺合成酶、谷氨酸脱氢酶和谷氨酸合成酶活性,且PBZ喷施时间越早效果越明显.在饱果期,HY25的各指标以主茎高25cm时喷施PBZ的效果最好,但HY20在主茎高25 cm时喷施PBZ的保护酶活性降低,化控时间过早导致植株早衰,叶绿素含量、根系活力以及碳代谢酶活性也略低于CK,HY20的指标以主茎高30 cm时喷施PBZ效果最好.适宜时期PBZ处理提高了2个品种的荚果产量和经济系数,提高了脂肪含量和油酸相对含量以及O/L值.高产条件下,HY25和HY20的最适多效唑处理时期分别为花生主茎高25和30 cm左右.     

麦套花生产量形成期固氮酶和保护酶活性特征研究

以小麦品种烟农23号"和花生品种花育22号"为材料,研究了大田条件下花生产量形成期套种和清种花生根瘤固氮酶活性及SOD、POD、CAT活性等指标变化情况.结果表明:(1)麦套和清种花生单株根瘤重量和固氮酶活性变化均呈单峰曲线,高峰期分别出现在结荚末期和结荚中期;前者固N能力明显高于后者.(2)花生根系中SOD、POD、CAT活性基本上均是先增后降趋势,但麦套花生后期下降速率明显缓于清种花生;叶片中SOD、POD、CAT活性变化规律性明显不及根系,后期麦套花生SOD、CAT活性高于清种花生,POD则相反.(3)麦套花生根系中可溶性蛋白含量一直较高,而清种花生后期下降较快;麦套花生叶片中可溶性蛋白含量的高峰约出现在结荚中期,清种花生整个结荚期呈下降态势,两者进入饱果期后均趋于稳定.可见麦套花生生育后期根系衰老速率明显迟于清种花生.     

南方红壤旱坡地花生植株对施用氮肥的响应

选用多年夏花生-冬蔬菜种植制度下的典型红壤旱坡地,通过田间试验,研究了5种氮肥水平下花生根系的形态特征、固氮能力、植株生物量以及荚果产量。结果表明:不同氮肥施用量对花生植株生物量及荚果产量影响均不显著(P=0.091);而不同处理的土壤固氮酶活性与氮肥施用量间呈极显著的负相关(R2=0.88,P=0.005);单株花生根系总长度、总表面积、总分叉数及根尖条数均随氮肥施用量的增加而减小,且与单株花生根瘤生物量呈极显著(P<0.001)正相关。     

固氮树种在混交林中的作用研究Ⅱ.固氮树木叶部N、P养分动态特征

研究了23种固氮与非固氮树种叶部N、P含量的季节变化、输出率以及叶片衰老过程中N、P的输出过程.结果表明,供试树种叶部N、P含量均存在着明显的季节变化,平均变化率为21～23%,最大变化率出现在叶片衰老期.在衰老期内不同树种表现出不同的N、P动态特征.固氮树种表现出低输出率,落叶中N含量是非固氮树种的1.6～3.7倍.固氮树种生长季叶部N含量在2.5%左右.     

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.     

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.     

1株高效花生根瘤菌的筛选与鉴定

从辽宁多地花生种植土壤及其鲜根瘤初步筛选到30株花生根瘤菌,进一步通过回接盆栽花生,测定花生根瘤数、根瘤干重,以及鲜根瘤固氮酶活性、植株全氮量等,筛选出1株结瘤固氮能力较强花生根瘤菌wz-6,通过16S rDNA序列分析,鉴定为圆明慢生根瘤菌(Bradyrhizobium yuanmingense)。为开发优质花生根瘤菌菌剂奠定基础。     

不同花生品种对旱涝胁迫的响应及生理机制

为评价花生对旱、涝胁迫的响应,本试验以4个旱、涝耐性差异明显的花生品种为材料,运用温室防雨盆栽方法,在苗期、花针期分别进行正常灌溉(对照)、干旱(7d,叶片萎蔫)、根部淹涝(土面水深2 cm,时间1d、3d、7d)和整株淹涝(水深至苗顶,时间1d、3d、7d)的处理,测定地上部及根系生物量、根冠比、根系活力、叶片超氧化物歧化酶(SOD)活性、丙二醛(MDA)含量。结果表明,苗期、花针期干旱均抑制地上部生长,提高根冠比;苗期干旱降低根系生物量,而花针期增加。2个时期淹涝均促进地上部生长、抑制根系生长、降低根冠比,并随淹水加深、延时而加重。旱、涝条件下根系活力均降低,SOD、MDA呈上升趋势。遭受相同时间(7d)的水分胁迫后,危害程度以干旱重于淹涝,花针期重于苗期。基于生物量、生理指标变化的综合分析进一步表明,4个花生品种的旱、涝耐性差异很大,湘花55号耐旱性强、耐涝性弱,豫花15号耐旱性弱、耐涝性强,中花4号耐旱、涝性均最弱,中花8号耐旱、涝性均最强。     

不同品种(系)小豆根系活力与叶片衰老的关联研究

以高产小豆品种(系)‘2000-75’、‘冀红9218’和低产品种(系)‘红宝1号’、‘湾选1号’为材料,测定小豆开花至成熟期,根系与始花节位叶片生长指标、保护酶活性、可溶性蛋白含量等变化,分析其根系与始花叶协同衰老的相关性,以揭示小豆根系活力与地上部叶片衰老之间的关系。结果表明:(1)各品种(系)开花后,植株根系伤流强度随着花后生育进程的推进呈单峰增长趋势,但根系活力的衰老起始期晚于叶片功能的衰退开始期。(2)从开花至成熟期,小豆根系活力与叶片中超氧化物歧化酶、过氧化氢酶、叶绿素含量、可溶性蛋白、叶片净光合速率都存在正相关关系,与丙二醛含量呈负相关关系。(3)与低产品种相比,高产小豆品种(系)‘2000-75’和‘冀红9218’的根系活力强,叶片功能期持续时间长,叶绿素含量下降速度慢,保护性酶含量高,使花后小豆的功能叶捕获光能的能力增强,从而形成较高光合能力的小豆群体,最终获得高产。     

外源乙烯利施用时期对花生源库形成的调控效应

为了解决源库关系不协调而限制花生产量提高的问题,在大田栽培条件下,以‘山花9号’花生为试验材料,设置花后10、20、30 d 3个喷施时期,以不喷施处理为对照,探讨不同时期喷施乙烯利对花生源库形成的调控效应。结果表明: 花后10和20 d喷施乙烯利可显著减少花生的开花数量、果针数、幼果数,提高秕果数和饱果数,而花后30 d喷施处理对开花数量、果针数和幼果数无抑制作用。喷施乙烯利可以增加花生单株叶面积,开花后10 d喷施处理的单株叶面积增幅最大,随着喷施时期的推迟增幅减小。花后10和20 d喷施乙烯利显著提高了花生叶片的光合速率,但花后30 d喷施处理只能在短期内提高光合速率,对生育后期的叶片光合速率无显著影响。从源库综合性状来看,花后20 d喷施乙烯利的源库关系最协调,有利于促进同化物向荚果的运输,提高有效果比例和荚果充实度,从而提高产量。因此,喷施乙烯利是解决花生“花多不实、果多不饱”源库失衡现象的有效措施,生产中使用乙烯利控花应选择在开花后20 d喷施。     

Characterization of leaf senescence and pod development in soybean explants

Excised soybean (Glycine max [L.] Merrill) cv Anoka leaf discs tend to remain green even after the corresponding intact leaves have turned yello on fruiting plants. We have found that explants which include a leaf along with a stem segment (below the node) and one or more pods (maintained on distilled H₂O) show similar but accelerated leaf yellowing and abscission compared with intact plants. In podded explants excised at pre-podfill, the leaves begin to yellow after 16 days, whereas those excised at late podfill begin to yellow after only 6 days. Although stomatal resistances remain low during the first light period after excision, they subsequently increase to levels above those in leaves of intact plants. Explants taken at mid to late podfill with one or more pods per node behave like intact plants in that pod load does not affect the time lag to leaf yellowing. Explant leaf yellowing and abscission are delayed by removal of the pods or seeds or by incubation in complete mineral nutrient solution or in 4.6 micromolar zeatin. Like chorophyll breakdown, protein loss is accelerated in the explants, but minerals or especially zeatin can retard the loss. Pods on explants show rates and patterns of color change (green to yellow to brown) similar to those of pods on intact plants. These changes start earlier in explants on water than in intact plants, but they can be delayed by adding zeatin. Seed dry weight increased in explants, almost as much as in intact plants. Explants appear to be good analogs of the corresponding parts of the intact plant, and they should prove useful for analyzing pod development and mechanisms of foliar senescence. Moreover, our data suggest that the flux of minerals and cytokinin from the roots could influence foliar senescence in soybeans, but increased stomatal resistance does not seem to cause foliar senescence.     

Transmission of the Monocarpic Senescence Signal via the Xylem in Soybean

During monocarpic senescence in soybean (Glycine max [L.] Merrill cv. Anoka) there is a remobilization of nitrogen from the leaves to the seeds, and it has been hypothesized that this loss of nitrogen from the leaves induces foliar yellowing. The phloem in a small segment of the petiole between the pods and the target leaf can be inactivated with a jet of steam. When a plant is depodded except for a single pod cluster in the center of the plant, the pod cluster induces yellowing of the nearest leaf even if the petiole contains a zone of dead phloem, whereas most of the rest of the plant remains green. The nitrogen content of these leaves with a dead phloem zone in their petioles does not decrease greatly, even though the leaves turn yellow. A similar treatment of a single leaf on a fully depodded plant (leaves stay green) does not cause that leaf to turn yellow. Since nutrients would have to be withdrawn from the leaves via the phloem, the pods do not induce yellowing by pulling nutrients out of the leaf and must be able to exert their influence via the xylem.     

Characterization and behaviour of 15-lipoxygenase during peanut cotyledonary senescence

Lipoxygenase (EC 1.13.11.12) (LOX), a ubiquitous plant enzyme which catalyzes the hydroperoxidation of unsaturated fatty acids (PUFA), plays an important role during the course of leaf and cotyledonary senescence. In the present study, senescence related changes in chlorophyll and protein content and lipoxygenase activity have been examined in peanut cotyledons. The chlorophyll content of the cotyledons increased from the 2nd to 8th day followed by a steady decline. In contrast, protein content of peanut cotyledons decreased continuously during senescence. Lipoxygenase activity, on the other hand, increased in early stages of germination followed by a decrease in the later course of senescing peanut cotyledons. Analysis of the product profile, the lipoxygenase with arachidonic acid as the substrate on HPLC, has shown a single peak comigrating with standard 15-Hydroperoxyeicosatetraenoic acid. The results on peanut cotyledonary 15-lipoxygenase activity in relation to abscisic acid and kinetin are discussed.     

Regulation of monocarpic senescence of Brassica campestris by the developing pods

Senescence of Brassica campestris L. cv. B-9 was studied with regard to seed maturation and source-sink relationships. In normal control plants leaf senescence (as determined by the change in chlorophyll level) started and proceeded in a progressive manner from base to apex during the period of early pod setting. Complete yellowing of the leaves occurred well before the seed maturation and pod wall senescence. The pod wall always senesced before the attainment of final seed weight. In two different sets of acrocarpous plants containing 65 pods and 10 pods, respectively, leaf senescence was delayed during the pod filling period. It started non-sequentially after complete yellowing and senescence of the pod wall. The degree of leaf senescence at the post-pod filling stage was almost proportional to the number of pods present. When peduncles of the acrocarpous 10-podded plants were removed after the pod filling stage of the plant, leaf senescence was delayed compared to plants whose pedicels were removed, although the senescence pattern of the upper three leaves was nonsequential in both cases. Defruiting at an early stage of development delayed leaf senescence, although the pattern of such senescence remained unaltered (i.e. nonsequential). Defoliation hastened the seed-filling process and pod wall senescence. Plants containing fewer pods had higher average seed weight, although yield per plant was reduced.
These results suggest that the pod wall serves as a temporary as well as intermediary storage organ and that foliar senescence is not directly related to seed maturation. The possible cause of uncoupling between foliar senescence and seed development is discussed.     

EFFECT OF PETIOLE PHLOEM DISRUPTION ON STARCH AND MINERAL DISTRIBUTION IN SENESCING SOYBEAN LEAVES

Normally, starch (sugars) and minerals are redistributed from the leaves to the pods during monocarpic senescence in maturing soybean plants. Petiole phloem destruction (steam girdling), which blocked this redistribution by interrupting export through the petiole, altered the foliar senescence pattern producing a distinctive interveinal yellowing with green areas along the veins on pod-bearing plants. This suggests that blockage of the petiole phloem may cause nutrients to accumulate in the green zones along the leaf veins instead of being redistributed to the pods. In the leaves of untreated plants, starch showed the same distribution pattern as chlorophyll; however, starch was preserved in yellow areas as well as the green zones of the steam-girdled leaves. Mineral analyses of the veinal and interveinal zones of treated leaves and controls showed that the veinal green zones and interveinal yellowing in treated plants were not respectively enriched and depleted in minerals corresponding to a redistribution of minerals within the leaves. Depodding also blocked leaf yellowing, net mineral redistribution and starch breakdown. Thus, the pods are able to induce chlorophyll breakdown without net mineral redistribution or starch loss in leaves with petiole phloem destruction. This shows that chlorophyll breakdown is not obligatorily coupled with mineral redistribution or starch breakdown.     

The effect of altered sink-source relations on photosynthetic traits and matter transport during the phase of reproductive growth in the annual herb <Emphasis Type="Italic">Chenopodium album</Emphasis>

Annual plants transport a large portion of carbohydrates and nitrogenous compounds from leaves to seeds during the phase of reproductive growth. This study aimed to clarify how reproductive growth affects photosynthetic traits in leaves and matter transport within the plant in the annual herb Chenopodium album L. Plants were grown in pots and either reproductive tissues or axillary leaves were removed at anthesis. Matter transport was evaluated as temporal changes in dry mass (as a substitute of carbohydrates) and nitrogen content of aboveground organs: leaves, axillary leaves, stems and reproductive tissues. Photosynthetic capacity (light-saturated photosynthetic rate under ambient CO₂ concentration), nitrogen, chlorophyll and soluble protein content were followed in the 20^th leaf that was mature at the start of the experiment. Removal of reproductive tissues resulted in accumulation of dry mass in leaves and axillary leaves, and accumulation of nitrogen in stem as nitrogen resorption from leaves and axillary leaves proceeded with time. Removal of axillary leaves proportionally reduced dry mass and nitrogen allocation to reproductive tissues, thus affecting the quantity but not quality of seeds. Removal treatments did not alter the time course of photosynthetic capacity, nitrogen, chlorophyll or soluble protein content during senescence in the 20^th leaf, but changed the photosynthetic capacity per unit of leaf nitrogen according to demand from reproductive tissues. Together, the results indicate that reproductive tissues affected carbon and nitrogen economy separately. The amount of carbon was adjusted in leaves through photosynthetic capacity and carbohydrate export from them, and the amount of nitrogen was adjusted by transport from stem to reproductive tissues. The plant’s ability to independently regulate carbon and nitrogen economy should be important in natural habitats where the plant carbon-nitrogen balance can easily be disturbed by external factors.     

Effects of pod removal on metabolism and senescence of nodulating and nonnodulating soybean isolines: I. Metabolic constituents

Field studies were conducted in 1981 and 1982 to ascertain the effects of pod removal on senescence of nodulating and nonnodulating isolines of soybean (Glycine max [L.] Merr. cv Harosoy) plants. Specifically, the test hypothesis was that nodules act as a nitrogen source and a carbohydrate sink which would in turn prevent or delay senescence in the absence of pods. Senescence was judged by changes in metabolite levels, in dry matter accumulation, and by visual observation.

For both nodulated and nonnodulated plants, pod removal had no effect on the magnitude or rate of dry matter and reduced-N accumulation by whole plants. Phosphorus accumulation was significantly less in both nodulated- and nonnodulated-depodded plants, compared with respective control plants with pods. These data suggested a role for pods in phosphorus uptake. Accumulation of dry matter, reduced N, and phosphorus ceased at approximately the same time for all treatments.

Pod removal did affect partitioning of plant constitments, with leaves and stems of depodded plants serving as a major alternate sink for accumulation of dry matter, reduced N, phosphorus, and nonstructural carbohydrates (primarily starch). While depodded plants eventually lost a significant amount of leaves, leaf drop was delayed relative to plants with pods; and depodded plants still retained some green leaves at 2 weeks past grain maturity of control (podded) plants.

The results indicated that senescence patterns of soybean plants were the same for nodulated and nonnodulated plants, and that pods did not control the initiation of senescence, but rather altered the partitioning of plant constituents and the visual manifestations of senescence.

     

Senescence-induced ectopic expression of the A. tumefaciens ipt gene in wheat delays leaf senescence, increases cytokinin content, nitrate influx, and nitrate reductase activity, but does not affect grain yield

The manipulation of cytokinin levels by senescence-regulated expression of the Agrobacterium tumefaciens ipt gene through its control by the Arabidopsis SAG12 (senescence-associated gene 12) promoter is an efficient tool for the prolongation of leaf photosynthetic activity which potentially can affect plant productivity. In the present study, the efficiency of this approach was tested on wheat (Triticum aestivum L.)-a monocarpic plant characterized by a fast switch from vegetative to reproductive growth, and rapid translocation of metabolites from leaves to developing grains after anthesis. When compared with the wild-type (WT) control plants, the SAG12::ipt wheat plants exhibited delayed chlorophyll degradation only when grown under limited nitrogen (N) supply. Ten days after anthesis the content of chlorophyll and bioactive cytokinins of the first (flag) leaf of the transgenic plants was 32% and 65% higher, respectively, than that of the control. There was a progressive increase in nitrate influx and nitrate reductase activity. However, the SAG12::ipt and the WT plants did not show differences in yield-related parameters including number of grains and grain weight. These results suggest that the delay of leaf senescence in wheat also delays the translocation of metabolites from leaves to developing grains, as indicated by higher accumulation of ((15)N-labelled) N in spikes of control compared with transgenic plants prior to anthesis. This delay interferes with the wheat reproductive strategy that is based on a fast programmed translocation of metabolites from the senescing leaves to the reproductive sinks shortly after anthesis.     

Studies on Genetic Male-Sterile Soybeans: I. Distribution of Plant Carbohydrate and Nitrogen during Development

Soybeans (Glycine max [L.] Merr. cv. NC 69-2774) were used to study the nonstructural carbohydrate and nitrogen content of plant tissues, and nitrogenase activity throughout the development of male-sterile and male-fertile plants. Male-sterile plants set approximately 85% fewer pods plus seed than the male-fertile siblings and retained green leaves until a killing frost at 145 days after emergence. Reduced pod set caused increased carbohydrate accumulation in the leaf and root systems of male-sterile plants. Total carbohydrate in roots of male-sterile plants increased from 1.7 to 7.6 times that in the male-fertile roots. A high proportion (60 to 70%) of the male-sterile root carbohydrate was starch. Apparently, root starch was not metabolized by the male-sterile plants. Late in plant development per cent nitrogen was higher in the male-sterile soybean tissues. However, no difference was found in the ability of the nodulated root systems from either genotype to fix nitrogen.