外生菌根菌对樟子松苗木生长的影响

以内蒙古大兴安林樟子松分布区较典型的6个乡土菌种与本实验室从法国引进的宿主范围较广的2个菌种及内蒙古地区分布广泛的土生空团菌为研究对象,采用固体和液体两种菌剂类型,对出苗30d左右的樟子松实生苗进行外生菌根菌接种试验,接种130d后观察菌根侵染情况及生长特性,同时对菌根化的樟子松苗木进行自然干旱胁迫,研究外生菌根菌接种对樟子松苗木生长及抗逆性的影响。结果显示:(1)5个乡土菌种和1个法国引进菌种均能够与樟子松实生苗共生菌根,菌根化苗木较对照的苗高增长10.5%～111.4%、地茎增长4.55%～92.8%、苗木干重增加6.8%～184.5%,且固体菌剂效果优于液体菌剂。(2)在干旱胁迫下,菌根化苗木叶绿素含量较对照增加5.82%～36.92%、净光合速率提高120.2%～217.03%,叶片推迟10.3～25h出现萎蔫,临界致死时间推迟13.8～38.2h。(3)接种菌种厚环乳牛肝菌和点柄乳牛肝菌的苗木菌根侵染率、苗木生长量、干旱胁迫下各项生理指标均显著优于其他菌种和对照。研究表明,樟子松实生苗菌根化对苗木生长有明显的促进作用,能够提高苗木对干旱胁迫的抵御能力;厚环乳牛肝菌和点柄乳牛肝菌是有潜在研究和应用价值的优良菌株,这两个菌株的固体菌剂可用于樟子松菌苗生产。     

黄山地区松树林外生菌根菌资源及生态分布

1998～2003年,对黄山地区松树林下外生菌根菌资源及生态分布进行了调查,鉴定出外生菌根菌43种,隶属于10科17属.其中马尾松林下有43种、黄山松林下有12种.马尾松幼林下的外生菌根菌种类单一,彩色豆马勃、硬皮马勃类为优势菌种;马尾松成熟林下外生菌根菌种类丰富,其优势种类为红菇科、鹅膏菌科、牛肝菌科和鸡油菌科的一些种类.并分析了树种植被对外生菌根菌分布的影响,菌根真菌的分布与温度、湿度及土壤条件的关系.     

辽东栎幼苗的外生菌根合成

 在温室花盆中播种辽东栎（Quercus liaotungensis）种子获得辽东栎幼苗,并对幼苗接种外生菌根真菌进行菌根合成试验。所用的外生菌根真菌有：铆钉菇（Gomphidius viscidus）、臭红菇（Russula foetens）、厚环乳牛肝菌（Suillus grevillei）、褐环乳牛肝菌（S. luteus）、彩色豆马勃（Pisolithus tinctorius）、美味牛肝菌（Boletus edulis）、赭丝膜菌（Cortinarius russus）、土生空团菌（Cenococ     

干旱胁迫对烟草叶片丙二醛含量和细胞膜透性的影响

对干旱胁迫下5个烟草品种(系)丙二醛含量和细胞膜透性进行测定表明,随着干旱胁迫的不断加重,烟草叶片丙二醛含量呈现先升后降的趋势,而细胞膜透性则表现为持续升高;复水后细胞膜透性能很快恢复正常,而丙二醛含量需要较长时间才略有恢复。细胞膜透性反应了烟草受干旱胁迫的程度,而丙二醛含量的稳定对烟草的抗旱性有重要意义。     

红花尔基樟子松优良抗旱菌树组合的筛选

为筛选红花尔基樟子松（Pinus sylvestris var.mongolica）优良抗旱菌树组合,采用樟子松林下5个优势外生菌根真菌菌株为接种体,分别对5个月龄樟子松实生苗进行人工接种,接种8个月后观察菌根侵染情况及菌根形态,并在非干旱胁迫和干旱胁迫条件下测定不同菌树组合的生长和生理生化指标。结果表明：5个乡土菌种均能成功侵染樟子松并形成典型的外生菌根;干旱胁迫下,菌根化樟子松的各项生长指标均显著高于对照（P<0.05）,且接种粘盖牛肝菌（Suillus bovinus）具有最高的菌根侵染率、苗高、地上及地下生物量和根茎比;外生菌根共生体可通过提高植物SOD活性与POD活性,同时降低MDA含量来提高樟子松对干旱的耐受力;干旱胁迫下,所有接种处理苗木的萎蔫时间较对照处理均推迟,推迟时间最长的是粘盖牛肝菌接种处理,较对照推迟96.3 h;另外,接种处理均能显著延长宿主临界致死时间,尤其是接种粘盖牛肝菌可延长113.8 h。因此,可以认为粘盖牛肝菌与樟子松是一个较为理想的抗旱菌树组合。     

6种外生菌根真菌对西南桦幼苗的接种效应

【背景】西南桦是兼具内生、外生菌根的典型菌根营养型树种,菌根化育苗是其壮苗培育的有效措施。【目的】揭示外生菌根真菌对西南桦无性系幼苗生长和养分含量的影响,为其菌根化育苗筛选优良外生菌根真菌提供科学依据。【方法】以BY1、FB4、FB4+和A5等4个西南桦优良无性系为研究对象,选用土生空团菌(Cenococcumgeophilum)、松乳菇(Lactariusdeliciosus)、黄硬皮马勃(Scleroderma flavidum)、多根硬皮马勃(S. polyrhizum)、褐环乳牛肝菌(Suillus luteus)和红绒盖牛肝菌(Xerocomuschrysenteron)6个外生菌根真菌进行盆栽接种试验,分析接种处理间及无性系间苗高、地径、生物量以及养分含量差异。【结果】6个菌种均能与西南桦无性系幼苗形成外生菌根共生体,接种多根硬皮马勃与黄硬皮马勃显著促进了幼苗生长和养分吸收(P0.05),说明其与幼苗的亲和力明显优于其它菌种。尽管菌根侵染率在4个无性系之间无显著差异(P≥0.05),但各菌种对FB4、BY1幼苗生长的促进作用显著强于其它2个无性系。【结论】多根硬皮马勃和黄硬皮马勃可作为西南桦菌根化育苗的优选菌种。     

丛枝菌根真菌对连翘幼苗抗旱性的影响

采用集球囊霉（Glomus fasciculatum Gerd.＆ Trappe emend.Walker ＆ Koske）、缩球囊霉（Glomus constrictum Trappe）单独接种和混合接种于连翘（Forsythia suspensa（Thunb.）Vahl）幼苗,研究丛枝菌根真菌对连翘抗旱性的影响.结果表明：在干旱胁迫条件下,随着菌根侵染率的提高,连翘幼苗叶绿素和脯氨酸含量增加,SOD活性增强,丙二醛含量和膜透性降低,苗木枯死率下降.菌根真菌通过促进苗木快速累积游离脯氨酸,提高SOD酶活性,减缓干旱对细胞膜的破坏,延缓了植物受伤害的速度,提高连翘幼苗的抗旱性;在不同接种处理间,混合接种效果最好,其次为缩球囊霉单独接种.     

菌根化技术在广西马尾松育苗中的应用

通过对马尾松苗木的菌根土接种及苗圃地选择的试验,可知培育马尾松菌根化苗木,应选择土壤中菌根菌含量丰富的马尾松疏残林地、近年采伐迹地、林中空地、林缘下方,以及前茬是马尾松或湿地松的老苗圃地作为马尾松苗圃地。在这些地类上,结合施以足量腐熟有机肥做基肥,培育的马尾松苗木菌根感染率一般都在85%以上,苗木质量好。上述地类外的新垦苗圃地,应在生长健壮,无病原菌,而且最好是生长有马勃子实体的马尾松林下,挖取0—20厘米表土层进行菌根土接种,培育的松苗也可获得较高的菌根感染率。历史上未种过松类、栎类,附近又无松林的荒山荒地,用作马尾松苗圃地,苗木的菌根感染率极低,质量差。     

外生菌根真菌对杉木的接种效应

对商南县2年生杉木苗木进行乳牛肝菌(Suillus bovines)、褐环乳牛肝菌(Suillus luteus)和褐黄牛肝菌(Boletus luridus)3种外生菌根真菌的接种试验.结果显示,外生菌根真菌对杉木苗木成活率、苗高和地径生长均有明显的促进作用,能明显提高苗木的菌根化水平,增加苗木体内叶绿素含量,促进其游离脯氨酸含量的累积,降低丙二醛含量.对不同坡向杉木苗木各项生长指标的分析显示,在杉木人工造林中,阳坡的综合效应明显优于阴坡.乳牛肝菌和褐黄牛肝菌可作为一种生物肥料,在杉木人工造林中应用.     

丛枝菌根对枳实生苗抗旱性的影响研究

在自然水分干旱胁迫和胁迫解除复水条件下,研究了丛枝菌根对1年生枳实生苗生长和抗旱性的影响.结果表明,接种丛枝菌根真菌Glomusmosseae93显著增加枳实生苗的株高、茎粗和鲜重,提高了幼苗移栽成活率.在自然水分干旱胁迫和胁迫解除复水过程中,丛枝菌根提高或者极显提高了叶片可溶性糖含量、叶片和根系的可溶性蛋白质含量、超氧化物歧化酶活性、过氧化物酶活性和过氧化氢酶活性,从而提高了枳实生苗的渗透调节能力,增强了其保护系统能力,降低了细胞膜脂过氧化,使枳实生苗抗旱能力增强.表明丛枝菌根真菌增强寄主植物抗旱能力的作用机制与保护系统相关.     

Terminal drought and seed priming improves drought tolerance in wheat

Plants retain the preceding abiotic stress memory that may aid in attainment of tolerance to subsequent stresses. This study was conducted to evaluate the influence of terminal drought memory (drought priming) and seed priming in improving drought tolerance in wheat (Triticum aestivum L.). During first growing season, wheat was planted in field under optimal (well-watered) and drought stress imposed at reproductive stage (BBCH growth stage 49) until maturity (BBCH growth stage 83). Seeds collected from both sources were subjected to hydropriming or osmopriming (with 1.5% CaCl₂ solution); while, dry seed was taken as control. Treated and control seeds, from both sources, were sown in soil filled pots. After the completion of seedling emergence, pots were maintained at 50% water holding capacity (drought) or 100% water holding capacity (well-watered). Drought stress suppressed the plant growth (2–44%), perturbed water relations (1–18%) and reduced yield (192%); however, osmolytes accumulation (3–14%) and malondialdehyde contents (26–29%) were increased under drought. The crop raised from the seeds collected from terminal drought stressed plants had better growth (5–63%), improved osmolyte accumulation (13–45%), and lower lipid peroxidation (3%) than the progeny of well-watered crop. Seed priming significantly improved the crop performance under drought stress as compared to control. However, osmopriming was more effective than hydropriming in this regard as it improved leaf area (9–43%), tissue water status (2–47%), osmolytes accumulation (6–48%) and grain yield (14–79%). In conclusion, terminal drought induced modifications in seed composition and seed priming improved transgenerational drought tolerance through improvement in tissue water status and osmolytes accumulation, and decrease in lipid peroxidation.     

Genetic basis of drought resistance at reproductive stage in rice: separation of drought tolerance from drought avoidance

Drought tolerance (DT) and drought avoidance (DA) are two major mechanisms in drought resistance of higher plants. In this study, the genetic bases of DT and DA at reproductive stage in rice were analyzed using a recombinant inbred line population from a cross between an indica lowland and a tropical japonica upland cultivar. The plants were grown individually in PVC pipes and two cycles of drought stress were applied to individual plants with unstressed plants as the control. A total of 21 traits measuring fitness, yield, and the root system were investigated. Little correlation of relative yield traits with potential yield, plant size, and root traits was detected, suggesting that DT and DA were well separated in the experiment. A genetic linkage map consisting of 245 SSR markers was constructed for mapping QTL for these traits. A total of 27 QTL were resolved for 7 traits of relative performance of fitness and yield, 36 QTL for 5 root traits under control, and 38 for 7 root traits under drought stress conditions, suggesting the complexity of the genetic bases of both DT and DA. Only a small portion of QTL for fitness- and yield-related traits overlapped with QTL for root traits, indicating that DT and DA had distinct genetic bases.     

Drought and drought tolerance

Drought tolerance is a nebulous term that becomes more nebulous the more closely we look at it, much as a newspaper photograph does when viewed through a magnifying glass. From the vantage point of an ecologist the features that distinguish xerophytic from mesophytic vegetation are clear. We can all tell that a cactus is more drought tolerant than a carnation. But when we look at crop plants, the features that confer drought tolerance are far from clear. The main reason for the contrast is that the traits we associate with xerophytes typically concern survival during drought, whereas with crops we are concerned with production—and insofar as the term drought tolerance has any useful meaning in an agricultural context, it must be defined in terms of yield in relation to a limiting water supply.Further, with the well-developed major crop plants, those of us trying to increase water-limited yield would be pleased to achieve improvements of just a few percent in environments that are highly variable in their water supply. This variability often means that several seasons are required to demonstrate the advantages of an allegedly improved cultivar. Traits that confer drought tolerance in such circumstances are subtle, and may manifest themselves in some types of drought but not in others. Indeed the most influential characters often have no direct connection to plant water relations at all, as I elaborate on below.I will concentrate on the agricultural rather than the natural environment (although there are no doubt lessons for us still to learn from analysing the behaviour of natural vegetation—see Monneveux, this volume), and will argue that drought tolerance is best viewed at an ontogenetic time scale—i.e. at the time scale of the development of the crop—weeks to months for an annual crop. The timing of the main developmental changes, like floral initiation and flowering, and the rate of development of leaf area in relation to the seasonal water supply, are the most important variables at this time scale. Occasionally though, rapid changes in the environment, such as a sudden large rise in air temperature and humidity deficit, perhaps associated with hot dry winds, make appropriate short-term physiological and biochemical responses essential for the survival of the crop. These short term responses may be amenable to cellular and sub-cellular manipulation, especially if the sudden environmental deterioration occurs at especially sensitive stages in development such as pollen meiosis or anthesis.Purists insist that drought is a meteorological term that refers only substantial to periods in which rainfall fails to keep up with potential evaporation. Within the spirit of this meeting it is appropriate to interpret the term more loosely than this definition, and to define it as circumstances in which plants suffer reduced growth or yield because of insufficient water supply, or because of too large a humidity deficit despite there being seemingly adequate water in the soil.     

A drought rarity and evapotranspiration-based index as a suitable agricultural drought indicator

Agricultural drought has a substantial impact on crop yields and, thus, food security within the context of global climate change. Therefore, efforts should focus on agricultural drought detection and monitoring. Agricultural drought is identified as unusually dry conditions in which severe water stress impedes crop growth. Thus, the crop water deficit severity and rarity are both key factors in agricultural drought detection and are rarely considered simultaneously in existing drought indices. To overcome this limitation, an integrated agricultural drought index (IADI) based on drought rarity and evapotranspiration is proposed. As an important grain production base, Northeast China has suffered from frequent droughts in recent years, demonstrating an urgent need for accurate drought monitoring. In this study, the superiority of the IADI as an agricultural drought indicator through the detection of the severity and rarity was tested using the drought disaster area (DDA) and grain yield, and its performance was compared to that of the evaporative drought index (EDI), an indicator that accounts for only the water deficit severity. The response of agricultural drought to meteorological drought and its impact on the grain yield were further analyzed. The results showed that (1) the IADI can effectively capture the drought variability and identify drought events by combining the detection of the severity and rarity. (2) The R² value between the DDA and IADI (0.72) was higher than that with the EDI (0.50), and the same result was found in a comparative analysis using the grain yield, showing that the IADI is a suitable indicator for agricultural drought assessment. (3) Severe and extreme meteorological droughts and extreme agricultural droughts in western Jilin and western Liaoning were more frequent than in other regions, highlighting the agricultural drought tendency and sensitivity to precipitation deficit in this region. (4) The impacts of agricultural drought on grain yield in three provinces of Northeast China vary greatly during the crop-growing period, with the most significant impacts occurring from May to July. Therefore, this period represents the critical crop water requirement period, and timely irrigation should be ensured during this period.     

花生幼苗对重复干旱胁迫的生理响应

防雨棚内设盆栽试验,设置对照(Control,75%田间持水量)、干旱胁迫(D,35%)、重复干旱胁迫(D_D,35%)3个处理,探讨花生幼苗对预干旱胁迫的适应和记忆响应,分析预干旱对缓解重复干旱胁迫危害的生理作用。结果表明,与干旱胁迫处理相比,重复干旱胁迫提高了叶片的相对含水量,减少脯氨酸的积累,降低MDA和O·_2~-含量;抗氧化酶SOD、CAT活性降低,其中POD活性降低最为明显,并在复水后恢复到与对照相同水平或低于对照。与正常水分的对照相比,干旱胁迫显著降低叶片光合速率(P_N)、最大光合势能(P_C)、最大光量子产量(Y_Q),但重复干旱处理在重复干旱胁迫时期和复水后P_N、P_C和Y_Q均高于干旱处理。预干旱胁迫导致光合和气孔导度滞后面积、滞后率(H_P和H_g)增加,经过预干旱胁迫后,重复干旱显著降低光合和气孔导度滞后面积和滞后率。预干旱胁迫提高植株在重复干旱胁迫下叶片含水量,减轻重复干旱对植株造成的生理伤害,在光合作用上提高对重复干旱的抵御能力,并在复水后快速恢复到正常水分条件下植株生长水平,减少干旱对植株的不利影响。因此,预干旱胁迫促使花生幼苗具备适应或可记忆初始胁迫的能力,重复干旱胁迫时表现更为迅速和强烈的生理防御和快速的生理恢复机制。     

水分胁迫对山黧豆萌发过程中β—ODAP和氨基酸的影响

山黧豆（Lathyrus sativus)种子在萌发过程中,根芽中β-N-草酰基-L-2,3-二氨基丙酸（β-ODAP）6d前逐渐增加,尔后不断下降;在水分胁迫条件下,β-ODAP和游离氨基酸含量随水分胁迫的增加而上升,子叶中β-ODAP在3d前高于根芽,然后下降并低于根芽,子叶中β-ODAP含量随着胁迫的增加而降低。