3种龙胆科植物的资源分配对策

选择青藏高原东缘同一生境类型下具有不同交配系统特点和不同传粉者丰度的3种龙胆科植物湿生扁蕾(Gentianopsis paludosa)(自花授粉)、祁连獐牙菜(Swertia przewalskii)(高昆虫访问异花授粉)和线叶龙胆(Gentiana farreri)(低昆虫访问异花授粉)为对象,研究其资源分配特征。结果表明,1)3种植物的花粉胚珠比例(P/O)存在显著差异(P0.05),湿生扁蕾的P/O显著低于另外两种异花授粉植物的(P0.05),祁连獐牙菜的P/O显著低于线叶龙胆的(P0.05);2)3种植物的繁殖分配比例存在差异,湿生扁蕾的繁殖分配比例显著高于另外两种异花授粉植物的(P0.05),线叶龙胆的繁殖分配比例显著高于祁连獐牙菜的(P0.05);3)在繁殖分配比例与个体大小关系上,湿生扁蕾与其个体大小不存在显著相关关系(P0.05),而另外两种异花授粉植物则与其各自个体大小之间存在显著负相关关系(P0.05)。研究表明,交配系统类型和传粉者丰度与植物的资源分配模式有关,尽管3种植物的繁殖绝对投入量都与其个体大小显著正相关(P0.05),但自花授粉植物相对于异花授粉植物具有较高的繁殖分配比例,并且这种较高的繁殖分配比例不受个体大小影响,这种高繁殖投入的资源分配模式可能与自花授粉植物具有繁殖保障,从而降低其繁殖代价有关。     

吉林省民营高等学校资源配置效率研究

民营高等学校是我国重要的人才培养渠道,自20世纪80年代以来,民营高等教育进入了飞速发展时期。吉林省民营高校经过多年的改革和探索已有了跨越式的发展,但如何使其从粗放型发展向内涵式发展转变,实现教育资源合理配置是关键。本文从调查研究吉林省民营高等学校资源配置的实际情况出发,采用数据包络分析方法（DEA）,评价民营高等学校资源配置效率问题,可以看出,吉林省民营高等院校在资源配置上依然存在着非效率的情况,本文据此提出相应建议。     

热处理对2种潜伏炭疽菌生长和致病性的影响

 通过测定热处理对潜伏侵染于芒果果实中的胶胞炭疽菌(Colletotrichum gloeosporioides Penz.)和香蕉果实中的芭蕉炭疽菌[C.musae(Berk.& Curt.)Arx.]离体培养菌的生长、繁殖和致病性的影响,结果表明:当温度达55℃和60℃,时间20 min时,对菌体的生长和孢子萌发可起明显抑制或杀伤作用,并降低其致病性。2种炭疽菌中,芭蕉炭疽菌比胶胞炭疽菌对热更敏感。作者认为,果实采后热处理时,应根据果实种类和不同菌,采用不同的处理温度和时间,才能得到更好的效果。     

Response of seedlings growth of Pinus sylvestriformis to atmospheric CO_2 enrichment in Changbai Mountain

IntroductionGIobaIchangehasbeenoneoftheimpoFtantis-suesandscientistspaycIoseattentiontoit.ThegreatimportanceofforestecosystemisreflectednotonlybytheirhUgebiomass,butaIsobytheirsignifi-cantroIeintheglobaIcarbonbaIance.Howtreesrespondtoclimaticchangesmightbeofgreatsig-nificance.ManystudiesindicatethattherisingatmosphericCo,leveIscanmakeasubstantialeffectonplantgroWthanddevelopment.SomeonethinkcommonlythattherisingCo,levelscanstimuIatepIantgroWthandbiomassproduction,sincephotosynthesisofC…     

一类p-Laplacian方程非平凡解的存在性

用山路引理得到了一类带有Dirichlet边值条件的p-Laplacian方程的非平凡解的存在性及多解性.     

牛乳过氧化物酶活性,电导率与隐性乳房炎的关系

对发情盛期、怀孕初期、怀孕中期、怀孕末期的泌乳奶牛的正常乳和隐性乳房炎阳性乳（简称隐乳），测定了其乳过氧化物酶活性及电导率，探讨了乳过氧化物酶活性和电导率的变化与隐性乳房炎的关系。结果表明，不同时期泌乳牛隐乳的乳过氧化物酶活性显著高于同期正常乳汁的酶值（Ｐ＜０．０１）；隐乳的电导率值比正常乳的亦明显升高（Ｐ＜０．０５）     

Further evidence of polygenic inheritance of partial resistance in barley to leaf rust,Puccinia hordei

Summary The latent period (LP) is a crucial component of partial resistance. Five cultivars, L94, Sultan (Su), Volla (Vl), Julia (Ju) and Vada (Va), representing the known range in partial resistance and LP were crossed in a diallel, and the F₁, F₂ and F₃ tested. The LP effectuated by the five cultivars is about 9, 10^1/2, 10^1/2, 13 and 15^1/2 days, respectively. The crosses Su×L94, Vl×L94 and Ju×L94 had an F₂ positively skewed. Their F₂ means were similar or only slightly larger than the F₁ means. The F₂ frequency distributions in the crosses Vl×Su, Ju×Su and Ju×Vl were normal or nearly so with F₁ and F₂ means similar to each other and to the mid-parent value. The crosses involving Va as a parent again showed a positive skewness but with F₂ means considerably larger than the F₁ moans.Most F₂'s ranged from the low parent to the high parent values without transgression. In the crosses Va×L94 (reported earlier) and Ju×L94 the parental values were not recovered among 216 and 154 F₂ plants, respectively. The cross Ju×Va showed transgression beyond the low parent, Ju.From these data it is concluded, assuming no linkage, that seven loci are involved. The + alleles (governing a longer LP) are thought to be distributed over the parents as follows: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacaqGmb% GaaeyoaiaabsdacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2caca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaa% b2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% iiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeyl% aiaabccaaeaacaqGtbGaaeyDaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae% 4kaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqG% RaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2% cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaa% qaaiaabAfacaqGSbGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeii% aiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGa% GaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUca% caqGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiai% aab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGa% aeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaaabaGaaeOs% aiaabwhacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaGaae% iiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2caaeaacaqGwbGaaeyyaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcaca% qGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae4kaiaa% bUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% 4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabc% cacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGGaGaaeiiaiaabUcacaqGRaaaaaa!1BBA!\[\begin{gathered} {\text{L94 - - - - - - - - - - - - - - }} \hfill \\ {\text{Su + + + + + + - - - - - - - - }} \hfill \\ {\text{Vl + + + + - - + + - - - - - - }} \hfill \\ {\text{Ju + + + + + + + + + + - - - - }} \hfill \\ {\text{Va + + + + + + + + - - + + + + }} \hfill \\ \end{gathered} \]The genes are supposed to act additively (intermediate inheritance) with the exception of one locus (the 6th or 7th locus) which shows dominance for the shorter LP (for the-alleles). The effect of this locus on LP seems considerably larger than that of the other loci. There are indications of physiological barriers, which means that LP's shorter than the one of L94 or much longer than that of Va are not possible.The effect of + genes in genotypes governing LP's close to these barriers (with very few or very many + alleles respectively) is smaller than in genotypes governing intermediate LP's.     

Does plant growth phase determine the response of plants and soil organisms to defoliation?

To test a hypothesis that the effects of defoliation on plant ecophysiology and soil organisms depend on the timing of defoliation within a growing season, we established a greenhouse experiment using replicated grassland microcosms. Each microcosms was composed of three plant species, Trifolium repens, Plantago lanceolata and Phleum pratense, growing in grassland soil with a diverse soil community. The experiment consisted of two treatment factors—defoliation and plant growth phase (PGP)—in a fully factorial design. Defoliation had two categories, i.e. no trimming or trimming a total of four times at 2 week intervals. The PGP treatment had four categories, i.e. 1, 3, 7 or 13 weeks growth following planting before the first defoliation (subsequently referred to as PGP1, PGP2, PGP3 and PGP4, respectively). In each PGP treatment category, microcosms were harvested 1 week after the final defoliation. Harvested shoot and root mass and total shoot production (including trimmed and harvested shoot mass) increased with time and were lower in defoliated than in non-defoliated systems. The fraction of root biomass of harvested plant biomass decreased with time but was increased by defoliation at PGP3 and PGP4. The proportion of T. repens in total shoot production increased and those of P. lanceolata and P. pratense decreased with time. Defoliation increased the proportions of P. lanceolata and P. pratense in total shoot production at PGP3 and PGP4. Root N and C concentrations increased and root C-to-N ratio decreased with time in non-defoliated systems. Defoliation increased root N concentration by 38 and 33% at PGP1 and PGP2, respectively, but decreased the concentration by 22% at PGP4. In contrast, defoliation reduced root C concentration on average by 1.5% at each PGP. As with the effects on root N concentration, defoliation decreased the root C-to-N ratio at PGP1 and PGP2 but increased the ratio at PGP4. Among soil animal trophic groups, the abundance of herbivorous nematodes was higher at PGP4 than at PGP1-3 and that of predacious nematodes higher at PGP2-4 than at PGP1, while the abundance of bacterivorous, fungivorous and omnivorous nematodes and that of detritivorous enchytraeids did not differ between the PGP categories. Among bacterivorous nematodes, however, Acrobeloides, Chiloplacus and Protorhabditis species decreased and that of Plectus spp. increased with time. Defoliation did not affect the abundance of soil animal trophic groups, but reduced the abundance of herbivorous Coslenchus spp. at each PGP and raised the abundance of herbivorous Rotylenchus spp. and bacterivorous Eucephalobus spp. at PGP4. Confirming our hypothesis, the results suggest that the effects of defoliation on the attributes of grassland plants, such as biomass allocation between roots and shoots and root quality, may depend on the timing of defoliation within a growing season. However, contradicting our hypothesis, the results suggest that significant changes in plant attributes after defoliation may not always lead to substantial changes in the abundance of belowground organisms.     

湖南报业资源配置现状与问题分析

以对湖南报业资源配置现状的调查为基础 ,从人力资源、媒体资源、信息资源、广告资源、受众资源等五个方面展开分析 ,探讨了湖南报业资源配置存在的主要问题 ,旨在为湖南报业资源的优化配置和湖南报业的发展提供借鉴。     

含蜡热油管道稳态与瞬态的温降计算

含蜡热油管道在设计及实际运行过程中,油品密度、粘度、比热容沿程随温度变化,沿线流型与流态也不断变化,这些都是计算管道温降必须考虑的因素.从能量方程出发,计入析蜡潜热的影响,推导出管道沿线流量变化不大时的瞬态温度方程,并利用三特征线方法进行求解,提高了含蜡热油管道的计算精度,并为其设计计算及仿真软件的开发提供了理论依据.