斑节对虾杆状病毒包涵体研究

利用显微图像分析技术,对斑节对虾肝胰腺正常细胞胞核和斑节对虾杆状病毒(MBV)感染细胞胞核横切面的直径、周长和面积进行了测量分析.结果表明:正常细胞胞核的直径为3.47±0.30μm、周长为13.03±1.36μm、面积为10.87±1.78μm²;MBV感染细胞胞核的直径为3.81±0.79μm、周长为14.00±2.87μm、面积为13.52±5.37μm²;两者的直径、周长和面积均存在极显著的差异(P<0.01).对3种类型的包涵体进行了测量,其中1类包涵体最大,2类包涵体次之,3类包涵体最小,并以1类包涵体占大多数.     

西瓜小叶脉超微结构研究

用透射电子显微技术研究了西瓜叶片小叶脉,结果表明,小叶脉是由大型维管束鞘细胞包围的维管束,维管束呈现大的头部和线形的柄部,柄部是单列细胞的木质部,由维管薄壁细胞和导管分子组成;头部是韧皮部,由维管薄壁细胞、伴胞和筛管分子组成。同一小叶脉内常见有超微结构特征显著不同的两种伴胞:一种伴胞体积小,与维管束鞘细胞接触面较小或不接触,细胞内有大液泡,细胞壁上没有胞间连丝或只有少数不分枝的胞间连丝,这种伴胞为2a型;另一种伴胞体积大,通常位于韧皮部两翼,不含大液泡而含大量小泡,与维管束鞘细胞接触面较大,接触面上有大量具分枝的胞间连丝,分枝部分比未分枝部分直径小,这种伴胞为中间细胞类型。显然,西瓜是小叶脉内兼具两种类型伴胞的植物。     

西瓜小叶脉超微结构研究

用透射电子显微技术研究了西瓜叶片小叶脉,结果表明,小叶脉是由大型维管束鞘细胞包围的维管束,维管束呈现大的头部和线形的柄部,柄部是单列细胞的木质部,由维管薄壁细胞和导管分子组成;头部是韧皮部,由维管薄壁细胞、伴胞和筛管分子组成。同一小叶脉内常见有超微结构特征显著不同的两种伴胞：一种伴胞体积小,与维管束鞘细胞接触面较小或不接触,细胞内有大液泡,细胞壁上没有胞间连丝或只有少数不分枝的胞间连丝,这种伴胞为2a型;另一种伴胞体积大,通常位于韧皮部两翼,不含大液泡而含大量小泡,与维管束鞘细胞接触面较大,接触面上有大量具分枝的胞间连丝,分枝部分比未分枝部分直径小,这种伴胞为中间细胞类型。显然,西瓜是小叶脉内兼具两种类型伴胞的植物。     

宁夏枸杞果实韧皮部及其周围细胞超微结构研究

应用透射电镜技术研究了宁夏枸杞果实韧皮部细胞的超微结构变化。结果表明:(1)随着枸杞果实的发育成熟,果实维管组织中的韧皮部筛分子筛域逐渐变宽,筛孔大而多,通过筛孔的物质运输十分活跃;筛分子和伴胞间有胞间连丝联系,伴胞属传递细胞类型,与其相邻韧皮薄壁细胞和果肉薄壁细胞连接处的细胞界面发生质膜内突,整个筛分子/伴胞复合体与韧皮薄壁细胞之间形成共质体隔离,韧皮部糖分的卸载方式主要以质外体途径进行。(2)韧皮薄壁细胞间的胞间连丝较多,而韧皮薄壁细胞与果肉薄壁细胞的胞间连丝相对较少,但果肉薄壁细胞间几乎无胞间连丝;果肉薄壁细胞之间胞间隙较大,细胞壁和质膜内突间形成较大的质外体空间,为质外体的糖分运输创造了条件。(3)筛管、伴胞、韧皮薄壁细胞和果肉薄壁细胞中丰富的囊泡以及活跃的囊泡运输现象,暗示囊泡也参与了果实糖分的运输过程。研究推测,枸杞果实韧皮部同化物的卸载方式以及卸载后的同化物运输主要以质外体途径为主。     

不同季节西双版纳热带雨林细罗伞幼树光合特性的变化

利用Li-6400光合作用测定仪,西双版纳热带季节雨林林下细罗伞幼树(Ardisia tenera)在雾凉季(1月)、干热季(4月)和雨季(7月)的光合光响应特征及光合速率日变化被测定.结果显示:人工光源下,细罗伞幼树Pn_max、c、a均以雨季中最大,分别为2.782μmol/(m²·s)、1.233μmol/(m²·s)和0.007,各季节中LSP、LCP均偏低;林下自然光照环境中,3个季节细罗伞幼树Pn均出现双峰型特征,雾凉季、干热季和雨季的最大峰值分别为1.288μmol/(m²·s)、1.919μmol/(m²·s)、2.5μmol/(m²·s),雨季中一天中的Pn和Gs最大,雾凉季的Tr最小,但WUE却最高.林下细罗伞幼树光合特性随季节而发生显著变化,且表现出耐荫的特性,总体上细罗伞幼树对CO₂的净吸收通量较低.     

苹果果实韧皮部及其周围薄壁细胞的超微结构观察和功能分析

利用透射电镜技术,对发育过程中的苹果（Ｍａｌｕｓ ｄｏｍｅｓｔｉｃａ Ｂｏｒｋｈ）果实韧皮部及其周围薄壁细胞的超微结构进行了观察研究。结果表明,在主脉和细脉的筛分子（ＳＥ）和伴胞（ＣＣ）之间存在胞间连丝,胞间连丝在筛分子一侧是单通道,在伴胞一侧呈多分枝通道。在细脉中筛分子小,伴胞大,在主脉中则是筛分子大,伴胞小。伴胞内胞质和核质稠密,富含线粒体、内质网和高尔基体,液泡内往往呈现多膜包被的囊泡结构,     

胞外H2O2及NADPH氧化酶参与了铜胁迫对植物细胞死亡的诱导

以烟草悬浮细胞BY-2(Nicotiana tabacum L.cv.Bright Yellow-2)为材料,探讨了在铜离子胁迫下植物细胞死亡发生过程中胞外H₂O₂及NADPH氧化酶所扮演的角色。实验结果表明,随着外源CuCl₂浓度的上升(从0~700 μmol·L^-1),细胞死亡水平不断上升,且胞外H₂O₂的水平也不断增加。在300 μmol·L^-1的CuCl₂诱导细胞死亡的过程中,加入H₂O₂清除剂N-N-二甲基硫脲(DMTU)降低了胞外CuCl₂胁迫下H₂O₂含量增加的同时也降低了细胞死亡水平的上升,这一观察表明了铜离子胁迫所导致的细胞死亡的发生和胞外H₂O₂的增加有关。进一步的研究表明,300 μmol·L^-1 CuCl₂的胁迫导致了NADPH氧化酶活性的显著性上升,而加入NADPH氧化酶的抑制剂（二亚苯基碘,DPI,)则降低了CuCl₂胁迫所导致的细胞死亡和胞外H₂O₂含量的上升。上述结果表明,胞外H₂O₂和NADPH氧化酶参与了CuCl₂对植物细胞死亡的诱导作用。     

动物体内海洛因代谢产物分析

将吗啡、海洛因分别给予大鼠,建立成瘾动物模型,用气相色谱联用质谱(Gas chromatography-mass spectrometry)方法分析大鼠体毛、尿液中吗啡及6-单乙酰吗啡水平。结果显示:连续给药14天后检测分析,大鼠体毛中吗啡、6-单乙酰吗啡水平分别为2.64±0.9ng·ng·mg^-1.88±0.6ng·mg·mg^-1,大鼠尿液中吗啡、6-单乙酰吗啡水平分别为27.7±0.6μg·mL^-1、5.2±0.2μg·mL^-1,与对照组比,有显著性差异(P<0.01)。海洛因在动物体内主要代谢产物为吗啡和6-单乙酰吗啡。     

秦岭南坡短柄枹栎和锐齿槲栎的种子产量和种子大小及其与昆虫寄生的关系

【目的】为了解昆虫寄生特征与短柄枹栎 Quercus glandulifera 和锐齿槲栎 Quercus aliena var. acuteserrata 的种子产量及种子大小的关系。【方法】本研究于2011和2012年在秦岭南坡佛坪国家自然保护区,对短柄枹栎和锐齿槲栎种群的种子产量和昆虫寄生特征进行了野外调查研究。【结果】2年中短柄枹栎、锐齿槲栎种子雨密度和种子产量均差异明显,2011年短柄枹栎种子雨密度和种子产量分别为145.76±24.56粒/m²和74.97±11.56粒/m²,分别显著高于2012年的64.09±9.61粒/m²和34.30±3.51粒/m²;2011年锐齿槲栎种子雨密度和种子产量分别为238.88±43.97粒/m²和117.34±18.76粒/m²,分别显著高于2012年的112.00±19.20粒/m²和55.96±19.20粒/m²。2011年短柄枹栎和锐齿槲栎的种子产量中完好种子所占比例分别为49.73%和50.73%,分别显著高于2012年的38.69%和44.28%;而2011年虫蛀短柄枹栎和锐齿槲栎种子所占比例分别为28.05%和19.31%,分别低于2012年的39.77%和26.63%,但并无显著差异。2011和2012年,短柄枹栎和锐齿槲栎虫蛀种子个体均显著大于完好种子,且2011年二者虫蛀种子所含幼虫数与种子大小的相关性显著,2012年二者相关性不显著。【结论】短柄枹栎和锐齿槲栎种子的虫蛀率与种子产量有一定的关系,即在种子产量较低年份,虫蛀率有升高趋势,反之有降低趋势。同时,昆虫对这两种栎树种子中个体大的种子有寄生选择偏好,同时虫蛀种子所含幼虫数与种子大小也有一定的关系,即种子越大,所含昆虫幼虫数就越多。     

模拟氮沉降对华西雨屏区苦竹林细根特性和土壤呼吸的影响

细根在森林生态系统地下碳循环过程中具有核心地位.2007年11月-2009年11月,对华西雨屏区苦竹人工林进行了模拟氮沉降试验.氮沉降水平分别为对照(CK,0 g N·m^-2·a^-1)、低氮(5 g N·m^-2·a^-1)、中氮(15 g N·m^-2·a^-1)和高氮(30 g N·m^-2·a^-1)处理,研究氮沉降对苦竹人工林细根和土壤根际呼吸的影响.结果表明：不同处理氮沉降下,<1 mm和1～2 mm细根特性差异较大,与< 1 mm细根相比,1～2 mm细根的木质素、磷和镁含量更高,而纤维素、钙含量更低;氮沉降显著增加了<2 mm细根生物量,对照、低氮、中氮和高氮处理的细根生物量分别为(533±89)、(630±140)、(632±168)和(820±161) g·m^-2,氮、钾、镁元素含量也明显增加;苦竹林各处理年均土壤呼吸速率分别为(5.85±0.43)、(6.48±0.71)、(6.84±0.57)和(7.62±0.55) t C·hm^-2·a^-1,氮沉降对土壤呼吸有明显的促进作用;苦竹林的年均土壤呼吸速率与<2 mm细根生物量和细根N含量呈极显著线性相关.氮沉降使细根生物量和代谢强度增加,并通过增加微生物活性促进了根际土壤呼吸.     

Modification of a Specific Class of Plasmodesmata and Loss of Sucrose Export Ability in the sucrose export defective1 Maize Mutant

We report on the export capability and structural and ultrastructural characteristics of leaves of the sucrose export defective1 (sed1; formerly called sut1) maize mutant. Whole-leaf autoradiography was combined with light and transmission electron microscopy to correlate leaf structure with differences in export capacity in both wild-type and sed1 plants. Tips of sed1 blades had abnormal accumulations of starch and anthocyanin and distorted vascular tissues in the minor veins, and they did not export sucrose. Bases of sed1 blades were structurally identical to those of the wild type and did export sucrose. Electron microscopy revealed that only the plasmodesmata at the bundle sheath-vascular parenchyma cell interface in sed1 minor veins were structurally modified. Aberrant plasmodesmal structure at this critical interface results in a symplastic interruption and a lack of phloem-loading capability. These results clarify the pathway followed by photosynthates, the pivotal role of the plasmodesmata at the bundle sheath-vascular parenchyma cell interface, and the role of the vascular parenchyma cells in phloem loading.     

Leaf structure and translocation in sugar beet

Anatomical and ultrastructural details of a translocating 10-cm leaf of sugar beet (Beta vulgaris L. var. Klein Wanzleben) were correlated with translocation rate data. The minor veins were found to be 13 times as extensive as the major veins and measure 70 cm/cm² leaf lamina. Measurements disclosed that a 33-μ length of minor vein services 29 mesophyll cells with the result that translocate moves an average of 73 μ or 2.2 cell diameters during transport from mesophyll cells to a minor vein. High-resolution, freeze-dry autoradiography revealed that assimilates accumulate in organelle-rich cells of the minor vein phloem. Correlation of phloem volume and loading rate for minor veins yielded an uptake rate of 735 μmoles of sucrose per g fresh weight of phloem. The arrangement and structural features of minor veins appeared to be consistent with the concept that vein loading precedes translocation.     

Minor vein structure and sugar transport in Arabidopsis thaliana

Leaf and minor vein structure were studied in Arabidopsis thaliana (L.) Heynh. to gain insight into the mechanism(s) of phloem loading. Vein density (length of veins per unit leaf area) is extremely low. Almost all veins are intimately associated with the mesophyll and are probably involved in loading. In transverse sections of veins there are, on average, two companion cells for each sieve element. Phloem parenchyma cells appear to be specialized for delivery of photoassimilate from the bundle sheath to sieve element-companion cell complexes: they make numerous contacts with the bundle sheath and with companion cells and they have transfer cell wall ingrowths where they are in contact with sieve elements. Plasmodesmatal frequencies are high at interfaces involving phloem parenchyma cells. The plasmodesmata between phloem parenchyma cells and companion cells are structurally distinct in that there are several branches on the phloem parenchyma cell side of the wall and only one branch on the companion cell side. Most of the translocated sugar in A. thaliana is sucrose, but raffinose is also transported. Based on structural evidence, the most likely route of sucrose transport is from bundle sheath to phloem parenchyma cells through plasmodesmata, followed by efflux into the apoplasm across wall ingrowths and carrier-mediated uptake into the sieve element-companion cell complex. Received: 5 October 1999 / Accepted: 20 November 1999     

Symplasmic Constriction and Ultrastructural Features of the Sieve Element/Companion Cell Complex in the Transport Phloem of Apoplasmically and Symplasmically Phloem-Loading Species

The ultrastructural features of the sieve element/companion cell complexes were screened in the stem phloem of two symplasmically loading (squash, [Cucurbita maxima L.] and Lythrum salicaria L.) and two apoplasmically loading (broad bean [Vicia faba L.] and Zinnia elegans L.) species. The distinct ultrastructural differences between the companion cells in the collection phloem of symplasmically and apoplasmically phloem-loading species continue to exist in the transport phloem. Plasmodesmograms of the stem phloem showed a universal symplasmic constriction at the interface between the sieve element/companion cell complex and the phloem parenchyma cells. This contrasts with the huge variation in symplasmic continuity between companion cells and adjoining cells in the collection phloem of symplasmically and apoplasmically loading species. Further, the ultrastructure of the companion cells in the transport phloem faintly reflected the features of the companion cells in the loading zone of the transport phloem. The companion cells of squash contained numerous small vacuoles (or vesicles), and those of L. salicaria contained a limited number of vacuoles. The companion cells of broad bean and Z. elegans possessed small wall protrusions. Implications of the present findings for carbohydrate processing in intact plants are discussed.     

<Emphasis Type="Italic">Amborella trichopoda</Emphasis>, plasmodesmata,and the evolution of phloem loading

Phloem loading is the process by which photoassimilates synthesized in the mesophyll cells of leaves enter the sieve elements and companion cells of minor veins in preparation for long distance transport to sink organs. Three loading strategies have been described: active loading from the apoplast, passive loading via the symplast, and passive symplastic transfer followed by polymer trapping of raffinose and stachyose. We studied phloem loading in Amborella trichopoda, a premontane shrub that may be sister to all other flowering plants. The minor veins of A. trichopoda contain intermediary cells, indicative of the polymer trap mechanism, forming an arc on the abaxial side and subtending a cluster of ordinary companion cells in the interior of the veins. Intermediary cells are linked to bundle sheath cells by highly abundant plasmodesmata whereas ordinary companion cells have few plasmodesmata, characteristic of phloem that loads from the apoplast. Intermediary cells, ordinary companion cells, and sieve elements form symplastically connected complexes. Leaves provided with ¹⁴CO₂ translocate radiolabeled sucrose, raffinose, and stachyose. Therefore, structural and physiological evidence suggests that both apoplastic and polymer trapping mechanisms of phloem loading operate in A. trichopoda. The evolution of phloem loading strategies is complex and may be difficult to resolve.     

Identification of phloem involved in assimilate loading in leaves by the activity of the galactinol synthase promoter

The definition of "minor" veins in leaves is arbitrary and of uncertain biological significance. Generally, the term refers to the smallest vein classes in the leaf, believed to function in phloem loading. We found that a galactinol synthase promoter, cloned from melon (Cucumis melo), directs expression of the gusA gene to the smallest veins of mature Arabidopsis and cultivated tobacco (Nicotiana tabacum) leaves. This expression pattern is consistent with the role of galactinol synthase in sugar synthesis and phloem loading in cucurbits. The expression pattern in tobacco is especially noteworthy since galactinol is not synthesized in the leaves of this plant. Also, we unexpectedly found that expression in tobacco is limited to two of three companion cells in class-V veins, which are the most extensive in the leaf. Thus, the "minor" vein system is defined and regulated at the genetic level, and there is heterogeneity of response to this system by different companion cells of the same vein.