Some Microscopical Observations of Functioning Sieve Tubes of Heracleum using Nomarski Optics

The study of isolated phloem in Heracleum has been extendedto intact functioning sieve tubes. Techniques of phloem dissectioncombined with Nomarski interference optics have been developedto permit useful visual observations, photomicrography, andciné photographs of sieve tubes which are apparentlynormal. In these preparations, plastids and organelles calledby us ‘marker particles’ are visible in rapid bouncingmotion, and the state of dispersal of these particles is relatedto the amount of damage done to the preparations. The movement of the marker particles and their subsequent fixationshows that they are apparently attached to or restrained byan invisible network in situ. The network is very sensitiveto disturbance and readily collapses around the sieve platesto form slime plugs upon damage to the sieve element. The markerparticles do not move through the cell nor across sieve platesin mature Heracleum. In young cells cyclosis is observable alongthe periphery and this suggests that a vacuole may then be present.In undamaged mature cells there was evidence neither of a vacuolenor of trans-cellular tubules of any size optically detectable. The motion of the particles was greater than Brownian movementand appeared to be under some physiological control. Their movementprobably indicated the presence of an operating transport phenomenon,either because solution was moving past them in the sieve tubeor because they were themselves attached to a contractile networkactively in pulsatory motion. Nearby companion and parenchymacells showed normal cytoplasmic streaming. Proposed mechanisms of translocation involving cytoplasmic streamingdo not seem to be applicable to the phloem of Heracleum. Themovement of the marker particles seemed to agree best with amechanism of ‘activated’ mass flow.     

中国蝶类新种小志Ⅳ

本文记述国产眼蝶科(Satyridae)的一个新属Sinonympha与它的一个模式种Sinonympha amoena(新种),这一蝶类最早是笔者于1939年7月在我国四川省西北部的杂谷脑(理县)发见的。为欲较全面地了解它们在分类系统上的亲缘关系,又于1963年和1964年在原产地采集了大量的成虫标本,并于1965—1966年在北京饲养了它的幼期。 新华新眼蝶属Sinonympha新属 新属属征 新华新眼蝶属Sinonympha(新属)与Coenonympha Hbner(1819)较为近似,但是某些形态特征和生物学特性(包括幼期)则与Ypthima Hbner(1818),OeneisHbner(1819)以及Mycalesis Hbner(1818)等属的种类互有相似之处,现将本新属的主要特征列述于下:     

Colony development and formation in halysitid corals

Lee, D.-J. & Noble, J. P. A. 1990 04 15: Colony development and formation in halysitid corals. Lethaia , Vol. 23. pp. 179–193. Oslo. ISSN 0024–1164.
Modes of colony formation and their relationship with colony morphology, size and substrate characteristics in species of halysitid corals have been studied. Two distinctive modes of colony formation in halysitids are proposed. In the monoplanulate mode. represented by Catenipora snnplex . the colony is developed from a single protocorallite and colony formation is achieved by a combination of asexual increase and intracolony fusions. In contrast, the polyplanulatc mode is demonstrated by C. escharoides . in which the early colony formation is achieved primarily by fusions of many 'incipicnt colonies' of more than a single planulate origin and of different generations. The latter mode has not previously been described in tabulates and has significant implications for coloniality, reproductive and life history characteristics, histo-compatibility and adaptative ecology. The colony size and morphology. and The distribution of halysitid species were primarily determined by the modes of colony formation and the substrate characteristics. Colonies of the monoplanulate mode. when developed on soft substrates, exhibit a small and spherical morphology with isolated distribution patterns, while those developed on hard substrates are tabular and variable in size. depending on the availability of substrate. In colonies of the polyplanulate mode, on the other hand. the size of the colony is largely dependent on The frequency and timing of allograft fusion. They are characteristically found on soft substrates. often as dense mono specific thickets. The mode of colony formation in halysitids is probably species-specific and results in the adaptation to substrates. * Colony development, halysitid corals, Anticosti Island. Gotland .     

Homologies to the tomato endopolygalacturonase gene in the peach genome

Abstract. Peach endopolygalacturonase was isolated from the mesocarp tissue of soft ripe, freestone peach fruit, but was not detectable in mature pre-ripening fruit. It is a basic protein with a M_r of approximately 45000 Da, and cross-reacts with antibody to tomato endopolygalacturonase. Using a cDNA to the tomato enzyme as a probe, a fragment of peach genomic DNA was isolated which encoded about 50% of the peach enzyme. The nucleotide sequence of the fragment was determined and the amino acid sequence of part of the peach endopolygalacturonase peptide derived. Coding regions of the peach gene show extensive homology with related regions of the tomato gene. Introns are dissimilar. Endopolygalacturonase activity occurs in ripe 'freestone'peaches but not in the firmer 'clingstone'varieties. Hybridization studies identified a similar gene fragment in freestone, semi-freestone and clingstone peach varieties.     

Sensitive detection of mycoplasmalike organisms in field-collected and in vitro propagated plants of Brassica, Hydrangea and Chrysanthemum by polymerase chain reaction

A polymerase chain reaction (PCR) protocol, previously designed for amplification of a DNA fragment from aster yellows mycoplasmalike organism (MLO), was employed to investigate the detection of MLO DNA in field-collected and in vitro micropropagated plants. PCR with template DNA extracted from symptomatic, naturally-infected samples of Brassica, Chrysanthemum and Hydrangea, each yielded a DNA band corresponding to 1.0 Kbp. However, no DNA product was observed when either infected Ranunculus (with phyllody disease) or Gladiolus with (symptoms of ‘germs fins’) was used as source of template nucleic acid for PCR; further experiments indicated absence of target DNA in the case of Ranunculus and the presence of substances in Gladiolus which inhibited the PCR. The MLO-specific DNA was detected by PCR using less than 95 pg of total nucleic acid (equivalent to total nucleic acid from 1.9, ug tissue) in the case of field-collected Hydrangea and less than 11.4 pg of nucleic acid (equivalent to total nucleic acid from 19 ng of tissue) in the case of field-collected Brassica. The findings illustrate highly sensitive detection of MLOs in both field-grown and in vitro micropropagated infected plants.     

The Interplay Between Life History and Environmental Stochasticity: Implications for the Management of Exploited Lizard Populations

SYNOPSIS. The sustainable use of wild species by local peopleis emerging as an important conservation strategy. The premiseis the economic value of species will justify their own preservationas well as the habitats they occupy. However, the lack of naturalhistory and demographic information for the majority of speciesbeing exploited or with potential uses presents challengingproblems for implementing sustainable use programs. Each yearin Argentina and Paraguay, an average of 1.9 million tegu lizardsof the genus Tupinambis are exploited for their skins. In spiteof the importance of tegus as a resource, their biology is poorlyknown and their populations have never been managed. The lifehistory of Tupinambis, like that of other exploited lizards,is characterized by a relatively long life span, a large clutchsize, several years of growth before reproduction, and highmortality of hatchlings. Importantly, the mortality of young-of-the-yearand the proportion of females reproducing each year are bothprobably strongly influenced by interannual environmental variation.Whenthese parameters were randomized in life table projections tosimulate the effects of environmental stochasticity, the populationgrowth rate was highly sensitive to environmental fluctuations.Monte Carlo simulations of different harvest strategies showedthat estimates of population growth rates were overwhelminglyinfluenced by environmental variation and the number of yearsincluded in the growth rate estimate, even in the face of seeminglylarge changes in adult mortality that would result from populationmanagement. These results are both encouraging and cautionaryfor Tupinambis conservation. On the one hand these patternscan help explain how Tupinambis populations may have persistedin spite of high and variable harvest levels during many years,but conversely, stochastic effects make it difficult to evaluatethe effects of conservation measures. Size and sex can be determinedfrom harvested skins, and pilot studies suggest that analysesof the annual harvest can provide valuable information for evaluatinglong-term population trends.     

Coordinated mRNA and Protein Expression of Human LAMP-1 in Induction of Melanogenesis After UV-B Exposure and Co-Transfection of Human Tyrosinase and TRP-1 cDNAs

In order to better understand the cascade of melanogenic events in melanocytes, this report has introduced our two recent approaches for the expression of melanogenesis/or melanosome-associated genes and encoded proteins in melanocytes (melanoma cells) after repeated exposure to UV -B and after cotransfection of two human genes, i.e., tyrosinase and tyrosinase-related protein-1 (TRP-1). Repeated exposure of UV B (2.5–5.0 mJ/cm²) caused not only upregulation of tyrosinase and TRP-1 genes but also coordinated increase in the gene and protein synthesis expression of Lamp-1 (lysosome-associated membrane protein-1). When COS-7 kidney cells and amelanotic melanoma (C32 and SKMEL-24) and melanotic melanoma (G361 and SK-MEL-23) cells were exposed to cotransfection of human tyrosinase and TRP-1 cDNAs, there was also an increased expression of Lamp-1 mRNA and protein along with tyrosinase activation and new melanin synthesis. Importantly, single transfectants of human tyrosinase cDNA revealed marked cellular degeneration, whereas this degeneration was not seen in single transfectants of TRP-1 cDNA or cotransfectants of human tyrosinase and TRP-1 cDNAs, indicating that TRP-1 prevented, along with Lamp-1, programmed death of melanocytes after transfection of tyrosinase gene. The coordinated expression of TRP-1 and Lamp-1 was further confirmed by antisense oligodeoxynucleotide hybridization experiment against Lamp-1 gene, showing the decreased expression of TRP-1 as identified by three different types of anti-TRP-1 monoclonal antibodies. We propose therefore that human tyrosinase and TRP-l, when activated or expressed together, will coordinate to upregulate the mRNA expression and protein synthesis of Lamp-1. The Lamp-1 molecules will, in turn, cover the inner surface of melanosomal membrane, together with TRP-1 molecules, thus protecting the melanosomal membrane from toxic melanin intermediates generated during melanogenesis in the presence of active tyrosinase. In contrast, the expression of other lysosome-related proteins, e.g., β-galactosidase and CD63 is not stimulated in new melanogenesis.     

Subcellular Distribution of Inorganic Phosphate, and Levels of Nucleoside Triphosphate, in Mature Maize Roots at Low External Phosphate Concentrations: Measurements with 31P-NMR

Maize plants were grown in nutrient solution without phosphate,or in which inorganic phosphate (Pi) was maintained at nearlyconstant concentrations of 1 µM, 10µM or 0·5mM. In vivo ³¹P-NMR measurements showed that there was no discernibledifference in the cytoplasmic Pi content (µmol cm^–3root volume) of the mature roots of plants exposed to 1 µM,10µM or 0·5 mM external phosphate for up to 12d. However, the vacuolar Pi content of the mature roots variedabout 10-fold between these three groups. The cytoplasmic Pi content of roots receiving no external phosphatedecreased significantly after about 7 d total growth, and atabout this time the vacuolar pool of Pi became too small foraccurate measurement. The presence of 1 µM Pi in the nutrientsolution completely prevented this decline in cytoplasmic Pi,and there was some evidence that it also raised the Pi contentof the root vacuoles above the almost undetectable level foundin the totally P-starved roots. During the first 7–9 d of growth, the nucleoside triphosphatecontent of the mature roots was unaffected by the concentrationof phosphate in the nutrient solution. The results highlight the close control of cytoplasmic concentrationsof certain important phosphorus metabolites in roots growingin soil of normal agricultural fertility. Key words: Vacuole, cytoplasm, intracellular compartmentation, NTP, P-nutrition     

高产杀粉蝶菌素的链霉菌鉴定及其拮抗水稻白叶枯菌活性研究

【目的】为保证农业生产可持续性发展,研发和使用环境友好的生物农药受到全社会的高度重视。微生物代谢产物农药是我国目前应用最广的生物农药,也是未来发展绿色农药的一个重要方向。【方法】利用包含水稻白叶枯菌(Xanthomonas oryzae pv. oryzae, Xoo) PXO99A的NA培养基琼脂平板,从水稻根际土壤中筛选能抑制Xoo生长的链霉菌。通过高效液相色谱和质谱分析活性代谢产物的化学结构;采用剪叶法接种Xoo到水稻叶片后,再喷施杀粉蝶菌素溶液(0.1 g/L),2周后测定叶枯症状;采用响应面分析法优化高产杀粉蝶菌素的发酵培养基;采用PacBio SMRT测序平台+Illumina HiSeq X Ten平台开展全基因组测序。平均核苷酸一致性(average nucleotide identity,ANI)用于比较HSW2009与其他链霉菌在全基因组水平的亲缘关系。【结果】分离到一株对Xoo生长有强抑制活性的链霉菌HSW2009,其活性代谢产物为杀粉蝶菌素A1(piericidin A1,简称PIE);喷施PIE可以减轻Xoo在水稻叶片内的侵染;优化HSW2009高产PIE的发...