高州油茶人工林碳储量分布特征

【目的】探明高州油茶Camellia gauchowensi人工林碳储量及分布特征,并估算评价其固碳效应。【方法】根据样地植株径级分布特征,选取不同径级样株各2～3株,取树叶、树干、树枝、树根、果实、花芽各器官测定生物量和碳含量,并建立各器官生物量模型;在标准地内按"S"形选取8个样点,沿土壤剖面分层采集0～20、20～40、40～60和60～100 cm土层的土壤样品,测定土壤容重与碳含量,计算碳储量。【结果】高州油茶中龄林植株各器官生物量分配比例依次为树干树根树叶树枝果实花芽,各器官生物量均随地径的增大而增大。试验林分总生物量为26.902 t·hm~(-2),树体平均碳质量分数为483.45 g·kg-1。同径级各器官的碳含量不同,其中,果实平均碳含量最高。林地100 cm深土层中,土壤碳含量随着土层深度的增加呈明显递减规律,其中,0～20 cm土层碳含量最高,碳质量分数为26.550 g·kg-1。高州油茶林地总碳储量为144.538 t·hm~(-2),其中,树体碳储量为12.857 t·hm~(-2),占总碳储量的8.90%;林地土壤碳储量为131.681 t·hm~(-2),占总碳储量的91.10%。根据中国生物多样性国情报告编写组数据,碳价格为260.90元·t-1,则本试验高州油茶林的碳汇经济效益约为3.8万元·hm~(-2)。【结论】高州油茶林分碳储量高于广东省经济林平均碳储量,林地土壤碳储量高于广东省平均土壤碳储量,林分总碳储量高于珠三角森林生态系统碳储量,具有较高的生态效益。高州油茶不仅有较好的生产效益,而且具有十分广阔的固碳前景。     

茶树CsSNAT基因的克隆与表达分析

为明确茶树SNAT基因的序列特征和表达特点,在茶树转录组测序的基础上以茶树(Camellia sinensis)品种舒茶早为试验材料,通过SMART^TM RACE技术克隆茶树褪黑素合成途径中关键限速酶5-羟色胺-N-乙酰转移酶CsSNAT基因的cDNA全长序列,并分析其基因结构和表达模式。结果表明,CsSNAT基因序列全长1 014 bp,其中包含742 bp的完整开放阅读框(ORF),编码247个氨基酸,预测等电点7.64,蛋白分子量27.36 kDa。氨基酸序列比对显示,CsSNAT蛋白与其他高等植物的SNAT蛋白具有较高同源性,与葡萄 VvSNAT(CBI31163)同源性最高,为66.19%。诱导蛋白最佳条件为温度28℃,异丙基-β-D-硫代半乳糖苷(IPTG)浓度0.5 mg·L^-1,诱导时间6 h,在上清液中可获得大量分子量为66 kDa的可溶性融合蛋白。实时定量 PCR 分析表明,CsSNAT在褪黑素处理6 h后表达量最高,为对照的3倍;茶尺蠖取食6 h后,CsSNAT表达显著上调。不同激素处理结果显示,CsSNAT受脱落酸(ABA)、茉莉酸甲酯(MeJA)和水杨酸(SA)诱导表达。本研究结果为5-羟色胺-N-乙酰转移酶功能研究奠定了一定的基础。     

茶树咖啡碱合成酶CRISPR/Cas9基因组编辑载体的构建

CRISPR/Cas9技术是一门新兴的基因组定点编辑技术,具有操作简单、高效的优点,可轻松实现对目标基因的敲除、替换和定点突变等操作。该技术刚诞生,就受到了全球生命科学领域研究者的关注,不到3年的时间就已经成功应用于多种动、植物当中。然而CRISPR/Cas9技术在茶树中的应用面临载体构建问题,本文以茶树咖啡碱合成酶为例,联合采用常规PCR、Overlapping PCR和Golden Gate Cloning技术,构建了包含茶树咖啡碱合成酶双靶点的CRISPR/Cas9基因编辑载体,为CRISPR/Cas9介导的基因组编辑技术在茶树中的应用奠定了坚实基础。     

不同激素对金花茶圈枝繁殖生根的影响

分析NAA、IBA及2种激素等体积混合溶液对金花茶圈枝繁殖生根成活率的影响。结果表明:采用萘乙酸和吲哚丁酸的等体积混合激素溶液1 000~1 500 mg/L能明显提高金花茶圈枝繁殖苗的生根率,达到95%以上。该技术简化了操作程序,可节省人力,在基质方面也节约了生产成本,可直接应用于金花茶苗木大规模生产。     

油茶高接换冠枯桩现象调查与研究

为了探寻影响油茶高接换冠后枯桩的相关因素,为今后油茶高接换冠技术改良提供理论依据,调查研究了嫁接方法、接穗品种、砧木粗度、留截高度和嫁接方位等因素对油茶高接换冠后枯桩现象的影响。结果表明:5种因素对油茶枯桩程度影响极显著。其中,采用插皮腹接、砧木直径2~6 cm枯桩程度最低;采用‘华硕’和‘湘林XLJ14’其枯桩程度显著低于其它品种;留截高度越低枯桩程度越低;嫁接方位在外侧枯桩程度最低。偏相关分析结果表明,留截高度对油茶枯桩程度的影响最大;其次是嫁接方法、砧木直径和嫁接品种;而嫁接方位对油茶枯桩程度的影响最小。     

叶用辣木新品种‘中林2号’

 ‘中林2号’是从缅甸引种的辣木中选育出的新品种。腋芽、附芽和潜伏芽排列密集，成枝率高。截干后的植株再生能力强。复叶长33.5 cm，宽21.7 cm。盛产期年均鲜叶产量可达30 000 kg · hm^-2。叶粉蛋白质含量可达293 g · kg^-1。适于营建叶用良种园。     

Changes in peroxidase activity and lignin content of cultured tea cells in response to excess manganese

Abstract

The present study was undertaken to identify the effects of manganese (Mn) on the activity of peroxidase (PO) and the amount of ascorbic acid (AsA) and lignin, as well as the cell viability of suspension-cultured tea cells (Camellia sinensis L. cv. Yabukita). Cells were grown in B5 medium (containing 0.06 mmol L^?1 Mn) and cultured for 24 h in medium with a Mn concentration of 0.9 mmol L^?1 as an excess treatment. No significant difference was observed between cellular growth and the viability of the cultured tea cells after treatment with excess Mn compared with cells grown under control conditions, although the content of Mn in cells in the excess Mn treatment was 12-fold higher than that of the control cells. The amount of total AsA was also not affected by the Mn treatment. The activity of ionically wall-bound peroxidase (IPO) increased in the presence of excess Mn, unlike the content of lignin. Conversely, the activities of soluble PO and covalently wall-bound PO decreased with excess Mn. These findings suggested that IPO might contribute to Mn tolerance in tea cells. However, its role in the mechanism(s) of Mn tolerance has not been elucidated.     

白菜型油菜DFR基因的克隆与序列分析

By using RACE (rapid amplification ofcDNA ends) based homologous cloning strategy, we have successfully isolated the genomic and full-length cDNA sequences of a gene encoding typical DFR (dihydroflavonol-4-reductase) from black-seeded Brassica campestris L. var. oleifera DC.. The gene, designated BcDFR here, is 1 722bp in length and harbors 5 introns with typical splice sites of plant DFR genes. BcDFR cDNA is 1311bp in length with a 1 158bp ORF as well as a 25bp 5‘ UTR and a 128bp 3‘ UTR. The encoded BcDFR protein is 385 aa with a calculated Mw of 42.85kD and a pI value of 5.55. The nucleotide and amino acid sequences of this gene share extensive homologies to plant DFR genes of wide origins especially high similarities to Cruciferous DFR genes. Sequence analyses such as phylogenetic analysis, conserved domain search and substrate specificity region detection all indicated that BcDFR gene is a quite potentially biofunctional gene. Its cloning enables us to further dissect the possible relatedness between DFR gene and Brassica seed coat color traits and to create transgenic novel yellow-seeded rapeseed germplasm through antisense- or RNAi-suppression of DFR gene expression in black-seeded elite cultivars.     

不同激素对碧云茶树丛生芽增殖培养的影响实验

为了获得碧云茶树的组培技术,加快其优良品种繁殖速度,2010～2011年进行了不同浓度的细胞分裂素6-BA和生长素NAA对碧云茶树丛生芽增殖培养的影响。结果表明,以MS为基本培养基,当6-BA为2.0 mg/L,NAA为0.2 mg/L时,对碧云茶树芽的诱导和增殖最有利,增殖率可达2.84;其中NAA差异不显著,6-BA差异显著。     

AM真菌对油茶生长和抗旱性的影响

AM（Arbuscular mycorrhiza）真菌能够促进植物生长，提高植物的抗逆性。AM真菌对油茶生长和抗旱性的影响的研究表明：接种AM真菌促进了油茶生长，改善了油茶叶片水分状况，增强了叶片细胞质膜的稳定性，使可溶性糖含量增加。