河流搬运花粉的初步研究

为进一步认识华北平原不同沉积相的孢粉组合特征和冲积物孢粉的沉积机制,作者对华北平原两条较大的河流——黄河、滦河的表层水样进行了孢粉分析１　材料和方法１．１　取样工具为容积１０００ｍＬ的塑料桶。将河流表层水灌入桶内,加盖封好带回实验室。将水样倒入２０００ｍＬ烧杯内,滴入现代石松孢子１３０００粒,以进行孢粉浓度计算［１］,同时加入少许冰醋酸,加速沉淀。将沉淀物置于离心杯中,用２．１和１．９的重液进行浮选,最后制成活动片在显微镜下进行鉴定、统计。１．２　冲积物的采集用一个圆筒形的铲,拴上绳子抛入河底,…     

有机壁藻类微体化石分析中的几个问题

藻类分析是藻类研究的前提。本文主要讨论以下几个问题：微体化石藻类分析与孢粉分析的异同、分析处理的时间掌握、超声波清洗机和筛选作用,重液浮选及药品用量等。     

周口店鬣狗(Hyaena)粪化石的孢粉分析

<正> 著名的北京猿人(Homo erectus pekingensis)化石产地周口店第一地点洞穴堆积物10—11层中,产有丰富的鬣狗(Hyaena)粪化石。通过对粪化石(编号 L:30:40,采于1949年;和 L:31:50采于1951年)进行盐酸浸泡,重液浮选,从而找到了148粒孢粉。经过鉴定、包括种属:     

云南泸沽湖及周边山地表层孢粉与植被关系研究

本文对云南泸沽湖周边山地不同植被类型下采集的32个表土样品和36个泸沽湖湖泊表层样品进行了孢粉分析,探讨了不同植被类型内的表土孢粉散布特征,对比分析了山地表土与湖泊表层孢粉分布特征的差异。结果表明,不同山地植被类型的孢粉组合具有不同的代表性成分与变化特征,能够较好地反映相应的植被类型。湖泊表层孢粉研究表明,湖泊内不同位置的孢粉组合差异较小,说明湖泊表层孢粉反映的是区域植被的平均分布状况。对比分析泸沽湖周边山地表土与湖泊表层样品的孢粉组合,两者存在一定的差异,表现为:湖泊表层的孢粉组合中乔木花粉(主要是松属)平均含量比表土高,但波动范围要小;草本花粉平均含量要低,且波动范围也小。这可能是由于乔木植物植株较高,而且有些乔木植物花粉具有气囊,更易借助风力将花粉传播到比较远的湖泊中的原因造成的。冷杉和铁杉花粉在所有样品中含量都相对较低,分别不高于6.5%和3.6%;桦属、桤木属、常绿栎类花粉的最高值出现在有这些母体植物生长的表土样品中,在其他样品中则明显较低。在表土孢粉样品中经常可以见到冷杉的气孔器,但在湖泊表层样品中却没有见到,说明气孔器不易到达湖泊中。该研究是对中国西南表层孢粉研究的有益补充,同时为泸沽湖新生代特别是第四纪化石孢粉解释提供了可靠的参考和依据。     

干旱区石羊河流域河水孢粉组合特征

石羊河流域初春和仲夏两季不同地点 ,洪水期、平水期 30个河水样孢粉分析显示 ,没有人类影响的情况下 ,河水样孢粉组合是由河流上游径流区的植物孢粉和采样点附近植被孢粉组成的 ,前者在孢粉组合中至少占30 %～ 6 0 %。河水搬运孢粉的能力非常强 ,可长距离、大量地搬运孢粉。孢粉组合中河水贡献孢粉的含量较高 ,如 :云杉属 (PiceaDietr.)花粉河水的贡献率在中下游可达 16 .5 %和 7.7%。采样时间、地点影响河水的孢粉组合和浓度 ,洪水期是孢粉搬运的主要时期。河水经过水库后 ,其中孢粉绝大多数沉积在水库中。     

干旱区石羊河流域河水孢粉组合特征

石羊河流域初春和仲夏两季不同地点,洪水期、平水期30个河水样孢粉分析显示, 没有人类影响的情况下,河水样孢粉组合是由河流上游径流区的植物孢粉和采样点附近植被孢粉组成的,前者在孢粉组合中至少占30%～60%.河水搬运孢粉的能力非常强,可长距离、大量地搬运孢粉.孢粉组合中河水贡献孢粉的含量较高,如:云杉属(Picea Dietr.)花粉河水的贡献率在中下游可达16.5%和7.7%.采样时间、地点影响河水的孢粉组合和浓度,洪水期是孢粉搬运的主要时期.河水经过水库后,其中孢粉绝大多数沉积在水库中.     

云南亚热带南部表土孢粉组合与植被间的定量关系

以云南亚热带南部沿温度带分布的35个表土孢粉样品和7个植被样方调查为基础,计算了代表性孢粉类型的百分比和孢粉浓度,及常见孢粉的R值,并分析了影响R值的因素;同时,研究了植物群落和样方内孢粉组合的相似度。结果表明,云南亚热带南部表土样品孢粉产量丰富,蕨类植物孢子产量较高,具有典型的亚热带特征,且山地垂直分异显著;木本、草本植物花粉基本代表了区域内乔木和草本植物特征,蕨类植物孢子则具有超代表性;表土孢粉组合与植物群落间的相似系数绝大部分都在70％以上,表土孢粉组合基本上可以反映植物群落面貌;表明云南亚热带地区表土孢粉与现代植被之间具有较好的对应关系,这对在该区利用化石孢粉资料定量恢复古植被和重建古气候有重要意义。     

南京低山丘陵区表土及捕捉器花粉谱的差异探究

选取南京丘陵地区29处样点,分别搜集表土及捕捉器样品,开展两种采样方式下孢粉组合与植被关系研究。结果表明,南京低山丘陵地区花粉类型以松属、栎属、枫杨属、榆属、蔷薇科、菊科、禾本科为主,表土花粉组合较好地反映了现代植被特征。主成分分析可以大致区分人工草坪区、农田区以及森林区的样品。农田区表土花粉浓度最低,每克仅为4 964粒,农田的翻耕以及微生物环境是造成其花粉浓度低的重要原因;森林区花粉浓度(每克29 176粒)及花粉通量(49 358粒/平方厘米/年)均很高。人类活动的增强可能会造成孢粉浓度的下降。在探究本地区历史时期人类活动时,可运用孢粉浓度以及与农作物相关的孢粉类型的变化来分析。所有捕捉器样品的乔木花粉百分比均低于其对应的表土样品,其中以松属尤为明显。     

神农架大九湖12．5kaBP以来的孢粉与植被序列

在神农架海拔1700m的大九湖盆地12．5kaBP以来晚第四纪中,高密度地取得3个钻孔的孢粉样品,建立起晚第四纪高分辨率孢粉组合序列,划分出15个综合孢粉带,代表15个不同时代类型的古植物群落,根据植被演替及其所反映的气候变化过程,本文还讨论了第四纪植被与气候阶段的划分问题,认为高分辨率孢粉－植被序列的建立与研究可以反映多种时间尺度,特别是小尺度的环境变化与事件,从而更详细地揭示其演变轨迹与特点。     

立地尺度植被重建模型MARCO POLO的应用分析——以柴达木盆地为例

立地尺度植被定量重建是对利用孢粉进行古气候和古环境研究的一个重要补充。一些新的定量重建模型相继提出,但其适用性仍需进一步验证。以柴达木盆地24个样方表土孢粉及4个湖泊表层沉积孢粉为研究对象,利用MARCO POLO模型重建立地尺度植被盖度并分析该模型的适用性。研究结果表明,由于地形开阔且风力较大,干旱区的大型湖泊沉积物中往往容易富集超代表性孢粉,使这些孢粉的区域信号增强,从而降低孢粉类型筛选的正确率。若湖泊与样方间的距离较近,湖泊表层孢粉能够更好地反映样方所在区域的孢粉特征,则有利于提高孢粉类型筛选的正确率。MARCO POLO模型中的孢粉代表性R值是将孢粉含量转化为植被盖度的关键参数。由于受到孢粉自身生产、传播、保存以及外部环境等多方面因素的影响,不同样方的R值可能差异很大。因此在运行该模型前需保证R值能够准确反映立地尺度中各孢粉类型与植被盖度的关系。仅在以柴达木盆地为代表的干旱区对该模型进行检验,今后仍需要在不同植被或气候区进行深入研究以全面了解该模型的适用条件。     

应用花粉分析预报板栗产量的研究

 1994～1996年河北省迁安县蔡园乡大气中板栗花粉散布特征研究表明,不同年份板栗花期有早有晚,大气中的花粉浓度变化悬殊;大气中板栗花粉浓度受花期气温和盛花末期前降水影响较大,受日照影响较小;盛花期花粉浓度与板栗产量的相关系数为0.998～0.999;根据两年相关关系建立的预报模式对第三年产量进行了预报,预报期比收获期提前2个月,预报结果最大误差5.7％,最小误差1.13％;多数误差均低于4％;运用花粉分析预报板栗和其它果品及农作物产量是一种投入少、预报期早、预报精度高的预测方法。     

多种被子植物花粉生殖细胞大量分离技术的比较研究

从11种植物的成熟花粉粒中分离出大量生活的生殖细胞。比较了四种分离方法(一步渗透压冲击法、二步渗透压冲击法、低酶法和花粉原生质体释放法)在不同植物中的效果。归纳出三类植物适于采用三种分离方法。研究了影响分离效果的若干重要因素。对5种植物的分离生殖细胞进行了纯化。经鉴定,纯化的细胞群体中80%以上的细胞是生活的。     

Airborne pollen calendar of the central region of Bursa (Turkey)

This report describes qualitatively and quantitatively the level of pollen in the atmosphere in the central region of Bursa. Turkey. In 1991, the season of maximum pollen concentration was from April to June, with a prevalence of arboreal pollen during the initial months, and of pollen from herbaceous plants in the latter months. During the year of research, 24 taxa of arboreal and 12 taxa of herbaceous pollen grains were collected and identified. In the region investigatedPinus, Cupressaceae/Taxaceae,Abies nordmanniana, Platanus orientalis, Olea europaea, Gramineae, Urticaceae, Chenopodiaceae/Amaranthaceae,Artemisia and Compositae were responsible for the greatest amounts of pollen. Some important allergenic pollens such asOlea europaea, Gramineae and Urticaceae were also found in high concentration. In this study, a pollen calendar for the region is presented.     

Isolation and Early in Vitro Development of Young Pollen Protoplasts in Nicotiana tabacum

For isolating young pollen protoplasts in Nicotiana tabacum. The authors had established two efficient enzymatic methods via anther preculture or pollen starvation pretreatment. Procedure of the first method included the following steps: 1. Cold pretreatment of flower buds with pollen at late unicellular to early bicellular stage; 2. Anther floating culture for pollen shedding into the culture medium followed by dehiscence of exine; 3. Enzymatic maceration of exine-dehisced pollen resulting in degradation of intine and release of pollen protoplasts in large quantity. Procedure of the second method involved the following steps: 1. Culture of pollen at middle bicellular in Kyo and Harada' B medium for starvation: 2. Enzymatic maceration of starvated pollen resulting in release of pollen protoplasts and subprotoplasts. Factors affecting the results of both methods as well as early in vitro developmental events of young pollen protoplasts were studied. The protoplasts could be induced either to trigger the first sporophytic division or to continue the gametophytic pathway leading germinatation of pollen tubes !ndicating their potentiality of inducing both sporophytic and gametophytic development of pathway. In rare instance a quite interesting phenomenon was observed that a pollen protoplast first divided into two daughter cells and one of which then germinated a pollen tube. It may insinuate that such pollen protoplasts initially induced a sporophytic pathway could reverse induce a gametophytic pathway.     

钙和硼对蓝猪耳花粉萌发及花粉管生长的影响

研究了钙(Ca^2 )和硼(H3BO3)对蓝猪耳花粉萌发和花粉管生长的影响。结果表明：(1)在一定范围内Ca^2 几乎不影响花粉萌发频率,而主要影响花粉萌发速度和花粉管生长速度;低Ca^2 不利于花粉管生长,而高Ca^2 抑制花粉萌发速度和花粉管生长;在稍高于最适Ca^2 浓度的条件下,花粉管生长早期呈现波浪形。(2)硼明显影响花粉萌发频率及花粉管形态;花粉管生长必需硼,但不同浓度的硼对花粉管生长速度影响不明显;在高浓度硼条件下,较长时间内花粉管均呈现出波浪形。(3)Cooled-CCD动态跟踪观察进一步证实Ca^2 影响花粉管生长速度,而硼则不明显。     

Isolation of Pollen Protoplasts in Nicotiana tabacum

A new method for isolation of quantities of mature pollen protoplasts in Nicotiana tabacum has been established. The first step was to germinate mature pollen in Brewbaker and Kwack medium containing 20% sucrose. When most of the pollen grains had just germinated short pollen tubes, they were transferred to an enzymatic solution for the second step. The enzymatic solution contained 1% pectinase, 1% cellulase, 0.5% potassium dextran sulfate, 1 mol/L mannitol, 0.4 mol/L sorbitol in Dx medium with or without 15% Ficoll. The enzymes firstly degraded the pollen tube wall and then the intine. As a result, intact pollen protoplasts were released with the isolation rate up to 50%-70%. Factors affecting pollen protoplast isolation during the germination and maceration of pollen grains were studied. The suceees depended on two key points:pollen germination duration and osmotieum concentration. The optimal germination duration was 30 rain at 30℃. When it was too long, long pollen tubes formed and subsequently, large number of subprotoplasts instead of whole protoplasts were yielded, as the case reported by previous investigators. The optimal concentration of mannitol and sorbitol in enzyme solution was as high as 1.4 mol/L in total. Lowering of the osmoticum concentration resulted in decrease of percentage of pollen protoplasts.     

大血藤科花粉形态及外壁超微结构的研究

对大血藤科及木通科的八月瓜属ＨｏｌｂｏｅｌｌｉａＷａｌｌ．和木通属ＡｋｅｂｉａＤｅｃｎｅ花粉进行了光镜及电子显微镜的观察研究。研究结果表明,其花粉形态具有较为明显的相似性,如花粉均为３沟,外壁表面具穴状纹饰,甚至大小也很近似。但从其外壁结构看,大血藤花粉的外壁内层为结均一的致密层组成     

Pollen Cryopreservation and Pollen Protoplast Isolation in Brassica carnpestris var.purpurea

The authors have investigated the factors affecting pollen cryopreservation in Brassica campestris var. purpurea, such as pollen development stages cryoprotectant and the process of freezing. A suitable procedure was established as follows :Pollen grains suspended in B5 medium containing 10X DMSO and 1SM sucrose were frozen by a three- –1℃/min – 1 ℃/min step method(0℃———→–10 ℃ ,standing for 15 min———→–40 ℃ , standing for 1 hr→liquid nitrogen)and later thawed in 40℃ water bath. During a period of 60, 90 days′preservation, the relative survival percentage of mature (at the day of anthesis)and nearly mature(2 days before anthesis, trinucleate stage)pollens maintained at ca. 91% that of young pollens(7-8 days before anthesis, late uninucleate stage to early binucleate stage)slightly declined from the original 91.6% to 84. 3%. Culture. experiment showed that the cryopreserved young pollen could be induced to cell division just as well as the fresh pollen. The method of isolating protoplasts from fresh mature pollen developed previously was improved and simplified. As a result, protoplasts were isolated more conveniently from mature pollen and young pollen for the first time. The protoplasts from cryopreserved mature and young pollen could be obtained as well with an isolation rate of 77.4% and 35.9% respectively. However, for isolation of protoplasts from preserved young pollen, an incubation in NLN medium at 35℃ after thawing was necessary.     

In vitro maturation and germination of <Emphasis Type="Italic">Orychophragmus violaceus</Emphasis> microspores

Microspores cultured in vitro can be regarded as a system to study gene regulation, cell fate determination and cell differentiation during pollen development as well as an alternative method of genetic transformation in plants. In our study, pollen development and viability in Orychophragmus violaceus in vivo were determined and then pollen from the late unicellular stage was cultured in vitro. MS liquid medium + White vitamins + 2% (V/V) coconut milk + 0.5 M maltose, pH = 7.0 was the most appropriate for in vitro culture of Orychophragmus violaceus microspores. With this medium, the rates of in maturation and germination were 19.3% and 4.7%, respectively. Liquid medium with 0.6 M maltose + 1.6 mM boric acid + 2.9 mM Ca(NO₃)₂ + 29.6 μM vitamin B1, pH = 7.0 was optimal for germination of pollen matured in vivo. The rate of germination was 70.7%. Pollen matured in vitro cultured in similar medium exhibited a rate of germination of 62.7%. Hence, the experimental study showed that in vitro maturation of microspores is feasible and this experimental system can be applied to further theoretical and practical research.     

黄土孢粉分析方法的研究

根据黄土的化学成分等特点,采取相应的化学及物理相结合的处理方法,把孢粉离析出来。在黄土最为发育的陕西、甘肃７ 个黄土剖面计９０ 多个样品中均获得丰富的孢粉,观察１—３ 张玻片,孢粉总数可达２０４—５９４ 粒以上,２５０ ｇ 的土样可获得３．９—５５．１ 万粒孢粉