长白山泥炭湿地主要植物植硅体形态特征研究

对长白山地区常见的泥炭地25个属31个种植物进行了植硅体形态鉴定统计,共发现植硅体类型15种,它们分别是硅化气孔、棒型、扇型、板型、硅质突起、尖型、导管型、帽型、齿型、哑铃型、鞍型、多边帽型、毛发型等。除禾本科和莎草科、菊科部分植物植硅体含量高外,木贼科、堇菜科、茜草科、蓼科等部分植物植硅体的含量也较高。禾本科植物的短细胞植硅体对植物分类有意义,但可能因采样环境和种类差异等原因,长白山泥炭湿地禾本科植物的植硅体在形态和数量上都与其他区域同类研究结果有所差异,如禾本科早熟禾亚科的菵草中新发现了含量丰富的枕木型植硅体,黍亚科的荩草和水稗中还发现少量帽型植硅体; 另外菊科兴安一枝黄花和齿苞风毛菊含有大量的特殊的尖形植硅体。硅化气孔宽度大小可指示环境湿度状况,对硅化气孔的数量和大小的深入研究将对古环境和古CO₂浓度的恢复有一定帮助。长白山泥炭湿地植物的植硅体与植物的分类关系密切,湿地植物植硅体中硅质突起、棒型、哑铃型和尖型植硅体特征组合代表湿冷组合,本研究中的5块泥炭湿地植硅体的组合特征受纬度变化影响不明显。     

长白山区湿地表土植硅体特征及其环境意义*

湿地在全球环境变化中扮演着十分重要的角色,湿地表土中的植硅体分析是恢复第四纪古环境的重要途径。文中选取长白山区的桦南到哈尼一线的6处湿地表土,并采用PCA和CA分析植硅体组合的环境指示意义,结果显示：温度因子是造成长白山不同湿地表土植硅体组合差异的第1环境因子,且植硅体的种类和含量与采样点上覆植被、湿度与海拔等环境条件都存在相关性。结合方差分析和植硅体大小变化趋势分析曲线可以看出,不同表土中符合方差分析条件的植硅体类型的大小随着温度的升高而增大。总体来看,长白山区6处湿地中,植硅体类型基本相同,但温暖指数和植硅体的大小差异较显著,说明植硅体大小及其组合对温度都有较敏感的响应。     

碳酸盐岩红土植硅体记录的指示意义

选取广西桂林市雁山碳酸盐岩红土剖面,对红土中的植硅体类型、分布及含量进行了定量分析。发现:(1)表土植硅体形态多样、含量丰富,含量从剖面表层向下迅速减少,20cm及其以下植硅体含量极少或没有;(2)除了0~0.1m内有植硅体富集外,其他深度再也没有发现新的植硅体富集层;(3)受淋滤和生物扰动作用影响,植硅体可能出现向下10~20cm的运移,但运移对其形态和大小没有明显的选择性,植硅体形态组合受运移影响不大,能够很好地反映上覆植被的组成和所处地区的气候总体特征;(4)研究区植硅体富集于红土表层,且为剖面中的唯一富集层,是红土形成过程植硅体运移的反映,支持了红土的碳酸盐岩风化成因;(5)植硅体运移选择性不明显的特点,为利用碳酸盐岩红土植硅体客观分析和重建古环境提供了基础和可能。      

长白山北坡垂直植被带表土植硅体组合研究

长白山垂直分布的植被是欧亚大陆从温带到寒带植被水平地带性的缩影。对其北坡不同海拔高度植被带土壤中的植硅体进行初次研究,结果发现,该山北坡海拔700m到2630m的土壤中发育了形态和数量丰富的植硅体。不同植被带植硅体组合的含量各不相同,主要特征表现为随海拔升高示冷型的植硅体含量整体呈上升趋势,而示暖型的植硅体含量整体呈下降趋势。温泉附近土壤中的植硅体则表现出明显的与其上下相邻地点不同的特点。它对中国东北第四纪沉积物中植硅体组合的研究及第四纪古植被和古环境的重建可提供重要的基础性资料。     

植硅体形态测量学研究与应用概述

植硅体形态测量学是植硅体研究的重要方向之一,随着学科交叉研究的深入,植硅体形态测量学在植物分类与生态学、环境考古学、全球变化与生态响应等领域得到快速发展。综合已有研究成果表明,长鞍型植硅体形态测量学在日本、中国的竹亚科属一级竹类生态学具有独特的指示作用,而扇型和长鞍型形态测量学在中国西南西双版纳竹亚科木本竹子属一级分类中具有重要的参考价值;稻亚科扇型形态测量学可以有效区分籼稻与粳稻,且扇型鱼鳞状纹饰与颖壳双峰植硅体形态测量学结合可以准确判别亚洲栽培稻与普通野生稻;黍亚科树状表皮长细胞形态测量学被成功运用到区分中国西北黍和粟及其亲缘物种的关系,葫芦科南瓜属刻面球型植硅体形态测量学揭示了野生种、半驯化种和驯化种之间植硅体形态大小及其关系,证实南美洲低地地区早全新世出现的南瓜驯化历史;中国东北不同环境条件下的禾本科羊草、芦苇植硅体形态测量学研究反映了陆生植物对全球变化的生理生态响应,为研究陆地生态系统对全球变化的响应及古环境重建提供了重要参考。     

植硅体稳定同位素生物地球化学研究进展

植硅体形态鉴定与组合分析广泛应用于古环境重建和农作物起源分析等.鉴于植硅体的抗腐蚀、抗降解,易保存,锢囚的碳不易污染,且保存了植物的原始信息等特性,其有机地球化学研究日益被重视.植硅体稳定同位素分析表明植硅体是植物通过吸收单硅酸,以蒸腾作用为主要动力,在植物的不同部位发生同位素分馏淀积形成,其稳定同位素组成具有丰富的植物生理和环境信息.植物不同部位植硅体稳定同位素组成具有差异,其含量和硅、氧同位素值沿蒸腾流通常有增加的趋势.沉积物植硅体碳同位素分析不仅可以用于恢复草本的C3、C4植物生物量的比例,并且有可能重建古大气的碳同位素构成,是三者中最具有潜力的考古学、古环境研究的指标.植硅体有机化学组成分析,特别是类脂物分析,有利于认识植硅体碳同位素值相对于总有机碳偏负,C3、C4草本植硅体同位素差值范围缩小的原因.     

植硅体化学组成研究进展

现代植物植硅体化学组成研究有利于揭示植硅体的化学组成与细胞形态、植物种类及植物生长环境之间的关系,认识植硅体形成机制、植物分类及生态意义。植硅体化学组成测试方法多种多样,主要涉及植硅体化学元素组成及Si、O和C元素同位素组成测定,研究表明植硅体主要含二氧化硅和水,封闭有少量的有机成分及多种矿质元素。在植硅体封闭有机成分存在形式,部分元素的形成、迁移等循环机理,稳定碳同位素组成、分布及其生态指示意义以及^14C测年研究等方面取得一定认识。植物种类、组织部位、细胞微环境以及植物生长的环境因子能够影响植硅体的化学组成。植硅体化学组成研究对植硅体形成机制及碳、硅等元素循环具有重要意义,植硅体部分化学元素、植硅体稳定同位素组成及^14C测年具有较好的古环境及考古研究潜力。现代植物植硅体化学组成及其与环境因子的关系,以及植硅体电子探针微区研究有待于进一步深入开展。     

增温、施氮、CO2浓度升高对羊草(C3)、芦苇(C4)植硅体组合的影响

研究未来全球变暖和氮沉降下C3、C4植物植硅体的变化规律,对松嫩草原优势群落演替方向的预判、古植被及古气候的重建和全球环境变化的预测等工作具有重要意义.本文选取松嫩草原的优势物种羊草(Leymus chinensis,C3)和芦苇(Phragmites communis,C4),对其进行模拟增温、施氮、CO2浓度升高处理,研究叶片部位植硅体的组合规律及形态变化特征,试图寻找在改变某一单一环境要素条件下,C3、C4植物所含各类型植硅体百分含量及形态的变化规律,以探究C3、C4植物植硅体对不同环境因素响应的异同.结果显示:CO2浓度升高、增温对羊草植硅体发育具有促进作用,对芦苇植硅体发育起抑制作用;氮素过高对羊草和芦苇植硅体的发育都不利,但增温能减轻施氮对羊草植硅体的负面效应.棒型、板型、方型、块状、蜂窝状植硅体对模拟增温、施氮、CO2浓度升高反应敏感,可作为指示环境变化的新指标.     

东北地区泥炭表层沉积中植硅体分布特征

表土沉积物中的植硅体分析是了解第四纪沉积物中植硅体组成的重要途径,也是重建第四纪古环境的基础。对东北地区跨越3个气候带、6个地区的41处泥炭地表土中的植硅体进行提取,鉴定出东北泥炭表土中主要发育哑铃型、扇型、鞍型、方型、长方型、梯型、尖型、帽型、齿型、棒型和其它等11种植硅体类型。分析显示,它们的分布与纬度、地形和温热条件具有明显关系,即哑铃型、鞍型、扇型、方型、长方型和梯型植硅体随纬度和海拔较高而含量较小,其余类型反之;较高温度条件对应扇型、哑铃型植硅体含量较高,较高湿度对应扇型植硅体含量较高。     

植硅体圈闭碳地球化学研究进展

植硅体是一种地球化学稳定性非常高的植源性非晶质二氧化硅颗粒物,在其形成过程中会圈闭一定量的有机碳。目前,植硅体圈闭碳(简称植硅体碳)被认为是一种稳定的碳汇机制,对调节全球气候变化具有重要意义,同时,植硅体碳同位素的研究对于古环境、古气候重建等研究领域具有重要的价值,因此,植硅体圈闭碳的地球化学研究受到许多学者的关注。基于国内外学者对植硅体、植硅体圈闭碳及其相关领域的研究成果,综述了植硅体的形成过程、化学元素组成、地球化学稳定性、植硅体碳汇以及植硅体碳同位素在古环境研究中的应用5个方面的研究进展,同时总结了当前植硅体及其圈闭碳在地球化学过程研究中所面临的主要问题,对于未来继续开展植硅体地球化学研究工作具有重要意义。     

Simultaneous thin section and phytolith observations of finely stratified deposits from Neolithic Çatalhöyük,Turkey: implications for paleoeconomy and Early Holocene paleoenvironment

Simultaneous thin section and phytolith observations of finely stratified anthropogenic deposits from the Neolithic settlement of Çatalhöyük, Turkey, dated between 7400 and 6000 BC provide evidence for both the depositional context and phytolith assemblage of these deposits. Although extracted phytoliths provide a general picture of vegetation that supports existing evidence of a local wet marshland environment, comparisons with observations of phytoliths in situ indicate a diverse range of microcontexts, as well as depositional and post‐depositional processes that influence phytolith size. This has implications for studies that use conjoined phytolith size as a proxy for water availability and early agricultural practices. Observations indicate a significant background noise of phytoliths and micro‐charcoal in the deposits, linked to the frequent use of fire, which has implications for interpreting assemblages where phytolith counts are low, such as from floors of buildings. This study confirms the usefulness of phytoliths in providing information on human plant use and environment where the taphonomy of the deposits is clear, and provides new evidence for wet farming of at least some of the wheat found at the site. It also suggests there needs to be greater consideration of phytolith taphonomy, which can be provided to an extent by combining phytolith analysis with thin section micromorphology. Copyright © 2011 John Wiley & Sons, Ltd.     

Potential of opal phytoliths for use in paleoecological reconstruction

Opal phytoliths, inorganic biogenetic plant particles of microscopic size, were investigated to determine the level at which their varied morphology is taxonomically significant. Extraction methods for the isolation of these particles from living plants and from soils were developed to provide maximum preservation of morphological features while remaining simple, rapid, and inexpensive. Extracts were made and microscopically viewed from 30 live specimens, of which 16 were systematically typed in order to develop taxonomic guidelines for their identification in soils. Clear taxonomic differentiation was noted between and within major plant groups with considerable indication that more detailed investigation will yield finer subdivisions. Since opal phytoliths are reported to be a particularly durable fossil found in deposits as far back as Tertiary Age, it appears that opal phytolith analysis can provide paleobotanical information comparable to palynological data in many areas where pollen is absent. When used in conjunction with pollen where present, they should serve to confirm pollen data as well as provide additional botanical data not available in pollen studies.     

Phytolith reference study for identifying vegetation changes in the forest−grassland region of northeast China

To provide a basis for tracing changes in vegetation and tree cover density, we studied the phytoliths of 129 common temperate plant species, and extracted the phytoliths from 75 surface soil samples from sites in grassland, forest−grassland ecotone and forest habitats in northeast China. From the analysis of shapes and morphological parameters of the plant samples, we developed a reference data set of herbaceous and woody phytoliths, and subsequently identified 21 herbaceous and 13 woody phytolith types in the surface soil samples. To test the reliability of soil phytolith analysis for distinguishing forest, grassland and the forest−grassland ecotone, we used principal components analysis (PCA) and discriminant analysis (DA) to summarize the soil phytolith assemblage characteristics of the different ecosystems. The results show that the grassland and forest samples are characterized by abundant herbaceous and woody phytoliths, respectively; and that forest−grassland ecotone habitats are characterized by low abundances of blocky polyhedral, multifaceted epidermal and sclereid phytoliths. In general, the surface soil phytolith assemblages can reliably differentiate samples from forest, grassland and the forest−grassland ecotone, with up to 92% of the samples classified correctly. We also tested the reliability of phytolith indices (W/G (1), W/G (2), W/G (3)) for discriminating different vegetation types in our study area, and found that W/G (2) was the most reliable index and corresponded well with the species inventory data. The W/G values for grassland ranged from 0 to 0.3, from 0.3 to 0.6 for the forest−grassland ecotone, and exceeded 0.6 for forest. We conclude that our study provides reliable analogues for phytolith assemblages from palaeoecological contexts, which can be used to reconstruct shifts in forest−grassland ecotones and vegetation succession in temperate areas.     

Effect of fire on phytolith coloration

Dark‐colored phytoliths are often found preserved in paleosols and archaeological sediments. Some practitioners believe these darkened phytoliths provide evidence of fire histories, while others suggest alternative reasons for their occurrence. This study examines the effect of fire on phytolith appearance and discusses the extent to which color may be used as proxy evidence for fire. The results of this study demonstrate that under oxidative conditions of openair fire, the color of phytoliths can be altered, although dark‐colored phytoliths also occur naturally in some unburned plant species. Despite some overlap observed between burned and unburned color in phytoliths, clear differences are apparent in the way this color appears optically. In particular, transparent and opalescent qualities were found to occur in nature as opposed to a dull opaque appearance of charred phytoliths. Although fire‐induced color change is probably limited to a portion of the phytolith assemblage, phytolith color remains a tool that can be confidently used to indicate the presence of fire in various sedimentary contexts. © 2006 Wiley Periodicals, Inc.     

Assessing modern arboreal phytolith sensitivity to vegetation variations in temperate forest regions

To assess the reliability of arboreal phytoliths for differentiating vegetation types in temperate forest regions, we systematically analysed arboreal leaf phytoliths from 72 arboreal plants and 49 modern soils from three forest types in northeast China. The arboreal leaf phytolith production and morphotypes were highly variable between species. The arboreal leaf phytolith assemblages could clearly distinguish between broadleaf and coniferous species, but they were much less successful in differentiating broadleaved trees into subtaxa. Coniferous leaf morphotypes were successfully used to differentiate coniferous trees into families and subtaxa, especially in the Pinaceae. Two diagnostic broadleaved and six coniferous phytolith morphotypes were recognized within the modern soil beneath forest ecosystems. These arboreal phytoliths comprised up to 10–15% of the total soil phytoliths, and were dominated by coniferous types. Arboreal phytolith concentrations and phytolith assemblages in the soils fluctuated substantially amongst the three forest types. Soil arboreal phytolith assemblages were successfully used to differentiate samples from Larix mixed forest, broadleaf forest and Pinus koraiensis mixed forest. In addition, the arboreal index quantitatively distinguished the three forest types, with B/BE values <0.4 for Larix mixed forest samples, values from 0.4 to 0.6 for broadleaf forest samples, and values from 0.6 to 0.9 for P. koraiensis mixed forest. Thus, our surface soil arboreal phytolith assemblages and arboreal index are a useful reference for differentiating forest ecotypes, and they also provide reliable analogues for arboreal phytoliths from palaeoecological contexts in temperate forest regions.