The Hekla 1947 tephra in the north of Ireland: regional distribution,concentration and geochemistry

A cryptotephra layer from the eruption of Hekla in 1947 has recently been discovered in Irish peatlands. This tephra layer represents the most recent deposition of volcanic ash in the UK prior to the eruption of Eyjafjallajökull in 2010. Here we examine the concentration and geochemistry of the Hekla 1947 tephra in 14 peat profiles from across Northern Ireland. Electron probe microanalysis of individual tephra shards (n = 91) reveals that the tephra is of dacitic–andesitic geochemistry and is highly similar to the Hekla 1510 tephra, although spheroidal carbonaceous particle profiles can be used for successful discrimination of the two layers. The highest concentrations of Hekla 1947 are found in western sites, probably reflecting the pathway of the ash fall event due to the prevailing wind direction. Comparable tephra concentrations from two cores (1 km apart) from a single bog and from nearby sites may suggest that tephra shard concentrations in peat profiles reflect ash fallout densities across a specific region, rather than site‐specific factors associated with peatlands. This paper firmly establishes Hekla 1947 as a useful chronostratigraphic marker for the twentieth century, although within a restricted zone. Copyright © 2012 John Wiley & Sons, Ltd.     

石榴石微量元素地球化学及其在沉积物源分析中的应用

石榴石是沉积物中常见的重矿物,其可来源于多种岩石,而且不同类型母岩中石榴石具有多样的地球化学组成,因此碎屑石榴石的地球化学分析在沉积物源研究中应用广泛。通过电子探针分析可以容易地获得单颗粒碎屑石榴石的主量元素地球化学组成,可借此探讨其母岩类型,但也存在一定的局限性,比如中酸性火成岩和部分变沉积岩来源的石榴石通常都具有高Fe、Mn的特征,不易于区分。本文系统地收集了不同岩石类型的石榴石微量元素数据,尝试利用微量元素地球化学的差异性对碎屑石榴石物源分析进行补充。最终得出以下结论:(1)石榴石的稀土元素(REE)组成与钇(Y)元素指标可区分中酸性火成岩和变沉积岩来源的碎屑石榴石;(2)基性岩(橄榄岩、辉石岩)及所对应的变基性岩石(榴辉岩)中石榴石的微量元素地球化学组成相近,但部分橄榄岩来源的石榴石在镨/钬(Pr_N/Ho_N)值和重稀土总量(ΣHREE含量)上与辉石岩和榴辉岩的有显著差别,这一特点可运用于以基性岩母岩为主的碎屑沉积物源研究中;(3)夕卡岩中的石榴石在主量元素地球化学组成上表现为高度一致的高Ca特征,而稀土元素组成具有两种典型的分配模式,岩浆型(指示富铁、氧化环境)与热液型(指示富铝、还原环境)。综上所述,石榴石微量元素地球化学可以有效地运用于沉积物源分析研究中,是其主量元素物源分析方法的重要补充。     

Effects of the peat acid digestion protocol on geochemically and morphologically diverse tephra deposits

Tephra shards for electron probe microanalysis are most efficiently extracted from peat using acid digestion, which removes organic material that hinders density separation methods. However, strong acids are known to alter glass chemical compositions, and several studies have examined how acid digestion affects rhyolitic volcanic glass. The focus on rhyolitic tephra in these studies leaves considerable uncertainty, as the dissolution rates of natural glasses (including tephra) are determined by the chemical composition and surface area/volume ratio, both of which vary in tephra deposits. Here, we use duplicate samples of basaltic, trachydacitic and rhyolitic tephra to examine physical and geochemical alteration following acid digestion. Scanning electron microscope imagery reveals no discernible degradation of glass surfaces, and electron probe microanalysis results from duplicate samples are statistically indistinguishable. These findings suggest the acid digestion protocol for organic peats does not significantly alter glass geochemistry regardless of shard morphologies or geochemical compositions.     

Glass geochemical compositions from widespread tephras erupted over the last 200 years from Mount St. Helens

Building reliable chronologies from lake sediments, peat and other paleoenvironmental archives can be challenging, especially for historical times where radiocarbon is unreliable. Nineteenth- and 20th-century eruptions from Mount St. Helens (MSH) provide important chronostratigraphic markers for regional paleoenvironmental studies within this time frame, but are constrained by poorly geochemically characterized tephra and/or limited published data. Here, we present glass geochemistry from the most significant eruptions from this time. This includes proximal, medial and distal deposits of the 18 May 1980 MSH eruption, layer T ( ad 1799/1800), a new tephra that we argue represents the ad 1842 eruption, and the 22 July 1980 eruption that had reported ashfall in Canada. Our results indicate that most tephras ejected during these eruptions, within a time frame of ~200 years, have distinct glass geochemical characteristics that can be used to identify distal deposits for tephrochronological studies. Layer T is on trend with analyses of the 1980 eruption but has a distinct dacitic glass population. The 1980 and ad 1842 eruptions are similar, both having rhyolitic glass compositions, but the ad 1842 event can be differentiated by a more constrained SiO₂ range in the main geochemical population, and the presence of a unique SiO₂ sub-population.     

The use of principle component analyses in characterising trace and major elemental distribution in a 55 kyr peat deposit in tropical Australia: Implications to paleoclimate

The Lynch’s Crater peat deposit in NE-Australia is a sensitive environmental archive located in the tropical Southern Hemisphere. This unique deposit illustrates that local and regional changes had a profound effect on the local Australian ecosystem over the past 55 kyr. To obtain a proxy of past climate changes, trace and major element geochemistry analyses were applied to a 13 m peat core from the crater. Principle component analysis (PCA) was used to identify the main factors that control elemental distribution in the peat and to add interpretative strength to the geochemical behavior of selected major and trace elements. For example, Sc, Al, Cu, and Pb were found to be related to increased erosion of the basin soils, and from this, several periods of significant flux from atmospheric input and/or terrigenous run-off were identified. Geochemically mobile elements during rock weathering and pedogenesis, such as Mg, Ca, and Sr helped to identify the peat ombrotrophic-minerotrophic boundary at ∼1.5 m depth and offered important information about fluxes of these nutrients to the mire and their dynamics within the deposit. Arsenic and V comparisons between the peat record (high concentrations in some peat sections) and in local basin rocks (very low concentrations), suggested the presence of a long range, atmospheric dust source early in the formation of the mire. The Lynch’s Crater peat record presents a continuous record of environmental change in tropical Australia and contributes new understanding to geochemical processes in peatlands.     

The influence of volcanism on paleoclimate in the northeast of China： Insights from Jinchuan peat, Jilin Province, China

Just like contemporary sediments, peat itself is a good repository of information about climate change, the effects of volcanic activity on climate change have been truly recorded in peat, since it is a major archive of volcanic eruption incidents. A section of sand was identified as tephra from the Jinchuan peat, Jilin Province, China, for the grains look like slag with surface bubbles and pits, characterized by high porosity, and loose structure with irregular edges and corners. According to the peat characteristics of uniform deposition, the tephra was dated at 2002–1976 a B.P. by way of linear interpolation, so the time of volcanic eruption was 15 B.C.–26 A.D. (the calibrated age). While the geochemical characteristics of tephra in this study are quite the same as those of tephra from the Jinlongdingzi volcano at Longgang and from alkaline basaltic magma, with the contents of SiO₂<55%, and the similar contents to Al₂O₃ and Fe, but the contents of Na₂O>K₂O. We speculated that the tephra in this study came from the Longgang volcano group. Compared with 11 recorded volcanic eruption events as shown on the carbon and oxygen isotope curves of the Jinchuan peat cellulose, it is obviously seen that adjacent or large-scale volcanic eruptions are precisely corresponding to the minimum temperature and humidity. It seems that these volcanic eruptions indeed affected the local climate, leading to the drop of regional temperature and humidity. As a result, there was prevailing a cold and dry climate there, and all these changes can be well recorded in peat. So the comparison of volcanic eruption events with information about climate change developed from peat, can provide strong evidence for the impact of volcanism on climate change.     

Diagenetic cycling of trace elements in the bottom sediments of the Swan River Estuary,Western Australia

Teflon strips were used in-situ in the bottom sediments at two sites in the Swan River Estuary to collect diagenetic Fe–Mn oxyhydroxides and monitor monthly changes in their morphology and trace element geochemistry. This study demonstrates that substantial concentrations of trace elements accumulate at the redox front during the formation of diagenetic Fe–Mn oxyhydroxides. It is likely that the Fe–Mn oxyhydroxides initially nucleate and grow on the Teflon strips via bacterial activity. Trace element geochemistry of the diagenetic Fe–Mn oxyhydroxides is influenced by changes in the supply of trace elements from either the bottom sediments and/or water column or changes in the physico-chemical status of bottom and porewaters. If sufficient diagenetic Fe–Mn oxyhydroxides are preserved in the upper layer(s) of the bottom sediment it is possible that diagenetic (secondary) trace element enrichment profiles may be produced which modify the historical input of natural or anthropogenic trace element sources. Alternatively, partial or complete dissolution of the diagenetic Fe–Mn oxyhydroxides in response to temporal changes in the redox status of the bottom sediment may lead to a substantial underestimate of trace element fluxes in historical bottom sediment profiles. This study highlights that considerable care must be taken when interpreting short- to long-term geochemical profiles in bottom sediments due to the possible occurrence of rapid, seasonally mediated diagenetic processes.     

高温下非传统稳定同位素分馏

过去十几年来,非传统稳定同位素地球化学在高温地质过程的研究中取得了的重大进展。多接收诱导耦合等离子质谱(MC-ICP-MS)的应用引发了稳定同位素分析方法的重大突破,使得精确测定重元素的同位素比值成为可能。本文总结了以Li、Fe和Mg同位素为代表的非传统稳定同位素在岩石地球化学研究中的应用。Li同位素目前被广泛地用于地幔地球化学、俯冲带物质再循环和变质作用的研究中,可以用来示踪岩浆的源区性质和扩散等动力学过程。不同价态的Fe在矿物熔体相之间的分配可以产生Fe同位素分馏,可以发生在地幔交代、部分熔融、分离结晶等过程中。岩浆岩的Mg同位素则大致反映其源区的特征,地幔的Mg同位素组成比较均一,这为研究低温地球化学过程中Mg同位素的分馏提供一个均一的背景。此外,Cl,Si,Cu,Ca,U等等同位素体系也具有广阔的应用前景。对同位素分馏机制的实验研究和理论模拟为理解非传统稳定同位素数据提供了必要的指导。实验表明,高温下具有不同的迁移速度的轻、重同位素可以产生显著的动力学同位素分馏,这一分馏可以在化学扩散、蒸发和凝华等过程中发生;同位素在矿物和熔体以及流体相中化学环境的差异使得不同相之间可以发生平衡分馏。而最近的硅酸盐岩浆的热扩散和热迁移实验则揭示了一种"新"的岩浆分异和同位素分馏机制。沿着温度梯度,硅酸盐岩浆可以发生显著的元素和同位素分异,湿的安山岩可以通过这种方式演变成花岗质成分,因此这个过程可能对陆壳的产生和演化有重大影响。如果温度梯度在岩浆作用中能长期存在,热扩散就可以产生稳定同位素的分馏,这一机制有别于传统的平衡和动力学同位素分馏。 而多个稳定同位素体系的正相关关系是示踪热迁移过程的最有力证据。在热扩散过程中,流体承载的物质的浓度和它的索瑞系数有关。但是这个系数对体系的很多参数非常敏感,变化极大,因此对热扩散效应的研究产生极大的困难。对热扩散实验的镁、钙和铁同位素测量表明,同位素比值的变化与体系的化学组成以及总温度无关,只和温度变化的幅度有关,这意味着即使元素的索瑞系数变化多端,某一元素的同位素之间的索瑞系数的差别总为常数。这一发现有助于简化对热扩散和索瑞系数这一基础物理问题的研究 。     

Using geochemistry as a tool for correlating proximal andesitic tephra: case studies from Mt Rainier (USA) and Mt Ruapehu (New Zealand)

Volcanic hazards assessments at andesite stratovolcanoes rely on the assessment of frequency and magnitude of past events. The identification and correlation of proximal and distal andesitic tephra, which record the explosive eruptive history, are integral to such assessments. These tephra are potentially valuable stratigraphic marker beds useful to the temporal correlation and age dating of Quaternary volcanic, volcaniclastic and epiclastic sedimentary deposits with which they are interbedded. At Mt Ruapehu (New Zealand) and Mt Rainier (USA), much of the detail of the recent volcanic record remains unresolved because of the difficulty in identifying proximal tephra. This study investigates the value of geochemical methods in discriminating andesitic tephra. Our dataset comprises petrological and geochemical analyses of tephra that span the late Quaternary eruptive record of each volcano. Our data illustrate that andesitic tephra are remarkably heterogeneous in composition. Tephra compositions fluctuate widely over short time intervals, and there are no simple or systematic temporal trends in geochemistry within either eruptive record. This complexity in tephra geochemistry limits the application of geochemical approaches to tephrostratigraphic studies, beyond a general characterisation useful to provenance assignation. Petrological and geochemical data suggest that the products of andesite systems are inherently variable and therefore intractable to discrimination by simple geochemical methods alone. Copyright © 2006 John Wiley & Sons, Ltd.     

Tephrological implications of beam size—sample‐size effects in electron microprobe analysis of glass shards

This paper concerns the potential consequences of varying procedures for the determination of tephra geochemistry by electron microprobe. Application of electron probe microanalysis to tephrostratigraphical methods has increasingly facilitated the resolution and refinement of Quaternary chronology associated with records of proxy‐environmental or proxy‐climatic change. The geographical range over which tephras are recovered has expanded significantly with the identification and analysis of crypto (or hidden) tephras in areas far removed from tephra sources. These tephras are dominated by glass shards, which, in many distal environments, may be either small in size (μm) or may be highly pumiceous with low glass:void ratios and thin (<10 μm) shard walls. We demonstrate that reducing the size of the electron beam used to analyse shard geochemistry cannot be used reliably to permit analysis of thin glass walls. This approach distorts the geochemical data, creating analytical differences that may generate inappropriate tephrogeochemical fingerprints. Additional distortion of the geochemical fingerprint in the form of hybrid analyses may be encountered in glass fragments containing micron‐sized crystalline phases such as feldspar. Copyright © 2001 John Wiley & Sons, Ltd.     

Tephra Discovered in High Resolution Peat Sediment and Its Indication to Climatic Event

Floating tephra was deposited together with ice core,snow layer,abyssal sediment,lake sediments,and other geological records.It is of great significance to interpret the impact on the climate change of volcanic eruptions from these geological records.It is the first time that volcanic glass was discovered from the peat of Jinchuan(金川)Maar,Jilin(吉林)Province,China.And it is in situ sediments from a near-source explosive eruption according to particle size analysis and identification results.The tephra were neither from Tianchi(天池)volcano eruptions,Changbai(长白)Mountain,nor from Jinlongdingzi(金龙顶子)volcano about 1 600 aBP eruption,but maybe from an unknown eruption of Longgang(龙岗)volcano group according to their geochemistry and distribution.Geochemical characters of the tephra are similar to those of Jingiongdingzi,which are poor in s.Jica,deficient in alkali,Na20 content is more than K20 content,and are similar to distribution patterns of REE and incompatible elements,which helps to speculate that they originated from the same mantle magma with rare condemnation,and from basaltic explosive eruption of Longgang volcano group.The tephra,from peat with age proved that the eruption possibly happened in 15 BC-26 AD,is one of Longgang volcano group eruption that was not recorded and is earlier than that of Jinglongdingzi about 1 600 aBP eruption.And the sedimentary time of tephra is during the period of low temperature alteration.which may be the influence of eruption toward the local climate according to the correlativity of eruption to local temperature curve of peat cellulose oxygen isotope.     

Three short essays from the soviet literature

Translations of three short essays from the Soviet literature are presented. All deal with aspects of electrogeochemistry as it applies to exploration for concealed ore. The first by V.P. Borovitskii describes field and laboratory measurements of electrical potentials induced by freeze-thaw cycles in solutions and in argillaceous rock. Some discussion of the relevance of this work to exploration geochemistry is given. The second essay, also by Borovitskii, describes advances in geochemical sampling technology in terrain covered by peat bogs and swamps. The influences on elemental dispersion of vegetative growth in peat bogs are described along with details of experiments conducted when electrical potentials were measured in tree trunks. The third essay, by S.L. Shvartsev, discusses electrochemical interactions which occur between coexisting sulphides and with moisture within orebodies. The relevance of these processes to elemental dispersion is discussed.     

Geochemistry of trace elements in surface waters of the Arno River Basin,northern Tuscany,Italy

Trace element geochemistry of the Arno River and its main tributaries was investigated on the basis of two sampling campaigns carried out in November 1996 and June 1997. By analyzing filtered and unfiltered water samples, Fe and Al are found in solution mainly as colloidal particles of size lower than 0.45 μm. In June (lower flow rate), Fe and Al are enriched in the filtered waters from the main river, and this feature was interpreted in terms of higher water temperature promoting the formation of smaller particles, thus reducing their aggregation properties. Iron and Al show perfectly synchronous downstream profiles along the Arno River, correlate quite well each to other, and display abrupt concentration increases near to Florence, where the lithology of the catchment changes from siliciclastic dominated to clay-sand (lacustrine-marine)-dominated. The same behaviour is shown by most of the other trace elements in the river, thus supporting a general lithological control. Trace elements in the final part of the Arno River are influenced by flocculation processes in addition to mixing. Adsorption phenomena on oxy-hydroxides are denoted by good elemental correlations with Fe (and Al). Sporadic anomalous concentration values, possibly related to anthropogenic contributions, may prevent such correlations. Referring to the quality of waters for potable use and fish life, toxic elements are below the acceptable limits of current European regulations, with few exceptions for Hg exceeding guideline values. Multivariate analysis groups trace elements according to geochemical affinities and natural or anthropogenic sources, thus distinguishing contaminated from uncontaminated samples. The results achieved in this work will help regional and national Authorities for compliance with the EU water policy, especially in assessing the water quality at the river basin scale and its vulnerability to human activities.     

Tephrochronology of the Toluca Basin,central Mexico

The major element glass geochemistry of 10 Late Pleistocene and Holocene tephras found in the Toluca Basin in the Trans-Mexican Volcanic Belt is reported for the first time, as a key step towards establishing a tephrochronology for the region. The context for this tephrochronology is provided by a review of Late Quaternary volcanism of the basin. New tephra samples were collected from reference profiles around the basin in order to establish major element glass geochemical data for tephras described in previous publications, but not previously analysed. In addition, cores were taken from the basin floor to extend the known spatial distribution of the tephra layers and establish correlations with the lacustrine record. Improved chronological control has been provided by seven new AMS and conventional radiocarbon dates on the major tephras. Geochemical data are presented for 10 tephras ranging in age from ca. 25,000 BP (Lower Toluca Pumice) to about 8500 BP (Tres Cruces Tephra). Based on geochemical data, it is possible to correlate between sites within the Toluca Basin and between the Toluca Basin and the Basin of Mexico. The basis for a tephrochronological framework has been established.     

Testing the reliability of the JEOL FEGSEM 6500F electron microprobe for quantitative major element analysis of glass shards from rhyolitic tephra

Coulter, S. E., Pilcher, J. R., Hall, V. A., Plunkett, G. & Davies, S. M. 2009: Testing the reliability of the JEOL FEGSEM 6500F electron microprobe for quantitative major element analysis of glass shards from rhyolitic tephra. Boreas , 10.1111/j.1502-3885.2009.00113.x. ISSN 0300-9483.
Electronprobe microanalysis is now widely adopted in tephra studies as a technique for determining the major element geochemistry of individual glass shards. Accurate geochemical characterization is crucial for enabling robust tephra-based correlations; such information may also be used to link the tephra to a specific source and often to a particular eruption. In this article, we present major element analyses for rhyolitic natural glass standards analysed on three different microprobes and the new JEOL FEGSEM 6500F microprobe at Queen's University Belfast. Despite the scatter in some elements, good comparability is demonstrated among data yielded from this new system, the previous Belfast JEOL-733 Superprobe, the JEOL-8200 Superprobe (Copenhagen) and the existing long-established microprobe facility in Edinburgh. Importantly, our results show that major elements analysed using different microprobes and variable operating conditions allow two high-silica glasses to be discriminated accurately.     

U-Th-Pb systematics of precambrian carbonate rocks: Dating of the formation and transformation of carbonate sediments

The current state in the Pb-Pb dating of the formation and epigenesis of Precambrian carbonate sediments has been reviewed. The geochemistry of admixture elements (U, Th, Pb, Rb, Sr, Mn, and Fe) constituting carbonate minerals and the redistribution of the elements in the course of early diagenesis and epigenesis have been considered. The advantages of choosing samples for Pb-Pb dating on the basis of geochemical criteria similar to those applied for Sr-isotope stratigraphy and the potentialities of applying different methods of decontamination of specimens, analyzed from surface contamination and possible epigenetic carbonate phases, were illustrated. By the example of a series of carbonate formations, distinctions in susceptibility of U-Pb and Rb-Sr systems of carbonate minerals to secondary transformations have been demonstrated. The prospects for using the method of step solution allowing noncogenetic carbonate generations to be separated and thus the accuracy and reliability of Pb-Pb dates to be upgraded were considered.     

Effect of permafrost on geochemistry in a Canadian peat plateau bog

Permafrost is a common feature in the Canadian Subarctic, resulting in the development of distinctive wetland forms, such as peat plateaux, which are perennially frozen peatlands. The geochemistry of a peat plateau bog in East Little Bear River Valley, Northwest Territories, is discussed, including variations in botanical and mineralogical composition, and the influence of permafrost. The riparian margin of the plateau bog is unfrozen, but permafrost occurs at 0.68 m depth 10 m inland. Cores taken in these 2 sites exhibit variations in peat stratigraphy, but possess a similar C-shape ash distribution. In the core not affected by permafrost, most elements studied (Al, Ba, Cr, Fe, K, Mg, Na, Si, Th, Ti, V) also display a C-shape distribution, and their concentration can be explained in terms of mineral matter abundance and variety. Halogens (Cl, I, Br), on the other hand, are mainly associated with the organic fraction, whereas Ca and Se appear to be associated with both the organic and inorganic fraction. In the permafrost-affected core, all elements, independently of their organic or inorganic affinity, exhibit a substantial enrichment immediately above the permafrost table, whereas they are depleted immediately below. This is inferred to be the result of solute redistribution linked with ice formation caused by upward permafrost growth and downward seasonal freezing.     

Geochemistry and origin of ferruginous nodules in weathered granodioritic gneisses, Mysore Plateau, Southern India

Fe-nodules occur within saprolites formed from weathering of granodioritic gneisses in the rain-shadow region of the Mysore Plateau adjacent to the Sahyadri Mountains in Southern India. These nodules and their host saprolites were studied for their geochemistry, including chemical speciation, to understand nodule formation and chemical redistribution processes during rock weathering. From their mode of occurrence, and mineralogical and geochemical data, we infer that the nodules originated by a two-stage process in which the initial extensive weathering of gneisses likely facilitated subsequent ferrolysis weathering and nodule formation. Nodules originated by precipitation of goethite, hematite and gibbsite along with several amorphous phases within the matrix of weathered gneisses. This is possible only under hydromorphic conditions, suggesting that parts of the plateau must have gone through a humid phase prior to the present aridity. In the saprolites, Al, Fe, and Ti become enriched because of the removal of Si, Ca, Na, and K. However within the nodule, Fe, Ti, Cr, and Ni are deposited after their chemical transport from the saprolite. Titanium, known for its immobile nature, was also mobilized and concentrated under the conditions of nodule formation. The most important elements in the nodule constitution are Fe, Al, Ti, and Mn, each having both crystalline and amorphous phases. Fe-Ti and Mn oxyhydroxides grain coatings in the saprolites and discrete amorphous Mn and Ti phases in the nodules seem to have scavenged trace elements from the weathering profile. REE were mobilized during weathering and nodule genesis in which Ce and Ti show a strong geochemical coherence. The enrichment of only HREE in saprolite, and both HREE and LREE with significant Ce in the nodule, indicate the control of evolving secondary minerals in the REE redistribution during rock weathering. Strong enrichment of Ce in the weathering profile and in nodules has important implications to the REE chemistry of river waters.     

Late Quaternary tephrostratigraphy,Ahklun Mountains,SW Alaska

Radiocarbon‐dated sediment cores from six lakes in the Ahklun Mountains, south‐western Alaska, were used to interpolate the ages of late Quaternary tephra beds ranging in age from 25.4 to 0.4 ka. The lakes are located downwind of the Aleutian Arc and Alaska Peninsula volcanoes in the northern Bristol Bay area between 159° and 161°W at around 60°N. Sedimentation‐rate age models for each lake were based on a published spline‐fit procedure that uses Monte Carlo simulation to determine age model uncertainty. In all, 62 ¹⁴C ages were used to construct the six age models, including 23 ages presented here for the first time. The age model from Lone Spruce Pond is based on 18 ages, and is currently the best‐resolved Holocene age model available from the region, with an average 2σ age uncertainty of about ± 109 years over the past 14.5 ka. The sedimentary sequence from Lone Spruce Pond contains seven tephra beds, more than previously found in any other lake in the area. Of the 26 radiocarbon‐dated tephra beds at the six lakes and from a soil pit, seven are correlated between two or more sites based on their ages. The major‐element geochemistry of glass shards from most of these tephra beds supports the age‐based correlations. The remaining tephra beds appear to be present at only one site based on their unique geochemistry or age. The 5.8 ka tephra is similar to the widespread Aniakchak tephra [3.7 ± 0.2 (1σ) ka], but can be distinguished conclusively based on its trace‐element geochemistry. The 3.1 and 0.4 ka tephras have glass major‐ and trace‐element geochemical compositions indistinguishable from prominent Aniakchak tephra, and might represent redeposited beds. Only two tephra beds are found in all lakes: the Aniakchak tephra (3.7 ± 0.2 ka) and Tephra B (6.1 ± 0.3 ka). The tephra beds can be used as chronostratigraphic markers for other sedimentary sequences in the region, including cores from Cascade and Sunday lakes, which were previously undated and were analyzed in this study to correlate with the new regional tephrostratigraphy. Copyright © 2012 John Wiley & Sons, Ltd.     

Tephrabase: tephrochronology and the development of a centralised European database

Tephrabase was launched on the World Wide Web in 1995 as a tool for tephrochronological research. In order to facilitate the identification, correlation and dating of tephra deposits, this database may be interrogated through multiple routes, including by source volcano, date, location, and tephra chemistry; datasets include stratigraphy, geochemistry, chronology and spatial information. Currently all the European data refer to Late Quaternary Icelandic‐sourced tephras, post‐12 k yr BP. The sites (62) where the tephra deposits are found include Iceland, the United Kingdom, Ireland, the Faroe Islands, Sweden and Russia. In addition, there are also data on tephra layers in central Mexico. Use of Tephrabase highlights the importance of selected geochemical data, but this has to be used with care as major element characteristics alone do not always produce unique definitions for single tephra deposits. For the most accurate results multiple criteria must be used. Tephrabase can be found at http://www.tephrabase.org . Copyright © 2007 John Wiley & Sons, Ltd.