黄海辐射沙洲沉积物地球化学特征及其环境意义

对黄海辐射沙洲烂沙洋水道区域的3个钻孔共81个沉积物样品进行了微量、常量元素分析和^14C测年分析．化学元素质量分数的变化与当时沉积环境的变化相对应。突发事件(如风暴潮)的发生不但在沉积物的岩性上有所体现,而且在微量元素质量分数的变化上也有很明显的体现。微量元素Zr可作为沉积能量变化的地化指示剂,潮汐通道北部的西太阳沙区域的沉积动力环境在4000a以前是较弱的。潮流通道的上段沉积物是来自水深较浅的区域,由于潮流和波浪的作用使其能够保持稳定的水深。     

The distribution of zinc,nickel, manganese,cadmium, copper,and iron in some surface waters from the world ocean

Determinations of Zn, Ni, Mn, Cd, Cu, and Fe have been carried out on 51 near-shore and 38 open-ocean surface seawaters from various regions of the World Ocean.The concentrations of the trace metals have been established in the open-ocean waters, and have been used as “baselines” to evaluate trace-metal enhancement in near-shore regions. The factors by which the trace metals are enriched in near-shore regions vary from one element to another and, according to the highest concentration factors found, decrease in the order Zn = Mn > Cd = Cu = Ni.These elements exhibit differences in their distributions between near-shore and open-ocean waters, and they have been divided into two types on this basis: Type I, in which the largest number of samples in both shelf and open-ocean waters lie in the same concentration range. Zinc, cadmium, and copper are Type I elements. Type 2, in which the largest number of samples of near-shore waters lie in a higher concentration range than the largest number of samples of open-ocean waters. Nickel and manganese are Type 2 elements.The concentrations of Mn, Cd and Zn are similar in open-ocean surface waters from the South Atlantic and Indian Ocean, but Cu and Ni have higher concentrations in the former ocean.There is considerable variation in the concentrations of the trace metals in near-shore surface waters from various regions of the World Ocean. These variations are discussed in detail.     

Concentrations of the elements Ag,Al, Ca,Cd, Cu,Fe, Mg,Mn, Pb and Zn,and the radionuclides 210Pb and 210Po in the digestive gland of the squid Nototodarus gouldi

Ag, Al, Ca, Cd, Cu, Fe, Mg, Mn, Pb and Zn concentrations and ²¹⁰Po and ²¹⁰Pb activities were measured in 26 specimens of the squid Nototodarus gouldi taken from the waters of Bass Strait in one jigging operation. All the elements show wide ranges in concentrations in specimens apparently subject to the same environmental conditions. Copper concentration was 27-1 200 μg/g, and ²¹⁰Po activity 4·8–24·2 Bq/g. The animal wet weights, the elements Ag, Al, Cd, Fe and Zn, and the radionuclide ²¹⁰Po have coefficients of variation in the range 40–60%; Ca, Mg and Mn show the smallest variability (CV = < 30%), and Cu the greatest (CV = 12%). Significant correlations (p < 0·001) were found between the following pairs of elements: Cd-Zn, Cd-Cu, Zn-Cu, Mg-Mn, Fe-Mn, Ca-Mg and Fe-²¹⁰Po.     

赣东–浙西下寒武统荷塘组稀土元素特征及其地质意义

为揭示下扬子下寒武统黑色岩系的物源属性、构造背景及其沉积环境等特征,对赣东-浙西地区下寒武统荷塘组野外露头及钻井岩心进行了系统采样与稀土元素分析测试。结果显示,荷塘组样品稀土元素总量变化波动大（16.83×10−6 ～ 321.22×10−6）,均值低（103.11×10−6）,轻稀土元素富集且分异明显,重稀土元素亏损但分异小,普遍存在Ce负异常和明显Eu正异常。研究表明：①荷塘组硅质泥页岩形成于缺氧还原的裂陷海盆环境,构造背景为被动大陆边缘,物源受陆源、海水和热液共同影响,横峰、上饶受热液和海水影响最大,受陆源碎屑影响最小,常山、江山与之相反;②沉积过程普遍有热液活动参与,在上饶存在热液活动中心,活动强度呈西强东弱特点,并发现低温热液活动有利于有机质的富集。     

Petrology, Geochemistry and Nd-Sr-Pb Isotopic Properties of Volcanic Rocks in Daheishan Island, Penglai, Shandong Province

The major elements, trace elements, K-Ar age and Sr-Nd-Pb isotopic systems of the Cenozoic volcanic rocks in Daheishan Island and Cishan, Penglai, Shandong Province are measured. The volcanic rocks ( olivine-nephelinite and nepheline-basanite ) in DaheishanIsland erupted periodically in an interval of 0.32 Ma, from 8.72 Mm 8.39 Ma, 8.08 Ma to 7.73Ma. The volcanic rocks are all rich in light REEs. They are similar to the OIB-type alkali basalt in the trace elements normalized model by primordial mantle: rich in high field elements such as Nb and Ta, and imcompatible elements such as Cs, Rb, Ba, Th, U. The volcanic rocks show a depletion of K and Rb elements. It is suggested by the trace elements that the olivine-nephelinite in Daheishan Island is originated fi‘om deep resources under the continental mantle, ε Nd (0) values of the volcanic rocks in Daheishan Island and Cishan are 5.31 - 8.51 and 7.33 respectively, suggesting that the volcanic rocks are from the depleted mantle resources, which have higher Sm/Nd ratios than the CHUR. ^143Nd /^144Nd ratios of Daheishan Island olivine-nephelinite and Cishan alkali basalts are 0.512 910 - 0.513 074 and 0.513 014 resoeetivelv. The ^87Sr /^86Sr of Daheishan lsland volcanic rocks are lower than that of Cishan, 0.703 427 - 0.703 482 and 0.703 895 respectively. The Daheishan Island olivinenephelinite has the Pb isotopic values as follows: ^206Pb /^204pb= 18.028 9 ～17.972 8,^207Pb /^204Pb= 15,435 8 - 15.402 2 and ^208Pb /^204Pb=38.087 6 - 37.997 5, lower than those of Cishan basanite. The Cishan basanite has ^206Pb / ^204Pb = 18.240 1, ^208Pb /^204Pb = 15.564 5 and ^208Pb /^204Pb=38.535. The authors suggest that the olivine-nephelinite in Daheishan Island is similar to the E-type MORB or Hawaii OIB, and the alkali basalts in Cishan similar to the Kerguelen OIB. The dominant mantle components of DM PREMA and perhaps DM( Dupal type ) are the dominant mantle components for volcanic rocks in Daheishan Island and Cishan. The PREMA component plays an important role.     

Phosphorus and metals bound to organic matter in coastal sediments - An investigation of complexes of P,Cu, Zn,Fe, Mn,Ni, Co and Ti by inductively coupled plasma-atomic emission spectrometry with sephadex gel chromatography

Phosphorus and metals bound to organic matter were separated from coastal sediments of Harima Sound in Seto Inland Sea, Japan by extraction with NaOH and fractionated by Sephadex G-25 chromatography. Phosphorus and metals were determined in the eluates by a multi-channel, inductively coupled plasma-atomic emission spectrometer. Phosphorus and Cu, Zn, Fe, Mn, Ni, Cr, Co and Ti bound to organic matter with high molecular weights (OMHMW) (MW ? 5000) were found to be present in the sediments, but no Mo or V were found. The technique provides minimum estimates of the amounts of P and metals bound to organic matter. These organic complexes show surface enrichment in a sediment core (0–20 cm) and their contents decrease with depth. Also, the amounts of eighteen elements, namely: P, Fe, Mn, Zn, Cu, Si, Al, Ti, Pb, Co, Ni, Cr, Mo, V, Na, K, Ca and Mg, in H₂O, ammonium acetate at pH 7 and 5, hydrogen peroxide, hydroxylamine hydrochloride and hydrogen fluoric acid soluble fractions have been determined with a selective chemical leaching technique for the ²¹⁰Pb-dated sediment core sample. Considerable amounts of P (6–19%) and Cu (5–21%) were associated with organic matter, in contrast to other metals such as Fe, Mn, Zn, Ni, Cr, Co and Ti which were associated with sulfide and silicate.     

Effects of salinity, temperature and food type on the uptake and elimination rates of cd, cr, and zn in the asiatic clamcorbicula fluminea

Laboratory radiotracer experiments were conducted to determine assimilation efficiencies (AE) from ingested algal food and oxic sediment particles, uptake rates from the dissolved phase, and the efflux rates of Cd, Cr and Zn in the Asiatic clamCorbicula fluminea. Among three elements, AE from both algal and sediment food was greatest for Cd, followed by Zn and Cr. The AEs of tested elements from algal food(Phaeodactylum tricornutum) were consistently higher than those from sediments at a given salinity and temperature. The influence of salinity (0, 4 and 8 psu) and temperature (5, 13 and 21¼) on the metal AEs was not evident for most tested elements, except Cd AEs from sediment. The rate constant of metal uptake from the dissolved phase (k _u was greatest for Cd, followed by Zn and Cr in freshwater media. However, in saline water, thek _u of Zn were greater than those of Cd. The influx rate of all tested metals increased with temperature. The efflux rate constant was greatest for Cr (0.02 d^-1), followed by Zn (0.010~0.017 d^-1) and Cd (0.006 d^-1). The efflux rate constant for Zn in clam tissues depurated in 0 psu (0.017 d^-1) was faster than that in 8 psu (0.010 d^-1). Overall results showed that the variation of salinity and temperature in estuarine systems can considerably influence the metal bioaccumulation potential in the estuarine clamC. fluminea. The relatively high Cd accumulation capacity ofC. fluminea characterized by the high AE, high dissolved influx rate and low efflux rate, suggested that this clam species can be used as an efficient biomonitor for the Cd contamination in freshwater and estuarine environments.     

冲绳海槽南部流纹岩中角闪石的化学特征及其对岩石成因的指示

为了揭示冲绳海槽西南端流纹岩成因,利用电子探针和LA-ICP-MS对该流纹岩中角闪石进行了主量和微量元素测定。所有角闪石主量元素成分变化范围小,晶体化学特征主要表现为:Ca_B>1.60,Ca_A=0,（Na+K）_A<0.33,Na_B介于0.23~0.39之间,均为钙质镁闪石。微量元素以富集Sc、V、Cr、Co、Ni和REE,亏损Rb、Sr、Ba、Zr、Th、U和Pb为特征,这些元素的富集与亏损与复杂的类质同象作用有关。由角闪石温压计得出其结晶时的温度范围为775~839℃,压力为0.12 GPa,大致相当于4 km的深度。角闪石的成因矿物学研究显示该流纹岩中角闪石为壳-幔混合成因,进一步表明冲绳海槽南部流纹岩由幔源玄武质岩浆与壳源长英质岩浆混合形成的中基性岩浆在浅层岩浆房中结晶分异而形成,且壳幔混合源很可能是冲绳海槽西南端火山岩岩浆的主要来源。     

Similarities between Mn,Ni and Co contents of deep-sea clays and manganese nodules from the south-west region of the North Atlantic

Recently published distribution patterns have shown that in the Atlantic Ocean Mn, Ni and Co tend to be concentrated in those deep-sea sediments deposited in a central zone which extends down the length of the ocean. The present paper shows that these trace elements are also concentrated in certain clays from the south-west region of the North Atlantic. This region is rich in manganese nodules, and analyses reveal that the non-lithogenous fractions of some of the clays approximate to those of the nodules in composition. It is suggested that these clays have acquired their relatively high concentration of non-lithogenous trace elements from sea water by processes associated with the formation of manganese nodules.     

Evidence for enhanced bioavailability of trace elements in the marine ecosystem of Deception Island, a volcano in Antarctica

This study assessed whether trace elements present at Deception Island, an active submarine volcano in the Antarctic Peninsula, show enhanced biological availability to the local marine community. Using a weak acid extraction method to dissolve organic material and leach associated but not constitutive trace elements of sediments, fifteen elements were measured from seafloor sediment, seawater particulates, and tissues of benthic (bivalves, brittlestars, sea urchins) and pelagic (demersal and pelagic fishes, krill) organisms collected in the flooded caldera. The highest element concentrations were associated with seafloor sediment, the lowest with seawater particulates and organism tissues. In the case of Ag and Se, concentrations were highest in organism tissue, indicating contamination through the food chain and biomagnification of those elements. The elements Al, Fe, Mn, Sr, Ti, and to a lesser extent Zn, were the most concentrated of the trace elements for all sample types. This indicates that the whole ecosystem of Deception Island is contaminated with trace elements from local geothermal activity, which is also reflected in the pattern of element contamination in organisms. Accordingly, element concentrations were higher in organisms collected at Deception Island compared to those from the neighboring non-active volcanic King George Island, suggesting that volcanic activity enhances bioavailability of trace elements to marine organisms. Trace element concentrations were highest in digestive tissue of organisms, suggesting that elements at Deception Island are incorporated into the marine food web mainly through a dietary route.     

Metalliferous Sediment and a Silica-Hematite Deposit within the Blanco Fracture Zone,Northeast Pacific

A Tiburon ROV dive within the East Blanco Depression (EBD) increased the mapped extent of a known hydrothermal field by an order of magnitude. In addition, a unique opal-CT (cristobalite-tridymite)-hematite mound was discovered, and mineralized sediments and rock were collected and analyzed. Silica-hematite mounds have not previously been found on the deep ocean floor. The light-weight rock of the porous mound consists predominantly of opal-CT and hematite filaments, rods, and strands, and averages 77.8% SiO₂ and 11.8% Fe₂O₃. The hematite and opal-CT precipitated from a low-temperature (≥ 115° C), strongly oxidized, silica- and iron-rich, sulfur-poor hydrothermal fluid; a bacterial mat provided the framework for precipitation.

Samples collected from a volcaniclastic rock outcrop consist primarily of quartz with lesser plagioclase, smectite, pyroxene, and sulfides; SiO₂ content averages 72.5%. Formation of these quartz-rich samples is best explained by cooling in an up-flow zone of silica-rich hydrothermal fluids within a low permeability system. Opal-A, opal-CT, and quartz mineralization found in different places within the EBD hydrothermal field likely reflects decreasing silica saturation and increasing temperature of the mineralizing fluid with increasing silica crystallinity.

Six push cores recovered gravel, coarse sand, and mud mineralized variously by Fe or Mn oxides, silica, and sulfides. Total rare-earth element concentrations are low for both the rock and push core samples. Ce and Eu anomalies reflect high and low temperature hydrothermal components and detrital phases.

A remarkable variety of types of mineralization occur within the EBD field, yet a consistent suite of elements is enriched (relative to basalt and unmineralized cores) in all samples analyzed: Ag, Au, S, Mo, Hg, As, Sb, Sr, and U; most samples are also enriched in Cu, Pb, Cd, and Zn. On the basis of these element enrichments, the EBD hydrothermal field might best be described as a base- and precious-metal-bearing, silica-Fe-oxide-barite deposit. Such deposits are commonly spatially and temporally associated with volcanogenic massive sulfide (VMS) ores. A plot of data for pathfinder elements shows a large hot spot at the northwestern margin of the field, which may mark a region where moderate to high temperature sulfide deposits are forming at depth; further exploration of the hydrothermal field to the northwest is warranted.     

Rare earth elements-rich phase and enriching mechanism in sediments from CC area, the Pacific Ocean

Compared to North American shale composition (NASC),REE contents of sediments from the CC area in the Pacific Ocean are obviously high except that cerium has equal content to that of NASC.Three-valence rare earth elements were completely enriched in phosphate-phase and cerium in iron-phase.Rare earth elements in the sediments were originally derived from seawater.During lithigenic and minerogenic processes of metalliferous nodules,three-valence rare earth elements in sediments mobilized and incorporated into sediments as authigenous biogenic-apatite,while cerium had change from Ce³⁺ to Ce⁴⁺ and directly precipitated from seawater and entered metalliferous nodules and caused Ceanomalies in REE pattern in sediments.     

西藏盐湖及其水系中的痕量金属

于1978年采集了西藏高原26个盐湖、6条河流、10处泉水及3地盐湖区的大气降水的水样,以ZCP等离子光谱仪测定所采水样中Fe,Mn,Al,Cu,Pb,Zn,Ni,Cr等痕量金属含量,结果表明,1.盐湖水及河流、泉水和大气降水等水系中的痕量金属均高度富集,但以盐湖水的最大;盐湖水中各痕量金属富集程度不一,其顺序:Pb>Mn>Cr>Fe>Zn>Cu>Al>Ni。2.区域出露的岩性、气候、湖盆及水文等为盐湖水中富集痕量金属创造了有利条件。3.高痕量金属浓度的河流、泉水及大气降水是控制和影响盐湖水中痕量金属富集的主要的直接因素。4.盐湖水的矿化度、pH及水化学类型也影响着水中痕量金属的富集。     

菲律宾海钱洲深海峡谷沉积物中元素的地球化学特征

作者研究了钱洲深海峡谷柱状沉积物中常量元素和微量元素的垂直分布及它们的相关关系。研究表明,大多数化学元素随岩芯深度的垂直分布变化不大,且元素明显的分为两组：Ca,Sr组和Al,Fe,Ti,Mg,Ni,V,Co,Li,Rb组,该区的物质来源为多源的,即生物来源、陆源和火山源。     

The Role of Primary-Producer-Mediated Organic Complexation in Regional Variation in the Supply of Mn,Fe, Co,Cu, Ni and Zn to Oceanic,Non-Hydrothermal Ferromanganese Crusts and Nodules

Oceanic, non-hydrothermal ferromanganese crusts and nodules are variably enriched in Mn, Fe, Co, Cu, Ni and Zn. Comparison of the content of these elements in crusts and nodules with the level of primary productivity in the South Pacific Ocean suggests that primary-producer-mediated complexation of several of these elements by organic ligands in solution may contribute to explaining a pattern of distinctive associations observed between compositional variations for these elements in these deposits and variations in the level of primary productivity.     

Major,Trace, and Rare Earth Elements in the Sediments of the Central Indian Ocean Basin: Their Source and Distribution

Abstract

A large number of surface sediments as well as short sediment cores collected in the Central Indian Ocean Basin have been subjected to various geochemical investigations during the last one and half decade. The studies varied, covering different aspects of sediments and resulting in a number of publications. In the present article, we have put together the data from 82 surface sediments and 14 short sediment cores, including 25 new analyses, to study the trend of their distribution and source at large. The distribution maps of elements show that highest concentrations of Mn, Cu, Ni, Zn, Co, and biogenic opal in the surface sediment occurs between 10°S and 16°S latitude, where diagenetic ferromanganese nodules rich in Mn, Cu, Ni, and Zn are present. The studies highlight that the excess element concentration (detrital unsupported) such as Mn, Cu, Ba, Ni, Co, Pb, and Zn have contributed >80% of their respective bulk composition. These excess elements exhibit strong positive correlation with each other suggesting their association with a single authigenic phase such as Mn oxide. Biogenic opal contributes 30–50% of the total silica in the siliceous sediment. Aluminum, Fe, and K have contributed >60% from terrigenous detrital source compared to their bulk composition. In calcareous ooze, Ca, and Sr excess contribute >95% while, in siliceous ooze it is only 50% of their bulk composition. Nearly 35% of structurally unsupported Al in the sediment raises doubt of using Al as a terrigenous index element to normalize the trace and minor elements. Biogenic apatite is evident by the positive correlation between Ca (<1%) and P. Calcium, Sr, and P depict a common source such as biogenic. Bulk element concentration such as Li, V, Cr, Sc, and Zr are positively correlated with Ti indicating their terrigenous detrital source. Rare earth element (REE) concentration increases from calcareous ooze to siliceous ooze and reaches a maximum in the red clay. Presence of positive Eu-anomaly in these sediments has been attributed to aeolian input. REE in these sediments are mostly carried by authigenic phases such as manganese oxide and biogenic apatite. Based on the distribution of transition elements in the sediment cores, three distinct zones—oxic at top, suboxic at intermediate depth, and a subsurface maxima—have been identified. Oxic and suboxic zones are incidentally associated with high and low micronodule abundance in the coarse fraction (>63 μm) respectively. Ash layers encountered at intermediate depth between 10 to 35 cm are correlative with the Youngest Toba eruption of ～74ka from Northern Sumatra. This ash is mainly responsible for the high bulk Al/Ti ratio up to 48.5 (three times higher than Post Archean Australian Shale), other than scavenging of dissolved Al by biogenic components.     

Carbon,nitrogen and phosphorus dynamics in nine sub-systems of the Sylt-Rømø Bight ecosystem,German Wadden Sea

Flow networks of nine sub-systems consisting of 59 components each of the Sylt-Rømø Bight, German Wadden Sea, were constructed depicting the standing stocks and flows of material and energy within and between the sub-systems. Carbon, nitrogen and phosphorous were used as currencies for each sub-system, thus resulting in 27 network models, which were analyzed by ecological network analytical protocols. Results show substantial variability in the dynamics of these elements within and between the nine sub-systems, which differ in habitat structure, species diversity and in the standing stocks of their constituent living and non-living components. The relationship between the biodiversity and selected information indices and ratios, derived from ecological network analysis, of individual sub-systems is variable and differ substantially between them. Ecosystem properties such as the structure and magnitude of the recycling of these elements, number of cycles, and total sub-system activity were calculated and discussed, highlighting the differences between and complexity of the flow of C, N and P in a coastal marine ecosystem. The average number of cycles increase from 179 for C, to 16,923 and 20,580 for N and P respectively, while the average amount of recycled material, as measured by the Finn Cycling Index (FCI), increase from 17% for C, to 52% for P and to 61% for N. The number of cycles and the FCI vary considerably between the sub-systems for the different elements. The largest number of cycles of all three elements was observed in the muddy sand flat sub-system, but the highest FCIs were computed for both C (32%) and N (85%) in the Arenicola Flats, and in sparse Zostera noltii sea grass beds for P (67%). Indices reflecting on the growth, organization and resilience of the sub-systems also showed considerable variability between and within the inter-tidal ecosystems in the Bight. Indices such as, for example, the relative ascendency ratios increase on average from C to N to P, whereas others, such as the Average Mutual Information and Flow Diversity indices, were found to be higher in the N models than in the C or P ones.     

南海北部湾东部海域表层沉积物地球化学特征

通过对南海北部湾东部海域61 个站位表层沉积物粒度和地球化学组成的相关分析和因子分析,探讨了其空间分布特征、元素相关性以及元素组合特征, 揭示了元素在区域上的分布规律和主控因素。结果表明: 绝大多数常微量元素具有相似的平面分布特征, 而MnO、Zr、CaO 和Sr 空间变异系数较大,在部分区域出现了异常高值, 表明其沉积环境受到正常陆源沉积以外其他因素的影响。元素和Al₂O₃的比值分布特征表明, 广西和海南岛近岸沉积物主要由陆源碎屑沉积组成, 在潮汐和近岸径流作用下,由近岸向远海输送; 而研究区西部海域沉积物主要为来自红河的物质。元素相关分析和因子分析结果表明, 研究区表层沉积物中绝大多数常微量元素主要受沉积物粒度的控制; CaO 和Sr 含量主要受生物活动活跃程度控制; Zr 含量分布主要受控于源区母岩矿物组成以及自源区的搬运距离; 而MnO 含量则受陆源、海底热液以及自生作用等多种来源共同影响。     

Geochemistry of rare earth elements in the dissolved,acid-soluble and residual phases in surface waters of the Changjiang Estuary

The concentrations of rare earth elements in the dissolved, acid-soluble and residual phases in surface waters of the Changjiang Estuary were determined using ICP-MS. The main purposes of the study are to understand the estuarine geochemistry of rare earth elements and to explore water-particle interactions in the Changjiang estuarine mixing zone. The results show that there are two distinct processes operating on dissolved rare earth elements in the estuary: large scale removal at low salinities due to salt-induced coagulation and remarkable release at mid to high salinities. These processes result in modification of the effective river water flux and the systematical fractionation of the dissolved rare earth elements toward the East China Sea. The increase in concentration of dissolved rare earth elements in the mid to high salinity waters of the Changjiang Estuary suggests a sediment source in the mixing zone of the estuary, which is located over a shallow, broad shelf where there is extensive physical contact between bottom sediment and estuarine waters. Acid-soluble rare earth elements, the concentrations of which also dropped sharply in the low salinity region, appear to be controlled by salt-induced coagulation process and intense deposition of suspended particulate matter in the low salinity region. In the mid to high salinities, all acid-soluble rare earth element concentrations increase slightly with increasing salinity, suggesting that resuspension of sediments occurred. In contrast, the residual rare earth element concentrations are relatively constant with salinity variation in the Changjiang estuarine surface waters.     

Hydrothermal Manganese Deposits from the Tonga-Kermadec Ridge and Lau Basin Region,Southwest Pacific

Hydrothermal Mn-oxide deposits from the Tonga-Kermadec Ridge and the Valu Fa Ridge back-arc spreading center in the Lau Basin have been studied mineralogically and by bulk and partition geochemical techniques. The Mn-oxides are present as three main morphological types; of these, a dense, grey submetallic material is most common. Common lamination of this material suggests an intermittent rate of formation. Mineralogically, the crusts comprise variable proportions of 10Å and 7Å manganite. Concentrations of some trace elements, including Li, Mo, and Zn are generally significantly higher than those observed in Mn-crusts of hydrogenous origin, suggesting that the observed trace element enrichments are due to a hydrothermal source. Both temporal and geographical controls are seen to affect these trace element concentrations. Although most of the hydrothermally enriched elements are associated with the Mn-oxide phases, Li appears to reflect either a surficial adsorption or the presence of a separate Li-rich phase. Observed variations in deposit composition could reflect differences in the geochemistry of the basement rocks from which the elements have been leached, the proximity of high-temperature sulphide deposits and temporal variability in the hydrothermal systems.