Particulate trace element fluxes in the deep northeast Atlantic Ocean

Particulate fluxes of trace elements (Al, Cd, Co, Cu, Fe, Mn, Ni, P, Ti, V and Zn) in the northeast Atlantic Ocean (three positions at latitudes from 33°N to 54°N along ∼20°W) were measured using time-series sediment traps between March 1992 and September 1994. Significant variabilities of fluxes with season and depth (1000 m to maximum of 4000 m) were observed only for ‘biogenic elements’, such as Cd, Ni, Zn or P. On the other hand, we found a distinct large-scale increase of fluxes into the deep-sea traps to the south for Al, Co, Fe, Mn and V. We attribute this latitudinal gradient to the increasing influence of the Saharan dust plume. The biogenic flux decreased towards the south. This trend was clearly visible for Cd and P only. The fluxes of other ‘nutrient-like’ elements, such as Ni or Zn, exhibited a general decrease between 53°N and 33°N. We compared our sedimentation flux data with published data from the western North Atlantic basins. For this purpose we corrected the deep-sea fluxes of Cu, Mn, Ni and Zn for their lithogenic fractions on the basis of Al, with average crustal material and granitic rocks as references. The comparison indicates that these ‘excess’ fluxes are a factor of at least 2 higher in the western basins for the selected elements. Estimated fluxes are in good agreement with reported atmospheric deposition in the two areas. The noted imbalance between the non-lithogenic atmospheric input of Mn and the determined ‘excess flux’ in the deep northeast Atlantic indicates an additional input in the form of a lateral flux of dissolved Mn(II) species and scavenging onto sinking particles. With respect to the mechanism of sedimentation, a unique behaviour is noticed for the refractory elements Co, Fe, Mn, Ti and V, which were found to correlate with the vertical transport of Al (clay). The ‘excess’ fluxes of Cu, Ni and Zn are linearly related to C_org, whereas the overall relation of Cd to P fluxes exhibits a molar Cd/P ratio of 2.0×10^-4, which is close to the ratio in the dissolved fractions in the northeast Atlantic.     

A study of the geochemistry of suspended particulate matter in coastal waters

The concentrations of Si, Al, Ti, Fe, K, Ca, Mg, P and Mn, before and after chemical leaching, in particulate matter from waters off the west coast of Scotland have been measured in vertical profiles at two seasons. The distribution of Si and Ca are shown partly to reflect temporal changes in biological production in different waters. The distributions of Al, Ti, Fe, K and Mg have been used to distinguish different sources and types of suspended alumino-silicates, and to trace probable circulation patterns in the water mass.While Si and Ti contents of the particulate matter are unaffected by mild chemical leaching, large amounts of other elements, notably Mg, K and Al, can be removed by this treatment. Presumably, these losses indicate preferential release of these elements from octahedral and interlayer sites in clay mineral lattices.The distribution of particulate P covaries with non-silicate Fe in the surface waters, while in bottom waters, high concentrations of particulate Fe and Mn are associated. The relationship of Fe and P is considered to be due to the presence of particulate ferriphosphates derived from runoff. The particulate Mn and Fe in deep waters is produced by the precipitation of dissolved metals released from bottom sediments by diagenesis.     

青岛近海秋末冬初悬浮颗粒物中部分金属元素的组成与影响因素研究

2008年11月末在青岛近海和胶州湾11个站点采集表层和底层海水中的悬浮颗粒物(SPM)样品,经消解后用等离子体发射光谱法测定了Al、Ca、Fe、Mg、Mn、Ti和Ba、Co、Cr、Cu、Ni、Pb、Sr、V、Zn共15个金属元素以及P的含量,结合SPM和元素含量聚类分析的结果探讨了秋末冬初青岛近海SPM的来源以及金属元素组成的影响因素.SPM含量范围在1.7～16.1mg/L之间,平均为7.9 mg/L;SPM来源以陆源风化产物为主,生物生产有较小的贡献.SPM中Ti、Fe、Mn、Mg、Al、V、Co、Sr和Ni的含量相对恒定,且主要受陆源输入的控制;Ca和P除受陆源影响外,生物生产亦有附加贡献.离陆地相对较远的区域表层海水SPM中Pb、Zn和Ba、Cr、Cu的含量较高,特别是Pb和Zn的富集因子较大,可能受到了潜在的污染影响.Ti的恒定性以及与SPM的良好相关性代表着在青岛近海可用Ti作为颗粒物陆源指示元素,且优于Al.     

MAJOR ION CHEMISTRY AND OCEANIC FLUX OF RIVERS IN SOUTHERN COASTAL CHINA

By analysing the major compounds of river water, it has been found that the water of the Xijiang River is dominated by the weathering products of carbonates, and its hydrochemical character is similar to that of the Changjiang River. Whereas the rivers in Fujian and Eastern Guangdong are characterized by the high contents of dissolved silica and low dissolved salt load, reflecting the typical siliceous rivers. A rough estimate of dissolved salt fluxes to the ocean by these rivers has been obtained. The chemical weathering rate of the Xijiang River basin is 3 times higher than the chemical weathering rates of Fujian and Eastern Guangdong which are close to the average value of rivers in the world.     

冲绳海槽北端表层沉积物过渡元素地球化学特征

利用原子吸收和等离子发射光谱等方法,对冲绳海槽北端184个表层沉积物中的Al和过渡元素(Ti、Cr、Mn、Fe、Co、Ni、Cu、Zn和Zr)进行了化学分析。结果表明,由于受生源碎屑稀释作用的影响,过渡元素在陆架砂质区含量较低,其分布呈北西-南东向舌状延伸;由于细粒组分的增加,在陆架细粒沉积区和海槽区过渡元素含量较高。Mn主要在海槽区富集,在陆架和陆坡区变化不大。除了Mn之外,Al和其他过渡元素均呈明显正相关。Al/Ti比值与陆壳平均值接近,说明二者主要来源于陆源碎屑。Mn/Fe比值与邻近海区沉积物类似,但在陆架区CaO含量大于20%的沉积物和海槽区沉积物中相对较高,这分别是生物富集作用和自生沉积的结果。过渡元素富集因子分析结果表明,研究区过渡元素部分来自于黄河、部分来自于长江物质。     

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。     

Dissolved and particulate aluminum in the Columbia River and coastal waters of Oregon and Washington: Behavior in near-field and far-field plumes

The distribution of dissolved (soluble and total) and particulate (leachable and total) aluminum was examined in the Columbia River and estuary, in near-field and far-field river plumes, and in adjacent coastal waters of Washington and Oregon during the River Influence on Shelf Ecosystems (RISE) cruise of May/June 2006. Dissolved and particulate aluminum (Al) concentrations were significantly greater in the river than in the coastal waters that mixed to form the plume. Dissolved Al concentrations in the Columbia River (∼80 nM) were low relative to other major rivers. Leachable and total particulate Al concentrations within the river reached concentrations greater than 1000 nM and 18,000 nM, respectively. Dissolved Al within the Columbia River estuary showed a significant removal (∼60%) at salinities between 0 and 10 with salt-induced flocculation of colloidal Al complexes and enhanced particle scavenging being probable explanations for aluminum removal. Dissolved and particulate Al concentrations were significantly greater in near-field plumes relative to surrounding coastal waters. As the plume advected from near-field to far-field away from the river mouth, dilution of the plume with lower dissolved Al surface waters as well as particle scavenging along the flow path appeared to be controlling dissolved Al distributions. Particle settling as well as dilution with lower particle-load waters led to observed decreases in particulate Al as the plume moved from near-field to far-field. However, the percent-leachable particulate aluminum in both near-field and far-field plumes was remarkably constant at ∼7%. Dissolved and particulate Al in a far-field plume over 100 km southwest of the Columbia River mouth were over an order-of-magnitude greater than surrounding waters, illustrating the importance of the Columbia River plume as a mechanism for transporting Al offshore. Aluminum could be used to trace the input of biologically-required elements such as iron into waters off the shelf.     

Metal distributions and their fluxes at the coastal boundary of a semi-enclosed ria

Water column samples have been collected in the outer channel of the Ferrol Ria (NW Spain) during four occasions over a tidal cycle. The objective was to study the exchange of dissolved and particulate Cd, Cu, Pb and Zn and particulate Al, Fe and Si between the ria and the adjacent coastal waters. This study provides the first extensive dataset on dissolved and particulate metal concentrations in the water column of a Galician ria. Typical concentrations of dissolved Cd (96 ± 31 pM), Cu (8 ± 4 nM), Pb (270 ± 170 pM) and Zn (21 ± 10 nM) were similar than in other European Atlantic shelf and coastal waters. The fraction of metals in the particulate phase followed the trend: Pb > Cu Zn > Cd. The outgoing water from the ria was enriched in dissolved and particulate Cu, Pb and Zn compared with incoming waters, whereas Cd concentrations were similar for both waters. The suspended particulate matter was composed of a mixture of marine and continental material. The latter end-member was found to arise from the metal-rich ria bed sediments, which is diluted by the dominant metal-poor marine end-member. The net output flux of Cu from the channel is balanced by the freshwater inputs to the ria, and the net Zn flux gave a positive output to coastal waters. For Pb, the net flux to the coastal waters is less than that input from the rivers, as a result of its particle reactivity and deposition in sediments. On the contrary, a net input flux of dissolved Cd from coastal waters was observed, highlighting the oceanic source of this metal in the Galician rias. Results from the budget calculations are in agreement with the differential geochemical behavior of these elements in coastal waters.     

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。     

Trace metals in seawater and copepods in the ocean outfall area off the northern Taiwan coast

The distribution, partitioning and concentrations of trace metals (Cd, Cr, Cu, Fe, Mn, Pb and Zn) in seawater, including dissolved and particulate phases, and in copepods in the ocean outfall area off the northern coast of Taiwan were investigated. Normalization of metal concentrations to the background metal concentration to yield relative enrichment factors (EF), which were used to evaluate the contamination of dissolved and particulate trace metals in seawater around the ocean outfall. The EF results indicated that the outfall area was significantly contaminated by dissolved Fe and Zn, and by particulate Fe, Cr, Cu, Pb and Zn. In addition, most trace metals were chiefly in the particulate phase. The average percentage of total metal concentrations (dissolved plus particulate phases) bound by suspended particulate matter followed the sequence Al(95%) = Mn(95%) > Pb(88%) > Cu(86%) > Fe(72%) > Zn(32%) > Cr(17.5%) > Cd(3.4%). Therefore, metal contamination is better evaluated in solid phase than in the dissolved phase. The concentration ranges of trace metals in the copepods, Temora turbinata, Oncaea venusta and Euchaeta rimana, near the outfall were: Cd, 0.23-1.81 microg g(-1); Cr, 16.5-195 microg g(-1); Cu, 14-160 microg g(-1); Fe, 256-7255 microg g(-1); Mn, 5.5-80.8 microg g(-1); Pb, 2.6-56.2 microg g(-1); Zn, 132-3891 microg g(-1); and Al, 0.21-1.13%. Aluminum, and probably Fe, seemed to be the major elements in copepods. The concentrations of trace metals in copepods, especially Temora turbinata, near the outfall were generally higher than those obtained in the background station. The mean increase in bioconcentration factor of metals in copepods ranged from 4 to 7 and followed the sequence Al(6.4) > Cu(6.2) > Fe(6.0) > Zn(5.7) > Pb(5.6) > Cr(5.5) > Cd(5.1) > Mn(4.7). Therefore, marine copepods in the waters of northern Taiwan can accumulate trace metals over background concentrations and act as contamination indicators.     

Fluxes and behavior of radium isotopes, barium, and uranium in seven Southeastern US rivers and estuaries

This paper demonstrates the importance of advective transport of water through permeable estuarine and salt marsh sediments. This transport delivers significant quantities of radium and barium to the coastal ocean; and, in some cases may remove significant quantities of uranium. These conclusions are based on repeated analyses of seven river–estuarine systems from North Carolina to Florida. Fluxes of radium and barium from these river systems are shown to be inadequate to balance the dissolved inventories of these elements in the South Atlantic Bight. The strong interactions that occur between surface and subsurface waters as these rivers encounter coastal marshes lead us to consider these river mouths as marsh-dominated in terms of their chemical fluxes to the ocean. Such interactions between the river and coastal marsh must be considered when estimating fluxes of material between the land and ocean.     

长江与黄河沉积物元素组成及地质背景

长江与黄河表层沉积物常量及微量元素组成特征明显不同。长江相对富Ｋ、Ｆｅ、Ａｌ等常量元素及绝大多数微量元素,且元素含量变化大;而黄河相对富Ｃａ、Ｎａ、Ｓｒ、Ｂａ、Ｔｈ、Ｚｒ、Ｈｆ等少数元素,元素含量变化较小;长江流域广泛分布的中酸性岩浆岩及复杂的源岩与强烈的化学风化作用决定了长江沉积物的特征元素组成及元素含量变化大的特点;而黄土高原的黄土化学成分与强烈的物理风化作用决定了黄河沉积物的特征元素组成。Ｃｕ、Ｚｎ、Ｓｃ、Ｔｉ、Ｆｅ、Ｖ、Ｎｉ、Ｃｒ、Ｃｏ、Ｂｅ、Ｌｉ等元素可较好地用来区分长江与黄河沉积物,以探索长江与黄河的入海物质在海域中的混合及扩散问题     

晚第四纪南海北部陆坡沉积物常量元素比值对气候变冷事件的指示意义

南海北部陆坡柱状沉积物的常量元素统计分析表明, 沉积物中的Ti、Al、Fe、K、Mn、Mg代表了陆源元素组合;而消除粒度效应的陆源元素比值Al/Ti、Fe/Ti和K/Ti等的变化曲线与浮游有孔虫氧同位素曲线对比表明, 在气候变冷事件(Heinrich事件、Younger Dryas事件、PME斜室普林虫低值等事件)期间, 陆源常量元素比值明显降低。这一对应特征, 一方面体现了气候变冷事件的发生对陆源区化学风化强度的制约, 另一方面也说明与指示长时间尺度气候相似, 陆源元素比值对短时间尺度的气候变化也具有明显的指示作用。     

Major- and trace-element composition of suspended matter in the north-east gulf of Alaska: Relationships with major sources

Seasonal variations of the distributions and chemical compositions of suspended particulate matter in the north-east Gulf of Alaska were studied during 1975–1976. Selected samples were analyzed for total suspended matter by gravimetry; particulate C and N by dry combustion gas chromatography; and particulate Al, Si, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu and Zn by thin-film X-ray secondary emission spectrometry. The results showed that suspended material from the Copper River and the coastal streams which drain the Bering, Guyot, and Malaspina glaciers was carried westward along the coast and deposited in nearshore environments. However, near Kayak Island, significant quantities of suspended material of terrestrial origin were deflected to the south-west, past the edge of the outer shelf, by an anticyclonic gyre.The distribution patterns of the major and trace elements in the particulate matter and their elemental ratios with aluminum indicated that: K, Ti, Mn and Fe were primarily associated with aluminosilicate material and C and N with organic material in all samples; and Si, Ca, Cr, Ni, Cu and Zn were primarily associated with aluminosilicate material in near-shore surface and near-bottom samples and with organic material in offshore surface samples. Only C, N, Ca, Cú and Zn showed significant seasonal variations which appeared to be related to biological production of organic matter.     

Chemical Fluxes of Asian Rivers into Oceans and their Controlling Factors

Chemical fluxes of Asian rivers into oceans bear different regional variations. Three zones are characteristic of distinct dissolved sediment loads and yields and ionic concentration.Rivers into oceans in China play an important role in Asia because of their different chemical fluxes, among which those draining the Loess Plateau have high ionic concentration, low water discharges and dissolved sediment loads and yields.Climate, vegetation, soil and strata lithology, chemical weathering intensity and tectonic activity dominate chemical fluxes of Asian rivers into oceans, and different factors have different effects on the chemical fluxes of separate regional rivers. Rising of the Tibet Plateau also exerts an important influence on chemical compositions of rivers originating from it.     

长江干流悬浮物中元素相态组成与环境指示

三峡水库蓄水后长江中下游干流和水库内悬浮物地球化学组成如何变化是一个重要科学问题。相态分析表明,在长江重庆至南通段干流悬浮沉积物中,不同元素在酸不溶相和酸溶相所占比例不同,且存在一定的区域变化,Ca和Mg在酸溶相中比例相当高,而Al、Fe、K、Na等元素主要赋存于酸不溶相中。长江悬浮沉积物元素组成的空间变化特征主要受流域风化物质的来源、风化程度和水动力环境控制。重金属元素组成研究显示,在三峡库区及下游地区由于受人类活动影响,Pb、Zn、Co、Cu等在悬浮沉积物中呈现明显的累积趋势。三峡水库内沉积动力环境的不均一性导致水体中元素组成的垂向变化。     

南海铁锰结核(壳)的元素地球化学研究

本文利用南海11个铁锰结核(壳)样品的化学分析资料,研究了铁锰结核(壳)中Fe,Mn,Cu,Co,Ni,Pb,Zn,Cr,K,Na,Ca,Mg,Si,P,Al,Ti,Sr,Ba及∑REE的元素地球化学特征。结果表明:(1)铁锰结核(壳)以高Fe,∑REE,低Mn,Cu,Co,Ni等元素为主要特征;(2)铁锰结核(壳)中Fe,Mn间无明显相关,而Fe与∑REE,∑Ce,∑Y呈弱的正相关,Mn与∑REE,∑Ce,∑Y呈明显的正相关,结壳中Fe,Mn与Si,Al,Cu Co Ni呈负相关;(3)结核(壳)中Mn/Fe与Cu/Ni,Ce/La呈负相关,Mn/Fe主要受Mn控制;(4)结核(壳)中Fe,∑REE等元素主要来自南海陆源中酸性岩类的风化、淋滤和沉积。     

南沙群岛珊湖礁潟湖垂直沉降颗粒物中主要元素的生物地球化学过程研究

本文首次报道用沉积物捕捉器（ＳＴ）研究南沙群岛珊瑚礁湖沉降颗粒物中主要元素垂直通量、垂直转移形态、再循环过程及垂直通量与表层海水温度的关系。结果显示,作为生物化学沉积标志的Ｃａ、Ｍｇ具有最高的垂直通量,达１．４和０．１ｇ／（ｍ２·ｄ）以上,作为生物富集标志的Ｂｒ、Ⅰ也有较高的垂直转移量;垂直转移形态的研究表明Ｎａ、Ｋ、Ｃａ、Ｍｇ、Ｓｒ主要以碳酸盐结合态向海底转移,其中Ｃａ、Ｍｇ、Ｓｒ占９９％以上,Ｆｅ、Ｉ、Ｂａ主要以铁锰氧化物结合态向海底输送,在垂直沉降颗粒物到达海底后,有相当部分的主要元素可再循环进入水体中,Ｂｒ、Ｉ、Ｋ、Ａｌ的绝大部分进入再循环,Ｍｇ、Ｎａ、Ｃｌ有一半左右进入再循环,Ｃａ、Ｓｒ、Ｂａ、Ｆｅ大部分被埋葬;Ｎａ等９种元素的垂直转移量随ＳＳＴ呈指数降低响应,对ＳＳＴ的敏感性Ｆｅ＞Ｂｒ＞Ｓｒ＞Ｃａ＞Ｎａ＞Ｃｌ＞Ｍｇ＞Ｉ＞Ａｌ,这再一次验证了ＣａＣＯ３随温度升高,其溶解度降低、化学沉积量增加这一自然界的普遍规律,表明在珊瑚礁海水的垂直沉降颗粒物中主要元素是作为珊瑚的重要成分与ＣａＣＯ３一同被沉积下来的,ＣａＣＯ３起到稀释剂的作用。     

Trace metal concentrations in the Ross Sea and their relationship with nutrients and phytoplankton growth

Dissolved and particulate trace metal concentrations (dissolved Fe, Zn, Cd, Co, Cu and Ni; particulate Fe, Mn and Al) were measured along two transects in the Ross Sea during austral summer of 1990. Total Fe concentrations in southern Ross Sea and inshore waters were elevated >3.5 times that of northern waters. Dissolved Zn, Cd and Co concentrations were lower by factors of 4.5, 3.5 and 1.6 in southern surface waters relative to northern waters. Dissolved Cu and Ni concentrations were similar in both areas. Elevated Fe concentrations coincided with areas of increased productivity, phytoplankton biomass and nutrient drawdown, indicating that Fe is an important factor controlling the location of phytoplankton blooms in the Ross Sea. Particulate concentrations of Fe, Mn and Al indicate two possible sources of iron to the Ross Sea, resuspension of continental shelf sediments and iron incorporated in annual sea ice and released with meltwaters.     

Seasonality of particle-associated trace element fluxes in the deep northeast Atlantic Ocean

In the framework of the German contribution to the Joint Global Ocean Flux Study (JGOFS), deep-water fluxes of particle-associated trace elements were measured in the northeast Atlantic Ocean. The sinking particles were collected almost continuously from 1992 to 1996 at three time-series stations, L1 (33°N/22°W), L2 (47°N/20°W), and L3 (54°N/21°W), using sediment traps. The focus of the present study is the temporal variability of the particle-associated elemental fluxes of Al, Ca, Cd, Co, Cu, Fe, Mn, Ni, P, Pb, Ti, V, and Zn at a depth of 2000 m.A clear seasonality of the fluxes that persisted for several years was documented for the southernmost station (L1) at stable oligotrophic conditions in the area of the North Atlantic Subtropical Gyre East (NASTE). At L2 and L3, an episodic nature of the elemental fluxes was determined. Mesoscale eddies are known to frequently cause temporal and spatial variability in the flux of biogenic components in that area. These events modified the simple seasonal pattern controlled by the annual cycle at L2, in the North Atlantic Drift Region (NADR), and at L3, which was influenced by the Atlantic Arctic province (ARCT). All stations were characterized by an additional episodic lithogenic atmospheric supply reaching the deep sea.The integrated annual fluxes during the multi-year study revealed similar flux magnitudes for lithogenic elements (Al, Co, Fe, Ti, and V) at L2 and L3 and roughly twofold fluxes at L1. Biogenic elements (Cd, P, and Zn) showed the opposite trend, i.e., two to fourfold higher values at L2 and L3 than at L1. For Mn, Ni, and Cu, the spatial differences were smaller, perhaps because of the intermediate behavior, between lithogenic and biogenic, of these elements. Similarly, among the three study sites, there were no noticeable differences in the total annual flux of Pb.The respective lithogenic fractions of the deep-sea fluxes of Cd, Co, Cu, Mn, Ni, V, and Zn were subtracted based on the amount of Al, with the average composition of the continental crust as reference. This procedure allowed estimation of the labile trace element fraction (TE_exc) of the particles, i.e., TE taken up or scavenged during particle production and sedimentation. The ratios of TE_exc/P clearly demonstrated an enrichment of TE over labile P from biogenic surface material to the deep sea for Zn (factor 4–6), Mn (12–27), Ni (3–5), and Cu (9–25); an intermediate status for Co (0.5–2.2); and depletion for Cd vs. P (0.2–0.4). Surprisingly, the recycling behavior of excess Co was found to be similar to that of P. Hence, Co_exc behaved like a biogenic element; this is in contrast to total Co, which is dominated by the refractory lithogenic fraction.Moreover, it is argued that these excess elemental fluxes caused a loss of the dissolved elements in upper waters, since their transport reaches the deep-sea waters at 2000 m, a depth far below of deep-winter mixing and upwelling. The annual amount of excess TE exported from surface waters was estimated to be 1.3×10⁹ mol Zn y^?1, 4.4×10⁹ mol Mn y^?1, 4.9×10⁸ mol Ni y^?1, 2.2×10⁷ mol Cd y^?1, 7.4×10⁸ mol Cu y^?1, and 2.7×10⁷ mol Co y^?1 for the whole North Atlantic Ocean. Important primary sources that could replenish these losses are the aeolian and fluvial supply processes.