Arsenic in sediments of the North Atlantic Ocean and the Eastern Mediterranean Sea

Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ～ 11 · 10^?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (～8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ～ 2 · 10^?4), but As/Fe ratios increase to ～ 13 · 10^?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ～ 20?50 · 10^?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (～ 6 μg cm^?2 10^?3 yr^?1) at sediments (～ 120 μg cm^?2 10^?3 yr^?1) at rate sufficient to balance river input input (～3 · 10¹⁰ g yr^?1). These estimates give an oceanic residence time for arsenic of 1–2 · 10⁵ yr.     

Particulate aluminium fluxes in the eastern Atlantic

The atmospheric, primary down-column and sedimentary fluxes of particulate aluminium (Al_p) have been calculated for a number of regions in the Atlantic Ocean.The vertical down-column flux of Al_p from Atlantic surface waters exhibits a strong geographical variation, and its magnitude is influenced by supply mechanisms, which control the surface Al_p concentrations, and primary production, which affects the rate of down-column transport. Overall, the down-column transport of Al_p is greatest in the marginal regions of the Atlantic. In the eastern margins the highest surface water concentrations are found in the region lying between ～30°N and ～10°N, i.e. under the general path of the northeast trades. In this region there is excellent agreement between the dry (i.e. 1 cm^?1 s^?1 deposition velocity) atmospheric flux (～80 000 ng Al_p cm^?2 y^?1), the primary vertical down-column flux ($\text{? 70 000}\text{ng Al}{}_{\mathrm{p}}\text{cm}{}^{\mathrm{?2}}\text{y}{}^{\mathrm{?1}}$) and the sediment flux (～90 000 ng Al_p cm^?2 y^?1). In the regions to the north (i.e. ～40°N to ～30°N) and to the south (i.e. ～10°N to ～5°S) the primary down-column Al_p flux decreases to an average of ～19 000 μg cm^?2 y^?1, which makes a direct maximum contribution of ～20% of the sediment Al_p requirement. In the open-ocean South Atlantic the primary down-column flux of Al_p is ～3300 μg cm^?2 y^?1, this is similar to the dry (i.e. 1 cm^?1 s^?1 deposition velocity) atmospheric flux, and contributes ～20% of the Al_p required by the underlying deep-sea sediment.     

Nutrient exchange across the sediment-water interface in the Potomac River estuary

The flux of ammonia, phosphate, silica and radon-222 from Potomac tidal river and estuary sediments is controlled by processes occurring at the sediment-water interface and within surficial sediment. Calculated diffusive fluxes range between 0·6 and 6·5 mmol m^?2 day^?1 for ammonia, 0·020 and 0·30 mmol m^?2 day^?1 for phosphate, and 1·3 and 3·8 mmol m^?2 day^?1 for silica. Measured in situ fluxes range between 1 and 21 mmol m^?2 day^?1 for ammonia, 0·1 and 2·0 mmol m^?2 day^?1 for phosphate, and 2 and 19 mmol m^?2 day^?1 for silica. The ratio of in situ fluxes to diffusive fluxes (flux enhancement) varied between 1·6 and 5·2 in the tidal river, between 2·0 and 20 in the transition zone, and from 1·3 to 5·1 in the lower estuary. The large flux enhancements from transition zone sediments are attributed to macrofaunal irrigation. Nutrient flux enhancements are correlated with radon flux enhancements, suggesting that fluxes may originate from a common region and that nutrients are regenerated within the upper 10–20 cm of the sediment column.The low fluxes of phosphate from tidal viver sediments reflect the control benthic sediment exerts on phosphorus through sorption by sedimentary iron oxyhydroxides. In the tidal river, benthic fluxes of ammonia and phosphate equal one-half and one-third of the nutrient input of the Blue Plains sewage treatment plant. In the tidal Potomac River, benthic sediment regeneration supplies a significant fraction of the nutrients utilized by primary producers in the water column during the summer months.     

The partitioning of organic carbon fluxes and sedimentary organic matter decomposition rates in the ocean

The partitioning of annual organic carbon fluxes from five stations located in the vicinity of the Pacific-Antarctic Ridge and the Peru continental margin suggests that 35–85% of the total near-bottom organic carbon flux is utilized at or near the sediment-water interface. These estimates have large uncertainties, but illustrate that assessments of organic carbon utilization can be made by several stepwise approaches which are generally applicable to a wide spectrum of marine environments.In one approach, the mineralization of organic carbon from the sediments was predicted from both sedimentary organic carbon and pore water nutrient profiles with comparable results. Neglecting sediment mixing, the rate constants of the anoxic sediments off Peru range from 0.1 × 10^?3 to 4 × 10^?3 y^?1, and rate constants derived for oxic SW Pacific sediments range from 3 × 10^?4 to 7 × 10^?4 y^?1. As with other values reported for sulfate reducing sediments by Toth and Lerman (1977) and for oxic central Pacific sediments by Müller and Mangini (1980), log-log plots of rate constants vs. sedimentation rate define two parallel linear relationships for oxic and anoxic sediments, respectively. The apparently enhanced rates for oxic environments may result from large benthic organisms which redistribute a portion of the available detritus and in doing so convert it into more easily accessible and metabolizable organic matter. In low-oxygen environments, bottom feeders and infauna are less abundant and more likely to irrigate rapidly accumulating sediments.     

210Pb in a tropical coastal lagoon sediment core

Excess ²¹⁰Pb in a core from a Mexican Coastal Lagoon, which has no connection with the sea shows a small but measurable decay over the length of the core, when different approaches were compared (excess and corrected ²¹⁰Pb activity with depth, total and inorganic cumulative weights) significant differences in the values for the sedimentation rate are obtained. The best coefficient correlation was calculated when corrected ²¹⁰Pb activity for the uneven distribution of organic matter and cumulative inorganic weight is considered ($\text{ω}\text{= 0·93 cm yr}{}^{\mathrm{?1}}$, R = ?0·86; ω = 0·51 cm yr^?1 for the top 13 cm, R = ?0·90 and 1·52 cm yr^?1 for the interval 14–46 with R = ?0·96).Time frames in the sedimentary column were in agreement between the ²¹⁰Pb calculated time and the appearance of shells fragments probably associated with the disturbances caused by the 1961 hurricane Tara.The surface accumulation rate is equivalent to a mean deposition of 262·5 g m^?2 yr^?1 or organic matter which is minor but comparable to some salt marshes of United States.     

The transport of bacteria in the sediments of a temperate marsh

The number of bacteria in sediments, interstitial water and overlying tidal water of an oligohaline marsh system are about 10⁹, 10⁶ and 10⁶ cells cm^?3, respectively. Average cell size in the overlying water (about 0·06 μm³), is much smaller than that in sediments and interstitial water (about 0·18 μm³). Most bacterial cells in sediments are bound to sediment particles and less than 1% of the cells were displaced by percolating water through sediment columns. Concentration of bacteria in flooding tidal waters is generally higher than that in ebbing waters. Movement of bacterial biomass does not appear to be a significant mechanism of particulate organic transport in marsh sediments and marsh sediments do not appear to be a source of suspended bacteria for estuaries.     

Intra-annual variability of extremely rapid sedimentation onto Gardar Drift in the northern North Atlantic

North Atlantic sediment drifts are valuable archives for paleoceanographic reconstructions spanning various timescales. However, the short-term dynamics of such systems are poorly known, and this impinges on our ability to quantitatively reconstruct past change. Here we describe a high-resolution 319-day time-series of hydrodynamics and near-bottom (4 m) particulate matter flux variability at a 2600 m deep site with an extremely high sediment accumulation rate on the southern Gardar Drift in the North Atlantic. We compare our findings with the actual deposits at the site. The total annual particle flux amounted to ～360 g m^?2 yr^?1, varied from ～0.15 to >5.0 g m^?2 day^?1 and displayed strong seasonal compositional changes, with the highest proportion of fresh biogenic matter arriving after the spring bloom in June and July. Flux variability also depended on the changing input of lithogenic matter that had been (re)suspended for a longer time (decades). Active focussing of material from both sources is required to account for the composition and the magnitude of the total flux, which exceed observations elsewhere by an order of magnitude. The enhanced focussing or increased delivery appeared to be positively related to current velocity. The intercepted annual particle flux accounted for only 60% of the sediment accumulation rate of 600±20 g m^?2 yr^?1 (0.20±0.07 cm yr^?1), indicating higher intra- and inter-annual variability of both the biogenic and lithogenic fluxes and/or advection of additional sediment closer to the seafloor (i.e. <4 m). This temporal variability in the composition and amount of material deposited highlights intra-annual changes in the flux of lithogenic material, but also underscores the importance of (reworked) sediment focussing and seasonality of the biogenic flux. All should be taken into account in the interpretation of the paleorecord from such depositional settings.     

A sediment budget for the Choptank River estuary in Maryland,U.S.A.

A sediment budget for the Choptank River, one of the three largest estuaries on the eastern shore of Chesapeake Bay, was developed from measurements of sediment carried in upland runoff, shore erosion, sedimentation, and levels of suspended sediments in estuarine waters. Shore erosion was the major source of sediment (340 × 10⁶ kg y^?1), contributing seven times more sediment than upland runoff. Low relief, the rural character of the Coastal Plain drainage basin, and the susceptibility of poorly consolidated shoreline materials to erosion contributed to the dominance of shore erosion over runoff as a sediment source. Box modelling indicated a net annual flux (14–44 × 10⁶ kg y^?1) of sediment from the Choptank River to Chesapeake Bay. A mass balance estimate of sedimentation, calculated as the difference between total inputs and loss at the mouth of the estuary, (350 × 10⁶ kg y^?1) agreed well with an estimate based on ²¹⁰Pb profiles (340 × 10⁶ kg y^?1) measured along the longitudinal axis of the estuary. Lead-210 sedimentation rates correspond to accumulation rates of 1·5–7·9 mm y^?1.     

A carbon budget for the Barents Sea

The first carbon budget constructed for the Barents Sea to study the fluxes of carbon into, out of, and within the region is presented. The budget is based on modelled volume flows, measured dissolved inorganic carbon (DIC) concentration, and literature values for dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations. The results of the budget show that ～5600±660×10⁶ t C yr^?1 is exchanged through the boundaries of the Barents Sea. If a 40% uncertainty in the volume flows is included in the error calculation it resulted in a total uncertainty of ±1600×10⁶ t C yr^?1. The largest part of the total budget flux consists of DIC advection (～95% of the inflow and ～97% of the outflow). The other sources and sinks are, in order of importance, advection of organic carbon (DOC+POC; ～3% of both in- and outflow), total uptake of atmospheric CO₂ (～1% of the inflow), river and land sources (～0.2% of the inflow), and burial of organic carbon in the sediments (～0.2% of the outflow). The Barents Sea is a net exporter of carbon to the Arctic Ocean; the net DIC export is ～2500±660×10⁶ t C yr^?1 of which ～1700±650×10⁶ t C yr^?1 (～70%) is in subsurface water masses and thus sequestered from the atmosphere. The net total organic carbon export to the Arctic Ocean is ～80±20×10⁶ t C yr^?1. Shelf pumping in the Barents Sea results in an uptake of ～22±11×10⁶ t C yr^?1 from the atmosphere which is exported out of the area in the dense modified Atlantic Waters. The main part of this carbon was channelled through export production (～16±10×10⁶ t C yr^?1).     

Seasonal distribution of bacteria in salt marsh sediments in North Carolina

The number and size of bacteria at four depths (0–1, 5–6, 10–11 and 20–21 cm) in a North Carolina salt marsh were minotored by direct counts for 13 months. The number of bacteria reached a maximum of about 1·4 × 10¹⁰ cells cm^?3 at the sediment surface in October, corresponding to the period of Spartina alterniflora die-back. Cell numbers were lowest and most consistent throughout the year at the 20 cm depth of sediment. Cell volumes averaged 0·2 μm³ at the marsh surface and decreased with depth. Mean standing crop of bacteria to a depth of 20 cm of sediment was about 14 g bacterial carbon m^?2. In surface sediments bacteria contribute up to 15% and algae up to 10% of total living microbial biomass as estimated by adenosine triphosphate (ATP). Bacteria were the major biomass component at sediment depths of 5, 10 and 20 cm. At all depths the microbial community contributes < 4% total organic carbon and < 8% of total nitrogen.     

Low calcification rates and calcium carbonate production in Porites panamensis at its northernmost geographic distribution

Porites panamensis is a hermatypic coral present in the eastern Pacific Ocean. Skeletal growth parameters have been reported, but studies of the relationship between annual calcification rates and environmental controls are scarce. In this study, we investigated three aspects of the annual calcification rates of P. panamensis: growth parameters among three P. panamensis populations; the sea surface temperature as a calcification rate control spanning a latitudinal gradient; and calcium carbonate production among three sites. Growth parameters varied among the sites due to the colony growth form. Massive colonies in the north showed a higher calcification rate than encrusting colonies in the south (mean: 1.22–0.49 g CaCO₃ · cm^?2 · yr^?1), where variations in calcification rates were related to growth rate (0.91–0.38 cm · yr^?1) rather than to skeletal density differences (overall mean ± SD, 1.31 ± 0.04 g CaCO₃ · cm^?3). Our results showed a positive linear relationship between annual calcification rates and sea surface temperatures within these P. panamensis populations. Differences were related to distinct oceanographic environments (within and at the entrance of the Gulf of California) with different sea surface temperature regimes and other chemical properties. Different populations calcified under different environmental conditions. Calcium carbonate production was dependent upon the calcification rate and coral cover and so carbonate production was higher in the north (coral cover 12%) than in the south (coral cover 3.5). Thus, the studied sites showed low calcium carbonate production (0.25–0.43 kg CaCO₃ · m^?2 · yr^?1). Our results showed reduced calcification rates, regional temperature regime control over calcification rates, different growth forms, low coral cover and low calcium carbonate production rates in P. panamensis.     

226Ra and 228Ra in the mixing zones of the Pee Dee River-Winyah Bay,Yangtze River and Delaware Bay Estuaries

²²⁶Ra and ²²⁸Ra have non-conservative excess concentrations in the mixing zones of the Pee Dee River-Winyah Bay estuary, the Yangtze River estuary, and the Delaware Bay estuary. Laboratory experiments, using Pee Dee River sediment, indicate desorption of ²²⁶Ra to increase with increasing salinities up to 20‰. In Winyah Bay desorption from river-borne sediments could contribute almost all of the increases for both isotopes. Desorption adds only a portion of the excess ²²⁸Ra measured in the Yangtse River and adjacent Shelf waters and Delaware Bay. In the Yangtze River the mixing zone extends over a considerable portion of the Continental Shelf where ²²⁸Ra is added to the water column by diffusion from bottom sediments, while ²²⁶Ra concentrations decrease from dilution. Diffusion of ²²⁸Ra from bottom sediments in Delaware Bay primarily occurs in the upper part of the bay (< 22‰ water) where fine grained sediments predominate. A diffusive flux for ²²⁸Ra of 0·33 dpm cm^?2 year was determined for Delaware Bay.     

Early diagenetic redistribution and burial of phosphorus in the sediments of the southwestern East Sea (Japan Sea)

This study was carried out in order to understand the early diagenetic redistribution of phosphorus and relevant mass balance in the sediments of the East Sea. In two cruises during May 1993 and October 1995, 11 box cores were collected in the southwestern part of the East Sea. Dissolved phosphorus and iron were analyzed in the porewater from the cores. Sediment samples were analyzed for solid-phase P species and solid-phase Fe oxyhydroxide by sequential extraction.Phosphorus speciation results show that organic P is the major chemical form of phosphorus in young sediments within the upper 50 cm of sediment. However, the authigenic fraction of total P increases with depth, indicating the precipitation of carbonate fluorapatite (CFA) in the sediments. The authigenic CFA (Ca₅(PO₄)_2.6(CO₃)_0.4F) was formed and buried at rates of 11–110 μmol cm⁻² kyr⁻¹. The main source of dissolved phosphorus for the precipitation of CFA is organic P. Dissolved phosphorus, released from the decomposition of organic P, diffuses upward to return to bottom water, or is sorbed to iron oxides in the oxidized sediments. As sedimentation proceeds, the iron oxide-bound P is released in the reduced layer and enters the dissolved phase, which contributes P to the formation of CFA in addition to that contributed by the organic P.The burial flux of reactive P (iron oxide-bound P+authigenic P+organic P) is 0.09–0.53 g P m⁻² yr⁻¹ that accounts for 18–58% of the reactive P arriving at the sediment/water interface. The burial flux of reactive P is high in the upper and lower continental margin sediment. The burial flux of reactive P in the Ulleung Basin sediment is less than those in the continental margin sites by a factor of 6, indicating that the reactive P burial flux is mainly dependent on sedimentation rate.     

The behavior of iron,manganese and silicon in the Peconic River estuary,New York

The behavior of dissolved and particulate iron and manganese and dissolved silicon has been studied as a function of chlorinity in the Peconic River estuary, New York. This study sought to identify important geochemical processes in a relatively pristine estuary facing increasing anthropogenic impact.Dissolved iron behaved in the classical non-conservative manner exhibiting removal of nearly 80% at very low chlorinities, while particulate iron increased by a corresponding amount over the same chlorinity range. Dissolved manganese was enriched by up to 200% over its predicted concentration at low and intermediate chlorinities by desorption from suspended particulates and by a probable benthic flux. Dissolved silicon was enriched by up to 100% at low and intermediate chlorinities also from a probable benthic flux. These fluxes were estimated to be 5 μg cm^?2 day^?1 for dissolved manganese and 70 μg cm^?2 day^?1 for dissolved silicon.The quantity of both particulate iron and manganese increased at high chlorinities due to an influx of suspended inorganic particulates. In the intermediate to high chlorinity region, oxidation of sediment-derived manganese is believed to contribute to the observed increase in particulate manganese.Total iron was essentially conservative throughout most of the estuary, while total manganese was non-conservative presumably due to extensive remobilization of dissolved manganese from the sediments.     

Sediment accumulation rates along the inner eastern Brazilian continental shelf

Box cores were collected close to river mouths along the eastern Brazilian shelf at water depths of 10–30 m. One core was taken from more than 1000 m depth at the shelf slope. ²¹⁰Pb and ²²⁶Ra activities were measured to establish sediment accumulation rates. Seven of the 10 cores exhibited an exponential decrease with depth of excess ²¹⁰Pb activities. The sediments from the sheltered Sudeste Channel off Caravelas revealed the highest sediment accumulation rate of 0.81 cm yr⁻¹. The sediments at the shelf slope seaward of the Rio Doce revealed the lowest accumulation rate of 0.13 cm yr⁻¹. Sediment accumulation rates increased towards the Caravelas Bank. Current patterns and the morphology of the seabed favor sediment deposition in this area.     

Seasonal dynamics of elemental sulfur in two coastal sediments

A spectrophotometric method for elemental sulfur (S⁰) analysis without interference from other reduced sulfur compounds was adapted for the use in reducing sediments. The S⁰ distribution in two coastal sediments was studied regularly from summer to winter and compared to factors regulating the S⁰ accumulation, such as redox potentials, the rate of bacterial sulfide production and the general sulfur chemistry. Dense coatings of sulfur bacteria developed on the sediment surface of a sulfuretum which had an S⁰ concentration of up to 41 μmol S cm^?3. The 2·5-mm thick bacterial coating contained 40% of all S⁰ in the sediment. A more typical marine sediment with a few cm thick oxidized surface layer had an S⁰ maximum of 1–3 μmol S cm^?3 at 2–4 cm depth. The S⁰ maximum in both sediments increased from summer to winter as the sediments gradually became more oxidized. The deeper layers maintained a low S⁰ concentration. Most of the S⁰ in the upper few mm of a laboratory sulfuretum was present inside sulfur bacteria and actively migrated up and down with the bacteria depending upon the changing light and oxygen conditions.     

Carbon dioxide emission and carbon accumulation in coastal wetlands

Direct measurements of CO₂ fluxes were made in salt, brackish and freshwater marshes and parallel adjacent open water areas in Barataria Basin, Louisiana. Vertical flux density was determined by monitoring the accumulation of CO₂ in aluminum chambers placed over the water or sediment surfaces. Annual CO₂ fluxes were 418, 180 and 618 g Cm^?2 from the salt, brackish and freshwater marsh, respectively. Water bodies adjacent to the marsh evolved 103, 54 and 242 g CO₂-Cm^?2yr^?1 to the atmosphere from saline, brackish and freshwater lakes, respectively. The role these marshes play in serving as a major carbon sink was determined from the carbon content of the sediment, vertical accretion rates and the bulk density of the sediment. Accretion rates were calculated from the depth in the sediment of the 1963 horizon, the year of peak ¹³⁷Cs fallout. Net carbon accumulation was essentially the same in all three marshes; 183, 296 and 224 g Cm^?2yr^?1 from the salt, brackish and fresh marsh, respectively. Data presented suggest a limited net export of carbon from these coastal marshes. A large percentage of fixed carbon remained on the marsh, being immobilized in accretionary processes or lost to the atmosphere as CO₂.     

Fine-grained sediment budget on the continental margin of the Bay of Biscay

Under present-day conditions, rivers are the main source of fine sediments dispersed to the Bay of Biscay. They deliver about 2.5×10⁶ t yr⁻¹ of continental fine sediments, 60% of which is derived from the Gironde estuary. Of this flux, 65% is believed stored on the shelf. Two kinds of mud fields can be found in the Bay of Biscay: coastal mud and shelf mud belts. The total mass of fine sediments stored during the past 2000 years is 3.2×10⁹ t. Consequently, about 0.9×10⁶ t yr⁻¹ could reach the shelf edge and eventually the open sea. From this amount of displaced material and the deposition surface areas, an evaluation of sediment fluxes across the margin during the late Holocene period is discussed. This evaluation is compared with results obtained from ECOsystéme du canyon du cap-FERret (ECOFER) data from sediment traps and surficial box cores.     

A sulfur budget for the Black Sea anoxic zone

A budget for the sulfur cycle in the Black Sea is proposed which incorporates specific biogeochemical process rates. The average sulfide production in the water column is estimated to be 30–50 Tg yr⁻¹, occurring essentially in the layer between 500 and 2000 m. About 3.2–5.2 Tg sulfide yr⁻¹ form during sulfate reduction in surface sediments of the anoxic zone. Total sulfur burial in anoxic sediments of 1 Tg yr⁻¹ consists of 10–70% (ca. 40–50% is the average) water column formed (syngenetic) component, the rest being diagenetic pyrite. As a maximum, between 3 and 5 Tg yr⁻¹ contribute sulfide to the bottom water or diffuse downward in the sediment. About 20–50 Tg yr⁻¹ sulfide is oxidized mostly at the chemocline and about 10–20% of this amount (4.4–9.2 Tg yr⁻¹) below the chemocline by the oxygen of the Lower Bosphorus Current. A model simulating the vertical distribution of sulfide in the Black Sea water column shows net consumption in the upper layers down to ca. 500 m, essentially due to oxidation at the chemocline, and net production down to the bottom. On the basis of the calculated budget anoxic conditions in the Black Sea are sustained by the balance between sulfide production in the anoxic water column and oxidation at the chemocline. On average the residence time of sulfide in the anoxic zone is about 90–150 yr, comparable to the water exchange time between oxic and anoxic zones. Hydrophysical control on the sulfur cycle appears to be the main factor regulating the extent of anoxic conditions in the Black Sea water column, rather than rates of biogeochemical processes.     

Incorporation rate measurements of <Superscript>10</Superscript>Be, <Superscript>230</Superscript>Th, <Superscript>231</Superscript>Pa,and <Superscript>239,240</Superscript>Pu radionuclides in manganese crust in the Pacific Ocean: A search for extraterrestrial material

In order to estimate the deposition rate of extraterrestrial material onto a manganese crust in a search for supernova debris, we analyzed the contents of ¹⁰Be, ²³⁰Th, ²³¹Pa, and ^239,240Pu in a sample of manganese crust collected from the North Pacific Ocean. On the basis of the depth profile of ¹⁰Be, the growth rate of the manganese crust was determined to be 2.3 mm Myr⁻¹. The uptake rates of ¹⁰Be, ²³⁰Th, and ²³¹Pa onto the manganese crust were estimated to be 0.22–0.44%, 0.11–0.73%, and 1.4–4.5%, respectively, as compared to the deposition rates onto the deep-sea sediments near the sampling station, while that for ^239,240Pu was 0.14% as compared to the total inventory of seawater and sediment column. Assuming that sinking particles represent 0.11–4.5% of the uptake rates, the deposition rate of extraterrestrial material onto the manganese crust was estimated to be 2–800 μg cm⁻²Myr⁻¹ according to the uptake of ¹⁰Be onto the manganese crust. Further, our estimate is similar to the value of 9–90 μg cm^{− 2}Myr⁻¹ obtained using the integrated global production rate of ¹⁰Be and the deposition rate of ¹⁰Be onto the manganese crust.