Silicon Cycle Research Articles

Sponge contribution to the silicon cycle of a diatom‐rich shallow bay

AbstractIn coastal systems, planktonic and benthic silicifiers compete for the pool of dissolved silicon, a nutrient required to make their skeletons. The contribution of planktonic diatoms to the silicon cycle in coastal systems is often well characterized, while that of benthic silicifiers such as sponges has rarely been quantified. Herein, silicon fluxes and stocks are quantified for the sponge fauna in the benthic communities of the Bay of Brest (France). A total of 45 siliceous sponge species living in the Bay account for a silicon standing stock of 1215 tons, while that of diatoms is only 27 tons. The silicon reservoir accumulated as sponge skeletons in the surface sediments of the Bay rises to 1775 tons, while that of diatom skeletons is only 248 tons. These comparatively large stocks of sponge silicon were estimated to cycle two orders of magnitude slower than the diatom stocks. Sponge silicon stocks need years to decades to be renewed, while diatom turnover lasts only days. Although the sponge monitoring over the last 6 yr indicates no major changes of the sponge stocks, our results do not allow us to conclude if the silicon sponge budget of the Bay is at steady state, and potential scenarios are discussed. The findings buttress the idea that sponges and diatoms play contrasting roles in the marine silicon cycle. The budgets of these two major silicon users need to be integrated and their connections revealed, if we aim to improve our understanding of the silicon cycling in coastal ecosystems.

Amorphous silica dissolution kinetics in freshwater environments: Effects of Fe2+ and other solution compositional controls

The availability of dissolved silicon (DSi) exerts an important control on phytoplankton communities in freshwater environments: DSi limitation can shift species dominance to non-siliceous algae and increase the likelihood of harmful algal blooms. The availability of DSi in the water column in turn depends on the dissolution kinetics of amorphous silica (ASi), including diatoms frustules and phytoliths. Here, batch dissolution experiments conducted with diatom frustules from three diatom species and synthetic Aerosil OX 50 confirmed the previously reported non-linear dependence of ASi dissolution rate on the degree of undersaturation of the aqueous solution. At least two first-order dissolution rate constants are therefore required to describe the dissolution kinetics at high (typically, ≥0.55) and low (typically, <0.55) degrees of undersaturation. Our results further showed aqueous ferrous ion (Fe2+), which is ubiquitous in anoxic waters, strongly inhibited ASi dissolution. The inhibition is attributed to the preferential binding of Fe2+ to Q2 groups (i.e., surface silicate groups bonded to the silica lattice via two bridging oxygen) which stabilizes the silica surface. However, further increasing the aqueous Fe2+ concentration likely catalyzes the detachment of Q3 groups (i.e., silicate groups bonded to the silica lattice via three bridging oxygen) from the surface. Overall, our study illustrates the manyfold effects the aqueous solution composition, notably the inhibition effect of Fe2+ under anoxic conditions, has on ASi dissolution. The results help to explain the controversial redox dependence of DSi internal loading from sediments, which is vital to quantitatively understanding silicon (Si) cycling in freshwater systems.

Hyalolithus didymus sp. nov. (Haptophyta): a late Miocene siliceous microfossil from Sicily, Italy

ABSTRACT Siliceous scales observed in an upper Miocene outcrop sample from the Caltanissetta Basin, Sicily, are similar to those of the extant haptophyte Hyalolithus neolepis and the fossil species H. tumescens. The newly discovered scales, examined by light and scanning electron microscopy, are sufficiently different to justify their assignment to H. didymus sp. nov. Like the two previously described species, the scales of H. didymus are elliptical, with a prominent marginal rim and numerous central openings (pores), separated by a submarginal hyaline area. However, the three species can be distinguished by slight (but visually recognizable) differences in the size and number of their central openings (pores). In distal view, the central area of the new species has two mounds, which are smaller and more distinct than in H. neolepis. Unlike the other two species, a swelling on the proximal side (and its corresponding depression on the distal side) has not been seen yet in H. didymus. This finding increases the knowledge of the fossil record of siliceous haptophytes, a poorly known phytoplankton group involved in the biogeochemical silicon cycle.

Benthic silicon cycling in the Arctic Barents Sea: a reaction–transport model study

Abstract. Over recent decades the highest rates of water column warming and sea ice loss across the Arctic Ocean have been observed in the Barents Sea. These physical changes have resulted in rapid ecosystem adjustments, manifesting as a northward migration of temperate phytoplankton species at the expense of silica-based diatoms. These changes will potentially alter the composition of phytodetritus deposited at the seafloor, which acts as a biogeochemical reactor and is pivotal in the recycling of key nutrients, such as silicon (Si). To appreciate the sensitivity of the Barents Sea benthic system to the observed changes in surface primary production, there is a need to better understand this benthic–pelagic coupling. Stable Si isotopic compositions of sediment pore waters and the solid phase from three stations in the Barents Sea reveal a coupling of the iron (Fe) and Si cycles, the contemporaneous dissolution of lithogenic silicate minerals (LSi) alongside biogenic silica (BSi), and the potential for the reprecipitation of dissolved silicic acid (DSi) as authigenic clay minerals (AuSi). However, as reaction rates cannot be quantified from observational data alone, a mechanistic understanding of which factors control these processes is missing. Here, we employ reaction–transport modelling together with observational data to disentangle the reaction pathways controlling the cycling of Si within the seafloor. Processes such as the dissolution of BSi are active on multiple timescales, ranging from weeks to hundreds of years, which we are able to examine through steady state and transient model runs. Steady state simulations show that 60 % to 98 % of the sediment pore water DSi pool may be sourced from the dissolution of LSi, while the isotopic composition is also strongly influenced by the desorption of Si from metal oxides, most likely Fe (oxyhydr)oxides (FeSi), as they reductively dissolve. Further, our model simulations indicate that between 2.9 % and 37 % of the DSi released into sediment pore waters is subsequently removed by a process that has a fractionation factor of approximately −2 ‰, most likely representing reprecipitation as AuSi. These observations are significant as the dissolution of LSi represents a source of new Si to the ocean DSi pool and precipitation of AuSi an additional sink, which could address imbalances in the current regional ocean Si budget. Lastly, transient modelling suggests that at least one-third of the total annual benthic DSi flux could be sourced from the dissolution of more reactive, diatom-derived BSi deposited after the surface water bloom at the marginal ice zone. This benthic–pelagic coupling will be subject to change with the continued northward migration of Atlantic phytoplankton species, the northward retreat of the marginal ice zone and the observed decline in the DSi inventory of the subpolar North Atlantic Ocean over the last 3 decades.

Comparing amorphous silica, short-range-ordered silicates and silicic acid species by FTIR

There is increased interest in the terrestrial silicon cycle in the last decades as its different compounds and species have large implications for ecosystem performance in terms of soil nutrient and water availability, ecosystem productivity as well as ecological aspects such as plant–microbe and plant-animal feedbacks. The currently existing analytical methods are limited. Fourier-transform infrared spectroscopy (FTIR) analysis is suggested being a promising tool to differentiate between the different Si species. We report here on the differentiation of varying Si-species/Si-binding (in synthetic material) using FTIR-analyses. Therefore, we collected FTIR-spectra of five different amorphous silica, Ca-silicate, sodium silicate (all particulate), a water-soluble fraction of amorphous silica and soil affected by volcanic activity and compared their spectra with existing data. A decrease of the internal order of the materials analyzed was indicated by peak broadening of the Si–O–Si absorption band. Peak shifts at this absorption band were induced by larger ions incorporated in the Si–O–Si network. Additionally, short-range ordered aluminosilicates (SROAS) have specific IR absorption bands such as the Si–O–Al band. Hence, SROAS and Si phases containing other ions can be distinguished from pure amorphous Si species using FTIR-analyses.

Stable silicon isotopes uncover a mineralogical control on the benthic silicon cycle in the Arctic Barents Sea

Biogeochemical cycling of silicon (Si) in the Barents Sea is under considerable pressure from physical and chemical changes, including dramatic warming and sea ice retreat, together with a decline in dissolved silicic acid (DSi) concentrations of Atlantic inflow waters since 1990. Associated changes in the community composition of phytoplankton blooms will alter the material comprising the depositional flux, which will subsequently influence recycling processes at and within the seafloor. In this study we assess the predominant controls on the early diagenetic cycling of Si, a key nutrient in marine ecosystems, by combining stable isotopic analysis (δ30Si) of pore water DSi and of operationally defined reactive pools of the solid phase. We show that low biogenic silica (BSi) contents (0.26–0.52 wt% or 92–185 μmol g dry wt−1) drive correspondingly low asymptotic concentrations of pore water DSi of ∼100 μM, relative to biosiliceous sediments (>20 wt% BSi) wherein DSi can reach ∼900 μM. While Barents Sea surface sediments appear almost devoid of BSi, we present evidence for the rapid recycling of bloom derived BSi that generates striking transient peaks in sediment pore water [DSi] of up to 300 μM, which is a feature that is subject to future shifts in phytoplankton community compositions. Using a simple isotopic mass balance calculation we show that at two of three stations the pore water DSi pool at 0.5 cm below the seafloor (+0.96 to +1.36 ‰) is sourced from the mixing of core top waters (+1.46 to +1.69 ‰) with the dissolution of BSi (+0.82 to +1.50 ‰), supplemented with a lithogenic Si source (LSi) (−0.89 ±0.16‰). Further, our sediment pore water δ30Si profiles uncover a coupling of the Si cycle with the redox cycling of metal oxides associated with isotopically light Si (−2.88 ±0.17‰). We suggest that a high LSi:BSi ratio and apparent metal oxide influence could lead to a degree of stability in the annual background benthic flux of DSi, despite current pressures on pelagic phytoplankton communities. Coupled with supporting isotopic evidence for the precipitation of authigenic clays in Barents Sea sediment cores, our observations have implications for the regional Si budget.

Seasonal, weathering and water use controls of silicon cycling along the river flow in two contrasting basins of South India

We present the first study of river water silicon isotopic composition from two contrasting basins in South India, the east flowing Kaveri river and the west flowing Netravathi river. Both rivers originate from the Western Ghats. River water samples were collected from mainstream, tributaries and reservoirs at different locations along the river flow during dry and wet (monsoon) seasons, with an additional post-monsoon sampling in Netravathi. High rainfall in Netravathi basin and upper reaches of Kaveri induce intense weathering in the region, with superposing contribution from anthropogenic controls in downstream Kaveri. The δ30SiDSi values range from +0.42 to +1.65‰ for Netravathi river basin and + 0.32 to +2.85‰ for Kaveri river basin. Silicate weathering index (Re) shows intense weathering associated with monosiallitization (kaolinite-gibbsite formation) in Netravathi basin and relatively moderate weathering with bisiallitization (smectite-kaolinite formation) in Kaveri basin. The seasonal changes in δ30SiDSi and Re in each basin shows similar patterns, with a likely higher and heavier contribution of soil water from deeper soil profiles closer to weathering front and bedrock, associated with significant secondary mineral formation during dry season and leaching of superficial soil profiles during the high discharge periods of monsoon. We provide a theoretical framework to estimate relative contribution of silicate weathering vs. anthropogenic processes on riverine δ30SiDSi. Re is broadly correlated with δ30SiDSi and an isotopic mass balance involving the whole rock composition (excluding the stable quartz and sericite) shows that the δ30Si in river water are well explained by silicate weathering and gibbsite-kaolinite formation in the Netravathi and upper upper reaches of Kaveri. However, silicate weathering explains only partially the heavier δ30SiDSi signatures in the middle and lower reaches of the Kaveri, and the additional enrichment of about +1.06‰ can be attributed to uptake of silicon and Si-depleted return flow through irrigated agriculture in the basin. This study confirms the major control of pedoclimatic conditions on the δ30Si of rivers and provides for the first time an estimation of the impact of human activities on the silicon isotopic signature of rivers.

A silicon isotopic perspective on the contribution of diagenesis to the sedimentary silicon budget in the Southern Ocean

Diatoms are known to fractionate silicon isotopes during the formation of their frustules causing the silicon isotopic composition of biogenic silica to track the degree of silicic acid consumption in surface waters. Despite a growing body of work that uses this proxy to reconstruct past changes in silicic acid utilization, the understanding of the benthic silicon cycle, particularly the identification and quantification of the processes that potentially alter the silicon isotopic composition of biogenic silica during early diagenesis is still lacking. We investigated these processes by comparing the silicon isotopic composition of pore water silicic acid, biogenic silica and, for the first time, lithogenic silica from five sediment cores collected in the deep basin of the Southern Ocean representing a diversity of sedimentation regimes. Silicic acid concentrations and the isotopic composition of Southern Ocean pore waters were the result of a dynamic balance between the dissolution of biogenic silica, reactive lithogenic silica phases and Si re-precipitation with the relative importance of each processes differing significantly between regions. The results are consistent with the formation of authigenic alumino-silicates derived from dissolved biogenic silica in the Sub-Antarctic Zone and in the Antarctic Zone (on average 12 ± 5% and 17 ± 13%, respectively). Since this latter process can fractionate silicon isotopes, this implies that, even if the silicon isotopic composition of diatoms preserved in the sediments is a reliable proxy for silicic acid utilization in the past ocean, care must be taken to extract a clean biogenic silica phase free of authigenic clays and lithogenic phases from sediments to eliminate this potential bias when interpreting isotopic records.

Peatland degradation in Asia threatens the biodiversity of testate amoebae (Protozoa) with consequences for protozoic silicon cycling

Anthropogenic peatland degradation is a global threat. As peatlands store large amounts of carbon (C) their potential for mitigation of climate change has been emphasized recently. Global C cycling is linked to silicon (Si) fluxes from the continents into the oceans. These fluxes in turn are driven by biosilicification, the incorporation of inorganic Si into living organisms, in terrestrial ecosystems. Biosilicification by testate amoeba (TA) communities and its potential for Si cycling has been highlighted since the beginning of the 21st century. However, the effects of peatland degradation on TA biodiversity and corresponding protozoic biosilicification on a continental scale remained unresolved so far. We show that TA biodiversity in Asian peatlands is strongly affected by the grade of human impact. This biodiversity decline was accompanied by an unexpected increase in protozoic biosilicification. Our findings provide new insights into the interactions between the biodiversity of soil microorganisms and biogeochemical Si cycling.

The Biotic‐Abiotic Control of Si Burial in Marine Carbonate Systems of the Pre‐Eocene Si Cycle

AbstractThe silicon (Si) cycle in the modern ocean might still be representative of some of the processes that occurred in the Si‐depleted post‐Eocene oceans resulting after the expansion of diatoms. However, silicon‐rich pre‐Eocene seas, where sponges and radiolarians were major Si users before the emergence of diatoms, were radically different from modern ocean scenarios. The spatial and temporal evolution of Si cycling in Earth history is recorded in geological deposits and could be reconstructed by petrographic and mineralogical analyses. The thick successions of carbonate siliceous rocks deposited in marine environments during the Paleozoic and Mesozoic indicate the significant role of Si outflow from the Si cycle via burial in sediments. The aim of this study is to fill an important gap in knowledge concerning the functioning of the main silicon sink in the oceans: burial in sediments. Si outflow from the marine biogeochemical Si cycle occurs via early diagenetic silica crystallization within seabed mud. The mechanisms leading to Si binding in silica minerals are a complex process controlled by abiotic global events, biological activity of silicifiers and geochemical conditions mediated by microbes. This study concentrates on reconstructions of the mechanisms of Si outflow from the Si cycle by silica polymorph crystallization below the seabed surface and was realized through mineralogical and microtextural analyses of the main components of Upper Cretaceous carbonate–siliceous rocks.

Carbon emission analysis of two crystalline silicon components throughout the life cycle

Take PERC P-type monocrystalline silicon and PERC P-type polycrystalline black silicon modules as examples to establish a life cycle carbon emission inventory of crystalline silicon modules. Study the contribution of five recycling technologies to the life cycle carbon emission reduction of two crystalline silicon modules, and the impact of the life cycle of 1MWP PERC P-type monocrystalline silicon and PERC P-type polycrystalline black silicon module systems on the environment. The results show that the carbon emissions of the two photovoltaic systems are concentrated in the production stage, and the carbon emissions of the crystalline silicon purification process are the highest, accounting for more than 41%. Through green low-carbon recycling technology to process waste photovoltaic modules to obtain glass, aluminum, silicon and other materials to achieve resource recycling, it can reduce the energy consumption of the module production process and life cycle carbon emissions. According to calculations, 1 MWp PERC P-type monocrystalline silicon system has 10% higher life cycle carbon emissions than PERC P-type polycrystalline black silicon system.

Composition of microorganisms in carbonated mineral waters of the Mukhen deposit (Khabarovsk territory)

The chemical composition, distribution, structure, number of physiological groups of cultivated bacteria and their biodiversity in the cold carbonic mineral waters of Mukhen and in microbial mats were studied. It is shown that the mineral waters are cold, hydrocarbonate-calcium-magnesium, enriched with iron, manganese, barium. Carbon dioxide predominates in the gaseous composition of waters. Microbiological studies have shown that no sanitary-indicative microflora was found in mineral waters, which indicates the purity of underground waters. Carbonic waters were characterized by a low number of physiological groups of autochthonous bacteria. Among the studied microorganisms, chemolithotrophic thionic bacteria predominated, which indicates the predominance of oxidation processes of reduced sulfur compounds with the participation of bacteria in groundwater. In the microbial mats, various chemolithotrophic and heterotrophic microorganisms were identified, participating in the geochemical cycles of carbon, nitrogen, sulfur, iron, manganese, and silicon. The number of physiological groups of bacteria was higher than in mineral waters, along with this saprophytic bacteria predominated significantly. A sufficiently high rate of protein and cellulose decomposition by microorganisms of microbial mats was shown. A low diversity of cultured heterotrophic bacteria with the dominance of microorganisms of the genus Bacillus was found in mineral waters and in microbial mats. By using the methods of X-ray phase analysis, the important role of microorganisms of microbial mats in the precipitation of silicate minerals and the formation of calcium carbonates was shown.

Simulations With the Marine Biogeochemistry Library (MARBL)

AbstractThe Marine Biogeochemistry Library (MARBL) is a prognostic ocean biogeochemistry model that simulates marine ecosystem dynamics and the coupled cycles of carbon, nitrogen, phosphorus, iron, silicon, and oxygen. MARBL is a component of the Community Earth System Model (CESM); it supports flexible ecosystem configuration of multiple phytoplankton and zooplankton functional types; it is also portable, designed to interface with multiple ocean circulation models. Here, we present scientific documentation of MARBL, describe its configuration in CESM2 experiments included in the Coupled Model Intercomparison Project version 6 (CMIP6), and evaluate its performance against a number of observational data sets. The model simulates present‐day air‐sea CO2 flux and many aspects of the carbon cycle in good agreement with observations. However, the simulated integrated uptake of anthropogenic CO2 is weak, which we link to poor thermocline ventilation, a feature evident in simulated chlorofluorocarbon distributions. This also contributes to larger‐than‐observed oxygen minimum zones. Moreover, radiocarbon distributions show that the simulated circulation in the deep North Pacific is extremely sluggish, yielding extensive oxygen depletion and nutrient trapping at depth. Surface macronutrient biases are generally positive at low latitudes and negative at high latitudes. CESM2 simulates globally integrated net primary production (NPP) of 48 Pg C yr−1 and particulate export flux at 100 m of 7.1 Pg C yr−1. The impacts of climate change include an increase in globally integrated NPP, but substantial declines in the North Atlantic. Particulate export is projected to decline globally, attributable to decreasing export efficiency associated with changes in phytoplankton community composition.

A lithium-isotope perspective on the evolution of carbon and silicon cycles.

The evolution of the global carbon and silicon cycles is thought to have contributed to the long-term stability of Earth's climate1-3. Many questions remain, however, regarding the feedback mechanisms at play, and there are limited quantitative constraints on the sources and sinks of these elements in Earth's surface environments4-12. Here we argue that the lithium-isotope record can be used to track the processes controlling the long-term carbon and silicon cycles. By analysing more than 600 shallow-water marine carbonate samples from more than 100 stratigraphic units, we construct a new carbonate-based lithium-isotope record spanning the past 3 billion years. The data suggest an increase in the carbonate lithium-isotope values over time, which we propose was driven by long-term changes in the lithium-isotopic conditions of sea water, rather than by changes in the sedimentary alterations of older samples. Using a mass-balance modelling approach, we propose that the observed trend in lithium-isotope values reflects a transition from Precambrian carbon and silicon cycles to those characteristic of the modern. We speculate that this transition was linked to a gradual shift to a biologically controlled marine silicon cycle and the evolutionary radiation of land plants13,14.

Impact of Holocene climate change on silicon cycling in Lake 850, Northern Sweden

Diatom-rich sediment in a small subarctic lake (Lake 850) was investigated in a 9400 cal. yr BP sediment record in order to explore the impact of Holocene climate evolution on silicon cycling. Diatom stable silicon isotopes ([Formula: see text]) and biogenic silica (BSi) indicate that high BSi concentrations in sediment throughout the Holocene are associated with a lighter Si isotope source of dissolved silica (DSi), such as groundwater or freshly weathered primary minerals. Furthermore, higher BSi concentrations were favoured during the mid-Holocene by low detrital inputs and possibly a longer ice-free period allowing for more diatom production to occur. The diatom [Formula: see text] signature shows a link to changes in regional climate and is influenced by length of diatom growth period and hydrological fluctuations. Lighter Si isotopic values occur during the mid-Holocene, when climate is inferred to be more continental and drier, with pronounced seasonality. In contrast, a heavier Si isotopic signature is observed in the early and late Holocene, when oceanic influences are thought to be stronger and the climate wetter. The [Formula: see text] values have generally lighter signatures as compared with other studies, which supports a light DSi source.

Silicon Isotope Signatures of Radiolaria Reveal Taxon-Specific Differences in Isotope Fractionation

The global silicon (Si) cycle plays a critical role in regulating the biological pump and the carbon cycle in the oceans. A promising tool to reconstruct past dissolved silicic acid (DSi) concentrations is the silicon isotope signature of radiolaria (δ30Sirad), siliceous zooplankton that dwells at subsurface and intermediate water depths. However, to date, only a few studies on sediment δ30Sirad records are available. To investigate its applicability as a paleo proxy, we compare the δ30Sirad of different radiolarian taxa and mixed radiolarian samples from surface sediments off Peru to the DSi distribution and its δ30Si signatures (δ30SiDSi) along the coast between the equator and 15°S. Three different radiolarian taxa were selected according to their specific habitat depths of 0–50 m (Acrosphaera murrayana), 50–100 m (Dictyocoryne profunda/truncatum), and 200–400 m (Stylochlamydium venustum). Additionally, samples containing a mix of species from the bulk assemblage covering habitat depths of 0 to 400 m have been analyzed for comparison. We find distinct δ30Sirad mean values of +0.70 ± 0.17‰ (Acro; 2 SD), +1.61 ± 0.20 ‰ (Dictyo), +1.19 ± 0.31 ‰ (Stylo) and +1.04 ± 0.19 ‰ (mixed radiolaria). The δ30Si values of all individual taxa and the mixed radiolarian samples indicate a significant (p &amp;lt; 0.05) inverse relationship with DSi concentrations of their corresponding habitat depths. However, only δ30Si of A. murrayana are correlated to DSi concentrations under normally prevailing upwelling conditions. The δ30Si of Dictyocoryne sp., Stylochlamydium sp., and mixed radiolaria are significantly correlated to the lower DSi concentrations either associated with nutrient depletion or shallower habitat depths. Furthermore, we calculated the apparent Si isotope fractionation between radiolaria and DSi (Δ30Si ∼ 30ε = δ 30Sirad − δ 30SiDSi) and obtained values of −1.18 ± 0.17 ‰ (Acro), −0.05 ± 0.25 ‰ (Dictyo), −0.34 ± 0.27 ‰ (Stylo), and −0.62 ± 0.26 ‰ (mixed radiolaria). The significant differences in Δ30Si between the order of Nassellaria (A. murrayana) and Spumellaria (Dictyocoryne sp. and Stylochlamydium sp.) may be explained by order-specific Si isotope fractionation during DSi uptake, similar to species-specific fractionation observed for diatoms. Overall, our study provides information on the taxon-specific fractionation factor between radiolaria and seawater and highlights the importance of taxonomic identification and separation to interpret down-core records.

High Productivity Makes Mangroves Potentially Important Players in the Tropical Silicon Cycle

Over the last two decades, recognition of the important role terrestrial plants play in regulating silicon (Si) cycling has emerged. Si improves plant fitness by protecting them from abiotic (e.g., desiccation) and biotic (e.g., fungal attack) stressors. Once incorporated into plant biomass this biogenic Si is more bio-available than the lithogenic material from which it was ultimately derived. Thus plants play a key function in regulating the amount and timing of Si availability in downstream ecosystems. Recent work has highlighted the importance of salt marshes in the temperate Si cycle. However, the role of their tropical counterparts, mangroves, has largely gone unexplored. Here we report foliar concentrations of plant Si (as %Si by dry weight) for four Caribbean mangrove species: Conocarpus erectus (buttonwood), Laguncularia racemosa (white mangrove), Avicennia germinans (black mangrove), and Rhizophora mangle (red mangrove). Overall, the median Si concentration was low (0.07%) and did not vary among plant part (e.g., foliage, twig, and propagule). There was also little variation in Si among species. Using literature values of aboveground net primary production, and the concentrations reported here, we estimate an aboveground mangrove Si uptake rate of 2–10 kg Si ha–1 year–1. These rates are on par with rates reported for temperate and boreal forests as well as low nutrient salt marshes, but lower than estimates for high nutrient salt marshes. Thus, despite the low Si concentrations observed in mangroves, their high productivity appears to make them a hot spot of Si cycling in tropical coastal systems.

Bacterial biosilicification: a new insight into the global silicon cycle.

Biosilicification is the process by which organisms incorporate soluble, monomeric silicic acid, Si(OH)4, in the form of polymerized insoluble silica, SiO2. Biosilicifying eukaryotes, including diatoms, siliceous sponges, and higher plants, have been the targets of intense research to study the molecular mechanisms underlying biosilicification. By contrast, prokaryotic biosilicification has been less well studied, partly because the biosilicifying capability of well-known bacteria was not recognized until recently. This review summarizes recent findings on bacterial extracellular and intracellular biosilicification, the latter of which has been demonstrated only recently in bacteria. The topics discussed herein include bacterial (and archaeal) extracellular biosilicification in geothermal environments, encapsulation of Bacillus spores within a silica layer, and silicon accumulation in marine cyanobacteria. The possible contribution of bacterial biosilicification to the global silicon cycle is also discussed.

Human influence on the continental Si budget during the last 4300 years: δ30Sidiatom in varved lake sediments (Tiefer See, NE Germany)

The continental silicon (Si) cycle, including terrestrial and freshwater ecosystems (lakes, rivers, estuaries), acts as a filter and modulates the amount of Si transported to the oceans. In order to link the variation in the terrestrial Si cycle to aquatic ecosystems, knowledge on changes in vegetation cover, soil disturbance and the impact of human activity are required. This study on varved lake sediments from Tiefer See near Klocksin (TSK) in northeastern Germany investigates Si isotope variations in diatom frustules (δ30Sidiatom) over the last ∼4300 years. δ30Sidiatom values vary between 0.37 and 1.63‰. The isotopic signal measured in centric (mostly planktonic) and pennate (mostly benthic) diatoms shows the same trend through most of the record. A decrease in δ30Sidiatom coinciding with early deforestation between 3900 and 750 a BP in the catchment area, points to an enhanced export of isotopically light dissolved silica (DSi) from adjacent soils to the lake. The burial flux of biogenic silica (BSi) observed in the lake sediments increases with cultivation due to enhanced nutrient supply (N, P and Si) from the watershed and nutrient redistribution caused by wind-driven increased water circulation. When the cultivation intensifies, we observe a shift to higher δ30Sidiatom values that we interpret to reflect a diminished Si soil pool and the preferential removal of the lighter 28Si by crop harvesting. Human activity influences the DSi supply from the catchment and appears to be the primary driver controlling the Si budget in TSK. Our data shows how land use triggers variations in continental Si cycling on centennial timescales and provides important information on the underlying processes.

Spatiotemporal dynamics of coupled dissolved silica and bicarbonate in a dam-induced urban lake system in the Three Gorges Reservoir Area

Dissolved silica (DSi) and bicarbonate (HCO3–) stoichiometric coupling is collectively regulated by chemical weathering and algal activity, and potentially indicates the aquatic silicon retention and carbon emission in aquatic systems. Damming markedly remodels the hydrological conditions and aquatic biological activity, however, its effects on the spatiotemporal dynamics of coupled DSi and HCO3– remain poorly understood. Here we deciphered a 2-year hydrological and water quality dataset collected at multiple sites within an urban lake, namely Hanfeng Lake, the largest pre-dam of the Three Gorges Reservoir, to unravel the spatiotemporal dynamics of DSi and HCO3– and selected hydrological and water quality variables using cluster analysis, and to explore the best predictors for DSi:HCO3– using partial least squares regression. The changes of DSi, HCO3– and selected water variables could be characterized by spatial east and west zones, and further by temporal periods 1, 2 and 3 corresponding respectively to fluctuation stage, fluvial stage and lacustrine stage in each zone based on the hydrographic features of Hanfeng Lake. Wet season presented higher flow velocity, permanganate index, concentrations of DSi, HCO3–, nitrate-nitrogen and total suspended solids, and lower water level, secchi depth and chlorophyll-a, but equal DSi:HCO3– relative to dry season. DSi was overall negatively correlated with HCO3–, highlighting the dominant role of chemical weathering rather algal activity. DSi:HCO3– exhibited significant relationships with various variables, but was the best predictable using water level, permanganate index and nitrogen-based variables, suggesting the strong effects of water level fluctuation and pollution discharge on the coupling of silicon and carbon. Our results have great significance for understanding and modeling the biogeochemical cycles of silicon and carbon in the dam-induced lake ecosystems worldwide.