Silicon pools, fluxes and the potential benefits of a silicon soil amendment in a nitrogen-enriched tidal marsh restoration

Tidal marshes are important sites of silicon (Si) transformation, where dissolved Si (DSi) taken up by macrophytic vegetation and algal species is converted to biogenic silica (BSi), which can accumulate in the soil, be recycled within the marsh, or be exported to adjacent coastal waters. The role of restored and created tidal marshes in these processes is not well understood, nor is the impact of nutrient enrichment at either the plant or ecosystem level. Here, Si fluxes were examined to develop a Si mass balance in a nitrogen (N)-enriched marsh created with fine-grained dredged material from the Chesapeake Bay, United States. In addition, the effectiveness of Si soil amendments to ameliorate the negative effects of excess nitrogen on Spartina alterniflora was examined through laboratory and field experiments. Silicon was exported to the estuary as DSi (49 g m−2 y−1) and BSi (35 g m−2y−1) in stoichiometric excess of nitrogen and phosphorus. Rapid recycling of Si within both marsh and the tidal creeks appeared to be important in the transformation of Si and export from the marsh. Enhanced macrophyte SiO2 tissue concentrations were observed in the field experiment, with end-of-season mean values of 2.20–2.69% SiO2 in controls and 2.49–3.24% SiO2 in amended plots, among the highest reported for S. alterniflora; however, improved plant fitness was not detected in either experiment. Thus, tidal marshes created with a fine-grained, N-rich dredged material appear to function as a rich source of Si to the restored marsh and local estuarine environment, an overlooked ecosystem service. Soil Si amendments, however, did not appear likely to alleviate N-induced stress in S. alterniflora.

[1]  M. Sommer,et al.  Spatial patterns of aboveground phytogenic Si stocks in a grass-dominated catchment – Results from UAS based high resolution remote sensing , 2021, Biogeosciences.

[2]  W. Boynton,et al.  The Fate of Nitrogen in Dredged Material Used for Tidal Marsh Restoration , 2021, Journal of Marine Science and Engineering.

[3]  C. Hopkinson,et al.  The Role of Marshes in Coastal Nutrient Dynamics and Loss , 2021, Salt Marshes.

[4]  R. Jones,et al.  Silicon , 2018, Reactions Weekly.

[5]  Defining events of 2020. , 2020, Science.

[6]  L. Staver,et al.  Tidal Marsh Restoration at Poplar Island I: Transformation of Estuarine Sediments into Marsh Soils , 2020, Wetlands.

[7]  K. Staver,et al.  Tidal Marsh Restoration at Poplar Island: II. Elevation Trends, Vegetation Development, and Carbon Dynamics , 2020, Wetlands.

[8]  W. Nardin,et al.  Empirical observations and numerical modelling of tides, channel morphology, and vegetative effects on accretion in a restored tidal marsh , 2019, Earth Surface Processes and Landforms.

[9]  W. Elmer,et al.  Interactions and consequences of silicon, nitrogen, and Fusarium palustre on herbivory and DMSP levels of Spartina alterniflora , 2017 .

[10]  Yongchao Liang,et al.  Silicon in Agriculture , 2015, Springer Netherlands.

[11]  J. Carey,et al.  Salt marsh tidal exchange increases residence time of silica in estuaries , 2014 .

[12]  J. Carey,et al.  Silica uptake by Spartina—evidence of multiple modes of accumulation from salt marshes around the world , 2014, Front. Plant Sci..

[13]  D. A. Barry,et al.  Use of Silicate Minerals for pH Control during Reductive Dechlorination of Chloroethenes in Batch Cultures of Different Microbial Consortia , 2014, Applied and Environmental Microbiology.

[14]  Floor I. Vandevenne,et al.  Silicon-vegetation interaction in multiple ecosystems : a review , 2014 .

[15]  E. Struyf,et al.  A Comprehensive Study of Silica Pools and Fluxes in Wadden Sea Salt Marshes , 2013, Estuaries and Coasts.

[16]  I. Mendelssohn,et al.  Sudden Vegetation Dieback in Atlantic and Gulf Coast Salt Marshes. , 2013, Plant disease.

[17]  Zhaoliang Song,et al.  Occluded C in rice phytoliths: implications to biogeochemical carbon sequestration , 2013, Plant and Soil.

[18]  A. Davy,et al.  Silicon alleviates deleterious effects of high salinity on the halophytic grass Spartina densiflora. , 2013, Plant physiology and biochemistry : PPB.

[19]  J. Carey,et al.  Nitrogen enrichment increases net silica accumulation in a temperate salt marsh , 2013 .

[20]  L. Deegan,et al.  Coastal eutrophication as a driver of salt marsh loss , 2012, Nature.

[21]  M. Gessner,et al.  Silicon supply modifies C:N:P stoichiometry and growth of Phragmites australis. , 2012, Plant biology.

[22]  O. Ragueneau,et al.  In situ biogenic silica variations in the invasive salt marsh plant, Spartina alterniflora: A possible link with environmental stress , 2012, Plant and Soil.

[23]  J. Carey,et al.  The ebb and flood of Silica: Quantifying dissolved and biogenic silica fluxes from a temperate salt marsh , 2011 .

[24]  H. Marschner,et al.  Marschner's Mineral Nutrition of Higher Plants , 2011 .

[25]  R. Turner Beneath the Salt Marsh Canopy: Loss of Soil Strength with Increasing Nutrient Loads , 2011 .

[26]  J. Cornwell,et al.  Quantifying Sediment Nitrogen Releases Associated with Estuarine Dredging , 2011 .

[27]  R. Marra,et al.  New species of Fusarium associated with dieback of Spartina alterniflora in Atlantic salt marshes , 2011, Mycologia.

[28]  W. Uddin,et al.  Soil silicon amendment for managing gray leaf spot of perennial ryegrass turf on golf courses in Pennsylvania , 2009 .

[29]  D. Conley,et al.  Silica: an essential nutrient in wetland biogeochemistry , 2009 .

[30]  P. Meire,et al.  Spatiotemporal aspects of silica buffering in restored tidal marshes , 2008 .

[31]  T. Behrends,et al.  Dissolution of biogenic silica from land to ocean: Role of salinity and pH , 2008 .

[32]  R. Eugene Turner,et al.  Below- and Aboveground Biomass of Spartina alterniflora: Response to Nutrient Addition in a Louisiana Salt Marsh , 2008 .

[33]  S. Temmerman,et al.  Dynamics of biogenic Si in freshwater tidal marshes: Si regeneration and retention in marsh sediments (Scheldt estuary) , 2007 .

[34]  J. Downing,et al.  Dry and wet atmospheric deposition of nitrogen, phosphorus and silicon in an agricultural region , 2006 .

[35]  J. Middelburg,et al.  Tidal marshes and biogenic silica recycling at the land‐sea interface , 2006 .

[36]  I. Tegen,et al.  Atmospheric Transport of Silicon , 2006 .

[37]  V. Ittekkot The silicon cycle : human perturbations and impacts on aquatic systems , 2006 .

[38]  D. Sauer,et al.  Methodologies for amorphous silica analysis , 2006 .

[39]  Michael R. Roman,et al.  Eutrophication of Chesapeake Bay: historical trends and ecological interactions , 2005 .

[40]  A. Mead,et al.  Phylogenetic variation in the silicon composition of plants. , 2005, Annals of botany.

[41]  Leigh A Sullivan,et al.  Soil carbon sequestration in phytoliths , 2005 .

[42]  M. Hemminga,et al.  The relationship between silicon availability, and growth and silicon concentration of the salt marsh halophyte Spartina anglica , 1999, Plant and Soil.

[43]  P. Cappellen Biomineralization and global biogeochemical cycles , 2003 .

[44]  J. Elser,et al.  Ecological Stoichiometry: The Biology of Elements from Molecules to the Biosphere , 2002 .

[45]  M. Weinstein,et al.  Use of dredge materials for coastal restoration , 2002 .

[46]  M. Jianfeng,et al.  Soil, Fertilizer, and Plant Silicon Research in Japan , 2002 .

[47]  L. Cahoon,et al.  Silicon is the Link between Tidal Marshes and Estuarine Fisheries: A New Paradigm , 2002 .

[48]  James T. Morris,et al.  Eco-Physiological Controls on the Productivity of Spartina Alterniflora Loisel , 2002 .

[49]  E. Takahashi,et al.  Chapter 2 Silicon as a beneficial element for crop plants , 2001 .

[50]  I. Lepsch,et al.  Chapter 7 Effect of silicon on plant growth and crop yield , 2001 .

[51]  E. Epstein Chapter 1 Silicon in plants: Facts vs. concepts , 2001 .

[52]  Christoph Humborg,et al.  Silicon Retention in River Basins: Far-reaching Effects on Biogeochemistry and Aquatic Food Webs in Coastal Marine Environments , 2000 .

[53]  C. Craft,et al.  TWENTY‐FIVE YEARS OF ECOSYSTEM DEVELOPMENT OF CONSTRUCTED SPARTINA ALTERNIFLORA (LOISEL) MARSHES , 1999 .

[54]  C. Hackney,et al.  Silica Content of a Mesohaline Tidal Marsh in North Carolina , 1999 .

[55]  D. Conley An interlaboratory comparison for the measurement of biogenic silica in sediments , 1998 .

[56]  D. Conley Riverine contribution of biogenic silica to the oceanic silica budget , 1997 .

[57]  D. Conley,et al.  A sediment chronology of the eutrophication of Chesapeake Bay , 1996 .

[58]  D. M. Nelson,et al.  The Silica Balance in the World Ocean: A Reestimate , 1995, Science.

[59]  D. Conley,et al.  Annual cycle of dissolved silicate in Chesapeake bay: implications for the production and fate of phytoplankton biomass , 1992 .

[60]  G. Brush,et al.  Long-Term History of Chesapeake Bay Anoxia , 1991, Science.

[61]  T. Church,et al.  The sedimentary flux of nutrients at a Delaware salt marsh site: A geochemical perspective , 1989 .

[62]  L. N. Eleuterius,et al.  Silica and Ash in Tissues of Some Coastal Plants , 1983 .

[63]  R. Good,et al.  DECOMPOSITION DYNAMICS OF SPARTINA ALTERNIFLORA AND SPARTINA PATENS IN A NEW JERSEY SALT MARSH , 1982 .

[64]  D. DeMaster The supply and accumulation of silica in the marine environment , 1981 .

[65]  L. N. Eleuterius,et al.  Silica and Ash in Several Marsh Plants , 1981 .

[66]  C. Officer,et al.  The Possible Importance of Silicon in Marine Eutrophication , 1980 .

[67]  I. Mendelssohn The influence of nitrogen level, form, and application method on the growth response ofSpartina alterniflora in North Carolina , 1979 .

[68]  R. Hesslein An in situ sampler for close interval pore water studies1 , 1976 .

[69]  T. Parsons,et al.  A practical handbook of seawater analysis , 1968 .