Abstract:This field and laboratory study examines whether regularly patterned biofilms on present‐day intertidal flats are equivalent to microbially induced bedforms found in geological records dating back to the onset of life on Earth. Algal mats of filamentous Vaucheria species, functionally similar to microbial biofilms, cover the topographic highs of regularly spaced ridge–runnel bedforms. As regular patterning is typically associated with self‐organization processes, indicators of self‐organization are tested and … Show more
“…At a small scale, within the vegetation patches, flow velocities and erosion are reduced (e.g., Nepf, 2012) resulting in improved plant growth (positive feedback van Wesenbeeck et al, 2008). At a larger scale, the water is partly forced to flow around the vegetation patches, leading there to increased flow velocities (Zong & Nepf, 2010), potential erosion (Bouma et al, 2007), and to inhibition of plant growth just next to the vegetation patch (negative feedback van Wesenbeeck et al, 2008). Scale-dependent biogeomorphic feedbacks have been studied extensively over the past decade.…”
Section: Introductionmentioning
confidence: 99%
“…Their strength is reported to depend on many characteristics, such as patch size (Licci et al, 2019;Vandenbruwaene et al, 2011), stem density (Bouma et al, 2009), stem height (Gu et al, 2018), stem stiffness (Bouma et al, 2013;Marjoribanks et al, 2019;Ortiz et al, 2013;Schwarz et al, 2015), interpatch distance (de Lima et al, 2015;Meire et al, 2014;Vandenbruwaene et al, 2011), lateral expansion rate (Schwarz et al, 2018), and flow velocity (Bouma et al, 2013;Marjoribanks et al, 2019;Vandenbruwaene et al, 2011). Several studies have also shown that strong scale-dependent feedbacks are needed to result in the self-organization of regular spatial biogeomorphic patterns at the landscape scale (Rietkerk et al, 2004;Schwarz et al, 2018;Temmerman et al, 2007;van de Koppel et al, 2012). Given the above description of the scale dependency of biogeomorphic feedbacks, it becomes evident that their representation within numerical models is highly dependent on the grid size, which raises a balance problem between domain size and computational time.…”
• Fine-scale flow-vegetation interactions can considerably impact large-scale biogeomorphic feedbacks • Current large-scale biogeomorphic models are too coarse to include these fine-scale interactions • Our computationally-efficient method allows large-scale models to account for fine-scale interactions
“…At a small scale, within the vegetation patches, flow velocities and erosion are reduced (e.g., Nepf, 2012) resulting in improved plant growth (positive feedback van Wesenbeeck et al, 2008). At a larger scale, the water is partly forced to flow around the vegetation patches, leading there to increased flow velocities (Zong & Nepf, 2010), potential erosion (Bouma et al, 2007), and to inhibition of plant growth just next to the vegetation patch (negative feedback van Wesenbeeck et al, 2008). Scale-dependent biogeomorphic feedbacks have been studied extensively over the past decade.…”
Section: Introductionmentioning
confidence: 99%
“…Their strength is reported to depend on many characteristics, such as patch size (Licci et al, 2019;Vandenbruwaene et al, 2011), stem density (Bouma et al, 2009), stem height (Gu et al, 2018), stem stiffness (Bouma et al, 2013;Marjoribanks et al, 2019;Ortiz et al, 2013;Schwarz et al, 2015), interpatch distance (de Lima et al, 2015;Meire et al, 2014;Vandenbruwaene et al, 2011), lateral expansion rate (Schwarz et al, 2018), and flow velocity (Bouma et al, 2013;Marjoribanks et al, 2019;Vandenbruwaene et al, 2011). Several studies have also shown that strong scale-dependent feedbacks are needed to result in the self-organization of regular spatial biogeomorphic patterns at the landscape scale (Rietkerk et al, 2004;Schwarz et al, 2018;Temmerman et al, 2007;van de Koppel et al, 2012). Given the above description of the scale dependency of biogeomorphic feedbacks, it becomes evident that their representation within numerical models is highly dependent on the grid size, which raises a balance problem between domain size and computational time.…”
• Fine-scale flow-vegetation interactions can considerably impact large-scale biogeomorphic feedbacks • Current large-scale biogeomorphic models are too coarse to include these fine-scale interactions • Our computationally-efficient method allows large-scale models to account for fine-scale interactions
“…The study of van de Vijsel et al . () reveals a striking similarity between present‐day sedimentary patterns in ridges and sedimentary patterns found in ancient stromatolites and Precambrian microbialite strata. Their laboratory study shows that biofilm sediment trapping and stabilization in ridges of present‐day intertidal flats is found to be characterized by indicators of self‐organization, suggesting an intriguing hypothesis whereby self‐organization dynamics might have been captured in fossil microbialites, a notion that may be important for paleoenvironmental reconstruction.…”
Section: Editorialmentioning
confidence: 58%
“…By analysing the effects of the impinging wind waves on the retreat of salt-marsh boundaries, and how the temporal evolution of wind-wave fields over the last centuries affects erosional dynamics, they highlight that relating salt-marsh lateral erosion rates to mean wave-power densities provides a valuable tool to address long-term tidal morphodynamics. The study of van de Vijsel et al (2020) reveals a striking similarity between present-day sedimentary patterns in ridges and sedimentary patterns found in ancient stromatolites and Precambrian microbialite strata. Their laboratory study shows that biofilm sediment trapping and stabilization in ridges of present-day intertidal flats is found to be characterized by indicators of self-organization, suggesting an intriguing hypothesis whereby self-organization dynamics might have been captured in fossil microbialites, a notion that may be important for paleoenvironmental reconstruction.…”
mentioning
confidence: 73%
“…The 17 collected contributions include four state-of-science papers concerning the most recent advances in computational morphodynamic modelling of coupled flow-bed-sediment systems (Shimizu et al, 2019), a critical analysis of existing data on vegetation-flow-sediment interactions obtained through both laboratory experiments and field campaigns (Tinoco et al, 2020), a review of existing moving-boundary theories of shorelines with two extensions to allow inclusion of firstorder effects of waves and tides (Voller et al, 2020), and an overall assessment of the role played by wave forcing on the hydro-morphodynamics in shallow nearshore areas and at river mouths (Brocchini, 2019). The other 13 papers cover different topics about morphodynamics, spanning multiple environments, tackling concepts and processes with the aid of refined theoretical and numerical tools (Redolfi et al, 2019;Tambroni et al, 2019), grounding the results on laboratory data (Finotello et al, 2019;Geng et al, 2019;Matoušek et al, 2019, Porcile et al, 2020 and field observations (Fogarin et al, 2019;Tommasini et al, 2019), and making use of interdisciplinary approaches (Calvani et al, 2019;Chen et al, 2019;Pivato et al, 2019;van de Vijsel et al, 2020) also to develop new conceptualizations (Schlömer et al, 2020).…”
The calcareous Halimeda bioherms of the northern Great Barrier Reef, Australia are the largest actively accumulating Halimeda deposits worldwide. They contribute a substantial component of the Great Barrier Reef neritic carbonate factory, as well as the geomorphological development of Australia's northeast continental shelf.Halimeda bioherm geomorphology is complex, expressing three distinct variations in morphotype patterns: annulate, reticulate and undulate. Similar regular and irregular geomorphological patterning often results from scale-dependent biophysical feedback mechanisms. Therefore, a better understanding of morphotype differentiation can inform the biotic and abiotic drivers of spatial heterogeneity in the bioherm ecosystem. Here, 3D LiDAR bathymetry is integrated with 2D sub-bottom profile datasets to investigate surface topography and internal sedimentary architecture of Halimeda bioherms through space and time. Using the ESRI ArcGIS 3D Analyst and Benthic Terrain Modeller extensions, the bioherm surface and subsurface geomorphometric characteristics were quantified for the annulate, reticulate and undulate morphotypes. Significant variation was found between the three bioherm morphotypes in their surface topography, internal structure, volume, slope gradients and terrain complexity. Therefore, their geomorphology is probably influenced by differing processes and biophysical feedback mechanisms. The complex surface topography does not appear to be inherited from the antecedent substrate, and preferred aspect orientations resulting from hydrodynamic forcing appear to be limited. It is suggested here that autogenic dynamics or biotic self-organization similar to patterns and processes in other marine organo-sedimentary systems modulates Halimeda bioherm geomorphology, and some hypotheses are offered towards future studies. Morphotype differentiation has implications for the development of the Halimeda bioherm carbonate factory, rates of sediment aggradation and progradation, and variable capacity to fill accommodation space. Self-organization dynamics and morphology differentiation in Modern bioherm systems could potentially inform | 177 MCNEIL Et aL.
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