FIGURE 8.1 Benthic diatom assemblages viewed by scanning electron microscopy (SEM). (a) Epipsammic diatoms (Achnanthes and Navicula) in the cavity of a.

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FIGURE 8.1 Benthic diatom assemblages viewed by scanning electron microscopy (SEM). (a) Epipsammic diatoms (Achnanthes and Navicula) in the cavity of a sand grain. (b) Vertical cut of a sediment surface at low tide photographed in a low Temperature SEM. Motile diatoms have moved to the sediment surface where they form a dense microalgal mat. Strings forming networklike patterns consist of extracellular polymeric substances (EPS) excreted by diatoms (the pattern is an artifact produced by the method). Source: Photograph (a) by H. Håkansson and K. Sundbåck, (b) by A. Miles, Sediment Ecology Research Group, University of St. Andrews, Scotland. ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.2 Different divisions of algae have adapted to the varied light regimes that occur along depth gradients in estuaries. ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.3 Comparison of minimum light requirements between macroalgae and seagrass. Depth limits are set by light attenuation in the water column. ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.4 Diel pattern of microphytobenthic primary production (bars) on a shallow-water subtidal sandy site (Kattegat, microtidal west coast of Sweden) and an intertidal muddy site (Tagus estuary, Portugal). Measurements were made by the 14 C technique with subsequent 2-h incubations during three full days. Filled circles show irradiance measured at sediment surface. Because of high turbidity, no light penetrated to the sediment surface during high tide in the Tagus estuary. Source: Redrawn from Miles and Sundbäck (2000). ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.5 Influence of microphytobenthos on oxygen distribution in surface sediment. (a) Oxygen profiles in light and dark measured by oxygen microelectrodes. Also shown is a vertical profile of modeled rates of primary production (bars). (b) and (c) Oxygen distribution in light and dark in bioturbated sandy silt measured by planar oxygen optodes (Section 8.7). The bright red spot indicates the high rate of photosynthetic oxygen production in light by an assemblage of benthic diatoms just below the sediment surface. Source: (a) Redrawn from Glud et al. (2009) and (b) redrawn from Fenchel and Glud (2000). ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.6 Maximum uptake rates of NH 4 -N versus concentration for macroalgae with different ratios of surface area to volume. Source: From Wallentinus (1984). ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.7 Periods of nutrient-limited growth (a) and storage capacity (ability to support growth in the absence of an external nutrient supply) (b) for phytoplankton and macroalgae in a Danish Fjord compared to ambient nutrient concentrations. Source: From Pedersen and Borum (1996). ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.8 Energy flow diagrams for different macroalgal communities. The size of the arrow represents the magnitude of flow in the different pathways. ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.9 Conceptual models of interactions between mats of benthic microalgae (microphytobenthos, MPB) and loose macroalgae (MA). Upper panel (a and b): macroalgal mat lying close to the sediment surface, a situation common on tidal coasts during low tide. Lower panel (c and d): macroalgal mat floating at the water surface, a typical situation in microtidal waters. In (a), the two closely coupled mats intercept nutrient release from the sediment to the overlying water, whereas in case (b) nutrients are released from the anoxic sediment and the coupled mats to the overlying water. When the two algal mats are spatially separated (c and d), there is no nutrient exchange between the two mats or between the sediment and water column. Instead, algal productivity is sustained by efficient recycling of nutrients within the mats themselves (c). This scenario applies particularly to autotrophic (often sandy) sediments in microtidal areas when nutrient levels in the overlying water column are low. At night, or when a thick floating macroalgal mat does not allow light to penetrate to the sediment surface (d), pore-water nutrients are released to the water column where they can be used by floating macroalgae. DFAA refers to dissolved free amino acids, and DCAA refers to dissolved combined amino acids. Source: Model drawings were inspired by the model in Astill and Lavery (2001) and redrawn from Sundbäck and McGlathery (2005). ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.10 The Nature of Community Collapse: Phase Shifts or Alternative Stable States? ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~

FIGURE 8.11 Many species of invasive red algae proliferate on Hawaiian coral reefs including (a) Acanthophora spicifera (b) Gracilaria salicornia, and (c) Kappaphycus alvarezii. (d) In some areas, such as the coast of Maui, blooms of Hypnea musciformis become so large that they detach, form floating rafts, and deposit on the beach. Source: Photographs by Jennifer Smith. ESTUARINE ECOLOGY, Second Edition. John W. Day JR, Byron C. Crump, W. Michael Kemp, and Alejandro Yánez-Arancibia. Copyright © 2013 by Wiley-Blackwell. All rights reserved ~