Abstract:The vast majority of organic matter in the world ocean is found in the dissolved pool. However, no evidence has been demonstrated for direct uptake of bulk dissolved organic matter (DOM) by organisms other than bacteria and some invertebrate larvae. The total organic carbon (TOC) is 10-30% higher in coral reefs than in adjacent open waters. The dissolved organic carbon (DOC) accounts for Ͼ90% of the TOC. Using a new in situ technique for clean sampling of the seawater inhaled and exhaled by benthic suspension … Show more
“…As organisms increase in size, SA/V drops and osmotrophy alone becomes insufficient to meet nutrient demands. Thus, strictly osmotrophic organisms tend to be microscopic (e.g., bacteria), although some macroscopic animals, including sponges, corals, brachiopods, bryozoans, molluscs, and echinoderms, use osmotrophic feeding on DOC as a supplemental food source (22)(23)(24)(25)(26).…”
The Ediacara biota include macroscopic, morphologically complex soft-bodied organisms that appear globally in the late Ediacaran Period (575-542 Ma). The physiology, feeding strategies, and functional morphology of the modular Ediacara organisms (rangeomorphs and erniettomorphs) remain debated but are critical for understanding their ecology and phylogeny. Their modular construction triggered numerous hypotheses concerning their likely feeding strategies, ranging from micro-to-macrophagus feeding to photoautotrophy to osmotrophy. Macrophagus feeding in rangeomorphs and erniettomorphs is inconsistent with their lack of oral openings, and photoautotrophy in rangeomorphs is contradicted by their habitats below the photic zone. Here, we combine theoretical models and empirical data to evaluate the feasibility of osmotrophy, which requires high surface area to volume (SA/V) ratios, as a primary feeding strategy of rangeomorphs and erniettomorphs. Although exclusively osmotrophic feeding in modern ecosystems is restricted to microscopic bacteria, this study suggests that (i) fractal branching of rangeomorph modules resulted in SA/V ratios comparable to those observed in modern osmotrophic bacteria, and (ii) rangeomorphs, and particularly erniettomorphs, could have achieved osmotrophic SA/V ratios similar to bacteria, provided their bodies included metabolically inert material. Thus, specific morphological adaptations observed in rangeomorphs and erniettomorphs may have represented strategies for overcoming physiological constraints that typically make osmotrophy prohibitive for macroscopic life forms. These results support the viability of osmotrophic feeding in rangeomorphs and erniettomorphs, help explain their taphonomic peculiarities, and point to the possible importance of earliest macroorganisms for cycling dissolved organic carbon that may have been present in abundance during Ediacaran times.erniettomorphs ͉ rangeomorphs ͉ Fractofusus ͉ Pteridinium
“…As organisms increase in size, SA/V drops and osmotrophy alone becomes insufficient to meet nutrient demands. Thus, strictly osmotrophic organisms tend to be microscopic (e.g., bacteria), although some macroscopic animals, including sponges, corals, brachiopods, bryozoans, molluscs, and echinoderms, use osmotrophic feeding on DOC as a supplemental food source (22)(23)(24)(25)(26).…”
The Ediacara biota include macroscopic, morphologically complex soft-bodied organisms that appear globally in the late Ediacaran Period (575-542 Ma). The physiology, feeding strategies, and functional morphology of the modular Ediacara organisms (rangeomorphs and erniettomorphs) remain debated but are critical for understanding their ecology and phylogeny. Their modular construction triggered numerous hypotheses concerning their likely feeding strategies, ranging from micro-to-macrophagus feeding to photoautotrophy to osmotrophy. Macrophagus feeding in rangeomorphs and erniettomorphs is inconsistent with their lack of oral openings, and photoautotrophy in rangeomorphs is contradicted by their habitats below the photic zone. Here, we combine theoretical models and empirical data to evaluate the feasibility of osmotrophy, which requires high surface area to volume (SA/V) ratios, as a primary feeding strategy of rangeomorphs and erniettomorphs. Although exclusively osmotrophic feeding in modern ecosystems is restricted to microscopic bacteria, this study suggests that (i) fractal branching of rangeomorph modules resulted in SA/V ratios comparable to those observed in modern osmotrophic bacteria, and (ii) rangeomorphs, and particularly erniettomorphs, could have achieved osmotrophic SA/V ratios similar to bacteria, provided their bodies included metabolically inert material. Thus, specific morphological adaptations observed in rangeomorphs and erniettomorphs may have represented strategies for overcoming physiological constraints that typically make osmotrophy prohibitive for macroscopic life forms. These results support the viability of osmotrophic feeding in rangeomorphs and erniettomorphs, help explain their taphonomic peculiarities, and point to the possible importance of earliest macroorganisms for cycling dissolved organic carbon that may have been present in abundance during Ediacaran times.erniettomorphs ͉ rangeomorphs ͉ Fractofusus ͉ Pteridinium
“…Corals may rapidly consume DOC and bacterioplankton (Sorokin, 1973), although many recent studies show corals to be sources, rather than sinks, for DOC (Ferrier-Pages et al, 1998;Van Duyl and Gast, 2001;Hata et al, 2002;Nakajima et al, 2009). Recent work has demonstrated the potential for sponges to consume both DOC and bacterioplankton at biogeochemically significant rates (Yahel et al, 2003;Van Duyl et al, 2006;de Goeij and Van Duyl, 2007;De Goeij et al, 2008). However, conspicuous sponge taxa, which exhibit the highest filtration rates (Southwell et al, 2008), are virtually absent from our study area, and even inconspicuous benthic sponges cover o1% of the reef benthos in Moorea on average (Adjeroud, 1997, http://mcr.…”
Coral reefs are highly productive ecosystems bathed in unproductive, low-nutrient oceanic waters, where microbially dominated food webs are supported largely by bacterioplankton recycling of dissolved compounds. Despite evidence that benthic reef organisms efficiently scavenge particulate organic matter and inorganic nutrients from advected oceanic waters, our understanding of the role of bacterioplankton and dissolved organic matter (DOM) in the interaction between reefs and the surrounding ocean remains limited. In this study, we present the results of a 4-year study conducted in a well-characterized coral reef ecosystem (Paopao Bay, Moorea, French Polynesia) where changes in bacterioplankton abundance and dissolved organic carbon (DOC) concentrations were quantified and bacterial community structure variation was examined along spatial gradients of the reef:ocean interface. Our results illustrate that the reef is consistently depleted in concentrations of both DOC and bacterioplankton relative to offshore waters (averaging 79 lmol l À1 DOC and 5.5 Â 10 8 cells l À1 offshore and 68 lmol l À1 DOC and 3.1 Â 10 8 cells l À1 over the reef, respectively) across a 4-year time period. In addition, using a suite of culture-independent measures of bacterial community structure, we found consistent differentiation of reef bacterioplankton communities from those offshore or in a nearby embayment across all taxonomic levels. Reef habitats were enriched in Gamma-, Delta-, and Betaproteobacteria, Bacteriodetes, Actinobacteria and Firmicutes. Specific bacterial phylotypes, including members of the SAR11, SAR116, Flavobacteria, and Synechococcus clades, exhibited clear gradients in relative abundance among nearshore habitats. Our observations indicate that this reef system removes oceanic DOC and exerts selective pressures on bacterioplankton community structure on timescales approximating reef water residence times, observations which are notable both because fringing reefs do not exhibit long residence times (unlike those characteristic of atoll lagoons) and because oceanic DOC is generally recalcitrant to degradation by ambient microbial assemblages. Our findings thus have interesting implications for the role of oceanic DOM and bacterioplankton in the ecology and metabolism of reef ecosystems.
“…Al− though typical sponges feed primarily on bacterial−sized parti− cles through the microvilli of their choanocytes (e.g., Reiswig 1971;Riisgård and Larsen 2000), in some cases (Leys and Eerkes−Medrano 2006) particle capture is through pseudo− podial extensions of these cells; larger particles (5-50 μm) are often captured by amoebocytes lining the incurrent canal walls (Reiswig 1971). There has also been an increasing apprecia− tion of the role of direct uptake of dissolved organic carbon (e.g., Reiswig 1981;Yahel et al 2003), but it is not yet clear to what extent symbiotic organisms are responsible for the up− take, and if the sponge itself is responsible, what is the mecha− nism of uptake. Other studies have also shown that sponge growth rate is independent of the supply of Dissolved Organic Carbon, suggesting a greater dependence on solid particle consumption (Koopmans and Wijffels 2008).…”
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