Extracellular Reef Metabolites Across the Protected Jardines de la Reina, Cuba Reef System

• Published in: Frontiers in Marine Science Vol. 7
• Main Authors: Weber, Laura, Armenteros, Maickel, Kido Soule, Melissa, Longnecker, Krista, Kujawinski, Elizabeth B., Apprill, Amy
• Format: Journal Article
• Language: English
• Published: Lausanne Frontiers Research Foundation 14-12-2020; Frontiers Media S.A
• Subjects: Algae; Amino acids; Archipelagoes; Benthos; Biogeochemistry; Chemical analysis; Composition; Coral reefs; Depth; DOM cycling; ecology; Ecosystems; Environmental changes; Environmental conditions; Extracellular; Intermediates; Investigations; Liquid chromatography; Marine ecosystems; Marine invertebrates; Mass spectrometry; Mass spectroscopy; Metabolism; Metabolites; Metabolomics; Microorganisms; Mineral nutrients; Nitrogen; Nutrient cycles; Nutrients; Oceanic analysis; Oxidation; Photochemicals; Photochemistry; Polls & surveys; Riboflavin; Seawater; Surveying; Vitamins; Water analysis; Cuba; United States > US
• ISSN: 2296-7745; 2296-7745
• DOI: 10.3389/fmars.2020.582161

Coral reef ecosystems are incredibly diverse marine biomes that rely on nutrient cycling by microorganisms to sustain high productivity in generally oligotrophic regions of the ocean. Understanding the composition of extracellular reef metabolites in seawater, the small organic molecules that serve as the currency for microorganisms, may provide insight into benthic-pelagic coupling as well as the complexity of nutrient cycling in coral reef ecosystems. Jardines de la Reina (JR), Cuba is an ideal environment to examine extracellular metabolites across protected and high-quality reefs. Here, we used liquid chromatography mass spectrometry (LC-MS) to quantify specific known metabolites of interest (targeted metabolomics approach) and to survey trends in metabolite feature composition (untargeted metabolomics approach) from surface and reef depth (6 – 14 m) seawater overlying nine forereef sites in JR. We found that untargeted metabolite feature composition was surprisingly similar between reef depth and surface seawater, corresponding with other biogeochemical and physicochemical measurements and suggesting that environmental conditions were largely homogenous across forereefs within JR. Additionally, we quantified 32 of 53 detected metabolites using the targeted approach, including amino acids, nucleosides, vitamins, and other metabolic intermediates. Two of the quantified metabolites, riboflavin and xanthosine, displayed interesting trends by depth. Riboflavin concentrations were higher in reef depth compared to surface seawater, suggesting that riboflavin may be produced by reef organisms at depth and degraded in the surface through photochemical oxidation. Xanthosine concentrations were significantly higher in surface reef seawater. 5′-methylthioadenosine (MTA) concentrations increased significantly within the central region of the archipelago, displaying biogeographic patterns that warrant further investigation. Here we lay the groundwork for future investigations of variations in metabolite composition across reefs, sources and sinks of reef metabolites, and changes in metabolites over environmental, temporal, and reef health gradients.