Dr. Mark L. Wells from University of Maine visited Institute of Oceanology
June 6th, Dr. Mark L. Wells, professor of School of Marine Sciences, University of Maine, visited Institute of Oceanology and gave the presentation on ‘Harmful Algal Blooms in Changing World’. Prof. Zhou Mingjiang of Key Laboratory of Marine Ecology and Environmental Science presided over the presentation. Dr. Mark L. Wells introduced the concept and status of HABs and detailed the current research about the effects on HABs of the global change. There were extensive and heated discussions between researchers and Dr. Mark L. Wells.
His research interests are introduced explicitly. Marine dissolved organic matter (DOM) is one of the largest reservoirs of organic carbon on the earth’s surface. Colored, or chromophoric organic matter (CDOM) is a variable component of the total DOM which interferes significantly with light propagation in surface and deep waters and greatly complicates the interpretation of remote sensing data. More importantly, the abundance and spectral characteristics of CDOM varies unpredictably over both temporal and spatial scales independently of traditional parameters (e.g. chl a, cell numbers, DOC, etc.). As a result, it is not possible to definitively correct remote sensing data for optical interferences arising from CDOM. Recent work in an adjacent oceanographic field has demonstrated that a major fraction (30-60%) of bulk marine DOM is colloidal (> 1 kDa) in nature, and preliminary evidence suggests that the optical signature of this organic colloidal matter differs markedly from the bulk CDOM. In addition, the colloidal organic fraction appears to cycle more rapidly than truly soluble organic matter. My working hypothesis is that a major part of the highly variable CDOM signal in surface waters can be explained mechanistically by short term fluctuations in the composition and cycling dynamics of colloidal CDOM. The two primary goals for this project are: 1) measure the optical signature of marine colloidal matter in near shore waters and determine the extent to which this signature changes in response to biological activity (the source and likely sink of marine colloids), and 2) determine the extent to which photochemical processes differentially affect the optical characteristics and residence time of soluble and colloidal CDOM in seawater. The work proposed here takes the first critical steps towards physically teasing apart marine CDOM components to better explain their nature and cycling in seawater.
