Phytoplankton chlorophyll-breakdown pathway: Implication in ecosystem assessment.

作者: K. Sathish , J.S. Patil , A.C. Anil

DOI: 10.1016/J.JENVMAN.2019.109989

关键词:

摘要: The chlorophyll-breakdown to pheophorbide is determined by biotic factors such as grazing (via chlorophyllide) or senescence pheophytin). So far, much of the information on available from sediments, but water column limited. This study addressed chlorophyll-breakdown-pathways (Chl-BP) a seasonal basis eight major ports (18-30 stations/port) representing freshwater, estuarine, and marine ecosystems. distribution chlorophyll its breakdown fractions (pheophytin, pheophorbide) exhibited distinct spatial variations. Fresh-water (except Haldia-port) estuarine are characterized high-biomass, high-pheophytin, low-pheophorbide, whereas marine-ports low-biomass Mangalore-port), low-pheophytin, high-pheophorbide. Pheophytin were biomass independent dependent, respectively. pheophorbide: pheophytin ratio indicated potential proxy for determining dominant pathway, i.e., herbivory (>1) not (<1). However, CHl-BP taxa-specific grazer's feeding habits. ratios apparent differences between different ecosystems, higher in (up 11.2) followed 0.9) freshwater 0.4; except Haldia) systems. diatoms (preferred grazer diet) contribution total phytoplankton was more low high suggested prevalence via mode, We proposed that scaling will have implications ballast management - BWM (ballast tank conditions (eg. dark) during voyages, post-voyage discharge including treated using approved systems, nature ports, point) algal bloom research (e.g. understanding fate control measures).

参考文章(53)
Jeffrey G. Allison, M.E. Wagner, M. McAllister, A.K.J. Ren, R.A. Snyder, SAND BOTTOM MICROALGAL PRODUCTION AND BENTHIC NUTRIENT FLUXES ON THE NORTHEASTERN GULF OF MEXICO NEARSHORE SHELF Gulf and Caribbean Research. ,vol. 25, pp. 1- 8 ,(2013) , 10.18785/GCR.2501.01
John W. Fleeger, Richard E. Condrey, M. Grippo, K. R. Carman, High Benthic Microalgal Biomass Found on Ship Shoal, North-central Gulf of Mexico Bulletin of Marine Science. ,vol. 84, pp. 237- 256 ,(2009)
Timothy Richard Parsons, Yoshiaki Maita, Carol M. Lalli, A manual of chemical and biological methods for seawater analysis ,(1984)
David A. Caron, Ee Lin Lim, Holly Kunze, Elizabeth M. Cosper, Donald M. Anderson, Trophic Interactions Between Nano- and Microzooplankton and the “Brown Tide” Springer, Berlin, Heidelberg. pp. 265- 294 ,(1989) , 10.1029/CE035P0265
URBAN TILLMANN, Interactions between Planktonic Microalgae and Protozoan Grazers1 Journal of Eukaryotic Microbiology. ,vol. 51, pp. 156- 168 ,(2004) , 10.1111/J.1550-7408.2004.TB00540.X
Doris Abele-Oeschger, Hans Theede, Digestion of algal pigments by the common periwinkle Littorina littorea L. (Gastropoda) Journal of Experimental Marine Biology and Ecology. ,vol. 147, pp. 177- 184 ,(1991) , 10.1016/0022-0981(91)90181-U
Robert R. Bidigare, Tamara J. Frank, Colleen Zastrow, James M. Brooks, The distribution of algal chlorophylls and their degradation products in the Southern Ocean Deep Sea Research Part A. Oceanographic Research Papers. ,vol. 33, pp. 923- 937 ,(1986) , 10.1016/0198-0149(86)90007-5