Deep chlorophyll maximum
Chlorophyll maximum layers, referred in the literature as deep chlorophyll maximum layers (DCM) or subsurface chlorophyll maximum layers (SCM), are common features of vertical stratified water columns. The term DCM is broadly used to describe a subsurface maxima of chlorophyll concentration. These are found throughout oceans, lakes, and estuaries around the world at varying depths, thicknesses, intensities, composition, and time of year.[1]
Location and Formation
The DCM depth varies both temporally and spatially; in many tropical gyres, this is a permanent structure within the water column, while in more temperate waters this feature can be seasonally formed. Many subtropical and tropical gyres, with minimal adsorption coefficients, contain strongly shade-adapted flora in the deeper euphotic zones forming the deep chlorophyll maximum. In this zone, generally around 100 m in tropical gyres, the net photosynthetic rate is still positive due to large concentrations of chlorophyll per cell resulting from shade adaptation.[2]
In several studies, the DCM layer was found to be located in the thermocline, adjacent to the nutracline, at the bottom of the euphotic layer, where light attenuation ranges from ~1-2%[3] [4] up to ~10%.[5] DCM’s can also be formed below the euphotic zone, where light levels are >1% and photosynthesis cannot actually occur. These layers are formed through purely physical processes due to the subduction of surface waters.
Plankton Community
The plankton community within the DCM is highly variable and diverse. One study in the western pacific gyre found over 223 major taxa, including alga, coccolithophorids, dinoflagellates, silicoflagellates, and diatoms.[6] This flora is not only the shade-acclimated plankton from higher up in the euphotic zone, but also includes widespread and populous species, such as Prochlorococcus. Through liquid chromatographic techniques used to distinguish difference in photosynthetic pigments, it was recently found that more than half of the pigment in DCM is divinyl chlorophyll a, which implies a dominance of Prochlorococcus in primary production.[7]
See also
References
- ↑ Cullen, JJ. (1982). "The Deep Chlorophyll Maximum: Comparing Vertical Profiles of Chlorophyll a". Canadian Journal of Fisheries and Aquatic Sciences 39 (5): 791–803. doi:10.1139/f82-108.
- ↑ Miller, Charles B. (2004). Biological Oceanography. Blackwell Science Ltd. pp. 56–58.
- ↑ Veldhuis, MJC; Kraay, G.W. (1990). "Vertical distribution and pigment composition of a picoplanktonic prochlorophyte in the subtropical North Atlantic: A combined study of HPLC-analysis and flow cytometry". Mar. Ecol. Prog. Ser. 68: 121–127. doi:10.3354/meps068121.
- ↑ Kononen, K.; Hallfors, S.; Kokkonen, M.; Kuosa, H.; Laanemets, J.; Pavelson, J. (1998). "Development of a subsurface chlorophyll maximum at the entrance to the Gulf of Finland, Baltic Sea". Limnology Oceanography 43: 1089–1106. doi:10.4319/lo.1998.43.6.1089.
- ↑ Mackey, D. J.; Parslow, J.; Higgins, H.W.; Griffith, F.B.; O'Sullivan, J.E. (1995). "Plankton productivity and biomass in the western equatorial Pacific:Biological and physical controls". Deep-Sea Research 42: 499–533. doi:10.1016/0967-0645(95)00038-r.
- ↑ Furuya, Ken; Marumo, Ryuzo (1983). "The structure of the phytoplankton community in the subsurface chlorophyll maxima in the western North Pacific Ocean". Journal of Plankton Research 5 (3): 393–406. doi:10.1093/plankt/5.3.393.
- ↑ Karl, D.M.; Bidigare, R.R.; Letelier, R.M. (2001). "Long-term changes in plankton community structure and productivity in the subtropical North Pacific Ocean: the domain shift hypothesis". Deep-Sea Research II 48 (8-9): 1449–1470. doi:10.1016/s0967-0645(00)00149-1.