Fróðskaparrit - 01.01.2005, Side 95

Fróðskaparrit - 01.01.2005, Side 95
LUTFALSLIGA ÁVIRKANIN AV PROTOZOOPLANKTON OG KOPEPODUM Á VÁRBLÓMING 93 AV PLANTUPLANKTON Á LANDGRUNNINUM í 1999 rate of 0.08 d'1 is based on a relatively high estimated ingestion rate from the copepod community during pre-bloom. This high estimated ingestion rate from the copepod community, can be interpreted in two dif- ferent ways: 1. The first possibility is that primary production during pre-bloom actually could have been high during this pe- riod, but due to grazing a build up of biomass was prevented. 2. The second possibility is that the copepod community during pre-bloom partly relies on lipid reserves to fuel gonad development and egg produc- tion. There has been some speculation in the past years as to what extent copepods are able to control the onset of the phytoplankton spring bloom. Yin et al. (1997) reported on the importance of the large oceanic co- pepod Neocalanus plumchrus during early spring from the Strait of Georgia, British Columbia. A large biomass of this cope- pod prior to spring-bloom, was able to suppress and thus delay the spring bloom development. Bathmann et al. (1990) found a large influence of copepods on the spring-bloom development in the Norwe- gian Sea, and postulated that if the upward migration of overwintering copepods oc- curred shortly before or concomitant with the diatom spring bloom, bloom forma- tion could be hindered. Other researchers have, however, stated the opposite, and concluded that the grazer community is not able to control or postpone a spring bloom (e.g. Smith et al., 1985; Hirche et al., 1991; Nielsen and Hansen, 1995). It is, however, not likely that the cope- pods were suppressing the phytoplank- ton spring bloom during our study. If the grazer community actually was suppress- ing the development of the phytoplankton spring bloom, we would have expected C. finmarchicus to graze at a maximum, and hence show a much higher egg production rate during this period. The most likely possibility for the high estimated ingestion rates during pre-bloom is probably that the females may have used stored lipids to fuel parts of the egg production during this period. There has been some debate about the importance of lipid storages during low productive pre- bloom periods. It is generally accepted that gonadogenesis and development of early oocyte in many Calanus species is partly fuelled by stored energy during winter (e.g. Hirche, 1996 and references therein), but to what extent these lipid re- serves actually are used for egg produc- tion in C. finmarchicus is not certain. This has been proposed for the closely related species Calanus helgolandicus (Gatten et al., 1979; 1980), and Hirche (1996) sug- gested that overwintering C. finmarchicus females might invest their lipid storages in egg production, since they may not have undergone the reported drastic lipid losses solely for maturing from the CV copepo- dite stage. This is supported by investiga- tions in the Faroe-Shetland Channel and northern North Sea (Richardson et al., 1999), the Labrador Sea (Cabal et al., 1997) and at station M in the Norwegian
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