PELAGIC-BENTHIC COUPLING IN THE OLIGOTROPHIC CRETAN SEA (NE-MEDITERRANEAN) - CINCS. VERTICAL FLUX OF PHYTOPLANKTON, MICROZOOPLANKTON AND FAECAL PELLETS. PRELIMINARY RESULTS
PELAGIC-BENTHIC COUPLING IN THE OLIGOTROPHIC CRETAN SEA (NE-MEDITERRANEAN) - CINCS. VERTICAL FLUX OF PHYTOPLANKTON, MICROZOOPLANKTON AND FAECAL PELLETS. PRELIMINARY RESULTS
Ypma, J. E. & Wassmann, P.
Norwegian College of Fishery Science (NCFS). University
of Tromsø, N-9037 Tromsø, Norway
Primary production in the open ocean of the Cretan Sea
is expected to be strongly coupled to pelagic heterotrophic
organisms with little flux to deeper waters. To test
this hypothesis PPS 3/3 Technicap sediment traps were
deployed at 200 m and 1500 m depth at a deep sea station
in the Cretan Sea.
The microscopical analysis of the collected material
from November 1994 to May 1995 revealed that faecal
pellets and amorphous material made up the bulk of
organic matter. Faecal pellets were grouped in four
size categories: cylindrical (250-2200 micrometer(s)),
elliptical/ spherical pellets of large (250-400 micrometer(s)),
medium (80-200 micrometer(s)) and small (30-75 micrometer(s))
size. In addition we observed that very large elliptical
pellets (400-800 micrometer(s)) were present in the
trap at 1500 m depth. The average faecal pellet flux
was calculated to 0.242 mg C m-2
d-1 (s.d
129) and 0.291 mg C m-2
d-1 (s.d
88) at 200 m and 1500 m depth, respectively. Biovolume
of faecal pellets was converted to carbon by using
a conversion factor of 0.0268 pg C micrometer(s)-3
according to Urrere and Knauer (1981).
Diatom remains and skeletons of silicoflagellates were
numerous, but very few intact cells were observed.
Coccolithophorids and unidentified cells (probably
cysts) made up the majority of phytoplankton carbon
flux to deeper waters. The vertical flux of polycystine
and phaeodarian radiolaria and foraminifera ranged
between 0.2-5 103 and 2-8 103
cells m-2
d-1,
respectively.
Swimmers were present in all samples from 200 m depth.
Copepodes were dominating, but pteropods (Thecosomata),
polychaete larva, malacostracan larva and small fish
larva were also present.
Material & Methods
Two Technicap PPS 3/3 cylindro-conical sediment traps
with a collecting area of 0.125 m2
were programmed with a collection sequence of 15 days
interval which gave 12 consecutive samples from November
1994 to May 1995. The traps were deployed at 200 m
and 1500 m at the deep sea station D7 in the Cretan
Sea. See Tselepides et al (this volume) for exact
location of the stations in the CINCS project. A volume
split of 1/16 were analysed in a Leitz IML inverted
light microscope at low magnification (40X). To count
smaller pellets and organisms the material was diluted
and a 1:10 subsample was taken out by a pipette and
analysed. Faecal pellets are reported in five categories
of cylindrical and spherical/oval forms. Biovolume
of faecal pellets were calculated from linear dimensions.
To convert faecal matter to carbon flux we used a factor
of 0.0268 pg C micrometer(s)-3
according to Urrere and Knauer (1981).
Results & Discussion
Foraminifera and radiolarians were found with highest
numbers in December with lower numbers in February
and March. Only the phaeodarians among the radiolarians
appeared to have intact protoplasma. The polycystine
radiolarians (Spumellaria and Nassellaria) were always
recorded as skeletons.
Two characteristics were evident when comparing the
pellet flux at 200 m and 1500 m depth. The vertical
flux increased with depth from December to February,
but was reversed from March to May. Secondly, the
presence of large elliptical pellets (400-800 micrometer(s))
at 1500 m depth. These pellets appeared very dense
and are probably produced by bathypelagic or interzonal
migrating zooplankton. Their contribution to the carbon
flux ranged from 3.5-20 mg C m-2 d-1
or < 10% of total faecal flux at 1500 m.
References
Tselepides et al. (this volume).
Urrere, M. A. & G. A. Knauer (1981). Zooplankton
fecal pellet fluxes and vertical transport of particulate
material in the pelagic environment.
J. Plankt. Res. 3: 369-387