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Prymnesiophytes
(Haptophytes)
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Characteristic
genus: Prymnesium

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Abundance:
primarily marine group, highest diversity
in oligotrophic water at greater depth
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Appearance:
Naked cells, mostly single and < 20 µm; motile, 2 flagella and
1 haptonema (therefore
also referred to as Haptophytes)
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Coccolithophorids
cells with scales of calcium carbonate (coccoliths) on the cell surface
(Coccolithophorids)
 
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Coccoliths
contribute ~25% of annual carbon transport to the deep-sea
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Fossil
records because coccoliths are well preserved
in sediments; coccolith deposits form white carbonate cliffs, e.g. White
Cliffs of Dover

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Phototrophic
and mixotrophic
forms; phagotrophy
abundant in cells that lack coccoliths
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Secondary
plastids with 4 membrane envelopes
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Pigments:
Chl.a, Chl.c, b-carotene, diatoxanthin, diadinoxanthin, fucoxanthin, 19-hexanoylfucoxanthin,
19-butanoylfucoxanthin; high diversity in accessory pigments, no pigment
characteristic for all prymnesiophytes
Prymnesiophyte Cell
Structure

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Coccosphere:
outer wall of coccoliths
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Coccoliths
are either produced with in the cell by the Golgi apparatus (heterococcoliths)
or outside the cell membrane (holococcoliths)
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Haptonema
is no flagellum, does not possess 9+2 microbubuli structure; it can be
as long as 160 µm
 
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Phagotrophy:
long haptonema are used for prey capture and attachement to substrates;
short haptonema mostly without function


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Coccolithophorids
lack haptonema
The Coccoliths
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Organic
scales occur in a few species together with
calcareous coccoliths

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Holococcoliths:
produced externally, simple shapes;
  
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heterococcoliths
are produced internally and possess a complex three-dimensional structure
  
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Great
variety of coccolith forms, used for taxonomy
and geological identifications

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Function:
defense of small grazers and infection by pathogenes; light focusing into
the cell has been discussed
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Coccolith
production is highly dependent on photosynthesis
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Calcification
is not a net sink for CO2!
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2 HCO3-
+ Ca2+ = CaCO3 + CO2 + H2O
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Atmospheric
CO2 partial pressure is higher than normal above oceanic coccolithophorid
blooms
Oceanic Blooms: Emiliania
huxleyi
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Prominent
blooms in temperate and polar areas of both
hemispheres
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Water
discoloration can be seen from satellites
 
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Three
life-cycle stages: non-motile C cells with
coccoliths, non-motile naked N-cells, motile S-cells with scales; DNA analyses
indicate that S-cells are haploid and C-cells are diploid


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Sexual
reproduction appears likely, given the presence
of diploid and haploid stages, but gamete fusion has not been observed
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DMS:
Emiliania huxleyi produces DMSP (dimethylsulfoniumpropionate); converted
to DMS (dimethylsulfide) upon release to air
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Climate
effects: DMS increases cloud formation; increased
clouds and coccolithsincrease water albedo ? cooling effect

Foamy Beaches: Phaeocystis
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Bloom
forming in the North Sea, Gulf of Maine, Antarctic
Ocean
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Foam
accumulates on the beaches during dense blooms because wave action destroys
the cells and wips the cells‘ proteins to foam

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Biogeochemically
of interest due to DMS production; ca. 10% of global DMS is produced by
Phaeocystis
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Growth
forms: as large (up to 1 cm), hollow, gelatinous
colonies with round cells lacking flagella, haptonema, and scales; or biflagellate,
single cells with short haptonema; blooms are formed by colonies
 
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Toxicity
is not reported from such blooms, but fish evades blooms, probably by detection
of the DMS in the water
Fisheries
are affected by net clogging
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