Phytoplankton Diversity and Evolution Flashcards

1
Q

Classification and taxonomy

A

Single celled 1um phytoplankton to 30m (kelp)
No tissue differentiation
Classification based on:
- Pigments
- Food storage products
- Variable cell wall composition
- Variable flagella position, length, form, number
- Other cellular features
- molecular analysis

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2
Q

Evolution of oxygenic photosynthesis

A

Photosystems in oxygenic photosynthesis very similar to the photosystems found in S bacteria

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3
Q

Prokaryotes and Eukaryotes

A

Cyanobacteria and Prochlorophytes
Euks:
Bacillariophyta - Diatoms
Dinophyta - Dinoflagellates
Crysophyta
Haptophyta
Cryptophyta
Chlorophyta - green algae
Euglenophyta

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4
Q

Evolution of eukaryotic phytoplankton

A

Primary symbiosis of a cyanobacterium with an apoplastidic host, rise to chlorophyte and red algae.
Chlorophyte line, second symbioses –> “green” line of algae, predecessor of all higher plants.
Secondary symbioses in the red line with various host cells gave rise to all chromophytes, diatoms, cryptophytes and haptophytes.

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5
Q

Prokaryotic cell

A

Photosynthetic apparatus in thylakoids

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6
Q

Eukaryotic cell

A

Outer cell covering of cellulose, silica, protein, calcite or organic scales
Nucleus
Mitochondria
Golgi, form waste material and polysaccharide production.
Endoplasmic reticulum and ribosomes
Chloroplast
Pyrenoid: proteinaceous area of chloroplast, site of carbon dioxide fixation
Vacuoles
Flagella

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7
Q

Cell walls

A

Silica in diatoms
Cellulose in dinoflagellates
Mucilage in Phaeocystis
Calcium carbonate in Coccolithophores

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8
Q

Pigments

A

Range of pigments across primary producers and therefore colours
Energy of the absorved photon modifies the electronic structure of pigment molecules
Auxiliary pigments can capture and utilise different wavelengths:
- Biliproteins found in cyanophyta, Rhodophyta and cryptophyta
- Carotenoids
Chlorophyll and carotenoids are soluble in lipid type solvents
Biliproteins are soluble in water.

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9
Q

Molecular phylogeny

A

Application of molecular methods to determine genetic diversity of organisms
Ribosomes are the sites of protein synthesis, have a slow evolutionary rate and are composed on two subunits, large and small
Prokaryotes 16S ribosomal RNA
Eukaryotes 18S ribosomal RNA
Ribosomal units can reveal phylogenetic relationships between bacterium types.

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10
Q

Sampling

A

Nets:
- large volume of water in short time
- Good for collecting large organims
- more difficult to sample quantitatively and to target discrete depths.
CTD:
- Samples a smaller volume of water, 5 to 20L
- Good for tageting discrete depths and collecting smalll to medium sized organisms
- largest organisms may be under sampled.
CPR/VPR:
- Continuous plankton recorder
- Captures samples on a silk, the preserved for future analysis
- Video plankton recorder.
- Captures images of larger images in situ.

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11
Q

Quantification

A

Light microscopy
Flow cytometry:
- individual cells counted and characterized according to optical characteristics
- Scatter (size)
- Chlorophyll a fluorescence and phycoerythrin fluoroescence

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12
Q

Pigments, HPLC

A

Pigments extracted into solvent
Pigments separated by High Performance Liquid
Chromatography then quantified by fluorescence and absorption,

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