Prof. Dr. Gamila H.
Ali
Water Pollution Research Department
National Research Centre
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Phytoplankton
The phytoplankton (microscopicalgae) occur as
unicellular, colonial or filamentous forms .
Biological methods used for assessing water
quality include the collection, counting,
identification, biomass measurements and
measurements of metabolic activity.
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I- Sample Collection:
Kem-meter Van Dorn
Structural features of common water samplers
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II- Concentration Techniques
Sample Fixation:
Lugol’s Solution:
20 gm potassium iodide (KI) and 10 gm iodine
crystals in 200 ml distilled water containing 20 ml
glacial acetic acid add 0.7 ml per each 100 ml
sample.
1- Phytoplankton net. 2- Sedimentation
3- Membrane Filtration. 4-Centrifugation.
5- Sand Filter.
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II- Concentration Techniques
Examples commonly used plankton sampling
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II- Concentration Techniques
Apparatus used in sand filtration method
A-cylindrical funnel: the graduations are commonly omitted except on
funnels that are to be used in the field, B-revolving stand for filter funnels.
C-concentrating attachment, showing U-tube in place. (From Whipple)
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III- Microscopes and Calibrations
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Calibration of Whipple Square
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V- Phytoplankton Counting Techniques
From the well mixed concentrated sample, a 1 ml
was drown and place into a Sedgwick- Rafter cell.
The cell was microscopically examined using
preadjusted eye piece and objective lens of the order
(x 15) for the eye piece and a 20-mm objective.
Counting was conducted on 50-fields of the cell using
a calibrated micrometer adjusted to the eye piece.
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phytoplanktonic organisms present in a sample
under investigation the following formula is
applied:
To calculate the number of
No. of phytoplankton/ml =
No. of fields in cell ml of concentrated sample
No. of fields counted ml of original sample
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V- Phytoplankton Counting Techniques
Counting cell (Sedgwick- Rafter), showing method of filling
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IV- Chlorophyll Content
Chlorophyll“a” is used as an algal biomass indicator.
Assuming that chlorophyll “a” constitutes on the
average, 1.5% of the dry weight of organic matter
(ash-free weight) of algae, estimate the algal biomass
by multiplying the chlorophyll “a”content by a factor
of 67.
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Spectrophotometric measurments of absorbance
and optical density at three different wave lengths
was the method adapted for estimation of
chlorophyll extracted via organic solvents. The
extracts represent the photosynthetic chlorophyll
pigments, namely, chl “a”, chl “b” and chl “c”
according to Standard Methods (1998).
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IV- Chlorophyll Content
The procedure involves the addition of 0.1 gm of
magnesium carbonate powder to one liter of water
sample in order to prevent chlorophyll degradation.
After shaking, the sample was filtered through
membrane filter (0.45 ) or centrifuged at 2000 r.p.m.
for 10 min. Following filtration, the membrane was
ground up and dissolved in 90% acetone (Ca 10-ml).
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The tightly capped tube was then placed in
refrigerator at 4oC for 18-24 hours to enhance complete
extraction.
. The material was mixed and centrifuged for
10 minutes at 1000 r.p.m
The clear extract was transferred to a 1-cm cuvette
and absorbance at 664, 647 and 630 nm were
determined using spectrophotometer. Measurements
at 750 nm were made for turbidity correction.
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IV- Chlorophyll Content
Calculation of chlorophyll concentration determined
as chlorophyll “a” was derived from equation:
Chl “a” = 11.85 (OD664) - 1.54 (OD647) + 0.08 (OD630)
OD663 , OD645 and OD630 Corrected optical denities (with a
1-cm light path) at the respective wavelengths. The final
calculation of the chlorophyll “a” content of sample
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under investigation is given by the formula:-
Chi “a” v
Chlorophyll “a” (mg/m3) = IV
in which v: is the amount of acetone extract in ml.
V: is the volume of the filtered water.
I : is the length of the cuvette used.
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IIV- Determination of Biomass (Standing
Crop)
1- Chlorophyll “a”
2- Biovolume (Cell Volume)
Plankton data derived on a volume per volume basis
often are more useful than numbers per milliliter.
Determine cell volume by using the simplest
geometric configuration that best fits the shape of the
cell being measured (such as sphere, cone, cylinder).
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IIV- Determination of Biomass (Standing
Crop)
3- Cell Surface Area
An estimation of cell surface area is valuable in
analyzing interactions between the cell and
surrounding waters. Compute average surface area in
square micrometers and multiply by the number per
milliliter of the species being considered.
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IIV- Determination of Biomass (Standing
Crop)
4- Displacement Volume
This method measure an equivalent volume of liquid
that is displaced by the sample.
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5- Gravimetric Methods
The biomass of the plankton community can be
estimated from gravimetric, although silt and organic
detritus interfere. (ashing the sample at 105ºC and
then at 500ºC).
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6- Adenosine Triphosphate (ATP)
Methods of measuring adenosine triphosphate (ATP)
in plankton provide the means of determining the total
viable plankton biomass. ATP occurs in all plants and
animals, but only in living cells. The ratio of ATP to
biomass varies from species to species.
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IIIV- Metabolic Rate Measurements
The physiological condition and spectrum of
biological interactions of the aquatic community must
be considered for evaluation of the state of natural
waters.
1 -Nitrogen Fixation
The ability of an organism to fix nitrogen is a great
competitive advantage and plays a major role in
population dynamics.
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2 -Productivity, Oxygen Method
Productivity is defined as the rate at which inorganic
carbon is converted to an organic form.
Photosynthesis ultimately results in the formation of
a wide range of organic compounds, release of
oxygen, and reduction of carbon dioxide (CO2) in the
surrounding waters.
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Primary productivity can be determined by measuring
the changes in oxygen and CO2 concentrations
CO2 + H2O -------- (CH2O)n + O2
Net photosynthesis = light bottle DO – initial DO
Respiration = initial DO – dark bottle DO
Gross photosynthesis = light bottle DO – dark bottle
DO
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IIIV- Metabolic Rate Measurements
3- Productivity, Carbon 14 Method
A solution of radioactive carbonate (14CO32-) is added to
light and dark bottles that have been filled with sample
as described for the oxygen method. The quantity of
carbon fixed is proportional to the fraction of
radioactive carbon assimilated.
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This procedure differs from the oxygen method in that
it affords a direct measurement of carbon uptake and
measures only net photosynthesis.
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