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Guidelines for
photographing, fixing and preserving corals and sponges
(To be used with
the Identification
Guide for corals and sponges for use by sea-going observers the
SEAFO Convention Area)
GENERAL
CONSIDERATIONS
Step 1.
For each trip observers are requested to photograph specimens of
a representative collection of the corals and sponges observed
in catches.
Step 2.
Where possible, a specimens collection should be frozen or
preserved using the methods described below. Only specimens in
good condition should be preserved. However, if all specimens
taken in catches are usually damaged then a representative
sample should be preserved.
PRESERVATION METHODOLOGY
a) For
corals – these should be preserved with 80% alcohol.
80%
alcohol: method of preparation.
Dilute 8
parts of 100% ethanol in 2 parts of fresh water.
b) For
sponges – these should be preserved with 4% formaldehyde
4%
formaldehyde: method of preparation.
Commercial
available formalin is a 37% solution of formaldehyde.
For a 4%
formaldehyde solution, dilute one part of the 37% (commercial)
formaldehyde in 9 parts of sea water. A buffering agent (Borax:
sodium tetraborate) should be added to prevent the dissolution
of calcareous material (one spoonful/litre).
Formaldehyde should be handled with extreme caution (toxic,
carcinogenic substance!)
Preparation of fixatives should be carried out ashore before
commencing the trip.
For
preservation using formaldehyde or alcohol, keep the specimens
in plastic containers of adequate size and add the preservative
solution until the specimens are completely submerged.
All
samples must be clearly labelled: A label including: vessel;
gear, best estimate of spatial position of capture (decimal
latitude and longitude to the nearest minute) date, depth and
taxon name must be placed inside each container. The labels,
made in resistant paper, should be written in pencil. Each
container should be also externally labelled with the same
information (using a permanent marker)
TABLE:
FIXATION AND PRESERVATION OF DIFFERENT INVERTEBRATES
|
Taxon |
Solution |
|
Porifera |
|
|
Hexactinellida (SHEET 1) |
4%
formaldehyde |
|
Demospongia (SHEET 2) |
4%
formaldehyde |
|
Calcarea |
80% alcohol |
|
Cnidaria |
|
|
Hydrozoa |
|
|
Anthoathecata – Leptothecata (SHEET 3) |
80% alcohol |
|
Stylasteridae (SHEET 3) |
80% alcohol |
|
Anthozoa |
|
|
Alcyonacea (SHEET 4) |
80% alcohol |
|
Gorgonacea (SHEET 5) |
80% alcohol |
|
Primnoidae |
80% alcohol |
|
Isididae (SHEET 5) |
80% alcohol |
|
Chrysogorgiidae (SHEET 5) |
80% alcohol |
|
Pennatulacea (SHEET 4) |
80% alcohol |
|
Antipatharia (SHEET 6) |
80% alcohol |
|
Scleractinia (SHEET 7) |
80% alcohol |
|
Bryozoa |
80% alcohol |
Other
preservation methods
When it is
not possible to use the above methods, samples should, where
possible, be stored frozen. In this case, each sample
must be placed in a plastic bag and clearly labelled internally
(resistant paper label) and externally (permanent marker) with
the information described above.
Specimens
of some groups: Stylasteridae, Gorgonacea (including Primnoidae,
Isididae and Chrysogorgiidae), Scleractinia and some Bryozoa,
can be preserved by drying. For storage, the dried specimens
must be placed in a plastic bag and clearly labelled (permanent
marker) with the information described above.
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