Samples should usually not exceed 20 mm
20 mm and there
must be at least 10 times the volume of fixative as there is tissue. Small carcasses can be fixed whole, following opening for processing
Tissues fixed in glutaraldehyde for
As above
Generally as above but only tiny samples are taken. Scanning electron
transmission electronmicroscopy
microscopy (SEM) employs different techniques and is not
(TEM)
considered here
Cytological
As above (histology)
Easy to take, cheap to process (readily done in any veterinary pr
actice
preparations
or in the field), and produce rapid results. Usually consist of touch preparations/impression smears which can give valuable informa
tion
about tissues within a few minutes. The samples must first be blotted onfilter paper in order to remove excess blood
Swabs, organ/tissue samples,
Live birds (superficial lesions, mouth or
Usually comprise swabs (in transport medium if they are t
o be sent
and other specimens for
cloacal swabs, or dead birds but also
elsewhere), portions of tissue, or e
xudates/transudates (Hunter 1
989;
microbiological and other
samples from internal organs)
Scullion 1989). If culture proves impossible for financial or other
investigations
reasons, an impression smear stained with Gram or other stains will often provide some useful information
Tissues for toxicological
Mainly dead birds but some small
Toxic chemicals may have been the cause of dea
th or could have
examination
samples can be taken from live birds,
contributed to the bird’s ill-health, either dir
ectly or by increasing its
for example, blood or muscle biopsies
susceptibility to infectious disea
se. Samples from wild bird casualties can
for certain pesticide analyses, feathers
be taken and stored routinel
y for toxicological analysis
(for heavy metal and other analyses)
Samples for toxicology ar
e usually kept frozen and can be analyzed
at a later date. As with formalin-fixed samples, such specimens should betaken and stored even when there is no immediate prospect of their beinganalyzed