[NHCOLL-L:5608] Fwd: FW: Rehydration of a sea anemone
Couteaufin at aol.com
Couteaufin at aol.com
Sun Aug 21 07:01:05 EDT 2011
From: Couteaufin at aol.com
To: dlauretta at gmail.com
CC: simmons.johne at gmail.com, abentley at ku.edu, nitellopsis at googlemail.com
Sent: 21/08/2011 12:00:02 GMT Daylight Time
Subj: Re: [NHCOLL-L:5600] FW: Rehydration of a sea anemone
Hi Daniel,
Andy forwarded your enquiry to me. Say hello to Daphne Fautin, she may
remember me from the days when I worked in the coelenterate section at the
NHM in London (early 1980s).
Alway rather ticklish when you have the holotype to perform such a radical
treatment!
Bear in mind also that rehydration will improve the appearance and texture
but it will compromise future DNA extraction/readings. If you need
further advice on this let me know.
I have also forwarded this to John Simmons who may also have some comments.
I tend to use Decon-90 at around 3 to 5% in deionised water as a
rehydrating agent.
The reaction is catalysed by warming it to no more than 50 deg. Centigrade
(hotplate) and make sure that the container has a loose lid to prevent
massive evaporation during warming.
Obviously photograph and weigh the specimen prior to treatment.
Start the process first thing as it can take some time and so that you can
monitor its progress during the day.
The fluid will start to yellow a bit and may smell rather fishy; the
specimen will gradually sink into the fluid - this will only happen in an ideal
situation, so if the specimen has expanded and feels soft and more flexible
like it should if not dry, then it will have reached its 'end-point'. If
it's still floating then it will have air trapped inside.
In which case.... place the specimen in clean water and place the
container inside a vacuum desiccator. Apply a mild vacuum to it and air should
bubble out of the specimen. After no more than a minute, stop the pump
(making sure that the hose is removed from the desiccator and that the tap is
closed before the pump is switched off - or it will suck the oil from the pump
all over the specimen!!)
Then release the vacuum slowly and the anemone should sink completely or
partly. Repeat the process until no more air bubbles out. Small amounts of
trapped air will often slowly diffuse out later in the alcohol
preservative (see below).
You should now have a fully rehydrated specimen. Place into formalin to
refix overnight and next day start to transfer into an alcohol dehydration
ladder so that by the end of the day, the specimen is preserved in IMS once
again. Ensure that the jar seal is good! Finally, make a note of the
treament for the specimen's record and reweigh the specimen, having drained off
excess fluid and re-photo.
That should hopefully be it!
With all good wishes, Simon
Simon Moore MIScT, FLS, ACR,
Conservator of Natural Sciences,
_www.natural-history-conservation.com_
(http://www.natural-history-conservation.com/)
_www.pocket-fruit-knives.info_ (http://www.pocket-fruit-knives.info/)
_http://uk.linkedin.com/in/naturalsciencespecimenconserve_
(http://uk.linkedin.com/in/naturalsciencespecimenconserve)
In a message dated 18/08/2011 16:31:29 GMT Daylight Time, abentley at ku.edu
writes:
Hi all
A question from someone not on this list about relaxing sea anemones for
dissection. Please respond directly to him with any help you may have.
Thanks
Andy
A : A : A :
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V V V
Andy Bentley
Ichthyology Collection Manager
University of Kansas
Natural History Museum & Biodiversity Institute
Dyche Hall
1345 Jayhawk Boulevard
Lawrence, KS, 66045-7561
USA
Tel: (785) 864-3863
Fax: (785) 864-5335
Email: _abentley at ku.edu_ (mailto:abentley at ku.edu) :
: :
A : A : A :
}<(((_°>.,.,.,.}<(((_°>.,.,.,.}<)))_°>
V V V
From: Daniel L [mailto:dlauretta at gmail.com]
Sent: Thursday, August 18, 2011 7:50 AM
To: Bentley, Andrew Charles
Subject: Rehydration of a sea anemone
My Name is Daniel Lauretta and I´m working with sea anemones (Cnidaria:
Anthozoa) in the argentinean museum of natural sciences. I have a holotype
of a sea anemone from a swedish Museum. The specimen was preserved in
formalin or etanol, but it has accidentaly dried and was put again in alcohol.
Now, I´m trying to study the specimen, but the tissue is hard and I can´t do
a disection. Do you know a way to soften the tissue? Or perhaps you can
tell me who could known how to do this. Daphne Fautin gave me the direction of
this website.
Thank you very much.
Lauretta Daniel M.
Museo Argentino de Ciencias Naturales Bernardino Rivadavia
Lab. 57
Av. Angel Gallardo 470 - C1405DJR - Buenos Aires - Argentina -
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