<div dir="ltr"><div class="gmail_default" style="font-family:tahoma,sans-serif;font-size:small;color:#000000">
<p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%">There are several drawbacks to using the suggested steps of
30-50-75. </span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><br></span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%">According to Waller and Strang (1996), transfer in concentration steps
greater than 20% risks causing cellular rupture to specimens because of the effect
of ethanol concentration on osmotic pressure (see figure 7 in Waller and
Strang). As stated in their paper, “…it is clear that the osmotic pressure rises
steadily with ethanol concentrations for solutions below about 75% v/v and
begins to rise more rapidly at concentrations above about 80% v/v. These facts
suggest that, from considerations of osmotic pressure, solutions with
approximately equal concentrations are appropriate for stepping specimens up to
higher ethanol concentrations, up to about 75%v/v.” This means that the abrupt
change from water to 30% ETOH should be avoided, and as the concentration of
ethanol nears 75% it is very close to the osmotic pressure shift, which should
also be avoided by not going above 70%. </span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><br></span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%">In addition, starting with the abrupt change to 30%
ETOH will cause more rapid dehydration than a 20% step, and rapid dehydration
is potentially destructive to tissues. </span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><br></span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%">Lastly, the assumption that using 75% ethanol
may result in a 70% concentration after stepping up may well be incorrect
(depending on the volume of fluid used and the specimen). The recommendation
for using 70% ethanol is based on the fact that 70%, ETOH is a very good
biocide, but ethanol preservation is balance between providing an antiseptic
environment and excessive dehydration of the specimens, so there is no reason,
but some risk, in using ETOH at concentrations greater than 70% (see figures 12
and 13 in Waller and Strang 1996).<span></span></span></p>
<p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><span> </span></span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><span>Referernce:<br></span></span></p>
<p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%">Waller and Strang. 1996. Physical chemical properties of preservative
solutions—I. Ethanol-water solutions. <i>Collection Forum</i> 13(2):70-85<span></span></span></p>
<p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><span> </span></span></p><p class="MsoNormal" style="margin:0in;line-height:107%;font-size:11pt;font-family:"Calibri",sans-serif"><span style="font-size:12pt;line-height:107%"><span><br></span></span></p></div><div><div dir="ltr" class="gmail_signature" data-smartmail="gmail_signature"><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><div><div dir="ltr"><font size="2"><span style="font-family:tahoma,sans-serif">John E. Simmons<br>Writer and Museum Consultant</span></font></div><div dir="ltr"><font size="2"><span style="font-family:tahoma,sans-serif">Museologica<br><i>and</i><br>Investigador Asociado, Departamento de Ornitologia<br>Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Lima</span></font><br></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><br></div><br><div class="gmail_quote"><div dir="ltr" class="gmail_attr">On Mon, Sep 30, 2024 at 3:53 PM Dirk Neumann <<a href="mailto:d.neumann@leibniz-lib.de">d.neumann@leibniz-lib.de</a>> wrote:<br></div><blockquote class="gmail_quote" style="margin:0px 0px 0px 0.8ex;border-left:1px solid rgb(204,204,204);padding-left:1ex"><u></u>
<div>
<div>Hi Dries and all,</div>
<div><br>
</div>
<div>also added offline that especially with these large specimens it would be worth keeping an eye on layering. The final concentration should be at 70%, and you are correct that it might be worth filling the jar up with 75% instead
of 70% to end up at 70% (and not 65%).</div>
<div><br>
</div>
<div>But I am not sure that the steep steps 30/50/70 are necessary for achieving this; if specimens have been sitting in formalin for long time, it might be worth considering lees steep steps (0/20/40/60/70-75) and allow for more time.<br>
</div>
<div><br>
</div>
<div>Pragmatically, when I had to handle a lot of large specimens (often large whitefish), there was the risk of what where cautioning, i.e. that specimens would arrive too fast at "70%" and the residual water could dilute the ethanol
concentration to well below 70%.</div>
<div><br>
</div>
<div>Therefore, I delayed labelling of specimens usually for some time and "added" the time it took to rearrange shelves to free space to monitor the freshly filled 70% jars if I could spot any layering. You could also exchange the 70%
after half a year to make sure that the concentration has not dropped significantly below 70%.</div>
<div><br>
</div>
<div>Both concentrations surely work, but I always preferred the slower option.</div>
<div><br>
</div>
<div>All the best</div>
<div>Dirk<br>
</div>
<div><br>
</div>
<div><br>
</div>
<div>Am 30.09.2024 um 20:28 schrieb <a href="mailto:a.j.van_dam@lumc.nl" target="_blank">
a.j.van_dam@lumc.nl</a>:</div>
<blockquote type="cite">
<div>
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Dear Vanessa,</div>
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There is a very simple way to monitor the progress of fluid exchange when transferring specimens from an aqueous solution of 4% formaldehyde to 70% ethanol.</div>
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</div>
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Since the density of ethanol (d=0.79) is much lower than the density of water (d=1.00) and the density of buffered formaldehyde 4% (d=1.02), during the time the specimen is in one of the transfer baths (ethanol 20-40-60-70), the density of the surrounding fluid
will slowly rise due its exchange with the heavier fluid inside the specimen.</div>
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</div>
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When measuring the surrounding fluid periodically (e.g. once a week) with a densimeter you will see a logarithmic decrease in density until there is hardly a significant change anymore, which indicates that the transfer step has been fully completed and the
specimen can be placed in the next bath. This way of monitoring will ensure correct transfer times without having to worry about the variables of type of specimen, shape, size, etc.</div>
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</div>
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Like Dirk and John, I would also recommend four baths, but with slightly different concentrations: 30-50-70-75, which gives after complete exchange an end concentration a little over 70%.</div>
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</div>
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Kind regards,</div>
<div style="margin:0cm;font-family:Aptos,Aptos_EmbeddedFont,Aptos_MSFontService,Calibri,Helvetica,sans-serif;font-size:12pt;color:rgb(0,0,0)">
</div>
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Dries</div>
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</div>
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<span style="color:rgb(5,99,193)"><u><a href="https://www.linkedin.com/profile/preview?vpa=pub&locale=en_US" id="m_786595444912941031OWA2886ea8c-54ee-7b44-2108-ef3d2d9ac85e" title="Originele URL: https://www.linkedin.com/profile/preview?vpa=pub&locale=en_US. Klik of tik als u deze koppeling vertrouwt." style="color:rgb(5,99,193)" target="_blank">Andries
J. van Dam</a></u></span> | curator-conservator</div>
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<span style="color:rgb(5,99,193)"><u><a href="https://www.lumc.nl/onderwijs/over-ons/anatomisch-museum/?setlanguage=English&setcountry=en" id="m_786595444912941031OWA4c0df347-2047-7f8f-52aa-ddf4bb7c20d5" title="Originele URL: https://www.lumc.nl/onderwijs/over-ons/anatomisch-museum/?setlanguage=English&setcountry=en. Klik of tik als u deze koppeling vertrouwt." style="color:rgb(5,99,193)" target="_blank">Anatomical
Museum</a></u></span> | Directorate of education | Leiden University Medical Center | Building 3 (V3-32)</div>
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P.O.Box 9600 | 2300 RC Leiden | Netherlands</div>
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<u><a href="mailto:A.J.van_Dam@lumc.nl" id="m_786595444912941031OWAe105eb1a-3631-f5fa-b59e-94e2aca94acb" style="color:rgb(5,99,193)" target="_blank">A.J.van_Dam@lumc.nl</a></u></span></div>
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<div style="margin:0cm;font-family:Aptos,Aptos_EmbeddedFont,Aptos_MSFontService,Calibri,Helvetica,sans-serif;font-size:12pt;color:rgb(0,0,0)">
Scientific associate | Natural History Museum London</div>
<div style="font-family:Aptos,Aptos_EmbeddedFont,Aptos_MSFontService,Calibri,Helvetica,sans-serif;font-size:12pt;color:rgb(0,0,0)">
<br>
</div>
<hr style="display:inline-block;width:98%">
<div id="m_786595444912941031divRplyFwdMsg" dir="ltr"><font face="Calibri, sans-serif" style="font-size:11pt" color="#000000"><b>Van:</b> Nhcoll-l
<a href="mailto:nhcoll-l-bounces@mailman.yale.edu" target="_blank">
<nhcoll-l-bounces@mailman.yale.edu></a> namens John E Simmons <a href="mailto:simmons.johne@gmail.com" target="_blank">
<simmons.johne@gmail.com></a><br>
<b>Verzonden:</b> maandag 30 september 2024 17:55<br>
<b>Aan:</b> Dirk Neumann <a href="mailto:d.neumann@leibniz-lib.de" target="_blank">
<d.neumann@leibniz-lib.de></a><br>
<b>CC:</b> <a href="mailto:nhcoll-l@mailman.yale.edu" target="_blank">
nhcoll-l@mailman.yale.edu</a> <a href="mailto:nhcoll-l@mailman.yale.edu" target="_blank">
<nhcoll-l@mailman.yale.edu></a><br>
<b>Onderwerp:</b> Re: [Nhcoll-l] [EXTERN] Removing specimens from formaldehyde</font>
<div> </div>
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<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
Vanessa,</div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
Dirk's advice is correct. <br>
</div>
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<br>
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<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
The reason we lack reliable recommendations for soaking time for each step is that there are too many variables to consider, such as the surface-to-volume ratio of the specimen, thickess of the specimen, whether the specimen has thin skin, scales, fur, a shell,
and so forth, and the density and structure of the dermal layers and internal tissues. </div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
<br>
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<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
There are several papers that give penetration times for formaldehyde or ethanol, but these rates should not be extrapolated for whole specimens. All of the published penetration rates that I have reviewed are based on small samples (often no more than 1
cubic cm in volume) of gels or agars, etc., so the penetration rates are not transferable to whole organisms. For example, the penetration rates of formaldehyde published by Steedman (1976) are based on gelatin and casein gels, Medawar (1941) used plasma clots,
and Baker (1958) used gelatin/albumin gels.</div>
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<br>
</div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
The rate of penetration of fixatives and preservatives is complicated by the fact that the chemicals modify the tissues as they penetrate them, which greatly impedes the rate of penetration of more of the fluid, and quickly limits the depth of penetration of
the fluid (this is why it is recommended to inject formaldehyde or other fixatives into specimens). In addition, penetration rates of preservative fluids are temperature dependent.
<br>
</div>
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<br>
</div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
I hope that someday we will have enough research on penetration, fixation, and preservation rates that we can come up with some general guidelines for time required for each soaking step, but until that day comes, Dirk's advice is the best we have.</div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
<br>
</div>
<div style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)">
--John<br>
</div>
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<div dir="ltr"><font size="2"><span style="font-family:tahoma,sans-serif">John E. Simmons<br>
Writer and Museum Consultant</span></font></div>
<div dir="ltr"><font size="2"><span style="font-family:tahoma,sans-serif">Museologica<br>
<i>and</i><br>
Investigador Asociado, Departamento de Ornitologia<br>
Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Lima</span></font><br>
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<div dir="ltr">On Mon, Sep 30, 2024 at 11:30 AM Dirk Neumann <<a href="mailto:d.neumann@leibniz-lib.de" target="_blank">d.neumann@leibniz-lib.de</a>> wrote:<br>
</div>
<blockquote style="margin:0px 0px 0px 0.8ex;border-left:1px solid rgb(204,204,204);padding-left:1ex">
<div>
<div>Dear Vanessa,</div>
<div><br>
</div>
<div>rising and staging times depends on the size of the specimens and how readily superfluous the formaldehydes is diluted from them. The specimens shown may require 2-3 days of rinsing, and then slowly going up 20/40/60/70. Each of these steps may take 1
week or longer, it depends how much formaldehyde comes out of them.</div>
<div><br>
</div>
<div>All together you should assume at least a month, but it can take you longer.</div>
<div><br>
</div>
<div>With all best wishes</div>
<div>Dirk <br>
</div>
<div><br>
</div>
<div><br>
</div>
<div>Am 30.09.2024 um 17:14 schrieb Vanessa Pitusi:</div>
<blockquote type="cite">
<div>
<div>
<p><span lang="NO-BOK">Dear all,</span></p>
<p><span lang="NO-BOK"> </span></p>
<p>Recently, I have discovered that most of our larger specimens kept in the large collection jars, are kept in formalin (photo for reference).</p>
<p> </p>
<p>I have looked into removing the specimens from formalin and placing them into ethanol. I understand the steps that have to be taken, but I was wondering if anyone has advice on the soaking time for each step. That is the only thing that
is kept vague in the texts that I have read. One reference mentioned that tortoises and racoons take two to three days.</p>
<p> </p>
<p>Most the specimens that I will work with a large fish, cephlapods, and birds.
</p>
<p> </p>
<p>In case any of you have done this, any advice on this or the process is appreciated!</p>
<p> </p>
<p>I am also open to having a quick chat via Teams or Zoom. <u>
</u></p>
<p> </p>
<p>Kind regards,</p>
<p>Vanessa</p>
</div>
</div>
<br>
<fieldset></fieldset>
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<p><br>
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<div>-- <br>
<div>
<p style="margin-bottom:0.0001pt;line-height:normal"><b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">****</span></b></p>
<p style="margin-bottom:0.0001pt;line-height:normal"><b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif"> </span></b></p>
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<p style="margin-bottom:0.0001pt;line-height:normal"><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">Collection Manager, Hamburg</span></p>
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<p style="margin-bottom:0.0001pt;line-height:normal"><span style="font-family:"Source Sans Pro",sans-serif">Martin-Luther-King-Platz 3</span></p>
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<p style="margin-bottom:0.0001pt;line-height:normal"><u><span style="font-family:"Source Sans Pro",sans-serif;color:blue"><a href="mailto:d.neumann@leibniz-lib.de" target="_blank">d.neumann@leibniz-lib.de</a></span></u></p>
<p style="margin-bottom:0.0001pt;line-height:normal"><a><span style="font-family:"Source Sans Pro",sans-serif">www.leibniz-lib.de</span></a></p>
<p style="margin-bottom:0.0001pt;line-height:normal"><span style="font-size:10pt;font-family:"Source Sans Pro",sans-serif"> </span></p>
<p style="margin-bottom:0.0001pt;line-height:normal"><span style="font-size:10pt;font-family:"Source Sans Pro",sans-serif">--
<br>
Stiftung Leibniz-Institut zur Analyse des Biodiversitätswandels<br>
Postanschrift: Adenauerallee 127, 53113 Bonn, Germany<br>
<br>
Stiftung des öffentlichen Rechts;<br>
Generaldirektion: Prof. Dr. Bernhard Misof (Generaldirektor), Adrian Grüter (Kaufm. Geschäftsführer)<br>
Sitz der Stiftung: Adenauerallee 160 in Bonn<br>
Vorsitzender des Stiftungsrates: Dr. Michael Wappelhorst</span></p>
<p><span style="font-size:10pt;line-height:107%;font-family:"Source Sans Pro",sans-serif"> </span></p>
</div>
</div>
-- <br>
Stiftung Leibniz-Institut zur Analyse des Biodiversitätswandels<br>
Postanschrift: Adenauerallee 127, 53113 Bonn, Germany<br>
<br>
Stiftung des öffentlichen Rechts;<br>
Generaldirektion: Prof. Dr. Bernhard Misof (Generaldirektor), Adrian Grüter (Kaufm. Geschäftsführer)<br>
Sitz der Stiftung: Adenauerallee 160 in Bonn<br>
Vorsitzender des Stiftungsrates: Dr. Michael Wappelhorst<br>
</div>
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NHCOLL-L is brought to you by the Society for the Preservation of<br>
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http://www.spnhc.org</a> for membership information.<br>
Advertising on NH-COLL-L is inappropriate.<br>
</blockquote>
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</blockquote>
<p><br>
</p>
<div>-- <br>
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<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">****</span></b></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif"> </span></b></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">Dirk Neumann</span></b></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">Collection Manager, Hamburg</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif"> </span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">Postal address:</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif">Museum of Nature Hamburg</span></b><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif"><br>
</span><span lang="EN-US" style="font-family:"Source Sans Pro",sans-serif;color:rgb(0,134,105)">Leibniz Institute for the Analysis</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-family:"Source Sans Pro",sans-serif;color:rgb(0,134,105)">of Biodiversity Change</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-family:"Source Sans Pro",sans-serif">Dirk Neumann</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-family:"Source Sans Pro",sans-serif">Martin-Luther-King-Platz 3</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-family:"Source Sans Pro",sans-serif">20146</span><span style="font-family:"Source Sans Pro",sans-serif">
</span><span style="font-family:"Source Sans Pro",sans-serif">Hamburg</span><span style="font-family:"Source Sans Pro",sans-serif"><br>
+49 </span><span style="font-family:"Source Sans Pro",sans-serif">40</span><span style="font-family:"Source Sans Pro",sans-serif">
</span><span style="font-family:"Source Sans Pro",sans-serif">238 3</span><span style="font-family:"Source Sans Pro",sans-serif">17 –
</span><span style="font-family:"Source Sans Pro",sans-serif">628</span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<u><span style="font-family:"Source Sans Pro",sans-serif;color:blue"><a href="mailto:d.neumann@leibniz-lib.de" target="_blank">d.neumann@leibniz-lib.de</a></span></u></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<a><span style="font-family:"Source Sans Pro",sans-serif">www.leibniz-lib.de</span></a></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-size:10pt;font-family:"Source Sans Pro",sans-serif"> </span></p>
<p class="MsoNormal" style="margin-bottom:0.0001pt;line-height:normal">
<span style="font-size:10pt;font-family:"Source Sans Pro",sans-serif">-- <br>
Stiftung Leibniz-Institut zur Analyse des Biodiversitätswandels<br>
Postanschrift: Adenauerallee 127, 53113 Bonn, Germany<br>
<br>
Stiftung des öffentlichen Rechts;<br>
Generaldirektion: Prof. Dr. Bernhard Misof (Generaldirektor), Adrian Grüter (Kaufm. Geschäftsführer)<br>
Sitz der Stiftung: Adenauerallee 160 in Bonn<br>
Vorsitzender des Stiftungsrates: Dr. Michael Wappelhorst</span></p>
<p class="MsoNormal"><span style="font-size:10pt;line-height:107%;font-family:"Source Sans Pro",sans-serif"> </span></p>
</div>
</div>
-- <br>
Stiftung Leibniz-Institut zur Analyse des Biodiversitätswandels<br>
Postanschrift: Adenauerallee 127, 53113 Bonn, Germany<br>
<br>
Stiftung des öffentlichen Rechts;<br>
Generaldirektion: Prof. Dr. Bernhard Misof (Generaldirektor), Adrian Grüter (Kaufm. Geschäftsführer)<br>
Sitz der Stiftung: Adenauerallee 160 in Bonn<br>
Vorsitzender des Stiftungsrates: Dr. Michael Wappelhorst<br>
</div>
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