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    <p>Dear Indah,</p>
    <p>Thanks for presenting this very interesting alterations. Are you
      certain that you are dealing with mold here? As already suggested,
      this two different alterations seem to be more of an efflorescence
      of some kind. The questions from John are indeed very helpful in
      trying to find out the cause. </p>
    <p>But, is it really necessary to remove the residues? For the
      specimen, it might be better to keep them on until you are sure
      that they need to go away, specially if you don't know what they
      exactly are. From the pictures I can't really detect an
      deterioration of the soft tissue, it seems to be more of an
      esthetic problem. </p>
    <p>And just from a conservation point of view: Its not really
      recommended to wash specimens with water if they are kept in
      ethanol, because it could damage the soft tissue due to osmotic
      shock. Besides you don't know how the efflorescence will react to
      water. And please don't use detergent either, you don't know what
      additive you might be adhering to the tissue and fluid, and adding
      surfactants to your mixture could cause a bigger issue as well. <br>
      If the alteration has to be removed because of an esthetic reason,
      you might first try to take a small sample of it and see how it
      react in different a different medium.</p>
    <p>And please send more pictures to the community if you find other
      interesting cases. Thanks!</p>
    <p><br>
    </p>
    <p>All the best,</p>
    <p><br>
    </p>
    <p><br>
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    <p><br>
    </p>
    <div class="moz-cite-prefix">Am 22.08.25 um 16:15 schrieb John E
      Simmons:<br>
    </div>
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cite="mid:CAF7GCDZ+7D6FWnCgTKff40ZOg_gAmVDmJBDmRvhZ3PWR74_dMw@mail.gmail.com">
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            class="gmail_default">I agree with Dirk, but I would add
            that it is also possible that some of the stuff could be an
            efflorescence due to anexcess of salts used to buffer the
            fixative (I have seen this happen when a formaldehyde
            fixative is buffered with an excess of borax and a few other
            buffers). </div>
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          <div
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            class="gmail_default">Following Dirk's recommendations
            should clear up the problem. Do be very careful if you need
            to brush away the white stuff so that you do not damage the
            skin of the specimen.</div>
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          <div
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            class="gmail_default">Thank you for sending these excellent
            photos, they are much better than the photos most us post of
            our problem specimens.\</div>
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          <div
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            class="gmail_default">You mentioned that you were new to the
            collection so you don't know the history of the specimen,
            but I do have a few questions that might help better
            diagnose the problem: </div>
          <div
style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)"
            class="gmail_default">1-Do you know how long it has been in
            the collection? </div>
          <div
style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)"
            class="gmail_default">2-Is denatured ethanol used in the
            collection?</div>
          <div
style="font-family:tahoma,sans-serif;font-size:small;color:rgb(0,0,0)"
            class="gmail_default">3-Is the alcohol diluted with tap
            water?</div>
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            class="gmail_default"><br>
          </div>
          <div
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            class="gmail_default">Thanks,</div>
          <div
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            class="gmail_default">John</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" class="gmail_attr">On Fri, Aug 22, 2025 at
          8:44 AM Indah Huegele <<a
            href="mailto:indahhuegele@isu.edu" moz-do-not-send="true"
            class="moz-txt-link-freetext">indahhuegele@isu.edu</a>>
          wrote:<br>
        </div>
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style="margin:0px 0px 0px 0.8ex;border-left:1px solid rgb(204,204,204);padding-left:1ex">
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            <div dir="auto">
              <div>Hello everyone,</div>
              <div dir="auto"><br>
              </div>
              <div dir="auto">I was wondering if I could get feedback on
                some scary-looking growths on a few herpetology
                specimens in our collection (photos attached here). Any
                thoughts on what these residues are and/or advice on how
                to treat them would be much appreciated!</div>
              <div dir="auto"><br>
              </div>
              <div dir="auto"><b>Orange-brown bumps.<i> </i></b><i>(images
                  143927 and 143900) </i>There are small, orange-brown,
                round bumps on one specimen that has had its tail
                exposed from fluid levels that are too low. I completely
                replaced the ethanol for this specimen and tried to
                gently scrape off the growth, but most of it was quite
                dried on, so I left it soaking in fresh 70% ethanol for
                the time being. Is this definitely fungal? Should I try
                to scrape the rest of the growth off the specimen's tail
                or leave it alone?</div>
              <div dir="auto"><br>
              </div>
              <div dir="auto"><b>White layer of residue.</b> <i>(all
                  other images) </i>On a few salamander specimens,
                there is this opaque, white layer of residue. This is
                occurring on salamander specimens that are completely
                submerged in ethanol. (However, I am not sure what the
                concentration of this ethanol is or the last time that
                it was changed out; I worry it might have lost ethanol
                concentration over time.) Any thoughts on what this
                might be and how to treat it? </div>
              <div dir="auto"><br>
              </div>
              <div dir="auto">I took over this collection a few months
                ago, so I am still discovering issues with specimens. I
                appreciate any suggestions that you folks have to offer
                on how to help these poor specimens!</div>
              <div dir="auto"><br>
              </div>
              <div dir="auto">Thanks,</div>
              <div dir="auto"><br>
              </div>
              <div dir="auto">Indah</div>
              <div dir="auto"><br>
              </div>
              <div><br>
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                  <p
style="margin-top:0px;margin-bottom:1rem;color:black;font-family:Roboto;font-size:12px"><span
                      style="font-size:14px;font-weight:bold">Indah B.
                      Huegele, PhD<br>
                    </span>Life Sciences Collection Manager | Idaho
                    Museum of Natural History</p>
                  <p
style="margin-top:0px;margin-bottom:1rem;color:black;font-family:Roboto;font-size:12px">Museum
                    Bldg | Room 220<br>
                    921 S 8th Ave, Stop 8096 | Pocatello, Idaho 83209<br>
                    (208) 282-2815 | <a
                      href="mailto:indahhuegele@isu.edu" target="_blank"
                      moz-do-not-send="true"
                      class="moz-txt-link-freetext">indahhuegele@isu.edu</a></p>
                  <p
style="margin-top:0px;margin-bottom:1rem;color:black;font-family:Roboto;font-size:12px"><img
                      width="200" height="37"
style="font-family: Arial, Helvetica, sans-serif; font-size: small; color: rgb(32, 33, 36);"
src="https://ci3.googleusercontent.com/mail-sig/AIorK4zpDKaE1A5p59nUvJJcaXwajw0Mg-6wzIW9yWbfX_lPRg5uhT10fU764DdL4hWwUnpkkchS-cL7YsEq"
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