﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Culture Journal, Species: Euterpina acutifrons</title><link>http://www.mbisite.org/Forums/</link><description /><copyright>(c) MBI Forums</copyright><ttl>30</ttl><item><title>Re:Culture Journal, Species: Euterpina acutifrons (road8514)</title><description>  These crashed. Will need to get another filter going. </description><link>http://www.mbisite.org/Forums/fb.ashx?m=96344</link><pubDate>Sun, 27 Sep 2015 22:40:30 GMT</pubDate></item><item><title>Re:Culture Journal, Species: Euterpina acutifrons (clayton447)</title><description>  &lt;div class="_container"&gt;
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			&lt;div class="_postedby"&gt;&lt;img title="Quote" alt="Quote" src="image/quote_icon.png"&gt; Originally Posted by &lt;strong&gt;road8514&lt;/strong&gt; &lt;/div&gt;
			&lt;div class="message"&gt;  &lt;br&gt;   &lt;br&gt;  I am not sure. But I will keep them in salt so I don't have issues using them for salt water fish. I don't think they would handle quick change in salinity from culture vessels to fry rearing vessel.  &lt;br&gt;  &lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt; &lt;br&gt;  &amp;nbsp; &lt;br&gt;  You could always perform some simple salinity stress tests and see how they respond.&amp;nbsp; Some copepods are more durable than others.&amp;nbsp; I work with &lt;i&gt;Tigriopus&lt;/i&gt; and the can easily tolerate going from 30ppt to 0ppt instantly, and stay in 0ppt for 30 minutes without mortalities.&amp;nbsp; It takes about 15 minutes for them to snap out of the stress after they are put back into 30ppt; it's remarkable either way.&amp;nbsp; I am also working with &lt;i&gt;Apocyclops&lt;/i&gt; and I will be testing them with salinity shock treatments.&amp;nbsp; That actually sounds barbaric! LOL &lt;br&gt;  &amp;nbsp; &lt;br&gt;  Chad&amp;nbsp; &lt;br&gt;  </description><link>http://www.mbisite.org/Forums/fb.ashx?m=95855</link><pubDate>Thu, 13 Aug 2015 11:21:53 GMT</pubDate></item><item><title>Re:Culture Journal, Species: Euterpina acutifrons (road8514)</title><description>  I am not sure. But I will keep them in salt so I don't have issues using them for salt water fish. I don't think they would handle quick change in salinity from culture vessels to fry rearing vessel. </description><link>http://www.mbisite.org/Forums/fb.ashx?m=95830</link><pubDate>Tue, 11 Aug 2015 21:41:31 GMT</pubDate></item><item><title>Re:Culture Journal, Species: Euterpina acutifrons (dave w)</title><description>  If I remember correctly, this species can acclimate in salinities almost all the way down to fresh water. &amp;nbsp;That might save you a little on the salt bill if you decide to use a low salinity algae as well. &lt;br&gt;  </description><link>http://www.mbisite.org/Forums/fb.ashx?m=95828</link><pubDate>Tue, 11 Aug 2015 20:30:40 GMT</pubDate></item><item><title>Re:Culture Journal, Species: Euterpina acutifrons   (road8514)</title><description>  &lt;a href="http://s105.photobucket.com/user/road8514/media/Fish%20stuff/A0F6F0E2-8FF3-4879-84A3-CD50F4CF1FF7.jpg.html" target="_blank" rel="nofollow"&gt;&lt;img src="http://i105.photobucket.com/albums/m227/road8514/Fish%20stuff/A0F6F0E2-8FF3-4879-84A3-CD50F4CF1FF7.jpg" /&gt;&lt;/a&gt; &lt;br&gt;  &lt;a href="http://s105.photobucket.com/user/road8514/media/Fish%20stuff/75B3BB09-F012-4159-9766-0A8C157A3D4B.jpg.html" target="_blank" rel="nofollow"&gt;&lt;img src="http://i105.photobucket.com/albums/m227/road8514/Fish%20stuff/75B3BB09-F012-4159-9766-0A8C157A3D4B.jpg" /&gt;&lt;/a&gt; &lt;br&gt;  &amp;nbsp; &lt;br&gt;  </description><link>http://www.mbisite.org/Forums/fb.ashx?m=95822</link><pubDate>Tue, 11 Aug 2015 15:16:34 GMT</pubDate></item><item><title>Culture Journal, Species: Euterpina acutifrons   (road8514)</title><description>  &lt;div align="center"&gt;&lt;u&gt;&lt;b&gt;&lt;font size="3"&gt;Culturing Journal DataSheet&lt;/font&gt;&lt;/b&gt;&lt;/u&gt;  &lt;br&gt;  &lt;font color="red"&gt;This first post should be updated regularly to include new information as events take place or changes are made to your system&lt;/font&gt;&lt;/div&gt;  &lt;br&gt;  &lt;font color="#000080"&gt;&lt;font size="3"&gt;&lt;u&gt;&lt;b&gt;General &lt;/b&gt;&lt;/u&gt;&lt;/font&gt;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Species:&lt;/b&gt;&amp;nbsp;&lt;font style="color: #339966;"&gt;Euterpina acutifrons&amp;nbsp; &lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Species description: &amp;nbsp;&lt;/b&gt;&lt;font style="color: #339966;"&gt;Harpacticoid&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Culture source (&lt;/b&gt;link if possible&lt;b&gt;):&lt;/b&gt;&amp;nbsp;&lt;font style="color: #339966;"&gt; Waldend at 2015 MBI Workshop&lt;/font&gt;&amp;nbsp;  &lt;br&gt;  &lt;b&gt;If algae, CCMP # (&lt;/b&gt;Optional&lt;b&gt;):&lt;/b&gt;&amp;nbsp;      &lt;br&gt;  &lt;a href="http://ccmp.bigelow.edu/" target="_blank" rel="nofollow"&gt;http://ccmp.bigelow.edu/&lt;/a&gt;  &lt;br&gt;  &lt;b&gt;Culture Establishment Date:&lt;/b&gt;&amp;nbsp; &lt;font style="color: #339966;"&gt;July 25, 2015&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Continuation Date:&lt;/b&gt;&amp;nbsp;    &lt;br&gt;   &lt;br&gt;  &lt;font color="#000080"&gt;&lt;font size="3"&gt;&lt;u&gt;&lt;b&gt;Culturing Vessel Details &lt;/b&gt;&lt;/u&gt;&lt;/font&gt;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Salinity:&lt;/b&gt;&amp;nbsp;&lt;font style="color: #339966;"&gt; 1.021&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Temperature:&lt;/b&gt;&amp;nbsp; &amp;nbsp;&lt;font style="color: #339966;"&gt;Room Temp&lt;/font&gt;&amp;nbsp;  &lt;br&gt;  &lt;b&gt;pH:&lt;/b&gt;&amp;nbsp; &lt;font style="color: #339966;"&gt;unknown&amp;nbsp;&lt;/font&gt;&lt;b&gt;  &lt;br&gt;  &lt;/b&gt;  &lt;br&gt;  &lt;b&gt;Vessel description:&lt;/b&gt;&amp;nbsp; &lt;font style="color: #339966;"&gt;1.75 liter used juice container.&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Lighting description:&lt;/b&gt;&amp;nbsp;&lt;font style="color: #339966;"&gt; light from the phyto cultures, single spiral CFL bulb.&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Lighting cycle:&lt;/b&gt;&amp;nbsp; &lt;font style="color: #339966;"&gt;14 on 10 off direct lighting&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Aeration description:&amp;nbsp;&lt;/b&gt;&amp;nbsp;&lt;font style="color: #339966;"&gt;Light air 1 bubble per second, just enough to keep water moving.&amp;nbsp;&lt;/font&gt;  &lt;br&gt;   &lt;br&gt;  &lt;font color="#000080"&gt;&lt;font size="3"&gt;&lt;u&gt;&lt;b&gt;Methodologies &lt;/b&gt;&lt;/u&gt;&lt;/font&gt;&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Split methodology:&lt;/b&gt; &lt;font style="color: #339966;"&gt;Culture is poured through a 23micron sieve to remove all copepods.&amp;nbsp; They are then backwashed into a container with fresh ASW. &lt;/font&gt;  &lt;br&gt;   &lt;br&gt;  &lt;b&gt;Culture medium description:&lt;/b&gt;&amp;nbsp;            &lt;br&gt;  &lt;font style="color: #339966;"&gt;Culture is feed Tetraselmis as needed to tint the water. &amp;nbsp;&amp;nbsp;&lt;/font&gt;  &lt;br&gt;   &lt;br&gt;  &lt;b&gt;Cell count:&lt;/b&gt;&lt;font style="color: #339966;"&gt;&amp;nbsp;unknown&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &amp;nbsp;(if known)            &lt;br&gt;   &lt;br&gt;  &lt;b&gt;Reference links:&lt;/b&gt; &amp;nbsp;            &lt;br&gt;   &lt;br&gt;  &lt;font color="#000080"&gt;&lt;font size="3"&gt;&lt;u&gt;&lt;b&gt;Additional Information &lt;/b&gt;&lt;/u&gt;&lt;/font&gt;&lt;/font&gt;  &lt;br&gt;  &lt;font color="red"&gt;(No Pictures or Videos in the Section Please)&lt;/font&gt;  &lt;br&gt;  &lt;b&gt;Notes:&lt;/b&gt;&amp;nbsp;            &lt;br&gt;  &lt;font style="color: #339966;"&gt;Water is sterilized using bleach and&amp;nbsp;and dechlorinated using sodium thiosulfate.&amp;nbsp;&lt;/font&gt;  &lt;br&gt;  &lt;font style="color: #339966;"&gt;Stock solution of sodium thiosulfate made following this info. &lt;/font&gt;  &lt;br&gt;  &lt;font style="color: #339966;"&gt;&lt;a href="http://www.mbisite.org/forums/tm.aspx?m=84959&amp;amp;mpage=1&amp;amp;print=true" target="_blank" rel="nofollow"&gt;http://www.mbisite.org/fo...print=true&amp;nbsp;&amp;nbsp;&lt;/a&gt;&lt;/font&gt;  &lt;br&gt;   &lt;br&gt;   &lt;br&gt;  &lt;font color="red"&gt;&lt;b&gt;You will be required to provide photographic evidence and as much detail as possible about your project in this thread.            &lt;br&gt;  If your thread does not contain detailed enough photos&amp;nbsp; and information the MBI Council will not be able to approve your reports.&lt;/b&gt;&lt;/font&gt; &lt;br&gt;  </description><link>http://www.mbisite.org/Forums/fb.ashx?m=95821</link><pubDate>Tue, 11 Aug 2015 15:11:18 GMT</pubDate></item></channel></rss>