BEE-L Archives

Informed Discussion of Beekeeping Issues and Bee Biology

BEE-L@COMMUNITY.LSOFT.COM

Options: Use Monospaced Font
Show Text Part by Default
Condense Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Sender:
Date:
Tue, 7 Aug 2012 09:57:39 +0200
Reply-To:
Informed Discussion of Beekeeping Issues and Bee Biology <[log in to unmask]>
Message-ID:
Subject:
MIME-Version:
1.0
Content-Transfer-Encoding:
quoted-printable
In-Reply-To:
Content-Type:
text/plain; charset=ISO-8859-1
From:
david quesada <[log in to unmask]>
Parts/Attachments:
text/plain (33 lines)
Randy, thanks for your extensive reply.
I know your articles, I´ve been collecting them and reading.

And about the following...

> David, it's simple math.  Hemacytometer count is simply the average count
per tiny square x 4 million.  You typically count 80 squares.  So one
single spore found among the 80 squares would give an average count of
50,000 spores per bee.  Thus, you'd be unlikely to find even a single spore
if infection level were only 10,000 spores.

Thanks!  Obviously!!...I´m sorry, I´m setting up the lab just now and
I´m still a bit "clumsy" ! If one nosema spore is observed in the
entire central square millimetre grid (25 x 16 = 400), is equal to an
average of 10.000 spores per bee...if level infection´s below 10.000
spores per bee...it´s really difficult find a spore!!


Thanks again

P. David Quesada
Honey Bee Pathology Lab
Extremadura, Spain
http://aym.juntaex.es/organizacion/centros/provincial/zafra/patologiaapicola.htm

             ***********************************************
The BEE-L mailing list is powered by L-Soft's renowned
LISTSERV(R) list management software.  For more information, go to:
http://www.lsoft.com/LISTSERV-powered.html

Guidelines for posting to BEE-L can be found at:
http://honeybeeworld.com/bee-l/guidelines.htm

ATOM RSS1 RSS2