[pestlist] (no subject)

2011-04-13 Thread WLouche
Please unsubscribe
 
_wlouche@aol.com_ (mailto:wlou...@aol.com) 


Re: [pestlist] Fwd: Fumigating cabinets - bug infestation

2010-10-13 Thread WLouche
Nitrogen is not totally inert, reacts with some metals that can  be used as 
pigments.. Fungi acceleration is after opening the chamber, not  in the 
chamber. More researchs needs to be done in this area, hopefully it will  be.
 
Bill
 
 
In a message dated 10/13/2010 9:53:11 A.M. Eastern Daylight Time,  
step...@stephan-schaefer.com writes:

Re:  Choice of Argon vs. Nitrogen for the treatment and control of insect  
infestation

In reference to the questionable statement, that inert  gases other than 
argon are likely to foster fungal growth I think it is  important to 
clarify some issues regarding the use of either gas for the  control of insect 
pests and the influence on microbiological activity. First  of all, both gases 
are entirely inert and scientific research has proven their  full efficacy 
in eliminating all types of insect pests in all life stages  (given that 
specific conditions are being maintained and controlled during  treatment). 
Second, fungal germination and growth depends upon the substrate  and ambient 
conditions. Actually, most of us will intuitively know that fungal  and 
bacterial development only occurs at higher humidity levels and where  there is 
lack of ventilation. Actually, the threshold level lies somewhere  around 70% 
relative humidity. Below about 65% there is literally no risk for  fungal 
and bacterial proliferation. My third and probably most important point  is 
why nitrogen anoxia will foster fungal growth although it is known to be  a 
strong inhibitor of microbiological activity?? From scientific research we  
only know, that some anaerobic microorganisms are able to survive under  
nitrogen anoxia conditions. The other more practical consideration is that  
during anoxia treatments, the humidity inside the bubble should always be  
controlled and certainly kept below 65% RH, so the likelihood of fungal 
growth  inside the bubble under anoxic conditions is absolutely zero, whether 
nitrogen  or argon is used. Furthermore, we are only speaking about a 
treatment period  of approximately 30 days, the time needed to kill all insects 
in 
all  developmental stages. Therefore, I think the issues of fungal growth 
are much  more related to the environment and ambient conditions where the 
objects in  question are being kept at all times, rather than the short period 
inside a  bubble where they remain during an anoxic treatment and where 
conditions  should be controlled anyway. In own experiments, where I sealed wet 
paper and  books in gas barrier bags with Ageless oxygen absorbers, where 
the remaining  gas is mainly nitrogen, no fungal growth was noticeable after 
about 50 days.  The bags were kept at about 20 - 22 °C and the control that 
was sealed with  atmospheric air inside has shown noticeable fungal and 
probably bacterial  growth after about 72 hours. This in itself proves that 
fungal growth is not  an issue with respect to the choice of the gas (argon or 
nitrogen) when  considering anoxia treatment in order to eliminate insect 
pests. Additionally,  it may be interesting to consider cost, as argon is a lot 
more expensive than  nitrogen which is the most abundant gas in our 
atmosphere. I would be very  interested in hearing other peoples comments on 
the  
subject.


Stephan Schäfer


STEPHAN SCHÄFER Conservação e Restauração  ltda. 

Rua Manduri, 400 - Jd.  Paulistano
01457-020 São Paulo, Brazil
Tel./Fax: 00 xx 11  3816-0489
Cel: 00 xx 11 8366-0230
e-mail: _step...@stephan-schaefer.com_ 
(mailto:step...@stephan-schaefer.com) 
-  

-
Prof. Dipl. Rest. Stephan  Schäfer

Universidade Nova de Lisboa  (UNL)
Faculdade de Ciências e Tecnologia (FCT)
Departamento de  Conservação  Restauro 
2829-516 Caparica -  Lisboa
PORTUGAL
e-mail: _sc...@fct.unl.pt_ (mailto:sc...@fct.unl.pt) 
-





At  19:22 08.10.2010, you wrote:

Dear Dr. Diego;

The  most reasonable option is to use anoxic system, specially with argon  
protocol. This is due to the fact other inert gases are likely to foster  
fungal growth.

Please give me a call when you can, and I'll be  pleased to help you as I'm 
using argon's anoxia systems here in Brazil for  over ten years.

Best regards,

Ulisses Mello, Dip.  Cons., PG
Art Care do Brasil
Mobile: +55 21 98979074
Office: +55 21  25587749
2010/10/8 Revelez, Marcia A. _mreve...@ou.edu_ (mailto:mreve...@ou.edu) 

Forwarding this for a colleague.  Please respond to Deigo (email  below). 

Thanks!



Marcia A. Revelez

Collection Manager

Department of Mammalogy

Division of Collections and Research

Sam Noble Oklahoma Museum of Natural History

University of Oklahoma

2401 Chautauqua

Norman, OK 73072

Phone: 405-325-7988

Fax: 405-325-7699





Begin 

Re: R: Re: [pestlist] Fwd: Fumigating cabinets - bug infestation

2010-10-13 Thread WLouche
Argon is a by product of collecting nitrogen, no extra cost involved. Yes,  
nitrogen is used most often based on cost and easier to contain in a 
chamber.  Nitrogen does not penetrate as well as argon, look at your periodic 
table for  weights. Use your FTIR to test argon verses nitrogen on real Art  
objects. You will be surprised.
 
Nitrogen chambers just like yours were being made by Rentokil long  before 
you were involved 10 years ago. Nitrogen was used during the Second World  
War to kill insects and rodents in food sources. There are some references  
dating to 1890's in Australia using nitrogen for insects. It was a by product 
in  ice making then. Rentokil followed Bob Koestler lectures before 
creating  their nitrogen generator system. Look back at the research papers in 
the  
mid 1980's early 1990's full of information in the beginning years
I have been working with anoxic chambers for 20+ years some of those  years 
in a Conservation department at a major museum. 
 
Why is the United State Constitution the most important document in our  
history stored under argon not nitrogen gas? Do your research learn about  the 
differences between argon and nitrogen its an interesting trip. I have 
about  5 years into the comparison still learning. 
 
 
Bill
Art Care International
 
 
 
 
In a message dated 10/13/2010 10:53:23 A.M. Eastern Daylight Time,  
rgi...@tiscali.it writes:

The  letter of Stephan Schaefer is simply perfect 
I have been the  
coordinator of the SAVE ART project of European Union and our team  
(Italy, Spain, Sweden and UK)  has certified the anoxia method  
(Nitrogen) to eradicate insect pests carried ot by VELOXY equipment  
(VEry Low OXY). It was almost ten years ago and until now I never heard  
about microrganisms problems This is a matter of humidity. There is  
no difference among Argon and N2 to kill  pests but there is a great  
difference in costs. Moreover, to separate Argon from air implies a  
great consumption of energy and to produce energy means pollution of  
environment.
Ercole Gialdi (rgi...@tiscali.it) 

Messaggio  
originale
Da: step...@stephan-schaefer.com
Data: 13/10/2010  15.44

A: pestlist@museumpests.net
Ogg: Re: [pestlist] Fwd:  Fumigating 
cabinets - bug infestation

Re: Choice of Argon vs.  Nitrogen for the 

treatment and control of insect infestation

In  reference to the 
questionable statement, that 
inert gases other than  argon are 
likely to 
foster fungal growth I think it is important to  
clarify 
some issues regarding the use of either 
gas for the  control of insect 
pests and the 
influence on microbiological activity.  First of 
all, 
both gases are entirely inert and scientific  
research has proven their 
full efficacy in 
eliminating all types  of insect pests in all life 

stages (given that specific conditions are  being 
maintained and 
controlled during treatment). 
Second, fungal  germination and growth 
depends 
upon the substrate and ambient  conditions. 
Actually, most of 
us will intuitively know that 
fungal  and bacterial development only 
occurs at 
higher humidity levels and  where there is lack of 

ventilation. Actually, the threshold level lies  
somewhere around 70% 
relative humidity. Below 
about 65% there is  literally no risk for 
fungal 
and bacterial proliferation. My third and  
probably most 
important point is why nitrogen 
anoxia will foster  fungal growth 
although it is 
known to be a strong inhibitor of  microbiological 

activity?? From scientific research we only know,  
that some anaerobic 
microorganisms are able to 
survive under  nitrogen anoxia conditions. 
The 
other more practical consideration  is that during 
anoxia 
treatments, the humidity inside the 
bubble  should always be 
controlled and 
certainly kept below 65% RH, so the  likelihood of 

fungal growth inside the bubble under anoxic  
conditions is absolutely 
zero, whether nitrogen 
or argon is used.  Furthermore, we are only 

speaking about a treatment period of  
approximately 30 days, the time 
needed to kill 
all insects in all  developmental stages. 
Therefore, I 
think the issues of fungal growth  
are much more related to the 
environment and 
ambient conditions  where the objects in question 
are 
being kept at all times, rather than  the 
short period inside a bubble 
where they remain 
during an  anoxic treatment and where conditions 

should be controlled anyway. In  own experiments, 
where I sealed wet 
paper and books in gas barrier  
bags with Ageless oxygen absorbers, 
where the 
remaining gas is  mainly nitrogen, no fungal 
growth was 
noticeable after about 50 days.  The 
bags were kept at about 20 - 22 °C 
and the 
control that was  sealed with atmospheric air 
inside has shown 
noticeable fungal and  probably 
bacterial growth after about 72 hours. 
This in 
itself  proves that fungal growth is not an issue 
with respect 
to the choice  of the gas (argon or 
nitrogen) when considering anoxia 

Re: [pestlist]

2010-06-09 Thread WLouche
Wood should not be frozen, it can crack. You may also lose part of the  
painted surface due to expansion and contraction.
In this case anoxic treatment is a better choice, less shock.
 
Bill
ACI
 
 
In a message dated 6/9/2010 1:33:22 P.M. Eastern Daylight Time,  
aa...@mindspring.com writes:

This is  a message from the Pest Management Database List.
To post to this list send  it as an email to pestlist@museumpests.net
To unsubscribe please look at  the footer of this  email.
---


































I  need some info asap.  My question is about low-temperature 
treatment  of icons - egg tempera on wooden panels.  I would like to 
hear from  anyone who has done freezing on these or similar items - 
polychrome  sculpture, for example - and how it turned out.  Any signs 
of  enhanced cracking?  Any indications of the thoroughness of the  
kill?

Many thanks.
Barbara Appelbaum
-- 
Appelbaum   Himmelstein
444 Central Park West
New York, NY   10025
Conservation of Works of  Art
212-666-4630
aa...@mindspring.com
www.AandHconservation.org
-
To  send an email to the list, send your msg to pestl...@museumpests.com

To  unsubscribe from this list send an email to
imail...@museumpests.net and in  the body put:
unsubscribe pestlist
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Re: [pestlist] detecting woodborers

2010-05-21 Thread WLouche
With training a stethoscope can be used. You need to discern background  
noise from insect sounds. Most of us have lazy ears.
 
Freezing and warming cycles are not good for wood Art, specially mixed  
media. Mixed media has different contraction rates, does not respond well to  
dramatic temperature change. Some will say they did it without consequences, 
may  be luck. You need to understand the risk and how much you are willing  
to gamble.
 
CO2 measurements can be obtained down to parts per billion. You can use  
this method to monitor one insect in an object. It does take time and  
experience. With newly developed equipments times have been cut to a few hours. 
 
Ten years ago almost 8 hours on a FTIR.
With good equipment a CO2 analyzer balanced with a O2 analyzer can offer  
some results without an FTIR.
 
Bill
ACI
 
 
In a message dated 5/21/2010 4:42:41 P.M. Eastern Daylight Time,  
bugma...@aol.com writes:



Katie -
 
Hydrogen phosphide is not a good penetrator of wood for control of  ppbs.  
If the items are small a freezing process, followed by a warming,  then 
plunging the materials again into freezing will elimiinate active  infestations 
in wood.
 
The first time do it at -20 degress F for 72 hours; then warm the object  
up to room temperature, then freeze 'em again for 3 days at -20 degress  F.  
Your problem will be elimanated.
 
Tom Parker





-Original  Message-
From: Katie Fisher kfis...@glenbow.org
To:  pestlist@museumpests.net pestlist@museumpests.net
Sent: Fri, May  21, 2010 2:02 pm
Subject: [pestlist] detecting woodborers

  
 
Hi, 
 
My name is Katie Fisher and I’m the new Pest Control  Technician at the 
Glenbow Museum. I just wanted to ask a somewhat out-there  question regarding 
the detection of wood borers… this museum has been battling  Powderpost 
Beetles for quite a while. Every 5 or so years a new wave will  appear, a 
large-scale treatment process will happen (phosphene), but it just  doesn’t 
seem to 
be effective in getting rid of the Powderpost population.  

Since it takes years for them to exit the wood, I feel  like I’m somewhat 
just twiddling my thumbs in the meantime, wondering if the  last treatment 
did the trick. A friend suggested that I might be able to use a  stethoscope 
to hear the larva inside the wood… does anyone do this, to detect  
woodborers? Does anyone think it would be at all effective in hearing  them?
 
Cheers,
Katie
 
Katie  Fisher
Pest  Control Technician
Glenbow  Museum
130-9th  Avenue S.E.
Calgary,  Alberta T2G 0P3
Tel  (403) 268-4235
Fax  (403) 265-9769

 



inline: image001.png

Re: [pestlist] Drywood Termites

2010-05-20 Thread WLouche
Anoxic treatment on a building is very possible. Grain silos were  purged 
with nitrogen during the Second World War preventing food lose to  rodent and 
insect populations.
Textiles from 1890's have changed color under Vikane,  off white to a 
yellow white from the acids. Most companies will tell you  your Art is safe, 
not 
always true.
 
Bill
ACI
 
 
In a message dated 5/20/2010 3:10:18 P.M. Eastern Daylight Time,  
toplad...@gmail.com writes:

Many  years ago conservation scientist Jim Duizak at the Getty Conservation 
 Institute did research on Vikane and found that the commercial formulation 
 contained residual organic acids that would tarnish and etch metals and 
affect  other acid sensitive materials. I talked to Jim about it and he told 
me that  the lab-grade Vikane was free of the acids but was too expensive to 
use  commercially. He recommended removing acid-sensitive collections before 
the  fumigation of a whole historic house with a commercial Vikane  
treatment.

I understand that Vikane is considered useful when a whole  structure 
requires fumigation / eradication such as with a termite infestation  in the 
structure. It does have deep penetration and once done and the tenting  removed 
it does not leave toxic residues. 

I have not heard of an  anoxic treatment for a whole building - is it even 
possible?

What are  the alternatives to the use of Vikane for a termite infested  
building?

Cheers!
Dave

David Harvey
Senior Conservator and  Museum Consultant
Los Angeles, CA

On Thu, May 20, 2010 at 10:43 AM, _bugma...@aol.com_ 
(mailto:bugma...@aol.com)  wrote:

Kristen -
 
Vikane gas, as it comes in its cylinder, has impurities in it,  which may 
damage collection materials.  It certainly will tarnish  silver and certain 
other metals.  It has amazing penetrating properties  and therefore would not 
be able to be confined to the lobby area of the  museum.  I like the dog 
suggestion; however, if they're in the ceiling  or walls, a dog would not be 
able to detect them.
 
In California, with small infestations, a type of ray-emitting gun is  used 
to fry 'em in their galleries.  I don't know if anyone in Florida  uses 
this device.
 
I agree with Mr. Louche - research, research.  A lot can go wrong  with a 
Vikane fumigation.
 
Thomas A. Parker, PhD
President, Entomologist
Pest Control Services, Inc.




 



-Original  Message-
From: Kristen Zimmerman _kzimmer...@cummer.org_ 
(mailto:kzimmer...@cummer.org) 
To: _pestl...@museumpests.net_ (mailto:pestlist@museumpests.net)  
_pestl...@museumpests.net_ (mailto:pestlist@museumpests.net) 
Sent: Thu, May 20, 2010  9:48 am
Subject: [pestlist] Drywood Termites


 
Hi All,
I am seeking advice on a termite  problem we are having at my museum.  We 
have determined that we have  drywood termites infested in the front lobby of 
our museum.  Our  extermination company of course wants to fumigate the 
entire museum.   We know that this not possible, so my questions are as 
follows:  The  exterminator wants to use Vikane Gas.  Is this the correct gas 
to  
use?  Will it harm artwork if the gas leaked into a gallery?  Is t  his the 
proper way to exterminate drywood termintes?   

This is definitely not something that  we have ever had to deal with 
before, so any suggestions on how to fix this  infestation would be greatly 
appreciated.  
 
Thanks,
Kristen 
 
Kristen  Zimmerman
Registrar
The Cummer  Museum of Art  Gardens
829 Riverside  Avenue
Jacksonville,  FL 32204
 
direct:  904.899.6020
fax:  904.353.4101
 
To engage and  inspire, through arts, gardens and education.
 

 












Re: [pestlist] can anyone help

2009-12-13 Thread WLouche
Is there frass ( powder or grains) , holes, soft spots or  rot in any of 
the wooden objects? Any prior infestation? Have you ever found  wings in the 
general area? Do you have sticky traps to monitor any  activity?
It is easier to associate damage to a particular insect than to identify an 
 insect by parts. I would continue to monitor the objects on a frequent  
basses until a determination is made.
Bill
 
 
In a message dated 12/12/2009 3:10:07 P.M. Eastern Standard Time,  
taisl...@hotmail.com writes:

I  understand I will take another one under the microscope and   
will send asap.


Cheers.

 

Date: Sat, 12 Dec 2009 15:34:12 -0200
Subject: Re: [pestlist] can anyone  help
From: ume...@gmail.com
To:  pestlist@museumpests.net

Tais;
It's hard to understand the  image.
Can you make a close up / macro?

Ulisses Mello 

2009/12/12 tais lima _taisl...@hotmail.com_ (mailto:taisl...@hotmail.com) 

I took some samples from a wooden object and found this.  


Does anyone recognize this??? I am not sure if is the  whole 
body or if is just the head.


Thank's

 

Quer conexões de rede mais fácil? _Clique  e conheça o Windows 7._ 
(http://www.microsoft.com/brasil/windows7/default.html?WT.mc_id=1539) 






 

Quer conexões de rede mais fácil? _Clique e conheça o Windows 7.._ 
(http://www.microsoft.com/brasil/windows7/default.html?WT.mc_id=1539)   =



Re: [pestlist] Grant for Walk-in Freezer/ CO2 Bubble

2009-10-02 Thread WLouche
You would be better off with an anoxic system that allows you  to make any 
chamber size. The systems I make allow you treat one  book or 100,000 books 
at one time. The system is portable and reads below 20 ppm  for mold issues.
 
I have been doing anoxic treatment for museums, institutions and  
universities since 1994
 
Bill
Art Care International
 
 
In a message dated 10/2/2009 5:26:20 P.M. Eastern Daylight Time,  
bridget.s...@dmns.org writes:

 
If anyone is replying with  specs and pricing about a CO2 chamber, would 
you please reply to the list? I  am interested in this information as well..  
Thanks very  much, 
Bridget  Sabo 
BRIDGET  SABO 
CONSERVATION  TECHNICIAN  
 (http://www.dmns.org/)   
bridget.s...@dmns.org 
W   303.370.8399
F   303.370.6313   
_Join the Museum’s Online  Community_ 
(http://community.dmns.org/content/OnlineCommunity.aspx)   
_www..dmns.org_ (mip://0658eee8/www.dmns.org)  
P  Please consider  the environment before deciding to print this e-mail. 
 
 
From:  pestlist-ow...@museumpests.net 
[mailto:pestlist-ow...@museumpests.net] On  Behalf Of Crumpton, Trey
Sent: Friday, October 02, 2009 2:26  PM
To: pestlist@museumpests.net
Subject: [pestlist] Grant  for Walk-in Freezer/ CO2 Bubble

I am looking into writing a grant for a walk-in freezer  and/or a CO2 
chamber to treat a large number of history and natural history  objects (I am 
considering a permanent apparatus that would be kept around for  future use by 
the museum, though a portable unit is always an option).  I  was wondering 
if anyone has gone through this process recently, or would have  specs and 
pricing on such items.  I’d like to have some insight into  issues or problems 
involved (i.e. finding a freezer that can get down to -25  and stay there).. 
Any comments will be appreciated, 
Trey Crumpton 
Assistant Collections Manager 
Mayborn Museum Complex 
Baylor University 
One Bear Place #97154 
Waco, Texas  76798-7154 
(254) 710-1190 
Fax:  (254) 710-1173 
_www.maybornmuseum.com_ (http://www.maybornmuseum.com/)  



inline: image001.jpg

Re: [pestlist] Pests and a Contemporary Installation

2009-10-01 Thread WLouche
Megan,
 
   The branches will need to be treated  no matter what country they 
come from. Freezing does not always work.  I re treated with anoxic treatment 
many branch items that were  frozen to prevent infestation.
 
Synthetic branches you may  want to consider treatment as well 
depending on material.
 
Bill
ACI
 
 
In a message dated 10/1/2009 12:20:38 P.M. Eastern Daylight Time,  
megan.em...@cincyart.org writes:

This is  a message from the Pest Management Database List.
To post to this list send  it as an email to pestlist@museumpests.net
To unsubscribe please look at  the footer of this  email.
---






Hello  everyone,

I am cross-posting this query to both OSG and the Pest-list  as I hope to 
find an answer to this dilemma soon.  Our Curator of Dec  Arts  Design 
approached me yesterday with a proposal from the designers  the Campana 
Brothers. 
 At the request of our institution, they have  proposed the design for an 
installation in our temporary exhibition space for  Contemporary Art.  They 
would like to fill the room with bare tree  branches- on the walls, floor, 
hanging from the ceiling, etc and then place  permanent collection objects 
throughout, including a carved bedroom set,  fashion arts, ceramics, paintings, 
and so on.

My initial reaction to  the curator was that this could work, but that the 
branches would have to be  bagged and frozen prior to arrival at the museum. 
 We do not have a  freezer for collections, therefore it would have to take 
place off-site and  for an unknown expense.  My suggestions have not been 
received well by  some.   Since the designers are located in Brazil, we also 
don't  know where the branches will be coming from.  Is it possible to 
purchase  treated bare branches?  I assumed freezing would be the low-cost 
option,  but am I overlooking another treatment?   Or am I overreacting to  the 
potential pest hazard of bringing a large number of tree branches into the  
museum?

The curator is drafting a contract as I type this, and I would  like to 
include some requirements if possible.  If anyone has had  experience working 
with artists using large quantities of fresh organics in  a museum setting, 
or if you have a solution to de-bugging the branches, I  would be grateful 
for any tips, advice, or suggestions!

Thank you so  much!
Megan

Megan J. Emery
Assistant Conservator of  Objects
cincinnati art museum
953 Eden Park Drive
Cincinnati, OH  45202
t: (513) 639-2869
f: (513) 639  2996
megan.em...@cincyart.org


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imail...@zaks.net and in the  body put:
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Re: [pestlist] Carpet beetle

2009-09-24 Thread WLouche
If you had an infestation in the past you may not have contained  it. 
Carpet beetle will hide under base boards, flooring and in walls where  dust 
accumulates. The new carpeting and drapes should have been  monitored before 
installation. Many new items come infested from  manufacture, warehouses, 
shippers or from retail outlets. Diligence in  cleaning is your best weapon. 
Others will offer solutions involving organic and  inorganic chemicals, baited 
traps etc Some will help others will aggravate  the problem. One 
solution, remove all the Art, anoxic treat and clean, heat the  building and 
contents to 140 degrees.
 
Bill
ACI
 
 
In a message dated 9/24/2009 12:25:24 P.M. Eastern Daylight Time,  
cgard...@mdah.state.ms.us writes:

This is  a message from the Pest Management Database List.
To post to this list send  it as an email to pestlist@museumpests.net
To unsubscribe please look at  the footer of this  email.
---






We  have carpet beetles at one of our sites that has recently reopened.   
We thought we had it under control, but yesterday the curtains in one  
room were covered in larvae.
What is the best way to treat carpet  beetles and larvae for an entire 
building?  The museum has three  floors with artifacts on all three 
floors.  So far the problem is  contained to the reproduction carpet and 
curtains and has not bothered the  few textiles on exhibit.
Thanks for any advice.

-- 
Cindy  Gardner
Director of Collections, Museum Division
Project Liaison, Museum  of Mississippi History
Mississippi Department of Archives and  History
P.O. Box 571
Jackson, MS 39205-0571
Telephone:  601/576-6901
Facsimile: 601/576-6815
Email:  cgard...@mdah.state.ms.us



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imail...@zaks.net and in the  body put:
unsubscribe pestlist
Any problems email  l...@zaks.com










Re: [pestlist] moths and carpet beetles

2009-07-09 Thread WLouche
_http://www.epa.gov/oppsrrd1/REDs/factsheets/permethrin_fs.htm_ 
(http://www.epa.gov/oppsrrd1/REDs/factsheets/permethrin_fs.htm)A good idea 
to read 
before use.
 
Bill
 
 
In a message dated 7/9/2009 9:48:08 P.M. Eastern Daylight Time,  
forr...@saintaubinbce.com writes:

Lisa, there  are several formulations of permethrin insecticide that are 
labeled for use on  clothing.  There are also several lines of outdoor and 
sports clothing  impregnated with permethrin.  Permethrin is used extensively 
by the armed  forces and, properly applied, will withstand several washing 
before  reapplication is necessary.

Permethrin would be ideal for use in a  working collection, such as 
theatre, as well as for museum  storage.

When applying permethrin, only apply to clothing, never  directly to the 
skin.. 


Forrest E. St. Aubin, BCE
Chair, ESA-ACE  Oversight Committee
Liaison, ESA/NPMA
12835 Pembroke Circle
Leawood,  Kansas 66209
Phone: 913.927.9588
Fax: 913.345.8008
E-mail:  forr...@saintaubinbce.com
Website:  www.saintaubinbce.com

Procrastination is opportunity's  assassin.
Victor Kiam, entrepreneur
1926-2001


-Original  Message-
From: Lisa Shockley  [shock...@unionstation.org]
Date: 07/01/2009 06:36 PM
To:  pestlist@museumpests.net
Subject: RE: [pestlist] moths and  carpet beetles

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Suggestion:
Check  the MSDS in detail.
It sounds as if the collection is worn or has the  possibility of being
worn.
If treated with such a residual pesticide,  make certain it is safe for
human contact for hours under very warm   moist (sweaty) conditions. If
it is, I would be very much interested in  knowing what the chemical is.


Lisa Shockley, Curatorial Specialist,  3-D Collections
Union Station/Kansas City Museum
30 W. Pershing  Road
Kansas City, MO 64108
816-460-2055
Where there is Peace; there  is Culture;
Where there is Culture; there is Peace.
Nicholas Roerich  (1874-1947



-Original Message-
From: _pestlist-ow...@museumpests.net_ 
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 ]  On Behalf Of Cindy Gardner
Sent: Wednesday, July 01, 2009 2:33 PM
To: _pestl...@museumpests.net_ 
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Subject:  [pestlist] moths and carpet beetles

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Hello  Everyone,

I apologize for this long-winded email. A local university  has asked me

for some help involving a pest infestation in a costume  collection and I

thought I would ask you. This is not a museum  collection but a 
working collection that is used in the theater program,  etc; however, 
it is comprised of period clothing from the 20th century.  There are 
about 1900 hanging textiles and another 2000 in boxes, and they  are kept

in a 12' X 60' room.

When the collection first came to  them, it showed evidence of 
moth/carpet beetle damage. At the suggestion  of an entomologist, the 
most vulnerable items in the collection were  frozen, the wool and silk 
items were vacuumed with a mesh screen, and the  room that houses the 
collection was periodically fogged with a fabric safe  pesticide.

However, the infestation has returned. An exterminating  company has 
recommended treating the room with a long lasting  micro-encapsulated 
chemical using controlled release technology to be done  on a regular 
basis for a year in 3 month intervals.

Are there any  other options or suggestions to be considered before this 
chemical  treatment of the room? Bear in mind, this is not a museum 
collection, and  the logistics and cost of freezing the almost 4000 items

prohibits  freezing the entire collection.

THANKS!


-- 
Cindy  Gardner
Director of Collections, Museum Division
Project Liaison, Museum  of Mississippi History
Mississippi Department of Archives and  History
P.O. Box 571
Jackson, MS 39205-0571
Telephone:  601/576-6901
Facsimile: 601/576-6815
Email: _cgard...@mdah.state.ms.us_ 
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