My WebLink
|
Help
|
About
|
Sign Out
Home
Browse
Search
SITE INFORMATION AND CORRESPONDENCE_FILE 2
EnvironmentalHealth
>
EHD Program Facility Records by Street Name
>
F
>
F
>
5491
>
3500 - Local Oversight Program
>
PR0545028
>
SITE INFORMATION AND CORRESPONDENCE_FILE 2
Metadata
Thumbnails
Annotations
Entry Properties
Last modified
12/6/2019 5:05:08 PM
Creation date
12/6/2019 2:55:44 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
3500 - Local Oversight Program
File Section
SITE INFORMATION AND CORRESPONDENCE
FileName_PostFix
FILE 2
RECORD_ID
PR0545028
PE
3528
FACILITY_ID
FA0003919
FACILITY_NAME
VAN DE POL ENTERPRISES
STREET_NUMBER
5491
STREET_NAME
F
STREET_TYPE
ST
City
BANTA
Zip
95304
CURRENT_STATUS
02
SITE_LOCATION
5491 F ST
P_LOCATION
99
P_DISTRICT
005
QC Status
Approved
Scanner
SJGOV\wng
Tags
EHD - Public
Jump to thumbnail
< previous set
next set >
There are no annotations on this page.
Document management portal powered by Laserfiche WebLink 9 © 1998-2015
Laserfiche.
All rights reserved.
/
219
PDF
Print
Pages to print
Enter page numbers and/or page ranges separated by commas. For example, 1,3,5-12.
After downloading, print the document using a PDF reader (e.g. Adobe Reader).
View images
View plain text
EXTOXNET PIP -PENTACHLOROPHENOL (PCP) Page 3 of 5 <br /> u Saw/ <br /> while another did find increases [71]. Weak mutagenic effects were seen in human lymphocyte <br /> cultures exposed to PCP [71]. The evidence suggests that PCP is nonmutagenic or weakly <br /> mutagenic. <br /> . Carcinogenic effects: Studies of two formulated PCP products (Dowcide and Penta) showed <br /> increases in cancers of the spleen, liver, and adrenal gland in test mice or rats at doses of about 17 <br /> to 18 mg/kg/day [71]. These findings were not replicated for Dowcide in mice in a second study <br /> [71]. There have been reports of a possible association between occupational exposures to <br /> technical PCP and Hodgkin's disease, acute leukemia, and soft-tissue sarcoma, but confounding <br /> factors such as concurrent exposure to other substances makes interpretation of these data <br /> problematic [71].No convincing evidence of PCP's caricinogenic effects in humans is available <br /> [71]. Current evidence is not sufficient to assess the potential of PCP to cause carcinogenic effects <br /> in humans. <br /> . Organ toxicity: Data from animal studies indicate that the major target organs for PCP are the <br /> liver, kidneys, and central nervous system. <br /> . Fate in humans and animals: PCP is rapidly absorbed through the gastrointestinal tract <br /> following ingestion [71]. Accumulation is not common,but if it does occur, the major sites are the <br /> liver, kidneys,plasma protein, brain, spleen, and fat [69,71]. Unless kidney and liver functions are <br /> impaired,PCP is rapidly eliminated from blood and tissues, and is excreted,mainly unchanged or <br /> in conjugated form, via the urine [71]. Single doses of PCP have half-lives in blood of 15 hours in <br /> rats, 78 hours in monkeys, and 30 to 50 hours in humans [69]. <br /> Ecological Effects: <br /> . Effects on birds: The compound is slightly toxic to practically nontoxic to bird species. The <br /> reported 5-day dietary LC50 value in Japanese quail is greater than 5139 ppm [54]. Reported <br /> acute oral LD50 values for PCP are 380 mg/kg in mallard duck and 504 mg/kg in pheasant [55]. <br /> . Effects on aquatic organisms: PCP may be highly to very highly toxic to many species of fish; <br /> reported 96-hour LC50 values are 68 ug/L in chinook salmon, 52 ug/L in rainbow trout, 205 ug/L <br /> in fathead minnow, 68 ug/L in channel catfish, and 32 ug/L in bluegill sunfish [55]. Several <br /> species of fish, invertebrates, and algae have had levels of PCP that were significantly higher(up <br /> to 10,000 times)than the concentration in the surrounding waters [71]. Once absorbed by fish, <br /> pure PCP is rapidly excreted as is its metabolite,with a biological half-life of only 10 hours [71]. <br /> Biomagnification,that is the progressively higher concentration of a compound as it passes up the <br /> food chain, is not thought to be significant because of PCP's rapid break down in living organisms <br /> [70]. <br /> . Effects on other organisms: Cattle and other farm animals have ingested PCP by chewing and <br /> licking outdoor wood structures, or from being housed in wooden pens that were treated with PCP <br /> solutions. This has caused sickness and death in some of these animals [17]. <br /> Environmental Fate: <br /> . Breakdown in soil and groundwater: PCP is moderately persistent in the soil environment, with <br /> a reported field half-life of 45 days [15]. PCP degrades most rapidly in flooded or anaerobic <br /> (airless) soils, at higher temperatures and in the presence of organic matter in the soil [12,15]. <br /> Breakdown is mainly by anaerobic biodegradation; breakdown by sunlight and hydrolysis do not <br /> appear to be significant processes [15]. It is poorly sorbed at neutral and alkaline conditions, and <br /> may be mobile in many soils [12,15]. Sorption will be slightly greater(and mobility slightly <br /> lesser) in soils with higher proportions of soil organic matter [12]. The compound has been found <br /> in groundwater in California, Oregon, and Minnesota at very low concentrations ranging from <br /> http://extoxnet.orst.edu/pips/pentachl.htrn 5/8/2008 <br />
The URL can be used to link to this page
Your browser does not support the video tag.