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SU0006554 SSCRPT
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SU0006554 SSCRPT
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Last modified
5/7/2020 11:32:32 AM
Creation date
9/9/2019 10:20:03 AM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2600 - Land Use Program
FileName_PostFix
SSCRPT
RECORD_ID
SU0006554
PE
2611
FACILITY_NAME
PA-0700181
STREET_NUMBER
13295
Direction
S
STREET_NAME
STEINEGUL
STREET_TYPE
RD
City
ESCALON
APN
20721011
ENTERED_DATE
5/8/2007 12:00:00 AM
SITE_LOCATION
13295 S STEINEGUL RD
RECEIVED_DATE
5/8/2007 12:00:00 AM
P_LOCATION
99
P_DISTRICT
004
QC Status
Approved
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SJGOV\rtan
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\MIGRATIONS\S\STEINEGUL\13295\PA-0700181\SU0006554\SSC RPT.PDF
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EHD - Public
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EXTOXNET PIP - COPPEi�,WULFATE 1-01 Page 2 of 4 <br /> triggered by its irritating effect on the gastrointestinal tract. Symptoms are severe, however, if <br /> copper sulfate is retained in the stomach, as in the unconscious victim. Some of the signs of <br /> poisoning which occurred after 1 to 12 g of copper sulfate was swallowed include a metallic taste <br /> in the mouth, burning pain in the chest and abdomen, intense nausea, repeated vomiting, diarrhea, <br /> headache, sweating, shock, discontinued urination leading to yellowing of the skin. Injury to the <br /> brain, liver, kidneys, and stomach and intestinal linings may also occur in copper sulfate <br /> poisoning [23]. Copper sulfate can be corrosive to the skin and eyes [8]. It is readily absorbed <br /> through the skin and can produce a burning pain, as well as the other symptoms of poisoning <br /> resulting from ingestion. Skin contact may result in itching or eczema [8]. It is a skin sensitizer <br /> and can cause allergic reactions in some individuals [24]. Eye contact with this material can cause <br /> conjunctivitis, inflammation of the eyelid lining, cornea tissue deterioration, and clouding of the <br /> cornea [23]. Examination of copper sulfate poisoned animals showed signs of acute toxicity in the <br /> spleen, liver, and kidneys [8]. Injury may also occur to the brain, liver, kidneys, and <br /> gastrointestinal tract in response to overexposure to this material [22]. The oral LD50 of copper is <br /> 472 mg/kg in rats [8]. <br /> • Chronic toxicity: Vineyard sprayers experienced liver disease after 3 to 15 years of exposure to <br /> copper sulfate solution in Bordeaux mixture [8]. Long term effects are more likely in individuals <br /> with Wilson's disease, a condition which causes excessive absorption and storage of copper [25]. <br /> Chronic exposure to low levels of copper can lead to anemia [8]. The growth of rats was retarded <br /> when given dietary doses of 25 mg/kg/day of copper sulfate. Dietary doses of 200 mg/kg/day <br /> caused starvation and death [8]. Sheep given oral doses of 20 mg/kg/day showed blood cell and <br /> kidney damage [8]. They also showed an absence of appetite, anemia, and degenerative changes <br /> [22]. <br /> • Reproductive effects: Copper sulfate has been shown to cause reproductive effects in test <br /> animals. Testicular atrophy increased in birds as they were fed larger amounts of copper sulfate. <br /> Sperm production was also interrupted to varying degrees [8]. Reproduction and fertility was <br /> affected in pregnant rats given this material on day 3 of pregnancy [23]. <br /> • Teratogenic effects: There is very limited evidence about the teratogenic effects of copper <br /> sulfate. Heart disease occurred in the surviving offspring of pregnant hamsters given intravenous <br /> copper salts on day 8 of gestation [8]. These data suggest that copper sulfate is unlikely to be <br /> teratogenic in humans at expected exposure levels. <br /> . Mutagenic effects: Copper sulfate may cause mutagenic effects at high doses. At 400 and 1000 <br /> ppm, copper sulfate caused mutations in two types of microorganisms [22]. Such effects are not <br /> expected in humans under normal conditions. <br /> • Carcinogenic effects: Copper sulfate at 10 mg/kg/day caused endocrine tumors in chickens given <br /> the material parenterally, that is, outside of the gastrointestinal tract through an intravenous or <br /> intramuscular injection [22]. However, the relevance of these results to mammals, including <br /> humans, is not known. <br /> • Organ toxicity: Long-term animal studies indicate that the testes and endocrine glands have been <br /> affected. <br /> • Fate in humans and animals: Absorption of copper sulfate into the blood occurs primarily under <br /> the acidic conditions of the stomach. The mucous membrane lining of the intestines acts as a <br /> barrier to absorption of ingested copper [8]. After ingestion, more than 99% of copper is excreted <br /> in the feces. However, residual copper is an essential trace element that is strongly <br /> bioaccumulated [8]. It is stored primarily in the liver, brain, heart, kidney, and muscles. <br /> Ecological Effects: <br /> s Effects on birds: Copper sulfate is practically nontoxic to birds. It poses less of a threat to birds <br /> httn://extoxnet.orst.edu/nips/connersu.htm 912112004 <br />
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