Pair / Group
Distinguishing Feature
Toxicity vs Exposure vs Hazard
Toxicity: capacity of the pesticide to cause injury or illness — combination of chemical properties + concentration. Exposure: pesticide gets onto or into the body via skin, lungs, mouth, or eyes. Hazard (risk): probability of harm from the COMBINATION of toxicity and exposure. Hazard = Toxicity x Exposure.
Acute vs Chronic vs Delayed effects
Acute: harm from a single exposure event, usually within 24 hours. Measured by LD50 + LC50. Chronic: harm from small, repeated doses over time (test typically 2 years = lifetime of test animal). NO single measure equivalent to LD50. Delayed: illnesses appearing weeks/months/years after exposure. Caused by EITHER acute OR chronic exposures. Signal word indicates ONLY acute toxicity.
Local (contact) vs Systemic effects
Local (contact): at the point of contact — skin (dermatitis: itching, redness, rashes, blisters, burns), eyes (swelling, stinging, burning, possibly blindness), nose/mouth/throat (swelling, stinging, burning). Systemic: after absorption + distribution throughout body — cholinesterase inhibition, nerve damage, blood clotting impairment, cancers, reproductive problems, organ damage (liver, kidney), hormonal effects.
Allergic effects vs Acute/chronic toxicity
Allergic effects: hypersensitivity reactions in some people — dermatitis, blisters, hives, itching eyes, asthma-like symptoms, life-threatening shock. CANNOT predict who will develop allergies. Allergic reactivity does NOT predict sensitivity to chronic/delayed effects (different mechanisms).
Dermal vs Ocular vs Inhalation vs Oral
Dermal: skin — primary route (97% during spraying); warm/moist body areas absorb more; oil-based formulations penetrate readily. Ocular: eyes — extremely absorbent, blood vessels close to surface, very rapid bloodstream entry; eye corrosion can cause blindness. Inhalation: lungs — rapid bloodstream entry; aspiration of EC/oil solvents during vomiting may be fatal. Oral: mouth — splashes during mixing/loading, eating/drinking/smoking with contaminated hands, accidental ingestion (children with rodent baits, food-container storage).
LD50 vs LC50
LD50 (Lethal DOSE 50%): dose required to kill 50% of test population. Expressed in mg toxicant per kg body weight (mg/kg). Oral LD50 (feeding) and Dermal LD50 (skin contact). LC50 (Lethal CONCENTRATION 50%): concentration in air or water required to kill 50% of test population. Expressed as parts per million or mg/liter. Common for fish + aquatic organisms, and inhalation toxicity.
DANGER-POISON vs DANGER (no skull)
DANGER-POISON (Hazard Class I systemic): "POISON" in RED + skull + crossbones; oral LD50 trace to 50 mg/kg; few drops lethal to 150-lb person; PELIGRO Spanish. Most fumigants, some insecticides + rodenticides, few herbicides. DANGER (without skull/POISON): Hazard Class I CONTACT injury — eye/skin/lung damage WORSE than systemic toxicity (LD50). Some herbicides, insecticides, antimicrobials.
WARNING vs CAUTION
WARNING (Hazard Class II; AVISO Spanish): moderately toxic; oral LD50 50-500 mg/kg; 1 teaspoon to 1 ounce fatal to 150-lb person — OR moderate eye/skin/respiratory irritation. CAUTION (Hazard Class III): slightly toxic; oral LD50 500-5,000 mg/kg — OR irritation of eyes/skin/respiratory tract.
Body absorption rates by region
Warm + moist areas absorb MOST: groin, armpits, head, neck, backs of hands, tops of feet. Palms + forearms absorb LESS but get the MOST exposure. Cuts, abrasions, rashes INCREASE absorption regardless of region. Time of contact matters too — longer contact = more absorbed.
Cholinesterase inhibitors: OP vs Carbamate
BOTH organophosphate and carbamate insecticides inhibit cholinesterase enzyme (controls nerve impulse transmission). They are the ONLY pesticide classes causing cholinesterase inhibition. Both have ANTIDOTES — administered ONLY by medical professionals. Anticoagulant-type rodenticides also have antidotes. No other class of pesticide has true antidotes.
Cholinesterase poisoning: Mild vs Moderate vs Severe
Mild: fatigue, headache, dizziness, blurred vision, excessive sweating/salivation, nausea, vomiting, stomach cramps, diarrhea. Moderate: inability to walk, weakness, chest discomfort, CONSTRICTION OF PUPILS, mild symptoms more severe. Severe: unconsciousness, SEVERE pupil constriction, muscle twitching, running nose + drooling, breathing difficulty, COMA + DEATH.
Pesticide poisoning vs Heat stress symptoms
Heat stress symptoms RESEMBLE pesticide poisoning (fatigue, weakness, dizziness, nausea, headache, confusion). PPE may INCREASE heat stress risk by restricting sweat evaporation. KEY heatstroke distinguisher: LACK OF SWEATING + body temperature above 105 degrees F. Severe heat stress kills 10%+ of victims.
Liver vs Kidneys vs Fatty deposits
Liver: primary organ that transforms toxic substances to nontoxic/less-toxic forms; makes them more water-soluble. Kidneys: filter water-soluble substances from blood into urine. Fatty deposits: store substances that cannot be made water-soluble — including breast milk. Pre-1970 pesticides: months-to-years elimination. Modern pesticides: hours-to-days elimination.
NEVER induce vomiting (3 cases)
(1) Victim is UNCONSCIOUS or CONVULSING; (2) victim swallowed CORROSIVE poison — strong alkali/acid burns going down AND coming up; (3) victim swallowed an EMULSIFIABLE CONCENTRATE or OIL SOLUTION — petroleum solvents may be fatally aspirated into lungs during vomiting. Otherwise, induce vomiting ONLY if the label says to.
Activated charcoal vs Antidotes
Activated charcoal: adsorbs many chemicals; pharmaceutical grade from drugstores; consult medical professional or poison control BEFORE administering. Antidotes: extremely dangerous if misused; available only for OP/carbamate insecticides + anticoagulant rodenticides; prescribed and administered ONLY by qualified medical professional; NEVER used to prevent poisoning.