Extensive damage is often caused by well-meaning individuals whose

attempts at first aid result in brutally deep incisions and tourniquets

applied too tightly and for too long a period of time; the resultant

damage in many instances exceeds that of the bite itself (Stimson and

Engelhardt, 1960:165). Stimson and Engelhardt also think that time

should be sacrificed to surgical cleanliness, and incisions should not

be made if a hospital can be reached within an hour.

The ligature-cryotherapy (L-C) method proposed by Stahnke (1953) has

been severely criticized by other workers. He stated that the ligature

should be tight enough to restrict completely the flow of venom until

the temperature of the area can be lowered sufficiently to prevent any

action of the venom. After 10 minutes the ligature may be removed and

the bitten area kept immersed in a vessel of crushed ice and water. If

the envenomized member is to be treated for more than four hours (which

is the case with almost all pit-viper bites), it should be protected by

placing it in a plastic bag. The venom action should be tested after 12

or more hours. This consists of a brief warming period to determine

whether or not the action of the venom can be felt. The patient should

be kept warm at all times; and the warming at the termination of

treatment should be done gradually, preferably by allowing the water to

warm slowly to room temperature.

Advocates of the L-C method warn against making incisions unless they

are absolutely necessary, the theory being that each cut permits

additional bacterial infection and does little good in removing venom.

However, McCollough and Gennaro (1963:963) demonstrated that, in bites

where the fangs had only slightly penetrated the skin, more than 50 per

cent of the venom was removed in some instances if suction was started

within three minutes after the injection. With deeper injection the

amount of venom recovered sometimes reached 20 per cent of the dose.

Stahnke suggested that an incision be made at the site of the bite only

after the site has been refrigerated for at least 30 minutes.

Stimson and Engelhardt (_loc. cit._) stated that two constricting bands

should be used between the bite and the body and that cracked ice in a

cloth should be applied to the bite before reaching a hospital. In

addition, they suggested the following procedure. Rings of incisions

should follow the swelling, and suction should continue for several

hours. After the edema has receded, the limb should be wrapped in a

towel containing crushed ice. Antivenin should be given only in severe

cases. Calcium gluconate and gas gangrene antitoxin as well as

antibiotics are helpful.

The most recent and up-to-date summary of snakebite treatment is that by

McCollough and Gennaro (1963). Following is a brief summary of their

suggestions:

1. Immobilization--Systemic immobilization is effected by body

rest and locally by splinting the bitten area.

2. Tourniquet--A lightly occlusive tourniquet during a 30- to

60-minute period of incision and suction would seem to possess

some advantages. In severe cases where medical attention is

hours away, a completely occlusive tourniquet may be necessary

to prevent death. Sacrifice of the extremity may be necessary

for the preservation of life.

3. Incision and suction--Suction should begin three to five

minutes after injection of venom if symptoms of poisoning are

present. Incisions one-fourth inch to an inch long across each

fang mark should be made in order to open the wound for more

efficient suction. Multiple incisions are not useful for the

removal of venom but may be employed under hospital conditions

to reduce subcutaneous tensions and ischemia.

4. Cryotherapy--An ice cap over the site of the bite for relief

of pain would seem to be permissible, especially prior to the

administration of antivenin. It must be remembered that cooling

during the administration of the antivenin radically reduces

the access of the antiserum to the bite area.

5. Antivenin--Antiserum is the keystone to the therapy of

snakebite. Careful evaluation of the severity of the bite and

the patient's sensitivity should be made before the use of

antivenin. In Grade II (moderate) bites, the intramuscular

injection on the side of the bite may suffice. In Grades III

(severe) and IV (very severe), shock and systemic effects

require intravenous injection. In bites producing symptoms of

this severity, antivenin must be given in amounts large enough

to produce clinical improvement. Ten to 20 units may be

necessary to prevent the relapse that sometimes occurs after

small doses of antivenin. Permanent remission of swelling and

interruption of necrosis are the therapeutic end point in the

clinical use of the antiserum.

In all cases of snakebite where there is any doubt as to the snake's

identity, it should be killed if possible and taken to the hospital for

positive identification. In many instances of actual bites by poisonous

snakes the only treatment needed was an injection of tetanus antitoxin

or toxoid and sedation, because physical examination revealed no

indication of poisoning (Stimson and Engelhardt, _loc. cit._).

Case History of a Bite

On July 29, 1963, at 8:20 a.m., I was treating a nine-month-old

cottonmouth for mites. As I dropped the snake into a sink, it twisted

its head and bit the tip of my right middle finger with one fang. The

fang entered just under the fingernail and was directed downward, the

venom being injected about five millimeters below the site of fang

penetration. After placing the snake back in its cage, I squeezed the

finger once to promote bleeding, wrapped a string around the base of the

finger, and drove to Watkins Memorial Hospital on the University of

Kansas campus. I began to feel a burning sensation in the tip of the

finger almost immediately. Upon my arrival at the hospital, an

additional ligature was placed around my wrist. At 8:30 a.m. a small

incision was made in the end of the finger, which by this time was

beginning to darken at the point of venom deposition. I sucked on the

finger until 8:35 a.m., when a pan of ice water that I had requested was

brought to me. No pain was felt except that caused by the ice. Fresh ice

was added as needed to keep the temperature low. By 9:30 a.m. the

finger had swollen and stiffened. At 10:00 a.m. the swelling had

progressed to the index finger and back of the hand. I experienced

difficulty in opening and closing the hand. Blood oozed slowly from the

incision. A dull ache persisted and about every two to four minutes a

sharp throb could be felt until nearly 11:00 a.m., when the pain

diminished. The rate and intensity of throbbing increased whenever the

hand was removed from the ice bath for more than a few seconds. Although

only the hand was immersed, the entire forearm was cold. Pain was felt

along the lymphatics on top of the arm when it was touched, and by 1:00

p.m. a slight pain could be felt in the armpit. Since swelling and pain

were almost nonexistent by 2:00 p.m., I was permitted to leave. After

walking to a nearby building, I again felt a burning sensation as the

hand warmed. I made another ice bath and again immersed the hand in it

until 4:10 p.m., at which time it was removed from the water. The pain

and swelling began anew, and the hand was placed back in an ice bath

from 5:30 p.m. until about 7:30 p.m. At this time cryotherapy was

discontinued. From 10:00 p.m. to 12:00 midnight my legs twitched

periodically, and pain could be felt in both armpits. A slight

difficulty in breathing also was experienced for a short time. The acute

pain and burning sensation remained in the finger until the following

morning, but swelling progressed only as far as the wrist. The only

discomfort that day was in the finger. The tip was darkened, the entire

first digit red and feverish, and the lymphatics still painful when

touched. By the third day the swelling had regressed. The incision

itself was the main cause of discomfort, and the soreness at the site of

the bite persisted for at least four days.

Although the L-C method of snakebite treatment has been vigorously

attacked by many, there is still need of much more data before it

can be unequivocally condemned or praised. It was preferred in the

treatment of this bite because: I knew that envenomation was minimal

and that there would be no need for antivenin; only one fang of a

snake less than one foot long had entered the tip of the finger; the

snake had bitten three frogs in the previous two days and had

possibly used up a considerable amount of its venom; the venom was

deposited at such a shallow depth that at least a portion of it

could be removed by suction; and the wound bled freely even before

suction was applied. The ice water was uncomfortably cold but was

not cold enough to cause frostbite, a major objection to the L-C

method. Ideally, fresh ice should be added little by little to

replace that which is melting, and the immersed area should be

protected from the water by a plastic bag. Pain and swelling can be

minimized by cryotherapy, but I would recommend its use only in

cases of mild poisoning such as the one described herein.

Snakebite in the United States

Many estimates have been made of the number of bites of poisonous snakes

that occur annually in the United States. The occurrence of poisonous

snakebite has been nearly as badly underestimated as fatal results of

their envenomations have been overrated. For important data on number of

persons bitten by poisonous snakes in the United States, see the

following: Allen and Swindell (1948:15); Githens (1935:172); Klauber

(1956:811); Parrish (1963); Sowder and Gehres (1963:973); Stimson and

Engelhardt (1960:153); Swaroop and Grab (1956:441); Swartzwelder

(1950:579); Willson (1908:530); and Wood (1954b:937).

Judging from estimates made in several states, the number of poisonous

snakebites in the United States would be about 5000 per year. In the

region where the cottonmouth occurs there are approximately 2000 persons

bitten annually by poisonous snakes. Of these approximately 39 per cent

are copperhead bites, 30 per cent each are cottonmouth and rattlesnake

bites, and I per cent are coral snake bites. These percentages vary

considerably from place to place, because of the distribution and

abundance of the eight species of poisonous snakes whose ranges overlap

that of the cottonmouth.

According to Parrish (1963), about 14 people die of snakebite each year

in the United States. Of these deaths, about 6.6 per cent are

attributable to cottonmouths, 77.0 per cent to rattlesnakes, and 1.6 per

cent to coral snakes; 14.8 per cent are unidentified. Almost half of the

fatalities are in persons less than 20 years of age, the high mortality

rate being partially due to the greater ratio of venom to body weight.

SUMMARY

In my study, 306 living and preserved cottonmouths were examined. This

species occurs throughout the coastal plains of the southeastern United

States, usually at altitudes of less than 500 feet but occasionally up

to altitudes of more than 2000 feet.

Two subspecies are recognized: the eastern cottonmouth, _A. p.

piscivorus_, occurring from extreme eastern Mississippi to southeastern

Virginia and Florida; and the western cottonmouth, _A. p. leucostoma_,

occurring from eastern Mississippi northward to southern Illinois and

Missouri and westward to central Texas. Intergradation occurs in eastern

Mississippi.

The northern edge of the range is probably limited by low temperatures

in winter, and the western edge by lack of available habitat resulting

from insufficient precipitation. Old records of occurrence indicate that

the range has decreased in the last 100 years. The species inhabits

mostly areas where water is found, but at times wanders a mile or more

from the nearest water.

The ground color is predominantly a brown, but varies from a

brownish-green to almost black with a pattern of 10 to 17 irregular

bands of a darker shade of brown. The pattern is better defined in the

eastern subspecies than in the western.

The scutellation resembles that of other species of _Agkistrodon_. In

the specimens examined supralabials ranged from 7 to 9, and infralabials

from 8 to 12. The number of dorsal scale rows on the neck, at mid-body,

and immediately anterior to the anus is relatively constant at 27-25-21,

respectively. Ventral scales of 34 males averaged 134.4 (128 to 139),

and those of 48 females 133.5 (128 to 137). The number of caudal scales

showed some degree of sexual dimorphism; the average was 45.4 (41 to 50)

in 34 males and 42.6 (39 to 49) in 44 females. In general, caudal scales

on the basal half of the tail are undivided, whereas those on the distal

half are divided. No marked geographical variation was found in any

scale character.

The poison fangs vary in length from 1.3 per cent of snout-vent length

in juveniles to 1.0 per cent in large adults. Fangs of captive

cottonmouths were shed and replaced at intervals of about 21 days, but

the interval was variable. Relationships in distance between the base of

fangs and between fang punctures in an actual bite indicate that

examination of the wound does not provide a good basis for judging

accurately the size of the snake that inflicted the bite.

In general, females less than 450 millimeters in snout-vent length were

juveniles; those more than 450 millimeters were classified as post

partum or reproductive on the basis of sizes of ovarian follicles. Since

about half the adult females were fecund, it was concluded that a

biennial reproductive cycle occurs in this species. An annual cycle may

occur in areas where temperature permits year-round activity. It was

estimated that females become sexually mature at an age of approximately

two and one-half years. Mating is probably most concentrated in early

spring at about the time when females ovulate, but copulation is not a

stimulus for ovulation. Sperm retention and delayed fertilization allow

young to be produced without copulation occurring in each breeding

season. The testes increase in size gradually rather than rapidly at

maturity or in each breeding season, but seasonal cycles in sperm

production occur.

The gestation period is three and one-half to four months. Determination

of sex in the embryos is possible by late June, because the hemipenes of

males are evaginated until the time of birth. Parturition generally

occurs in August or September, but captivity may delay birth for a month

or more. From one to 16 young per litter are born, depending on size of

the mother and other factors; but the average is between six and seven.

Mortality rate at birth is high in captive individuals but has not been

determined in natural populations. The sex ratio in embryos and adults

examined revealed about 53 per cent females. Because sufficient

information on population composition is not available, an estimate of

the percentage of adults in a natural population was based upon the

number found in my study. The reproductive potential was estimated from

these figures.

Normal young at birth are 230 to 240 millimeters in snout-vent length,

but their size is influenced by the condition of the mother. Comparison

of newborn young with those captured in spring indicates that little

growth occurs during winter. Early growth is largely dependent upon

feeding before winter quiescence.

The umbilical cord is broken at birth and the navel closes within a few

days, but the scar remains throughout life. Sexual dimorphism in the

position of the scar is characteristic of some snakes but is minimal in

cottonmouths.

In those snakes more than 700 millimeters in length, males outnumber

females three to one. The maximum age of cottonmouths in nature is

unknown, but one has been kept in captivity for more than 18 years.

Allometric growth is striking in cottonmouths. The head and tail are

proportionately longer in young individuals than in adults; and in males

the tail is, on the average, slightly longer than in females of the same

size.

Shedding of the skin provides for growth and wear in snakes. The young

shed within a few days after birth and generally shed more frequently

than adults. Frequency of shedding depends mostly on amount of food

consumed, and there is some evidence that injuries on the head and neck

increase the frequency of shedding. Before shedding, the eyes become

cloudy for about five and one-half days, then clear up again for about

four days before the skin is shed.

The food of cottonmouths consists mainly of small vertebrates and

occasionally invertebrates that are found near water. Fish, amphibians,

and reptiles make up nearly 70 per cent of the diet. Carrion is also

eaten and cannibalism occurs occasionally. Food is obtained by lying in

ambush or by active searching. The young are known to lure their prey

within striking range by waving their yellow tails in a manner

suggestive of writhing grubs. The method of obtaining prey differs

according to the kind of prey. Generally, cottonmouths retain their hold

on fish or frogs but release mice and larger prey after delivering a

bite.

The major causes of mortality of cottonmouths are obscure. Predators are

known to include alligators, indigo snakes, king-snakes, largemouth

bass, and blue herons; there are probably numerous others. Heavy

parasitic infestations were found among the snakes examined. Snake

mites, _Ophionyssus natricus_, became increasingly abundant on almost

all captive snakes in April and May of 1963. Lung flukes (_Ochetosoma_

sp.) were in 16 of 20 captive snakes, and many preserved specimens

contained nematodes (_Kalicephalus_ sp.) in the stomach and/or tapeworms

(_Ophiotaenia_ sp.) in the intestine. Although parasitic infestation

causes discomfort and may lower resistance to other detrimental factors,

it is difficult to attribute death to the effect of any particular kind

of parasite. Miscellaneous causes of death of some captive snakes also

were discussed.

The maximal body temperatures tolerated by four cottonmouths were

between 38 deg. and 40 deg. C., but a temperature of 38 deg. was lethal to a fifth

individual. Cottonmouths have been found on occasion when other snakes

were inactive because of low temperatures, but minimal temperatures

tolerated by this species are not known. The annual cycle of activity is

dependent upon temperature and thus varies from north to south.

Cottonmouths generally migrate inland in autumn, usually to dry forested

hillsides, where they den along with other species of snakes. After a

few warm days in spring they migrate back to the water's edge. The diel

activity cycle likewise depends upon temperatures but is influenced by

other factors as well. In spring and autumn, the snakes are active

mostly on warm, sunny days, whereas in summer they are active mostly at

night. In order to maintain adequate internal temperatures, much time is

spent basking mostly in a characteristic flat, resting coil either

beside a body of water or above water on limbs of dead trees. In this

position the snake is ready either for a short strike or a hasty

getaway.

Juveniles appear particularly aggressive and strike repeatedly when

approached, a behavioral pattern definitely favoring survival. Adults

vary in disposition, usually appearing sluggish and lazy, but they are

capable of striking rapidly when disturbed. The typical threat display

consists of lying in a coiled position with the mouth opened widely,

exposing the white interior, and with the tail vibrating rapidly. The

striking posture resembles the resting coil except that the anterior

part of the body is raised off the ground and the mouth is sometimes

opened. Musk is often ejected in a fine spray from glands in the tail as

a further defensive action.

"Head bobbing," more properly described as spastic contractions of the

body, was observed in captives when food was introduced into a cage

containing several individuals or when one of the snakes was returned to

the cage after being handled. Reports in the literature also have

connected these jerking movements with courtship. The response appears

to be elicited whenever a nervous state is recognized in another

individual and may serve to protect the jerking individual from

aggressive advances of the former.

The relatively heavy appearance of the body, sluggish habits, and

cryptic coloration are correlated with the development of venom and

fangs. The poison apparatus has developed primarily as a means of

causing rapid death in prey and secondarily, perhaps, to begin the

digestion of small animals that are the usual prey, but it is also

important as a defensive device. The venom contains at least eight

constituents that aid in its action on prey. Toxicity of the venom is

difficult to determine because of numerous variables, but cottonmouth

venom is generally believed to be less potent than that of most

rattlesnakes and more potent than that of the copperhead. Snakes in

general are more resistant to snake venoms than other vertebrates of

similar size, but there is no immunity even to their own venom.

About ten per cent of the approximately 5000 bites of poisonous snakes

per year in the United States are attributable to cottonmouths, and

about seven per cent of the approximately 14 deaths per year are caused

by cottonmouths.

LITERATURE CITED

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1937. Florida snake venom experiments. Florida Acad. Sci., 2:7 pp.

ALLEN, E. R., and SWINDELL, D.

1948. Cottonmouth moccasin of Florida. Herpetologica, 4:1-16 (first

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ALLEN, M. J.

1932. A survey of the amphibians and reptiles of Harrison County,

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ANDERSON, P.

1941. The cottonmouth in northern Missouri. Copeia, 1941(3):178.

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ANON.

1953. Snake collecting hobby of Colonial Heights lad. Virginia

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1963. The fossil snakes of Florida. Tulane Studies Zool.,

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1948. Winter mortality in the snake _Storeria dekayi_. Copeia,

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BARBOUR, R. W.

1956. A study of the cottonmouth, _Agkistrodon piscivorus

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1958. Reproduction, young, eggs, and food of Oklahoma snakes.

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CARR, A. F., JR.

1936. The gulf-island cottonmouths. Proc. Florida Acad. Sci.,

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CARR, A. F., JR., and CARR, M. H.

1942. Notes on the courtship of the cottonmouth moccasin. Proc. New

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CLARK, R. F.

1949. Snakes of the hill parishes of Louisiana. Jour. Tennessee

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CONANT, R.

1933. Three generations of cottonmouths, _Agkistrodon piscivorus_

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1958. A field guide to reptiles and amphibians. Houghton Mifflin

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CORRINGTON, J. D.

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DARLINGTON, P. J.

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DIDISHEIM, P., and LEWIS, J. H.

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