Crotalus cerastesSidewinder

Ge­o­graphic Range

Sidewinder rat­tlesnakes (Cro­talus cerastes) in­habit the south­west cor­ner of the United States of Amer­ica, ex­tend­ing as far west as the Mo­jave Desert in south­ern Cal­i­for­nia and as far east as the Sono­ran Desert in Ari­zona. These rep­tiles also re­side on the east­ern coast of Baja Cal­i­for­nia, and the north­ern coast of Gulf of Cal­i­for­nia, and the Isla del Tiburon. (Frost, et al., 2007; Web­ber, et al., 2016)

Habi­tat

Sidewinders re­side in ter­res­trial, desert land­scapes such as sandy washes, sand dunes, and the open ter­rain of warm deserts. These snakes are highly con­cen­trated near mam­malian bur­rows—close to sandy washes and thickly veg­e­tated areas. Sidewinders live in areas rang­ing from deserts below sea level to 1830 m. On av­er­age, most sidewinders re­side in areas less than 1,200 m be­cause moun­tain­ous ter­rains in­hibit their lo­co­mo­tion. (Babero and Em­mer­son, 1974; Freymiller, 2016; Frost, et al., 2007; Mosauer, 1935; Secor, 1994; Secor and Nagy, 1994)

  • Range elevation
    0 to 1830 m
    0.00 to 6003.94 ft
  • Average elevation
    1200 m
    3937.01 ft

Phys­i­cal De­scrip­tion

Sidewinders are dis­tin­guished among rat­tlesnakes by their horn-like su­pe­r­oc­u­lar scales on their heads. This horn­like struc­ture is why sidewinders are also called horned rat­tlesnakes. They also have a rat­tle on their tails; the num­ber of seg­ments of the rat­tle equates to the num­ber of sheds the in­di­vid­ual has com­pleted.

Adult sidewinders have a snout-vent length av­er­ag­ing 50 cm (range 44.6 -61.5 cm). Sidewinders also ex­hibit sex­ual di­mor­phism. Fe­males grow larger than males, an un­usual trait be­cause most rat­tlesnakes are monomor­phic. Fe­male sidewinders are slightly larger when they reach adult­hood, greater than 38cm, whereas male sidewinders must be greater than 34 cm to reach the same stage. Adult can weigh 93.8 - 304 g (av­er­age 250 g), with older snakes weigh­ing more than younger snakes. Sidewinders are cam­ou­flaged in a va­ri­ety of earthen col­ors, such as light-brown, grey, and cream de­pend­ing on their habi­tats.

Sidewinders subadults can have masses up to 65.0 g be­fore they are clas­si­fied as adults. Snout-vent length ranges from 16.5cm-43.6cm in subadults.

Sidewinders and other rat­tlesnakes are soleno­glyp­hous, mean­ing they have front-fac­ing, hinged ven­omous fangs that can fold down in their mouths.

The stan­dard meta­bolic rate for sidewinders was mea­sured 0.01 mL/g*h car­bon diox­ide pro­duced at 20 de­grees Cel­sius. Ad­di­tional stud­ies con­ducted on other rat­tlesnakes such as west­ern di­a­mond­backs (Cro­talus atrox), black-tailed rat­tlesnakes (Cro­talus molos­sus), and mot­tled rock rat­tlesnakes (Cro­talus lep­idus) pos­tu­late that rat­tlesnakes have a frac­tion (0.2-0.5) of the meta­bolic rate of all other snakes. (Beaupre, et al., 1998; Beaupre and Du­vall, 1998; Beaupre, et al., 1998; Bul­lock and Fox, 1957; Cohen and Myres, 1970; Ernst, 1964; Lewis, 1949; Secor, 1994; Woz­niak, et al., 1994)

  • Range mass
    93.8 to 304 g
    3.31 to 10.71 oz
  • Average mass
    250 g
    8.81 oz
  • Range length
    44.6 to 61.5 cm
    17.56 to 24.21 in
  • Average length
    50 cm
    19.69 in

De­vel­op­ment

Sidewinders are vi­vip­a­rous rat­tlesnakes. Dif­fer­en­ti­a­tion of the em­bryo in­creases at the be­gin­ning of em­bry­onic for­ma­tion (neu­ru­la­tion arises), but grad­u­ally slows by the end of the de­vel­op­men­tal stage. This is fol­lowed by two con­sec­u­tive se­ries of growth, which is fol­lowed by live birth.

Like most snakes, sidewinders ex­hibit in­de­ter­mi­nate growth. They grow faster as ju­ve­niles, and growth rate de­creases as the sidewinders age. Be­cause rat­tles in­crease in the num­ber of seg­ments each time the rat­tlesnakes shed, the num­ber of seg­ments does not equate to age, but in­stead to the num­ber of sheds. Fe­male sidewinders are slightly larger when they reach adult­hood, greater than 38cm, whereas male sidewinders must be greater than 34cm to reach the same stage. (An­drews and Math­ies, 2000; Beaupre, et al., 1998; Blom­sten, et al., 2016; Cochran, 2010)

Re­pro­duc­tion

Male sidewinders show an­nual sex­ual mo­ti­va­tion re­gard­less of am­bi­ent tem­per­a­ture. Fe­male sidewinders’ re­pro­duc­tion is con­tin­gent on the tem­per­a­ture of the re­gion. The dis­tri­b­u­tion of fe­males through­out the ge­o­graphic range forces males to en­hance their lo­co­mo­tion by search­ing for fe­males by straight-line paths through the desert. Males fed more often dur­ing the re­pro­duc­tive sea­son, as the de­mands for en­ergy are high when dis­tances trav­eled to fe­males is high.

Upon find­ing a mate, by dis­tin­guish­ing scents via the vomeronasal organ and tac­tile ef­forts, the two will re­pro­duce after courtship. Tem­po­ral dis­tri­b­u­tion of fe­males causes local polyg­yny, and fe­males will fight for males to mate. (Beaupre and Du­vall, 1998; Cochran, 2010; Macart­ney and Gre­gory, 1988; Web­ber, et al., 2016)

Sidewinder males can mate up to three times a year, while fe­males are de­pen­dent on warm tem­per­a­tures (which occur from April-July) to de­ter­mine if they are suit­able for mat­ing.

Fe­male sidewinders con­tin­u­ously feed dur­ing vitel­lo­ge­n­e­sis (the be­gin­ning of their re­pro­duc­tive cycle) but show a ten­dency to lower their con­sump­tion dur­ing ges­ta­tion (which typ­i­cally last 4-5 months in rat­tlesnakes). This early feed­ing by fe­males helps pre­pare them for the en­er­getic de­mands for ges­ta­tion and par­tu­ri­tion. How­ever, males in­crease food con­sump­tion to meet en­er­getic needs for move­ment to find po­ten­tial part­ners.

Fe­male sidewinders typ­i­cally have lit­ters rang­ing from 4-11 young born alive. They are in­de­pen­dent within 3 hours of live birth. Age of re­pro­duc­tive ma­tu­rity for the genus Cro­talus is 3 years for both sexes. (Keen­lyne, 1978; Macart­ney and Gre­gory, 1988; Web­ber, et al., 2016)

  • Breeding interval
    Sidewinders males can mate up to three times a year, while females are dependent on warm temperatures to determine if they are suitable for mating.
  • Breeding season
    April-July
  • Range number of offspring
    4 to 11
  • Range gestation period
    4 to 5 months
  • Average time to independence
    3 hours
  • Average age at sexual or reproductive maturity (female)
    3 years
  • Average age at sexual or reproductive maturity (male)
    3 years

While most snakes do not pro­vide ma­ter­nal care, fe­male sidewinders will guard new off­spring up to 3 hours after birth be­fore aban­don­ing their young. Be­cause this is en­er­get­i­cally costly for fe­males after giv­ing birth, they have po­ten­tial to die after strain­ing them­selves by pro­tect­ing their young. Be­yond the act of mat­ing, males pro­vide no parental care. (Keen­lyne, 1978; Macart­ney and Gre­gory, 1988)

Lifes­pan/Longevity

Fe­male sidewinders typ­i­cally only live 5 years, whereas, males can live up to 13 years in the wild. How­ever, in cap­tiv­ity, both male and fe­male sidewinders can live up to 20 years. Fe­males have a shorter lifes­pan be­cause birthing ex­hausts the fe­males to the point of death. Males and fe­males are also sub­jected to nat­ural deaths such as lill­nesses and pre­da­tion. Sidewinders also die from get­ting hit by motor ve­hi­cles. It has been es­ti­mated that 2383-4000 sidewinders get killed per year from ve­hi­cles. (Reis­erer and Schuett, 2008; Rosen and Lowe, 1994; Secor, 1994)

  • Typical lifespan
    Status: wild
    5 to 13 years
  • Average lifespan
    Status: captivity
    20 years
  • Average lifespan
    Status: captivity
    27.3 years
    AnAge

Be­hav­ior

Sidewinders' home ranges are not in cir­cu­lar areas, but in­stead are con­vex poly­gons con­form­ing to the land­scape. Males typ­i­cally have a larger home range than fe­males be­cause they travel greater dis­tances over mat­ing sea­son. Av­er­age dis­tance trav­eled in a 24-h block av­er­aged 185.4m for males and 122.9m for fe­males across all ages. Subadult males trav­eled the far­thest, on av­er­age, 223 m per day. They can travel via their name­sake, sidewind­ing, but also have been ob­served using rec­ti­lin­ear mo­tions and lat­eral undulations.​The sidewind­ing mo­tions min­i­mize their con­tact with the hot sands.

Sidewinders, es­pe­cially males dur­ing mat­ing sea­son, are con­stantly on the move for new ter­ri­to­ries. To op­ti­mize move­ment through­out home range, males and fe­male will typ­i­cally move in straight lines to cover more dis­tance, but this type of move­ment is en­er­get­i­cally costly for sidewinders if they can­not find a mate.

Bouts be­tween male rat­tlesnakes (be­tween sin­gle or mul­ti­ple species) can last over a day when it comes to ter­ri­to­r­ial or mat­ing dis­putes. Sidewinders are non-gre­gar­i­ous snakes, but group to­gether dur­ing den­ning. Sidewinders ex­hibit di­ur­nal and noc­tur­nal pe­ri­ods through­out the year, but are strictly noc­tur­nal dur­ing the warmest parts of the year. When try­ing to stay cool, they spend 80% of their time den­ning in ro­dent bur­rows, and 20% coiled up on the sur­face of the sand.

Sidewinders hi­ber­nate in the desert habi­tats, mi­grat­ing to sandy-al­lu­vial de­posits when fall hi­ber­na­tion be­gins. They typ­i­cally hi­ber­nate in the bur­rows of ro­dents or desert tor­toises. When hi­ber­na­tion is com­plete, these snakes move to purely sandy areas of the desert. They also re­main in­ac­tive for days at a time in two in­stances: after con­sum­ing prey (in­ac­tive for 5-10 days there­after), or just be­fore molt­ing (3-5 days prior). (Beaupre and Du­vall, 1998; Beck, 1995; Cowles, 1938; Cowles, 1956; Cun­ning­ham, 1959; Frost, et al., 2007; Secor, 1994; Young and Morain, 2003)

  • Range territory size
    7300 to 61000 m^2
  • Average territory size
    23000 m^2

Home Range

Home ranges for sidewinders in the Mo­jave Desert were the largest among rat­tlesnake species, about 23 ha for for sexes (range 7.3-61 ha). Al­though sidewinders are ter­ri­to­r­ial, pop­u­la­tion den­si­ties are 0.48-1.18 per ha, mean­ing that some ter­ri­to­ries over­lap. (Beaupre and Du­vall, 1998; Beck, 1995; Cowles, 1938; Cowles, 1956; Cun­ning­ham, 1959; Secor, 1994)

Com­mu­ni­ca­tion and Per­cep­tion

Rat­tlesnakes have pits on the sides of their heads that de­tect in­frared ra­di­a­tion, which sidewinders use to iden­tify prey in their sur­round­ings. Sidewinders, like all snakes, use their nose and flick their tongues (tac­tile) to smell their sur­round­ings.

Sidewinders and other rat­tlesnakes have a vomeronasal organ, which is used from chem­i­cal recog­ni­tion. Using the vomeronasal organ, sidewinders can de­tect chem­i­cal in prey, and have been shown to de­tect sub­stances within the skin of kingsnakes Lam­pro­peltis to avoid con­fronta­tion with them.

Sidewinders typ­i­cally rely on the vomeronasal organ to de­tect prey in­stead of using sight, but sight is used as a lesser sense.

Tac­tile senses are used by male sidewinders dur­ing mate-search­ing, courtship, catch­ing prey, and de­tect­ing preda­tors like kingsnakes. They also move in a va­ri­ety of meth­ods (sidewind­ing, rec­ti­lin­ear mo­tion, lat­eral un­du­la­tions) and each method re­quires the snakes' tac­tile senses to feel body parts touch­ing the sand (or al­ter­nate sub­strate).

They shake their rat­tles on their tails when they feel threat­ened, which could be per­ceived as an acoustic, vi­sual, or vi­brat­ing ef­fort as a way to com­mu­ni­cate with the preda­tor. (Jayne, 1988; Moore, 1978; Secor, 1994)

Food Habits

Sider­winders pri­mar­ily con­sume desert rep­tiles such as glossy snakes (Ari­zona el­e­gans), west­ern ground snakes (Sonora semi­an­nu­lata), and west­ern ze­bra-tailed lizard (Cal­lisaurus dra­conoides), west­ern whip­tail (Cne­mi­dopho­rus tigris), and Col­orado desert fringe-toed lizards (Uma no­tata). Sidewinders also con­sume mam­mals such as house mice (Mus mus­cu­lus), desert pocket mice (Chaetodi­pus peni­cil­la­tus), Botta’s pocket go­pher (Tho­momys bot­tae). Large sidewinders also con­sume birds such as lark spar­rows (Chon­destes gram­ma­cus), house spar­rows (Passer do­mes­ti­cus), and cac­tus wrens (Campy­lorhynchus brun­ne­icapil­lus). Lizards con­sist of over 50% of the sidewinders’ diet, and mam­mals con­sist of over 40% of the diet. Sidewinders in­gest a greater pro­por­tion of mam­mals when they are noc­tur­nal dur­ing late spring and sum­mer. Dur­ing early spring and fall, sidewinders con­sume more di­ur­nal lizards be­cause the tem­per­a­ture is cool enough for them to hunt dur­ing the day. (Freymiller, 2016; Funk, 1965; Mosauer, 1935; Woz­niak, et al., 1994)

  • Primary Diet
  • carnivore
    • eats terrestrial vertebrates
  • Animal Foods
  • birds
  • mammals
  • reptiles

Pre­da­tion

Cal­i­for­nia kingsnakes, Lam­pro­peltis getula cal­i­for­niae, coy­otes Canis la­trans, and red-tailed hawks Buteo ja­maicen­sis are com­mon preda­tors of sidewinders in the south­west United States. Sidewinders typ­i­cally react to these preda­tors by puff­ing them­selves up to ap­pear larger, and strike preda­tors with their ven­omous fangs.

Be­cause sidewinders re­side in dry, desert en­vi­ron­ments, hu­mans rarely in­ter­act with sidewinders, much less harm them. (Beaupre and Du­vall, 1998; Cochran, 2010; Cowles, 1938; Cowles, 1956; Fitch, et al., 1946)

Ecosys­tem Roles

Sidewinders can con­tain blood par­a­sites from gen­era Haemogre­ga­rina and He­pata­zoon. Both of these gen­era are from the phy­lum Api­com­plexa. A ne­ma­tode re­ported in sidewinders is Thub­naea cne­mi­dopho­rus, which can be found in the esoph­a­gus, stom­ach, and in­testines. (Babero and Em­mer­son, 1974; Woz­niak, et al., 1994)

Com­men­sal/Par­a­sitic Species
  • Api­com­plexan Haemogre­ga­rina
  • Api­com­plexan He­pata­zoon
  • Ne­ma­tode Thubunaea cne­mi­dopho­rus

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive im­pacts of sidewinders on hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Sidewinders uti­lize their ven­omous fangs for hunt­ing prey, and as a mech­a­nism of de­fense against preda­tors. More­over, sidewinder venom has in­creased lev­els of pro­tease ac­tiv­ity com­pared to other ven­omous snakes which al­lows these snakes to be ac­tive dur­ing day or night. Hu­mans rarely en­counter sidewinders, there­fore, lit­tle is known about how sidewinder venom af­fects the human body. Anec­do­tal blog post­ings de­pict necrotic tis­sue, painful swellings, black and blue ap­pendages, and vic­tims de­scribe in­tense burn­ing for days, fol­lowed by painful joints weeks after the ini­tial bite. An­tivenom treat­ments are still being stud­ied and tested in hu­mans. (Cowles, 1938; Cowles, 1956; Crump, 2010; Rosen and Lowe, 1994; Web­ber, et al., 2016)

  • Negative Impacts
  • injures humans

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List, sidewinders are a species of “Least Con­cern.” Fur­ther­more, no spe­cial sta­tus is given to sidewinders via the U.S. Fed­eral List, CITES, and the State of Michi­gan List. No con­ser­va­tion ef­forts are being made to pro­tect sidewinders at this time. These snakes re­side in many pro­tected areas such as Death Val­ley Na­tional Park, Se­quoia Na­tional Park, Desert Na­tional Wildlife Refuge, Mo­jave Na­tional Pre­serve, Joshua Tree Na­tional Park, Kofa Na­tional Wildlife Range, Organ Pipe Cac­tus Na­tional Mon­u­ment and the Gila River In­dian Reser­va­tion. (Frost, et al., 2007)

Con­trib­u­tors

Cole Faulkner (au­thor), Rad­ford Uni­ver­sity, Alex At­wood (ed­i­tor), Rad­ford Uni­ver­sity, Layne DiBuono (ed­i­tor), Rad­ford Uni­ver­sity, Lind­sey Lee (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Joshua Turner (ed­i­tor), Rad­ford Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

acoustic

uses sound to communicate

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

desert or dunes

in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.

diurnal
  1. active during the day, 2. lasting for one day.
ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

female parental care

parental care is carried out by females

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

hibernation

the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

infrared/heat

(as keyword in perception channel section) This animal has a special ability to detect heat from other organisms in its environment.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

migratory

makes seasonal movements between breeding and wintering grounds

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

polygynous

having more than one female as a mate at one time

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

sexual ornamentation

one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.

solitary

lives alone

tactile

uses touch to communicate

terrestrial

Living on the ground.

venomous

an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

An­drews, R., T. Math­ies. 2000. Nat­ural his­tory of rep­til­ian de­vel­op­ment: Con­straints on the evo­lu­tion of vi­vipar­ity. Bio­science, 50/3: 227-238.

Babero, B., F. Em­mer­son. 1974. Thubunaea cne­mi­dopho­rus in Nevada rat­tlesnakes. The Jour­nal of Par­a­sitol­ogy, 60/4: 595.

Beaupre, S., D. Du­vall, J. O'Leile. 1998. On­to­ge­netic vari­a­tion in growth and sex­ual size di­mor­phism in a cen­tral Ari­zona pop­u­la­tion of the west­ern di­a­mond­back rat­tlesnake (Cro­talus atrox). Copeia, 1998/1: 40-47.

Beaupre, S., D. Du­vall. 1998. In­te­gra­tive bi­ol­ogy of rat­tlesnakes. Bio­Science, 48-7: 531-538.

Beck, D. 1995. Ecol­ogy and en­er­get­ics of three sym­patric rat­tlesnake species in the Sono­ran Desert. Jour­nal of Her­petol­ogy, 29/2: 211-223.

Blom­sten, P., G. Schuett, M. Hog­gren, R. Reis­erer. 2016. Fif­teen con­sec­u­tive years of suc­cess­ful re­pro­duc­tion in a cap­tive fe­male sidewinder (Cro­talus cerastes). Her­peto­log­i­cal Re­view, 47/1: 69-72.

Bogert, C. 1947. Rec­ti­lin­ear lo­co­mo­tion in snakes. Copeia, 1947/4: 253-254.

Bul­lock, T., W. Fox. 1957. The anatomy of the in­fra-red sense organ in the fa­cial pit of pit vipers. Jour­nal of Cell Sci­ence, 3/98: 219-234.

Cochran, P. 2010. Rat­tlesnake eggs and the pass­ing of a torch in Winona County, Min­nesota. Archives of nat­ural his­tory, 37/1: 19-27.

Cohen, A., B. Myres. 1970. A func­tion of the horns (supraoc­u­lar scales) in the sidewinder rat­tlesnake, Cro­talus cerastes, with com­ments on other horned snakes. Copeia, 1970/3: 574-575.

Cowles, R. 1956. Sidewind­ing lo­co­mo­tion in snakes. Copeia, 1956/4: 211-214.

Cowles, R. 1938. Un­usual de­fense pos­tures as­sumed by rat­tlesnakes. Copeia, 1938/1: 13-16.

Crump, D. 2010. "Sono­ran sidewinder bite (Cro­talus cerastes)" (On-line). Ven­om­list. Ac­cessed April 16, 2018 at http://​venomlist.​com/​forums/​index.​php?/​topic/​27466-sonoran-sidewinder-bite-crotalus-cerastes/​.

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Ernst, C. 1964. A study of sex­ual di­mor­phism in Amer­i­can Agk­istrodon fang lengths. Her­peto­log­ica, 20/3: 214.

Fitch, H., F. Swen­son, D. Tillot­son. 1946. Be­hav­ior and food habits of the red-tailed hawk. The Con­dor, 48/5: 205-237.

Freymiller, G. 2016. Ac­tiv­ity cy­cles and for­ag­ing be­hav­iors of free-rang­ing sidewinder rat­tlesnakes (Cro­talus cerastes): The on­togeny of hunt­ing in a pre­co­cial ver­te­brate. Zo­ol­ogy, 119/3: 196-206.

Frost, D., G. Ham­mer­son, H. Gads­den. 2007. "Cro­talus cerastes" (On-line). The IUCN Red List of Threat­ened Species 2007: e.T64315A12764960.. Ac­cessed Feb­ru­ary 01, 2018 at . http://​dx.​doi.​org/​10.​2305/​IUCN.​UK.​2007.​RLTS.​T64315A12764960.​en.

Funk, R. 1965. Food of Cro­talus cerastes lat­erorepens in Yuma County, Ari­zona. Her­peto­log­ica, 21/1: 15-17.

Gilling­ham, J., C. Car­pen­ter, J. Mur­phy. 1983. Courtship, male com­bat and dom­i­nance in the west­ern di­a­mond­back rat­tlesnake, Cro­talus atrox. Jour­nal of Her­petol­ogy, 17/3: 265-270.

Jayne, B. 1988. Mus­cu­lar mech­a­nisms of snake lo­co­mo­tion: An elec­tromyo­graphic study of the sidewind­ing and con­certina modes of Cro­talus cerastes, Nero­dia fas­ci­ata and Elaphe ob­so­leta. Jour­nal of Ex­per­i­men­tal Bi­ol­ogy, 1998/4: 1-33.

Keen­lyne, K. 1978. Re­pro­duc­tive cy­cles in two species of rat­tlesnakes. The Amer­i­can Mid­land Nat­u­ral­ist, 100/2: 368-375.

Lewis, T. 1949. Dark col­oration in the rep­tiles of the Tu­larosa Mal­pais, New Mex­ico. Copeia, 1949-3: 181-184.

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