Cyanocoraxtufted jays

Di­ver­sity

Cyanoco­rax is a genus of New World jays lo­cated pri­mar­ily in South Amer­ica. Cyanoco­rax con­tains sev­en­teen species that are very di­verse in their mor­phol­ogy and col­oriza­tion. They are known to act like typ­i­cal jays with sim­i­lar vo­cal­iza­tions. Many live in co­op­er­a­tive groups. There is even hy­bridiza­tion be­tween some species. They live in drier neotrop­i­cal forests rang­ing from the south of North Amer­ica to Ar­gentina. Due to their di­ver­sity, Cyanoco­rax has gone through many changes in the for­mat of their phy­lo­ge­netic tree. Today, they have two clades with Psilorhi­nus morio and Calocitta part of one of the clades. With such a large di­ver­sity, there is more in­for­ma­tion about Cyanoco­rax that still hasn't been dis­cov­ered. (Apoli­nario and Fabio Sil­veira, 2019; Bar­ros, et al., 2014; Bonac­corso, 2007; Bonac­corso, et al., 2010; Hope, 1989)

Ge­o­graphic Range

Cyanoco­rax can be found from the south­ern United States to the west side of Ecuador and east of Brazil all the way south to Ar­gentina. (Bonac­corso, 2007; Bonac­corso, et al., 2010)

Habi­tat

Cyanoco­rax live in drier neotrop­i­cal forests. They build nests in the trees or thick brush. The nests are typ­i­cally cir­cu­lar and are built with twigs, roots, branches, fiber. Some­times, they will add lit­ter to the nest. Cyanoco­rax for­age in the trees and the ground. Not much is known on how they for­age but some species are known to fol­low ants. They eat the in­sects the ants chase out and the ants them­selves. (Bar­ros, et al., 2014; Bonac­corso, 2007; Bonac­corso, et al., 2010; Gor­don and Or­nelas, 2000; Gus­tavo Ro­drigues França and Da Silva Braz Biotemas, 2009; Hope, 1989; Lasky and Keitt, 2010; Ue­jima, et al., 2012)

Sys­tem­atic and Tax­o­nomic His­tory

Due to the di­verse mor­phol­ogy, Cyanoco­rax has un­der­gone many changes. At first it was split into four groups Xan­thoura, Cis­silopha, Uroleuca, and Cyanoco­rax. Calocitta and Psilorhi­nus were once con­sid­ered to be sub­gen­era to Cyanoco­rax but are now con­sid­ered to be their own taxa and sis­ter to Cyanoco­rax. Re­cently, re­searchers have been using mol­e­c­u­lar data to try to piece to­gether a tree using five dif­fer­ent genes. These genes are used as synapo­mor­phies for the tree since mor­pho­log­i­cally, Cyanoco­rax are too di­verse. Cyanoco­rax is pa­ra­phyletic but ends up being mono­phyletic if Calocitta and Psilorhi­nus are in­cluded. (Bonac­corso, 2007; Bonac­corso, et al., 2010; Reich, et al., 2010)

  • Synonyms
    • Xanthoura
    • Cissilopha
    • Uroleuca
    • Calocitta
    • Psilorhinus
  • Synapomorphies
    • ND2
    • cytb
    • AK5
    • ßfib7
    • TGFß2.5

Phys­i­cal De­scrip­tion

Cyanoco­rax species have a large va­ri­ety in sizes, mor­phol­ogy, and col­oration. Some species are small jays with bright fa­cial mark­ings and long, spiked frontal crests ex­cept Cyanoco­rax chrysops which have a long bristly frontal crest. These small jays are dark blue ex­cept for Cyanoco­rax yncas which are green. The rest are large jays with planer fa­cial mark­ings and short, lax frontal crests ex­cept for Cyanoco­rax cristatel­lus which have a curly frontal crest. These big jays are dark blue, pur­ple, or brown. (Hope, 1989; Ridgely and Tudor, 1989)

  • Sexual Dimorphism
  • sexes alike

Re­pro­duc­tion

Cyanoco­rax are co­op­er­a­tive breed­ers where there is one pri­mary fe­male that mates with mul­ti­ple males. Ju­ve­niles from pre­vi­ous broods will stay with the group to help with fu­ture broods. Fe­males will typ­i­cally stay with the group for their en­tire lives as helpers while males leave to join a dif­fer­ent group after one to two years. The old­est fe­male is the breeder and will sup­press the other fe­males from breed­ing. Es­tab­lish­ing a breed­ing pair is unique in each species but there are some sim­i­lar­i­ties. The most com­mon ways for a pair to bond is through al­lo­preen­ing and allofeed­ing. The mat­ing dances are done on a perch and are a mix of head and body bob­bing, feather fluff­ing or erect­ing, tail move­ments, and vo­cal­iza­tions. De­fenses are done as a group by mob­bing a preda­tor until it re­treats. (Apoli­nario and Fabio Sil­veira, 2019; Bosque and Molina, 2002; Reich, et al., 2010; Ue­jima, et al., 2012; Williams, 2004)

Re­pro­duc­tion in Cyanoco­rax has only been stud­ied in a few species but there are sim­i­lar­i­ties. These jays do com­mu­nal breed­ing where there is one breed­ing pair. The rest of the jays are fam­ily mem­bers that stay with the breed­ing pair to pro­tect and raise the young. In­cu­ba­tion lasts about 20 days while fledg­ing oc­curs around one month. It can take about two years after fledg­ing for a ju­ve­nile to ma­ture into an adult. The sea­son of breed­ing is in the spring and some­times sum­mer. The size of the clutch is around two to five eggs. Fer­til­iza­tion oc­curs in­ter­nally in the pri­mary fe­male. The pri­mary fe­male is the only one that breeds with mul­ti­ple males. Some­times sec­ondary fe­males are able to breed but it rarely oc­curs. Mul­ti­ple birds have ac­cess to the nest with no ag­gres­sion oc­cur­ring in the group. There has been some hy­bridiza­tion recorded be­tween sis­ter species but it rarely oc­curs. (Apoli­nario and Fabio Sil­veira, 2019; Bosque and Molina, 2002; Reich, et al., 2010; Ue­jima, et al., 2012; Williams, 2004)

Cyanoco­rax par­ents put a lot of in­vest­ment into their young. They are co­op­er­a­tive breed­ers where pre­vi­ous off­spring help their par­ents raise fu­ture off­spring. All mem­bers of the group pro­vide food and pro­tec­tion to the brood. The pri­mary fe­male will in­cu­bate the eggs and will some­times switch with other fe­males. The young are com­pletely de­pen­dent on the group until they fledge. After fledg­ing, they learn how to hunt and pro­tect the nest from the older group mem­bers. They still have to be fed and pro­tected by the group for one to two months. After two years, the males leave to find a dif­fer­ent group while the fe­males stay as helpers. (Apoli­nario and Fabio Sil­veira, 2019; Bosque and Molina, 2002; Reich, et al., 2010; Ue­jima, et al., 2012; Williams, 2004)

  • Parental Investment
  • altricial
  • pre-fertilization
    • provisioning
    • protecting
  • pre-hatching/birth
    • provisioning
    • protecting
  • pre-weaning/fledging
    • provisioning
    • protecting
  • pre-independence
    • provisioning
    • protecting
  • post-independence association with parents
  • maternal position in the dominance hierarchy affects status of young

Lifes­pan/Longevity

Cyanoco­rax species have a va­ri­ety of lifes­pans based on size. Small species like Cyanoco­rax yncas can live up to 12 years while large species like Cyanoco­rax caeruleus can live up to 40 years. (Planck-Gesellschaft, 2002; Reich, et al., 2010)

Be­hav­ior

Cyanoco­rax species are so­cial birds that live in co­op­er­a­tive groups. They for­age and travel to­gether. Some species form mixed species flocks. There is a so­cial hi­er­ar­chy based on who gets to breed in the group. There is usu­ally one mat­ing pair, where the mat­ing fe­male has dom­i­nance over other fe­males. They build nests in trees and for­age in the trees and ground. Their nests are built with sticks and twigs on the out­side with roots and fiber on the in­side. The sticks pro­vide strength while the roots make the nest more com­fort­able. Some­times they will use other ma­te­ri­als based on what is avail­able. Some species fol­low groups of ants as a food source. They will eat the in­sects that the ants chase out of their homes or the ants them­selves. Only the young are known to face pre­da­tion be­cause they can­not fly and have no phys­i­cal de­fenses that are fully de­vel­oped. Adults pro­tect young by mob­bing preda­tors until they re­treat. Cyanoco­rax species are noisy and com­mu­ni­cate using unique vo­cal­iza­tions. Each species have their own way to find a mate. They will bob their head and body, move their feath­ers, and make spe­cific vo­cal­iza­tions. Some­times the male will bring the fe­male food and they will al­lo­preen. They are most ac­tive in the day. (Apoli­nario and Fabio Sil­veira, 2019; Bar­ros, et al., 2014; Bonac­corso, 2007; Bosque and Molina, 2002; Gus­tavo Ro­drigues França and Da Silva Braz Biotemas, 2009; Hope, 1989; Reich, et al., 2010; Ridgely and Tudor, 1989; Ue­jima, et al., 2012; Williams, 2004)

Com­mu­ni­ca­tion and Per­cep­tion

Cyanoco­rax species com­mu­ni­cate and per­ceive the world pri­mar­ily through vi­sion and sounds. They can see the color spec­trum but they can also see UV light. Vi­sion is used for for­ag­ing and com­mu­ni­ca­tion. Vi­su­als are mostly used for courtships where both sexes bob their head and body, move their feath­ers, and turn their head. Each type of dance is unique to each species. For vo­cal­iza­tions, it is their main form of com­mu­ni­ca­tion. Adults use vo­cal­iza­tions as alarms, mim­icry, or to find mates. Young Cyanoco­rax use it to beg for food or seek pro­tec­tion. Each species has a unique set of calls that can help dis­tin­guish them from other species. Cyanoco­rax species are known to be loud dur­ing the day due to how so­cial they are. They can range from ring­ing to chit­ter­ing to click­ing. (Bar­ros, et al., 2014; Berger, 2012; Bosque and Molina, 2002; Hope, 1989; Reich, et al., 2010; Ridgely and Tudor, 1989; Ue­jima, et al., 2012)

Food Habits

Cyanoco­rax species have a di­verse diet. They are om­ni­vores that feast on arthro­pods, berries, other small fruits, nuts, acorns, and seeds. Some species will even eat the eggs of other bird species and lizards. Some are also known to fol­low army ants so that they can eat the in­sects the army ants flush out of their hid­ing places or the ants them­selves. Some species store and cache their food. (Bar­ros, et al., 2014; Gus­tavo Ro­drigues França and Da Silva Braz Biotemas, 2009; Reich, et al., 2010; Ue­jima, et al., 2012)

Pre­da­tion

Cyanoco­rax species have many preda­tors. They are mainly hunted when they are ju­ve­niles and are un­able to pro­tect them­selves. This is why adults stay with young until they are ma­ture. Cyanoco­rax species live in so­cial groups and mob preda­tors. Nest­ing adults send out a warn­ing call if a preda­tor is near so that for­ag­ing adults can re­turn to mob the preda­tor. Com­mon preda­tors are snakes(Lep­i­dosauria), hawks(Ac­cip­itri­dae), owls(St­rigi­dae), tree squir­rels(Sci­uri­dae), igua­nas(Iguanidae), and crows(Corvi­dae). (Bosque and Molina, 2002; Reich, et al., 2010)

Ecosys­tem Roles

Cyanoco­rax species are om­ni­vores that help con­trol the arthro­pod pop­u­la­tions. They are also a source of prey for snakes, hawks, owls, crows, igua­nas, and tree squir­rels. Cyanoco­rax species are com­men­sal­is­tic with army ants. They fol­low army ants and eat the prey they flush out and some­times the ants them­selves. Cyanoco­rax species are also a host to ne­ma­todes such as Vik­toro­cara species. Since they eat seeds, this helps with the dis­per­sal of seeds of smaller fruits and nuts. (Pinto, et al., 1997; Reich, et al., 2010)

  • Ecosystem Impact
  • disperses seeds
Com­men­sal/Par­a­sitic Species
  • Vik­toro­cara

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Due to how col­or­ful Cyanoco­rax species are, they helped in­crease eco­tourism in South Amer­ica. Sci­en­tists re­cently have started to get mol­e­c­u­lar data on them to trace back their his­tory and fig­ure out their tree due to how often it is changed. Their feath­ers are also a valu­able ma­te­r­ial used for fash­ion and dec­o­ra­tions. Since they eat arthro­pods, Cyanoco­rax species help con­trol pest pop­u­la­tions in their range. (Reich, et al., 2010)

  • Positive Impacts
  • body parts are source of valuable material
  • ecotourism
  • research and education
  • controls pest population

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Cyanoco­rax species are a main rea­son to stop de­for­esta­tion but at an eco­nomic cost to the com­mu­nity who have to use more eco­nomic meth­ods that tend to be more ex­pen­sive. (Reich, et al., 2010)

Con­ser­va­tion Sta­tus

Most Cyanoco­rax species are con­sid­ered Least Con­cern by BirdLife In­ter­na­tional with some being Near Threat­ened on the 2009 IUCN Red List Cat­e­gory and some being Threat­ened or En­dan­gered under Mex­i­can Law. The biggest threats to the Cyanoco­rax species are de­for­esta­tion, un­sus­tain­able log­ging, and clear­ing for agri­cul­tural, drug, and graz­ing pur­poses. Cur­rently, some Cyanoco­rax species are being pro­tected by dif­fer­ent com­mu­ni­ties as a way to pro­mote eco­tourism. Cyanoco­rax dick­eyi is a good ex­am­ple of a com­mu­nity com­ing to­gether to form a con­ser­va­tion plan in Con­cor­dia to pro­tect it. Some species like Cyanoco­rax vi­o­laceus have ben­e­fited from de­for­esta­tion be­cause they pre­fer to live in for­est edge habi­tats. (Gor­don and Or­nelas, 2000; Reich, et al., 2010)

  • IUCN Red List [Link]
    Not Evaluated

Other Com­ments

Cyanoco­rax species have been a good taxon to use for mol­e­c­u­lar re­search. This is due to its di­verse mor­phol­ogy and lit­tle re­search on be­hav­ior. Ge­nomic in­for­ma­tion has helped in­crease the un­der­stand­ing of the re­la­tion­ships within Cyanoco­rax species and its sis­ter taxa. Re­searchers are now start­ing to focus on the breed­ing, so­cial, and for­ag­ing be­hav­iors of each Cyanoco­rax species. (Reich, et al., 2010)

Con­trib­u­tors

My­chaela Hodous (au­thor), Col­orado State Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

acoustic

uses sound to communicate

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

arboreal

Referring to an animal that lives in trees; tree-climbing.

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

choruses

to jointly display, usually with sounds, at the same time as two or more other individuals of the same or different species

cooperative breeder

helpers provide assistance in raising young that are not their own

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

ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates

duets

to jointly display, usually with sounds in a highly coordinated fashion, at the same time as one other individual of the same species, often a mate

ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

fertilization

union of egg and spermatozoan

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

frugivore

an animal that mainly eats fruit

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

insectivore

An animal that eats mainly insects or spiders.

internal fertilization

fertilization takes place within the female's body

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).

mimicry

imitates a communication signal or appearance of another kind of organism

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.

omnivore

an animal that mainly eats all kinds of things, including plants and animals

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

polyandrous

Referring to a mating system in which a female mates with several males during one breeding season (compare polygynous).

rainforest

rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.

scrub forest

scrub forests develop in areas that experience dry seasons.

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

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

social

associates with others of its species; forms social groups.

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

tactile

uses touch to communicate

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

visual

uses sight to communicate

Ref­er­ences

Apoli­nario, C., L. Fabio Sil­veira. 2019. Hy­bridism be­tween Cyanoco­rax chrysops and Cyanoco­rax cyano­pogon (Aves: Corvi­dae) in Brazil. Zo­olo­gia (Cu­ritiba), 36: 1-7. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi.​org/​10.​3897/​zoologia.​36.​e32138.

Bar­ros, R., C. Costa, M. Pas­cotto. 2014. Diet and feed­ing be­hav­ior of the White-naped Jay, Cyanoco­rax cyano­pogon (Wied, 1821) (Aves, Passer­i­formes, Corvi­dae) in a dis­turbed en­vi­ron­ment in cen­tral Brazil. Brazil­ian Jour­nal of Bi­ol­ogy, 74(4): 899-905. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi.​org/​10.​1590/​1519-6984.​09313.

Berger, C. 2012. "True Col­ors: How Birds See the World" (On-line). Ac­cessed Feb­ru­ary 22, 2020 at https://​www.​nwf.​org/​Magazines/​National-Wildlife/​2012/​AugSept/​Animals/​Bird-Vision.

Bonac­corso, E. 2007. Evo­lu­tion of the New World jays (Corvi­dae): Phy­logeny, bio­geog­ra­phy, and ecol­ogy. Ann Arbor: Pro­Quest Dis­ser­ta­tions Pub­lish­ing. Ac­cessed Feb­ru­ary 01, 2020 at https://​search-proquest-com.​ezproxy2.​library.​colostate.​edu/​docview/​304856261/​abstract/​961208F8645549FCPQ/​1?​accountid=10223.

Bonac­corso, E., A. Pe­ter­son, A. Navarro-Siguenza, R. Fleis­cher. 2010. Mol­e­c­u­lar sys­tem­at­ics and evo­lu­tion of the Cyanoco­rax jays. Mol­e­c­u­lar Phy­lo­ge­net­ics and Evo­lu­tion, 54: 897-909. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi.​org/​10.​1016/​j.​ympev.​2009.​11.​014.

Bosque, C., C. Molina. 2002. Com­mu­nal breed­ing and nest de­fense be­hav­ior of the Cayenne Jay (Cyanoco­rax cayanus). Jour­nal of Field Or­nithol­ogy, 73(4): 360-362. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi.​org/​10.​1648/​0273-8570-73.​4.​360.

Gor­don, C., J. Or­nelas. 2000. Com­par­ing en­demism and habi­tat re­stric­tion in Mesoamer­i­can trop­i­cal de­cid­u­ous for­est birds: im­pli­ca­tions for bio­di­ver­sity con­ser­va­tion plan­ning. Bird Con­ser­va­tion In­ter­na­tional, 10(4): 289-303. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi-org.​ezproxy2.​library.​colostate.​edu/​10.​1017/​S0959270900000241.

Gus­tavo Ro­drigues França, F., V. Da Silva Braz Biotemas. 2009. Pre­da­tion on the lizard Poly­chrus acu­tirostris (Squa­mata, Poly­chroti­dae) by the curl-crested jay Cyanoco­rax cristatel­lus (Aves, Corvi­dae) in the Cer­rado of Cen­tral Brazil. Biotemas, 22(3): 243-245. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi.​org/​10.​5007/​2175-7925.​2009v22n3p243.

Hope, S. 1989. Phy­logeny of the avian fam­ily Corvi­dae. Ann Arbor: Pro­Quest Dis­ser­ta­tions Pub­lish­ing. Ac­cessed Feb­ru­ary 01, 2020 at https://​search-proquest-com.​ezproxy2.​library.​colostate.​edu/​docview/​303702253/​abstract/​3771EE14A09C4F94PQ/​1?​accountid=10223.

Lasky, J., T. Keitt. 2010. Abun­dance of Pana­man­ian dry-for­est birds along gra­di­ents of for­est cover at mul­ti­ple scales. Jour­nal of Trop­i­cal Ecol­ogy, 26(1): 67-78. Ac­cessed Feb­ru­ary 01, 2020 at https://​doi-org.​ezproxy2.​library.​colostate.​edu/​10.​1017/​S0266467409990368.

Pinto, R., V. Júlio, D. Noronha. 1997. Ne­ma­tode Par­a­sites of Brazil­ian Corvid Birds (Passer­i­formes): A Gen­eral Sur­vey with a De­scrip­tion of Vik­toro­cara brasilien­sis n. sp. (Acuari­idae, Schis­torophi­nae). Memórias do In­sti­tuto Os­waldo Cruz, 92(2): 209-214. Ac­cessed March 01, 2020 at 10.1590.

Planck-Gesellschaft, M. 2002. "Longevity Records" (On-line). Ac­cessed Feb­ru­ary 22, 2020 at https://​www.​demogr.​mpg.​de/​longevityrecords/​0303.​htm.

Reich, S., A. Kumar, M. Baran, A. Bran­dreth Pot­ter, S. Brady, D. Molfetto, C. Gha­lam­bor, L. Power, A. Du­vall, K. Adams, M. Kit­tel­son. 2010. "Neotrop­i­cal Birds On­line" (On-line). Ac­cessed Feb­ru­ary 22, 2020 at https://​neotropical.​birds.​cornell.​edu/​Species-Account/​nb/​home.

Ridgely, R., G. Tudor. 1989. The Birds of South Amer­ica: Vol­ume 1: The Os­cine Passer­ines. Austin, Texas: Uni­ver­sity of Texas Press. Ac­cessed Feb­ru­ary 15, 2020 at https://​books.​google.​com/​books?​hl=en&​lr=&​id=tRBb15pk4w0C&​oi=fnd&​pg=PR9&​ots=TwTtPLJrKc&​sig=o4kd6AN2CeZMrtVZ07N-0YVy1TE#​v=onepage&​q&​f=false.

Ue­jima, A., A. Boesing, L. Dos Anjos. 2012. BREED­ING AND FOR­AG­ING VARI­A­TION OF THE PLUSH-CRESTED JAY (CYANOCO­RAX CHRYSOPS) IN THE BRAZIL­IAN AT­LANTIC FOR­EST. The Wil­son Jour­nal of Or­nithol­ogy, 124(1): 87-95. Ac­cessed Feb­ru­ary 01, 2020 at https://​www-jstor-org.​ezproxy2.​library.​colostate.​edu/​stable/​41932804?​seq=1#​metadata_​info_​tab_​contents.

Williams, D. 2004. Fe­male con­trol of re­pro­duc­tive skew in co­op­er­a­tively breed­ing brown jays (Cyanoco­rax morio). Be­hav­ioral Ecol­ogy and So­cio­bi­ol­ogy, 55(4): 370-380. Ac­cessed Feb­ru­ary 16, 2020 at https://​doi.​org/​10.​1007/​s00265-003-0728-7.