|Mexican jay from Madera Canyon, Arizona,
Aphelocoma wollweberi arizonae.
note bill color not entirely black, this is a character of the Arizona race
5, see text
The Mexican jay (Aphelocoma wollweberi)  formerly known as the gray-breasted jay, is a New World jay native to the Sierra Madre Oriental, Sierra Madre Occidental, and Central Plateau of Mexico. It reaches north to eastern Arizona, western New Mexico and western Texas in the United States. Its preferred habitat is montane pine-oak forest.
Note, in May 2011, the American Ornithologists' Union voted to split the Mexican jay into two species, one retaining the common name Mexican jay and one called the Transvolcanic jay (see below).
The Mexican jay is a medium-large (~120 g) passerine similar in size to most other jays, with a blue head, blue-gray mantle, blue wings and tail, and pale gray breast and underparts. The sexes are morphologically similar, and juveniles differ only in having less blue coloration and, in some populations, a pink/pale (instead of black) bill that progressively becomes more black with age (Brown and Horvath 1989). Some field guides misreport this color as yellow because the pale bill becomes yellow in museum study skins. The iris is brown and legs are black. It is most readily distinguished from the similar western scrub-jay by the plain (unstreaked) throat and breast, and the mantle contrasting less with the head and wings. Its range somewhat overlaps with the western scrub-jays, but, where they co-occur, the two species seem to show ecological and morphological character displacement (Curry et al. 2002).
In the winter, the Mexican jay's diet consists mainly of acorns and pine nuts, which are stored in the autumn. However, they are omnivorous in all seasons and their diet includes a wide variety of plant and animal matter, including invertebrates, small amphibians and reptiles, and birds' eggs and nestlings (McCormack and Brown 2008).
It has a cooperative breeding system similar to that of the related Florida scrub-jay, with several birds helping at a nest; these "helpers" are usually immature offspring of the dominant pair from the previous 1–2 years, but also include apparently unrelated flock members.
A recent decision by the American Ornithologists' Union Check-list Committee elevated some populations of the Mexican jay to a separate species, called the Transvolcanic jay (A. ultramarina), based on diagnosable phenotypic differences in plumage and morphology, millions of years of genetic divergence, and no evidence for interbreeding with Mexican jays. The Transvolcanic jay inhabits montane forest in the Transvolcanic Belt of central Mexico. Populations to the north retained the common name Mexican jay, but the Latin name changed to A. wollweberi. This was because the type specimen was a Transvolcanic jay, meaning that this species had precedent for the original Latin name A. ultramarina.
Thus, as of this decision, there are now five described subspecies of Mexican jays that are divided into three divergent groups (see below). Marked differences in size, color, vocalizations, and genetics have led some authors to consider at least two of these groups as separate species (East and West; Navarro-Sigüenza and Peterson 2004). The three groups inhabit three distinct mountainous regions in northern and central Mexico. Genetic breaks in mitochondrial and microsatellite DNA occur abruptly between the groups, indicating some barriers to genetic exchange (McCormack et al. 2008). Size variation among the groups does not always follow Bergman's Rule, with more southerly populations in the Sierra Madre Oriental being larger than populations to the north. Mexican jays do not seem to follow Gloger's rule either as populations in arid habitat in southwestern Texas are very blue. On the other hand, Mexican jays in Arizona - also arid habitat - have a washed-out appearance, in accordance with Gloger's rule.
Sierra Madre Occidental in northern [Jalisco] north to central Arizona and southwestern New Mexico. Southern and eastern limits in Jalisco deserve further study. Juveniles have a pink/pale base to the otherwise black bill for up to two years. Eggs are pale green-blue and unspeckled, unlike Eastern group where speckled eggs are common.
- Aphelocoma wollweberi gracilis
- E Nayarit and N Jalisco
- Smallest of the Western subspecies with a distinct, high-pitched vocalization* Aphelocoma wollweberi wollweberi
- Durango and Zacatecas
- Intermediate in size
- Aphelocoma wollweberi arizonae
Sierra Madre Oriental in Nuevo León and W Tamaulipas north to Texas (Chisos Mountains). Juveniles have an all-black exterior to the bill after fledging, but roof of inner upper mandible can remain partially white for up to two years. Reports of less social behavior compared to other groups are over-stated and credible accounts of cooperative breeding (Ligon and Husar 1974) and large flock sizes (Bhagabati and Horvath 2006) exist. Plain, speckled, and even white eggs have been observed in a single study area (McCormack and Berg 2010).
- Aphelocoma wollweberi couchii
- Smaller than preceding. Population of latter species distinguishable by more contrasting markings and ecological preferences (lowland birds). Egg color may range from plain blue to nile blue with pale brownish speckling, most heavy on blunt half. Gives rattle call similar to Cyanocitta and western scrub-jays.
Central Plateau group
Central Plateau in Queretaro, Guanajuato, San Luis Potosi, and eastern Jalisco. Similar to Eastern group but larger in most features. Distinguishable in morphology and plumage in ~80% of specimens. There is an area of apparent hybridization in San Luis Potosi that deserves study.
- Aphelocoma wollweberi potosina
- BirdLife International (2013). "Aphelocoma wollweberi". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 26 November 2013.
- Etymology: Aphelocoma, from Latinized Ancient Greek apheles- (from ἀφελής-) "simple" + Latin coma (from Greek kome κόμη) "hair", in reference to the lack of striped or banded feathers in this genus, compared to other jays. wollweberi, Name: "collector Mr. Wollweber".
- Bhagabati, N. K. & Horvath, E. G. (2006): Mexican jay social group size varies with habitat in northeastern Mexico. Journal of Field Ornithology 77: 104-110.
- Brown, J. L. & Horvath, E. G. (1989): Geographic Variation of Group Size, Ontogeny, Rattle Calls, and Body Size in Aphelocoma ultramarina. Auk 106: 124-128.
- Curry, Robert L.; Peterson, A. Townsend & Langen, T.A. (2002): Western Scrub-Jay (Aphelocoma californica). In: Poole, A. & Gill, F. (eds.): The Birds of North America 712. Academy of Natural Sciences, Philadelphia, PA & American Ornithologists' Union, Washington, D.C. Online version, retrieved 2007-FEB-25. doi:10.2173/bna.712 (requires subscription)
- Ligon, J. D. & Husar, S. L. 1974 Notes on the behavioral ecology of Couch's Mexican jay. Auk 91: 841-843.
- Madge, Steve & Burn, Hilary (1994): Crows and jays: a guide to the crows, jays and magpies of the world. A&C Black, London. ISBN 0-7136-3999-7
- McCormack, JE & Brown, JL. (2008) Mexican jay (Aphelocoma ultramarina). In The Birds of North America Online (A Poole, ed.). Cornell Laboratory of Ornithology: Ithaca, NY.
- McCormack, JE & Berg, EC (2010): Small-scale divergence in egg color along an elevation gradient in the Mexican Jay: a condition-dependent response? Auk 127: 35-43.
- McCormack, John E., Peterson, A.T, Bonaccorso, Elisa, & Smith, Thomas B. (2008): Speciation in the highlands of Mexico: Genetic and phenotypic divergence in the Mexican jay (Aphelocoma ultramarina). Molecular Ecology 17: 2505-2521.
- Navarro-Sigüenza, A. & Peterson, A. (2004) An alternative species taxonomy of the birds of Mexico. Biota Neotropica 4.
- Pitelka, Frank A. (1951): Speciation and ecological distribution in American jays of the genus Aphelocoma. University of California Publications in Zoology 50: 195-464.
- Rice, Nathan H.; Martínez-Meyer, Enrique & Peterson, A. Townsend (2003): Ecological niche differentiation in the Aphelocoma jays: a phylogenetic perspective. Biol. J. Linn. Soc. 80(3): 369–383. doi:10.1046/j.1095-8312.2003.00242.x PDF fulltext