Species of Mabrya are herbaceousperennials with fibrous roots. They have brittle stems, usually pendant and forming mats, although more upright in M. erecta. The stems branch and become woody at the base with age. Unlike related genera, such as Maurandya and Lophospermum, the leaf stalks (petioles) are straight and do not twine. The leaves are rounded or kidney shaped, generally with broad, somewhat rounded teeth.[2]
The flowers are borne individually on stalks (peduncles) that are usually horizontal or ascending. The sepals are joined at the base; where their margins become free, they curve back on themselves. Together the sepals form an urn-shaped calyx. The flowers consist of five petals joined at the base to form a tube. The free lobes of the petals are differentiated into two upper ones that curve backwards and three lower ones that either point forward or also curve backward. The flower tends to be whitish at the base and is then cream, yellow, pink, red or reddish violet. There are four fertile stamens, of two different lengths, and one rudimentary infertile stamen. The stamens and style are either held inside the flower or protrude. The stigma is forked. After fertilization, the two-chambered capsule contains tan or dark brown seeds.[2]
Taxonomy
The genus Mabrya was created by Wayne J. Elisens in 1985 to separate out a number of species previously placed in the genus Maurandya. The type species is Mabrya acerifolia. The generic name honours Tom J. Mabry for his contributions to phytochemistry and chemotaxonomy, which Elisens says "have substantially increased our understanding of the North American flora."[3]
Mabrya is placed in the tribe Antirrhineae. The drooping or upright habit of the brittle stems distinguishes Mabrya (together with Holmgrenanthe) from the closely related genera Lophospermum, Maurandya and Rhodochiton, which have longer, flexible stems and climb by means of twining leaf stalks (petioles). The ovary of Mabrya is bilocular (i.e. has two compartments) unlike the unilocular ovary of Holmgrenanthe.[2]
Phylogeny
A number of molecular phylogenetic studies have shown that subtribe Maurandyinae, defined by Elisen to consist of the five North American genera Holmgrenanthe, Lophospermum, Mabrya, Maurandya and Rhodochiton, forms a monophyletic group, which is related to the Old World genera Cymbalaria and Asarina.[4][5][6] Gehebrehiwet et al. suggested that the Maurandyinae could be expanded to include Cymbalaria and Asarina.[4] Vargas et al. presented the following cladogram in 2013:[6]
Vargas et al. concluded that the Antirrhineae evolved in the Old World and subsequently colonized North America more than once, probably in the Miocene epoch (23 to 5 million years ago). One such colonization led to the evolution of the Maurandyinae (in Elisen's sense).[6]
Elisens treated Mabrya flaviflora as a subspecies of Mabrya geniculata; it was later raised to a full species by David A. Sutton.[8]
Distribution and habitat
All the species are found in very dry areas, typically in shaded cliffs or canyons. Mabrya acerifolia is native to the Sonoran Desert in a small area about 80 km (50 miles) across in south central Arizona. All the other species are only found in Mexico, in the Sonoran Desert (M. geniculata and M. flaviflora, the latter only in Baja California Norte), the Chihuahuan Desert (M. coccinea and M. erecta) and in the states of Jalisco and Zacatecas (M. rosei).[2]
Ecology
Although observations of pollinators are limited, Elisens suggests that most Mabrya species are pollinated by hummingbirds; other possible pollinators are long-tongued bees.[10] The nectar composition of most species resembles that of related species known to be hummingbird-pollinated, being high in sucrose and low in glucose compared to fructose.[11]
^ abcdeElisens, Wayne J. (1985), "Monograph of the Maurandyinae (Scrophulariaceae-Antirrhineae)", Systematic Botany Monographs, 5: 1–97, doi:10.2307/25027602, JSTOR25027602
^ abGhebrehiwet, Medhanie; Bremer, Birgitta & Thulin, Mats Thulin (2000), "Phylogeny of the tribe Antirrhineae (Scrophulariaceae) based on morphological and ndhF sequence data", Plant Systematics and Evolution, 220 (3–4): 223–239, Bibcode:2000PSyEv.220..223G, doi:10.1007/bf00985047
^Vargas, P; Rosselló, J.A.; Oyama, R. & Güemes, J. (2004), "Molecular evidence for naturalness of genera in the tribe Antirrhineae (Scrophulariaceae) and three independent evolutionary lineages from the New World and the Old", Plant Systematics and Evolution, 249 (3–4): 151–172, Bibcode:2004PSyEv.249..151V, doi:10.1007/s00606-004-0216-1
^ abcVargas, Pablo; Valente, Luis M.; Blanco-Pastor, José Luis; Liberal, Isabel; Guzmán, Beatriz; Cano, Emilio; Forrest, Alan & Fernández-Mazuecos, Mario (2013), "Testing the biogeographical congruence of palaeofloras using molecular phylogenetics: snapdragons and the Madrean–Tethyan flora", Journal of Biogeography, 41 (5): 932–943, doi:10.1111/jbi.12253
^Sutton, David A. (1988), A Revision of the Tribe Antirrhineae, London; New York: The Natural History Museum; Oxford University Press, ISBN978-0-19-858520-6, cited in "Mabrya flaviflora (I.M. Johnst.) D.A. Sutton", Tropicos.org, Missouri Botanical Garden, retrieved 2014-07-15
^Elisens, Wayne J. & Freeman, C. Edward (1988), "Floral Nectar Sugar Composition and Pollinator Type Among New World Genera in Tribe Antirrhineae (Scrophulariaceae)", American Journal of Botany, 75 (7): 971–978, doi:10.2307/2443763, JSTOR2443763