Abstract

Zea Mays L., one of the most highly evolved of all grasses, is still botanically much of an enigma. Commonly known as Indian corn or maize, it was a very important plant to the peoples of the New World long before the arrival of Columbus. It formed the basis of the highly developed Inca, Maya, and Aztec civilizations and was the staple crop from Canada to Chile for several thousand years. It is, of course, quite important to the present-day inhabitants of Central and South America, and agriculture and industry in the United States uses three and one-quarter billion bushels annually. Botanists have until recently followed almost exclusively Sturtevant's (1899) classification of contemporary races of maize by kernel types. Although this classification is an artificial one, it has proven to be of practical commercial worth. Archaeologists have long known the value of maize kernels found at excavation sites for determining types of maize grown and the uses to which they were put. Until the last few years, other parts of the maize plant have been quite generally neglected as a source of historical data, chiefly because of the complexities involved in determining and evaluating such evidence as they contain. Evidence from maize tassels has been used with promising results (Alava, 1952; Anderson, 1944Ab, 1944c, 1949a, 1951; Anderson and Brown, 1948; Anderson and Cutler, 1942; Brown et al, 1952; Cutler, 1946; Wellhausen et at, 1951, 1952). Prat (1948) showed that in maize and other grasses hairs and other epidermal emergences can be used as a basis for identification and classification. Internode patterns have been studied by several workers (Anderson, 1943, 1949a; Anderson and Brown, 1948; Anderson and Schregardus, 1944; Stonor and Anderson, 1949; Wellhausen et al, 1951, 1952). Ear and tassel ontogeny have been studied by Bonnett (1940, 1948) and Kiesselbach (1949). Esau studied the ontogeny of the maize vascular bundle. Surprisingly little has been done to measure and evaluate those morphological structures which are present on a maize cob after the kernels have been removed. Weatherwax, a pioneer in the study of the maize cob, pointed out (1918) the need and value of accurate morphology in understanding this structure, and demonstrated (1920) the orderly spikelet behavior underlying changes in kernel rowing. Fujita (1939) observed that an even number of pairs of kernels resulted in straight rows, and an odd number in spiral rows. Cutler (unpublished work) made many histological studies of the cobs of both North and South American maize, as well as of several closely related genera. Lenz (1948) indicated the types

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