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Maize forms the center of a series of cultural traits illustrative of the interrelationships of man and plants. More than 20 racial types of maize have been collected in northwest Mexico. Phenotypic analysis of more than 600 collections from the area indicates constant intercrossing among maize populations.
Maize forms the center of a series of cultural traits illustrative of the interrelationships of man and plants. More than 20 racial types of maize have been collected in northwest Mexico. Phenotypic analysis of more than 600 collections from the area indicates constant intercrossing among maize populations.
Maize forms the center of a series of cultural traits illustrative of the interrelationships of man and plants. More than 20 racial types of maize have been collected in northwest Mexico. Phenotypic analysis of more than 600 collections from the area indicates constant intercrossing among maize populations.
Source: Economic Botany, Vol. 39, No. 4 (Oct. - Dec., 1985), pp. 416-430 Published by: Springer on behalf of New York Botanical Garden Press Stable URL: http://www.jstor.org/stable/4254793 . Accessed: 29/04/2013 13:50 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. . New York Botanical Garden Press and Springer are collaborating with JSTOR to digitize, preserve and extend access to Economic Botany. http://www.jstor.org This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions Maize and Man in the Greater Southwest1 EFRAIM HERNANDEZ XOLOCOTZI2 In northwest Mexico, along the Sierra Madre Occidental and the adjacent slopes and plains, maize forms the center of a series of cultural traits illustrative of the interrelationships of man and plants. Here more than 20 racial types have been collected. This diversity is related to the variation in climate and soil conditions, to human migrations from the Mesoamerican cultural center to the Greater South- west area, and to the differential selection by the ethnic groups in the region. The agricultural practices of the farmers are reviewed to illustrate how different aspects of environment, economic needs, food preference, manner of utilization, and cer- emonial concepts constitute continuing forces of selection and motivation for in- troduction of varieties from other areas. It is suggested that color of the grain is utilized as an indicator of physiological characteristics. A phenotypic analysis of more than 600 collections from the area indicates the occurrence of constant in- tercrossing among maize populations. Maize, the basic subsistence element of Mesoamerican cultures, forms the center of a series of cultural traits illustrative of the interrelationships of man and plants. Although the topic of this symposium is limited to the Greater Southwest, the maize populations of this region form a constellation of closely allied racial groups that occupy an immense arc from the northeastern United States to the semiarid fields of Arizona and New Mexico, and then south along the Sierra Madre Oc- cidental in western Mexico to the Tehuacan area in the southeastern end of the Mexican Central Plateau. According to the map included in the National Geographic Society Magazine (1972), the Sierra Madre Occidental in Mexico is occupied, from the United States border to the south, by the following Indian groups within the Greater Southwest: Papago, Pima Alto, Opata, Pima Bajo, Tarahumar, Tepehuan, Huichol, Tepecan, Colotlan, and a cluster of small groups around the Rio Mayo headwaters (109W long., 27N lat.). A closer study of field data gathered by the author and collaborators during the 1968-1969 exploration of the Sierra Madre Occidental and of published infor- mation (Bennett and Zingg, 1935; Wellhausen et al., 1952; Pennington, 1969; Hemrnandez X. and Alanis F., 1970) permits the identification of the racial com- ponents of maize in the Mexican part of the Greater Southwest. This presentation will be based on general ecological regions (from south to north and from east to west). The Eastern Region includes the northern limits of Michoacan, eastern Jalisco, western Guanajuato, and the plains and foothills of western Zacatecas, Durango, and Chihuahua; it lies at an elevation of 1,600-2,000 m and has a mild temperate, 1 Received 25 October 1984; accepted 17 May 1985. Presented at the Symposium on Ethnobotany of the Greater Southwest, Twenty-fifth Annual Meet- ing, Society for Economic Botany, Texas A&M University, College Station, TX, 11-13 June 1984; symposium organized and chaired by Dr. Robert A. Bye, Jr. 2 Profesor-Investigador, Centro de Botanica, Colegio de Postgraduados, 56230 Chapingo, Mexico. Economic Botany, 39(4), 1985, pp. 416-430
1985, by the New York Botanical Garden, Bronx, NY 10458 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN humid climate. The maize races found are: Dulce (Fig. l a), Bofo (Pozolero), Reventador (Fig. 1 b), C6nico Norteiio, Tablilla de Ocho, Chalquefio, Cristalino Chihuahua (Fig. 4k), Apachito (Fig. 5n), Gordo (Fig. 5m), Blando (Fig. 3i), and Palomero Toluquefio (Fig. 41). The Central Region is formed by the valleys and slopes of the Sierra Madre Occidental whose southern limits lie at the Jalisco-Nayarit state boundary; to the north it extends slightly into New Mexico. Isolated agricultural fields are generally found at 2,000 m elevation and have a cool temperate, humid climate. In Chi- huahua, the mountainous area usually receives snows in winter, which delay maize planting in spring until drying and warming of the soil has occurred. From south to north, the maize races are: Conico Nortefio, Jala (Fig. 2e), Tabloncillo, Cris- talino Chihuahua, Gordo, Apachito, Azul, Onavefio (Fig. 4j), and Blando. The Western Region includes the plains along the Pacific Ocean and the Gulf of Baja California and the flood plains and slopes along the western limits of the Sierra Madre. The agricultural lands are generally below 500 m elevation and have a warm, humid climate up to the southern limits of Sonora. Farther north the coastal plains are semiarid and arid, restricting maize cultivation to the flood plains and the areas closer to the mountains. The maize races are: Dulce, from Jalisco to northern Sinaloa; Dulcillo del Noroeste (Fig. 3h); Harinoso de Ocho (Fig. 3g) only in Sonora and Nayarit; Blando in Sonora; Bofo (Fig. 2d, a form of which is called Pozolero in northeastern Jalisco) from Nayarit to Sonora; Tab- loncillo Perla (Fig. 1 c) from Jalisco to Sonora; Onavefio, only in Sonora; Reven- tador, from Jalisco to northern Sinaloa; Chapalote (Fig. 2f) in Sinaloa, and Sonora. We might now visualize the distribution of the races along latitudinal bands indicating the texture of the grain. This would give us: Along a southern band (northern Jalisco, Nayarit, southern Zacatecas) dents: Tabloncillo, Jala, Conico Nortefio, Chalqueiio flints: Tabloncillo Perla floury: Bofo, Pozolero pops: Reventador sweet: Dulce Along a central band (Sinaloa, northern Zacatecas, Durango) dent: Conico Norteio flint: Tabloncillo Perla floury: Bofo (ceremonial maize) pop: Reventador, Chapalote sweet: Dulce Along a northern band (Sonora, Chihuahua) dent: C6nico Nortefio flints: Onavefio, Azul, Cristalino Chihuahua, Apachito floury: Blando, Gordo, Harinoso de Ocho pops: Chapalote, Palomero Toluquefio, Lady Finger sweets: Dulcillo Noroeste, Dulce The south-north regions might give us an idea of the migration routes followed by cultural traits from the Mesoamerican center to the northwest of Mexico. The latitudinal sections should give an idea of the ecological variations encountered. 1985] 417 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY To understand what these raw data represent, we should recognize that maize has been the basic food of the Mesoamerican ethnic groups since the origin and spread of agriculture. Before the introduction of domesticated animals, all parts of the maize plant were used: the grain and the male inflorescence for food; the cane of the earless plants for sweet juice; the leaves and corn husks for wrapping tamales (small loaves of maize dough and other ingredients); the dry canes for construction material or for fuel; the cobs, stumps, and roots for fuel; corn smut for food. With the introduction of farm animals the vegetative parts and grain of maize have become important for their feed but human consumption is still by far the dominant purpose of production. As a result of this relationship, deep- rooted ceremonial beliefs will show their influence in the production practices, seed selection, and resulting plant populations of maize. We will work under the assumption that the migration of this domesticated plant northward has occurred with a high proportion of the cultural traits related to its cultivation, use, and ceremonial practices. We might now ask some ethnobotanical questions related to: 1. the farmer's understanding of his environment in regard to the production of maize; 2. the existence of maize populations of practically all types of texture of grain; 3. the maintenance of the seedstock; 4. the artificial selection by the farmer; and 5. the migration of maize populations. In case you expect the full answers now, may I anticipate that the purpose of this exercise is to call attention to some relevant points of ethnobotany in need of further inquiry, not to give solutions. Our field observations in fairly isolated regions indicate that the Indian farmers know the climatic regimes and their vagaries in their territories, the soils and their qualities, especially in regard to water retention and fertility, and an ample spec- trum of the biological nature of the maize populations they handle. For instance in Bahia de Banderas, Jalisco, at 40 m elevation with a warm humid climate, we found the following agricultural habitats, method of use, and reasons: Rainfed lands, plowed, spring plantings: Tabloncillo Perla (human consumption); "Criollo de Ocho," early for forage and human consumption of corn on the cob. Criollo is a term used to indicate a local variety; Criollo de Ocho is similar to Tabloncillo. Fig. 1. Races of maize found in northwest Mexico: a. Dulce (1 = 1.5),* Jalisco, Zacatecas, Sinaloa; b. Reventador (1 = 2.11), Jalisco; c. Tabloncillo sub-race Perla (1 = 1.65), Nayarit, Sinaloa. * Scale in centimeters, i.e., 1 cm in Fig. la = 1.5 cm in actuality; 1 cm in Fig. lb = 2.11 cm in reality, etc. Fig. 2. Races of maize found in northwest Mexico: d. Bofo (1 = 1. 7),* Jalisco, Nayarit and Durango; e. Jala (1 = 2.30), Nayarit; f. Chapalote (1 = 1), Nayarit and Sinaloa. * Scale in centimeters-see above for explanation. Fig. 3. Races of maize found in northwest Mexico: g. Harinoso de Ocho (1 = 1.25),* Sonora; h. Dulcillo del Noroeste (1 = 1.7), Sonora and Sinaloa; i. Blando de Sonora (1 = 1.27), Sonora. * Scale in centimeters-see above for explanation. 418 [VOL. 39 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN a b C 1985] 419 b a c This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions CD _j^^^^^^^.P , ,rppfrrsrv^. "' |^ ^-Al:/U" 'Atb\ t A n -* ,.... 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This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN 9 h 1985] 421 h i g This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY i k 422 [VOL. 39 I This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN Soils with high water table, plowed, winter plantings: "Criollo Amarillo" (early), Criollo de Ocho early commercial production. Criollo Amarillo is a yellow-grained form of Criollo de Ocho. Irrigated, plowed: "Arriaga" introduced from Chiapas; commercial crop. Arriaga is a variety similar to Tuxpenio. Old slash-bum fields, spring planting: Tabloncillo; subsistence. New slash-bum fields, spring planting: Criollo Amarillo; early, subsistence. Fields with drier soils, spring planting: Criollo Amarillo; early, subsistence. These observations appear repeatedly where various microhabitats occur. In Valparaiso, Zacatecas, where humid winds penetrate from the Pacific, early plant- ings are made at 2,090 m elevation in Jan.-Feb.; regular rain-fed plantings are made in June-July. At Madera, Chihuahua, 2,000 m elev., when rains are delayed, Apachito is planted because it is fast-growing. It should be mentioned that the best indications of an understanding by the farmer of the ecological conditions available for his agricultural activities are the decisions he makes in regard to the best combination of seed and conditions. This in turn is related to the choices of seed available. With regard to the seed found in the various areas, this includes not only representatives of the main variants in texture, but also a color series of glassy white, enamel white, yellow, pink, red, dark blue, and black (Table 1). The main- tenance of the various textures is related to the constant consumption of maize and the need for variety in the monotonous diet. Capsicum has a similar reason for being (Hernandez X., 1970). Several studies (Bennett and Zingg, 1935; Kelly and Anderson, 1943; Anderson, 1944; Foster, 1946; Beals, 1946; West, 1946; Pennington, 1969; Echeverria and Arroyo, 1982), have given ample information on maize recipes. I shall limit myself to a few examples from the area, as recorded in my field notes: dents: Tabloncillo: tortillas, piznate (flint grain with floury capping, cooked in water until it pops, dried, roasted over a clay grill, ground, the flour screened, water added, allowed to ferment) (colors: glassy white; yellow) flints: Amarillo Cristalino: elotes (corn on the cob), tortillas, animal feed Tab.-Perla: tortillas, pinole (flour maize roasted, ground, sugar or cinnamon added) Azul: "el mejor para tesgtiino" (maize grains germinated under fresh pine leaves, young plants dried, boiled in water, cooled, fermented in clay pots used previously for same purpose). Cristalino Chihuahua: tortillas (colors: white, yellow, blue) floury: Blando: pinole, coricos (cookies of various shapes made of floury maize) Pozolero: pinole, elotes, huachales (cooked corn on the cob, dried, stored for later use), pozole (floury, usually pink maize, cooked until it bursts) Bofo: gordas (floury maize, uncooked grains ground, cookies made adding brown sugar and putting in oven), huajatole (grains broken in large pieces, these and the cobs put in water until they sour; cooked; cobs removed and liquid drunk cold), pozole (colors: enamel white, yellow, pink, red, blue, black) pops: Chapalote: pinole, ponteduro (popped maize grains made into balls by adding brown sugar), flores (pop corn), esquite, coricos Palomero Toluquefio: flores Reventador: flores, ponteduro Fig. 4. Races of maize found in northwest Mexico: j. Onavefio (1 = 2.23),* Sonora; k. Cristalino de Chihuahua (1 = 1.97), Durango and Chihuahua; 1. Palomero Toluquefno (1 = 1), Durango and Chihuahua. * Scale in centimeters-see above for explanation. 1985] 423 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY m I [VOL. 39 424 m n This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN TABLE 1. USE OF COLOR OF GRAIN AS INDICATOR OF ECOLOGICAL, DIETARY, AND MEDICINAL CHARACTERISTICS. Medicinal-ceremonial Color of grain Ecological adaptation Dietary use and characteristics significance yellow early; for drier oily, good for hogs and areas; for poorer chickens soils pink on floury intermediate or sweet corn on the cob; background late-growing pe- sweet pinole; sweet riod canes dark purple on intermediate-grow- blue tortillas, softer and floury back- ing period tastier; atole; best for ground tesguino; coloring other dishes red on floury intermediate-grow- pozolero, the grain pops background ing period on boiling white, yellow, red, guardians of the milpa black, all floury among the Huicholes with enameled color red on different protection of the milpa backgrounds against disease, hail, drought and "eclipse" dark red on floury remedy against "pujos" background (dysentery), for luck Lady Finger: flores (colors: glassy white, yellow, dark brown, red) sweets: Dulce: roasted, esquite, pinole Dulcillo Noroeste: pinole, esquite (colors: glassy yellow, pink, red) Farmers in all areas cultivate a type suitable for tortillas and accepted for sale. In isolated communities the floury, pop and sweet types are cultivated in a few rows separate from, but adjacent to, the main varieties. They are considered very ancient varieties that are fast disappearing. On slopes, the colored and sweet varieties are grown along the upper limits of cultivation to prevent out-crossing to the prevailing dents or flints. If one observes the piles of maize harvested in different places, one can appre- ciate some very heterogeneous mixtures and some surprisingly uniform lots. With the special color and texture types there is usually less mixture. It is understood that there are both careful and careless Indian farmers. If one has the privilege of examining the maize granary of a farmer reputed to be careful, one will see maize ears separated in piles according to race, color, and texture, and clusters of ears hung separately for seed, including a sufficient quantity of red-grained ears for safeguarding the fields. Since the rainy season varies, a series of varieties must be available to meet the particular conditions of a given year: very early, white; Fig. 5. Races of maize found in northwest Mexico: m. Gordo (1 = 2),* Chihuahua; n. Apachito (1 = 2), Chihuahua. * Scale in centimeters -see above for explanation. 1985] 425 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY early, yellow; intermediate, various colors; late, white. That this relationship holds true has been shown experimentally in the Puebla-Tlaxcala area of the Central Mexican Plateau (Lopez Herrera, 1975). But the farmer can manipulate part of the environmental factors so that he may give his plants a longer growing season by early plantings in soils that have stored moisture, and in this way separate the flowering periods of his maize varieties, fostering genetic isolation between varieties. The reason for seeking longer periods of growth seems to be related to an understanding that this is correlated with a higher yield (Bucio Alanis, 1954). This has been demonstrated by the planting of the late-maturing, higher-yielding Chalqueiio at Valparaiso, Zacatecas, and Victoria, Durango. Basic to the maintenance of seed pure (homozygous) in color and texture is the farmer's appreciation and response to the phenomenon of xenia in the kernel. Weatherwax (1942) reports that Indians in New England apparently had no un- derstanding of pollination. I am not in a position to say that the farmer knows the full process of pollination. Present-day farmers say that when one color type affects another color, it has been "married," and, in selecting their seed of the color and texture varieties, they shell the ears and select grains with the full expression of the character desired. Apparently the specific needs of the ethnic groups are not fully met in certain cases, or the human trait of curiosity lies behind the constant introductions of new varieties from short and from long distances. Some examples: 1. sweet corn, from San Joaquin, California, to Sahuaripa, Sonora; "didn't do so well." 2. pop corn, from U.S. to Yecora and Sahuaripa, Sonora. 3. Palomero Toluqueiio (pop) from the Mesa Central, to Las Varas, Madera, and Guachochic, Chihuahua. 4. Chalquefno, from Mexico State, to Zacatecas and Durango. 5. Tabloncillo, from the coast of Nayarit, to Amatlan de Jara, Nayarit. 6. Dulce, from central Jalisco northward, to southern Sonora. 7. Tuxpeiio, in Amatlan, Nayarit, from Torreon, Coahuila, and Tampico, Tamaulipas; in Ixtlan del Rio, Nayarit, from Tampico, Tamaulipas; "Tor- reon" at Puente Camotlan, Nayarit, from Bolanios, Jalisco. 8. Celaya, the variety "Argentino" from southern Guanajuato to Huazamota, Durango. 9. Chapalote, ca. Culiacfan, Sinaloa, "Chapalote" from Tamazula, Durango. 10 Cuarenteno, ca. CuliacLan, Sinaloa from Mocorito ca. La Angostura, Sonora. 11. Hibrido, Badiraguato, Sinaloa, 600-800 m, from Los Mochis, Sinaloa; Tamazula, Durango, 500 m, H-503 from Mexico City. With the presence of such a large number of races and the introduction of a few additional ones, it is not surprising that an analysis based on the phenotypic characters of the ears should give a high number of reciprocal hybrids, as shown in Table 2 taken from Hemrnandez X. (1973). Apparently unsuccessful migrations of maize populations may nevertheless donate genes involving simple genetic characteristics of the endosperm and be selected through the phenomenon of xenia. Apparently this explains the probable formation of Dulcillo del Noroeste from Dulce de Jalisco; Gordo, Azul and Po- 426 [VOL. 39 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN TABLE 2. GENETIC VARIABILITY FOUND IN SIERRA MADRE OCCIDENTAL IN NORTHWEST MEXICO, ACCORDING TO PHENOTYPIC CHARACTERS OF EARS OF 660 COLLECTIONS AND INDI- CATED BY RACES AND RECOMBINATIONS. Grain texture Tablon- Reven- C6nico Cristalino typeb Race Tuxpefio cillo tador Nortenio Chih. Bolita Apachito 1, 3 Tabloncillo + + + + 1, 3 C6nico Norteiio + + + Ia 2 Bofo I | + 5 Reventador + 1 San Juanc + + + + 4 Dulcillo N.O. I I I 5 Lady Finger 5 Dulce l I I 2 Harinoso-8 | 1 Tuxpenio + + + 1 Tablilla-8 I 3 Cristalino Chih. + + I l l 2 Gordo - + 5 Apachito + 3 Azul | | - + 5 Palomero Tol. + 1, 3 Celaya 1, 3 Bolita (Cafime) + - - - 1, 3 Chalquefio + a Vertical line refers to apparent genetic flow from a race in the upper row to a race in the left column; horizontal line to flow in reciprocal manner. A + indicates genetic flow in both directions. This series is the one registered above 1500 m (Hernandez X., 1973). bGrain types: 1, dent; 2, floury; 3, flint; 4, sweet; 5, pop. c San Juan, undescribed, early, 12-row; small white dented grain; like Nal-Tel, from southwestern Tamaulipas. zolero from Bofo and this in turn from Harinoso de Ocho; the presence of sweet and floury in Onave-no, which is normally a flint. Schuster and Bye (1983) report the results of an experiment designed to test the effect of long distance transport of exotic races to a new geographic area. Material from the Tarahumara region of Mexico and from southern Arizona was grown in southwestern Colorado. Although the maize plants had problems of growth in their new setting they shed pollen and all produced viable seed. From our study of the Mexican northwest, we emphasize the permanent contribution that might be made through the influ- ence of pollen by the exotics on the local population. Bucio Alanis (1954) did a study with the Mexican races comparing the F1 of crosses among said races and their progenitors. He indicates that in the majority of instances the hybrids tended to be as early as the earlier parent and in various cases they were earlier. In addition, there was a marked effect on yield: the hybrids showed an increase, probably due to heterosis. Finally we come to the problem of maize classification in the area, initiated in its modem, biosystematic approach by Anderson and Cutler (1942), Kelly and Anderson (1943), Anderson (1944, 1946), Carter and Anderson (1954), Wellhau- sen et al. (1952), and Hernandez X. and Alanis Flores (1970). The use of statistical and chemical analyses has resulted in new efforts at phylogenetic classifications (Goodman and Paterniani, 1969; Goodman and Bird, 1977; Benz, 1981; Yakoleff G. et al., 1982). There are several reasons for continuing this important taxonomic 1985] 427 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY TABLE 3. MAIN MORPHOLOGICAL CHARACTERISTICS OF RACES OF MAIZE FOUND IN NORTH- WEST MEXICO. Length and diameter Race Ear shapea of ear, cm Row number Grain textureb Grain color Dulce 1 13.7-4.5 14.5 a yellow, red Dulcillo del 2 16.1-3.4 10.0 a glassy yellow Noroeste Reventador 2 16.5-3.2 12.0 b glassy white, pink Chapalote 2 11.0-2.9 12.3 b dark brown Blando de 2 18.7-3.7 12.0 c enamel white Sonora Onavefio 2 20.0-4.4 12.0 d, c glassy white Bofo 2 18.0-3.8 14.0 c white, red, dark purple Cristalino 3 26.6-4.9 12.0 d white Chihuahua Harinoso de 3 11.9-3.8 8.0 c enamel white Ocho Gordo 3 16.0-4.0 14.0 c enamel white Tabloncillo 3 16.4-4.1 9.0 e white, smoky Tabloncillo Perla 3 17.0-3.7 8.3 d white Tuxpefio 3 19.7-4.4 12.6 e white Jala 3 30.5-5.9 14.7 e white Palomero Toluquefio 4 10.2-3.4 23.0 b glassy white Chalquefio 4 16.0-4.9 16.6 e glassy white C6nico 4 13.1-4.6 16.0 e glassy white Nortefio Apachito 5 15.0-3.5 12.0 d white, pink a Ear shape: 1, oblong; 2, ellipitcal; 3, cylindrical; 4, conical; 5, big butt. b Grain texture: a, shrunken; b, pop; c, floury; d, flint; e, dent. task both at the micro and macro level: the need for a logical classification to handle the populations under study, the need for a basis for analyzing possible phylogenetic trends and, the need to monitor genetic changes in critical areas to discover their possible causes (Table 3). In this respect, probably one of our errors has been to disregard Edgar Ander- son's (1946) recommendation to undertake more population studies of maize in the different indigenous areas of production. Such studies would give us a better understanding of the crop as managed by the local farmers and would provide periodic records for comparison. This broad analysis, plus information derived from plant breeding programs, would help to define the best material represen- tative of a given race. This might help avoid the confusion created by the similarity of phenotypic characters on different genetic backgrounds, as suggested by some of the results of research mentioned above. Perhaps a study similar to that conducted by Ortega Paczka (1973) in Chiapas should be programmed for part of the Sierra Madre Occidental. Since a rather extensive collection had been obtained by Hernandez X. from Chiapas in 1946 and maintained in the germplasm bank in Mexico, a new collection was made in 1971 to evaluate the changes that had occurred in maize (Ortega Paczka, 1973). The same basic and speciality types found in 1946 were recovered 25 yr later. 428 [VOL. 39 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions HERNANDEZ X.: MAIZE & MAN New types were found corresponding in general to recombinations of regional types with introduced populations from bordering states and Guatemala. One widespread type in 1971 could be traced via Guatemala to an improved open- pollinated variety, Rocamex 521, released during the initial years of the Rocke- feller Foundation Agricultural Program in Mexico and now found very suitable for newly opened slash-bum areas. The new populations found were occupying newly worked areas in the Chiapas Central Basin and the Lacandon territory. The persistence of the original races was due to the apparent cultural cohesion of the Indian groups of the central depression and mountain areas of the state. ACKNOWLEDGMENTS I wish to thank Dr. Robert D. Osler of the Centro Internacional para el Mejoramiento de Maiz y Trigo (CIMMYT), L6ndres 40, Mexico, D.F. 06600, for all photographs except Fig. 2d and Fig. 5m and n. Fig. 1 a is reproduced by permission from the Missouri Botanical Garden (Kelly and Anderson, 1943). LITERATURE CITED Anderson, E. 1944. Maiz Reventador. Ann. Missouri Bot. Garden 31: 301-314. 1946. Maize in Mexico-A preliminary survey. Ann. Missouri Bot. Garden 33: 147-247. , and H. Cutler. 1942. Races of Zea mays: Their recognition and classification. Ann. Missouri Bot. Garden 29: 69-89. Beals, L. 1946. Cheran: A Sierra Tarascan Village. Inst. Soc. Anthropol. Publ. no. 2. Smithsonian Inst., Washington, DC. Bennett, W. C., and R. M. Zingg. 1935. The Tarahumara, an Indian Tribe of Northern Mexico. Chicago Univ. Press, Chicago, IL. Benz, B. F. 1981. Five Modem Races of Maize from Northwestern Mexico: Archaeological Impli- cations. Master's Thesis, Dept. Anthropol., Univ. Colorado, Boulder, CO. Bucio Alanis, L. 1954. Algunas observaciones del comportamiento de la F, de las cruzas entre las razas de maiz descritas en Mexico. Tesis profesional, Escuela Nacional Agricultura, Chapingo, Mexico. Carter, G. F., and E. Anderson. 1945. A preliminary survey of maize in the Southwestern United States. Ann. Missouri Bot. Garden 32: 297-323. Echeverria, Ma. E., and E. Arroyo, coord. 1982. Recetario mexicano del maiz. Museo Nacional de Culturas Populares, Secretaria Educaci6n Pfiblica, Mexico, D.F. Foster, G. 1946. Empire's Children: the People of Tzintzuntzan. Inst. Soc. Anthropol. Publ. no. 6. Smithsonian Inst., Washington, DC. Goodman, M. M., and R. McK. Bird. 1977. The races of maize. IV: Tentative grouping of 219 Latin American races. Econ. Bot. 31: 204-221. , and E. Paterniani. 1969. The races of maize: III. Choices of appropriate characters for racial classification. Econ. Bot. 23: 265-273. Hernmndez X., E. 1970. Exploraci6n etnobotanica y su metodologia. Rama Botanica, Colegio Post- graduados, ENA, Chapingo, Mexico. , and G. Alanis Flores. 1970. Estudio morfolo6gico de cinco nuevas razas de maiz de la Sierra Madre Occidental de Mexico. Implicaciones filogeneticas y fitogeograficas. Agrociencia 5: 3- 30. 1973. Genetic resources of primitive varieties of Mesoamerica: Zea spp., Phaseolus spp., Capsicum spp., and Cucurbita spp. In Frankel, 0. H., ed, Survey of Crop Genetic Resources in Their Center of Diversity (first report), p. 76-115. FAO, Int. Board for Plant Genetic Re- sources, Rome. Kelly, I., and E. Anderson. 1943. Sweet corn in Jalisco. Ann. Missouri Bot. Garden 30: 403-412. Lopez Herrera, A. 1975. Fechas de siembras en Valles Altos para comprobar la relaci6n de la coloracion del grano de maiz con la precocidad y la produccion. Tesis profesional, Escuela Nacional Agricultura, Chapingo, Mexico. 1985] 429 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions ECONOMIC BOTANY ECONOMIC BOTANY National Geographic Society. 1972. Indians of North America. Map supplement. Natl. Geogr. Mag. 142: 739 A. Ortega Paczka, R. 1973. Variaci6n en maiz y cambios socioecon6micos en Chiapas, Mex. 1946- 1971. M.C. tesis, Colegio Postgraduados, Chapingo, Mexico. Pennington, C. W. 1969. The Tepehuan of Chihuahua. Their Material Culture. Univ. Utah Press, Salt Lake City, UT. Schuster, R. A., and R. A. Bye, Jr. 1983. Patterns of variation in exotic races of maize (Zea mays, Gramineae) in a new geographic area. J. Ethnobiol. 3: 157-174. Weatherwax, P. 1942. The Indian as a corn breeder. Proc. Indiana Acad. Sci. 51: 13-21. Wellhausen, E. J., L. M. Roberts, and E. Hernmndez X. in collaboration with P. C. Mangelsdorf. 1952. Races of Maize in Mexico, Their Origins, Characteristics and Distribution. Bussey Inst., Harvard Univ., Cambridge, MA. West, R. C. 1946. Cultural Geography of the Modern Tarascan Area. Inst. Soc. Anthropol. Publ. no. 7. Smithsonian Inst., Washington, DC. Yakoleff G., V., E. Hernmndez X., C. Rodjind de Cuadra, and C. Larralde. 1982. Electrophoretic and immunological characterization of pollen protein of Zea mays races. Econ. Bot. 36: 113- 123. Book Review Plant Chemosystematics. J. B. Harborne and B. L. Turner. Academic Press, Orlando, FL 32887. 1984. 562 pp. $95.00. When Biochemical Systematics was published in 1963, R. E. Alston and B. L. Turner wrote that ".. . no significant taxonomic dispositions of higher plants rest primarily upon biochemical criteria. We consider that an important objective of this book is to develop ... an appreciation of the diversity of applications of biochemistry to systematics." Clearly the authors achieved this goal, for in the decades following publication of their text one is impressed by the large numbers of biochemical articles dealing with systematic problems which have appeared in botanical and other journals. Without doubt, ". . . the plant sys- tematist is carrying out the chemical work necessary to help resolve his particular taxonomic problem," and this is the chief objective of the revised edition: to review the state and potential of this approach to plant systematics through 1982. And how admirably the authors accomplish their purpose. Divided into three parts, Introduction, Secondary Metabolites, and Macromolecular Approaches, and 21 chapters, they first outline the biochemical characters of application in plant systematics. Thus, secondary metabolites which are volatiles (e.g., sesquiterpenes, aromatic volatiles), defence agents (e.g., alkaloids, cyanogenes, steroids), pigments (e.g., anthocyanins, betalains, ca- rotenoids), and storage metabolites (e.g., fatty acids, sugars, polyols), variations in metab- olism involving primary, secondary, and degradative pathways, and macromolecules (pro- teins, nucleic acids, polysaccharides), are all of potential value towards improving classification and phylogenetic schemes, particularly at the family level and lower. They cite numerous infraspecific, specific, generic, and familial examples where applications of chemistry along with exomorphic and other characters have been important in improving, highlighting, and confirming existing systems. They do this succinctly and objectively with an unparalleled mastery of their subject. This is a first-rate reference for all biologists who utilize or wish to refer to biochemistry as it applies to classification and phylogeny/evolution of plants. WALTER H. LEWIS, WASHINGTON UNIVERSITY, ST. Louis, MO 63130 National Geographic Society. 1972. Indians of North America. Map supplement. Natl. Geogr. Mag. 142: 739 A. Ortega Paczka, R. 1973. Variaci6n en maiz y cambios socioecon6micos en Chiapas, Mex. 1946- 1971. M.C. tesis, Colegio Postgraduados, Chapingo, Mexico. Pennington, C. W. 1969. The Tepehuan of Chihuahua. Their Material Culture. Univ. Utah Press, Salt Lake City, UT. Schuster, R. A., and R. A. Bye, Jr. 1983. Patterns of variation in exotic races of maize (Zea mays, Gramineae) in a new geographic area. J. Ethnobiol. 3: 157-174. Weatherwax, P. 1942. The Indian as a corn breeder. Proc. Indiana Acad. Sci. 51: 13-21. Wellhausen, E. J., L. M. Roberts, and E. Hernmndez X. in collaboration with P. C. Mangelsdorf. 1952. Races of Maize in Mexico, Their Origins, Characteristics and Distribution. Bussey Inst., Harvard Univ., Cambridge, MA. West, R. C. 1946. Cultural Geography of the Modern Tarascan Area. Inst. Soc. Anthropol. Publ. no. 7. Smithsonian Inst., Washington, DC. Yakoleff G., V., E. Hernmndez X., C. Rodjind de Cuadra, and C. Larralde. 1982. Electrophoretic and immunological characterization of pollen protein of Zea mays races. Econ. Bot. 36: 113- 123. Book Review Plant Chemosystematics. J. B. Harborne and B. L. Turner. Academic Press, Orlando, FL 32887. 1984. 562 pp. $95.00. When Biochemical Systematics was published in 1963, R. E. Alston and B. L. Turner wrote that ".. . no significant taxonomic dispositions of higher plants rest primarily upon biochemical criteria. We consider that an important objective of this book is to develop ... an appreciation of the diversity of applications of biochemistry to systematics." Clearly the authors achieved this goal, for in the decades following publication of their text one is impressed by the large numbers of biochemical articles dealing with systematic problems which have appeared in botanical and other journals. Without doubt, ". . . the plant sys- tematist is carrying out the chemical work necessary to help resolve his particular taxonomic problem," and this is the chief objective of the revised edition: to review the state and potential of this approach to plant systematics through 1982. And how admirably the authors accomplish their purpose. Divided into three parts, Introduction, Secondary Metabolites, and Macromolecular Approaches, and 21 chapters, they first outline the biochemical characters of application in plant systematics. Thus, secondary metabolites which are volatiles (e.g., sesquiterpenes, aromatic volatiles), defence agents (e.g., alkaloids, cyanogenes, steroids), pigments (e.g., anthocyanins, betalains, ca- rotenoids), and storage metabolites (e.g., fatty acids, sugars, polyols), variations in metab- olism involving primary, secondary, and degradative pathways, and macromolecules (pro- teins, nucleic acids, polysaccharides), are all of potential value towards improving classification and phylogenetic schemes, particularly at the family level and lower. They cite numerous infraspecific, specific, generic, and familial examples where applications of chemistry along with exomorphic and other characters have been important in improving, highlighting, and confirming existing systems. They do this succinctly and objectively with an unparalleled mastery of their subject. This is a first-rate reference for all biologists who utilize or wish to refer to biochemistry as it applies to classification and phylogeny/evolution of plants. WALTER H. LEWIS, WASHINGTON UNIVERSITY, ST. Louis, MO 63130 430 430 [VOL. 39 [VOL. 39 This content downloaded from 132.248.181.49 on Mon, 29 Apr 2013 13:50:53 PM All use subject to JSTOR Terms and Conditions