Ban Chiang Pottery and Rice

A Discussion of the Inclusions in the Pottery Matrix

By: Douglas E. Yen

Originally Published in 1982

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Rice (Oriza sativa) remains are hardly novel discoveries in Asian archaeology. Reported as grain husks or glumes, charred endosperms or as husk impressions in ce­ramics from north and south China, Japan, India, Pakistan and Southeast Asia includ­ing Indonesia, their influence on the inves­tigation of agricultural origins has been considerable. (Figure 1).

With the possible exception of some of the materials from the Indian subcontinent (Vishnu-Mittre, 1974) the identification of oryza (rice) from archaeological remains in Thailand has undergone more critical scru­tiny than other such Asian finds. The reader will note the writer’s consciousness in these opening sentences, in which refer­ence to rice remains has changed to the more non-committal identity of the generic Oryza. The amplified attention to the Thai material was due to the date of 3500 B.C. or earlier given to charred grain and husk impressions in pottery recovered by Donn Bayard (1970, 1971) from the site of Non Nok Tha. At the time, the only comparable date for early rice was in the 4th millen­nium B.C. from a Chinese site south of the Yangtse, reported secondarily by K-C. Chang (1973). The identification of possibly domesticated plants, none of them major grain crops like rice, in Hoabinhian levels some ten thousand years old (Gorman 1969, 1970) at Spirit Cave, together with the Non Nok Tha recoveries suggested a continuum of domestication that prompted Solheim (1972) to propose the controversial ‘earlier agricultural revolution’ for Southeast Asia. The much disputed theory of Carl Sauer (1952) advocating the primacy of Southeast Asian origins of Old World agriculture had found further material basis.

This formed the background against which Chet Gorman and I continued our collaboration in late 1973. He had begun work in northwest Thailand by excavating Spirit Cave, as well as two other cave sites in this region, prior to undertaking his major research program at Ban Chiang. My role was to complete an ethnobotanical study of the modern flora and its possible relation­ship to the Hoabinhian plant remains, whose preliminary identifications on publi­cation (Gorman, 1969) had produced stir and scorn (Harlan and De Wet, 1973). The new excavations yielded more plant mate­rial for identification. This included nearly whole specimens from Banyan Valley Cave which the archaeologist had jubilantly labelled “RICE!!!” The results of the whole study were published (Yen, 1977), with due caution, and submitted to the eminent rice geneticist T.-T. Chang. He concluded (1976: 146) that they possessed “surface features more indicative of a wild form of rice.” This is most significant since the mere mention of “rice” often implied its cultiva­tion. Of course, in 1974 when I visited Gorman at Ban Chiang, we were not yet aware of Dr. Chang’s determination, nor indeed that the carbon dating of the Banyan Valley Cave site would yield occu­pation dates extending only from 3500 B.C. to A.D. 700.

During the 1974 excavations at Ban Chiang, we could see, with limited equip­ment, that the pottery contained inclusions similar to those in Bayard’s Non Nok Tha ceramics. The pronouncement of the geneticist Otsuka (1972) that the Oryza fragments were undifferentiable as wild or cultivated forms was to be confirmed by the palaeobotanist Vishnu-Mittre (1973). Subsequently, T.-T. Chang (1976:146) diag­nosed a photomicrograph of Otsuka’s sam­ple as representing the husk fragments of an Oryza form ‘intermediate between a wild race and the weed race.’ That is, a plant that was disposed to colonize places where the soil has been disturbed, such as takes place with cultivation. The expecta­tion that the sophisticated culture repre­sented at Non Nok Tha—as judged by the richness of its artifacts—should be accom­panied by an advanced subsistence base was somewhat dashed by this identifica­tion. Indeed, the ‘wild’ or non-cultivated identity of the Oryza remains from recent excavations in Thailand could have been construed to mean that a hunting/gathering economic base for the late Hoabinhian techno-complex of the Northwest was shared by the pottery-making, metal-forging people of the Northeast.

This unpromising start was nearly the finish of any extension of my collaboration in the Thai project to the northeast, but anyone who had the good fortune to work with Chet Gorman also knew of his powers of persuasion. In 1976, I found myself carrying a package of sherds from The Uni­versity Museum where the laboratory anal­ysis of the Ban Chiang material was pro­ceeding (Gorman and Charoenwongsa, 1976). Final stratigraphic associations had not yet been worked out, but the random sample of 80 sherds from the various levels of excavation all showed evidence of Oryza husks (Yen, 1980).

With this result, I asked for a further series of sherds, this time with as accurate as possible a calibration with the Ban Chiang cultural sequence so that each sherd could be assigned to one of the phases Gorman defined. We were also interested in the organic content of the rough ceramic crucibles. These appear roughly at the time of the first iron and are of considerable interest in terms of organic inclusions and what may have been heat resistant temper.

Our hope was that this sequence might reveal a transformation of Oryza husk remains from ‘wild’ forms to those resem­bling the cultivated 0. sativa. This opti­mism was ‘tempered’ however, by an immovable botanical fact—tiny fragments of grain husks cannot produce unquestion­able Linnean identifications which gen­erally require a complete herbarium speci­men. We had to look for micro-characters within the limited archaeological material that might give us some approximations to species identity, and even more remotely, of the wild/cultivated differentiation. Most work of this sort, after the initial stages, produces an hypothesis to prove or dis­prove. Ours, which was partially stated by Yen (1980:142), can now be expanded as a prelude to the description of the material.

For the non-specialist who may find I Dr. Yen’s discussion too technical, the following explanation may be helpful. In general the situation has been sug­gested to be something like this. Wild rites have an irregular pattern of cells on the husk. This irregularity exists in terms of both cell shape and the arrangement between cells. Domesticated rice (Oryza sativa) is different. Here the husk cellular pattern is regu­lar.

Cells tend to be squarish and arranged in a regular ‘checkerboard’ pattern. It is presumed that the more regular the cellular pattern the more domesticated an individual sample can be said to be.

The Influence of The Modern View of Rice Origins

“The Asian rice (0. sativa) evolved from an annual progenitor over a broad belt that extended from the Ganges plains below the foothills of the Himalayas, across Upper Burma, northern Thailand, and Laos, to North Vietnam and south China” (T.-T. Chang, 1976:143).

Our adoption of this scheme (Fig. 1) is possible only because of the splendid research done by plant geneticists of south and east Asia. The very wide geographic origin that transcends modern political and cultural boundaries, however, conforms to the definition by Harlan (1971,1975) of a ‘non-center’ (in its more debatable relation­ship with the true ‘centers,’ in this case north China), where the domestication of one plant could occur many times within human history, and be dispersed over many thousands of square kilometers. A corollary to Harlan’s theory may be that the direc­tions of selection in the process, and the genetic nature of the subject species, were not necessarily the same in each location since they may have been separated not only spatially but temporally. This may find some support in the differentiation of modern races of rice into the groups Indica, Japonica or Sinica and Javanica (Fig. 1). Each of these has distinctive characters involving some genetic isolation between groups as well as anatomical and quantita­tive contrasts and geographic separation. Thus, at a very particular scale of study, rice remains recovered from-several archae­ological sites could exhibit significant inter-site differences. It may well be that such variation would be expressed in the wild characteristics of cellular structure possibly detectable in the fragmentary husk inclu­sions in pottery. Such an hypothesis takes literal cognizance of the long held view that domestication is a process rather than an event—and thus evidence of domestication should include intermediate stages between wild and cultivated states. In the adoption of such an approach, the study of the mate­rial requires control comparisons, not only of domesticated rice but of the recognized close Oryza relatives as well. In terms of the identifications that have been made of the recently excavated Thai materials, this may suggest that the Banyan Valley Cave and Non Nok Tha materials represent dif­ferent directions of domestication, different stages that yet did not form a connected series. Chang’s identifications (see earlier), read carefully, may further suggest that the Non Nok Tha material could represent the man-guided evolutionary pathway towards rice that was closer than that from the northwestern site. Indeed, it may be that as more ‘rice’ remains are found in late Hoabinhian sites, examples of the blind alleys of domestication may be found—remains with wild characters, or those inseparable from wild Oryza forms. In other words, these would represent the dis­cards in the progress of the dispersed process of rice domestication, which, in their day, held promise for their domesti­cators—early or incipient farming groups of Southeast Asia.

It is hoped that this digression into the sometimes vexing questions of agricultural origins may show its relevance in this re­port on Gorman’s Ban Chiang pottery mate­rial. In the course of this study, we were able to include similar pottery material from the site of Ban Nadi. This is 25 km. southwest of Ban Chiang, and was exca­vated by Charles Higham (1981), one of the leading participants in Gorman’s earlier work.

Descriptions of Material

During the 1974-75 excavations at Ban Chiang, occasional charred grains were re­covered which Gorman identified as ‘rice’ (personal communication). These were often, but not always, associated with burial goods, the earliest of which, because of the incidence of painted pottery, could have been as early as 1600-1200 B.C. or Phase IV on the approximate chronology of Gorman and Pisit (1976). Inspection of this material confirmed that it was Oryza but its con­sistently small size possibly indicated that it was wild. On the other hand, three things suggest that the rice could have been cultivated:

(1)    There is ample evidence that rice was already cultivated at this time in India and China.

(2)    Shrinkage through the firing of the pottery and due to archaeological depo­sition could neither be eliminated nor allowed for. Experiments reported by Renfrew (1973:11) comparing fired and unfired grain samples of wheat, barley, oats and rye, offer us a cautionary note in this consideration of Oryza.

(3)    Cultivated rices collected from indig­enous subsistence farmers of northwest Thailand, include varieties that are no larger in grain size than those identified as ‘wild’ in the archaeological husk samples that had been excavated from Banyan Valley Cave (Yen, 1977:587).

In citing (3) we are obviously deferring to our previous discussion of the nature of rice origins in a non-center.

To further investigate this question of whether the Ban Chiang and Non Nok Tha rices were domesticated or not, we turned to the pottery sherds once again and the anatomy of cell structure as a possibility for identification. This is similar to the experience of Buth and Saraswat (1972) working on Indian archaeological materials, who stated that charred caryopses are better material for identification than charred grains, because of the preserved cellular details. Unfortunately, they did not specify ‘the morphological and anatomical details to enable classification at least up to groups of species’ (p. 33), other than to indicate the ‘typical chess-board pattern of cells of husk in surface view’ (pl. 1) as diag­nostic of Oryza sp. As will be seen, this criterion was to prove inadequate in terms of our materials.

The study of the first 80 sherds from Ban Chiang allowed us to settle on a technique for the investigation of the second set of 67. We adopted three initial approaches: 1, Low-power light microscopy: At 18-20x magnification, we could distinguish two predominant forms of Oryza remains: impressions that were of a chess-board pattern, and the still identifiable, actual remains of husks. Generally, only the impressions were detectable on the inner and outer surfaces of sherds. The direct evidence of husks themselves, first found on the broken edges, as well as further impressions, could be more consistently seen by making new breaks across the sherds. Figure 2 shows a par­ticularly productive sherd, with a con­centration of impressions and burnt husk on a broken facet.

2, X-ray inspection: Owen Rye suggested an adaptation of an x-ray technique that he had used (Rye, 1977) in the study of pottery temper, to quickly detect organic content. We found that although all the Ban Chiang sherds contained organic matter, there was considerable variabil­ity in content or density, but we could not associate these differentials with position on the pot of which the sherd was originally a part. It was noted, how­ever, that the four rim sherds in the first sample of 80 were among the lowest in density scores for organic matter.

3. Scanning electron microscopy (SEM): John Preston of the SEM Facility at Australian National University sug­gested the use of this form of micro­scopy to overcome the difficulties that

we were having in defining the cellular structures in our material using a normal light microscope. After we had coated the freshly broken sherd fragments with gold, the high resolution capability of the SEM enabled us to see clearly husk and impression with associated struc­tures. Figure 3 exemplifies the utility of this approach to the material, All frag­ments of husk as represented in the pottery were of minute proportions, the maximum being 1000µ at their longest dimensions.

It was obvious that the SEM would be the major tool for the study of the second, calibrated group of sherds requested of Gorman. Some limitation, however, re­stricted the choice of sherds. Gorman had to be certain that he did not require the sherds later for thermoluminescence dating, since both x-ray (Rye, 1977) and SEM (John Head, personal communication) would have adverse effects on the material for that purpose.

By using the photographic attachments of the SEM, it was not only possible to obtain a permanent record of the scanning of each sherd but, standardized at three magnifications, the prints could be used for more extended, detailed observations and measurements.

An integral part of the study was, of course, the determination of cellular characteristics of contemporary wild and culti­vated forms of Oryza as control compari­sons with the archaeological material. We coated whole grains as we had coated the sherds and scanned them at the same mag­nifications. Table 1 incorporates the control samples used, representing species recog­nized as having an ancestral role in the evolution of rice. The problems of tax­onomy, such as the questionable separation of Oryza rufipogon and Oryza perennis, are here skirted by simply presenting the iden­tification of the donor, and the provenience of each sample. The Table also includes the anatomical features provided by T.-T. Chang (personal communication) as possible dif­ferentiating features between wild species and cultivated rice. For the latter, we used modern, highly bred varieties and cultivars collected from subsistence farmers of northeast and northwest Thailand.

An ancillary control was the SEM pho­tography of plant parts other than the husks, which we thought might be found in the pottery. These included sterile glumes (the husk glumes with which we are dealing are called ‘fertile’), awns (the usually elongate attachments at the distal end of the husk, often characteristic of wild species and subsistence varieties of domes­tic rice), petioles or the stemlet attachments of the grain to the main stems of the plant, stems and leaves. We were also prepared for the identification of grain fragments—and less so for the remains of other species —but we have controls available of two of the commonest weeds, Chenopodium and Amaranth us, associated with modern rice paddies and swiddens (wet- and dry-land traditional cultivations).

As far as parts of Oryza other than husks are concerned, they are virtually absent in the pottery, except for the very occasional inclusion of grain fragments (Fig. 5). While, perhaps due to frequency of differ­ential preservation through firing, the husks predominate, it is highly likely that this reflects the condition of the grain after har­ vest. The significance of this innocuous observation is treated in the following sec­tion on pottery making.

Oryza Husks and Ban Chiang Pottery

Although it may not seem so, we already have data on which some implications re­garding the manufacture of Ban Chiang pottery may be drawn:

(1)  Since Oryza husk particles have been found in every sherd we have examined, it is a justifiable contention that such inclu­sion was a part of pottery-making tech­niques throughout the cultural sequence. Rye (1981:33) has noted the use of crop plant waste as temper, citing straw remains in southern Arabian ceramics. He states that its function is to reduce shrinkage and improve the workability of clays that are too plastic. He also notes that much organic matter is burnt out in firing, leaving voids which interrupt cracking in cooking vessels due to thermal stress.

(2)  Again, according to Rye, uniformity and fineness of inclusions of organic matter indicate that they are more likely to be deliberate additives to the paste than natural occurrences in the original clay matrix.

(3)  The relative purity of the organic remains indicates something of the nature and derivation of the husks prior to inclu­sions as temper. Its most likely condition is that they are the winnowed byproduct of milled grain or caryopses. Such a procedure conforms to agricultural practice with rice in modern Thai villages where stored grain, from threshing floors after harvest, is milled according to individual household require­ments prior to each meal. Since the large wooden mortars for milling are seldom moved from their position near houses, stockpiles of husks accumulate from win­nowing. The earlier threshing process, by which the dried bundles of spikes brought in from the field at harvest are divested of the whole grain (with husk still intact for storage), also eliminates most of the ap­pended structures of the grain (awns, if any, petioles, leaves, stems) through the first winnowing. This contrasts with other Southeast Asian practices, such as in the Philippines, where such hill people as the Bontoc (Jenks, 1905) and Ifugao (Conklin, 1980) store their grain as dried bundles. Milling consists of the pounding of these  bundles. If these winnowings were used for pottery making, fragments of grain append­age material would be expected in the paste components.

Rye (1981:34) makes the suggestion that the inclusion of such post-harvest material indicates the seasonality of pottery making, but agricultural storage is a factor that may limit adoption of this idea in the Ban Chiang case. What we do not know is whether such storage techniques existed any time in prehistory, whether any of the archaeologi­cal evidence for structures is mute testa­ment of the presence of specialized or un­specialized granaries (e.g. granaries are a part of residence structures in lfugao, whereas they are smaller discrete and spe­cialized structures in modern north Thai­land). Be that as it may, the paucity of evi­dence for plant genera other than Oryza in the Ban Chiang pottery reflects not only the deliberate nature of its inclusion, but also the careful nature of grain harvesting which excluded contaminants such as weed species at the milling stage.

Of course, one may suggest that such contaminants are destroyed differentially on firing. However, if modern village prac­tice is considered relevant, collections of winnowed husk material from northwest Thailand made by the writer from freshly milled grain were notable for the absence of other species. However, despite the vigor­ous pounding, the surviving husk remains were considerably larger than those found in the archaeological sherds. Further and more direct ethnographic observations have been made on the association of rice husks with pottery making in the region of Ban Chiang. Observations by Gorman and Joyce White indicate that the incorporation of rice husk into matrices of modern pottery is done in two stages: first, a mixture of clay and rice husk in approximately equal proportions by volume is fired in regular shapes, round, cylindrical or brick-like, and then stored. When pot making is under­taken, these are crushed and added to fresh clay, again in the same proportion, as a sort of ‘grog,’ which is strictly defined as crushed damaged pottery sherds (Rye, 1981:33). Gorman collected small samples of three stages of pottery manufacture—the fired primary mixture of clay and husk, the crushed grog, and a body sherd of a finished pot. The first sample was the most revealing, since the husk fragments and im­prints were much larger than those in the archaeological pottery, with many nearly whole pales and lemma (the two separate parts of the glumes enclosing the rice grain). The grog however, had been so thor­oughly ground that there were only a few structures confidently identifiable as rice husk. In the SEM scanning of the sherd, we were unable to find evidence equivalent to that in the excavated pottery.

On this sampling then, admittedly a small representation of modern northeast Thai potting technique, it would seem that the prehistoric incorporation of husk material into the pottery paste was effected by some similar secondary reduction of its size, not as drastically as evidenced in the ethno­graphic example. Perhaps this reflects something of the function of pots, for in modern times, with the universal adoption of metal culinary gear, the heat resisting property in cooking use is hardly an imperative.

Whatever kind of economy we are ad­dressing at any stage in the prehistoric Ban Chiang sequence, whether grain agriculture or a form of grain harvest in a hunting/ gathering pattern, one thing seems certain. The conversion of a subsistence byproduct to an ‘industrial’ use is a constant from the beginning of the sequence, through all of its cultural transformations.

Towards Identification

This section describes, in summary, the survey of the Ban Chiang sherds represent­ing Phases I to VI in the cultural sequence and comparisons with the control—wild species and cultivated rice. The husk im­pressions, whose frequency was greater than the actual husk remains, had to be included in the study, despite the possibility that some qualitative and quantitative fea­tures of the cells might be obscured during the original process of pottery manufacture, e.g. flattening by pressure, or indeed, the effects of firing. However, the husks them­ selves would also undergo undefinable dis­tortional influences. Figure 5 illustrates, with both impression and husk responsible for the imprint, that spacing of cells at least corresponded. The characters studied (see Table 1) then, are differentiated on this basis in this description and comparison with controls.

Cell shape: The surface structure of the grain husk cells is recognized as an impor­tant taxonomic character but, generally, such criteria have been applied only to the differentiation of sectional partition of rice (e.g. Kihara and Katayama, 1959), using an impression method on fresh material. The choice of ‘control’ species (Table 1) for our project was based on the characteristics of the preliminary electron microscope scan­ning of the pottery material from Ban Chiang. Since the cells all showed a square or rectangular basic construction, with rela­tively smooth tubercular projections, we knew that the archaeological material would be represented in the Sativae section of Oryza. It may be seen from inspection of the photographs of the pottery material, however, that there is abundant variability in cell structure nevertheless, but, as we have already noted, we cannot assign all of this to the intrinsic nature of the Oryza material it represents, any more than to the possible distortions that could be the result of the ceramic manufacturing process.

Cell size: The variability of shape is paral­leled in size. On representative testing of individual cells, the square shape of the archaeological material was confirmed, so that we attempted to quantify size by meas­uring along the cell rows to obtain an index of cell size (rather than across cell rows that might incorporate error in some exam­ples due to breakage along the inter-row axis). Wherever possible we tried to meas­ure as many rows of ten cells; but as the illustrations show, often that number was not attainable, and normally three was the maximum row number. All measurements were made on the 100 µ magnification. Table 2 shows the range of variability in the pot­tery inclusions for each Phase, compared with controls. Despite the uneven sampling of the archaeological material, it is obvious that its quantitative range exceeds the total range represented by modern wild species putatively involved in rice parentage. We might indulge in speculations of the manu­facturing effects in terms of shrinkage at one end of the range of variations of the size index, and expansion due to compres­sion at the other. The clustering of the cell measurements of most of the pottery husk fragments towards the middle of the range, however, may be more significant. Perhaps controlled experiments on pottery making —the effects of the working and firing on rice husk particle inclusions—may be war­ranted to elucidate the seemingly greater variability of measurable cell size in the archaeological material than observable in control species. If, however, we could accept the results at their face value, it might be possible to account genetically for what is, after all, an asychronic comparison For the control species have been through some 2000 years longer process of ‘natural’ selection than the archaeological material. We do not know the quantitative character. istics of those species at that, and earlier, times. The wide variability of cell size in the pottery inclusions may then be reflec­tions of a wider range of variability in the parental material of 5,000+ years ago, or it may be that hybridizations of wild species, some perhaps gathered for grain, produced segregation for the cell size character that was transgressive of the parental range. Such expectabilities are theoretical config­urations that may well be applicable to the early phases of domestication.

Trichomes: In our first SEM survey of the Ban Chiang pottery, we did not notice the hair development on the husk fragments, so that the indication, on this criterion alone (see Table 1), was that the inclusions rep­resented cultivated rice. However, with the use of higher magnifications, nearly every husk fragment showed signs of breakage of the inter-row trichome features. Moreover, it was in a few examples of husk impres­sions that actual detached trichomes could be detected, while other impressions showed long indentations that could repre­sent trichomes, the actual tissues being lost in the firing process. The potential reversal of ‘identification’ of all specimens as wild Oryza was soon qualified by the observa­tions in the control cultivated rice samples from northern Thailand, when a high percentage were found, even under normal light microscopy, to evidence the presence of trichomes. While it seemed that densities of hair development were lower in culti­vated varieties than in wild species (Figs. 9, 10), the small dimensions of the pottery-included fragments, in relation to their position of origin on original husks, made such relative values meaningless. This can be illustrated in reference to Figure 9. If a husk fragment is extracted from the center or sides of the caryopsis, trichome develop­ment is dense; from the intermediate posi­tions, trichomes are less frequent. This applies to all material—wild species, or those cultivated varieties with hair development.

Towards Interpretation

The differentiation within the Sativae section of Oryza through husk cell compari­son can only rely on the most brittle of comparison, a discovery that had to be made in this project since, as T.-T. Chang (personal communication) has said, every worker with SEM ‘has skipped the hull [husk] and only studied the endosperm and embryo.’ Should we rue the absence of other associated plant structures in our material, or, ideally, comparisons of herbarium standard (virtually whole) plants, let us see what one rice authority says: “In point of fact, there is no character which distinguishes 0. rufipogon Griff. from 0. sativa except that of early and complete shedding of the grain even before it is fully ripe and dry.” (Grist, 1953:265).

Our pottery ‘rice,’ if it had contained recognizable grain attachment structures (pedicels and rachillae), might have told us more; whether the grain ‘shattered,’ that is, fell to the ground before harvest, or was non-shattering, which is generally regarded as an advance due to gene selection. This argument for advanced genetic composition is based on the more-or-less common sense notion that ‘wild’ species of cereals includ­ing rice would be predominantly shattering types since this would promote the seeding process under untended ‘wild’ conditions. When man entered the picture and began to harvest these plants he would tend to select the non-shattering varieties since the seeds on the head of grain would be likely to remain together when plucked or hit by a sickle. Thus, over long periods of harvest we believe that gradually plant populations were shifted from being predominantly shattering to non-shattering. It must be remembered however, that the perennial rufipogon form is not thought to be the immediate progenitor of the annual sativa. That status is reserved for the annual and wild nivara, so what are the possibilities of distinguishing sativa from it?

Indeed, T.-T. Chang’s identification of the Non Nok Tha material as intermediate be­tween a wild race (presumably sativa, a further complication) and a weed race may be as serviceable (and non-committal) an identification as we can apply to our study material. We may hypothesize that what we are looking at is a mixture of quantitative genes affecting the expression of husk cell structures, some of which were retained (e.g. large, squarish, thicker walled cells) in more developed rice varieties, some subject to negative selection that was never com­pletely eliminative (e.g. trichome formation).

There is abundant testament (e.g. Grist, 1953; Oka, 1980 in a collection of his earlier essays on rice evolution) that modern pop­ulations of rice, not subject to pure line selection but grown in proximity to wild Oryza populations, will often exhibit gene exchanges. It is thus not unlikely that popu­lations of ‘rice’ already cultivated 5,000 years ago should show a similar effect of hybrid­ity. As stated elsewhere (Yen, 1980), early domestications (and not necessarily the first or only) must be hard to identify, especially when they are evolved, and still evolving through a process of hybridization and selection. In a non-center situation, the directions of selection may be narrow in terms of total variability, but broad in terms of human preference and the element of chance in the unconscious aspects of selec­tion. Perhaps the Ban Chiang rice in those early times was relatively uniform in the utilitarian characters of yield constancy and satisfaction of human preferences—the variability being a desirable feature of genetic buffering against environmental amplitudes. We may never recover husks from early Asian sites that are exactly like those of modern commercial varieties, but we contend that the difference between our archaeological material and some of today’s indigenous subsistence rites is narrower than would be expected from some model of simple lineal progression of evolution of wild to cultivated. That plant domestication is a process rather than an event is a theo­retical concept hard-won since the early studies of de Candolle (1886). Perhaps it is a part of this process that Ban Chiang reflects.

We return to the archaeological context of the Ban Chiang finds. To this writer, it would be incredible for that civilization to have been founded and maintained for over 3,000 years on a grain gathering economy. We have described the culture as sophisti­cated as evidenced by the material manifes­tation of the structure of the society—metallurgy, ceremonial burial practices, animal husbandry, pottery making, and the elaboration of elements of personal adorn­ment that utilize more than natural mate­rials for their effect. Changes there were, not of structure, but within the elements of the components of that structure (style, iron added to bronze, etc.). That Ban Chiang could parallel the Near Eastern examples of Flannery (1969), in which sedentary vil­lage life in early settlements occurred before plant domestication, is unsupported by our plant evidence—for the persistence of ‘wild’ characters through our sequence contrasts with the evidence of wild-to­cultivated conversion in the Iran and other western Asian examples. Flannery (1973: 274 fn) himself, however, conditions his original argument with the caution that wild characters in plants do not prove their non-cultivation . .. our very point.

A classic criterion in archaeology for the presence of cultivation is the quantity of direct plant evidence. We may not have weights and numbers to support our con­tention of agriculture throughout the Ban Chiang sequence, but the quantitative implication is there, embedded by con­sistency and persistency of rice husk frag­ments through the stylistic modulations of the surfaces of the pottery through nearly 4,000 years.

The final question is the provenience of Ban Chiang rice one notes the increasing boldness of the identification), and subjec­tive caution prevails. The immediate origin could have been the next village; the ulti­mate origins could have been nearby or thousands of miles away in the vastness of the Southeast Asian non-center. We turn directly to the prehistorian, for what we seek is inevitably bound to the tracing of the origins of Southeast Asian civilizations in the archaeological records that surely must be forthcoming.

Cite This Article

Yen, Douglas E.. "Ban Chiang Pottery and Rice." Expedition Magazine 24, no. 4 (August, 1982): -. Accessed February 29, 2024. https://www.penn.museum/sites/expedition/ban-chiang-pottery-and-rice/


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