Abstract
Research has generally outlined that the Neolithic East Asian farmers expanded into Southeast Asia, leading to substantial social and cultural transformations. However, the associated archaeobotanical evidence until now has been insufficient to clarify the exact timing, dispersal route, and farming package of the emergence of agriculture in Mainland Southeast Asia. To clarify these issues, the micro-plant remains of phytolith and starch from three Neolithic sites in Ha Long Bay were extracted and analyzed. This study validates the earliest evidence of co-cropping in northern Vietnam, involving the cultivation of rice together with foxtail millet at 4000 years BP or slightly earlier. Moreover, the results indicate that at least two patterns of subsistence strategy were practiced simultaneously during the initial farming phase in the region. The Trang Kenh people, a regional variant of the Phung Nguyen cultural group often have been seen as the first farmers in northern Vietnam, and they mainly practiced a cereal-based subsistence strategy with more vital cultural characteristics of southern China origin. Meanwhile, the Ha Long people, mainly composed of indigenous hunter-gatherer descendants, continued to utilize a wide range of their preferred plant resources such as taros, yams, and acorns, while they absorbed and incorporated new elements such as millet and rice into their food system. This study provides solid information to understand the diverse economic systems among different cultural groups in Vietnam.
Introduction
Several studies based on archaeology, linguistics, and genetics have suggested that farming groups with rice and/or millet domestication originated from central China and expanded into Mainland Southeast Asia through southern China, admixing with or replacing the indigenous hunter-gatherers around 4000 years BP (Before Present) (e.g., ; ; ; ; ; ; ). The arrival of rice and millet agriculture and their domesticators led to significant social, cultural, and economic transformations in Mainland Southeast Asia, including technological advancement, demographic expansion, and cultural complexity.
Recent archaeobotanical studies have confirmed that both rice and millet agriculture occurred in southern China at about 5000-4800 cal. years BP. For instance, phytoliths from rice (Oryza sativa) and broomcorn millet (Panicum miliaceum) were discovered from the Tanshishan cultural layer (ca. 5000-4500 cal. years BP) at Baitoushan in coastal Fujian (). Gancaoling in the Pearl River Delta of Guangdong documented the co-cultivation of rice and foxtail millet (Setaria italica) around 4800-4600 cal. years BP (). In the inland terrain of southwest China, rice and millet mixed cropping emerged in Guijiabao in southern Sichuan about 5000 cal. years BP (; ). The earliest crop package comprising foxtail millet, broomcorn millet, and soybean began around 4650 cal. years BP in Baiyangcun in northwestern Yunnan (; ). Until now, the southernmost Neolithic site with evidence of rice-millet cultivation in Yunnan was from Shifodong, where rice and foxtail millet were retrieved from a context dated to ca. 3400-3100 years BP (; ) (Figure 1).
Figure 1
In Mainland Southeast Asia, evidence related to rice comes from a few Phung Nguyen sites in northern Vietnam () and much farther south in the Mekong Delta region, such as at An Son and Loc Giang, dating back to 4200-3150 cal. years BP (; ). Additional early rice remains were recovered from the Neolithic coastal site of Khok Phanom Di in Thailand, dated 4000-3500 cal. years BP (; ; ). So far, the earliest evidence of foxtail millet has been from Non Pa Wai in the Khao Wong Prachan Valley, where a single foxtail millet grain was dated to 4470-4200 cal. years BP, but rice was dated no earlier than 3000 BP at this same site (). Before this study, Rach Nui (3500-3300 cal. years BP) in coastal southern Vietnam was the only known site with rice and foxtail millet, both from the same cultural layer. However, these crops were more likely acquired through trade or exchange from other farming societies () (Figure 1 and Table 1).
Table 1
| Country | Site | Province | Age (BP) | Collecting method | Rice | Foxtail millet | Broomcorn millet | Reference |
|---|---|---|---|---|---|---|---|---|
| Vietnam | Dong Dau | Vinh Phuc | 3400-2800 | Flotation | × | ; ; | ||
| Thanh Den | Vinh Phuc | 3700-2600 | Flotation | × | ||||
| Xuan Kieu | Hanoi | 3500-3200 | Impression | × | ; | |||
| Tu Son | Bac Ninh | 3500-3200 | Impression | × | ||||
| Bai Cu | Thanh Hoa | 4000-3500 | Impression | × | ||||
| Bai Man | Thanh Hoa | 3500-3200 | Impression | × | ||||
| Thach Lac | Ha Tinh | 4000-3500 | Pollen | × | ||||
| Rach Nui | Long An | 3500-3300 | Flotation, phytolith | × | × | ; | ||
| An Son | Long An | 4200-3150 | Impression, microCT | × | ; | |||
| Loc Giang | Long An | 4000-3300 | Impression, microCT | × | ||||
| Cambodia | Krek 52/62 | Kompong Cham | 4620-3690 | Impression | × | ; | ||
| Samrong Sen | Kampong Chhnang | 3800-3200 | Impression | × | ||||
| Mlu Prei | Preah Vihear | 3500-1300 | Impression | × | ||||
| Thailand | Banyan Valley Cave | Mae Hong Son | 5500-1300 | Dry-sieving | × | |||
| Ban Chiang | Udon Thani | 3600-3100 | Flotation, dry-sieving, pollen, impression | × | ; ; | |||
| Non Nok Tha | Khon Kaen | 3500-3000 | Impression | × | ; ; | |||
| Khok Charoen | Lopburi | 3500-3150 | Impression | × | ||||
| Non Pa Wai | Lopburi | 4470-2700 | Flotation | × (after 3000 BP) | × | × | ; | |
| Non Mak La | Lopburi | 4100-2700 | Flotation, phytolith | × (after 3000 BP) | × | × | ; | |
| Nil Kham Haeng | Lopburi | 3350-2500 | Flotation, phytolith | × (after 3000 BP) | × | × | ; | |
| Tha Kae | Lopburi | 3700-3100 | Phytolith, impression | × | ; ; | |||
| Ban Lum Khao | Nakhon Ratchasima | 3400-2600 | Flotation, impression | × | ; ; | |||
| Khok Phanom Di | Chonburi | 4000-3500 | Impression, dry-sieving, hand-picked | × | ; ; |
Major sites with evidence of rice and millets (mark as ×) in Mainland Southeast Asia during the Neolithic period.
Overall, uncertainty has surrounded whether rice and millet domesticates had appeared in Mainland Southeast Asia simultaneously in the first place. The archaeobotanical work has been insufficient to reconstruct the initial dispersal of the timing, route(s), and the combination of crops for early farming into Mainland Southeast Asia. Presumably, the spread of Neolithic farmers and their farming cultures from southern China to Mainland Southeast Asia occurred rapidly and through both inland river systems and coastal roads (; ; ; ; ). The northeastern regions of Mainland Southeast Asia, neighboring both inland and coastal southern China, must have been the first accommodation for the early farmers from the north. Therefore, the Red River floodplain and coastal areas around the Gulf of Tonkin are crucial for understanding the dispersal of early rice and millet and their domesticators into Mainland Southeast Asia.
In northern Vietnam, despite some sporadic reports of pottery impressions from rice husks, or a few carbonized rice (; ; ), the systematic archaeobotanical work to authenticate the evidence of agriculture in this region has been somewhat limited. In this regard, two of the most representative Neolithic groups, Trang Kenh and Ha Long, both coexisted around 4000 cal. years BP in the northeastern coast of Vietnam, and therefore they are ideal for investigating the emergence of rice and millet cultivation in Mainland Southeast Asia. This study investigates micro-plant remains (phytolith and starch) extracted from stone tools excavated from three sites belonging to these two cultural groups in northeastern Vietnam. The new data obtained from this study are incorporated with previously collected data from the Cai Beo site on Cat Bat Island (). All four sites discussed in this study were excavated when the floatation method for collecting macro-plant remains was not yet applied in Vietnam.
Site description
About 4000 years ago, two cultural groups, Ha Long and Trang Kenh, coexisted around the Gulf of Tonkin. The Ha Long group (ca. 4500-3000 cal. years BP) was a developed maritime-oriented society, supported mainly by fishing and hunting, augmented by perhaps a small amount of farming (). Many archaeologists have suggested that a deep root of the Ha Long group can be traced back to the earlier Cai Beo group in the same region, which had developed from the Late Pleistocene Hoabinhian-Bacsonian tradition (; ). Overlaping in time with the Ha Long group, the Trang Kenh group (ca. 4000-3200 cal. years BP) contains strong characteristics of the Neolithic Phung Nguyen (ca. 4100-3200 cal. years BP), often regarded as the most thriving early farming society in northern Vietnam that likely could be traced back to a southern China origin (Figure 2).
Figure 2
While the Trang Kenh group concentrated in the Red River Delta in Hai Phong Municipality, the Ha Long group ranged through the coastal areas and nearby islands of the Ha Long Bay. These two groups, defined by the Vietnamese archaeologists, show differences in many ways, such as their artifact assemblages, burial practices, and other cultural aspects. For example, most of the human burials of the Ha Long group are in the flexed position, the typical practice of hunter-gatherers in Vietnam since the Hoabinhian cultural phase more than 10,000 years ago (; ; ). Some Ha Long burials contain goods such as typical shouldered axes/adzes, pebble pointed tools, grinding stone "Ha Long Mark", bracelets with D/rectangular section and pottery. In contrast, the burial position of the Trang Kenh group is extended, like the cemeteries in early farming societies in southern China and Phung Nguyen sites. Moreover, these burials often contain grave goods such as pottery vessels, lithic tools, and shell or jade ornaments.
To collect the ancient micro-plant remains, this study analyses 20 stone tools excavated from two Ha Long cultural sites, Bai Ben and Bai Cat Don, and the representative Trang Kenh cultural group site, the Trang Kenh site itself.
Bai Ben site
Bai Ben site (N20°46’44”, E106°58’20”) is located in a present-day fishing port surrounded by limestone mountains on the west side of Cat Ba Island () (Figure 1). The site covers an area of 5000 m2 distributed along the main road of the island and the western seashore. An area of 142.5 m2 was excavated over two seasons in 1999 and 2001 (). Excavations at Bai Ben consistently have uncovered a single cultural layer of about 80 cm in thickness. In addition, the site has yielded tens of thousands of drill points, cores, and flakes, suggesting it was a workshop specializing in drill point manufacture ().
Six 14C dates obtained from mollusc shells and plant fragments in Bai Ben suggest an occupation at 4100-3100 cal. years BP (; ) (Figure 3 and Table 2). Bai Ben has yielded ground shouldered and stepped or rectangular axes/adzes, sandstone saw blades, chert ground/flaked pointed tools, grinding stones, stone hammers, anvils, a stone spearhead, and a small number of ornaments including slate and nephrite beads and bracelet fragments (). In addition, earthenware vessels and fragments with rectangular everted rims, curved rims with outer roofs, stamped, incised with “S” shape, and short parallel line motifs, present the typical pottery characteristics of the Ha Long group.
Figure 3
Table 2
| Site name | Sample No. | 14C dates BP | Material | Cal. BP (2σ) | Context | Reference |
|---|---|---|---|---|---|---|
| Bai Ben | HNK-92 | 3900 ± 80 | marine mollusc shells (species unknown) | 3950 - 3453 | Layer 4 | |
| HNK-91 | 3380 ± 55 | marine mollusc shells | 3262 - 2852 | Sterile bottom | ||
| HNK-87 | 3180 ± 55 | marine mollusc shells | 3021 - 2664 | Sterile bottom | ||
| HNK-86 | 3150 ± 55 | marine mollusc shells | 2981 - 2611 | Layer 4 | ||
| HNK- L1 | 3450 ± 120 | plant fragments | 4078-3411 | plant fragments in pottery | ||
| HNK- L2 | 3590 ± 140 | plant fragments | 4346-3493 | plant fragments in pottery | ||
| Trang Kenh | AA-2772 | 3250 ± 55 | charcoal | 3616-3362 | 160-180 cm, M1 Trench 1, 1986 excavation | |
| AA-2773 | 3340 ± 70 | charcoal | 3821-3400 | 180-200 cm, M2 Trench 2, 1986 excavation | ||
| Bln-3710 | 3260 ± 150 | charcoal | 3884-3079 | 160-180 cm, M1 Trench 1, 1986 excavation | ||
| Bln- 891 | 3405 ± 90 | charcoal | 3885-3451 | 190 to 210 cm, Trench 1A, 1969 excavation | ||
| ZK-307 | 3005 ± 100 | charcoal | 3442-2885 | 140 cm, Trench 1B, 1969 excavation | ||
| ANU-10884 | 3440 ± 60 | charcoal | 3868-3495 | Layer 5, 175 to 190 cm | ||
| BA-97005 | 2390 ± 60 | charcoal | 2706-2332 | layer L2 | ||
| BA-97006 | 3330 ± 90 | charcoal | 3827-3377 | layer L2 | ||
| BA-97007 | 3910 ± 60 | charcoal | 4519-4153 | layer L2 | ||
| BA-97008 | 3080 ± 60 | charcoal | 3445-3080 | layer L3 | ||
| BA-97009 | 3190 ± 60 | charcoal | 3561-3250 | layer L3 | ||
| BA-97010 | 3000 ± 60 | charcoal | 3354-3002 | layer L3 | ||
| BA-97011 | 3390 ± 60 | charcoal | 3827-3469 | layer L4 | ||
| BA-97012 | 3440 ± 60 | charcoal | 3868-3495 | layer L4 | ||
| BA-97013 | 3530 ± 70 | charcoal | 4066-3591 | layer L5 | ||
| BA-97014 | 3220 ± 60 | charcoal | 3573-3267 | layer L5 | ||
| HNK-1/1 | 3035 ± 160 | charcoal | 3570-2789 | 140 to 160 cm | ||
| HNK-KT3L1 | 2970 ± 115 | plant fragments | 3441-2851 | plant fragments in pottery | ||
| HNK-KT3L2 | 3120 ± 135 | plant fragments | 3680-2960 | plant fragments in pottery |
Radiocarbon dates from Bai Ben and Trang Kenh.
Calibrated through OxCal v4.4.2 (
Vietnamese archaeologists generally regard Bai Ben as a late Ha Long cultural site. However, much evidence from the site has reflected the cultural interactions between Ha Long and other groups, such as Phung Nguyen in the Red (Hong), Da, Lo, and Day River, Hoa Loc in northwestern Thanh Hoa Province, and some contemporary workshop sites like Trang Kenh in Hai Phong (
Figure 4

Stone tools from Bai Ben (A–E), Bai Cat Don (F–O), and Trang Kenh (P–T) for this study; (A, F–K, P) Grinding stone, (B, C, L, Q, R) Muller/Pounder, (D, O) Grinding stone tools “Ha Long Mark”, (E) Short axe, (M) Pitted pebble, (N) Shouldered axe fragment, (S) Chopper, (T) Adze.
Table 3
| Tool | Field number | Tool type | Starch Type | Total | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Aroid | Yam | Palm | Ginger | Millet | Acorn | Bean | Rice | ||||||
| Ia | Ib | IIa | IIb | III | IV | V | VI | VII | VIII | ||||
| Bai Ben site | |||||||||||||
| 1 | 01 BB H11 L3 a2: 141 | Grinding stone | 5 | 1 | 1 | 3 | 10 | ||||||
| 2 | BB 99. TS2. T1 M1 L3. e2: 410 | Muller/Pounder | 11 | 6 | 1 | 18 | |||||||
| 3 | BB 99. TS2. T1 L5 b4: 1242 | Muller/Pounder | 6 | 2 | 1 | 1 | 10 | ||||||
| 4 | 01 BB H11 L3 c2: 220 | Grinding stone tool “Ha Long Mark” | 1 | 1 | 2 | ||||||||
| 5 | 01 BB H11 L3 b4. 87 | Short axe | 6 | 2 | 3 | 11 | |||||||
| Total | 29 | 11 | 3 | 3 | 1 | 4 | 51 | ||||||
| Total % | 56.86% | 21.57% | 5.88% | 5.88% | 1.96% | 7.84% | 100.00% | ||||||
| Bai Cat Don site | |||||||||||||
| 1 | 13 CD H1 L1 b3. 32 | Grinding stone | 1 | 1 | 2 | ||||||||
| 2 | 13 CD H1 L1 b5 | Grinding stone | 6 | 3 | 9 | ||||||||
| 3 | 03 CD H1 L4 A1: 94 | Grinding stone | 9 | 2 | 3 | 1 | 1 | 16 | |||||
| 4 | 03 CD H1 L4 D5 | Grinding stone | 3 | 1 | 4 | ||||||||
| 5 | 03 CD H1 L3 D2. 76 | Grinding stone | 1 | 1 | 2 | 4 | |||||||
| 6 | 03 CD H1 L3 D1 | Grinding stone | 1 | 2 | 2 | 1 | 6 | ||||||
| 7 | 13 CD H1 L1 a5.8 | Muller/Pounder | 1 | 1 | |||||||||
| 8 | 03 CD H1 L4 A4 | Pitted pebble | 1 | 1 | 2 | 4 | |||||||
| 9 | 13 CD L1 a3. 56 | Shouldered axe fragment | 1 | 2 | 3 | ||||||||
| 10 | 03 CD H1 L2 b2 | Grinding stone tool “Ha Long Mark” | 11 | 1 | 12 | ||||||||
| Total | 32 | 2 | 7 | 1 | 4 | 11 | 2 | 2 | 61 | ||||
| Total % | 52.46% | 3.28% | 11.48% | 1.64% | 6.56% | 18.03% | 3.28% | 3.28% | 100.00% | ||||
| Trang Kenh site | |||||||||||||
| 1 | 35 D18 C | Grinding stone | 6 | 4 | 5 | 15 | |||||||
| 2 | H1 L7 d4 734 D18 | Muller/Pounder | 5 | 1 | 10 | 2 | 18 | ||||||
| 3 | 96 TK L3 (5) D4 552 | Muller/Pounder | 2 | 2 | |||||||||
| 4 | 96 TK L5 (5) D622 | Chopper | 2 | 2 | |||||||||
| 5 | 86 TK H1 L5 60 | Adze | 1 | 1 | |||||||||
| Total | 14 | 1 | 16 | 7 | 38 | ||||||||
| Total % | 36.84% | 2.63% | 42.11% | 18.42% | 100.00% | ||||||||
Identification of starch grains recovered from the studied sites.
Bai Cat Don site
Bai Cat Don site (N20°44’43.40”, E106°59’33.74”) is a residential site located in the southwestern corner of Cat Ba Island in Ha Long Bay, about 4 km from Bai Ben (
So far, no radiocarbon dates are available from the Bai Cat Don site. During this study, we intended to carbon-14 date samples from Bai Ben and Bai Cat Don, but no dateable materials were available in the curation storage. Still, the similar stone tools and ceramic wares in both the manufacturing materials and stylistic output indicate a context equivalent with Bai Ben and belonging to the late Ha Long cultural phase (
This archaeobotanical study includes ten stone tools collected from 2003 and 2013 excavations at Bai Cat Don. They are six grinding stones, one muller/pounder, one pitted stone, a one-shouldered axe, and one “Ha Long Mark” artifact (Figures 4F–O and Table 3).
Trang Kenh site
Trang Kenh site (N20°57’10”, E106°45’10’’) is located near the estuary of the Bach Dang River in Hai Phong City (Figure 1). It was discovered in 1968 and excavated five times, opening a total of 380.5 m2 (
Many nephrite gouges and adzes were found at Trang Kenh. The most remarkable findings here were the thousands of pieces of debris and debitage from the manufacture of nephrite (jade) ornaments such as bracelets, small rings, and beads, and the associated crafting tools such as saws, chisels, and jasper drills (Figure 5). Trang Kenh is the largest nephrite workshop site known so far in Southeast Asia. It was a specialized manufacturing settlement for making ornaments for exchange with other communities of the Phung Nguyen and Dong Dau groups in the Red River Valley.
Figure 5

Jade ornaments excavated from the Trang Kenh jade workshop.
Burial features frequently contained finished jade ornaments (
Materials and methods: Micro-plant extraction and identification
All the stone tools analyzed in this study had been excavated by Kim Dung Nguyen and colleagues, and the objects have been stored in the Hai Phong Museum and Institute of Archaeology (VASS), Hanoi. As the major goal was to understand their staple food, grinding stone tools were preferred for this study, but other types of lithic tools were tested to investigate their functions. Sediments adhering to the stone tools and dust from the storerooms were collected as comparative samples to exclude the possibility of modern contamination.
The sediments and dust on each tool’s surface first were rinsed with distilled water and then cleaned in an ultrasonic bath with distilled water for five minutes to recover the residues. Next, the ultrasound mixtures were transferred into test tubes and processed to recover the micro plant remains, including starches and phytoliths, in the laboratory at the Department of Archaeology and Natural History, the Australian National University.
The extraction process of starches and phytoliths followed the procedures of previous studies (
The identification of ancient starches was based on the modern reference collections from Vietnam (collected by the authors of this study), the database (http://cmsgd.igsnrr.ac.cn/) built by the Institute of Geographic Sciences and Natural Resources Research (IGSNRR) that contains more than 200 species of plants, particularly the rich morphological data of cereal crops and their wild relatives (
Results
Bai Ben site
A total of 56 starch grains were recovered from the Bai Ben lithic tools (N=5), of which five starch grains could not be classified due to the lack of identifiable features. More than half of the other 51 starch grains were identified as edible Aroids (Table 3). They usually were round or sub-round in shape with multiple flat facets and centric hilum (Figures 6, Group 1A, B;7A, B) (Table 4). The facet starch grains appear widely in many plants with underground organs, so they are difficult to identify into species, especially when the number of recovered starches is small. However, integrated with the former large findings of these types of starches from the Cai Beo site (
Figure 6

Ancient starches recovered from residues on the stone tools (under polarized and brightfield light). Group 1 from Bai Ben site: (A, B) Type Ia, Colocasia spp./Alocasia spp., (C) Type IIa, Dioscorea alata, (D) Type IIb, Dioscorea spp., (E) Type III, Arenga sp., (F) Type IV, Zingiber sp., (G) Type V, Setaria italica,; Group 2 from Bai Cat Don site: (A) Type Ia, Colocasia spp./Alocasia spp., (B) Type Ib, Colocasia esculenta, (C) Type IIa, Dioscorea alata, (D) Type III, Arenga sp., (E) Type V, Setaria italica, (F) Type VI, Quercus sp., (G) Type VII, Vigna sp.; Group 3 from Trang Kenh site: (A) Type Ia, Colocasia spp./Alocasia spp., (B) Type IV, Zingiber sp., (C–E) Type V, Setaria italica, (F) Type VIII, Oryza sativa. Scale bar = 20μm.
Figure 7

Modern starch references relevant to this study (under polarized and brightfield light). (A)Colocasia konishii, (B)Alocasia macrorrhizos, (C)Dioscorea esculenta, (D)Arenga pinnata, (E)Zingiber officinale, (F)Setaria italica, (G)Colocasia esculenta, (H)Quercus francheti, (I)Vigna umbellata, (J)Oryza sativa subsp. japonica. Scale bar = 20μm.
Table 4
| Type | Subtype | Granule shape | Size range (μm) | Mean size (μm) | Hilum | Fissures | Lamellae | Extinction cross | ID |
|---|---|---|---|---|---|---|---|---|---|
| I | Ia | Spherical/Sub-rounded/Rounded polygonal | 5.64-20.42 | 12.69 ± 3.4 | Centric | Absent | Absent | Straight | Colocasia spp./Alocasia spp. |
| Ib | polygonal/round | < 5 | < 5 | Centric | Absent | Absent | Straight | Colocasia esculenta | |
| II | IIa | Triangular/Elliptical | 15.82-40.17 | 27.53 ± 7.71 | Highly eccentric | Rare | Visible on large grains | Bent arms | Dioscorea alata |
| IIb | Ovoid/Elongated ovoid | 12.05-33.06 | 21.41 ± 6.51 | Highly eccentric | Absent | Absent | Bent arms | Dioscorea spp. | |
| III | Elongated ovoid | 12.33-35.83 | 23.77 ± 7.24 | Extremely eccentric | Absent | Absent | Bent arms | Arenga sp. | |
| IV | Ovoid | 13.3-16.26 | 14.78 ± 1.48 | Extremely eccentric | Absent | Absent | Bent arms | Zingiber sp. | |
| V | Polygonal | 7.44-18.12 | 11.75 ± 2.92 | Centric | Lined fissures | Absent | Straight | Setaria italica | |
| VI | Irregular ovoid | 11.16-12.95 | 12.51 ± 0.9 | Slightly eccentric | Absent | Absent | Bent arms | Quercus sp. | |
| VII | Kidney | 29.68-34.66 | 32.17 ± 3.49 | Centric | Small fissures | Absent | Bent arms | Vigna sp. | |
| VIII | Polygonal | 4-6.67 | 5.75 ± 0.83 | Centric | Absent | Absent | Straight | Oryza sativa |
Morphology of starch grains from the studied sites.
Fourteen starch grains with oval or long oval shapes, highly eccentric hilum, and curved cross-arms shared similar morphological features with Dioscorea. Apart from three starch grains lacking the relative references to identify them into species, the other 11 starch grains, ranging from 12.05 to 38.48 μm in size, best matched with the features of the greater yam (Dioscorea alata) (Figures 6, Group 1C, D; 7C). Three starch grains from the palm (Arecaceae) were recovered; they were narrow, elongated ovoid in shape with extreme eccentric hilum, resembling those from Arenga sp. (Figures 6, Group 1E; 7D). One starch grain, 10.3 μm in length and 13.3 μm in width, ovoid in shape, was from ginger (Zingiber sp.) (Figures 6, Group 1F; 7E).
Four starch grains with polygonal shapes exhibited characteristics of millets; they were classified into foxtail millets for more comparable morphological features (Figures 6, Group 1G; 7F).
Bai Cat Don site
Among the 74 starch grains recovered from the stone tools (N=10) of Bai Cat Don, 61 starches could be categorized into six groups, and the remaining 13 starch grains were unidentified. The starches from Aroids accounted for 56% of the total findings (Table 3). This result is consistent with our recent study from the Cai Beo site, where the edible Aroids accounted for half of the total findings (
Compared to our modern references, two clusters of compound grains with the most lengths smaller than 5 μm and faint cross arms under polarized light were identified as taro (Colocasia esculenta) (Figures 6, Group 2B; 7G). Eight ovoid starch grains with eccentric hilum were from Dioscorea, among which six were the best match with Dioscorea alata (Figures 6, Group 2C; 7C). Four starch grains with elongated ovoid shapes were identified as Arenga sp. (Figures 6, Group 2D; 7D).
Starch grains from acorns were rare, represented in merely two granules, 12.95 μm and 11.16 μm in size, and they shared the typical physical features with Quercus sp. (Figures 6, Group 2E; 7H).
Eleven starch grains with polygonal or spherical shape and centric hilum, ranging from 9.17 to 18.12 μm in size, sometimes with linear fissures, exhibited the distinctive features of foxtail millet (Setaria italica) (Figures 6, Group 2F; 7F).
Two starch grains, 29.68 μm and 34.66 μm in length with an ovoid shape and small linear fissures in the hilum part, came from Vigna sp. (Figures 6, Group 2G;7I), found on the shouldered axe in Bai Cat Don.
Trang Kenh site
In the Trang Kenh site, 38 starch grains were recovered from lithic tools (N=5), among which the cereal crops seemed quite crucial as more than half of the total starch grains were identified as millets and rice (Table 3). On the other hand, except for 14 starch grains from edible Aroids (Colocasia spp.; Alocasia spp.) (Figures 6, Group 3A; 7A, B), no starch was found from yams, acorns, or palms at Trang Kenh, reflecting a different plant consumption mode apart from the other two sites mentioned above.
One starch grain from Ginger (Zingiber sp.) is 16.26 μm in size with a nearly round shape, extremely eccentric, and protruding hilum (Figures 6, Group 3B; 7E).
Sixteen starch grains with polygonal shapes fall into sizes between 9.09 μm and 16.52 μm; their morphologies were most comparable with foxtail millet (S. italica) after being compared with modern millets and their wild relatives (Figures 6, Group 3C; 7F) (
Notably, two groups of compound starch grains that shared the typical features of rice (Oryza sativa) (Figures 6, Group 3F; 7J) were discovered on one grinding stone and one muller, reflecting the combination of use as a toolset for processing cereals. The individual starch grains of rice are difficult to identify due to their small sizes and lack of unique attributes. However, when they occur in agglomerations, their unique morphological characteristics with a flat surface, tightly grown together, and clearly defined margin between particles confidently could distinguish rice from other plants (
Discussion
Through this micro-botanical study, two modes of subsistence strategy were revealed in ancient Ha Long Bay, corresponding with the different cultural backgrounds in the mainland and offshore areas separately attributed to Ha Long and Trang Kenh cultural assemblages.
A wide range of plant resources was exploited by Bai Ben and Bai Cat Don residents on Cat Ba Island, including taros, yams, acorns, palm, ginger, and beans, as well as foxtail millet, suggesting that the site’s occupants relied heavily on wild plants or horticulture while using limited amounts of rice and millet products. They may have practiced cropping on a small scale or managed exchange activities with neighboring farming groups, as some archaeologists suspected previously (
Indigenous hunter-gatherers and their tropical plants
The underground storage organs (U.S.O.s) from several species of edible aroids (Colocasia spp.; Alocasia spp.) and yams (Dioscorea spp.) were crucial food resources for inhabitants in Ha Long Bay, which could trace back to Cai Beo culture phase about 7000-5000 years BP (
The cultural use of aroids and yams extends deep into the local traditions of Southeast Asia and the Pacific regions, and aroids are regarded as fundamental in supporting the development of pre-farming societies (
The starches from the pith of Arenga sp. in Bai Cat Don and Bai Ben indicate the continued exploitation or management of palms by the Neolithic inhabitants on Cat Ba Island. Palms were ubiquitous in southern China and Southeast Asia Neolithic sites that have shown their distinctive phytolith and starch morphologies (
The exploitation of tree nuts, such as Quercus, Canarium, and Castanopsis was common practice throughout Southeast Asia and southern China from late Pleistocene to late Holocene, supported by pollen, macro-botanical findings, and starch grain analysis (
Acorn is a time-consuming, high-cost, and low-return economic resource that would have entered into the diet only when people are forced to expand their diet breadth (
Farmers brought the new plants and new recipes
Millets usually have been absent in the early farming sites in Mainland Southeast Asia (Figure 8). In the past decade, the ancient starch grain analysis based on detailed comparative morphological studies on modern millets and their wild relatives has been applied effectively to reconstruct the origins and domestication process of millets in northern China (
Figure 8

Major sites with the evidence of rice and millets in Mainland Southeast Asia during the Neolithic period. 1. Dong Dau, 2. Thanh Den, 3. Xuan Kieu, 4. Tu Son, 5, Trang Kenh, 6. Bai Ben, 7. Bai Cat Don, 8. Cai Beo, 9. Bai Cu, 10. Bai Man, 11. Thach Lac, 12. An Son, 13. Loc Giang, 14. Rach Nui, 15. Krek 52/62, 16. Samrong Sen, 17. Mlu Prei, 18. Banyan Valley cave, 19. Ban Chiang, 20. Non Nok Tha, 21. Khok Charoen, 22. Ban Lum Khao, 23-25. Non Pa Wai, Non Mak La, Ni Kham Haeng (labeled as millet sites, because no rice was found in the Neolithic period of these three sites), 26. Tha Kae, 27. Khok Phanom Di (see details in Table 1).
Foxtail millet (S. italica) has been found at all three study sites, and Trang Kenh has yielded both foxtail millet and rice, showing the earliest multi-cropping in Mainland Southeast Asia. During this time, with the sea level falling near the present level around 4000 years BP, flatlands with fresh water supply appeared in the upper streams of the coastal basins in northern Vietnam (
No clear evidence of broomcorn millet has yet been found in northeastern Vietnam; a similar multi-cropping pattern and lacking broomcorn millet have been reported on the Guangdong coast. Broomcorn millet has been discovered more frequently in southwest China and central Thailand (
As mentioned, individual starch grains from rice are small and not easy to identify, but the confidence is much higher when they are found in sheets or clusters. The starch grains from rice were documented successfully in many sites dating from 9000 to 7000 cal. years BP in China’s Huai River and Yangtze River region (
The presence of starch grains from Vigna sp. at Bai Cat Don suggests the region-wide behavior of exploiting beans in Neolithic southern China and Mainland Southeast Asia. For instance, rice bean (Vigna umbellata) and azuki bean (Vigna angularis) are locally essential legumes that have been domesticated in Southeast and East Asia (
Although the bean starch from Bai Cat Don is too little to determine species, two possibilities are proposed with the newest genetic and archaeobotanical study. First, they were collected locally, noting that the wild progenitors of Vigna umbellata have been found in the most extraordinary genetic diversity in Mainland Southeast Asia (
Spatial-tempo transition of subsistence patterns along with cultural transformation
The plant consumption history from 7000 through 3000 years BP in Ha Long Bay could be reconstructed by integrating our previous findings (
Figure 9

The proportions of different plants recovered from the four studied sites (multicolor histogram correlate to the left coordinate axis), and the average number of starch grains recovered (gray dots and solid line correlate to the right coordinate axis). The average number of starch grains found on each stone tool from the Cai Beo and Early Ha Long phases was 100, but the number dropped in the Late Ha Long and Phung Nguyen phases to below 10 grains on each tool. Clearly, the numbers of rice and millet increased through time.
As presented in this study, the transition of subsistence strategies became more apparent in the Late Ha Long culture around 4000 years BP. The average starch grains recovered on stone tools from Bai Ben and Bai Cat Don experienced a sharp decrease compared with the preceding phases in the Cai Beo site (Figure 9). The number of grinding stone tools from this period gradually declined, representing another cultural indicator of a possible subsistence transition. Although the diversity of utilized plant species became less (
In a broader context in prehistoric southern China and Southeast Asia, hunting and gathering often continued as essential subsistence activities even after the arrival of animal and plant domesticates (
Given that the majority of Ha Long cultural inhabitants were descendants of indigenous hunter-gatherers and exhibited distinct cultural contexts with other farming groups in northern Vietnam, the foxtail millets discovered in Bai Ben and Bai Cat Don were perhaps acquired through exchanges or trades. As mentioned, from an archaeological perspective, the Ha Long group appears to have sustained contacts and exchanges with other groups, such as Phung Nguyen, Ha Giang, Mai Pha (Lang Son), Hoa Loc, and offshore islands along the South China Sea coast (
At Trang Kenh, which represented a typical Neolithic farming site with extensively worked jade remains, the discovered plant resources showed that people relied on cereal-based farming (Figure 9). This subsistence pattern coincided with a cultural background of agricultural communities that depended heavily on cultivated crops, which contrasts with hunter-gatherers that explored a broad range of wild plant resources. The limited discovered amount of rice and foxtail millet from Trang Kenh may have been due to stone artifacts from this site mainly related to nephrite ornaments manufacturing. The stone tools associated with daily life were far fewer. More findings undoubtedly will be recovered in the residential areas in future work.
Conclusion
The archaeobotanical studies from three Neolithic sites in Ha Long Bay reveal that rice and millets already existed in northern Vietnam around 4000 years BP. Based on the comparison of cultural assemblage and chronology in the study and neighboring regions, the multi-cropping likely can be traced back to 4500- 4000 years BP in the northern part of Mainland Southeast Asia. The coastline along the South China Sea probably contributed a role in expediting the early cultural interaction and rapid movement of farming groups into northern Vietnam. However, the cultural contacts with southwest China through inland routes are apparent as well, which could be exemplified by the discoveries of Yazhang jade blades and other identical pottery and lithic tools of southwest China characteristics from the Phung Nguyen cultural sites (
Based on this study, we can reconstruct two plant-based subsistence patterns, which coexisted in northeastern Vietnam from 4000 through 3000 years ago, and two different cultural groups practiced them, perhaps with their own cultural and biological backgrounds (
Funding
This study was funded in part by the Australian Research Council (Grant Number: DP190101839), the National Natural Science Foundation of China (Grant No. 41930323), and the Chinese Scholarship Council (Grant Number: E94962376).
Acknowledgments
We appreciate Director Dr. Doi Nguyen (Institute of Archaeology, Vietnam Academy of Social Science, Hanoi) and Deputy Director Mr. Do Xuan Trung (Hai Phong Museum) for their support of this study.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Statements
Data availability statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Author contributions
H-CH, WW, and KN conceived and designed the study. KN and HL provided the archaeological samples. H-CH, WW, KN, HL, and CZ collected the study samples. WW completed sample identification and data analysis. XY assisted with the starch identification. WW and H-CH wrote the manuscript. MTC edited the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
agriculture, phytolith, starch, rice, millet, Ha Long Bay, Vietnam, Southeast Asia
Citation
Wang W, Nguyen KD, Le HD, Zhao C, Carson MT, Yang X and Hung H (2022) Rice and millet cultivated in Ha Long Bay of Northern Vietnam 4000 years ago. Front. Plant Sci. 13:976138. doi: 10.3389/fpls.2022.976138
Received
23 June 2022
Accepted
10 October 2022
Published
02 November 2022
Volume
13 - 2022
Edited by
Jianping Zhang, Key Laboratory of Cenozoic Geology and Environment, (CAS), China
Reviewed by
Chinyung Chao, Academia Sinica, Taiwan; Yuchao Jiang, Zhengzhou University, China
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Copyright
© 2022 Wang, Nguyen, Le, Zhao, Carson, Yang and Hung.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Hsiao-chun Hung, Hsiao-chun.Hung@anu.edu.au
This article was submitted to Plant Systematics and Evolution, a section of the journal Frontiers in Plant Science
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