Background

The Tibetan speaking population inhabits highland areas of Central Asia in five countries of the region, namely China, India, Bhutan, Nepal and Pakistan. Most Tibetans live in the People’s Republic of China. Due to the inaccessibility of many Tibetan-inhabited areas and the political isolation of the region throughout the 20th century, the number of ethnobotanical studies among Tibetans has been disproportionally small relative to the biocultural diversity present in the Tibetan Plateau and adjacent areas [17].

So far the wild food plants used by Tibetans have been documented in only a few studies. A team of scholars from Beijing recorded them in the Shangri-La region in Yunnan [2], Boesi researched Litang, Sichuan [1], and Kang and colleagues the Zhouqu county in Gansu [3]. We know even less about the edible fungi used by Tibetans, though existing publications show that in some communities at least a few taxa are widely collected and eaten [1, 3, 4, 8, 9].

One of the least ethnobotanically explored parts of China is the province of Gansu, which lies in the north-eastern part of the range of Tibetan languages and dialects. In previous expeditions some of the authors of this paper explored another area of western-central China, namely two valleys on the northern slope of the Qinling Mountains in Shaanxi [10, 11], and one mountain valley in south-western Gansu inhabited by Tibetans [3]. Our previous study among the Tibetan people was performed in very unusual surroundings for this ethnic group, i.e., a relatively low elevation of around two thousand m a.s.l. In contrast, the study whose results we present in this article concerns a population of Gansu Tibetans living at higher altitudes (around 3000 m a.s.l.), among highland spruce forests.

The documentation of traditional wild foods is important for an understanding of traditional food systems [1217] and for the cultural heritage of minorities living in China, as rapid economic progress increases food availability, and many lesser-used wild vegetables are becoming forgotten. Nowadays we still can interview many people who have good expertise on the emergency foods used during the 1959–61 famine (see e.g., [10, 11]). These people are 60–80 years old now, so in a few years there will be less of them and those remaining may be too old to go to the forest and show these foods. Eastern Asia is a particularly interesting region for the study of wild foods since nowhere in the world are such large numbers of species of wild vegetables used as in China, Thailand, Japan, Korea and neighbouring countries [1724]. Tibetans living at high elevations, in areas with species-poor floras, do not use as many species of wild vegetables, but their skill in utilizing local food resources is remarkable and worth documenting.

Tibetans are classified in China as one minority (Zangzu). However a mosaic of several Tibetan languages and dialects exists. In the study area Thebo (Diebu) Tibetan is spoken, which is not mutually intelligible with any of the neighbouring varieties, neither Amdo Tibetan, Chone (Zhuoni) nor Mbrugchu (Zhouqu). Few reliable sources exist on this dialect [25].

To fill the gap in the ethnobotanical exploration of the north-western part of China we aimed at documenting the use of wild food plants in one Tibetan valley in SW Gansu.

Methods

Study site

The province of Gansu in northwest China (Fig. 1.) has very diverse vegetation. It changes from desert in the north and centre through dry grasslands to deciduous forests in the mountainous south. In the south-west of Gansu, inhabited mainly by Tibetans, the Gannan Tibetan Autonomous Region was established.

Fig. 1
figure 1

The map of the studied area

Tibetans in Gannan constitute a very diverse collection of subsistence economies and speak a variety of dialects/languages, still not sufficiently explored linguistically. In the northern part of the territory, in the grasslands, animal herders predominate. The Diebu (Tebo, Tewo) Tibetans, although living among forests, live both from animal husbandry and farming, whereas in the southern part of the region (Zhouqu), at lower elevations, plant cultivation is the main source of subsistence.

The studied valley is located along a small river valley (the river Yiwa), which is a tributary of Bailongjiiang (the White Dragon River). Bailongjiang valley and its surrounding areas constitute a mountainous forefront of the Tibetan Plateau. The dominant vegetation in the study area is forest, composed of Picea crassifolia Kom., Picea asperata Mast., Picea wilsonii Mast. Sabina tibetica Kom., Sabina saltuaria (Rehd. et Wils.) Cheng et W. T. Wang, Betula platyphylla Suk.etc. Other frequent types of vegetation are grassland and scrub (Beberis, Ribes, Rosa, Clematis and Rubus).

We studied Tibetan villages called Zhagana, near the source of Yiwa River, which is part of the township (zhen) of Yiwa, famous for its picturesque landscape (Figs. 1 and 2). These are: Daiba, Yeri, Dari and Dongwa (with a range of coordinates from: N 34°14ʹ13″, E 103°09ʹ54″ to N34 °14ʹ14″, E 103 °10ʹ 58″).

Fig. 2
figure 2

A general view of Zhagana valley

The Yiwa Township covers an area of 365 km2. The average annual rainfall is 447–762 mm (mainly in summer months), the annual average temperature is 5.7 °C (at altitude 2500 m a.s.l.) and 2.8 °C (at altitude 3000 m), and the frost-free period lasts on average 142 days per year [26]. The studied villages are purely Tibetan. The altitude at which the houses are located ranged from 2800 to 3300 m a.s.l.

The studied population consists of subsistence farmers cultivating oats, barley and potatoes and keeping some yaks, cattle and pigs. Tourism has become an important part of the local economy as the valley has been voted one of the most picturesque places in China. This is causing a suddenly increasing influx of tourists (mainly from the capital of Gansu, Lanzhou). Over the last three years the local population have shifted their main activity from farming to building ad-hoc hiking shelters near many of the village homesteads. Apart from the pristine beautiful landscape, tourists are attracted to the fact that the village of Daiba was one of the headquarters of the famous American botanist explorer Joseph Rock who came to live there in 1925 or 1926 during his expedition to Tewo country (the house where he lived is marked and advertised as a tourist attraction – Fig. 3). Unfortunately Rock’s materials from Gansu sunk with the ship which carried them from Calcutta to the USA during World War II [2729].

Fig. 3
figure 3

The homestead where Joseph Rock once stayed

Data collection

The field research was conducted in August 2015 using the Rapid Rural Appraisal approach [30, 31], and included 30 freelisting interviews (14 interviews – with 11 men and 3 women as single informants and 16 group interviews), which altogether involved 63 people (43 men and 22 women). The mean age of the participants was 55 (median 49, aged from 21 to 83). The research was carried out following the code of ethics of the American Anthropological Association [32] and the International Society of Ethnobiology Code of Ethics [33]. Oral prior informed consent was acquired.

The listed taxa (Table 1) were identified using specimens collected by informants in the forest or in the village. During freelisting we separately asked which species of wild vegetables (including underground organs), wild fruits and wild mushrooms were used. Making three separate freelists enabled comparison of the use of these categories and helped elicit answers from the respondents, who categorized the studied wild products in a similar way [34, 35]. Freelists were made orally and written down on the spot by our team. The conversations were additionally recorded using a digital sound recorder. The interviews were carried out in the local Thebo Tibetan dialect with the use of a local translator, or in Chinese if the interviewee could fluently speak this language. Many older men and nearly all middle-aged and elder women speak only Tibetan, whereas teenagers and young people in their twenties learned Mandarin Chinese at school and could facilitate communication. In contrast to their parents and grandparents they could also write down the plant names using Tibetan script. We recorded the local Tibetan names and transcribed them according to the International Phonetic Alphabet, and sound recordings of plant names were deposited in the Digital Repository of the University of Rzeszów [36].

Table 1 The list of fungi and plants used for food in Zhagana valley

Voucher specimens of fungi were deposited in the herbarium of the University of Warsaw (WA), and plants were deposited in the Herbarium of the Northwest A&F University in Yangling (WUK). Plants were identified using the standard identification key concerning local floras, and their names follow the Plant List [37]. Fungi names follow the Index Fungorum [38].

Around half of the fungi specimens (those whose specimens were gathered) were successfully identified using the DNA barcoding technique [39, 40]. Fungal DNA was extracted from a small part of each fruiting body using a Plant and Fungi DNA Purification Kit (Eurx), following standard protocol. The PCR cocktail was composed of 4 ml DNA extract, 0.5 ml each of the primers (ITS5 and ITS4 in 10 nmol concentration) and 5 ml Type-it Microsatellite PCR Kit (Qiagen). PCR was performed using the following thermocycling conditions: an initial 15 min at 95 °C, followed by 35 cycles at 95 °C for 30 s, 55 °C for 30 s, 72 °C for 1 min, and a final cycle of 10 min at 72 °C. PCR products were estimated by running 5 ml DNA amplicon on 1.5 % agarose gel for 30 min. The PCR products were sequenced with the use of ITS4 primers at the Laboratory of Molecular Biology of Adam Mickiewicz University (Poznań). The obtained sequences were verified visually on chromatograms using BIOEDIT. Nuclear ITS sequences obtained in this study are deposited in GenBank [41], with the accession numbers listed in Table 2.

Table 2 The results of DNA barcoding

Results

Among the twelve most frequently mentioned wild foods are five species of wild vegetables – Pteridium aquilinum (L.) Kuhn (Fig. 4), Notopterygium incisum K.C.Ting ex H.T.Chang (Fig. 5), Allium chrysanthum Regel (Fig. 6), A. cyaneum Regel and Chenopodium album L., two taxa of fungi Lactarius deliciosus and Ramaria spp. (Fig. 7), three species of fleshy fruits (Fragaria orientalis Losinsk, Rubus spp., Ribes alpestre Wall. ex Decne) and two species used as staple foods (Persicaria vivipara (L.) Ronse Decr. syn. Polygonum viviparum L., edible seeds) and Potentilla anserina L. (edible tubers, Fig. 8).

Fig. 4
figure 4

Fried Pteridium fronds. The fronds were dried and reconstituted in water before frying

Fig. 5
figure 5

Nothopterigium is sometimes planted in home gardens as it is appreciated for its celery-like fragrance

Fig. 6
figure 6

Allium chrysanthum flowers dried in the sun for winter

Fig. 7
figure 7

Potentilla anserina tubers boiled and served with butter and sugar. This is an expensive traditional dish served on important holidays

Fig. 8
figure 8

A collection of edible and non-edible mushrooms ready for sorting

We recorded the use of 54 species of vascular plants (Table 1). We also recorded the use of 22 mushroom taxa (Tables 1 and 2), which formed the largest category of wild foods. Fruits formed the largest category of food plants, with 21 species, larger than the wild greens category, which included 20 species eaten after boiling or frying and 7 as raw snacks. We also recorded the alimentary use of 10 species of edible flowers and 3 species with underground edible organs. On average, 20.8 edible taxa were listed per interview (median – 21). The most-listed category of wild foods was green vegetables (mean – 7.5 species, median – 8 species), but fruits and mushrooms were listed nearly as frequently (mean – 6.3, median – 6 and mean – 5.8, median – 6 respectively). Other category lists were very short: flowers (mean – 1.3, median – 1), underground edible parts (mean – 0.7, median – 1).

Most wild vegetables and mushrooms are usually boiled, sprinkled with hot oil and served as side-dishes. Wild fleshy fruits are collected mainly by children and eaten raw. Some green parts of plants are eaten as raw snacks: plants with a sour taste (Rumex leaves, Rheum peeled stalks), solidified spruce sap and nectar sucked out of flowers.

In times of famine or grain scarcity Persicaria vivipara fruits were mixed with barley and used to make flour. This was practiced even up until the 1980s. Other wild staples are the small tubers of Potentilla anserina. They are still gathered now, but are treated only as ceremonial foods, being served during New Year celebrations, funerals and other ceremonial occasions. Their rarer use stems from a very tedious gathering procedure. The tubers are dug out by women in late autumn or early spring. One woman can gather 0.5–1 kg of tubers per day. In the past they also constituted emergency food. Several informants observed changes in the frequency with which wild foods are collected: adults collect and eat less wild vegetables and children snack less on wild fruits. Most people usually use only a few wild vegetables, such as Allium spp., Pteridium and Notopterygium. Some people have stopped eating Chenopodium and Urtica. Due to the increasing involvement of tourism in the valley in the last 5 years, people do not have time to gather fungi in summer, at the peak of the tourist season.

Practically all families dry wild vegetables for later use, however they do not lacto-ferment them. People usually dry bracken (Pteridium) fronds, Nothopterigium leaves and wild garlic (Allium) flower heads. They also dry a few species of mushrooms, mainly morels (Morchella conica; Fig. 9) and milk velvet caps (Lactarius deliciosus var. deterrimus). Morels are an important article of commerce, as is the medicinal Cordyceps sinensis mushroom, which was regarded by our informants as medicinal and not an edible mushroom. Some of our informants stored a few large sacks of morels for sale.

Fig. 9
figure 9

Dried Morchella elata for winter use or for sale

Discussion

The few plant names available in the only other existing paper dealing with Thebo vocabulary [25] are very close to those recorded during the field trip, for instance Potentilla anserina (tsõL in [25], tsõL in the recordings, from Old Tibetan gro.ma) and the word for mushroom (xhawũ in [25], χõ in the recordings, from Old Tibetan ɕa.mo). Note that the sound change from Old Tibetan gr- to Thebo ts- in the word for Potentilla anserina is unique, among the varieties spoken in this region, to the Thebo language (Chone Tibetan for instance has tɕũ:Lwa:H, [42]).

The number of wild taxa eaten in the studied valley is relatively low, much lower than in the lower elevations and in the Qinling Mountains. However the main reason for this is the lower number of species available in a landscape dominated by nearly pure spruce forests. The average length of freelisted wild foods is quite long and similar to other places in the mountains of western-central China. On the other hand, a particularly large number of fungi are eaten, and in this case, the spruce forests are a favourable habitat for many mycorrhizal edible taxa.

Interestingly, the composition of the list of edible taxa highly resembles many areas of Eastern Europe [4350]. The following similarities may be noted:

  • the large number of fungi taxa consumed,

  • similar genera or even species eaten (e.g., Rumex acetosa, Urtica dioica, Chenopodium album, Lactarius deliciosus, Agaricus campestris, Fragaria, Rubus, Sorbus, Ribes, Agaricus, Russula and Morchella),

  • similar length of lists of fungi, fruits and wild vegetables consumed,

  • a high appreciation of the sour taste, in contrast e.g., to Chinese people in the Qinling Mts. [7, 8].

However, the list of the collected taxa and their processing also displays features typical for other east Asian communities – e.g., the use of Pteridium aquilinum, drying wild vegetables for winter, a lack of preserves made of fruits and fungi. The list of species is quite similar to the edible plants used by Tibetan communities recorded by Boesi in the vicinity of Litang (Sichuan) [1]. The people in Litang also eat Potentilla roots, Allium, Rosa shoots, Berberis flowers, Rheum stalks, Sinopodophyllum fruits (Fig. 10), Urtica, Chenopodium and Thlaspi shoots, food is spiced with Carum fruits etc. and Persicaria vivipara is used there under a nearly identical name (rambu). A very similar composition of wild foods was also recorded in south-central Tibet in another study [4]. There, Rheum spp. stalks, P. anserina bulbs, Chenopodium album, Allium and Urtica are also eaten.

Fig. 10
figure 10

Sinopodophyllum hexandrum is called ‘toy pig’ as apart from being eaten it is used for making miniature pigs, as children’s toys

It should be emphasized that although edible mushrooms are highly appreciated in China, it is only in Yunnan that larger numbers of mushroom species are used for food (e.g., [51, 52]). In the areas east of our study area, at lower elevations, in Gansu and Shaanxi, we recorded much lower numbers of species used and the very rare occurrence of drying mushrooms for winter use. For the moment, the use of over 20 fungi taxa in a wild valley makes the studied communities the most mycophilous places outside Yunnan. However this may simply result from the low number of ethnomycological studies in central Asia. For example it is worth noting that the number of edible fungi taxa recorded in this study (22) is similar to that used by Sherpa people in Nepal, on the other edge of the Tibetan Plateau (26 species) [53].

Conclusions

The studied community uses a nearly equal number of fungi, fruit and wild vegetable species. The list of taxa used is not very long for a rural mountain community in Asia, but this stems mainly from the low species richness of the vegetation surrounding the villages.

The ZhaganaTibetans are probably the most mycophilous ethnic group in China outside Yunnan.

The composition of wild food plant taxa is typical for Tibetan speaking areas (e.g., the use of rhubarb shoots, Potentilla anserina, Persicaria vivipara).