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Traditional food plants of the upper Aswa River catchment of northern Uganda—a cultural crossroads

Abstract

Background

In the parkland agroforestry system of northern Uganda, smallholder farming households rely on a diversity of plant species to fulfil their nutritional requirements, many of which also serve a range of medicinal, cultural, and livelihood functions. The purpose of the study was to assemble an inventory of indigenous plant species used as food in four districts within the Aswa River catchment of northern Uganda, and to document their utilization and management by rural communities.

Methods

From July 1999 to August 2000, a series of 61 community-based focus group discussions on the utilization of plant biodiversity were conducted in the vernacular language at 34 sites in four districts of northern Uganda, with participation by key informants self-selected on basis of their technical knowledge and personal interest. Of these, 232 respondents subsequently contributed to a collection of herbarium specimens, which were submitted to the Makerere University Herbarium for identification. On receipt of each specimen collected, a structured interview was conducted to document the botanical, ecological, seasonal, and alimentary attributes of each identified taxon, and details of its processing and utilization by the community from which it was obtained. The data analysis was undertaken during 2019 and 2020, including statistical tests to assess the relative importance of the cited taxa using the Relative Importance Index (RI), and to determine the similarity of edible plant use between the four cultures using the Jaccard Index of similarity (JI).

Results

Key informant interviews yielded 1347 use reports (URs) for 360 identified specimens of 88 indigenous edible plant species. The data describes patterns of use of indigenous edible plants of four cultures of the Aswa River catchment of northern Uganda. RI scores ranged from 0.93 to 0.11, with fruit trees occupying the top 25 taxa (RI 0.45 and above). Jaccard similarity scores ranged from 25.8% between Lango and Acholi, to 15.8% between Acholi and Ethur, indicating that cultural factors appear to be more significant than shared ancestry as determinants of cultural similarity of plant use.

Conclusions

The data constitute an inventory of on-farm plant species, including cultivated, semi-cultivated, and wild plants, integrated into a parkland agroforestry system in which useful trees and other plant species are sustained and managed under cultivation. Agricultural and on-farm plant biodiversity may be seen as a food security resource, and a nutritional buffer against increasing risks and stressors on low-input smallholder agriculture. Further studies should assess the intra-species biodiversity of these resources, with respect to farmer-valued traits and vernacular (folk) classification systems.

Background

If the best time to plant a tree was 20 years ago, then there is no time like the past in which to document traditional technical knowledge.

This study is based on data collection undertaken during 1999 and 2000, as an inventory of species and a situation assessment of plant utilization and management in the parkland agroforestry system of northern Uganda, characterized by a range of landrace crops and a wide distribution of multipurpose tree species, which are selectively retained by farmers when fallow woodland is cleared for cultivation.

Globally, food plants have been assessed in context of agrobiodiversity (or agricultural biodiversity), a vastly inclusive category that includes the cultivated crop plants, semi-domesticated species, wild crop relatives and other, associated biota [1]—occupying trophic niches extending from soil mycorrhiza and other microorganisms to the ‘charismatic megaflora’ of parkland tree species of noted cultural import (such as the baobab, the shea butter tree, tamarind, and fig).

The indigenous plant biodiversity of Uganda has been well documented historically—classified and mapped according to vegetation type [2], and on the species level [3, 4]. Utilization of wild and semi-cultivated food plants has been considered in Uganda as a whole [5, 6], in specific regions [7], and in a number of regional studies [8, 9], some in northern Uganda [10], and one proximate to the study area [11].

According to Harlan’s reprise of the Vavilovian classification, northern Uganda lies within the ‘African noncenter’ of agricultural origin [12], distinguished by landrace cultures including finger millet (Eleusine coracana (L.) Gaertn.), Sorghum bicolor (L.) Moench, pigeon pea (Cajanus cajan (L.) Millsp.), cowpea (Vigna unguiculata (L.) Walp.), and simsim or sesame (Sesamum indicum L.), all of which comprise the major food crops of the study area, well recognized in the literature and addressed by agricultural policy and research.

The initial impetus for this study arose during a regional food shortage observed by the author in 1994, during which it was evident that households within the study area had little to fall back on during times of hardship [13], and that the elderly held—and passed on—a body of traditional technical knowledge of edible wild plants, which was observed to contribute to more favorable food security and nutritional outcomes in their communities. Significantly, this knowledge often involved the processing methods by which potentially harmful secondary compounds in the wild plants eaten only during times of hardship could be neutralized, rendering these ‘famine foods’ more palatable.

The aim of the broader study, conducted under the auspices of an integrated conservation and development project (ICDP) aimed at documenting and reinforcing sustainable use of the tree and other woodland plant species, was to compile a full inventory of plant species traditionally utilized by rural communities, drawing upon the expertise and interest of key informants, and leveraging tacit knowledge from those motivated to share it in order to codify utilization and management of plant resources. This was achieved through a series of multi-dimensional studies (cultural, ethnographic, socioeconomic, ecological, and botanical) of plant diversity, its use, and management by smallholder farming households across the project area, of which this paper presents the results relevant to edible plants.

The operational hypothesis driving the study was that use patterns of some plant species within and between the four cultures surveyed are similar, but that plant use within each culture bears a distinctive profile of plant use—and that, given that they inhabit similar geographies, the relative degrees of relatedness of edible plant use between the four communities might be expected to reflect ethnic as well as cultural dimensions.

Methods

The study area, communities, and landscapes

The study area occupies the southern catchment of the Aswa RiverFootnote 1, a major tributary of the Nile, which takes in the rivers Agago and Moroto as it descends the northern Uganda plateau to merge with its larger confluent at Nimule. Situated between 1 and 3° North, and from 33 and 34° East (see Fig. 1), the study area is characterized by wooded savanna standing on sandy loams overlaying a lateritic ironstone layer. Annual rainfall of between 800 and 1500 mm is unimodal, distributed between two peaks from April to September [14].

Fig. 1
figure 1

Map of the study area

The peoples of the study area, residing in the four current districts of Otuke, Agago, Amuria, and Abim, represent four different cultures—the Acholi, Lango, Teso, and Ethur—each with a complicated and interlinked history of migration dating back over a thousand years—some details of which have been transmitted by oral tradition into living memory [15]. The inselberg ranges of the Agoro and Labwor hills, and the long massif of Mount Otuke (1600 m) provide geographic and cultural landmarks within oral tradition, from which a chronology of migrations has been derived according to the royal genealogies of Acholi. Although no such framework exists for the acephalous societies of the Ethur, Lango, and Teso, the historical famines recalled by all four cultures have been correlated to historical data recorded at the Rodah nilometer, near Cairo, which provides a chronology of eastern African rainfall over the past thirteen centuries [16], in confirmation of the oral histories.

There is a fundamental and audible distinction between the Ateso language and the other three languages of the study area—Acholi, Lango, and Thur—which share many words and structures, although the four tongues ultimately derive from the Nilotic branch of the Nilo-Saharan language group, estimated to be over 15,000 years old [17]. Whereas the oral histories of the LwoFootnote 2 cultures of Acholi and Ethur recall a migration from north to south, the Lango and Teso recall an east to west movement, the four groups ultimately settling together around Mount Otuke for a period, before dispersing into their current homelands [18]. Several hundred grinding pits can be observed on the granite face at the southern end of the mountain, along the Abim to Lira road; the author has been unable to locate any archeological assessment regarding the dates of these structures, which seem to indicate a substantial population residing in what today is a wilderness of deep cultural import.

While there is historical linguistic evidence for Lwo language being spoken in northern Uganda since before 1000 BCE [19], the migrations of the Lwo people are recalled to have begun in response to a drought dated to 1031–1058 CE. This event is remembered as resulting in a ‘breakup of the Nilotic cradleland’ along the Nile Valley [20] or the Bahr el Ghazal region of present day South Sudan, and sequential southern migrations of Sudanic and Nilotic peoples [21]. The Lwo people, common ancestors of the Acholi and the Ethur, seem to have moved south into the study area from the sixteenth century, while the ancestral Lango and the Teso migrated west from a homeland in present day Ethiopia, splitting off from the Jie clan of the Karimojong cluster between 1780 and 1840 [22]. The study area includes the eastern clans of Acholi and Lango (as indicated by the historical sub-regional designations East Acholi and East Lango respectively), comprised of clans distinct from their western counterparts in their enjoying more harmonious cross-cultural social relations, and, in the case of the Lango, by very different cultural and geographic origins [23].

While cattle genetic studies provide some triangulation regarding these human migrations [24], many of which can be linked to climatic events, for the most part cattle have been an intermittent and secondary factor in each of the four cultures of the study area. Each of the four cultures consider themselves to be agricultural rather than pastoral societies—‘people of the hoe’ for whom cultivation was supplemented by hunting, as reflected in many place names—Adwari signifying a place of hunting, other places indicating presence of prey, such as Bar Jobi, place of the buffalo. Historically, the cattle herds of the study area were devastated by several rinderpest epidemics from the 1890s, and again by a series of well-organized cattle raids a hundred years later. As a consequence, the first recorded observations of livelihoods in the study area, made during the early twentieth century, describe food systems based on cultivation, hunting and gathering of wild foods including plants, mushrooms, and termites [25, 26].

The communities of the study area are distinguished socially by widespread participation in community-based farming groups, many of them women’s groups, many of which are said to have been formed to facilitate distribution of relief food during a drought of the early 1980s. Culturally, these ‘self-help’ groups draw from traditional shared labor work groups, known in the Lango language as wang tic (for ‘burn the work’), in which groups of neighbors rotated between the household farms of their fellows, the group performing collective tasks to be compensated at day’s end with a shared pot of millet beer [25].

The landscapes of the study area are characterized by the parkland agroforestry system [27], in which useful tree species are conserved when land is cleared for cultivation, allowing for regeneration of woody species during fallow, and semi-domestication of some of these species through generational selection of farmer-favored attributes over time [28] (e.g., reliable yield, sweetness of fruit, palatability of leaves, and cooking or processing attributes of grains and pulses) [29]. The gathering, processing, and sale on local markets of woodland products, including wild foods, has been observed to be a gendered activity—the returns to which remain largely controlled by rural women in their custodial role within rural households [13].

Data collection

Data collection began with a period of participative personal observation from 1992, with substantial time spent by the author in rural areas of the then Otuke County, Lira District, (now Otuke District), with the engagement, hospitality, and support of community-based groups. Formal research instruments were developed during 1999, and were administered from August of that year to September of 2000.

Sampling was undertaken as widely as possible within each of the four focus districts, each of which represents a different ethnicity and culture, during a time of increasing insecurity. The study area is typified by hamlets in which land use is traditionally allocated by the clan, and agricultural labor undertaken by groups of neighbors, of which many are formally constituted as farming groups, women’s groups, and youth groups.

The data collection was undertaken several years into an integrated conservation and development project which began in 1992, eventually engaging over 10,000 smallholder farmers affiliated to over 400 community-based groups in a range of program activities at the interface between plant biodiversity and rural livelihoods. This context allowed for mutual familiarity, credibility, and trust to be well established between the interviewers and respondents, and within the broader communities surveyed, and also provided opportunities for triangulation and confirmation of data during subsequent visits.

As a means of identifying key informants, the engagement of these community-based groups provided a logistical channel for the engagement of whole communities, and an invaluable social infrastructure, facilitating establishment of trust-based personal relationships between interviewers and respondents. On basis of their technical knowledge and personal interest in participation, key informants volunteered their time as subject matter experts on the foodways of tradition (tekwaro), and of the ‘early times’ (ikare me con), a pre-historical period known as the aconya (Lango, Acholi, Ethur) or asonya (Ateso).

From July 1999 to August 2000, a series of 61 focus group discussions on the topic were conducted in the local vernacular language at 34 sites (see Fig. 1), in order to introduce the study objectives, and to identify potential key informants. Discussions followed formal introductory meetings hosted by local leadership, with participation by one or more community-based groups of smallholder farmers representing 67 locations of origin (Local Councils, or LCs). Participants notably included the elders of an area, community leadership, and the members of one or more farming or women’s groups. Each exchange began with a general discussion of plant use, during which those with relevant knowledge and interest were encouraged to provide botanical specimens of plant species of interest.

Respondents were requested to provide botanical samples of food plants of interest to them, each of which was documented by completion of a questionnaire indicating the location, date, local names, seasonal availability, palatability classification (i.e., traditional food or famine food), habitat, plant type, part(s) eaten, a description or the plant, its harvesting and processing, storage time, and manner of consumption. Further information was recorded documenting the morphological characteristics, geographical distribution according to vegetation type for each specimen, according to its vernacular name.

Following their engagement on basis of prior informed consent, 232 key informants were identified on basis of prior specialist knowledge, their participation was determined by self-selection based on individual motivation and interest. With prior guidance on the requirements of botanical sampling provided during the focus group discussions, interested respondents were requested to collect one or more specimens of plants of interest for subsequent identification by the Makerere University Herbarium. Use of plant specimens as a focal point for structured interviews has been referred to as the ‘plant interview’ method of ethnobotanical research [30].

Each informant was interviewed individually, to complement the collection of one or more herbarium specimens. For each specimen collected, a separate sub-interview was conducted with the informant, and a separate entry was made on each specimen, for which multiple use reports were recorded by a single key informant. The data was recorded on interview sheets which were numbered sequentially. The results of each interview were subsequently digitized as a line in a spreadsheet shortly after the interview.

The study was conceived as an inventory of species use for the four districts, with a hypothesis that patterns of use would differ significantly between the four cultures represented therein, i.e., East Lango, East Acholi, Teso, and Ethur (Labwor). Data was recorded according to eight use categories—edible, medicinal, ritual, agricultural (including livelihood and environmental services), fodder (animal food), wood, and fuel (firewood and charcoal), and 52 sub-categories including 10 edible applications.

A distinction was attempted to be drawn between plant foods commonly consumed throughout the year or in season, and those foods which are only consumed in times of food shortage and hardship, due to their relative unpalatability and often rigorous processing methods required to reduce or mitigate the presence of anti-nutritional factors.

Botanical specimens were prepared by the researchers at the Shea Project offices in Corner Adwari and in Lira Town, and presented to the Makerere University Herbarium for identification by Latin binomial, for which local vernacular names were recorded during the interviews conducted in the four languages of the study area.

Taxonomic data were compiled on basis of contemporary botanical identification of each herbarium specimen as per the contemporary botanical nomenclature. Since that time, a number of species have been reclassified, necessitating verification of each identified species by cross-checking the original identification with the Plant List (http://www.theplantlist.org/), a comprehensive online database of plant names for all described plant species, maintained in collaboration between the Royal Botanic Gardens, Kew and the Missouri Botanical Garden [31].

Data analysis

Given the differing sample sizes between the four districts, Spearman’s rho coefficient (rs) and statistical significance (p value) tests were run in order to determine whether there was a significant correlation between the number of respondents per district and the number of use reports per district, significant difference being defined as p < 0.05.

Relative Importance Index (RI) was calculated for each species, and separate RI values were obtained for the taxa cited by respondents from each district, in order to evaluate the relative importance of each species by culture, based on frequency of citation and number of use categories. Originally developed for ranking of medicinal plants by their pharmacological properties and body systems affected [32], the RI was subsequently adapted for the ranking of multiple-use species by use category [33].

$$ {\mathrm{RI}}_{\mathrm{s}}=\frac{{\mathrm{RFC}}_{\mathrm{s}\left(\max \right)}+\kern0.5em {\mathrm{RNU}}_{\mathrm{s}\left(\max \right)}}{2} $$

where RFCs(max) is obtained by dividing the relative frequency of citation (RFC) for the species (FCs) by the maximum value in all edible species surveyed [RFCs(max) = FCs/max (FC)], and RNUs(max) is the relative number of use categories (RNU) for the species divided by the maximum number of use categories in all edible species surveyed [33].

In order to test the operational hypothesis, the Jaccard Index of similarity (JI) was calculated as an indicator of the relative commonality (or similarity) of edible plant citation between each of the four cultures [34]. This metric represents the relative degree of confluence (similarity) of plant utilization among and between the four cultures of the study area.

In considering the degree of similarity between any two populations, JI = a / (a + b + c), where a is the number of taxa cited by both populations, b is the number of taxa cited only by the first of the two populations, and c the number of taxa cited by the second of the two populations [35].

Results and discussion

Species diversity, relative importance, and cultural comparisons

Table 1 presents a summary of interview data and herbarium specimens collected from 232 respondents in 67 locations within the four districts, languages, and cultures of the study area. The key informant interviews yielded 391 edible use reports for 620 herbarium specimens, identified as 88 species of 66 genera within 36 plant families. Of the 36 plant families listed, the 10 most frequently cited families account for 58.3% of all use reports.

Table 1 Results Summary by District

Spearman’s rho coefficient was calculated as rs = 0.8, the p value of 0.2 shows no correlation between the number of respondents by district and the number of edible use reports.

Table 2 presents the total number of use reports according to all use categories considered by respondents, indicating the relative importance of edible plants within each culture, comprising 29% of all use reports. While this paper considers only the edible uses, the total number of use reports is the basis for calculation of the RI of each species, as indicated in Table 3.

Table 2 All plant use reports by use category and culture
Table 3 Edible Species of the Study Area

Table 3 lists the indigenous plant species used as food within the study area, providing the overall RI value of each species indicated, while Table 4 presents the ranked list species with an RI greater than 0.50. Species ranking by RI was further calculated for each of the four cultures of the study area. As a basis for cross-cultural comparison, Table 5 provides the twelve highest RI values for each of the four cultures. There results show a cultural confluence in the very highest ranked species, notably Bridelia scleroneura, Annona senegalensis Grewia mollis, Tamarindus indica, and several species of genus Ficus. Although cited by three of the four cultures, Balanites aegyptiaca was highly ranked only by the Ethur, possibly reflecting a cultural preference for the edible leaves.

Table 4 Edible Taxa with RI greater than 0.5
Table 5 Twelve highest ranked taxa by RI in each of the four cultures studied

Figure 2 charts the edible taxa cited by each of the four cultures, indicating the number of taxa cited uniquely by each culture, and the number of cited taxa shared between each of the four cultures, as listed in Table 6. Using these figures, Table 7 provides the Jaccard Similarity Index for each cultural interface, ranging from 15.5% (Acholi and Ethur) to 25.8% (Lango and Acholi). Taken together, these values indicate relative commonality of edible plant use between cultures, providing a basis for comparison of one aspect of cultural similarity (see Fig. 2).

Fig. 2
figure 2

Edible taxa cited by language and inference n = 88

Table 6 Proportion of Edible Taxa by Culture and Interface
Table 7 Commonality of edible taxa

Historically, the Acholi and Ethur (JI of 15.8%) share common (if temporally distant) ethnic origins, as do the Lango and Teso (JI of 19.2%), but the cultural divergence between each of these pairs is exemplified by their distinctly divergent languages. By contrast, the more recent cultural confluence between the Lango and Acholi (JI of 25.8%) is exemplified by the historical adoption by the Lango of a Lwo-based language quite distinct from their original tongue [22, 36]. These results could be interpreted as indicating that a more recent cultural affinity is a stronger determinant of cultural similarity than shared ethnic origins of the more distant historical past, but on the other hand, there is no direct cultural (nor geographic) proximity between the Acholi and Teso, despite their relatively high JI of 22.0%.

Drawing from descriptive statistics as a further basis for cross-cultural comparison, Fig. 3 shows the proportion of edible use reports by plant part for each of the four cultures. These results seem to indicate that leaf and seed protein are of relatively greater nutritional importance to the Ethur than the other three cultures, and that leaf protein is of higher importance to the Teso than to the Lango and Acholi, whose similar profiles are consistent with their notably high Jaccard similarity index.

Fig. 3
figure 3

Proportion of edible use reports by plant part and culture n = 391

Species utilization

Drawn from 1447 use reports based on an herbarium collection of 630 specimens, the broader data set documents the nutritional, economic, medicinal, and cultural uses of 213 plant species, from annual herbs to trees, with local names recorded in the Lango, Acholi, Ateso, and Thur languages.

Noting that most species are used in multiple ways by respondents, the results describe the edible plants (29%, with 391 use reports); medicinal plants (19.3%, with 260); plants with cultural uses (18.7%, with 252) and plants utilized for their wood (24.1%, with 324) or as fuel (8.9% with 120 use reports). While only the edible plant applications are relevant here, the other use categories of application have been used to generate the RI value for each species, as described in the Methods section above.

The overall on-farm plant biodiversity of the study area includes cultivated and semi-cultivated species, many of which are indigenous, along a broad interface between cultivated plants, wild plants, and wilding crops from earlier rotations. The most heavily sampled species, Bridelia scleroneura with 13 specimens, yielded the greatest number of individual use reports—42, across each of the four broader categories, comprising two medicinal applications, six cultural uses, 21 use reports for the wood, and 13 edible use reports (all involving the fresh fruit).

Species used as food include plants bearing edible leaves, fruits (eaten fresh, or used in cooking), roots and tubers, and seeds, including commonplace cultivated species and those collected as wildings or weeds in cultivated fields, and gathered from woodland, wetland, and fallow. Not all of the taxa listed in Table 3 can be considered wild species sensu stricto. While graminoid seeds and leaves and fruits from trees and shrubs in particular are collected from the wild, indigenous plants which occur in the wild are sometimes cultivated as minor crops (often called underutilized or ‘orphan’ crop species), are considered here, including a range of leafy vegetables—Amaranthus spp., Hibiscus spp., African spider-plant (Cleome gynandra)—and seed crops including Bambara groundnut (Vigna subterranea), the wild sesame relatives Sesamum calycinum subsp. angustifolium and Ceratotheca sesamoides, and the ‘proto-sesame’ Hyptis spicigera.

To understand the convergent foodways of the four cultures of the study area, it is useful to consider the form of a typical meal. While porridge is often taken in the morning, an afternoon or evening meal is commonly based on a starch component, a pulse component, and a leafy green (vegetable component), based around finger millet, Eleusine coracana, a landrace crop, and a staple food. Finger millet grain is ground to a fine flour between stones, and stirred (‘mingled’) into boiling water to form a porridge, or, with further flour added, into a boiled bread (kwon in the Lwo languages, atap in Ateso), which outsiders might refer to as a ‘stiff porridge,’ though it is eaten as a solid, pasty ‘cup’ in which the relish is scooped by hand.

A standard meal combination would consist of the boiled bread eaten with ground pigeon pea over which shea butter has been drizzled. The same bread can be made with sorghum or maize flour, or can be substituted with mashed cassava tubers or sweet potato. This basic dish is served alongside a cooked green vegetable, or a vegetable sauce, depending upon palatability of the leaves.

Plant parts used

Leaf vegetables

Respondent classification of leafy green vegetables is based on the distinction between the more unpalatable species, from which the secondary compounds must be removed, from others which may be ‘fried’ directly, without such prior processing. For greens with a more pronounced sour or bitter taste, the leaves are processed by parboiling in the ‘first water,’ which is discarded.

Notable on all types of ground throughout the study area are wilding or relict Cleome gynandra, which appears in cultivation from around March to October. Its leaves are characteristically bitter with secondary compounds, so the water in which it is parboiled is discarded prior to assembling the final configuration, in which the cooked leaves are combined with an alodi paste of sesame and groundnut to sweeten the sauce. The leaves may be served alone, or combined with Hibiscus spp., Amaranthus graecizans, Curcurbita pepo, or Cyphostemma adenocaule.

Likewise frequent as wilding or relict individuals are several types of Hibiscus, known generically as malakwang (Lango, Acholi, and Thur) or emalakany (Ateso), from which leaves are constitute a popular dish. Whereas Cleome is bitter, Hibiscus is characteristically sour due to its flavonoids and phenolics [37]; as with Cleome, the parboiling water is discarded prior to mixing with alodi paste, although fermented Hibiscus seeds known as toke were formerly used in the manner, as a means of sweetening the sauce.

While four of the samples collected were identified as Hibiscus cannabinus, commonly known as kenaf, two specimens were only identified as Hibiscus sp. Several other studies [5, 38] identify vegetable Hibiscus as H. sabdariffa (commonly known as roselle), from which the calyces are harvested for the tea known in Arabic as karkade. Katende et al. include H. cannabinus, H. diversifolius, as well as H. sabdariffa as malakwang species, with H. acetosella designated as malakwang kulo in Lango [6].

Vegetable species which may be eaten directly and without parboiling include Crassocephalum vitellinum, which is usually mixed with Solanum nigrum—in Lango (Otuke District); it is eaten alone only in times of famine. Other vegetables which may be fried directly include Curcurbita pepo; the young tender leaves are picked, the rough surface trichomes are removed, the leaf wilted, and then fried or boiled. Vegetables which require parboiling include Cyphostemma adenocaule, Oxalis corniculata, Oxygonum sinuatum, Sesamum calycinum subsp. angustifolium (the leaves of which are mixed with other vegetables to reduce the cooking time, and to ‘make better soup’), and Solanum nigrum.

Commelina africana is eaten alone, or mixed with Hibiscus spp. or Corchorus trilocularis, of which there are two types, commonly mixed; it is not eaten alone, but is combined with other leafy greens such as cowpea or Crotalaria ochroleuca, which is commonly interplanted with cereals and simsim (sesame), and may be boiled fresh, or dried and stored.

The young leaves of Senna bicapsularis are commonly eaten as a sauce in Abim, but are considered a famine food in Agago; in Amuria, Senna obtusifolia is described as ‘one of the traditional vegetables liked best by the Iteso,’ where the first cooking water is discarded ‘due to its black color,’ the leaves eaten with groundnut paste. In Otuke, it is boiled in water and ‘cooked down to dry,’ then added to a Cleome sauce, while in Agago, the leaves can be fried directly, as they are not considered bitter—a distinction suggestive of cultural or individual preference, with possible implication of intra-species diversity within the study area.

Trees which provide edible leaves include Balanites aegyptiaca, the young leaves of which are boiled twice (the initial water being discarded as ‘too sour’), pounded, ground, re-boiled, and mixed with groundnut paste. The species is considered a famine food by some respondents, but a palatable regular food by others (e.g., those of Abim). In Amuria, the tree is reportedly lopped to that young branches may develop, from which the tender new leaves are picked. According to respondents in Agago and Abim, the pounded young leaves of Securidaca longipedunculata are likewise prepared and eaten as sauce. Whether these distinctions reflect cultural rather than individual preferences is not clear.

Other trees and shrubs providing edible leaves include Grewia mollis (commonly combined with other vegetables, e.g., Cleome or Hibiscus) and Justicia exigua. In Amuria, the young leaves of Tamarindus indica are boiled, pounded, and boiled again, to make a ‘juice’ for flavoring porridge or bread (atap).

In Otuke, the young leaves of Harrisonia abyssinica are put into a sauce of pigeon peas, and given to a woman who has just given birth—but this is considered as a medicinal or ‘nutraceutical’ use, and not a regular food.

Fruits

A total of 48 fruit species were documented, providing a wide range of fruits mostly eaten fresh, particularly by children.

With a few notable exceptions, fresh fruits are collected from trees which have been conserved when cultivated land is cleared for fallow. Ripe fruits are usually gathered from the ground under the tree canopy, with the notable exception of Syzygium guineense—fruits picked from the tree by children, as the fallen fruits are normally rotten. Other fruit-bearing species include shrubs (e.g., Carissa edulis) and annual herbs (notably Afromomum spp. and Solanum spp.).

A number of fruits are commonly processed, some of which may be stored for extended periods, either pre- or post-processing. Of these, most are processed into pulp or juice and are eaten with porridge, in which a sour taste is appreciated—as when lemon juice is added to porridge made from finger millet flour.

Fruits eaten in this manner include Aframomum alboviolaceum, the fruit pods of which are crushed, its juice squeezed into flour for making porridge. Water is used to extract fruit pulp from the peeled fruit pods of Tamarindus indica (which can be stored for half a year or more); the pulp is then added to the flour from which a porridge or bread is mingled. Other fruits consumed this way include Ficus spp., Searsia spp., Saba comorensis, and Strychnos innocua.

Fruits which may be dried and conserved for later consumption include those of Vitellaria paradoxa subspecies nilotica, from which the fruit pulp may be formed into discs and dried as yao adanya (‘patted shea’ in leb Lango), a traditional delicacy which was commonly served, with shea butter, to honored guests. Rarely seen on local markets, the discs can be stored up to 2 years.

Of the several Ficus species cited, F. sur fruits are eaten fresh, or squeezed with fresh grass to make juice; they may also be dried and stored for later consumption. Ficus glumosa, F. sycomorus, and F. thoningii fruits may also be eaten fresh, or they may be dried. Other fruits which may be dried and conserved include those of Cucumis aculeatus, Balanites aegyptiaca, Tamarindus indica, and Ziziphus mucronata—the fruits of which may also be eaten fresh, or dried, and later pounded to separate the seeds from the seed-coat (pulp), which is used as a sweetener, sometimes added to porridge ‘as sugar.’

The fibrous coconut-shaped fruit of Borassus aethiopum may be beaten, to soften it, then eaten fresh, or grated and rinsed with water to make a drink; the harvested fruit can be stored for several months. In the mid-1990s, a concentrated Borassus fruit syrup was sold as a squash on the roadside at the Kafu river bridge; sweet, but not overly so, its taste was distinctively resinous, with a slightly soapy aftertaste suggesting the presence of saponins [39]. Similar products have been commercialized in Burkina Faso, and in Ghana [40].

Of the Cucurbitaceae, Cucumis aculeatus and Curcurbita pepo fruit may be dried and stored up to 3 months, kept separately from the dried leaves and seeds, which may be conserved for a longer time.

Seeds

While Hibiscus spp. have been considered above in the form of malakwang or emalakany (the vegetable sauce made from its tender leaves, harvested year-round ‘if there is rain’), in the dry season the vegetative plant is cut, bundled, and dried, the calyces threshed to obtain the seed, which can be stored up to 2 years prior to consumption.

Known as toke in all of the four language groups, the seed of Hibiscus was traditionally a stored food commodity of significance, used even as bride-price within the past few generations, following a series of cattle epidemics around the 1890s, which devastated the cattle herds [24]. Among the grandmothers of current adults were not a few ‘toke brides’ (A. Achen, personal communication 1992).

To prepare toke, the seeds are first dry-roasted, then allowed to cool before being rinsed with water, strained, and pounded into a puree or paste, which is boiled in water as a base for sauces; the watery remnant may be allowed to ferment before being used in place of the alodi paste to cook malakwang [41]. Fermented seed flour of H. sabdariffa features prominently in traditional diets of the poor in Sudan, where it has been described as a ‘meat substitute’ [42] analogous to the fermented proteinaceous flavoring product dawadawa in West Africa.

As noted above, the study area is within the ‘non-center’ of origin or diversity for sesame (Sesamum indicum) and its wild crop relatives [12]. Sesame in northern Uganda is widely considered a cash crop, and that as a food it is consumed not as an extracted oil, but primarily as a component of sauces and stews. This is also the case for the wild crop relatives of sesame Sesamum calycinum syn. S. angustifolium and Ceratotheca sesamoides, occurring as weeds or crop relicts in cultivated fields in the study area.

Another seed crop, which occurs wild and as a relict crop in cultivation and in fallow, is Hyptis spicigera, known in Lango as amola (lamola, Acholi), an ancient crop which has been classified as a ‘proto-sesame’ in western and central Africa [28]. Due to its similar form and alimentary function, Hyptis is closely associated with sesame, to which it is culturally associated [43] (if not botanically related), and with which may be conflated [44]. While consumption of the crop was not noted in Teso, it is well documented in Lango agricultural history [25]; Tarantino lists it among the first food crops planted by the Lango [26], and is known to be appreciated in the Madi culture of northwest Uganda [8] and in the Western Equatoria region of South Sudan [45]. Hyptis seed may be stored up to 2 years.

At maturity, stems are cut for dried in the compound, then and threshed and winnowed. Like simsim seeds pounded with ‘local salt and usual salt,’ the preparation of Hyptis in Lango and Acholi culture goes well beyond a generic paste. Following the dry roasting of the seeds, the half-cooked seeds are pounded to a flour using a mixture of conventional and vegetable salt, then mixed with warm water and molded into a saucer-shaped patties a hand’s breadth in diameter, called agilgili (Lango) or akilikili (Acholi), which is gently boiled into a semi-moist cake, following which sesame paste is added to the broth [5, 41].

This dish, which may be served with smoked beef (olel, Lango), is considered a traditional delicacy, and its place on the cultural menu is quite distinct; the taste of the Hyptis patty is pleasant, slightly nutty with a hint of umami, and despite the small size of the patty; it is very filling, and not more than two are likely to be eaten at a sitting (personal observations).

Actual sesame relatives which are eaten in a similar manner to that crop are Ceratotheca sesamoides and Sesamum calycinum subsp. angustifolium, both of which occur as wild plants or crop relicts, and may be inter-planted with cereals. While specimens of these plants were obtained only in Otuke and Amuria districts respectively, both were observed to be well-represented in the fields of Agago District during the 2019 agricultural season.

As with sesame, Hibiscus spp. and Hyptis spicigera, the mature stems are cut and bundled, let stand to dry, and then threshed and winnowed; seeds of both species are said to keep 1–2 years, and are pounded and then stone-ground into a paste which is served as is (as a type of alodi), or is used as a base for sauces.

Purely wild species providing edible seeds include the graminoids Dactyloctenium aegyptium and Pennisetum glaucum. Both grasses are cut and threshed to yield a grain which is ground into flour. In Amuria, the flour of D. aegyptium is mingled into boiling water as a porridge ‘when condition is serious’ (i.e., in times of famine), while in Abim the porridge may eaten with Tamarindus indica pulp.

In Agago, P. glaucum provides a boiled bread (kwon), and is sometimes fermented into beer. D. aegyptium is one of the more ancient grains harvested from wild species, known generically as kreb across the Sahara, with a notably high nutritional profile [46]—particularly in terms of the essential amino acids [47].

Other edible seeds include Aspilia pluriseta, Bidens sp. and Cucumis figarei (from which the seeds are roasted and ‘pounded with salt’ to form a paste), and Hypoxis angustifolia, the seeds of which are eaten fresh as a snack in Otuke.

Trees providing edible seeds include Balanites aegyptiaca and Sclerocarya birrea, from which the seed kernel is pounded and ground to paste as a base for sauces. In Amuria, the seeds of Ficus glumosa may be ground with cassava to make bread (atap) during times of hunger, while in times of hardship in Otuke, the dried seeds of Ficus sur are winnowed, then mixed with dried beer residue and ground into flour which is mingled into bread (kwon).

Tubers, bulbils, and shoots

Species from which edible tubers are obtained include two Dioscorea species, D. alata and D. bulbifera, of which the latter (also known as ‘aerial yam’) produces edible bulbils at the leaf axils. The list also includes one unidentified species, originally identified as belonging to the genus Cissus, but subsequently (if tentatively) identified as Cissampelos mucronata.

One species with edible tubers well documented elsewhere is Hypoxis, which was only noted for its edible seeds, although the bulb is reportedly considered edible by the Maasai and Kipsigis of Kenya [48]; at one cave site in South Africa, evidence for consumption of the cooked rhizome has recently been dated to 170,000 BP [49].

Beyond the above categories, other plant foods include the hypocotyl axis of the germinated seed of Borassus aethiopum, which is sometimes offered for sale on local markets or by the roadside. Germination may be stimulated in pits dug for that purpose, a practice also common in the Eastern Equatoria region of South Sudan [50].

Other plant foods

Plant foods other than the vegetative products mentioned above include the flower nectar of Leonotis nepetifolia, and the food oil shea butter, expressed from the seed kernel of Vitellaria paradoxa (as distinct from the solid fats of West African origins, the eastern subspecies nilotica yields an oil stable to about 20 °C).

Seasonal availability

The seasonal availability of each taxon is indicated in Table 3, and the availability of product types throughout the year (species per month by product type) is indicated in Fig. 4.

Fig. 4
figure 4

Seasonality of availability of product type (plant part)

Seasonality data collected from each informant per species diverged in some cases, perhaps due in part to sub-regional ecologies including hydrological factors as well as rainfall patterns—noting again the precipitation gradient extending across the Aswa river valley, as described above. It is also possible that in some cases, informants indicated the occurrence of the developing plant within the growing cycle (particularly for annual forbs and graminoids), rather than the availability of harvested food products to which the question refers. For this reason, seasonality was triangulated against the literature [6].

Seasonality of edible plants can loosely be classified according to their occurrence in three separate seasons: the onset of rains (April through July), wet season (August through October), and dry season (November through March). By contrast to the complex seasonality of availability described by the data, the agricultural cycle is more narrowly pegged to the seasonality of precipitation. The availability of foods derived from agriculture corresponds to harvests undertaken during the wet season, roughly July to December, dried and stored foods being consumed through the dry season from January to June. The onset of rains at the end of the dry season, when food stores are depleted and agricultural labor (particularly women’s labor) is needed for planting and weeding the crops, is considered the ‘hungry season’—a period extending roughly from April to July.

Edible leaves tend to be harvested when young and soft, beginning shortly following onset of the rains. Edible leaves are harvested primarily from forbs (25 species) and creepers (2), which generally become available shortly after the onset of rains in March and April. Edible leaves are also collected from 4 tree species, from which young leaves from new growth are preferred, thus following a similar availability cycle to the annuals. While many leaves can be dried and stored up to 6 months, providing a potential buffer of availability during the dry season, freshly harvested leaves are significantly more palatable and nutritious than dried.

Edible fruit are gathered primarily from trees (21 species) and shrubs (7), and from forbs (4) and creepers (3). While storage of fruits is limited to a few exceptional cases (e.g., the processed and dried pulp of Vitellaria paradoxa, and the pods of Tamarindus indica), the availability of fresh fruits is evenly distributed throughout the year, with availability classified according to their availability as dry season or wet season fruits [41].

Dry season fruits, which mature alongside cultivated crops and are harvested concurrently, include Aframomum spp., Balanites aegyptiaca, Bauhinia thonningii, Borassus aethiopum, Cucumis aculeatus, Gardenia ternifolia, Grewia arborea, Oncoba spinosa, Phoenix reclinata, Sarcocephalus latifolius, Solanum spp., Tamarindus indica, and Vangueria apiculata.

More relevant to food security during the annual ‘hungry season’ are the wet season fruits, including Ampelocissus africana, Annona senegalensis, Antidesma venosum, Bridelia spp., Carissa spinarum, Diospyros mespiliformis, Fadogia glaberrima, multiple Ficus species (F. dicranostyla, F. glumosa, F. sycomorus, F. sur), Grewia mollis and G. villosa, Hoslundia opposita, Physalis minima, Saba comorensis, Searsia pyroides, Syzygium guineense, Vitellaria paradoxa, and Ximenia americana.

Of these, the relative abundance and nutritional value of Vitellaria paradoxa was specifically mentioned by informants as a valued nutritional resource during the annual food deficit, when agricultural labor requirements are highest. The fruit is collected in the early morning by women and young children on their way to the fields, where the pulp will provide a snack during the work-day, the remainder and cleaned seeds carried home for de-husking and drying at the end of the day.

For species such as Vitellaria paradoxa with multiple edible uses, the availability of different products at different times of year provides another layer of nutritional diversity by edible use—fresh fruit from May to July, edible oil (and dried fruit) from October to March. Other notable examples include Borassus aethiopum (fresh fruit October to December, edible shoot April to June), Ficus dicranostyla (leaf March to May, fruit June to August), and Hibiscus spp. (fresh leaf from March to November, seed from October to December).

Limitations of the study

Design of the study was somewhat ad hoc, partly as a result of overlapping areas of inquiry common to multiple studies serving the program objectives of a donor-supported integrated conservation and development project with an applied research component focused on on-farm biodiversity.

Although the state of ethnobotanical research at that time involved hypothesis testing and quantitative methods of data analysis which were largely based on informant consensus and ranking of species [51], the study was undertaken under the applied research component (on-farm biodiversity program) of an integrated conservation and development project (ICDP) with specific development-oriented objectives, as an inventory of species and their utilization, without regard to ranking.

As such, the purpose of the broader study was to document the ethnobotanical knowledge held by subject matter experts locally recognized for their expertise at the community level. The study did not aim to assess the awareness and knowledge of the broader population, nor generate any ranking of species by their relative importance.

As the core area of program emphasis was the Shea Butter Tree Vitellaria paradoxa subspecies nilotica, the study was conceived to supplement and complement the greater depth of data on that species. As an apparently compensatory consequence, relatively little attention was paid to that species by study informants, with only for specimens provided and only one medicinal application noted, against a vastly longer list of medicinal and cultural uses of the tree and its products documented through other project applied research [52].

The study was conceived as an inventory of species and their uses, and thus no attempt was made to assess preferences or rankings of the species, either within the respondent population or between cultures or locations. Respondents were not asked to list, nor prioritize, other food plants of significance beyond those for which they provided a herbarium specimen.

Botanical specimens were provided by the informant at the time of the interview, and as such the availability of this material determined in part the frequency of mention by individual informants. As a result, some plants were over-sampled (with more than a dozen vouchers for several species), while plants which were not easily sampled due to seasonality, or to physical limitations, may be under-represented in the collection. Although its value and use were very evident in the as multiple edible and other uses, just three specimens of Borassus aethiopum were collected—probably due to the impracticality of sampling the tree, in which the vegetative and floral parts are high above the ground.

During the data collection, it was not possible to draw a clear distinction between foods commonly consumed at present, in the past, and specifically in times of food shortage (‘famine foods’), since the personal tastes and circumstances of the informants could not be calibrated according to the data collection instruments.

Although it is tempting to read into the data, developing cultural generalizations (‘people of Labwor eat Balanites leaf and Dactylotenium porridge often, while those of Lango consider them famine foods’), there is insufficient data here to justify such conclusions.

Beyond the inventory of species by edible use, there were inconsistencies in the classification of species by designation, i.e., as a former food of the ‘old times’ (ikare me aconya), a famine food, or ‘common today’); there was likewise a degree of subjective disagreement regarding a species within the same district as regards habitat, abundance, establishment and even plant type (herb, creeper or vine—tree or shrub?), which prevents any meaningful consideration of these attributes.

Over the year of the study, each of the four interviewers displayed a different ‘style’ of data collection, with varying degrees of detail provided—some respondents seem to have been more forthcoming at sharing details of tradition and culture than others, possibly depending upon the tenacity of the interviewer, as well as factors such as gender and ethnicity, and the personality and mood of both interviewer and respondent.

Phenotypic diversity between sampled individuals was not evaluated, nor were questions asked about local classification of product types or favored characteristics of a given product. Areas of potential for further study include the intra-species biodiversity of the inventoried species, and how it is classified according to farmer selection criteria.

Contemporary studies of diversity and use of Vitellaria paradoxa subspecies nilotica within the study area revealed traditional classification systems by which the morphological and organoleptic attributes of shea fruit were known in the four languages of the study area [53]; a subsequent study provided an expanded this ‘folk classification’ framework to include the West Nile region [54]. Diversity in the morphology, proximate composition, and nutritional parameters of Tamarindus indica fruit and seed from different geographic origins of Uganda, including the study area, has also been assessed as significant [55,56,57].

Clearly, there is scope for assessment of the morphological, phenotypic, and nutritional parameters of intra-species diversity of the food plants presented here, preferably linked to locally and culturally specific evaluative frameworks.

Conclusions

The data describe patterns of use of plants used as food in four districts of northern Uganda, including an inventory of species consumed by plant part, type of food, and seasonality. This study documents an inventory, and perhaps an archive, of traditional food plants—the use of which may or may not have changed during the last two decades since it was compiled.

Subsequent to the study, civil conflict brought wholesale displacement of communities in much of northern Uganda, including Agago and Otuke districts in particular, suffering massive social and cultural disruption as entire communities were displaced to military camps for half a decade [58, 59]. As many elders did not survive the hardships of war, and the youth who emerged from the camps 5 years later had no eagerness to return to subsistence agriculture, these events disrupted the chain of generational transmission of technical knowledge in a precipitate process of cultural erosion. The data presented here may thus have been drawn from a more extant body of traditional knowledge than that of today.

The extent to which the identified species are currently used as food is unknown. But there are recent indications that the plant species described here are still strongly represented on the farms of the study area. Observations made by the author within the study area during 2019 indicate both negative and positive impacts of the war and displacement on the ecological integrity of the agroforestry parkland. Many large, mature trees were cut to meet urban charcoal demand during the war, but a cohort of young trees established itself during the years of displacement which has been protected into maturity by returning communities. Under the canopy, and throughout cultivated fields, traditional food plants remain well represented in the cultivation mosaic, though relatively scarce on local markets.

The results of this study are intended as a reference for policy-makers engaged in support to agricultural systems in northern Uganda, and as a resource for further development of the plant foods described herein as a nutritional buffer serving systemic resilience at the local, national and regional levels.

It is hoped that diffusion of these results back to the informant communities may serve as a codified record of this knowledge, which might provide a measure of encouragement to farmers interested in the ancestral crops and wild foods described herein.

Availability of data and materials

The data from which this study is drawn will be freely shared with interested researchers by request.

Notes

  1. Also written as Acwa, Acwaa, Achwa or Acaa

  2. Also written as Luo

Abbreviations

BCE:

Before the Common Era

BP:

Before the Present

FAO:

Food and Agriculture Organization of the United Nations

JI:

Jaccard Index of similarity

RI:

Relative Importance Index

UR:

Use report

References

  1. Jackson LE, Pascual U, Hodgkin T. Utilizing and conserving agrobiodiversity in agricultural landscapes. Agric Ecosyst Environ. 2007;121(3):196–210.

    Article  Google Scholar 

  2. Langdale-Brown I, Osmaston HA, Wilson JG. The vegetation of Uganda and its bearing on land use, Government of Uganda, Entebbe; 1964.

    Google Scholar 

  3. Eggeling WJ, Dale IR. The indigenous trees of the Uganda Protectorate. Entebbe: Government Printer; 1952.

    Google Scholar 

  4. Lind EM, Tallantire AC. Some common flowering plants of Uganda. Entebbe: Oxford University Press: Londonon, The Vegetation of Uganda and Its Bearing on Land Use, Government of Uganda; 1964.

    Google Scholar 

  5. Goode PM. Edible plants of Uganda: The value of wild and cultivated plants as food: FAO; 1989.

  6. Katende AB, Ssegawa P, Birnie A, Holding C, Tengnäs B. Wild food plants and mushrooms of Uganda. Nairobi: Regional Land Management Unit, RELMA/Sida; 1999.

  7. Agea JG, Okia CA, Abohassan RA, Kimondo JM, Obua J, Hall J, Teklehaimanot Z. Wild and Semi-Wild Food Plants of Bunyoro-Kitara Kingdom of Uganda: growth forms, collection niches, parts consumed, consumption patterns, main gatherers and consumers. Environ Res J. 2011;5(2):74–86.

    Article  Google Scholar 

  8. Tallantire AC, Goode PM. A preliminary study of the food plants of the West Nile and Madi Districts of Uganda: The utilization of leaves and fruits of local and mainly indigenous plants in supplementing the staple foods. East Afri Agric For J. 1975;40(3):233–55.

    Article  Google Scholar 

  9. Tabuti JRS. Status of non-cultivated food plants in Balumogi County, Uganda. Afr J Ecol. 2007;45(Suppl 1):96–101.

    Article  Google Scholar 

  10. Ojelel S, Mucunguzi P, Katuura E, Kakudidi EK, Namaganda M, Kalema J. Wild edible plants used by communities in and around selected forest reserves of Teso-Karamoja region, Uganda. J Ethnobiol Ethnomed. 2019;15(1):3.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Ojelel S, Kakudidi EK. Wild edible plant species utilized by a subsistence farming community in Obalanga sub-county, Amuria district, Uganda. J Ethnobiol Ethnomed. 2015;11:7. https://doi.org/10.1186/1746-4269-11-7.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Harlan JR. Agricultural origins: centers and noncenters. Science. 1971;174(4008):468–74.

    Article  CAS  PubMed  Google Scholar 

  13. Masters ET, Puga A. Conservation of woodland of Butryospermum paradoxum for local conservation and development. Kampala: Cooperative Office for Voluntary Organizations of Uganda; 1994.

    Google Scholar 

  14. Farbrother HG, Muro JM. Water. In: Jameson JD, editor. Agriculture in Uganda. 2nd ed. London: Oxford University Press; 1971.

  15. Onyango-Odongo JM, Webster JB. Chronology for the Lwo-Speaking Peoples: Introduction. The Central Luo during the Aconya; 1976. p. 39–40.

    Google Scholar 

  16. Herring RS. Hydrology and chronology: the Rodah nilometer as an aid in dating interlacustrine history. In: Chronology, migration and drought in interlacustrine Africa; 1979. p. 38–86.

    Google Scholar 

  17. Gomes V, Sánchez-Diz P, Amorim A, Carracedo Á, Gusmão L. Digging deeper into East African human Y chromosome lineages. Hum Genet. 2010;127(5):603–13.

    Article  PubMed  Google Scholar 

  18. Uzoigwe GN. The beginnings of Lango Society: a review of evidence. J Hist Soc Nigeria. 1973 Jun;1:397–411.

    Google Scholar 

  19. Atkinson, RA. The evolution of ethnicity among the Acholi of Uganda: The Precolonial Phase Source: Ethnohistory, Ethnohistory and Africa (Winter, 1989), Vol. 36, No. 1, pp. 19-43

  20. Webster JB. Noi! Noi!: Famines as an Aid to Interlacustrine Chronology. In: Webster JB, editor. Chronology, migration and drought in interlacustrine Africa. Longman; 1979. p. 1–37.

    Google Scholar 

  21. Jameson JD, editor. Agriculture in Uganda. 2nd ed. London: Oxford University Press; 1971.

  22. Herring RS. The view from Mount Otuke: migrations of the Lango Omiro. In: Webster, editor. Chronology, Migration and Drought. Longman; 1979. p. 283–316.

    Google Scholar 

  23. Ogot BA. History of the Southern Luo: Migration and settlement, 1500-1900. Nairobi: East African Publishing House; 1967.

  24. Rege JE, Tawah CL. The state of African cattle genetic resources II. Geographical distribution, characteristics and uses of present-day breeds and strains. Anim Genet Resour. 1999;26:1–25.

  25. Driberg JH. The Lango: A Nilotic Tribe of Uganda. London: T Fisher Unwin Ltd; 1923.

    Google Scholar 

  26. Tarantino. Notes on the Lango. Uganda J. 1949;13(2):1949.

    Google Scholar 

  27. Pullan RA. Farmed parkland in West Africa. Savanna. 1974;3(2):119–51.

    Google Scholar 

  28. Seignobos C. Végétations anthropiques dans la zone soudano-sahélienne: la problématique des parcs. Rev Géographie Cam. 1982;3(1):1–23.

    Google Scholar 

  29. Boffa JM. Agroforestry parklands in sub-Saharan Africa. Rome: FAO; 1999.

  30. Alexiades MN, Sheldon JW. Selected guidelines for ethnobotanical research: a field manual; 1996.

    Google Scholar 

  31. Royal Botanic Gardens, Kew and the Missouri Botanical Garden. The plant list. A working list of all plant species. [Internet] 2013; Online at: http://www.theplantlist.org/.

  32. Bennett BC, Prance GT. Introduced plants in the indigenous pharmacopoeia of Northern South America. Econ Bot. 2000;54(1):90–102.

    Article  Google Scholar 

  33. Tardío J, Pardo-de-Santayana M. Cultural importance indices: a comparative analysis based on the useful wild plants of Southern Cantabria (Northern Spain). Econ Bot. 2008;62(1):24–39.

    Article  Google Scholar 

  34. Jaccard P. Nouvelles recherches sur la distribution florale. Bull Soc Vaud Sci Nat. 1908;44:223–70.

    Google Scholar 

  35. Höft M, Barik SK, Lykke AM. Quantitative ethnobotany. Applications of multivariate and statistical analyses in ethnobotany. People Plants Work Paper. 1999;6:1–49.

    Google Scholar 

  36. Bavin EL. Aspects of morphological and syntactic divergence in Lango and Acholi. Stud Afr Linguistics. 1982;13(3):231–48.

  37. Mungole A, Chaturvedi A. Hibiscus sabdariffa L. a rich source of secondary metabolites. Int. J Pharm Sci Rev Res. 2011;6(1):83–7.

    Google Scholar 

  38. Purseglove JW. Some Uganda Vegetables. East Afri Agric J. 1943;9(2):25-8–98-101.

    Google Scholar 

  39. Umaru HA, Adamu R, Dahiru D, Nadro MS. Levels of antinutritional factors in some wild edible fruits of Northern Nigeria. Afr J Biotechnol. 2007;6(16):1935–8.

  40. Adzinyo OA, Kpodo FM, Asimah VK, Asante-Dornyinah D. Sensory and physicochemical characteristics of naturally flavoured Borassus aethiopum syrups for potential applications in food products. Food Sci Qual Manag. 2015;45:109–13.

    Google Scholar 

  41. Epila-Otara JS. Ecoculture of the Langi: the plains nilotes of central-northern Uganda. Kampala: Fountain Publishers; 2013.

    Google Scholar 

  42. Dirar HA. The indigenous fermented foods of the Sudan: a study in African food and nutrition. Wallingford: CAB International; 1993.

  43. p'Bitek O. Artist, the ruler: essays on art, culture, and values. Nairobi: East African Publishers; 1986.

  44. Bedigian D. Feeding the Forgotten: Wild and Cultivated Ceratotheca and Sesamum (Pedaliaceae) that Nourish and Provide Remedies in Africa. Econ Bot. 2018;72(4):496–542.

    Article  Google Scholar 

  45. Banja GA, Beatrice KM, Kanensi OJ. Effect of soaking and germinating techniques on the macronutrient content of Hyptis spicigera Lamiaceae seeds in Morobo County, South Sudan. Sky J Food Sci. 2016;5(3):19–23.

    Google Scholar 

  46. Harlan JR. Wild-grass seed harvesting in the Sahara and Sub-Sahara of Africa. In: Harris DR, Hillman GC, editors. Foraging and farming: the evolution of plant exploitation. London: Unwin Hyman; 1989. p. 40.

    Google Scholar 

  47. Ahmed MI, Sulieman AA, Xu X, Na Y, Mahdi AA, Mohammed JK. Effect of preprocessing methods on the physicochemical and functional properties of koreeb (Dactyloctenium aegyptium) seeds. J Cereal Sci. 2019;87:280–5.

    Article  CAS  Google Scholar 

  48. Burkill HM. The useful plants of west tropical Africa, vol. 2. 2nd ed. Kew: Families E-L; 1994.

  49. Wadley L, Backwell L, d’Errico F, Sievers C. Cooked starchy rhizomes in Africa 170 thousand years ago. Science. 2020;367(6473):87–91.

    Article  CAS  PubMed  Google Scholar 

  50. Grosskinsky B. Study on wild food plants of Eastern Equatoria, South Sudan, Final report to German Agro Action, Nairobi; 1998.

    Google Scholar 

  51. Phillips O, Gentry AH. The useful plants of Tambopata, Peru: I. Statistical hypotheses tests with a new quantitative technique. Econ Bot. 1993;47(1):15–32.

    Article  Google Scholar 

  52. Bratcher V. Cultural values of the Lango and Iteso concerning the Shea tree: An ethnographic study. B.A. Dissertation, 79.

  53. Nkuutu D, Lovett PN, Masters ET, Ojok P, Obua J. Tree management and plant utilisation in the ‘Agroforestry Parklands’ of Northern Uganda. In: The Shea Butter Tree (Vitellaria paradoxa subspecies nilotica): Proceedings from the First Regional Conference for Eastern and Central Africa, Lira, Uganda; 2000. p. 26–30.

    Google Scholar 

  54. Gwali S, Okullo JB, Eilu G, Nakabonge G, Nyeko P, Vuzi P. Folk classification of Shea butter tree (Vitellaria paradoxa subsp. nilotica) ethno-varieties in Uganda. Ethnobot Res Appl. 2011;9:243–56.

    Article  Google Scholar 

  55. Okello J. Morphological and nutritional characteristics of Tamarindus indica (Linn) fruits in Uganda. Unpublished Master's thesis, Makerere University, Uganda; 2010.

    Google Scholar 

  56. Okello J, Okullo JB, Eilu G, Nyeko P, Obua J. Morphological variations in Tamarindus indica Linn. fruits and seed traits in the different agroecological zones of Uganda. Int J Ecol. 2018;2018:1–12.

  57. Okello J, Okullo JB, Eilu G, Nyeko P, Obua J. Physicochemical composition of Tamarindus indica L. (Tamarind) in the agro-ecological zones of Uganda. Food Sci Nutr. 2018;6(5):1179–89.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Nannyonjo J. Conflicts, poverty and human development in Northern Uganda. UNU-WIDER. Round Table. 2005;94(381):473–88.

  59. Gelsdorf K, Maxwell D, Mazurana D. Livelihoods, basic services and social protection in Northern Uganda and Karamoja. ODI Secure Livelihoods Research Consortium Working Paper; 2012.

    Google Scholar 

  60. International Society of Ethnobiology. International Society of Ethnobiology Code of Ethics (with 2008 additions); 2008 Online at: http://ethnobiology.net/code-of-ethics/

Download references

Acknowledgements

The author is most grateful to the study participants, in particular the 232 informants who gave generously of their time and knowledge—and often of their hospitality—and to the staff of the Makerere University Herbarium for their diligence in specimen identification.

The author acknowledges the project staff of the Cooperative Office for Voluntary Organisations of Uganda (COVOL Uganda), including a team of five interviewers who covered countless kilometers under conditions of uncertainty and outright insecurity, and the supportive role played by the student interns from the Makerere University College of Agricultural and Environmental Sciences.

Special thanks to Patrick Abwango, Anna Awio, Leonora Okello, Patrick Lomumba, and Charles Erongot, who made initial contact with the study informants, informed of the aims and purposes of the study, and arranged for focus group discussions, and to the interviewers Simon Atyang, Lilliane Akot, Charles Erongot, Paul Ojok, and David Nkuutu, who also developed collaboration with the Makerere University Herbarium. Special thanks as well to Perpetua Apili, who entered all data, and arranged follow-up visits within the study area during September and October 2019.

Funding

Funding from 1995 to 2003 was provided by the US Agency for International Development under cooperative agreements 623-0124-A-00-5113-00, 617-G-00-98-00001-00 and 617-A-00-98-00007-00; by the European Commission under INCO Contract No. IC18-CT98-0261, and by the McKnight Foundation under Grant No. 98-798. Additional observations were made, and interviews conducted, during a regional seed fair at Lacekocot, with support from FAO Uganda under LOA No. 030/08, and in a series of follow-up visits in 2019 with funding from the Nelson Marlborough Institute of Technology (NMIT).

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EM conceived and designed the study, assembled an applied research team under the auspices of The Shea Project for Local Conservation and Development (The Shea Project), and subsequently undertook data cleaning and analysis, and writing up of all results for publication. The author has read and approved the final manuscript.

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The author is a permanent academic staff member of the Nelson Marlborough Institute of Technology (NMIT) at Nelson, New Zealand, and a Senior Associate of World Agroforestry (ICRAF) at Nairobi, Kenya.

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Correspondence to Eliot T. Masters.

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Prior informed consent was obtained from each informant. Informants were informed of the scope and purposes of the study, and were assured that all contributions, made on a voluntary basis, would be kept confidential, and that no commercial use would be made of any of the results of the study.

The author attests that the data collection and analysis was undertaken in accordance with the International Society of Ethnobiology Code of Ethics [60].

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Not applicable.

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The author declares that he has no competing interests.

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Masters, E.T. Traditional food plants of the upper Aswa River catchment of northern Uganda—a cultural crossroads. J Ethnobiology Ethnomedicine 17, 24 (2021). https://doi.org/10.1186/s13002-021-00441-4

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