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Indigenous biosystematics of yams (Dioscorea spp.) in Southwest Ethiopia: folk taxonomy, ethnolinguistic analysis, and folk descriptors

Abstract

Background

In Southwest Ethiopia, various plant species are coexisting in wild and cultivated forms. This provides an ideal setting for studying folk biosystematics of neglected species. One of such species is the Dioscorea species, in which we studied to assess the commonly applied folk wisdom of identifying, naming, and classifying yams by Sheko and Bench farmers.

Methods

This study was conducted in Bench-Maji and Sheka Zones using 272 farmers. Data on the lists of local names and system of folk taxonomy; the inherent logic, etymons, and consistency of names; and the folk descriptors and other criteria involved in taxonomy were collected. Data were collected by establishing participatory research appraisal tools, i.e., informant interviews and researcher direct observation.

Results

The result suggests that there exists a well-developed folk taxonomic system in Sheko and Bench. This is evident in the recognition of four distinct folk ranks: sub-variety, variety, supra-variety, and folk generic. Taxa assigned to each ranks have distinct features that mark them as members of a separate categories. Farmers over-differentiate 58 individual taxa at the intraspecific levels. Of these, 37 represented varietal taxa while the rest are sub-varietal taxa. Structurally, over 78% of the varieties are labeled with unitary names while all the sub-varieties consisted of binomial names. Farmers used a total of 26 characters and 74 character states for identifying the different taxa. More than 84% of these refer to aspects of plant characteristics. Tuber characters played a key role in the local identification of varietal and sub-varietal taxa while contexts and gender played a key role in the recognition of supra-variety groups.

Conclusions

This study documented a great wealth of knowledge on indigenous biosystematics of yams, constitutes an essential step towards setting development priorities aimed at in situ conservation. The study clearly demonstrated the value of folk biosystematics for assessing the actual extent and spatial dynamics of yam diversity in traditional farming.

Background

Root and tuber crops such as potato, sweet potato, enset, cassava, and yam play an enormous role in feeding the world. They are among the most adaptable staples addressing food security for millions of peoples globally and are nutritionally rich staples that contribute towards the dietary demands of the society. Thus, they serve as an important safety net against starvation. Many of these crops are grown primarily for subsistence, under traditional farming systems, which still represent much of world agriculture. These agro-ecosystems retain a great diversity potential for future use, yet studies on the evolution and conservation needs of these crops are few. Evolution under domestication is affected by the management of folk cultivars, mainly when humans act as agents of selection and is thus said to be linked with the knowledge of indigenous biosystematics of crop plants [1,2,3]. Yam is one of such crops which needs high conservation concern.

The word yam is applied only to members of the genus Dioscorea that belong to the family Dioscoreaceae classified under the monocotyledons [4]. Dioscorea is one of the largest genera in this family comprising over 600 species [5]. It is a pantropical genus, and different species have been independently domesticated in three separate continents [6]. The genus Dioscorea was first described by Linnaeus in 1753, when he considered three species, but its division into botanical sections was much more recent. In 1924, Knuth established the prevailing systematic and then, Dioscorea is divided into 5 sections: Enantiophyllum, Opsophyton, Macrogynodium, Combilium, and Lasiophyton. Of these, the section Enantiophyllum is the largest in terms of number of species and includes all the species with a rightward stem twining direction [7]. Of the important yam species, D. alata and D. cayenensis complex belong to this section [5].

Yams in Ethiopia are hardly known to the scientific community, and in fact, the country is generally regarded to as an isolated center of yam belt [8]. Yet, several yam species might have their origin in Ethiopia and are one of those crops with wild relatives in the country [9, 10]. Miege and Sebsebe [11] reported that the genus Dioscorea has 11 species in Ethiopia. Regarding the intra-specific diversity of yam in Ethiopia, at least 134 non-synonymous landraces have been reported by previous works ([12,13,14,15], Tsegaye B, Bizuayehu T, Wendawek A: Diversity, Distribution and Farmers Management of Yams (Dioscorea spp.) in Southwest Ethiopia, submitted). Over 97% of these landraces belong to the section Enantiophyllum, and within this section, high degree of polymorphism has been identified in the D. cayenensis complex. Though this species complex shows a very wide range of variation, it has not been studied throughout its range.

This paper presents the indigenous biosystematics of yams. Indigenous biosystematics can be defined as the commonly applied and recognized folk wisdom of identifying, classifying, naming, and relating living organisms as practiced by a particular ethnic group [16]. Scientific studies of indigenous biosystematics seek to unravel the classification of folk ranks and taxa, the morphological character states applied in classification and native nomenclatures. In earlier works, the term folk taxonomy is more widely used [17,18,19]. Though it is a more widely used term, its use in literature may relate to different components of taxonomy ranging from a mere list of local names to a hierarchical system of taxonomy [16]. Its common use does not necessarily address how particular cultures classify living organisms. Moreover, a basic linguistic analysis, i.e., questions concerning the inherent logic and consistency of folk names, are not always considered as part of folk taxonomy. Here, folk taxonomy is considered as one component of folk biosystematics, which involves a broader set of subsystems.

Studying indigenous biosystematics is thus essential at least for two reasons. First and more notably, it provides a better understanding to the nature and extent of diversity and how this diversity is perceived and valued by farmers. Second, by detailing the inherent subsystems of indigenous biosystematics, an insight to its relation with the taxa recognized in the domain of formal science can be obtained. The insight that this provides is valuable for the improvement and conservation of yam in Ethiopia. Finally, it is of utmost importance because it is not only the unit of diversity that they recognize but also the unit of how they actually manage and conserve.

The far Southwest Ethiopians maintain large numbers of intraspecific yam diversity [12, 14]. Each of these is perceived as distinct and given a separate name. But, studies on how farmers identify, name, and classify yams are poorly studied. Accounts on the consistency of folk names and their importance as part of indigenous biosystematics of yams is scarce. Formal descriptors for yam had already been developed early in the nineteenth and twentieth century [20, 21] and have been improved at several instances [22,23,24]. Equally important but poorly studied aspect is accounts on the use of folk descriptors. The descriptors recognized by farmers have been little studied. The few attempts made in South and Southwest Ethiopia [12, 25] have focused only on folk taxonomy and have not covered the multiple dimensions of folk biosystematics.

This study aimed to test the following hypotheses. Classification of yam by some Southwest Ethiopian farmers is over-differentiated at the intraspecific level [12]. Knowing that such over-differentiation is rare, and is often related with crops of great importance [26], we hypothesized that this knowledge is widely shared within the community and across locations. Assuming that farmers manage a wide range of descriptors and other criteria for classification [12, 14, 25], we hypothesized that classification is based on a consistent sets of descriptors and can influence practical decisions of maintaining diversity. Considering that some locally recognized taxa are consistent to a considerable extent with the variability obtained in studies using standard markers [25, 27, 28], we assumed that folk taxonomy has a clear biological and functional implication. The present study was thus conducted with the objective (i) to investigate how yam species are named, identified, and classified by Sheko and Bench farmers, (ii) to identify a set of orders of folk ranks recognized by local farmers, and (iii) to assess consistency of folk taxonomy across locations and compare it with the formal taxonomy.

Methods

Population size and ethnic compositions

The study was conducted in Bench-Maji and Sheka Zones of southwest Ethiopia. They are part of the Southern Nations, Nationalities, and Peoples Region (SNNPR) of Ethiopia. The Regions are sub-divided into 13 zones, which are organized into woredas. Kebeles are the smallest administrative units within woredas. Bench-Maji Zone is sub-divided into 11 woredas. Based on the population projection values of 2017, this Zone has a total population of 847,168 of whom 687,212 or 81.12% are rural inhabitants [29]. Bench-Maji Zone is well-known by its multi-ethnic diversity consisting of six main ethnic groups namely Bench (45.11%), Me’enit (21.36%), Surma (3.88%), Dizzi (5.17%), Sheko (4.21%), and Zilmamo (0.22%). The remaining 20.05% comprises a diverse mix of other ethnic groups. Sheka Zone is sub-divided into 3 districts. Based on the population projection values of 2013, this Zone has a total population of 269,243 of whom 196,524 or 72.99% are rural inhabitants [29]. Sheka Zone is also well-known by its multi-ethnic diversity consisting four main ethnic groups namely Shakacho (32.41%), Bench (5.23%), Sheko (4.24%), and Majang (1.73%). The remaining 56.39% of the population comprises a diverse mix of other ethnic groups. Figure 1 presents map of the study area, indicating the surveyed points in Bench-Maji and Sheka Zones.

Fig. 1
figure 1

Map of the study areas, indicating the surveyed points in Bench-Maji and Sheka Zones

Sample and sampling procedure

This study was conducted in five districts of Bench-Maji and Sheka Zones. Yam-growing farmers were purposively considered for this survey. Secondary data regarding the accessibility and culture of yam farming were assessed in Bench-Maji and Sheka Zones. The secondary data obtained from each Zone were used to select yam-growing districts. A total of five yam-growing woredas (districts) were considered in this study. Within these districts, informal survey was conducted to identify yam-farming kebeles. In addition, secondary information regarding the accessibility of yams was assessed in each district. Based on the result of informal survey and secondary data, three kebeles were chosen in each woreda, bringing the total number of sampled households to 272. Informant interviews were adapted from ethnobotanical field inquires as suggested by [30]. Field visits in combination with individual farmer interviews using a standard questionnaire were carried out during the period from December 2016 to November 2017. The data collection procedures employed for recording folk biosystematics is given below.

Folk taxonomy

Folk taxonomy was researched with the use of informant interviews, researcher observations, and comparison of farmers’ recognized taxa with formal taxonomy. Folk ranks and taxa were recorded according to the universal scheme proposed by Berlin et al. [26] and Berlin [31]. Accordingly, there are at least five, perhaps six, ethnobiological folk categories which appear to be highly general if not universal in folk biological science. Applying the basic principles proposed by the preceding authors, the categories can be reduced into a set of four general nomenclatural orders as follows:

  1. 1)

    Farmers were asked to free list generic names to all kinds of yams they knew at and above species level. Taxa satisfying these conditions are generic; their labels are generic names.

  2. 2)

    A category called intermediate taxa included the fact that farmers recognized supra-variety categories that are labeled by names. Taxa satisfying these conditions are sub-generic (specific); their labels are supra-variety names.

  3. 3)

    Farmers were asked to free list the names of individual taxa that they perceive as a distinct unit. Taxa satisfying these conditions are varietal; their labels are variety names.

  4. 4)

    Some taxa are marked only by binary lexemes, containing further divisions of a variety. Taxa satisfying these conditions are sub-varietal; their labels are sub-variety names.

Ethnolinguistic analysis

A basic linguistic analysis, i.e., questions concerning the inherent logic and consistency of folk names, was researched with the use of farmers’ interview and researcher observations. Individual farmers were asked to free list the local names of yam varieties and sub-varieties they grew or knew. All the folk names were registered, and translation considering meaning, origin, and structures of folk names was made with the use of elderly farmers. The consistency of folk names was assessed with the use of fixed landrace samples. Of the total farms surveyed, landraces that were encountered in more than ten farms were selected as a fixed sample. Accordingly, 15 landraces were identified as fixed samples.

Folk descriptors

Folk descriptor was researched based on the farmers’ free listing of individual taxa along with their descriptors, according to informants’ own order of priority without major researcher intervention. Informants were asked to free list the names of (both known and actually grown) individual taxa. For each of the names, farmers were asked how they were able to identify it. All the folk descriptors were registered and supplemented with field observation by the researcher to verify the information gathered.

Results

Folk taxonomy

Names and naming of yams at and above species level

Farmers have used a broader set of subsystems in naming and classifying yams. Despite their separate taxa in scientific terms, at and above species level, all underground yam types have been merged into Sheko concepts of “Kachi”. The Bench, upland Omotic-speaking peoples to the east of Sheko, knew yam by the folk generic name “Boyye”. But, Bench still credits the Sheko with having initiated yam culture; some of the Bench farmers knew it by the Sheko generic name, “Kachi”. The cultivated bulbifera plant has different generic names. In Sheko, it is usually called “Ama”, whereas it is called “Oake” in Bench. Farmers also provide the generic names for wild yams. The prefixes such as “Karka” and “Shah” added to the names of wild yams are referring to location names in the wild places (Table 1). Thus, “Kachi” is a generic term that is usually used to refer to the underground yam types at the genus level, but not entirely applied to yam species. When farmers were asked to free list all kinds of yams they grew or knew, they linked plants of other species to yams though they are not yam. For instance, cassava (Manihot esculenta) is to some extent linked to yams and commonly known as Enchet-Kachi (Table 1).

Table 1 Sheko and Bench folk classification of yams at and above the species level

Names and naming of sub-variety, variety, and supra-variety

At least two well-recognized species (D. bulbifera and D. alata) and one species complex (the D. cayenensis complex) grow in the study area. The far Southwest Ethiopians classify these species into at least 37 varietal taxa. Some varieties are further composed of a number of subordinate units (sub-varieties), each of which are reported to differ from all the others at least in one feature. In our study, ten varieties consisted of 21 sub-varieties, bringing the total numbers of locally recognized individual taxa to 58 (Table 2). Of these, 34 represented actually grown landraces [16]. Besides these, six additional landraces were found in farms of unsampled households while the rest reported verbally. Yams in the lowest taxonomic levels, i.e., at varietal and sub-varietal ranks, are further grouped into distinct supra variety categories. These categories are labeled by names and usually group several varieties and sub-varieties together by a single criterion; they thus constitute intermediate ranking. Table 3 presents a description of nine supra-variety groups that are common in Sheko and its environs.

Table 2 Lists of variety and sub-variety names and the underlying basis of the classification
Table 3 Sheko and Bench intermediate folk categories of yams at the sub-generic level

Ethnolinguistic analysis of folk names

Meaning and origin of names

Names of yam varieties are derived from a wide range of sources. The sources from which names are originated include locations where it grows or comes from, attributes of a persons, or social groups, name of animals or pests, plant morphological characteristics, and others. Translation of names revealed that 49% of the names have meanings while the rest have no meanings, or their word origin is lost. The lists of names and their implied meanings are presented in Table 2. Naming is based on a consistent set of linguistic categories. A survey with 15 fixed landrace samples showed that about 88% of the landraces are consistently named across locations. Naming was considered consistent if more than 80% of the seed lots to which a particular name was attached represented the same variety [32]. Identification and distinction of the taxa assigned to different categories is also made based on a consistent set of characters and character states. Throughout the region, names and naming of varieties and sub-varieties of yams are often relying on specific plant traits.

Structures of names

Structures of variety names

Naming of varieties takes place in two structures: those that are composed of a single word (unitary names), and those that are consisted of two words (binary names). Unitary names can be divided into two obvious classes. Some unitary names such as Chabsha and Yasind are linguistically unanalyzable in form, containing unique words which can be shown to be semantically unitary and linguistically distinct. These expressions are known as simple unitary names. Others such as Karka-Kachi, Shah-boy, and Kaibab-kachi are analyzable linguistically. They are noticeable in that their expression shows the origin of a subordinate category. For instance, Karka-Kachi is kind of wild Kachi obtained from wild area, and Kaibab-kachi is a kind of domestic Kachi originated from Kaibab area, and so on. These forms are known as productive unitary names. Few yam varieties are also labeled with binary structures. Binary forms, like productive unitary forms, are identifiable in that each of the expression carries a modifier that marks a characteristic of the subordinate category. But, binary forms differ from productive unitary forms in that the modifiers they carry are related to specific plant characteristics. These forms are known as simple binary names. Examples of simple binary names include Tsid boy and Dal boy. Over 78% of the varieties are labeled with unitary names whereas the rest are binary names, indicating that the labeling system used for naming a given variety is skewed to uninominal (Table 2).

Structures of sub-variety names

Examination of the naming structure used for labeling sub-varieties shows that all consisted of binary names (Table 2). Two forms of binary names can be recognized. One group contains simple unitary names of a given variety in a modified form such as Tsid Chabsha and Dal yasind are noticeable in that the modifiers they carry are related with specific characteristics of a sub-variety. These forms are known as simple binary names. Other groups such as Karka-kachi submseb and Kaibab-kachi ga’nseb are identifiable in that they carry modifiers of a variety plus modifiers related with the characteristics of a sub-variety. These forms are known as productive binary names. The basic name of a sub-variety is often a binomial structure consisting of a word designating the variety plus a prefix/suffix added to it. The prefix/suffix is meaningless alone because several sub-varieties in different varieties may have the same specific prefix/suffix (Table 2).

Folk descriptors

Identification of varieties and sub-varieties

A total of 37 named varieties are recognized by farmers as distinct. The lists of names of varieties together with descriptions of the characters that the farmers used to distinguish them are presented in Table 2. Farmers used a total of 14 characters and 43 character states for distinction and identification of varietal categories (Table 4). More than half of these refer to aspects of a variety’s morphology, thus showing that morphological characters played a key role in the local distinction of yam varieties. Of these, tuber characteristics such as shape, color, size, and texture played a key role in the local identification of varieties. In some cases, non-tuber traits such as stem or leaf characters are also used. Non-plant characters such as location where it grows or comes from and attributes of persons or social groups can also be used to distinguish between varieties. For example, classification of a bulbifera variety does not depend on the physical traits of a plant but of its location. Farmers described that Ama/oake grows in gardens, whereas Karka-ama/Balakay-oake grows in wild places (Table 2).

Table 4 Comparison of Sheko and Bench folk classification of yams with the formal divisions

The lowest level of yam taxonomy is the sub-variety, i.e., composed of further divisions of a given variety. The lists of names of sub-varieties together with the description of the descriptors that the farmers used to distinguish sub-varieties are presented in Table 2. Altogether, 21 sub-varieties are recognized by farmers as distinct. Some sub-varieties of a given variety were reported to have the indicative features of the main variety; each was also reported to differ from all the others and the main variety at least in one aspect. Distinction and identification of sub-varietal category is principally or sometimes exclusively relying on the color of the tuber.

Supra-variety categories

Farmers have a number of additional systems for grouping yam varieties. Two major ways of groupings can be identified. One grouping distinguishes yams by cultivation contexts, describing them as cultivated, wild, or wild transplant. A second grouping distinguishes yams by gender describing them as female or male. Each of these groupings is formed by assembling several varieties and sub-varieties together; they are thus supra-variety categories, i.e., are groupings higher than the folk variety. Farmers used a total of 19 characters and 54 character states while grouping of yams by contexts and gender (Tables 3 and 4). The characteristics of the different supra-variety categories and the underlying basis of the classification are presented below.

Groupings on the basis of contexts

On the basis of contexts, yam varieties fall into three main supra-variety groups. These are (a) yams of the D. cayenensis complex or D. bulbifera that are growing wild; (b) yams of the D. cayenensis complex that have been recently transplanted from wild location to garden; and (c) yams of the D. cayenensis complex, D. bulbifera, or D. alata that are of under cultivation.

Wild-growing yams

Wild yams are morphologically related to some domestic yams, but unlike domestic yams, they have not been domesticated yet and exist in wild contexts. The term “wild” here refers to plants that are growing wild in the forest and had no known history of human manipulations. It also assembles volunteer plants growing in uncultivated areas without farmers’ help. In the studied area, wild growing yams are found in degraded forests, field margins, river banks, and disturbed habitats. Such yam types are known in Sheko as Karka-Kachi as a general category, with different one word names for smaller categories. In Bench, such yam types are known as Shah-boy as a general category, with no smaller categories (Table 2). The folk basis and the characteristics of this supra-variety category are presented in Table 3.

Wild transplant yams

Wild transplant yams are those yams transplanted from wild contexts and grown in home garden beneath a large tree. Unlike the cultivated yams that are replanted in an annual cycle, yams in this supra-variety group are left in the same place for many years. Hence, this group of yam qualifies as yams under domestication and not just as yams under cultivation. We therefore designate this supra-variety group as “wild transplants” to differentiate it from wild and cultivated yams. Across the study area, many gardens contain a few yams that seem on the state of transition, yams transplanted from wild contexts where many of them had no known history of cultivation in an open field along row of stakes. In Sheko, such yams are usually known as Karka-kachi while it is called Yasind in Bench as a general category, with each of them has different one word names for smaller categories (Table 2). The folk labels and the characteristics of this supra-variety category are presented in Table 3.

Farmers did not provide consistent morphological grounds for differentiating between wild and wild transplant yams. Yet, some farmers are able to describe the distinction between the two contexts. According to farmers, wild transplant yam retains its wild traits for the first few years after transplantation, and thus, they knew it by the name of wild places though it grows in a home garden. It begins to take on the traits of domestic yam, and in fact, farmers credit wild transplant yams as having broader and tasty tubers over the course of 3 to 5 years of cultivation. If they are satisfied with the modifications, they may rename it to a variety of domestic yam it resembles most closely. Sheko usually renames Karka-Kachi as Torbay or Kaibab-Kachi, whereas the Bench renames Yasind as Chabsha or Tolubab. There is no strict rule in naming, and renaming to a variety of other domestic yam is also possible.

Cultivated yams

This group of yams is further divided into two main supra-variety categories: those known to be recent transplants and those regarded as longtime variety.

Those known to be recent transplants

This group represented a variety of cultivated yams, but their morphotype is closely related with wild transplant yams. Some individual plants are known to be recently transplanted to open field. Farmers reported four varieties that belong to this supra-variety category, namely Kaibab-kachi, Chabsha, Torbay, and Tolubab (Table 2). Some of these names can also be used interchangeably for yams that have been recently transplanted from wild contexts and grow beneath a large tree. The name Kaibab-Kachi is sometimes used as a gloss for all varieties in this supra-variety category (Table 3).

Those regarded as longtime varieties

Of all yam varieties recorded, 27 have a longtime history of cultivation by humans (Table 2). They are usually grown in small plots of open field along rows of stakes. This group of yams can be further divided into three obvious classes. The first class assembles 22 varieties, most of which seem to have similarity to the D. cayenensis complex (Table 2). Of all the yam species, this complex is the most economically important, but also has the greatest number of locally threatened varieties. Six varieties, namely Shure, Don, Kappar, Dal boy, Zansul, and Kuchuu’bai are undergoing erosion. Others such as Kachi-kundi, Kachi-Kuch’ai, Kalu, Bud boy, Tush boy, and Bunkri are already abandoned. Farmers usually labeled them by the name Kachi/Boyye (Table 3). Despite the scientific taxa that describe their origins to separate areas in Africa, farmers regarded all of them as native to their area.

A second class comprises four longtime varieties belonging to D. alata (Table 2). Of these, Baday is the most common, both in terms of its distribution and relative abundances. Farmers usually labeled them by the name Baday-Kachi (Table 3). The names Baday and Ongubay are used interchangeably for one another and sometimes used as a gloss for all varieties of D. alata. This species is not native to Ethiopia, and in Ethiopia, it grows only in cultivated forms [11]. Farmers readily distinguished a variety of D. alata due to its large-sized foliages and four-winged stems. D. alata varieties had no known history of introduction to these areas, but farmers regarded all of these varieties as native to their area. D. alata, thus, must have first entered these areas as a cultivar well before the time periods known in local oral historic memory [12]. The meaning of the names of Baday, one of the most common variety (Table 2), also confirm the speculation made by Hildebrand [12] and suggests that farmers are aware of the distinct nature of this yam in relation to other kinds of domestic yam.

A third group comprises a single cultivar of bulbifera that is labeled by the name Ama-/Oake. It has two sub-varietal categories. Distinction between the two categories is relied on traces of dark pigmentation on the portions of the bulbils. The bulbifera plant also occurs in wild form. Farmers did not provide consistent morphological grounds for discriminating between the two contexts. Identification of a bulbifera variety as wild vs. cultivated does not depend on the physical traits of the plant but of its location and edibility of the bulbils (Tables 2 and 3).

Groupings on the basis of gender

On the basis of gender, yam varieties fall into two supra-variety groups: female (Mine/Baye) and male (Babu/Eyane). The distinction of varieties as male or female is not related to the biological reproduction of varieties. Farmers’ distinction most of the time depends on maturity stage, time of harvest, growth habit, taste of the tubers, and tolerance to stress. Some farmer claims early maturing, less vigorous, double harvest, and tasty varieties as female, while they are male otherwise. For instance, late maturing domestic yams such as Chabsha, Torbay, and Tolubab are among others that farmers considered as a male variety. All the wild and wild transplant yams were also considered as male varieties. Others such as Dizzu-Kachi and Tsid boy are among others that are recognized as female varieties (Tables 2 and 3).

Comparisons between folk and formal taxonomy

Sheko and Bench classification and naming of yam allows for the recognition of four distinct folk ranks. Each of these can be considered as belonging to different levels and thus arranged hierarchically. In order from the least to the most inclusive group, the categories are sub-variety, variety, supra-variety, and folk generic. Table 4 provides comparison of formal and folk botanic systems. Applying Berlin et al. [26] and Berlin [31] schemes, the folk-recognized ranks can be assigned to four formal biological divisions such as sub-varietal, varietal, sub-generic, and generic. Taxa assigned to the folk generic and varietal categories correspond to the formally recognized divisions at the genus and varietal levels, respectively. Taxa assigned to supra-variety category may also correspond to formally recognized ranks at the sub-generic level.

One interesting observation between the two system is that formal taxonomy focuses at and above species level, while folk taxonomy concentrates on intraspecific diversity, i.e., at the folk varietal and sub-varietal ranks. We found the highest number of taxa at the folk varietal and sub-varietal ranks. The recognition of rich taxa at the lowest folk ranks can be taken as a clear evidence for the existence of a moderate overlap between the two systems. Yet, the overlap is far from perfect, and the standards in folk taxonomy are not expected to be absolutely consistent across locations and different social domains; there are thus some anomalies. In view of this, the two systems can be combined in order to obtain insights into the links of classification rationale and systems applied to the management and utilization of on farm genetic resource.

Discussion

Indigenous biosystematics of yam

The folk taxonomic systems reported in Sheko and Bench show a pattern of hierarchy starting from the least to the most inclusive groups. Farmers recognize at least 58 individual taxa (Table 2). This suggests that Sheko and Bench taxonomy of yam is over-differentiated at the intraspecific level, i.e., at varietal and sub-varietal ranks. Such over-differentiation is rare and is often related with crops of great importance [26, 30, 31]. A similar distinction has been made to yam in South and Southwestern Ethiopia [12,13,14]. The same trend of using folk biosystematics was reported for enset in Southern Ethiopia [33, 34] and for sorghum in Eastern Ethiopia [35].

We also found nine supra-variety categories that are labeled by names (Table 3). Applying Berlin [31] scheme, these categories constitute mid-level ranking rather than separate taxa. The recognition of labeled intermediate taxa is highly relevant in order to obtain insights into the basic principles of native taxonomy and should not be ignored by placing too much stress solely on the named groups at smaller ranks. It is rare in most formal taxonomic system, and only a few works has yet reported such taxa. Such ranks have been reported in folk taxonomy of potatoes by the Quechua communities in the Andes [17, 18]. At and above species level, Sheko and Bench recognize four generic taxa (Table 1). Growing location was used as the main differentiating criterion for recognizing and naming of yams at the generic level. Our result is in accord with other reports on yam in Ethiopia [12] and in Oceania [36, 37], enset in Ethiopia [34], and species of Mesoamerican columnar cacti [3, 38] and potato in the Andes [17,18,19], where the local farmers in each of these areas recognize the genus level folk taxa in a similar way.

A basic ethnolinguistic analysis of folk names unraveled the meaning, origin, and structure of naming categories applied to yams. The meaning of the names is quite descriptive of the plant characteristics or its geographic origin. Besides, knowledge of the names and the characteristics of locally recognized taxa is widely shared within the community and across locations. This is evident in the recognition of a consistent set of folk names across locations as well as in the use of a consistent set of characters and character states for recognizing the different taxa. This suggests that there appears to be strong relationships between the ethnolinguistic forms of naming and the characters with which it labels. But, for the majority of the recorded names, their implied etymology was not explained by farmers. In Ethiopia, similar unexplained names were reported in these and other areas for yam and enset varieties [12, 14, 33, 34]. Examination of the labeling systems revealed that they are of two types structurally. Unitary structure was found to be predominant in variety names while all the sub-varieties were labeled with binary names. The existence of two distinct structures at the lowest botanic levels can be taken as a clear evidence of the existence of two separate folk groups. Studies from Ethiopia [12, 25, 33] reported a similar labeling system for varieties and sub-varieties of yam and enset.

Farmers used a wide range of folk descriptors for identification of taxa at varietal and sub-varietal ranks (Table 2). The lowest level of folk rank is sub-variety, where the primary contrast is between tuber colors. The folk descriptors identified in this study are comparable with descriptors reported for yam in Ethiopia [12] and in Oceania [37], where farmers relied on tuber color for sub-varietal distinction. Folk descriptor recognized in our study is also comparable with that reported for potato in the Andes [16,17,18, 39], where the only distinction between sub-varieties of potato is color of the tubers. The determination of a variety’s identity is made by considering a number of specific plant characteristics. Of these, variety is mainly distinguished by the shape, color, and size of the tubers. Non-tuber characters such as location, attributes of persons, or social groups are also used to distinguish yam varieties. The folk descriptors recorded in this study are comparable with those reported for yam in Ethiopia [12, 13, 25]. Folk descriptors recognized for yam also share the descriptors reported for enset in Sidama and Wolaita [33, 34].

Analysis of the ethnobotanical data showed that the individual units are further grouped into a number of named categories. Sheko and Bench recognize three main supra-variety categories by contexts, describing them as cultivated, wild, or wild transplant. Four additional subordinate groups are recognized within the cultivated groups, bringing the total number of labeled groups to seven. Each of these categories is made up of small subpopulations that are morphologically distinct, yet share some overlapping character states that the farmers used to group them (Table 3). This reflects the diversity forms of cultivated yams through which farmers drive its evolution under domestication. A similar distinction has been made in Ethiopia with yam [12]. Sheko and Bench also recognize two main supra-variety groups of yam on the basis of gender, describing them as male or female. Gender can thus be considered as a distinct way of classifying supra-variety groups and, hence, influence practical decisions of maintaining diversity. Gender-based classification system was reported for yam in Ethiopia [14, 25]. This gender-related classification is not limited to yam, where similar studies [33, 34, 40] reported gender-based classification of enset, showing that different social groups in Ethiopia classify crop plants in a similar way.

Comparison between formal and folk taxonomy

The local classification system allows for the recognition of a folk biological category consisting of four ranks (Table 4). Sheko and Bench taxonomy of yam shares the general classification schemes reported for enset in Ethiopia [33], potato and cassava in the Andes [16, 17, 39, 41, 42], columnar cacti in Mexico [38], and folk botanical classification of plants in Switzerland [43]. A closer look of the two systems shows a moderate overlap, the most frequent being difference in scales. In the formal taxonomy, varietal taxa occur in contrast sets of few members, while in folk taxonomy it occurs in contrast sets of many members. Contrast sets of more than two members tend to refer to plants of major cultural importance [26]. Though there is a modest overlap, they are arguably complementary at least for two reasons. First and more notably, the folk-recognized taxa are consistent to a considerable extent with the variability obtained with standard markers (Tsegaye B, Bizuayehu T, Wendawek A: Assessing Morphological Diversity in Ethiopian Yams (Dioscorea spp.) and its Correspondence with Folk Taxonomy, forthcoming), confirming earlier reports from Ethiopia [25, 27, 28, 44] and West Africa [45,46,47]. This suggests that biological and functional consideration constitutes the basis of folk taxonomy. Second, farmers manage a wide range of descriptors, each of which contains several character states with inherent labeling systems. This provides additional support to the view that plant classification is not an activity confined to the domain of formal science only.

Conclusion

A number of conclusions can be drawn from the study. First, analysis of the local classification systems in Southwest Ethiopia suggests that within the province where cultivation of yam is feasible, Sheko and Bench botany of yam is unique. It is polytypic in Sheko, as is also in Bench. This is evident in the recognition of four taxonomic ranks. Second, farmers used a wide range of descriptors for recognizing the different taxa, most of which correspond to the formal descriptor list. As a result, the two systems can be treated as complementary, and conservation efforts should take both systems into account.

Third, farmers recognize various individual taxa. Each of these is perceived as distinct and given a separate name. The recognition of rich intraspecific taxa is prima facie evidence for great diversity and can be used as the unit of on farm diversity. Individual households are the primary management unit of selection and maintaining diversity. Assessment of diversity kept by diverse households is essential to obtain insights into the nature and spatial dynamics of diversity, and this assessment can rely on folk-recognized taxa. Research on diversity can draw directly on folk biosystematics as long as the unit of analysis is the household.

More generally, this study documented folk biosystematics of yams by the far Southwest Ethiopians, constitutes a complex of dynamic indigenous knowledge that is highly relevant for conservation efforts. Yet, the study is not exhaustive; no objective generalizations can thus be drawn regarding the actual extent of diversity in Ethiopia. The problem is further complicated by the fact that for the majority of the recorded names, their etymons and implied descriptions are incomplete. Thus, more detailed ethnobotanical studies in these and other areas are of paramount importance to unravel such difficulties.

Availability of data and materials

The ethnobotanical data gathered during the current study are included in the manuscript. Other supplementary materials such as photographs and field notes of varieties are available by request to the authors.

References

  1. Emshiwller E. Evolution and conservations of clonally propagated crops. Insights from AFLP data and folk taxonomy of Andean tuber Oca (Oxalis tuberosa). In: Motley TJ, Zerega N, Cross H, editors. Darwin’s harvest: new approaches to the origins, evolution, and conservation of crops. USA: Colombia University Press; 2006. p. 308–32.

    Google Scholar 

  2. Motley TJ, Zerega N, Cross H, editors. Darwin’s harvest: new approaches to the origins, evolution, and conservation of crops. USA: Colombia University Press; 2006.

    Google Scholar 

  3. Parra F, Casas A, Peñaloza-Ramírez JM, Cortés-Palomec AC, Rocha-Ramírez V, González-Rodríguez A. Evolution under domestication: ongoing artificial selection and divergence of wild and managed S. pruinosus populations in the Tehuacan Valley, Mexico. Ann Bot. 2010;106:483–96.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Alexander J, Coursey DG. The origins of yam cultivation. In: Peter UJ, Dimbleby GW, editors. The domestication and exploitation of plants and animals. London: Cerald Duckworth; 1969. p. 405–25.

    Google Scholar 

  5. Burkill IH. The organography and evolution of Dioscoreaceae, the family of yams. J Linn Soc. 1960;56(367):319–412.

    Article  Google Scholar 

  6. Coursey DG. YAMS: an account of the nature, origins, cultivation and utilization of the useful members of the Dioscoreaceae. London: Longmans and Green; 1967. p. 222.

    Google Scholar 

  7. Degras L. The yam: a tropical root crop. London: The Technical Centre for Agricultural and Rural Cooperation (CTA), Macmillian; 1993.

    Google Scholar 

  8. Norman MJT, Pearson CJ, Searle PGE. The ecology of tropical food crops. 2nd ed. Cambridge: Cambridge University Press; 1995.

    Book  Google Scholar 

  9. Harlan JR. Ethiopia: a centre of diversity. Econ Bot. 1969;23:309–14.

    Article  Google Scholar 

  10. Edwards S. Crops with wild relatives found in Ethiopia. In: Engels JMM, Hawkes JG, Melaku W, editors. Plant genetic resources of Ethiopia. New York: Cambridge University Press; 1991. p. 42–75.

    Chapter  Google Scholar 

  11. Miège J, Sebsebe D. Dioscoreaceae. In: Edwards, S. Sebsebe D. and Hedberg, I. (eds). Flora of Ethiopia and Eritrea. A Joint publication of the National Herbarium, Biology Department, AAU, Ethiopia and the Department of Systematic Botany, Uppsala University, Sweden; 1997. p. 55–62.

  12. Hildebrand EA. Motives and opportunities for domestication: an ethnoarchaeological study in Southwest Ethiopia. J Anthropol Archaeol. 2003;22:358–75.

    Article  Google Scholar 

  13. Tamiru M, Becker HC, Maass BL. Diversity, distribution and management of yam landraces (Dioscorea spp.) in Southern Ethiopia. Genet Resour Crop Evol. 2008;55:115–31.

    Article  Google Scholar 

  14. Sisay T. Diversity and management of yam landraces (Dioscorea spp.) in Bench-Maji Zone, Southwest Ethiopia. Lap Lambert Academic publishing; 2012.

  15. Tewodros M. Genetic diversity, path coefficient analysis, classification and evaluation of yams (Dioscorea spp.) in Southwest Ethiopia. Haramaya: PhD thesis, Haramaya University; 2016.

    Google Scholar 

  16. Haan S, Bonjerbale M, Ghislain M, Nunez J. Indigenous biosystematics of Andean potatoes: folk taxonomy, descriptors, and nomenclature. Acta Hort. 2007;745:89–115.

    Article  Google Scholar 

  17. Brush SB. Ethnoecology, biodiversity, and modernization in Andean potato agriculture. J Ethnobiol. 1992;12:161–85.

    Google Scholar 

  18. Brush SB. Farmers’ bounty: locating crop diversity in the contemporary world. New Haven: Yale University Press; 2004.

    Book  Google Scholar 

  19. Zimmerer KS. Changing fortunes: biodiversity and peasant livelihood in the Peruvian Andes. Berkeley: University of California Press; 1996.

    Book  Google Scholar 

  20. Poiret IC. Dioscorea rotundata. In: Encyclopediae Methodique. Suppl. III. Paris; 1813.

  21. Chevalier A. Contribution a retude de quelques especes africaines du genre Dioscorea. Bulletin du Museum National d’Histoire Naturelle 2eme Serie. 1936;8:520–51.

    Google Scholar 

  22. Ayensu ES, Coursey DG. Guinea yams. The botany, ethnobotany, use and possible future of yams in West Africa. Econ Bot. 1972;26:301–18.

    Article  Google Scholar 

  23. Martin FW, Rhodes AM. The relationship of D. cayenensis/rotundata. Trop Agric. 1978;55:193–206.

    Google Scholar 

  24. IPGRI/IITA. Descriptors for yam (Dioscorea spp.). Ibadan: International Plant Genetic Resource Institute (Rome)/International Institute of Tropical Agriculture; 1997.

    Google Scholar 

  25. Tamiru M, Becker HC, Maass BL. Comparative analysis of morphological and farmers’ cognitive diversity in yam landraces (Dioscorea spp.) from Southern Ethiopia. Trop Agric Dev. 2011;55:28–43.

    Google Scholar 

  26. Berlin B, Breedlove DE, Raven PH. General principles of classification and nomenclature in folk biology. Am Anthropol. 1973;75:214–42.

    Article  Google Scholar 

  27. Wendawek A, Demissew S, Fay FM, Smith RJ, Nordal I, Wilkin P. Genetic diversity and population structure of Guinea yams and their wild relatives in South and South West Ethiopia as revealed by SSR marker. Genet Resour Crop Evol. 2013a;60:529–41.

    Article  Google Scholar 

  28. Wendawek A, Demissew S, Fay FM, Smith RJ, Nordal I, Wilkin P. Genetic diversity and species delimitation in the cultivated and wild Guinea yams from Southwest Ethiopia as determined by AFLP markers. Genet Resour Crop Evol. 2013b;60:1365–75.

    Article  Google Scholar 

  29. CSA. Population projection of Ethiopia for all regions at zone and woreda levels from 2014 – 2017. Addis Ababa: Central Statistical Agency; 2013.

    Google Scholar 

  30. Martin GJ. Ethnobotany: a method manual. London: Earthscan Publications; 2004.

    Google Scholar 

  31. Berlin B. Ethnobotanical classification; principles of categorization of plants and animals in traditional societies. Princeton: Princeton University Press; 1992.

    Book  Google Scholar 

  32. Nuijten E, Almekinders CJM. Mechanisms explaining variety naming by farmers and name consistency of rice varieties in the Gambia. Econ Bot. 2008;62(2):148–60.

    Article  Google Scholar 

  33. Bizuayehu T. On Sidama folk identification, naming, and classification of cultivated enset (Ensete ventricosum) varieties. Genet Resour Crop Evol. 2008;55:1359–70.

    Article  Google Scholar 

  34. Olango TM, Tesfaye B, Catellani M, Enrico PM. Indigenous knowledge, use and on-farm management of enset (Ensete ventricosum (Welw.) Cheesman) diversity in Wolaita, Southern Ethiopia. J Ethnobiol Ethnomed. 2014;10:41.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Mekbib F. Infra-specific folk taxonomy in sorghum (Sorghum bicolor) in Ethiopia: folk nomenclature, classification, and criteria. J Ethnobiol Ethnomed. 2007;3:38.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Hayes TE. Plant classification and nomenclature in Ndumba, Papua New Guinea highlands. Am Ethnol. 1976;3:253–70.

    Google Scholar 

  37. Malapa R, Noyer JL, Marchand JL, Lebot V. Genetic relationship between Dioscorea alata L. and D. nummularia Lam. as revealed by AFLP markers. In: Motley TJ, Zerega N, Cross H, editors. Darwin’s harvest: new approaches to the origins, evolution, and conservation of crops. USA: Colombia University Press; 2006. p. 239–68.

    Google Scholar 

  38. Casas A, Pickersgill B, Caballero J, Valiente-Banuet A. Ethnobotany and domestication in Xoconochtli, S. Stellatus, In Tehuacan Valley and La Mixteca Baja, Mexico. Econ Bot. 1997;51:279–92.

    Article  Google Scholar 

  39. Zimmerer KS. The regional biogeography of native potato varieties in the highland of Peru. J Biogeogr. 1991;18:165–78.

    Article  Google Scholar 

  40. Almaz N, Niehof A. The significance of enset culture and biodiversity for rural households’ food and livelihood security in Southwestern Ethiopia. Agric Human Values. 2004;21:61–71.

    Article  Google Scholar 

  41. Quiros CF, Brush SB, Douches DS, Zimmerer KS, Huestis G. Biochemical and folk assessment of variability of Andean cultivated potatoes. Econ Bot. 1990;44:254–66.

    Article  CAS  Google Scholar 

  42. Boster JS. Selection for perceptual distinctiveness: evidence from the Aguaruna cultivates of Manihot esculenta. Econ Bot. 1985;39:310–25.

    Article  Google Scholar 

  43. Poncet A, Vogl CR, Weckerle CS. Folkbotanical classification: morphological, ecological and utilitarian characterization of plants in the Napf region, Switzerland. J Ethnobiol Ethnomed. 2015;11:13.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Tamiru M, Becker HC, Maass BL. Generic diversity in yam germplasm from Ethiopia and their relatedness to the main cultivated yam species assessed by AFLP markers. Crop Sci. 2007;47:1744–53.

    Article  CAS  Google Scholar 

  45. Dansi A, Mignouna HD, Zoundjihekpon J, Sangare A, Asiedu R, Quin FM. Morphological diversity, cultivar groups and possible descent in the cultivated yams (D. cayenensis complex) of Benin Republic. Genet Resour Crop Evol. 1999;46:371–88.

    Article  Google Scholar 

  46. Dansi A, Mignouna HD, Zoundjihekpon J, Sangare A, Asiedu R, Ahoussou N. Using isozyme polymorphism to assess genetic variation within cultivated yams (D. cayenensis complex) of the Benin Republic. Genet Resour Crop Evol. 2000a;47:371–83.

    Article  Google Scholar 

  47. Tostain S, Agbangla C, Scarcelli N, Mariac C, Daïnou O, Berthaud J, Pham J. Genetic diversity analysis of yam cultivars (D. rotundata Poir.) in Benin using simple sequence repeat (SSR) markers. Genet Resour Crop Evol. 2007;5:71–81.

    CAS  Google Scholar 

Download references

Acknowledgements

We duly acknowledge Hawassa University, School of Graduate Studies, for facilitating the grant funded by Ethiopian Ministry of Science and Higher Education. We also acknowledge the immense contribution made by Mizan-Tepi University, College of Agriculture and Natural Resource, for facilitating the field survey and Institute of Research and Community Development Support for subsidizing the research.

Funding

This study was funded by the Ethiopian Ministry of Science and Higher Education. The funding body has no role in the design of the study, analysis, and interpretation of the data and in writing the manuscript.

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Field survey, interpretation and analysis of the data and writing the original draft were made by the corresponding author; while the co-authors contribute in conceptualization, review and editing the paper. All authors have read and approved the final version of the manuscript.

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Correspondence to Tsegaye Babege Worojie.

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Worojie, T.B., Asfaw, B.T. & Mengesha, W.A. Indigenous biosystematics of yams (Dioscorea spp.) in Southwest Ethiopia: folk taxonomy, ethnolinguistic analysis, and folk descriptors. J Ethnobiology Ethnomedicine 17, 1 (2021). https://doi.org/10.1186/s13002-020-00427-8

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