Potato (Solanum tuberosum L.) is the world’s third most important food crop in overall production after rice and wheat, and is a food security crop (Devaux et al. 2014) in some countries, including Ethiopia. The past few decades have seen a dramatic increase in potato production and demand in many developing countries (FAO 2014). In Ethiopia, potato production area has increased more than fivefold from 30,000 ha during the 1970s (Kidane Mariam 1979) to more than 169,000 ha today (CSA 2014). The climate of the Ethiopian highlands is well-suited for potato production. That, combined with the need for a crop that can be harvested in August and September to meet seasonal food shortages, are two reasons why potato production has expanded so dramatically.

Although the International Potato Center (CIP) has worked with Ethiopian partners to introduce many new cultivars over the past three decades, most Ethiopian farmers still grow older local cultivars (Labarta et al. 2012; Kolech et al. 2015). The origin of these cultivars is not well understood, although it is clear that local cultivars differ considerably from each other in terms of adaptation to the numerous ecological zones of the country, as well as for many important traits (e.g., storability, drought tolerance, marketability, suitability for making stew) (Abebe et al. 2013; Kolech et al. 2015). Seventy to 90 % of Ethiopian farmers report growing at least two local cultivars each year. Nationally, about 77 % of Ethiopian potato land is planted to local cultivars each year (Kolech et al. 2015).

Kidane Mariam (1979) suggested that Ethiopian local cultivars may have originated from a small number of introductions and reported that local cultivars were low yielding. Because of the perception of poor yield, local cultivars have received relatively little attention from the research community. Instead, cultivar improvement has centered on evaluating clones developed by outside sources, primarily CIP. Using this approach, the Ethiopian potato cultivar development program has released at least 29 potato cultivars since 1987 (MOA 2013). In addition, three Dutch cultivars have been registered in Ethiopia by a private company, SolaGrow. Nonetheless, only 23 % of the production area is allocated to new cultivars (Kolech et al. 2015), and only a few of the new cultivars have been adopted (Woldegiorgis 2013).

Potato has been cultivated in Ethiopia since its introduction by a German botanist, Wilhelm Schimper, in about 1858 (Pankhurst 1964). The next known introduction was over 100 years later, in 1971–72, when several Dutch cultivars were tested in the country (Kidane Mariam 1979). There may have been introductions between 1858 and 1971, e.g., by missionaries, but we know of no documentation supporting this. After 1972, several authors reported the introduction of additional cultivars (Yilma 1987; Lemaga et al. 1994; Woldegiorgis et al. 2001). In 1981, 27 commercial cultivars were introduced from the Netherlands and tested under Ethiopian conditions (Lemaga et al. 1994). From these introductions only one cultivar, ‘Krolisa’, was released in Ethiopia, under the name ‘Wechecha’ (Kolech et al. 1998). According to Woldegiorgis et al. (2001), drought in 1985 resulted in the importation of more than 2340 tons of seed of European potato cultivars, some of which could have been saved for seed. Because Ethiopia lacks a cultivar registration system for local cultivars, and does not have an advanced seed certification system, it is very difficult, if not impossible, to trace back the origins of current local cultivars through historical records alone.

The first step in crop improvement in a developing country should be a full assessment of the local material (Williams et al. 1991). Similarly, Ortiz (2001) argued that including locally adapted potato germplasm in crossing would help ensure that the resulting cultivars could be produced in a sustainable and environmentally-friendly manner. Molecular markers are playing an increasingly important role in the management and utilization of plant genetic resources (Karp 2002). The recent development of a single nucleotide polymorphism (SNP) chip for potato has made it possible to assess genetic variation in a dosage-sensitive manner at thousands of loci simultaneously (Hirsch et al. 2013). Using the potato 8303 SNP chip, we evaluated genetic variation in local cultivars collected from the two major potato production zones of Ethiopia (Northwest and South) as well as from cultivars developed in America and Europe, and cultivars developed by CIP. Our objectives were to: 1) assess the extent to which cultivars in Ethiopia are known by different names (not uncommon in countries without a strong, formalized seed system); 2) examine the genetic diversity of Ethiopian potatoes; and 3) assess the relationship between Ethiopian cultivars and cultivars/advanced clones developed in other parts of the world (CIP, America and Europe).

Material and Methods

Plant Materials

Forty-four local cultivars were collected from Northwest (Amhara region) and Southern (Oromia and SNNPR) Ethiopia (Fig. 1) during 2012 and 2013. Ten to twenty-five tubers of each local cultivar were collected from either markets or farmers’ fields, and their names recorded based on the knowledge of growers, traders and/or marketers. Details of the collections are shown in Table 1. Passport data including cultivar characteristics and estimated time of introduction were also collected at the time of collection but these data were not comprehensive. Each cultivar was planted in a screen house at the Adet Agricultural Research Center for morphological observation and genetic fingerprinting. At the same time, DNA was isolated from 31 CIP genotypes (17 ‘improved’ cultivars and 14 advanced clones) from research fields at the Adet and Holetta Agricultural Research Centers. The improved cultivars represent those introduced into Ethiopia from CIP research sites in Peru and Kenya at different times, which were subsequently tested and ultimately officially released for production in Ethiopia. The CIP advanced clones represent new introductions from CIP for evaluation as possible new cultivars. Details of the CIP materials are shown in Table 2. SNP data of 22 widely grown American cultivars were generated previously (Hirsch et al. 2013). SNPs from European cultivars were collected using the same SNP chip as for the Ethiopian, American and CIP germplasm. The American and European cultivars evaluated are summarized in Table 2, and represent several market classes (chipping, French fries and table), as well as old and newer cultivars.

Fig. 1
figure 1

Local cultivar collection sites

Table 1 List of Ethiopian potato cultivars sampled along with their collection sites
Table 2 List of CIP potato cultivars and advanced clones, as well as European and North American cultivars

Morphological Assessment

The vines, flowers and tubers of local cultivars were characterized using descriptors for cultivated potato (Huaman et al. 1977) to complement the results of DNA analysis. For leaf and stem characteristics, stem color, shape of stem cross section, abaxial and adaxial leaf pubescence, leaf dissection, leaf size, leaf color, growth habit and branching habit were recorded. Flower characteristics measured included flower color, degree of flowering, and tendency to premature flower abscission. Tuber characteristics recorded after harvest include tuber skin color, tuber flesh color, tuber skin texture, secondary tuber color, tuber shape, and storability.

DNA Extraction and SNP Genotyping

DNA was extracted from two young leaves of each cultivar/advanced clone (from screen house plants for local cultivars, and from field grown plants of CIP advanced clones) using the CTAB method of Mace et al. (2003). The quality of each DNA sample was checked by agarose gel electrophoresis and a Nano Drop spectrophotometer (Thermo Fisher Scientific, USA). Later, the DNA was sent to Cornell University and clarified using a QIAGEN DNeasy Plant Minikit (QIAGEN, Germantown, MD). The DNA was then sent to Michigan State University and genotyped at 8303 SNP loci using the potato Illumina Infinium array developed by the SolCAP project (Hirsch et al. 2013). Loci with low-signal intensity or that displayed no polymorphism, or that did not cluster well into discrete dosage categories were filtered out. Of the 8303 markers genotyped, data from 3696 were retained for evaluation of potato diversity.

Genotypic Data Analysis

To study the genetic relationship of Ethiopian local cultivars to each other, as well as to cultivars/advanced clones from North America, Europe and CIP, a neighbor joining analysis was performed. The SplitsTree4 program version 4.13.1 was used to construct an unweighted pair group method with arithmetic mean (UPGMA)-based tree (Huson and Bryant 2006). Archaeopteryx version 0.9901 beta was then used to generate the tree image (Han and Zmasek 2009). Principal component analysis was conducted using JMP software (JMP 2012). The SNP data were first converted into numeric data (AAAA = −1, AAAB = −0.5, AABB =0, ABBB =0.5, BBBB =1), then the principal component analysis was computed from the correlation matrix.

Genetic diversity among Ethiopian cultivars and between Ethiopian cultivars and germplasm from America, Europe and CIP was calculated using a custom R script based on the method described by Thrall and Young (2000). After minor allele frequencies for each locus were calculated for a subgroup of all cultivars and advanced clones combined, expected heterozygosity values (chromosome inheritance model) for each allele were calculated as

$$ \mathrm{H}=2*{\mathrm{p}}^3*\mathrm{q}+4*{\mathrm{p}}^2*{\mathrm{q}}^2+2*{\mathrm{q}}^3*\mathrm{p} $$

Where p is the major allele frequency, q is minor allele frequency, p + q = 1, the AAAB and ABBB genotypes are given a heterozygosity weight of 0.5, and AABB is given a heterozygosity weight of 0.667 (Bever and Felber 1992). Expected heterozygosities for each subgroup (HS), and for all cultivars/advanced clones combined (HT) were calculated by averaging expected heterozygosities across all loci. Genetic differentiation of each group relative to all potato cultivars/advanced clones (FST) was calculated as FST = (HT-HS)/HT). Expected heterozygosity of each of the 3696 loci for each of the four groups were arranged in four columns in Excel and exported to JMP software (JMP 2012). Then, t statistics were computed to test whether expected heterozygosity between groups was significantly different. Genetic differentiation between groups was arranged in the same way as expected heterozygosity, and t statistics similarly computed to test pairwise differentiation between groups. Expected heterozygosity, rather than observed heterozygosity, was used in this study as the former provides a framework for comparing genetic variation across groups, while the latter is better suited for detecting deviations from Hardy-Weinberg equilibrium.


Identifying Cultivars by Morphological and Molecular Characterization

In the course of growing out samples of cultivars collected from farmers’ fields and markets, we observed that seven of the 44 samples were cultivar mixtures, where the phenotypes of some plants in a sample were strikingly different from other plants in the same sample. Morphological descriptions collected from farmers or marketers during the course of collecting were used to identify which of the two cultivars in a mixture would be subjected to further analyses.

We also detected mislabeling in cultivars handled by Ethiopian research centers. SNP analysis revealed that samples of the new cultivars ‘Awash’ and ‘Gabisa’ were identical, as were samples of ‘Tolcha’ (UK-80.3) and ‘Shenkolla’. We used CIP potato catalogue and Ethiopian cultivar registry booklets to determine which cultivars these actually were (‘Gabisa’ and ‘Shenkolla’, respectively).

Our genotyping and morphological evaluations further revealed that ‘Sisay’, a CIP-bred cultivar, is one of the most widely grown cultivars in Yilmana (Northwest Ethiopia). When we collected this cultivar, there was no reason to believe it was anything other than a local cultivar, because it was not documented in the Ethiopian potato cultivar registry. We later noticed that CIP had recently released a cultivar by the name of ‘Sisay’ in Ethiopia (Acquisition and Distribution Unit 2008). The morphological features used to define ‘Sisay’ in the CIP catalog are identical to the morphological characteristics of the cultivar we had collected.

Duplications within Ethiopian Collections

Farmers name potato cultivars based on varietal characteristics that they readily perceive. Most Ethiopian local cultivar names are based on descriptors such as texture, flower and tuber color, taste, or productivity. However, after conducting morphological and SNP comparisons, we found that some cultivar are known by many different names across the country. Of the 44 samples of local cultivars, described with 33 unique names, we found only 15 unique genotypes. The names and known synonyms of each of the 15 unique genotypes are shown in Table 3. For instance, a widely grown cultivar in Northwest Ethiopia (West Amhara region) is known as ‘Deme’ or ‘Demas’ in Sinan, as ‘Ater Abeba’ and ‘Siquare’ in Yilmana, Quarit and some districts of the Awi zone, as ‘Mirt’ in Banja, and as ‘Key Dinch’ in Laigaint. The same cultivar is known as ‘Key’ in Bekoji and ‘Woyra’ in Southern Ethiopia. A cultivar with the same morphology as ‘Siquare’ is known as ‘Abateneh’ at Sekela, and ‘Rejim Siquare’ at Yilmana and Quarit. A surprising observation was that two improved cultivars, ‘Jalene’ and ‘Guasa’, were found to be identical by both SNP and morphological analyses. These two cultivars have long been considered siblings in Ethiopia, as it is known that both originated from the same CIP cross (Table 2). ‘Jalene’ was released by the Holeta Agricultural Research Center while ‘Guasa’ was released by the Adet Agricultural Research Center. It is remarkable that these two cultivars were not known to be identical until now. Similarly, two CIP advanced clones, CIP-393382.44 and CIP-393385.39 were found to be identical.

Table 3 Proposed names for Ethiopian local cultivars, along with known duplicate names, cultivar characteristics and areas of adaptation

These duplications have misled previous authors, who reported the names of these cultivars as if they represented different genotypes (Woldegiorgis et al. 2008; Tesfaye et al. 2008; Yazie et al. 2009; Labarta et al. 2012). For example, Tesfaye et al. (2008) reported ‘Demie’, ‘Siquare’ and ‘Key Abeba’ as if these names represented different cultivars but our DNA and morphological analysis showed that they are identical. Adding to the confusion, the Hawassa Agricultural Research Center released a new cultivar in 2005 known as ‘Bulle’ (MOA 2006) which, unfortunately, was already the name of a widely grown local cultivar.

In a few cases we observed distinct genotypes known by the same name. Traders at Hawassa refer to the distinct genotypes of ‘Durame’ and ‘Agazer’ as ‘Durame’, whereas all farmers in Shashemene (who supply the Hawassa markets) correctly identify these as different cultivars with different names. Similarly, consumers and traders in the city of Bahir Dar used the name ‘Key Dinch’ for both ‘Siquare’ and ‘Abateneh’.

It is important for future cultivar identification, research and breeding if each cultivar is known by one, and only one, unique name. Our proposed unique names for local cultivars that are currently known by one or more duplicate names are shown in Table 3; in all cases, we propose the name that is most widely used at present. To differentiate the local ‘Bulle’ cultivar from the new ‘Bulle’ cultivar, which are genotypically and morphologically distinct, we propose renaming the local cultivar as ‘Bulle Local’.

Genetic Relationships among Ethiopian Local Cultivars and Relationship to Cultivars from CIP, America and Europe

After removing duplicate genotypes, cluster analysis was performed again. Data from 3696 polymorphic SNPs were analyzed to construct the neighbor-joining dendrogram shown in Fig. 2. With a few exceptions, potato cultivars and advanced clones from America (n = 22), Europe (n = 17) and CIP (n = 26) separated into three distinct branches. Ethiopian cultivars (n = 15) localized to the European and CIP branches; none clustered with American cultivars. The oldest cultivars from northwest Ethiopia (‘Enat Beguaro’, ‘Abalo’ and ‘Samune’) and Southern Ethiopia (‘Durame’) all grouped within the European branch. The southern Ethiopian local cultivar ‘Key Shule’, the widely grown local cultivar ‘Siquare’, and the less widely grown local cultivars ‘Feleke’ and ‘Gedigala’ group in a separate sub-cluster of the European branch.

Fig. 2
figure 2

Clustering of cultivars and advanced clones using neighbor-joining analysis of 3696 SNP markers. American cultivars are shown in black, European cultivars are shown in green, CIP (International Potato Center) cultivars and advanced clones are shown in blue, and local Ethiopian cultivars are shown in red

Two cultivars from Northwest Ethiopia (‘Kuchibiye’ and ‘Abadamu’) and major cultivars from southern Ethiopia (‘Holland’, ‘Nech Abeba’, ‘Agazer’ and ‘Bulle’) group together with several of the CIP cultivars and advanced clones evaluated. ‘Kuchibiye’ and ‘Bulle’ are also similar morphologically, both being known by their pink tuber color and pigmented leaf veins. ‘Abateneh’ (from northwest Ethiopia) is the only Ethiopian cultivar that grouped in a distinct sub-cluster of CIP cultivars and advanced clones.

Genetic relationships were further assessed using principal components analysis, which showed that American, European and CIP-bred cultivars and advanced clones group into three distinct clusters with relatively little overlap (Fig. 3). Most local cultivars of northwest Ethiopia cluster with the European group while the dominant cultivars of Southern Ethiopia cluster with the CIP group.

Fig. 3
figure 3

Principal components of the simple matching coefficient matrix, calculated from 80 potato cultivars genotyped with 3696 polymorphic SNP markers. American cultivars are represented by black dots, European cultivars are represented by green rectangles, CIP cultivars and advanced clones are represented by blue diamonds, and local Ethiopian cultivars are represented by red stars. The percent variation explained by the first and second components is shown in parentheses

Heterozygosity in Ethiopian Potatoes Compared to American, European and CIP Cultivars and Advanced Clones

3696 polymorphic SNP markers were used to calculate expected heterozygosity (HS and HT). There are small but statistically significant differences in heterozygosity between Ethiopian, American, European and CIP cultivar groups (Table 4). Even though the Ethiopian cultivar group did not contain any unique SNP alleles (Fig. 4), higher heterozygosity was observed in the Ethiopian group compared to the CIP group. The American group is the most heterozygous, and had more unique alleles than any other group, possibly because the SNPs on the chip were chosen for their polymorphism in American cultivars. The CIP group exhibited the lowest heterozygosity of all four groups.

Table 4 Mean SNP diversity for 3696 SNP markers
Fig. 4
figure 4

Venn diagram illustrating how SNPs are distributed among Ethiopian, North American, European and CIP cultivars and advanced clones. Individuals of each group were genotyped with 3696 polymorphic SNP markers. The Ethiopian, North American, European and CIP cultivars and advanced clones are represented by red, black, green, and blue rectangles, respectively

Genetic Differentiation

Genetic differentiation was analyzed for each of the four cultivar groups compared to all potato cultivars and advanced clones combined, as well as between groups, as shown in Table 4. Pairwise genetic differentiation between groups showed that each group is statistically different from every other group, but the magnitude of each pairwise difference was small. The Ethiopian cultivar subgroup is more closely related to CIP and European germplasm than to American cultivars.


Causes of Duplications among Ethiopian Cultivar Collections

Of the 44 local potato cultivars evaluated in Ethiopia, we found only 15 distinct genotypes. Most of these 15 genotypes are known by different names in different parts of the country. The high frequency of duplications likely exists because the dominant seed system in Ethiopia is informal (Gildemacher et al. 2009; Hirpa et al. 2010): seed tubers are produced and disseminated without any regulations. The movement of seed tubers is common in Ethiopia (Samberg et al. 2013; Kolech et al. 2015). Agents for seed movement can be individuals, non-governmental and governmental organizations, and farmer’s cooperatives. During the Derg regime (1974–1991), farmer’s cooperatives played a major role in moving planting material.

Farmers in different districts name potato cultivars based on characteristics that they perceive. Most cultivar names are based on descriptors related to texture, color, taste, productivity and time to maturity. For instance, one widely grown cultivar in northwest Ethiopia (‘Siquare’ from Table 1) is currently known by many different names, where each name represents an attribute of this cultivar. ‘Siquare’ means sugary taste in Yilmana, Quarit and some districts of the Awi zone; ‘Deme’ or ‘Demas’ means dark red tuber color in the Sinan district; ‘Ater Abeba’ means that the flower color is similar to the flower color of field peas; ‘Mirt’ means best in the Banja district; and ‘Key Dinch’ means red colored potato in the Laigaint district. Similarly, ‘Abateneh’ means “father” in Sekela while in Yilmana this cultivar is known as ‘Rejim Siquare’ because it is taller than ‘Siquare’. The name ‘Ayito’ means colored like a mouse because tubers are blue-black in color, while this cultivar is called ‘Kuchbiye’ in Sinana, which means late maturing.

The genotyping results reported here can serve as a first step in developing officially recognized names for local cultivars. Our proposed names for each unique genotype, summarized in Table 3, can be taken as a starting point, since we know of no reliable historical records to determine the original name for each cultivar.

Origin and Relationships among Ethiopian Cultivars

Although potato has been grown in Ethiopia for over 150 years, the origin of current local cultivars is not known. Based on genetic relationships gleaned from molecular marker data (Figs. 2, and 3), it appears likely that most local cultivars in the northwest originated in Europe. Several authors have reported that many cultivars have been introduced over the past 40 years from European countries as well as the International Potato Center (Peru) (Kidane Mariam 1979; Yilma 1987; Lemaga et al. 1994). Some of these introductions may have become the local cultivars grown today. Alternatively, or in addition, it is possible that Ethiopian farmers selected local cultivars from naturally occurring crosses. The long growing season of the Belg and Belmehr seasons in the cool agroecological zones of Ethiopia favors the development of mature true potato seeds (TPS). Any seed that germinates can, in principle, become a new cultivar if it meets farmer’s needs. Many Andean potato cultivars are believed to have been produced by farmer selection from naturally occurring variation (Bradshaw et al. 2006).

According to Ethiopian farmers, some local cultivars have been grown for more than 40 years. These old cultivars include ‘Abalo’, ‘Samune’, ‘Enat Beguaro’ and ‘Durame’. All four of these cultivars are most closely related to the European cultivars tested. Some recent cultivars, such as ‘Siquare’, are also most closely related to European cultivars. According to farmers, ‘Siquare’, the most commonly grown cultivar in northwest Ethiopia, has been grown for the last 25 years. Morphologically, ‘Siquare’ looks like an andigena type, as it has small leaves and flowers profusely. Despite its similarity to European cultivars, it is not possible to confidently conclude that ‘Siquare’ originated from Europe, as CIP also uses European cultivars as parents.

Unlike northern cultivars, the predominant southern cultivars (‘Nech Abeba’, ‘Agazer’, ‘Bulle’ and ‘Holland’) are most closely related to germplasm developed by CIP. According to farmers, these cultivars are also not as old as most of the cultivars in the Northwest. Thus, the major cultivars of the south are likely of different origin than the Northwest. One or more of these cultivars may represent direct adoption of advanced clones introduced by CIP. Cultivar introduction from CIP began 32 years ago (Lemaga et al. 1994). According to Kidane Mariam (1979), the first CIP cultivars were tested in 1976 in central, Southern and Eastern Ethiopia (Holetta, Nazreth, Alemaya, Endiber, Chencha, Areka and Kulumsa).

Within Ethiopia it is believed that potato cultivars introduced into the country during the past 23 years can all be traced back to their initial introduction, since a National Seed Industry Policy was issued by the government in 1992 to regulate seed import and export (Bishaw et al. 2008). Even so, there are some cases, like ‘Abateneh’, a local Ethiopian cultivar that has been grown for the last 10 years, where it is impossible to find information about its origin. Molecular genetic characterization shows that ‘Abateneh’ is related to ‘Gorebella’ and ‘Bulle’ (new cultivars that originated at CIP). It may be that tubers were taken from research fields during cultivar testing; advanced CIP clones are tested in research plots in many parts of Ethiopia. It is also possible, but less likely, that ‘Abateneh’ was selected from TPS by farmers, where one or both parents were CIP cultivars.

Divergence and Population Differentiation

It has been suggested that maximum heterozygosity leads to maximum heterosis and thus high yield in potato (Mendoza and Haynes 1974). Increasing the heterozygosity of Ethiopian local cultivars and widening their genetic base are both likely to be important breeding activities as new Ethiopian cultivars are developed that possess desired combinations of abiotic and biotic stress tolerances and high yield. An unexpected result of this study is that Ethiopian cultivars are more heterozygous than the CIP clones tested. Our naïve expectation was that since CIP cultivars and advanced clones have genes from many different species, they would contain many unique alleles, and be more heterozygous. The reduced heterozygosity compared to Ethiopian cutlivars, as well as lower numbers of unique alleles, compared to North America, may be due entirely, or in part, to ascertainment bias, as the SNPs evaluated were pre-selected for being informative in US germplasm. As Hamilton et al. (2011) noted, novel alleles in CIP sources derived from wild species may not have been detected because SNPs for the infinium array were derived exclusively from cultivated potato. Indeed, Vos et al. (2015) have demonstrated that relatively few of the SNPs evaluated by the SolCAP 8303 array represent SNPs introduced into potato after 1945, i.e., recent introgressions. When SSR markers were used to compare CIP germplasm with that from Kenya and Europe, the CIP germplasm was found to have the most within-group diversity (Lung’aho et al. 2011).

It is abundantly clear from the heterozygosity analyses, and evaluation of private and shared SNPs, that Ethiopian cultivars harbor considerable genetic diversity; this in turn negates the belief that Ethiopian potato cultivars are derived from a markedly narrower genetic base than American, European or CIP cultivars and advanced clones.

Implications for Future Potato Breeding and Conservation

Breeders require sufficient genetic variation when developing new cultivars adapted to changing environmental conditions and emerging pests and diseases. Such cultivars are especially important for Ethiopian farmers, where low input agriculture is the norm, and weather variability has increased in recent years. This study is the first to characterize Ethiopian potato genetic resources in relation to cultivars from the International Potato Center, America and Europe, using molecular genetic and morphological methods. We have found that current Ethiopian cultivars harbor considerable genetic variation, comparable to that found in CIP, European and American germplasm. American germplasm differs the most from Ethiopian material, suggesting that crossing with American cultivars could help broaden the genetic base in Ethiopia. Moreover, establishing a consistent name for each unique genotype is undoubtedly the first step in registering these cultivars for future development of the crop and for conservation of these genotypes.