|Common Names||Ck’ipa ch’ogue, Ita papa, Lluttu papa|
|Synonyms||S. flavoviridens, S. tarijense, S. trigalense, S. x litusinum, S. x zudaniense|
|Ploidy||Diploid (2x), Triploid (3x)|
|Tuberization Photoperiod||Short Day|
|Cytoplasmic Genome||W, T|
|Citation||Hawkes: Bull. Imp. Bur. Pl. Breed. Genet., Cambridge 45, 122. 1944|
Solanum berthaultii is native to central Bolivia. It forms large plants, three feet tall or more. The berries are green and speckled. Tubers are round and white. Most accessions produce tubers less than an inch in diameter, but some are much larger, reaching more than two inches. Flowers blue to purple or sometimes white (Correll 1962). It grows in dry areas, primarily between 6500 and 8500 feet in elevation (2000 and 2600 m) (Ochoa 1990). The specific epithet, berthaultii, honors French potato expert Pierre Berthault.
S. berthaultii is thought to be the wild ancestor of the domesticated Chilean potato (S. tuberosum group Chilotanum) and crosses between the two, using S. berthaultii as the female parent and Andean domesticated tetraploids as the male parent have produced long day adapted progeny with characteristics similar to Chilean potatoes (Hosaka 2018, as S. tarijense).
S. berthaultii is of interest to modern potato breeders because its leaves are covered in glandular hairs that can immobilize small insects. This feature could be valuable for controlling aphid infestations and thereby reducing the transmission of viruses. Gibson (1971) reported that 30% of aphids were completely immobilized within 24 hours of introduction onto the leaves. The same mechanism works to deter potato leafhoppers by gumming up their mouth parts, leaving them unable to feed (Tingey 1978). Gibson (1983) found that the leaf hairs also exude a substance that mimics the aphid alarm pheromone and causes them to avoid the plants.
S. berthaultii appears to deter the Colorado potato beetle by emitting a semiochemical (signalling chemical) that the beetles can detect (Pelletier 1999). On S. berthaultii, CPB lay fewer eggs (Wright 1985), the larvae take longer to develop, and larval mortality is higher than for S. tuberosum (Groden 1986).
This species can survive frosts down to 27.5 degrees F (-2.5 C) (Li 1977). Vega (1995) found that this species is less frost tolerant than domesticated potato. Because it grows in dry environments, it may also be a useful source of drought tolerance.
In a study of early blight resistance, Jansky (2008) found that S. berthaultii (as S. tarijense) was one of the top three most resistant species tested.
|Condition||Type||Level of Resistance||Source|
|Alternaria solani (Early Blight)||Fungus||Resistant||Prasad 1980|
|Alternaria solani (Early Blight)||Fungus||Somewhat resistant||Jansky 2008 (as S. tarijense)|
|Empoasca fabae (Potato Leafhopper)||Invertebrate||Somewhat resistant||Tingey 1978|
|Epitrix harilana (Flea Beetle)||Invertebrate||Somewhat resistant||CIP 1979|
|Globodera rostochiensis (Potato Cyst/Golden Nematode)||Invertebrate||Somewhat resistant||Castelli 2003|
|Globodera pallida (Pale Cyst Nematode)||Invertebrate||Somewhat resistant||Castelli 2003|
|Globodera rostochiensis (Potato Cyst/Golden Nematode)||Invertebrate||Somewhat resistant||Rothaker 1961|
|Leptinotarsa decemlineata (Colorado Potato Beetle)||Invertebrate||Somewhat resistant||Machida-Hirano 2015|
|Leptinotarsa decemlineata (Colorado Potato Beetle)||Invertebrate||Resistant||Pelletier 1999|
|Liriomyza huidobrensis (Potato Leaf Miner)||Invertebrate||Somewhat resistant||CIP 1977|
|Macrosiphum euphorbiae (Potato Aphid)||Invertebrate||Not resistant to resistant||Alvarez 2006|
|Meloidogyne spp. (Root Knot Nematode)||Invertebrate||Somewhat resistant||Machida-Hirano 2015|
|Myzus persicae (Green Peach Aphid)||Invertebrate||Somewhat resistant||Gibson 1971, Gibson 1983, Machida-Hirano 2015|
|Phytophthora infestans (Late Blight)||Fungus||Not resistant||Gonzales 2002|
|Phytophthora infestans (Late Blight)||Fungus||Somewhat resistant||Machida-Hirano 2015|
|Phytophthora infestans (Late Blight)||Fungus||Not resistant||Bachmann-Pfabe 2019|
|Polyphagotarsonemus latus (Broad Mite)||Invertebrate||Somewhat resistant||CIP 1977|
|Potato Spindle Tuber Viroid (PSTVd)||Virus||Somewhat resistant||Machida-Hirano 2015|
|Potato Virus X (PVX)||Virus||Somewhat resistant||Machida-Hirano 2015|
|Synchytrium endobioticum (Wart)||Fungus||Somewhat resistant||Machida-Hirano 2015|
|Tetranichus urticae (Red Spider Mite)||Invertebrate||Somewhat resistant||Gibson 1976|
|Tetranichus urticae (Red Spider Mite)||Invertebrate||Somewhat resistant||CIP 1977|
|Thrips tabaci (Potato Thrips)||Invertebrate||Somewhat resistant||CIP 1977|
Tingey (1982) found that accessions of S. berthaultii had different TGA compositions, with 51 of 65 accessions having primarily solamarine and the remainder primarily solanine and chaconine. The lower limit of TGA detected was 5 mg / 100 g and the upper limit was unstated. Gregory (1981) counted the TGA levels in S. berthaultii foliage as undetectable, which does not necessarily correlate with the tuber content. Van Gelder (1988) found 16mg / 100 g for this species. It seems that S. berthaultii varies quite a bit in TGA composition. In my experience, tubers taste bitter more often than not and sometimes very bitter.
I have found seeds of this species easy to germinate using the standard conditions for S. tuberosum.
Towill (1983) found that seeds of this species stored at 1 to 3 degrees C germinated at 52% after 12 years and 4% after 23 years.
Bamberg (2017) found a 275% increase in seed set in this species with supplemental applications of liquid fertilizer at four and seven weeks after potting.
This species typically has five to six months of dormancy.
Gibson (1979) found that sticky tipped leaf hairs are a single-gene, dominant trait in S. berthaultii.
Crosses with S. tuberosum
Gibson (1974) reported that four crosses of S. tuberosum x S. berthaultii produced aphid trapping hairs and that one of the plants produced substantially more of these hairs than either parent. Gibson (1979) found that, in reciprocal crosses between S. berthaultii and diploid S. tuberosum, first generation progeny did not develop sticky leaf hairs, but some crosses made from among the progeny did, suggesting that there is an additional recessive gene at work.
|Female||Male||Berry Set ||Seed Set||Germ||Ploidy||Source|
|S. berthaultii (including S. tarijense)||S. tuberosum||None||None||Jackson (1999)|
|S. tuberosum 4x||S. berthaultii||Moderate||Minimal||Jackson (1999)|
Crosses with other species
Jackson (1999) found 0-13% 2n pollen for varieties of this species.
|Female||Male||Berry Set ||Seed Set||Germ||Ploidy||Source|
|S. berthaultii||S. brevicaule (as S. alandiae)||High||High||Ochoa (1990)|
|S. berthaultii||S. brevicaule 6x (as S. oplocense)||Yes||None||Ochoa (1990)|
|S. berthaultii (as S. litusinum)||S. candolleanum||Yes||Yes||Ochoa (1990)|
|S. berthaultii||S. chacoense||Yes||Yes||Ochoa (1990)|
|S. berthaultii (as S. tarijense)||S. infundibuliforme||Moderate||Low||Ochoa (1990)|
|S. brevicaule (as S. alandiae)||S. berthaultii||High||High||Ochoa (1990)|
|S. brevicaule 6x (as S. oplocense)||S. berthaultii||Yes||None||Ochoa (1990)|
|S. commersonii ||S. berthaultii (as S. tarijense) ||Yes||No||Hawkes 1969|
|S. infundibuliforme||S. berthaultii (as S. tarijense)||High||High||Ochoa (1990)|