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Morphological and genetic variability in wild potato species from northwest Argentina

                    

   

Clausen, AM1, Ispizúa, VN1, Camadro, EL1,2, Larrosa, F1.
1Unidad Integrada EEA Balcarce, INTA-FCA, UNMdP. 2CONICET. C.C.276, (7620). Balcarce, Argentina.

 

email:aclausen@balcarce.inta.gov.ar

 

Figure 1. Click on the picture to enlarge

Introduction

 

Populations of wild potato species identified as S. infundibuliforme (ifd, 2n=2x=24; 2NBE) and S. gourlayi (grl, 2n=4x=48; 4NBE) and probable interspecific hybrids (grl-ifd; opl-ifd) were collected in a narrow dry Andean gorge at 3600m known as Incacuevas in the province of Jujuy. Morphological variability was detected in the accessions collected (Fig. 1).

 

Materials and Methods

 

Twelve populations were collected as plants and tubers in the site and accession of S. oplocense (opl), S. gourlayi (grl) and S. Infundibuliforme (ifd) from neighboring valleys were included in this study (Table 1).

 

Click to enlarge

 

Table 1: Accessions studied.

 

Accessions

Species

Coordinates
Lat. S-Long. W

Oka 4837

S. gourlayi

24º 32' - 66º 12'

Oka 4314

S. gourlayi

23º 37' - 65º 32'

Oka 7565

S. gourlayi

23º 58' - 65º 38'

ClI 1705

S. oplocense

23º 11' - 65º 19'

ClI 1706

S. oplocense

23º 11' - 65º 19'

ClI 1707

S. gourlayi

23º 00' - 65º 27'

ClI 1708

S. gourlayi x ?

23º 00' - 65º 27'

ClI 1709

S. infundibuliforme x ?

23º 00' - 65º 27'

ClI 1710

S. gourlayi

23º 00' - 65º 27'

ClI 1711

S. infundibuliforme

23º 00' - 65º 27'

ClI 1712

S. gourlayi x ?

23º 00' - 65º 27'

ClI 1713

S. gourlayi x ?

23º 00' - 65º 27'

ClI 1714

S. oplocense ?

23º 00' - 65º 27'

ClI 1715

S. gourlayi x infundibuliforme?

22º 59' - 65º 27'

ClI 1716

S. gourlayi x ?

22º 59' - 65º 27'

ClI 1717

S. infundibuliforme

22º 59' - 65º 27'

ClI 1718

S. gourlayi

22º 59' - 65º 27'

ClI 1720

S. infundibuliforme

23º 03' - 65º 24'

 

 
   

The material was planted in a screenhouse, with a variable number of genotypes of each accession. 36 morphological characters (Table 2) were determined on 172 plants and the results were analyzed by a Principal Components Analysis (PCA). Chromosome numbers were determined on root tips using the standard technique. Percentage of pollen viability was estimated according to Alexander (1980) and 76 genotypes were screened for 2n pollen. Controlled crosses were made for 362 combinations of genotypes on selected genotypes. 5 flowers were pollinated per combination of genotypes and styles were fixed in FAA (8:1:1), processed according to Martin (1958) and microscopically observed with UV light. Fruit and seed set were recorded.

Table 2: Morphological characters registered.

 

1 Plant height

19 Leaf color

2 Color of stem

20 Leaf pubescence

3 Presence of wings

21 Peduncle length

4 Leaf length

22 Number peduncle forks

5 Leaf width

23 Pedicel length

6 Length of terminal leaflet

24 Pedicel length from base to articulation

7 Width of terminal leaflet

25 Number of flowers/

inflorescence

8 Length petiole terminal leaflet

26 Calyx length

9 Length primary lateral leaflet

27 Length of calyx acumen

10 Width primary lateral leaflet

28 Radius of corolla

11 Length petiolule primary lateral leaflet

29 Width of corolla lobe at the base of corolla lobe

12 Width second lateral leaflet

30 Length of corolla lobe from base to acumen

13 Length second lateral leaflet

31 Corolla acumen length

14 Number lateral leaflets

32 Primary adaxial corolla color

15 Number interjected leaflets

33 Secundary adaxial corolla color

16 Adaxial pubescence

34 Anther length

17 Abaxial pubescence

35 Style length

18 Color leaf veins

36 Length of style exsertion

 

 
     

Table 3. Click to enlarge

 

Results and Discussion

 

Chromosome numbers were determined on a variable number of genotypes and only tetraploids have been detected so far in the probable hybrid populations. Variable results were obtained as a result of the crosses performed; a high percentage of the combinations were compatible in both directions (Table 3). Some combinations did not produce seeds, indicating the probable existence of post-zygotic barriers. Variable results for pollen fertility and a high number of plants with 2n pollen were found (Table 4).

 
   

Table 4. Pollen fertility and 2n pollen production.

 

Species

Accession

Nº plants

Fertility
(%) x range

Nº plants with 2n pollen

% 2n pollen 2n
x range

grl

ClI 1710

11

80(87,5-73,6)

11

7,3 (16,4-1,9)

grl

ClI 1718

1

91,7

1

0,9

grl?

ClI 1712

3

76,9(80,9-73,5)

3

7,5(8,7-5,7)

grl

ClI 1707

6

67,3(80-34,8)

6

4,8(7,2-2,5)

ifd

ClI 1717

2

59,7(64,3-55,2)

2

3,5(4-3,1)

Hybrid?

ClI 1715

27

93,4(99,3-50,9)

16

4,2(15,6-0)

Hybrid?

ClI 1716

26

57,6(86,4-22,61)

24

4,1(13,4-0)

 

 

Figure 2a y 2b. Click to enlarge


Figure 3. Click on the picture to enlarge

The morphological analysis of the entire data set by means of PCA (Fig. 2a) revealed that only opl from outside Incacuevas formed a group, overlapping with grl in a few cases.

The PCA performed with the mean values of each accession (Fig. 2b) differentiated opl, grl and ifd. Populations suspected to be hybrids as ClI 1715, with many plants with a strong resemblance to ifd (Fig 3), clustered close to this species, although the wide dispersion of individual plants of this accession can be observed in Fig. 2a. The characters with a major contribution to PCA axis I were width of primary lateral leaflet, leaf width, width of second lateral leaflet, length of primary lateral leaflet and length of petiolule of primary lateral leaflet.

The majority of the accessions from Incacuevas, presented intermediate values for these characters.

Conclusions
 

  • The morphological variability observed in the different populations of the wild potato species found in Incacuevas may be the result of gene flow by hybridization, considering the varying levels of pollen fertility, 2n pollen production in diploids and tetraploids and the results of the crosses performed and compatibility analysis.

 

 
     
    
 
 

 

 

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