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Table 3 Characterisation of 15 dinucleotide microsatellite loci for the Greater Water Parsnip Sium latifolium, all tested on 24 individuals sampled at Wickhampton Marshes, reveals tetraploidy in this species

From: The characterisation of microsatellite markers reveals tetraploidy in the Greater Water Parsnip, Sium latifolium (Apiaceae)

Locus

Fluoro dye

Exp. I50 (bp),

Obs. I50 (bp).

N

K

Observed allele size range (bp)

Number of individuals with 1–2 alleles

Number of individuals with 3–4 alleles

Ho

Sla01

[6FAM]

192

191, 193, 195

23

12

189–213

0

23

1.000

Sla02

[HEX]

154

132, 150, 154, 164

24

17

132–180

4

20

1.000

Sla03

[6FAM]

241

230, 232, 240

23

16

202–242

10

13

1.000

Sla04

[HEX]

196

180, 188, 194*

24

9

180–204

9

15

1.000

Sla05

[6FAM]

248

244, 248, 250

23

8

242–254

8

15

0.958

Sla06

[6FAM]

154

130, 138, 150, 154

23

9

130–158

5

18

0.958

Sla07

[6FAM]

228

203, 207, 224*

24

12

203–224

2

22

1.000

Sla08

[HEX]

115

104, 110, 112*

24

15

94–136

3

21

1.000

Sla09

[HEX]

180

168, 182*

24

10

166–186

21

3

0.875

Sla10

[HEX]

142

132, 141

23

13

128–170

14

9

1.000

Sla11

[6FAM]

148

136, 142, 148

22

11

128–156

8

14

1.000

Sla12

[6FAM]

107

92, 106, 108, 112

22

13

90–116

3

19

1.000

Sla13

[HEX]

121

117, 128*

23

11

110–136

11

12

1.000

Sla14

[6FAM]

161

158, 160, 168

22

14

134–176

4

18

1.000

Sla15

[6FAM]

106

101, 105, 107, 119

23

12

83–119

7

19

1.000

  1. Microsatellite loci, expected and observed allele sizes (with the sequenced allele underlined*; bp) of individual from which the microsatellite sequences were isolated (individual I50, sampled at Wickhampton Marshes, Norfolk), number of individuals successfully genotyped (n), number of alleles (k), allele size range (bp), observed heterozygosity (Ho). Exp. I50 (bp), Expected allele size of I50, Obs. I50 (bp), Observed amplified allele sizes of individual, I50, *Minor size differences (bp) were observed between the expected size of the allele (based on sequencing) and observed allele size (based on ABI genotyping). This error is caused by (1) the presence of the fluorescent dye label (6FAM and HEX) and/or (2) sequence misalignment due to the repeat region when creating the consensus sequence from the two paired-end complementary sequences