December 2012 Number 1 - Utah Native Plant Society
December 2012 Number 1 - Utah Native Plant Society
December 2012 Number 1 - Utah Native Plant Society
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<strong>Utah</strong> <strong>Native</strong> <strong>Plant</strong> <strong>Society</strong><br />
4<br />
Family 7<br />
4<br />
Family 11<br />
4<br />
Family 14<br />
4<br />
Family 16<br />
2<br />
2<br />
2<br />
2<br />
0<br />
0<br />
0<br />
0<br />
-2<br />
-2<br />
-2<br />
-2<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
Family 17<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
Family 21<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
Family 24<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
Family 26<br />
PRINCIPAL COMPONENT 2<br />
0<br />
-2<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
0<br />
-2<br />
4<br />
2<br />
0<br />
-2<br />
Family 27<br />
-4<br />
-4<br />
-6 -4 -2 0 2 4 -6 -4 -2 0 2 4<br />
Family 39<br />
-4<br />
-6 -4 -2 0 2 4<br />
0<br />
-2<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
0<br />
-2<br />
4<br />
2<br />
0<br />
-2<br />
Family 33<br />
Family 41<br />
-4<br />
-6 -4 -2 0 2 4<br />
0<br />
-2<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
0<br />
-2<br />
Family 35<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
0<br />
-2<br />
Family 42<br />
-4<br />
-6 -4 -2 0 2 4<br />
PCA 2<br />
0<br />
-2<br />
-4<br />
-6 -4 -2 0 2 4<br />
4<br />
2<br />
0<br />
-2<br />
Family 37<br />
-4<br />
-6 -4 -2 0 2 4<br />
One Individual<br />
Two Individuals<br />
Three Individuals<br />
Four Individuals<br />
Five Individuals<br />
PRINCIPAL COMPONENT 1<br />
Figure 4. Scores on the first two axes from Principal Components Analysis of AFLP (amplified fragment length<br />
polymorphism) data for greenhouse-grown individuals belonging to 15 half-sib familes collected from the P. argillacea<br />
Tucker population in 2004. Point size reflects number of individuals with identical AFLP genotypes.<br />
argillacea indicated that individuals tended to group<br />
together by year much more than by population. These<br />
data suggest a persistent seed bank, which means a fraction<br />
of the seeds not only remain in the soil, but are viable<br />
for at least one year after production (Thompson<br />
and Grime 1979). A site characterization study of P.<br />
argillacea supported this hypothesis by suggesting that<br />
the seed bank reservoir contains an accumulation of<br />
seeds from many different years (Armstrong 1992).<br />
Preliminary results from a long term seed retrieval study<br />
with P. argillacea also support the existence of a longlived<br />
seed bank in this species. Few or no seeds have<br />
germinated in the field during the first two years, and<br />
most are still in a state of primary dormancy (Meyer<br />
unpublished data). This type of seed bank structure has<br />
also been reported in Phacelia secunda. Seeds from P.<br />
secunda were collected and allowed to germinate, and<br />
after three years a considerable fraction of the seeds remained<br />
viable but ungerminated (Cavieres 2001).<br />
PCA also suggests that collections from a single year<br />
and population of P. argillacea would depict a very narrow<br />
genetic diversity within the organism. A persistent<br />
seed bank can function as a genetic memory by accumulating<br />
seed genotypes from different years (Cabin et al.<br />
1998). In the case of the rare annual Clarkia springvillensis,<br />
analysis of seed bank samples illustrated significantly<br />
higher within-seed bank genetic diversity when<br />
compared to the adult population (McCue and Holtsford<br />
1998). The same could be true for P. argillacea, as evidenced<br />
by the pattern seen in the PCA (Figure 3). The<br />
seed bank must have a higher genetic diversity than the<br />
established plants in any one year, because of the wide<br />
range of diversity seen when comparing years. A similar<br />
situation was found in Phacelia dubia, which has small<br />
132