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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 />

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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 />

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-2<br />

4<br />

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-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 />

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-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 />

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-6 -4 -2 0 2 4<br />

4<br />

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0<br />

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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

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