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Results of the Study
As the data are still being analyzed, only preliminary results are presented here.
We request that these data not be used for any purpose without permission and proper
aknowledgment. We are currently working on publications and will send manuscripts
on request.
Sarracenia purpurea
There was significant among-site variation in the appearance of the plant itself
and in their habitats. Populations of Sarracenia purpurea in the north were
more likely to be in very wet bogs or along pond margins, often in deep sphagnum,
while plants in the south could be found in sandy soil in seepege bogs that could
be quite dry for periods of time. Plants in the north had significantly more leaves
and were shorter (as measured from the ground surface to the top of the tallest leaf).
The mean leaf length did not significantly change with latitude, suggesting that
the plants in the north have a more prostrate form or may be nestled down into sphagnum,
decreasing their apparently height. There were no significant trends in the size
of the keel or aperture. Naczi et al. (1999) had suggested that there may also be
differences in the morphology of the pitcher, such as in lip width, that justify
dividing Sarracenia purpurea into two species. We found no significant pattern
in lip width with latitude, although the southern-most population did tend to have
somewhat thicker leaf lips.
We hope to further analyze these data to understand how aspects of the habitat
or climate may affect morphology. The plant shape may vary in more subtle ways, such
as generaly shape or color. All leaves were photographed and will be analyzed for
such differences, as well as looking for specific differences among the proposed
subspecies and species.
Invertebrates
The invertebrate species composition seems fairly constant over the 39 sites. Virtually
all sites contained the major known invertebrates: the mosquito Wyeomyia smithii,
the midge Metriocmenums knabi, the mite Sarraceniopus gibsoni, and
the rotifer Habrotrochus rosa. This suggests interesting questions about the
relative stability of this species group. In addition, 11 other invertebrate taxa
were recorded (Table 1), most of which were relatively rare. At the among-pitcher
scale, the presence of the four most abundant taxa (midges, mites, mosquitoes, and
bdelloid rotifers) was more variable; each occurred in less than 62% of the pitchers
collected. The other eleven taxa occurred in less than 10% of pitchers.
Table 1. Number of sites (out of the 39) and pitchers (out
of the 780) in which each invertebrate taxon occurred.
Taxon |
Number of sites
|
Percentage of sites
|
Number of pitchers
|
Percentage of pitchers
|
Midges |
38
|
97
|
480
|
61.5
|
Mites |
38
|
97
|
474
|
60.8
|
Mosquitoes |
37
|
95
|
461
|
59.1
|
Bdelloid rotifers |
38
|
97
|
370
|
47.4
|
Flesh flies |
23
|
59
|
67
|
8.6
|
Copepods |
16
|
41
|
43
|
5.5
|
Loricate rotifers |
12
|
31
|
23
|
2.9
|
Nematodes |
8
|
21
|
15
|
1.9
|
Unknown rotifers |
9
|
23
|
13
|
1.7
|
Cladocerans |
8
|
21
|
10
|
1.3
|
Gastropods |
3
|
8
|
3
|
0.4
|
Gastrotrichs |
2
|
5
|
2
|
0.3
|
unknown Mosquitoes |
2
|
5
|
2
|
0.3
|
Amphipods |
1
|
3
|
1
|
0.1
|
Tardigrades |
1
|
3
|
1
|
0.1
|
Protozoans
In all, 50 different types of protozoa were distinguished. We are now confirming
identifications of many of these species. As with the invertebrates, several types
were relatively common across the 39 sites. We do not know whether these are exactly
the same species across all sites or whether they are specialists in pitcher plants
or just common environmental types. Many types were rare; just over half of the taxa
were found only at one or two sites (Table 2). Most of the taxa were rare at the
pitcher scale; only 6 of the 50 taxa occurred in more than 10% of the pitchers.
Table 2: Number of sites (out of the 39) and pitchers (out
of the 780) in which some of the most abundant protozoan taxon occurred
Genus |
Number of sites
|
Percentage of sites
|
Number of pitchers
|
Percentage of pitchers
|
Bodo |
39
|
100
|
402
|
51.5
|
Colpoda |
37
|
94.9
|
141
|
18.1
|
Colpidium |
34
|
87.2
|
100
|
12.8
|
Chrysomonas |
32
|
82.1
|
149
|
19.1
|
Cyclidium |
32
|
82.1
|
126
|
16.2
|
Peranema |
17
|
43.6
|
32
|
4.1
|
unknown |
16
|
41.0
|
44
|
5.6
|
unknown |
15
|
38.5
|
88
|
11.3
|
Cryptomonas |
14
|
35.9
|
25
|
3.2
|
Anisonema |
13
|
33.3
|
22
|
2.8
|
Tachysoma |
10
|
25.6
|
12
|
1.5
|
Paramecium |
9
|
23.1
|
18
|
2.3
|
Petalomonas |
9
|
23.1
|
19
|
2.4
|
Euglena |
8
|
20.5
|
24
|
3.1
|
Menoidium |
8
|
20.5
|
11
|
1.4
|
Bacteria
We identified 30 different colony types of bacteria. Because we identified types
on the basis of colony growth on agar, we cannot yet confirm species identifications
across sites. We have preserved the 5-8 most abundant colony types at each site and
hope to use 16S sequencing or fingerprint data to identify species at a later date.
The colony types were often highly colored, a common feature of bacteria in stressed
environments.
Colony-type composition was more variable than that of invertebrates and protozoa;
only 9 out of the 30 types occurred in more than 90% or less than 10% of sites. At
the pitcher scale, however, nearly half of the taxa occurred in less than 10% of
the pitchers.
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