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Contributions to the Study of Biological Diversity Vol. 3<br />

employed by Kelloff <strong>and</strong> Funk (2004). The<br />

classifications are illustrated <strong>in</strong> the map <strong>in</strong><br />

Figure 2.3.<br />

The Guiana Shield distribution (1) <strong>in</strong>cludes<br />

species that are, fairly strictly, restricted to that<br />

geologic formation’s igneous <strong>and</strong> sedimentary<br />

bedrock <strong>and</strong> areas <strong>in</strong>fluenced by that area’s<br />

outwash. It <strong>in</strong>cludes southern Venezuela, most<br />

of the three Guianas, <strong>and</strong> parts of northern Brazil<br />

<strong>and</strong> scattered outliers <strong>in</strong> southeastern Colombia.<br />

The Northern South America distribution<br />

(2) <strong>in</strong>cludes species found <strong>in</strong> the Guiana Shield<br />

as well as the Northern Andes, the cont<strong>in</strong>ent’s<br />

Pacific coast south to the arid Peruvian coast,<br />

<strong>and</strong> much of the Amazon Bas<strong>in</strong> lowl<strong>and</strong>s to<br />

about 7 degrees south. The Andes reach much<br />

higher elevations than the Guiana Shield<br />

highl<strong>and</strong>s. Many of the habitats <strong>in</strong> this zone are<br />

wet to extremely wet.<br />

The Neotropical distribution (3) <strong>in</strong>cludes<br />

all of the Americas between approximately 23.5<br />

degrees north <strong>and</strong> 23.5 degrees south, with<br />

subclasses either <strong>in</strong>clud<strong>in</strong>g or exclud<strong>in</strong>g<br />

distribution <strong>in</strong> the Antilles (3a). Follow<strong>in</strong>g<br />

climate patterns, this unit is mapped to the south<br />

of the Tropic of Capricorn on the Atlantic coast<br />

of South America, <strong>and</strong> to the north of that<br />

latitude on the Pacific coast, which is <strong>in</strong>fluenced<br />

by strong, cool ocean currents from the south.<br />

The Trans-Atlantic distribution (4)<br />

accommodates species native to both the<br />

Neotropics <strong>and</strong> tropical Africa. Here this<br />

distribution is applied predom<strong>in</strong>antly to<br />

mangrove species, thus the mapp<strong>in</strong>g <strong>in</strong> Figure<br />

2.3 is adapted from the Atlantic-east Pacific<br />

distribution from mangroves by Toml<strong>in</strong>son<br />

(1986)<br />

The South American distribution (5) is<br />

essentially self-explanatory, <strong>and</strong> is <strong>in</strong>dicated on<br />

Figure 2.3 only by the l<strong>and</strong>mass of the cont<strong>in</strong>ent.<br />

The Western Hemisphere distribution (6)<br />

<strong>in</strong>cludes species adapted to a broad climate<br />

range. It <strong>in</strong>cludes species that extend <strong>in</strong>to the<br />

subtropics <strong>and</strong> temperate zones of North <strong>and</strong><br />

South America.<br />

The Pantropical distribution (7) covers<br />

tropical areas nearly worldwide, from 23.5<br />

degrees north to 23.5 degrees south.<br />

Cosmopolitan (8) species are those known<br />

from both tropical, sub-tropical, <strong>and</strong> <strong>in</strong> some<br />

cases temperate areas, nearly worldwide. Here<br />

39<br />

the Neotropical <strong>and</strong> Pantropical classifications<br />

both <strong>in</strong>clude species that might to some degree<br />

extend <strong>in</strong>to the Subtropics.<br />

RESULTS<br />

Quackal <strong>and</strong> Manicole Communities<br />

Forty-four species were shared between the<br />

126 Wa<strong>in</strong>i species recorded <strong>and</strong> the list of all<br />

species recorded by van Andel for the entire<br />

District. That 35% overlap <strong>in</strong>cludes 5 species<br />

that are either cultivated or escaped from<br />

cultivation, Cocos nucifera L., Luffa cyl<strong>in</strong>drica<br />

M.Roem., Pedilanthus tithymaloides (L.)Poit.,<br />

Gossypium barbadense L., <strong>and</strong> Jatropha<br />

gossypiifolia L..<br />

Only seven taxa were shared between the<br />

Wa<strong>in</strong>i Pen<strong>in</strong>sula (126 species) <strong>and</strong> van Andel’s<br />

Quackal <strong>and</strong> Manicole plots (138 species ). That<br />

is approximately a 5.5 % overlap relative to the<br />

species of the Wa<strong>in</strong>i Pen<strong>in</strong>sula. Of 240 total<br />

plant taxa for all sites, only 51 were shared <strong>in</strong><br />

any way among the seven vegetation types.<br />

Considered separately, collections result<strong>in</strong>g<br />

from this research on the Wa<strong>in</strong>i Pen<strong>in</strong>sula <strong>and</strong><br />

other sites <strong>in</strong> the Northwest added 99 species to<br />

the basel<strong>in</strong>e list formed from historic collections,<br />

while van Andel (2000a) collections added 308<br />

species to the basel<strong>in</strong>e list. Thirteen of those<br />

species were added by both efforts.<br />

The similarity matrix <strong>and</strong> tree matrix,<br />

displayed as a phenogram (similarity-based<br />

dendrogram), from the UPGMA cluster<strong>in</strong>g of<br />

the seven coastal pla<strong>in</strong> communities are shown<br />

<strong>in</strong> Figure 2.4. A cophenetic matrix was formed<br />

from the UPGMA tree matrix <strong>and</strong> run aga<strong>in</strong>st<br />

the orig<strong>in</strong>al matrix to test the goodness of fit of<br />

the cluster<strong>in</strong>g results to the orig<strong>in</strong>al data set,<br />

us<strong>in</strong>g a Mantel test for matrix correspondence<br />

(Rohlf 1997). That resulted <strong>in</strong> a high probability<br />

(p = 0.995) that a r<strong>and</strong>om Z-value would be less<br />

than the Z-value derived from the comparison<br />

of matrices, <strong>in</strong>dicat<strong>in</strong>g a close fit <strong>in</strong> the UPGMA<br />

cluster<strong>in</strong>g. Alternate tests of s<strong>in</strong>gle-l<strong>in</strong>k <strong>and</strong><br />

complete-l<strong>in</strong>k cluster<strong>in</strong>g methods yielded<br />

phenograms very similar to those from UPGMA<br />

cluster<strong>in</strong>g, <strong>in</strong>dicat<strong>in</strong>g that the clusters are quite<br />

dist<strong>in</strong>ct (Rohlf 1997).<br />

Coastal Mangrove <strong>and</strong> River<strong>in</strong>e Mangrove<br />

swamps clustered together. The two mangrove<br />

swamp types differed <strong>in</strong> part because different

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