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Download the publication - Tropenbos International

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Diversity patterns in <strong>the</strong> flora of <strong>the</strong> Campo-Ma’an rain forest, Cameroon: do tree species tell it all?<br />

The species richness was also significantly different between growth forms (GLM:<br />

F3, 33.2 = 221.889, P < 0.001 for layer and F10, 30 = 2.973, P < 0.01 for vegetation type<br />

included as a random factor), with similar relative difference. Overall, <strong>the</strong>re was a<br />

decrease in diversity and <strong>the</strong> total number of species recorded/plots with decreasing<br />

sampling resolution (Figures 3.5 & 3.6). About 30% of <strong>the</strong> total number of species<br />

recorded was lost when <strong>the</strong> sampling design only took into account all vascular<br />

plants with DBH ≥ 5 cm and more than 50% were lost when only vascular plants<br />

with DBH ≥ 10 cm are collected. Moreover, <strong>the</strong>re was a very strong significant<br />

positive correlation between <strong>the</strong> number of stems/ha and <strong>the</strong> total number of species<br />

recorded (R 2 = 0.956, P < 0.0001), and a considerable drop in diversity when <strong>the</strong><br />

sampling was limited to all vascular plants with DBH ≥ 10 cm. In terms of sampling<br />

effort, less than 30% of <strong>the</strong> total number of stems/ha were recorded when <strong>the</strong><br />

sampling design only took into consideration all vascular plants with DBH ≥ 5 cm.<br />

Fur<strong>the</strong>rmore, only 15% of <strong>the</strong> total number of stems/ha were recorded for all<br />

vascular plants with DBH ≥ 10 cm.<br />

Species richness within families<br />

Overall, shrubs/small trees show <strong>the</strong> highest number of families (75) followed by<br />

medium trees (61), herbs and hemi-epiphytes (58), large trees (54) and woody<br />

climbers (37). Rubiaceae was by far <strong>the</strong> most species rich family (204 species)<br />

followed by Euphorbiaceae (88), Leguminoseae-Caesalpinioideae (85), Annonaceae<br />

(63), Sterculiaceae (50), Apocynaceae (47) and Sapindaceae (40). Leguminoseae<br />

(especially <strong>the</strong> sub-family Caesalpinioideae) was <strong>the</strong> dominant family for <strong>the</strong> large<br />

trees species (DBH ≥ 30 cm) in terms of relative density and frequency in <strong>the</strong><br />

Campo-Ma’an area (Table 3.7). Dominant large tree species included Brachystegia<br />

cynometroides, Calpocalyx heitzii, Desbordesia glaucescens, Erythrophleum<br />

ivorensis, Lophira alata, Lovoa trichilioides, Piptadeniastrum africanum,<br />

Pterocarpus soyauxii, Pycnanthus angolensis, Sacoglottis gabonensis and<br />

Terminalia superba. Common shrubs and small tree species included Jollydora<br />

duparquetiana, Lasian<strong>the</strong>ra africana, Massularia acuminata, Podococcus barteri<br />

and many species of <strong>the</strong> genera Campylospermum, Cola, Crotonogyne, Diospyros,<br />

Drypetes, Microdesmis, Psychotria, Rinorea and Scaphopetalum. Common large<br />

woody climber species were from <strong>the</strong> genera Agelaea, Dichapetalum, Combretum,<br />

Laccosperma, Landolfia, Millettia, Salacia and Strychnos. The most important herb<br />

species were Costus englerianus, Haumania danckelmaniana, Leptaspis zeylanica,<br />

Marantochloa monophylla, Microcalamus barbinodis, Puella ciliata, P.<br />

schumanniana, and many species of <strong>the</strong> genera Asystasia, Begonia, Cercestis,<br />

Culcasia, Dorstenia, Geophila, Hymenocoleus, Mapania, and Palisota.<br />

51

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