THE IMPORTANCE OF PTERIDOPHYTES IN THE EPIPHYTIC FLORA OF SOME PHOROPHYTES OF THE CAMEROONIAN SEMI-DECIDUOUS RAIN FOREST

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Selbyana 7: 76-8 THE IMPORTANCE OF PTERIDOPHYTES IN THE EPIPHYTIC FLORA OF SOME PHOROPHYTES OF THE CAMEROONIAN SEMI-DECIDUOUS RAIN FOREST DCpartement de Biologie et Physiologie VCgCtales, UniversitC de YaoundC I, B.P. 8 2, YaoundC, Cameroun Fax: (237) 23 53 88 Museum National d'histoire Naturelle, Laboratoire de Phankrogamie, 6, Rue de Buffon-F-75005 Paris, France. The Marie Selby Botanical Gardens, 8 South Palm Avenue, Sarasota, Florida 34236, USA. -.-. ABSTRACT. Epiphyte diversity and abundance were surveyed in trees that were felled by a logging operation in the Cameroonian semi-deciduous rain forest to determine the importance of pteridophytes. Six host tree species were surveyed, including 50 individual phorophytes. Triplochiton scleroxylon hosted the greatest number of pteridophytes while Canarium schweinfurthii and Terminalia superba hosted the fewest. Of the 78 epiphytic species recorded, the largest groups were the monocotyledons (5 species) and the pteridophytes (20 species), while the dicotyledons (7 species) were the smallest. Regardless of the host, pteridophytes represented over 25% of the epiphytic flora. More than 5 pteridophytes were always hosted by each of the individual host trees. Within the pteridophytes, Polypodiaceae (8 species) was the most diversified family, followed by Davalliaceae (5 species) and Aspleniaceae (4 species). Factor analysis showed no strict specificity between tree species and pteridophytes. are a characteristic feature of forest in tropical regions. They are used as a bioindicator of different types of forests. In the flora of Cameroon, Tardieu-Blot (964) recorded 256 species belonging to 6 orders, 25 families and 69 genera. In the semi-deciduous rain forest, more than 40 epiphytic pteridophytes were recorded (Zapfack 993). In this paper, we studied the importance of pteridophytic flora in the canopy of 6 host species: Gossweilerodendron joveri, Triplochiton scleroxylon, Detarium macrocarpum, Canarium schweinfurthii, Terminalia superba and Erythrophloeum suaveolens. The tree trunks of most individuals had low numbers ofepiphytes. The few species observed belonged to the families of Hymenophyllaceae (genera Hymenophyllum and Trichomanes), Lomariopsidaceae (genera Lomariopsis) and Aspleniaceae (genera Asplenium). We documented the pteridophyte species on each of the six host tree species; determined the percentage of pteridophytes in the epiphytic flora of these host species; and assessed the relationship, if any, between pteridophytes and phorophytes, and between pteridophytes and tree species. This study was conducted in the semi-deciduous rain forest located in the southern part of Cameroon, between longitudes E and 2' 5'W, and latitudes 4' 5'N and 2'30's. This site was situated between Biafran and Congolian forests and the grass land of the northern region (Letouzey 968). Six tree species were selected in 8 timberyards. They were the most abundant species within this region, and subsequently also the most exploited by timber companies. Epiphytes were surveyed in timber camps for two reasons: access to the canopy was easy, and errors in the determination of species were very low. Epiphytes were collected from 25 individuals of each tree species that had been felled. The number of pteridophytes in the epiphytic flora was then determined. On the 25 individuals of each timber species, the presence or absence of the different pteridophytes was noted. Only phorophytes with D.B.H. (Diameter at Breast Height) > 60 cm were considered. Frequencies were determined for all pteridophyte species observed, first by tree species and then on all 50 individuals. The percentages of each epiphytic group and family were calculated.

996 ZAPFACK ET AL.: FERN EPIPHYTES IN CAMEROON 7 7 The mean number of epiphytes per tree was also determined. In this way, we determined the number of the most common species and of pteridophytes that were related to a specific tree species. Data were subjected to factor analysis in order to determine the affinity between pteridophytes and host species. Gossweilerodendron joveri Forty-nine epiphytes were recorded on 25 individuals, of which 4 epiphytes were pteridophytes. Some individuals hosted as many as 20 ephiphytes, while some as few as 3 (mean ). Of the most common species, 6 were pteridophytes: Arthropteris orientalis, Asplenium laurentii, Phymatosorus scolopendria and Plafycerium angofense. The pteridophytic flora of.gossweilerodendron ioveri re~resented 28.6% of the ~j. epiphytic flora ( ~ L E In order ofdecreasing 'abundance, the most common species found on this host tree were Arthropteris orientalis, Asplenium africanum, A. laurentii, Davallia chaerophylloides, Drynaria laurentii, Loxogramme lanceolata, flicrogramma owariense, Microsorium punctatum, Oleandra distenta, Phymatosorus scolopendria, Platycerium angolense, Pyrrosia mechowii, Vittaria guineense and V. schaeferi. Triplochifon scleroxylon Forty two epiphytes were collected on 25 individuals, and 7 species (among the 42) were pteridophytes. Epiphyte abundance ranged from 3-24 individuals with a mean of 0. There were 0 common species on this host tree. Among them, 5 were pteridophytes: Phymafosorus scolopendria, Arthropteris orientalis, Microsorium punctatum, Platycerium angolense and P. stemaria. The pteridophytes on Triplochiton sclero-lsylon represented 40.5Oh (TABLE B) of the epiphytic flora. The most common species included: A rthropteris orientalis, Asplenium africanum, A. laurentii, Davallia chaerophylloides, Drynaria laurentii, Lycopodium ophioglossoides, Microgramma owariense, Microsorium punctatum, Nephrolepis biserrata, Oleandra distenta, Phymatosorus scolopendria, Platycerium angolense, P. stemaria, Pyrrosia mechowii, and Vittaria guineense. Detarium macrocarpum Of 43 epiphytes counted on 25 individuals of this tree species, 2 were pteridophytes. Abundance ranged from 7-29 epiphytes per tree. Of the 3 commonest species, five were pterido- phytes: Phymatosorus scolopendria, Asplenium laurentii, Arthropteris orientalis, Drynaria laurentii, and Asplenium africanum. The pteridophytes represent 27.9% of the flora. The following species were collected: Arthropteris orientalis, Asplenium africanum, A. laurentii, Microsorium punctafum, Phymafosorus scolopendria, Platycerium angolense, P. sfemaria, Pyrrosia mechowii and Viffaria guineense. Pte- ridophytes were the second commonest group of epiphytic flora of this host species (TABLE C). Canarium schweinfurthii Of 34 epiphytes counted on 25 trees of this species, ten were pteridophytes. Individuals hosted between 6 and 3 of the commonest epiphyte species; but only one, Drynaria laurentii, was a pteridophyte. The entire checklist of ferns collected on this host tree was: Arthropteris orienfalis, Asplenium laurentii, Davallia chaerophylloides, Drynaria laurentii, Loxogramme lanceolafa, Microsorium punctatum, Phymatosorus scolopendria, Platycerium angolense, P. stemaria and Vif faria guineense. represented 29.4% of the epiphytic flora of Canarium schweinfurthii (TABLE D and 2). Terminalia superba On 25 phorophytes, 38 epiphytes were recorded of which 2 ~ere~pteridophytes. Epiphyte abundance ranged from 4-5, with a mean of 7. There were seven common species, and two were pteridophytes: Phymatosorus scolopendria and Platycerium stemaria. formed 3.6% of the epiphytic flora of this host species (TABLE E). Species collected were Arthropteris orientalis, Asplenium a$ ricanum, A. laurentii, Davallia chaerophylloides, Microsorium punctatum, Nephrolepis biserrata, Oleandra distenta, Phymatosorus scolopendria, Platycerium angolense, P. stemaria, Pyrrosia mechowii, and Vittaria guineense. Erythrophloeum suaveolens Thirty-eight epiphytes were collected on this host tree. Of these, 6 were pteridophytes. Trees averaged 5-2 epiphytes. Of the commonest species, seven were ferns: Drynaria laurentii, Microgramma owariense, Microsorium punctatum, Platycerium angolense, Oleandra distenta, and Arfhropferis orienfalis. formed 42.% of the flora (TABLE F), including Arthropteris orienfalis, Asplenium africanum, A. hemmitomum, A. laurentii, Davallia chaerophylloides, Microsorium punctatum, Nephrolepis undulata, Platycerium angolense, P. stemaria,

7 8 SELBYANA [Volume 7 TABLE. Systematic partitioning of species of epiphytes in groups, families and genera: A: Gossweilerodendron joveri, B: Triplochifon scleroxylon. C: Defarium rnacrocarpum. D: Canarium schweinfurrhii; E: Terminalia superba; F: Eryfhrophloeum suaveolens. Number of Number of Groups % Families genera species % species A 28.6 Polypodiaceae 7 7 4.2 Davalliaceae Aspleniaceae 3 3 2 6.2 4... Ptendophytes Ptendophytes Vittariaceae 2 4. r Orchidaceae 6 3 63.2 Begoniaceae 3 6.2 Cactaceae 2.0 Poly podiaceae 6 7 6.7 Davalliaceae 4 4 9.5 Aspleniaceae 3 7. Vittariaceae 2 4.8 Lycopodiaceae 2.4 Orchidaceae 9 20 47.6 Begoniaceae I 3 7. Cactaceae 2.4 Piperaceae 2.4 Polypodiaceae 6 7 6.3 Davalliaceae 2 4.6 Aspleniaceae 2 2 4.6 Vittariaceae I 2.3 Orchidaceae 5 29 67.4 Begoniaceae I 2.3 Cactaceae I 2.3 Polypodiaceae 5 6 7.7 Davalliaceae 2 2 6 Aspleniaceae I., 2.9 vittariacdae I I' 2.9 Orchidaceae 0 2 6.8 Begoniaceae 2.9 Cactaceae 2.9 Moraceae 2.9 Polypodiaceae 5 6 5.9 Davalliaceae 3 3 7.9 Aspleniaceae I 2 5.3 Vittariaceae 2.6 Orchidaceae 2 23 60.5 Begoniaceae 2.6 Cactaceae 2.6 Urticaceae 2.6 Polypodiaceae 6 7 8.5 Davalliaceae 4 4 0.5 Aspleniaceae 3 7.9 Vittariaceae 2 5.3 Orchidaceae 9 50 Begoniaceae 2.6 Cactaceae 2.6 Urticaceae 2.6 Moraceae 2.6 Pyrrosia mechowii, Vittaria guineense and V. axis and the other on the positive side of axis schaeferi.. The following epiphytes have higher fre- The factor analysis revealed two groups quences and therefore influenced the disposition ): one located on the negative side of of species into two groups: Arthropteris orien- (FIGURE

996 ZAPFACK ET AL.: FERN EPIPHYTES IN CAMEROON 7 9 TABLE 2. Number of epiphytes in the different groups and families. Epiphyte groups Total Families Aspleniaceae Davalliaceae Lycopodiaceae Polypodiaceae Vittariaceae Orchidaceae Begoniaceae Cactaceae Moraceae Piperaceae Urticaceae Number of Epiphytes 4 5 8 2 5 3 78 talis, Phyrnatosorus scolopendria. Drynaria laurentii, Davallia chaerophylloides and Loxograrnrne lanceolafa. The group located at the negative side of axis were Canariurn schweinfurthii, Terrninalia superba and Erythrophloeurn suaveolens. Around these host;s"pecies, 3 pteridophytes were'correlated with them. In the second group located at the positive side of axis, Arthropteris orientalis and Phyrnatosorus scolopendria have the higher frequences. This group showed two poles with respect to axis 2: the first pole at the positive side of the axis 2, with species related to Triplochiton scleroxylon; and the second pole, located at the negative side of the axis regroups Gossweilercdendron joveri and Detariurn macrocarpurn. In all the phorophytes surveyed, the percentage of pteridophytes collected was always > 25%. Erythrophloeum suaveolens was the richest host for pteridophytes (42.%) while Detariurn macrocarpurn was the poorest (27.9%). The pteridophytes represented 28.6% of the epiphytic flora, distributed into 5 families. Among them, Polypodiaceae was the most diverse family (TABLE E and FIGURE 2). D~scussroN AND CONCLUSION This study illustrated the variability of pteridophytes between host canopies (TABLE 3). Johanson ( 974) made similar studies in the Nimba area, and found 5 pteridophytes on Canariurn schweinfurthii, 9 on Triplochiton scleroxylon, and 5 on Terrninalia superba. In the Cameroonian semi-deciduous rain forest, we counted 0, 7 and 2 pteridophytes, respectively, on these host species of Mt. Nimba. In these two cases, it was noted that Triplochiton scleroxylon hosted the greatest number of pteridophytes. Both Wee ( 978) and Handerson ( 935) noted that ceqain species of epiphytes were found on specific host trees, while Piers (968), Rupp ( 969) and Moris (970) demonstrated a specificity between tree species and orchids. In this study, no clear relationship between pteridophytes and tree species was found. We noted in this tropical rain forest that certain pteridophytes had affinity for certain hosts. For instance, Drynaria laurentii grew on 6 of 25 individuals of Gossweilerodendron joveri, Detariurn rnacrocarpum, Canariurn schweinfurthii and Eryfhro- \ Tri I Can MI Ev - \ Det Axis (46.60%) FIGURE. Factor analysis of the distribution of pteridophytes and their hosts. Projection on the plane formed by Axis and 2.

SELBYANA [Volume 7 G. joveri T. Scleroxylon Hi D. macrocarpum C. schwinhrthii T. superba Wl E. suaveolens Orch. Poly. Dam As@. Vitt BCgo. Cact. Wra Lyco. Pi* W. Families FIGURE 2. Proportion of epiphytes in each family encountered on the six host species. Orch. = Orchidaceae; Poly. = Polypodiaceae; Dava.. = Davalliaceae; Aspl. = Aspleniaceae; Vitt. = Vittariaceae; BCgo. = Begoniaceae; Cact. = Cactaceae; Mora. = Moraceae; Lyco. = Lycopodiaceae; Pipe. = Piperaceae; Urti. = Urticaceae. TABLE 3. Occurrence of pteiidophytes on the six host trees. The arabic number represents the pteridophyte frequencies on 25 individuals of each host species. - - 'Host species I Code Epiphytes Gos Tri Det Can Ter Ery Total % Ps Phymatosorus scolopendria 6 22 8 9 87 58 Dl Drynaria laurentii 7 6 8 8 8 78 52 Ao Arthropteris orientalis 9 9 7 7 7 7 76 50.6 Pa Platycerium angolense 8 4 9 9 8 9 67 44.6 A Asplenium laurentii 22 6 6 5 4 54 36 Sp Platycerium stemaria 0 4 0 2 3 2 4 27.3 Mp Microsorium punctatum 8 4 6 5 35 23.3 Mo Microgramma owariense 4 3 9 0 2 29 9.3 Vg Vittaria guineense 5 6 6 3 3 24 6 Aa Asplenium africanum 4 3 3 0 2 4 Od Oleandra distenta 5 3 7 0 3 9 2.6 Dc Davallia chaerophylloides 3 0 6 6 7.3 Pm Pyrrosia mechowii 3 9 0 0 3 08.6 MI Loxogramme lanceolata 0 0 3 0 3 7 04.6 Vs Vittaria schaeferi 0 0 0 0 2 0.3 Ah Asplenium hemmitomum 0 0 0 0 0 00.6 Ag Asplenium geppii 0 0 0 0 0 00.6 Lo Lycopodium ophioglossoides 0 0 0 0 0 00.6 Nb Nephrolepis biserrata 0 0 0 0 0 00.6 Nu Nephrolepis undulata 0 0 0 0 0 00.6 Total 32 5 3 70 54 7 573 Percentage 23.0 20.02 22.8.2 9.4 2.5 00 Total number of pteridophytes/ host species 4 7 2 0 2 6 Gos: Gossweilerodendron joveri, Tri: Triplochiton scleroxylon, Det: Detarium macrocarpa, Can: Canarium scweinfurthii, Ter: Terminalia superba, Ery: Erythrophloeum suaveolens.

996 ZAPFACK ET AL.: FERN EPIPHYTES IN CAMEROON 8 phloeum suaveolens. In contrast, this fern was seen only once on 25 phorophytes of Triplochiton scleroxylon (TABLE 3). The percentage of pteridophytes in the epiphytic flora has been calculated by some authors: 8.9% in the Nimba region (Johanson 974), 27.4% by Kiew and Anthonysamy (987), and 23% in the epiphytic flora of Dipterocarpzu oblongifolizu (Henderson 935). In the semi-deciduous rain forest, pteridophytes comprised an average of 28.6% in the epiphytic flora (Zapfack 993). They always represented more than 25%, regardless of host species. Catling and hfkovitch (989) recorded 20 pteridophytes belonging to 3 families on 327 tree trunks in the Guatemalan cloud forest (Hymenophyllaceae, Lycopodiceae and Polypodiceae). Within the semi-deciduous rain forest canopy of South Cameroon, we recorded 20 pteridophytes on 6 tree species belonging to 5 families: Aspleniaceae, Davalliaceae, Lycopodiaceae, Polypodiaceae and Vittariaceae. On their trunks, we found only 3 families: Aspleniaceae, Hymenophyllaceae and Lomariopsidaceae. As in Guatemalan cloud forest, Polypodiaceae was also the most diversified family in the tropical rain forest. It has been noted that the percentages of these familics do not vary regardless of the phorophytes. We are grateful for the logistic support given by timber companies, COCAM, SFID, ECAM PLACAGE, in providing comfortable facilities in base camp. Specimens were identified or con- firmed by the persons of the National Herbarium of Cameroon. This project was presented as a poster at The First International Conference on Forest Canopies at the Marie Selby Botanical Gardens in Sarasota, FL (November 9-3, 994). CATLING P.M. AND L.P. LEFKOVITCH. 989. Association of vascular epiphytes in a Guatemalan cloud forest. Biotropica 2 (): 3540. H~DERSON M. R. 935. The epiphytic flora of Dipterocarpus oblongifolius B. ("Nerram"). Gardens' Bull. Str. Scttl. 9: 93-97. JONHANSON D.R. 974. Ecology of vascular epiphytes in west African rain forests. Acta Phytogeogr. Snec. 59: -29. KIEW R. AND S. ANTHONYSAMY. 987. A comparative study of vascular epiphytes in three epiphyte rich habitats at Ulu Endan, Johore, Malaysia. Malayan Nature Journal 4: 303-3 5. LETOUZEY R. 968. Etude phytogeographique du Cameroun. Editions Paul Lechevalier Paris. 5 P. Moms B. 970. The epiphyte orchids of Malawi. The society of Malawi, Blantyre. PIERS P. 968. Orchids of East Africa. 2nd ed. Cramer, Lehre. R m H.M.R. 969. The Orchids of New South Wales. National Herb., Sydney. TARDIEU BLOT, M.-L. 964. Flore du Cameroun. Pttridophytes. Mus. Nat. Hist. Nat 6, nu. Buffon, Paris 5e. 250 p.. WEE Y.C. 978. vascular epiphytes of Singapore's wayside trees. Gardens' Bull. Singapore 3: 4 24. ZAPFACK L. 993. Flore et vtgttation epiphytique de quelques phorophytes de la For& dense stmi-dtcidue. Thtse. Univ. Yaoundt I. 209 P.