DataPDF Available

Species Composition, Richness and Diversity in Miombo Woodland of Bereku Forest Reserve, Tanzania

Authors:
  • Forestry Training Institute
  • Ministry of Natural Resources and Tourism, Tanzania

Abstract

There is increased interest in the academic world with regards to tree and shrub species richness and diversity within the Miombo Woodlands and to determine the potential for biodiversity conservation. This study assessed species richness, diversity, dominance and exploitation of tree and shrub in Bereku Forest Reserve. Plant inventory was carried out in 80 systematically selected sample plots. The information recorded includes: diameter at breast height, species name and frequency of regenerants. Analysis of inventory data was done by using Microsoft Excel. A total of 110 species belonging to 53 families were identified. Results showed Shannon-Wiener Index and Simpson Diversity Index of 4.27 and 0.043 respectively for the Miombo woodland of Bereku. Moreover, the findings in this study show mean stems density and mean total density of regenerants of 616 stems per hectare and 2780 stems per hectare respectively. The paper concludes that despite the Miombo Woodland providing products and services to the surrounding communities the woodland is still fairly stocked with high tree and shrub species diversity. The study recommends in-depth forest inventory, preparation of management plan and promotion of good governance in management of Bereku forest reserve.
Species Composition, Richness and Diversity in Miombo
Woodland of Bereku Forest Reserve, Tanzania
Richard A. Giliba1, Emmanuel K. Boon2, Canisius J. Kayombo1, Emmanuel B. Musamba3,
Almas M. Kashindye1 and Philipina F. Shayo1
1Forestry Training Institute, Olmotonyi, Tanzania
E-mail: richiea78@yahoo.com
2Vrije Universiteit Brussel, Belgium, 3Ministry of Natural Resources and Tourism, Tanzania
KEYWORDS Species Diversity. Species Dominance. Species Composition. Miombo Woodland
ABSTRACT There is increased interest in the academic world with regards to tree and shrub species richness and diversity
within the Miombo Woodlands and to determine the potential for biodiversity conservation. This study assessed species
richness, diversity, dominance and exploitation of tree and shrub in Bereku Forest Reserve. Plant inventory was carried
out in 80 systematically selected sample plots. The information recorded includes: diameter at breast height, species name
and frequency of regenerants. Analysis of inventory data was done by using Microsoft Excel. A total of 110 species
belonging to 53 families were identified. Results showed Shannon-Wiener Index and Simpson Diversity Index of 4.27 and
0.043 respectively for the Miombo woodland of Bereku. Moreover, the findings in this study show mean stems density
and mean total density of regenerants of 616 stems per hectare and 2780 stems per hectare respectively. The paper concludes
that despite the Miombo Woodland providing products and services to the surrounding communities the woodland is still
fairly stocked with high tree and shrub species diversity. The study recommends in-depth forest inventory, preparation of
management plan and promotion of good governance in management of Bereku forest reserve.
1. INTRODUCTION
Miombo Woodland is the most extensive veg-
etation type in Africa, covering an estimated 2.7
million km2 in regions receiving greater than 700
mm mean annual rainfall on nutrient-poor soils
(Campbell et al. 1996). Miombo Woodland is
distinguished from other African savanna, wood-
land and forest formations by the dominance of
tree species in the family Fabaceae, subfamily
Caesalpinioideae, particularly in the genera
Brachystegia, Julbernardia and Isoberlinia
(Frost 1996). These genera are seldom found
outside Miombo. Although this dominance by
Caesalpinioideae is characteristic, their contri-
bution to numbers and biomass varies extensively
within and between communities (Frost 1996).
What factors favour this dominance is an inter-
esting but as yet largely unanswered question,
though the widespread occurrence of ectomy-
corrhizae in their roots may enable them to ex-
ploit porous, infertile soils more efficiently than
groups lacking ectomycorrhizae (Högberg and
Nylund 1981). The composition and structure of
Miombo Woodland appears superficially to be
relatively uniform over large regions, suggest-
ing a broad similarity in key environmental con-
ditions. Woody plants comprise 95-98% of the
aboveground biomass of undisturbed stands;
grasses and herbs make up the remainder (Chi-
dumayo 1993a). The woodlands typically com-
prise an upper canopy of umbrella shaped trees;
a scattered layer, often absent, of subcanopy
trees; a discontinuous understorey of shrubs and
saplings; and a patchy layer of grasses (Campbell
1966). The uniformity in appearance is due in
part to the remarkably similar physiognomy of
the dominant canopy trees, no doubt a reflection
of their origins in the Caesalpinioideae. Differ-
ences in species composition, diversity and struc-
ture are more apparent at a local scale. The ori-
gin of these differences is unclear: geomorphic
evolution of the landscape (Cole 1986); edaphic
factors, principally soil moisture and soil nutri-
ents (Campbell et al. 1988) and past and present
land use and other anthropogenic disturbances
(Chidumayo 1987c), have all been implicated.
According to Chidumayo (1989a), anthropoge-
nic activities play a big role in the dynamics of
miombo woodlands. The species diversity and
composition have been shaped in many ways by
human beings, and it is believed no part of it re-
mains absent of human influence (WWF-SARPO
2001). Knowledge of the extent to which tree
and shrub diversity have been shaped is inad-
equate. This study assessed species richness, di-
versity and dominance of tree and shrub in
Bereku Forest Reserve (BFR). BFR is a Central
Government owned forest located in Manyara
region. It is managed through Joint Forest Man-
© Kamla-Raj 2011J Biodiversity, 2(1): 1-7 (2011)
agement (JFM). It is against this background that
the area is selected for this study since it is a
good representative of a forest managed jointly
in Northern part of Tanzania and as such it is
worthy assessing species diversity under this for-
est management regime.
2. MATERIAL AND METHOD
2.1 The Study Area Description
Babati district is located at latitude 4°132
South and longitude 35°452 East, 1300-1800
m.a.s.l, Manyara Region, northern part of Tan-
zania. The district has a total area of 6069 km2.
It is bordered to the north by the Arusha Region,
to the southeast by the Simanjiro District, to the
south by the Dodoma Region, to the southwest
by the Hanang District, and to the northwest by
the Mbulu District. The Bereku forest has a total
area of about 5670 ha (Fig. 1). The forest is typi-
cal dry Miombo woodland located within the Rift
valley, about 20 km south of Babati township,
accessed by road.
According to the 1988 population census of
Tanzania, the district hosts 208,000 people com-
pared to 95 411 people in 1928. Currently, more
than 379 000 people live in Babati district.
Bereku forest reserve is surrounded by 9 villages
with a total population of about 17 000 people.
Most of the villages are linked by paths except
Babati
NN
Legend
Bereku_forest
02050 4100 8200 Kilometers0187.5 375 750 Kilometers
Fig. 1. The study area map
for a few that link the main roads. The main socio-
economic activities of the people in study area
include agricultural production and livestock
keeping. Other activities include: beekeeping,
fishing and lumbering. Cultivated food crops in-
clude: maize, beans, simsim, paddy and ground-
nuts. Cash crops which are given high priority in
the area include: pigeon peas and sunflower.
Livestock keeping is mainly extensive though
there are some zero grazing and semi-intensive
systems. Part of the grazing is done in the forest
reserve, which is a key contributor to land deg-
radation.
2.1 Data Collection
Forest inventory was conducted to understand
tree and shrub species diversity, their distribu-
tion and estimate the available stock in the wood-
land. Forest inventory is defined as the proce-
dure for obtaining information on the quantity
and quality of the woodland resources and other
characteristics of the land on which the trees and
shrubs are growing (Malimbwi 1997). The ac-
tual inventory was preceded by a reconnaissance
survey which involved establishing transects and
plot laying-out on the map of the forest reserve.
To cover the whole woodland area and variation
between vegetation cover. Systematic sampling
design was adopted in this study. In this study,
systematic sampling design ensured an even
RICHARD A. GILIBA, EMMANUEL K. BOON, CANISIUS J. KAYOMBO ET AL.
2
spread of the samples throughout the woodland
area and thus increase the chances of including
all vegetation types in the woodland (Philip
1994).
This study adopted a sampling intensity of
0.1% which is equivalent to 80 sample plots.
Reasons behind this include limited finances and
time constraint. Synnot (1979) recommended
sampling intensity within a range of 0.5% to 0.7%
for tropical natural forest inventories. However,
according to Malimbwi and Mugasha (2002) and
Malimbwi et al. (2005), financial and time con-
straints and purpose of the forest inventory may
dictate the sampling unit to be as low as 0.01%.
Circular shaped sample plots were adopted be-
cause they are easy to use, they reduce edge ef-
fects in the samples and counting errors during
inventory of border trees are minimised. The ef-
fects are less on the circle plots than in square
and rectangular plots (Krebs 1989). The sample
plot was divided into three areas of 5m, 10m and
15m radius. The information that was recorded
from each sample plot includes: diameter at
breast height (dbh), tree and shrub species names,
regenerants frequency, Geographical Positioning
System (GPS) readings, indicators of human dis-
turbances such as trees cut, poles cut, charcoal
kilns, pit sawing, burnt areas and grazing.
2.3 Data Analysis
The data were analysed for species composi-
tion, richness, diversity, Species Importance
Value Index (IVI). Species importance values
were computed as the average of the relative
basal area, density and frequency. The IVI for a
species is a composite of three ecological pa-
rameters – density, frequency and basal area,
which measure different features and character-
istics of a species in its habitat. Ecologically,
density and frequency of a species measure the
distribution of a species within the population
while basal area measures the area occupied by
the stems of trees. Species diversity was com-
puted using Shannon’s and Simpson’s diversity
indices. The Shannon Diversity Index was com-
puted as (H’ = ΣPi*ln Pi) where H’ is the index
of diversity, Pi is the importance value of a spe-
cies as a proportion of all species. Simpson’s
Diversity Index was computed as C = ΣPi2 where
C is the index number and Pi as defined above
(Munishi et al. 2008). The knowledge of species
diversity is useful for establishing the influence
of biotic disturbance, and the state of succession
and stability in the environment (Misra 1989).
This species diversity index increases with the
number of species in the community (Krebs
1989).
3. RESULT AND DISCUSSION
3.1 Species Composition and Richness
Table 1 shows the general characteristics of
Bereku tree resources. A total of 110 tree and
shrub species were identified, out of these trees
constituted 75% while shrubs were 25%. The
species richness (110) of trees and shrub obser-
ved in this study compares well with the Miom-
bo forest occurring in other areas. Luoga (2000)
enumerated 79 species in Kitulanghalo Forest
Reserve while Backeus (2006) found 86 species
around Ihombwa village. Njana (2009) and Ma-
fupa (2006) found 82 and 46 species in Urumwa
forest reserve and Igombe river forest reserve
respectively. The high number of species rich-
ness in the study area is attributed to the pres-
ence of the riverine forest that contributes to the
growth of many species. Climatic, edaphic vari-
ability and anthropogenic activities are other fa-
ctors associated to the difference in species ri-
chness. Chidumayo (1989a) reported that anth-
ropogenic activities play big role in the dynam-
ics of Miombo Woodlands.
Table 1: Characteristics of tree and shrub resources in
the Bereku forest reserve
Parameter Values
Richness (Total number of species) 110
Density (stems/ha) 616
Density of regenerants (stems/ha) 2780
Shannon’s Index 4.27
Simpson’s Index 0.04
3.2 Species Diversity
The study revealed Shannon-Wiener Index of
diversity (H’) of 4.27 for the Miombo Wood-
land (Table 1). This index tells about species rich-
ness (number of species) and evenness (species
distribution) (Magurran 1988), the larger the
value of H’ the greater the species diversity and
vice versa. An ecosystem with H’ value greater
than 2 has been regarded as medium to high di-
SPECIES COMPOSITION, RICHNESS AND DIVERSITY IN MIOMBO WOODLAND 3
verse in terms of species (Barbour et al. 1999).
Thus, Miombo Woodland of Bereku has ratio-
nally high species diversity. Species noted to ha-
ve contributed to high species diversity include:
Brachystegia microphylla Harms (0.42), Bra-
chystegia spiciformis Benth (0.22), Julbernadia
globiflora (Benth.) Troupin (0.24), Combretum
molle R.Br ex G. Don (0.17) and Markhamia
obtusifolia (Baker) Sprague (0.14). Comparative
studies elsewhere in Miombo Woodlands by a
number of scholars have shown small values.
Nduwamungu (1997) and Zahabu (2001) re-
ported H’ value of 3.79 and 3.13 respectively in
Miombo Woodlands of Kitulangalo forest re-
serve in Morogoro, Tanzania. Recent studies in
Miombo Woodlands of Urumwa forest reserve
Tabora, Tanzania by Njana (2008), Igombe river
forest reserve, Tabora, Tanzania by Mafupa
(2006) and Handeni Hill forest reserve, Tanga,
Tanzania by Mohamed (2006) reported H’ val-
ues of 3.40, 2.90 and 3.10 respectively. The big-
ger the value (4.27) from present study is associ-
ated with the presence of riverine forest that
found rich in species composition and diversity
in miombo woodland of Bereku forest reserve.
3.3 Species Dominance
The study came up with index of dominance
(ID) of 0.043 for Miombo Woodland (Table 1).
The lower the index value, the lower the domi-
nance of a single or few species (Edward 1996).
Misra (1989) reported the greater the value of
index of dominance the lower the species diver-
sity and vice versa in the scale of 0 to 1. The
index of dominance value in this study is rela-
tive smaller compared to what has been found
by other studies in Miombo Woodlands imply-
ing that the probability of picking randomly two
individuals belonging to the same species is very
low or the probability that any species encoun-
tered at random would be different species. Njana
(2008) reported ID value of 0.056 in miombo
woodlands of Urumwa forest reserve Tabora,
Tanzania, Mafupa (2006) reported ID value of
0.088 and 0.135 in undisturbed and disturbed
strata of miombo woodlands of Igombe river for-
est reserve, Tabora, Tanzania respectively while
Malimbwi and Mugasha (2002) and Mohamed
(2006) recorded ID values of 0.073 and 0.063
respectively in miombo woodlands of Handeni
Hill forest reserve, Tanga, Tanzania.
3.4 Importance Value Index (IVI)
Importance value index provides knowledge
on important species of a plant community. Based
on IVI Brachystegia microphylla Harms was
most dominate species followed by Brachyste-
gia spiciformis Benth, Julbernadia globiflora
(Benth.) Troupin, Combretum molle R.Br ex G.
Don, Parinari curetellifolia Planch. Ex Benth
and Markhamia obtusifolia (Baker) Sprague.
Others were Dombeya rotundifolia (Hochst.)
Planch., Vernonia amygdalina Delile, Faurea
rochetiana (A. Rich.) Pic.Serm and Bridelia
micrantha (Hochst.) Baill. Figure 2 shows the
distribution of important tree and shrub species
in the woodland. These results disclose that, the
most important species in Bereku forest reserve
have high diversity in the scale of Shannon-
Weiner Index of Diversity. The IVI rank species
in a way as to give an indication on which spe-
cies come out as important element of the
miombo trees (Munishi et al. 2008).
3.5 Stem Density of Standing Trees and
Shrubs (N)
The total mean stems density in UFR was
found to be 616 ± 46 for trees and shrubs with
greater than 4 cm diameter at breast height. Fig-
ure 3 shows an inverted ‘J’ shape which is com-
mon for natural forests with active regeneration
(Phillip 1983) and recruitment. Accordingly, ac-
tive regeneration and recruitment in miombo
woodland of BFR as portrayed in this study is a
good sign of sustainability of the woodland stock
which has chances of insuring sustainable sup-
ply of products and services; and hence sustained
livelihoods of the woodland dependants.
3.6 Stem Density of Regenerants
The results show that, mean total density of
regenerants was 2780 ± 20 stems per hectare.
Figure 3 shows the distribution of regenerants in
the miombo woodland. It shows that,
Brachystegia microphylla (19%), Brachystegia
spiciformis (14%), Jubernadia globiflora (11%),
Brachystegia utilis (8%), Parinari curatellifolia
(5%), Dodonea viscosa (5%), and Markhamia
obtusifolia (4%) are among the most regenerat-
ing species in Bereku forest reserve (Figure 4).
From these results it suffices to conclude that,
the most regenerating species are possibly the
RICHARD A. GILIBA, EMMANUEL K. BOON, CANISIUS J. KAYOMBO ET AL.
4
% Importance value index
0
5
10
15
20
25
30
35
40
45
50
Brachy-
stegia
micro-
phylla
Brachy-
stegia
speci-
formis
Julber-
nadia
globi-
flora
Comb-
retum
molle
Parinari
curatelli-
folia
Markhamia
obtusifolia Dombeya
rotundi-
folia
Bridelia
micrantha Vernonia
amigda-
lina
Faurea
rochetiana
Species
Fig. 2. Tree and shrub species richness according to IVI in Bereku forest
Stems/ha
0
50
100
150
200
250
300
350
400
450
500
1-10 11-20 21-30 31-40 41-50 >50
Diameter class
Fig. 3. Distribution of number of stems per hectare of
standing trees by diameter class (Sample plots = 80)
most exploited species by local communities in
their daily livelihood activities and the ones
browsed by domestic animals. Regeneration in
miombo is mainly from stump coppices, stump/
root sucker shoots and recruitment from old
stunted seedlings already present in grass layer
at the time of tree cut, fall or death (Chidumayo
1993, 1997). Moreover, comparing Figure 4 with
Figure 2, it can be deduced that the forest is
moving towards a more balanced one with a dif-
ferent composition of species, as the regenerants
of B. microphylla, which seems the “dominant”
species as a tree, give place to other species (38%
of trees against 19% of regenerants).
3.5 Tree and Shrub Species Exploitation
Regardless of high plant diversity in Bereku
forest reserve, valuable timber tree species have
been harvested illegally to the extent that it was
very occasional to encounter mature stems in the
forest during forest inventory. The tree species
include: Pterocarpus angolensis, Pterocarpus
rotundifolius, Albizia verscolor and Dalbergia
melanoxylon. This was evident in the number of
coppices observed from the stumps, indicating
that stems were cut. Presence of pits and wooden
platform for sawing in the forest also justifies
illegal harvesting of the mentioned tree species.
This is in line with study by Malambo and
Syampungani (2008) in Miombo Woodlands of
Zambia who reported that illegal and selective
logging of valuable species such as Pterocarpus
angolensis, Afzelia quanzensis, Dalbergia
melanoxylon and Isoberlinia angolensis contrib-
ute to over exploitation of these tree species.
Furthermore, the presence of cut stumps and old
earth kilns in the forest revealed that charcoal
making is crucial activity in the study area. Spe-
cies frequently used for charcoal were Combre-
tum molle, Brachystegia and Julbernadia spe-
cies. A study in western Tanzania by Monela et
al. (2007) reported that charcoal production
venture is growing high because it is taken as
part time job to supplement farmers’ income.
Sandalwood (Osyris lanceolata) was found to
be vulnerable plant species in the reserve. This
is because people illegally harvest entire plant
SPECIES COMPOSITION, RICHNESS AND DIVERSITY IN MIOMBO WOODLAND 5
Markham
i
a
obtusifo
l
i
4%
Dodenea viscose
5%
Brideliamicrantha
5%
P
a
r
i
n
a
r
i
c
u
r
a
t
e
l
l
i
f
o
l
i
a
5
%
J
u
b
e
r
n
a
d
i
a
g
l
o
b
i
f
l
o
r
a
1
0
%
Brachystegia utilis
13%
Others
30%
Brachystegia
microphylla
16%
B
r
a
c
h
y
s
t
e
g
i
a
s
p
i
c
i
f
o
r
m
i
s
1
2
%
Others 30%
Brachystegia
microphylla 16%
Brachystegia
spiciformis 12%
Jubernadia
globiflora 10%
Parinari
curatellifolia 5%
Markhamia
obtusifolia 4%
Dodenea viscose 5%
Bridelia micrantha 5%
Brachystegia utilis 13%
Fig. 4. Distribution of regenerant species in BFR (Number of species = 48)
body (root and stem) for sale. This limits the re-
generation of this species by seeds and coppices
from the stumps and roots. Sandalwood oil is
used for perfume manufacture and it is one of
the oldest known perfume materials.
4. CONCLUSION
The study revealed that the Miombo Wood-
land of Bereku forest reserve has a reasonably
good tree and shrub species composition and
richness. Species noted to be both dominant and
with high species diversity indices include:
Brachystegia spiciformis (0.41), Brachystegia
spiciformis (0.23), Julbernadia globiflora (0.24),
Combretum molle (0.18). These dominant as
well as highly diverse tree and shrub species fit
quite well within the general definition of Mio-
mbo Woodlands. However, species richness for
some timber tree species such as Pterocarpus
angolensis, Dalbergia melanoxylon, Pterocar-
pus rontundifolius, and Albizia verscolor was
very poor due to overexploitation. The harvest-
ing involves wood fuel collection and building
materials like timber, poles and withies. Gener-
ally, the regeneration of the Miombo Woodland
was found to be good. This indicates a good si-
gn of sustainability of the woodland stock which
has chances of ensuring sustainable supply of
products and services and hence sustains liveli-
hoods of the surrounding communities.
5. RECOMMENDATION
The study recommends in-depth forest inven-
tory, preparation of management plan and pro-
motion of good governance in management of
Bereku forest reserve.
ACKNOWLEDGEMENTS
We are grateful to the Flemish Interuniver-
sity Council (VLIR) of Belgium for providing
financial support for this study. We are also thank-
ful to all people who assisted in the data collec-
tion in the study area as well as village leaders,
household heads, key informants and the Dis-
trict forest officers for providing the required
information and data for this study.
REFERENCES
Backéus I, Pettersson B, Strömquist L, Ruffo C 2006. Tree
communities and structural dynamics in Miombo
(Brachystegia-Julbernadia) Woodland, Tanzania.
Forest Ecology and Management, 230: 171 - 178.
Barbour M, Burk JH, Pitts WD, Gillians FS, Schwartz
MW 1999. Terrestrial Ecology. Chicago, Illinois:
Addson Wesley Longman, Inc.
Campbell BM, Swift MJ, Hatton J, Frost PGH 1988. Small-
scale vegetation pattern and nutrient cycling in
Miombo Woodland. In: JTA Verhoeven, GW Heil,
MJA Werger (Eds.): Vegetation Structure in Relation
to Carbon and Nutrient Economy. The Hague: SPB
Academic Publishing, pp. 69-85.
Chidumayo EN 1989a. Land use, deforestation and re-
forestation in the Zambian Copperbelt. Land Degra-
dation and Rehabilitation, 1: 209-216
Campbell BM 1996. The Miombo in Transition:
Woodlands and Welfare in Africa. Bogor, Indonesia:
CIFOR.
Chidumayo EN 1993a. Silvicultural Characteristics and
Management of Miombo Woodlands. Paper Presen-
ted in the Conference on International Symposium
on Ecology and Management of Indigenous Forest
in Southern Africa, Victoria Fall Zimbabwe, July 27
–to 29, 1992.
RICHARD A. GILIBA, EMMANUEL K. BOON, CANISIUS J. KAYOMBO ET AL.
6
Chidumayo EN 1993b. Responses of Miombo to Harvesting:
Ecology and Management. Stockholm: Stockholm
Environment Institute.
Chidumayo EN 1997. Miombo Ecology and Management:
An Introduction. Intermediate Technology Publica-
tions. Sweden: Stockholm Environment Institute, pp.
22 – 30.
Cole M 1986. The Savannas: Biogeography and
Geobotany. London: Academic Press.
Frost P 1996. The ecology of Miombo Woodlands. In: B
Campbell (Ed.): The Miombo in Transition:
Woodlands and Welfare in Africa. Bogor, Indonesia:
Center for International Forestry Research (CIFOR),
pp. 11 – 57.
Högberg P, Nylund JE 1981. Ectomycorrhizae in coastal
miombo woodland of Tanzania. Plant and Soil, 63:
283-289.
Krebs CJ 1989. Ecological Methodology. New York:
Hamper Collins Publishers, P. 654.
Luoga EJ 2000. The Effect of Human Disturbances on
Diversity and Dynamics of Eastern Tanzania Miombo
Arborescent Species. Ph.D. Thesis, Unpublished.
Johannesburg: University of Witwaterrand.
Mafupa CJ 2006. Impact of Human Disturbances in
Miombo Woodlands of Igombe River Forest Reserve,
Nzega District, Tanzania. M.Sc. Thesis, Unpublished.
Morogoro: Sokoine University of Agriculture.
Malambo MF, Syampungani S 2008. Opportunities and
challenges for sustainable management of Miombo
Woodlands: The Zambian perspective. Paper Presen-
ted in the Conference on Research and Development
for Sustainable Management of Semiarid Miombo
Woodlands in East Africa. Tanzania, March 3 to 8,
2008.
Magurran EA 1988. Ecological Diversity and Its Measure-
ment. Princeton: Princeton University Press, P. 179.
Malimbwi RE 1997. Fundamentals of Forest Mensuration.
Morogoro: Department of Forest Mensuration and
Management.
Malimbwi RE, Mugasha AG 2002. Reconnaissance Timber
Inventory for Handeni Hill Forest Reserve in Han-
deni District, Tanzania. Morogoro: FOCON-SULT.
Malimbwi RE, Shemweta DTK, Zahabu E, Kingazi SP,
Katani JZ, Silayo DA 2005. Inventory for Mvomero
and Morogoro Districts, Tanzania. Morogoro
FOCONSULT.
Misra KC 1989. Manual of Plant Ecology. 3rd Edition. New
Delhi: Oxford and IBH Publishing Co. Pvt. Ltd.
Mohamed BS 2006. Impact of Joint Forest Management
on Handeni Hill Forest Reserve and Adjacent Com-
munities, Tanga, Tanzania. M.Sc. Thesis, Unpublished.
Morogoro: Sokoine University of Agriculture.
Monela GC, Abdallah JM 2007. Principle Socio-economic
Issues in Utilization of Miombo Woodlands in
Tanzania. Paper Presented in the Conference on
Management of Indigenous Tree Species for
Ecosystem Restoration and Wood Production in
Semi-Arid Miombo Woodlands in Eastern Africa,
Tanzania, February 6 to 12, 2007.
Munishi PKT, Philipina F, Temu RPC, Pima NE 2008. Tree
species composition and local use in agricultural
landscapes of west Usambaras Tanzania. African
Journal of Ecology, 46: 66–73
Nduwamungu J 1997. Tree and Shrub Diversity in Miombo
Woodlands. A Case Study at SUA Kitulanghalo Forest
Reserve, Morogoro, Tanzania. M.Sc. Thesis, Unpub-
lished. Morogoro: Sokoine University of Agriculture.
Njana MA 2008. Arborescent Species Diversity and
Stocking in Miombo Woodland of Urumwa Forest
Reserve and their Contribution to Livelihoods,
Tabora, Tanzania. M.Sc. Thesis, Unpublished,
Morogoro: Sokoine University of Agriculture.
Philip SM 1994. Measuring Trees and Forests. 2nd Edition.
Wallingford: CAB International.
Philips O, Gentry AH 1993. The useful plants of Tam-
bopata, Peru: Statistical hypothesis tests with a new
quantitative technique. Economic Botany, 47: 15 –
32.
Synnott TJ 1979. A Manual of Permanent Plot Procedures
for Tropical Rainforests. University of Oxford: Tropical
Forestry Papers.
WWF-SARPO 2001. Conserving the Miombo Eco-region.
Reconnaissance Summary. WWF-Southern Africa
Regional Programme Office, Harare, Zimbabwe.
Zahabu E 2001. Impact of Charcoal Extraction to the
Miombo Woodlands: The Case of Kitulangalo area,
Tanzania. MSc. Thesis, Unpublished. Morogoro:
Sokoine University of Agriculture.
SPECIES COMPOSITION, RICHNESS AND DIVERSITY IN MIOMBO WOODLAND 7

File (1)

Content uploaded by Emmanuel Musamba
Author content
... In Zimbabwe the woodlands cover approximately 42% of the country [5], but the biodiversity composition and structure are mostly poorly documented. Miombo woodland dynamics is strongly influenced by anthropogenic factors [6][7][8]and most ecosystems are being threatened by the increased demand for services by the burgeoning human population [9]. Woodland ecosystems and their valuable biodiversity resources are being lost at an accelerated rate [10][11][12] , thereby altering ecosystem function and consequently threatening the provision of services and goods especially to poor rural communities [13]. ...
... Reference [44] reported that Shannon-Wiener index values fall between 1.5 and 3.5 for tropical woodlands, so the value obtained here is within the expected range. Ecosystems with Shannon-Wiener values greater than 2 are regarded as medium to highly diverse in terms of species [7]. Reference [45] attributed the high species diversity in miombo woodlands to the wide diversity of habitats present. ...
... Our results are relatively larger than those found by [46] (Shannon 2.8) in Zambia, [29] (Shannon 1.05) in Tanzania, and [34] (Shannon 1.25) in Mozambique. Higher Shannon values have also been recorded from Tanzanian study [7] (Shannon 4.27). Differences in richness and diversity possibly result from differences in rainfall regimes [12] and disturbance history [1]. ...
Article
Full-text available
The diversity, structure, species composition, and above ground biomass of woody plants on Ngomakurira mountain in Zimbabwe were studied. A systematic random sampling approach was adopted to establish 52 sampling plots measuring 10 × 10 m across 3 study strata in the 1266 ha study area. Woody species occurring in each plot were identified and the circumferences of trees with diameters >8.0 cm at 1.3 m height were measured. A total of 91 species belonging to 74 genera and 39 families were identified in the sample plots. A Shannon-Wiener index mean value of 3.12 was obtained indicating high species diversity on the mountain. The DBH size class distribution showed inverse J distribution patterns across the three study strata, but with only 3 individual plants with DBH > 30 cm. Mean basal area was 15.21 m 2 ha −1 with U. kirkiana and J. globiflora contributing approximately 30% of the basal area. The estimated above ground biomass ranged from 34.5 to 65.1 t ha −1 . Kruskal-Wallis- H test showed no significant differences in species richness, stem density, basal area, above ground biomass, and evenness, across the study strata ( p < 0.05 ). Ngomakurira woodland has potential to regenerate due to the presence of many stems in the small diameter size classes.
... (2014), Tang et al. (2012), Grand and Lavkulich (2011), Djukic et al. (2010), Hattar et al. (2010), Egli et al. (2009, Seibert et al. (2007) and Yoo et al. (2006) established that the SOC stock increase with an increase in elevation. This has been explained by variations in dominant vegetation types and species richness with elevation (Yao et al., 2010; Giliba et al., 2011; Grand and Lavkulich, 2011; Sreekanth et al., 2013). Studies by Cambule et al., (2014) in Mozambique, Wiesmeier et al., (2012in Germany and Aticho (2013) in Ethiopia have reported soil thickness to be among the important factors that affect SOC stocks. ...
... Studies in different parts of the world by Hoffmann Yoo et al. (2006) established that the SOC stock increase with an increase in elevation. This has been explained by variations in dominant vegetation types and species richness with elevation (Yao et al., 2010; Giliba et al., 2011; Grand and Lavkulich, 2011; Sreekanth et al., 2013). Studies by Cambule et al., (2014) in Mozambique, Wiesmeier et al., (2012 in Germany and Aticho (2013) in Ethiopia have reported soil thickness to be among the important factors that affect SOC stocks. ...
Article
Full-text available
The organic carbon stock (SOC) (t/ha) was calculated in different approaches in order to enhance the differences among methods and their utility regarding specific studies. Using data obtained in Romania (2000-2012) from 4,500 profiles and 9,523 soil horizons, the organic carbon stock was calculated for the main forest soils (18 types) using three different methods: 1) on pedogenetical horizons, by soil bulk density and depth class/horizon thickness; 2) by soil type and standard depths; 3) using regression equations between the quantity of organic C and harvesting depths. Even though the same data were used, the differences between the values of C stock obtained from the three methods were relatively high. The first method led to an overvaluation of the C stock. The differences between methods 1 and 2 were high (and reached 33% for andosol), while the differences between methods 2 and 3 were smaller (a maximum of 23% for rendzic leptosol). The differences between methods 2 and 3 were significantly lower especially for andosol, arenosol and vertisol. A thorough analysis of all three methods concluded that the best method to evaluate the organic C stock was to distribute the obtained values on the following standard depths: 0 - 10 cm; 10 - 20 cm; 20 - 40 cm; > 40 cm. For each soil type, a correlation between the quantity of organic C and the sample harvesting depth was also established. These correlations were significant for all types of soil; however, lower correlation coefficients were registered for rendzic leptosol, haplic podzol and fluvisol.
... However, little is known about the effectiveness of PAs in containing deforestation and forest degradation. This expansion led to an exponential increase in studies of forest cover, structure, diversity and species composition in the miombo woodlands PAs (Banda et al., 2008(Banda et al., , 2006Giliba and Boon, 2011;Green et al., 2013;Mwakalukwa et al., 2014;Paul et al., 2013;Ribeiro et al., 2013Ribeiro et al., , 2008. Such studies were conducted either to meet the demand and agenda of different conservation actors (Cobbinah et al., 2014) or to assess whether the best way of conserving natural resources was by restricting access in to PAs (Banda et al., 2006;Hall et al., 2003). ...
Poster
Niassa National Reserve (NNR) is the most extensive conservation area in Mozambique and the third largest in Africa, Encompassing 42,000 Km2 of miombo woodland. Due to the importance of the dambos formation in the maintenance of forest, fauna and aquatic diversity in the miombo woodlands, in 2015 we assessed the vegetation structure and composition of dambos in the NNR. Six dambos were selected using Google earth, MODIS satellite images and exploratory visit in the site. The field data was collected using fixed area and systematic sampling process in two stages: the first, consisted in transects lines of 100 x 10m, laying perpendicular to the dambos flow, whereas the second stage consisted in use systematic sub-transects. In total 5.8 hectares were sampled, summing up 109 inventoried wood species in the main dambos transects. The most common species were Vitex doniana, Burkea africana, Syzygium cordatum and Annona senegalensis, while the most dominant species in the Importance Value Index (IVI) were Vitex doniana, Pseudolachnostylis maprouneifolia, Annona senegalensis and Syzygium cordatum. The diversity index was 3.55, the Simpson’s dominance index was 0.05 and the heterogeneity index (H) was 2.99, indicating high diversity and heterogeneity in the NNR dambos.
... In Tanzania, the number of tree species in miombo woodlands exceeds 100 (e.g. Giliba et al., 2011; Mugasha et al., 2013a). The structure of miombo woodlands may also vary significantly. ...
Research
Malimbwi, R.E., Eid, T. & Chamshama, S.A.O (Eds.). 2016. Allometric volume and biomass models in Tanzania. Department of Forest Mensuration and Management, Sokoine University of Agriculture, Morogoro, Tanzania. 129 pp. ISBN: 978-9976-9930-1-1.
Chapter
Understanding woody plant species composition and structure is fundamental to design and optimize the needed conservation measures for Ethiopian church forests. The aim of this study was to describe the composition, structure, and regeneration status of woody species in church forests in southeast of Lake Tana, Ethiopia. Data were collected from twenty-four church forests. Four plots (20 m × 20 m) were established in each church forest. Plots were located in four cardinal directions (north, east, west, and south) at different distances from the forest center. Four subplots (5 m × 5 m) were established in each plot to assess seedlings and canopy cover. In each plot, all woody plants were identified and counted, and diameter at breast height (DBH) was measured. Species and family importance values were computed to characterize the species composition. Additionally, population structural features were analyzed through the variation of tree size classes. Species richness (SR), Pilou evenness (Jʹ), and Shannon–Wiener index (Hʹ) were used to determine species diversity. A total of 115 woody species representing 53 families and 97 genera were found. Of these, 62% were trees, 36% shrubs, 1.89% climber, and 0.06% reed species. Species richness differed among forests, ranging between 16 and 38 species. Fabaceae, Sapotaceae, and Rubiaceae were the dominant families with a high family importance values of 41, 28, and 22, respectively. The church forests have relatively high indices of species diversity (SR = 26 ± 1.25), (Jʹ = 0.75 ± 0.02), and (Hʹ = 2.42 ± 0.07), indicating that they play a major role in the conservation of woody species. However, a relatively high densities of Eucalyptus spp. ranging from 13 to 1925 individuals ha−1 were recorded, and these exotic tree species, thus, form a potential threat to the conservation of native species. The diameter class distribution of some selected keystone and dominant species formed four main shape types, of which the irregular-shaped pattern was most predominant, which suggests missing cohorts and regeneration problems for most species. Higher densities of Eucalyptus plantations were recorded in more recently established than old church forests. Therefore, effective measures should be taken to address the major pressures, such as plantation of exotic species that negatively affect the species composition and vegetation structure of these church forests, which, in turn, affect their ecosystem functions and services.
Article
Full-text available
It is important to understand how species distributions will shift under climate change. While much focus has been on species tracking temperature changes in the northern hemisphere, changing precipitation patterns in tropical regions have received less attention. The aim of the study was to estimate the current distribution of wet and dry miombo woodlands of sub-Saharan Africa and to predict their distributions under different climate change scenarios. A maximum entropy method (Maxent) was used to estimate the distributions and for projections. Occurrence records of dominant tree species in each woodland were used for modeling, together with altitude, soil characteristics, and climate variables as the environmental variables. Modeling was done under all four representative concentration pathways (RCPs) and three general circulation models. Three dominant tree species were used in models of dry miombo while seven were used for wet miombo. Models estimated dry miombo to cover almost the entire known distribution of miombo woodlands while wet miombo were estimated to predominate in parts of Angola, southern Democratic Republic of Congo, Malawi, Tanzania, Zambia, and Zimbabwe. Future climate scenarios predict a drier climate in sub-Saharan Africa, and as a result, the range of dry miombo will expand. Dry miombo were predicted to expand by up to 17.3% in 2050 and 22.7% in 2070. In contrast, wet miombo were predicted to contract by up to − 28.6% in 2050 and − 41.6% in 2070. A warming climate is conducive for the proliferation of dry miombo tree species but unfavorable for wet miombo tree species.
Article
Full-text available
Ecological restoration of degraded riparian Tugai forests is a key driver to combat desertification in arid regions. Previous studies have focused mainly on changes in groundwater as the underlying mechanisms of Tugai forest’s decline. We evaluated species composition and diversity of Tugai forest and their relationship to groundwater, soil salinity, and soil nutrient. Using 73 quadrats (100 m × 100 m) from 13 transects located perpendicularly to river in the upper reaches of the Tarim River. Eighteen plant species belonging to sixteen genera and eight families were recorded, and the dominant species included Populus euphratica, Phragmites communis, and Tamarix ramosissima. Three P. euphratica stand ages were detected: young stand, mature stand, and old stand. There were significant differences in species diversity, groundwater depth, groundwater salinity, distance from the quadrat to the river channel, soil moisture content, pH, electrical conductivity, total salt, Cl⁻, SO4²⁻, Ca²⁻, Mg²⁺, Na⁺, K⁺, soil organic carbon, and soil organic matter across the stand ages. Seven species were identified as indicators of the three stand ages. Redundancy analysis indicated that the Tugai forest diversity indices were negatively correlated with groundwater depth, groundwater salinity, and distance from the river, and positively associated with electrical conductivity, total salt, pH, Cl⁻, SO4²⁻, CO3²⁻, soil organic matter, soil organic carbon, and soil moisture content. Plant diversity was the highest at 3–6 m groundwater depth, followed by 0–3 m and then 6–9 m, with the lowest recorded at > 9 m. The appropriate groundwater depth for herbs was about 1–4 m, whereas the depth for trees and shrubs was about 3–6 m. The groundwater depth < 6 m was deemed suitable for the growth of desert riparian forests. This results provide a scientific reference for the ecological restoration and protection for Tugai forests in arid areas.
Article
Full-text available
Scientific research on plant biodiversity is the only one to identify and develop the potential for innovations derived from plant richness, particularly those of the developing countries. In order to valorize the wild phytogenetic resources for the efficient conservation and sustainable use in sudano-zambezian, a study was carried out in eastern part of National Park of Sena Oura (Chad) assessing the floristic composition, specific abundances and assessing the stand diversity. The systematic inventory of all trees and shrubs (diameter ≥ 5 cm) was done in 10 linear transects (1000 m × 20 m = 20 ha). In total, 84 species grouped in 58 genera and 29 families were found. Combretaceae was the most diverse family (16 species) and the most diverse genus was Terminalia (9 species). The most abundant species was Isoberlinia doka (pi*100 = 12.13% and D = 23 stems/ha) followed by Burkea africana (pi*100 = 7.91% and D = 15 stems/ha). The Simpson index (E= 0.95), the Shannon index (H= 3.41) and the equitability index of Pielou (J= 0.76) indicated that there was moderate stand diversity with more or less equitable species in the Park. The values of diversity and equitability were sufficient for sudanian vegetation. Combretaceae, Caesalpiniaceae, Fabaceae, Meliaceae, Anacardiaceae, Mimosaceae, Rubiaceae were most dominant families according to the Family Importance Value index (FIV). These results contribute to the valorization of the wild phytogenetic resources for efficient in situ conservation and sustainable use.
Thesis
Full-text available
The contribution of local knowledge in natural resource management has been widely reported. However, only a few study cases have focused on the role of local knowledge in overcoming the challenges associated with technical design of forest management plans (under Participatory Forest Management). Notable are the cases reported of Asia’s community forestry systems where community forest users, based on their understanding of their environmental history, ecological theories behind forest regeneration and understanding of simple silvicultural practices, have resorted to application of locally-situated knowledge as opposed to being informed by flawed technical management plans in their forest management practices. Their understandings have subsequently proven adequate in achieving sustainable forest management objective under Participatory Forest Management (PFM). Technically-designed management plans characterize PFM systems in most Sub-Saharan African countries. Yet the contributions of local knowledge in such context remain rather unexplored. It is therefore imperative to investigate the role local knowledge can play in overcoming the reported challenges associated with technical designing of forest management plan. This invites for investigations into understanding of local forest users about their forest condition, their capacity to make independent rational decisions that enhance the intended objectives of PFM and their consciousness in observing the changes or outcomes of their practices thereby making it possible to suggest appropriate intervention during the management process. The current study seeks to unravel these issues by focusing on the following research objectives namely: one, to explore the understanding of local forest managers/users (hereafter referred to as locals) of their forest disturbances and underlying principles of forest regeneration and growth; two, to explore the understanding of local forest managers of their current and future management practices; three, to explore understanding of local forest managers about the changes and trends in forest condition including and lastly, to determine the current biophysical outcome of forest under PFM management. A mixed method approach is adopted using both qualitative data (Focus group discussions, direct observation, forest walk, document reviews and semi structured interviews with key informants) to elicit data on locals’ perceptions and quantitative data from forest survey to elicit data on forest condition. The different sources of data were triangulated not just for convergence/ match, but also for complementarity and divergence (mismatch). Results indicate that local forest managers and users understand to a greater extent the underlying forest ecological principles of forest management, and therefore to some extent consciously undertake relevant management practices which aim both at sustainable supply of forest products, as well as conservation of valued species. Their understanding of the Miombo indicator species such as Mushrooms’ association with Brachystegia could potentially be a less-technical way in monitoring the population trends of Miombo woodland species. However, their knowledge of the forest stock is very little and is less reliable in estimating the forest stock and the harvesting level. Consequently, decision made on the annual harvesting levels are neither dependent on their understanding of the forest stock nor is it dependent directly on the Annual allowable cut amount directives from the experts (District Forest officer) but indirectly dependent on expert knowledge by taking Annual allowable Cut issued by the experts as a point of reference below which they determine the annual harvested amount after taking into account the interest of a few forest-dependent groups-local firewood buyers at the expense of other local charcoal producers. A practice that may be explaining the reason for success in forest conservation (sustainable supply of forest products) efforts with negative effects in access to forests resources to all community members through or unequal distribution of forest resources/benefits. This study contributes in assessing the level of local participation in participatory forest management with their simple and cost effective local knowledge. The findings in Iringa do not indicate that local forest managers have sufficient knowledge of quantifying the harvesting level and cannot possibly be tasked to determine the harvesting level, therefore an integration of local and expert knowledge is recommended to complement the partial nature of both forms of knowledge to ensure the sustainable forest management. Key words: Community forestry, PFM, local knowledge, biophysical outcome,
Article
Full-text available
Studying interactions between elephant and habitats is valuable for assessing the welfare of elephant populations and their habitats. The study was carried out in RINP between March and July 2014 constituting wet and dry seasons to assess the feeding preference of the African elephant (Loxodonta africana) on woody plant species. Purposive sampling was used for gathering data from 26 sample plots, sized 50m x 50m each. Plots were designed immediately after the herd (s) had passed on the various habitats. Frequency and percentage was used to estimate utilization of individual plant species and their parts. Chi-square test and excel were used to analyze feeding pattern preference. The present study found 22 species of plants in 13 families foraged by African elephants in Rubondo Island National Park. Plant species observed to be utilized mostly by elephants included Croton sylvaticus (13.33%), Croton macrostachyus (11.11%), Aeschynomene elaphroxylon (8.88%), Chaetacme aristata (8.88%), Ekerbegia capensis (8.88%), Saba comorensis (6.67%), and Phoenix reclinata (6.67%). There was difference in feeding preference between stem and leaves in woody plant species (χ2=86.462, P < 0.05) which suggested that elephants prefer more leaves than stem. This study presents useful information in understanding the interaction between the African elephant and vegetation in RINP.
Article
Full-text available
Species richness and diversity in agricultural landscapes are important characteristics of agro-ecosystems that determine their potential for biodiversity conservation. This study assessed species composition, richness, diversity and local use of on-farm trees in predominantly agricultural landscape in the Usambaras, north-eastern Tanzania. Assessments were carried out in 90 randomly selected individual farmlands. We identified 47 tree species belonging to 23 families and used by local people for various purposes. The most dominant species were Albizia gummifera (Gmel) C. A. Sm. (mkenge), Parinari excelsa Sabine ssp holstii (Engl.) R. Grah. (muula), Newtonia buchananii (Bak.) Gilb. and Bout (mkufi), Syzygium guineense (Willd) D.C. (mshihwi), Ficus capensis L. (mvumo) and Casearia engleri (Gilg) (mkokoko). These species are indigenous and were retained from existing ones during farm clearing. The species diversity (by the Simpson’s and Shannon–Wiener diversity indices of 0.07 and 2.8 respectively) is comparable with that of adjacent natural forests. There are apparently high on-farm tree species richness and diversity, the conservation of which can contribute to ex-situ biodiversity conservation. On-farm tree management should be encouraged, especially where there is population pressure on the existing natural forests. Research to enhance sustainability of the farming system is important for biodiversity management on farmlands.
Article
Full-text available
This paper describes a new, simple, quantitative technique for evaluating the relative usefulness of plants to people. The technique is then compared to the quantitative approaches in ethnobotany that have been developed recently. Our technique is used to calculate the importance of over 600 species of woody plants to non-indigenous mestizo people in Tambopata, Amazonian Peru. Two general classes of hypotheses are formulated and tested statistically, concerning (1) the relative importance of different species, and (2) the importance of different families. The plant families are compared with respect to all uses, and with respect to five broad groups of uses. Palms, Annonaceae, and Lauraceae were found to be the most useful woody plant families. On average, the 20 largest woody plant families are most important to mestizos for subsistence construction materials, followed in descending order by commercial, edible, technological, and medicinal uses. En éste estudio se describe una nueva técnica cuantitativa para la evaluation de la relativa utilidad de plantas a la gente. Esta técnica se compara con aquellas técnicas cuantitativas recientemente desarrolladas en etnobotánica. Con ésta técnica nosotros estimamos la importantia que las plantas lenosas, más de 600 especies, tienenpara los mestizos de Tambopata de la Amazonia del Peru. Estadisticamente, se prueban dos hipótesis generates concernientes a (1) la relativa importantia de especies diferentes, y a (2) la importantia de diferentes familias. Las familias de plantas son comparadas entre ellas en relation a todos los usos, y con respecto a cinco grupos amplios de usos. Se descubrió que lasfamilias leńosas mas útiles son las palmeras, Annonaceas, y Lauraceas. En término promedio, las 20 familias mas grandes de plantas leñosas tienen prioridad como materiales de constructión de subsistencia, seguidas en orden descendiente por sus usos comerciales, comestibles, tecnológicos, y medicinales.
Chapter
A quick dip into the literature on diversity reveals a bewildering range of indices. Each of these indices seeks to characterize the diversity of a sample or community by a single number. To add yet more confusion an index may be known by more than one name and written in a variety of notations using a range of log bases. This diversity of diversity indices has arisen because, for a number of years, it was standard practice for an author to review existing indices, denounce them as useless, and promptly invent a new index. Southwood (1978) notes an interesting parallel in the proliferation of new designs of light traps and new permutations of diversity measures.
Article
Tree vegetation and size structure was sampled in a miombo woodland area in E Tanzania and related to environmental factors, particularly soil and disturbance history. A total of 86 tree species was found. Four plant communities were distinguished through multivariate classification. Community 1 was dominated by Brachystegia boehmii, Brachystegia bussei and Julbernardia globiflora, and community 2 by B. boehmii and Brachystegia spiciformis. Community 1 was found on grey, eroded soil and community 2 on red, residual soil, a fact that opens up possibilities to use soil signals of satellite data for vegetation mapping. Community 3 is heavily disturbed miombo woodland near villages and community 4 was found on more clayey soil where miombo woodland is not expected.At our 42 sampled sites, density ranged from 74 to 1041 individualsha−1 and basal area from 3.9 to 16.7m2ha−1. Regeneration is generally good but large sized trees are less prominent in communities 3 and 4 due to harvesting. With reduced disturbance miombo species may rapidly resume dominance in community 3. A higher than expected representation by the size class 30–40 (−50)cmdbh in community 2 is probably related to disturbance history. Prevalence of certain species (Pseudolachnostylis maprouneifolia, Pterocarpus angolensis and Diplorhynchos condylocarpon) may be related to frequent fires. Selective logging will soon cause extinction of Dalbergia melanoxylon, whereas Pterocarpus angolensis still has good regeneration, possibly because individuals below logging size have a good seed set.A way to get an easy overview of size classes in all species in an area using PCA is discussed.
Article
Temporal and spatial changes in land use, vegetation cover, deforestation and reforestation in the Zambian Copperbelt were studied using a combination of aerial photograph analysis, literature review and inquiries among relevant government institutions. The study showed that between 1937 and 1984 loss of natural woodlands in the Copperbelt of Zambia (total area of Copperbelt: 9,615 km2) amounted to 41 per cent woodland area (8,419 km2). The major causes of this deforestation are woodfuel collection (for firewood and charcoal), cultivation and replacement of natural woodland with forest plantations. These accounted for 38 per cent, 37 per cent and 15 per cent of the total deforestation, respectively. Before 1962 the copper mining industry used large quantities of firewood to generate electricity and this resulted in the loss of 150,413 ha of woodland between 1937 and 1961. When the mining industry switched to hydroelectricity, urban households became the major users of woodfuel. The urban population in the Copperbelt increased from 0.412 million in 1960 to 1.400 million in 1984 and its consumption of woodfuel led to the deforestation of at least 89,436 ha between 1962 and 1984. Deforested areas are left to regenerate naturally. However, due to poor management about 34 per cent of the area deforested before 1962 has failed to regenerate. Although 50,200 ha have been reforested with exotic trees, only 5,020 ha of this is on land previously deforested. Thus only about 10 per cent of reforestation efforts have contributed to the rehabilitation of damaged land. Ninety per cent of the reforestation has actually replaced standing indigenous woodland. Uncontrolled bushfires have destroyed forest plantations and have also caused the failure of woodland regeneration in deforested areas. These observations indicate that if forest resources in the Copperbelt of Zambia are to be properly managed it will be necessary:
Article
Ectomycorrhizae were found in root samples of the treesAfzelia quanzensis Welw. andBrachystegia spiciformis Benth. (Caesalpiniaceae), collected in the coastal miombo type woodland 50 km west of Dar-es-Salaam, Tanzania. Root nodules with a structure resembling that of nitrogen-fixing root nodules of other leguminous plants were observed in theA. quanzensis material. The climate of the locality is rather dry, and strongly seasonal. In the tropics, ectomycorrhizae have previously been found only in humid or rain forest climate zones.
Article
Ectomycorrhizae were found in root samples of the trees Afzelia quazensis Welw. & the Brachystegia spiciformis Benth.(Caesalpiniaceae), collected in the coastal miombo type woodland 50km west of dar-es-Salaam, Tanzania. Root nodules with a structure resembling that of nitrogen-fixing root odules of other leguminous plants were observed in the A.quazensis material. The climate of the area is rather dry, & strongly seasonal. In the tropics, ectomycorrhizae have been previously only found in humid or rain forest climate zones