Termites (Blattodea Latreille 1810, Termitoidae Latreille 1802) of Abuko Nature Reserve, Nyambai Forest Park and Tanji Bird Reserve (The Gambia)

From 28 October to 5 November 2013, a termite study was undertaken in 3 protected sites in The Gambia (West Africa). The aim of the study is to investigate the diversity of termites in three protected areas in the western region of the country. Termite sampling is carried out in 100 m × 2 m transects that are replicated three (3) times in each site. A total of thirty-one (31) termite species, that belong to fungus growing (11), harvester (1), humuvorous (12) and xylophagous (7), were recorded. The following nineteen (19) species are new to The Gambia: Coptotermes intermedius, Astalotermes near quietus, Ancistrotermes cavithorax, Macrotermes bellicosus, Microtermes grassei, M. lepidus, M. subhyalinus, Odontotermes erraticus, O. pauperans, O. sudanensis, Basidentitermes sp., Euchilotermes tensus arcuata, Noditermes cristifrons, Amitermes evuncifer, Amitermes spinifer, Microcerotermes fuscotibialis, Microcerotermes near parvulus, Microcerotermes near solidus and Promirotermes holmgreni. Additional description and/or ecological information on Odontotermes erraticus, Cubitermes severus, Cubitermes n. proximatus, Euchilotermes tensus arcuata, Basidentitermes sp., and Noditermes cristifrons are given.


Introduction
The termite fauna of The Gambia is still poorly known. One single termite collection trial carried out by Sands in 1966 in the country has been documented [1].
Prior to this date, only one termite species, Odontotermes capensis, referred to as Termes fatalis, was wrongly reported to The Gambia by Walker in 1845 [2]. The occurrence of T. fatalis in both South Africa and The Gambia is objected to by Sjöstedt [3]. The African species referred to as O. capensis is restricted to South Africa and does not occur in The Gambia [4].
In this study, the objective is to investigate the diversity of termite species and functional groups in the three protected areas of The Gambia, namely Abuko Nature Reserve, Nyambai Forest Park, and Tanji Bird Reserve.

Study Sites
The Gambia is a small country in West Africa enclosed by the Senegalese territory except on its Atlantic coast (Figure 1). The climate is characterized by a short rainy season from July to September and a dry season during the rest of the year. From the coast to the inland, the rainfall (900-1300 mm) declines and temperatures increase. In the dry season, the inland regions have an average temperature as high as 35 °C, whilst the average temperature in the coastal regions ranges between 25 °C and 28 °C. In the wet season, the average temperature can be below 25 °C at the coast and up to 30 °C in the inland.
The Termites were sampled from the Abuko Nature Reserve, Tanji Bird Reserve and the Nyambai Forest Park, which are protected areas in the coastal region ( Figure 1).

Abuko Nature Reserve
The Abuko Nature Reserve is located outside the village of Lamin (13°23′00.45″ N, 16°38′37.9″ W) in the Kombo North District, about 25 km away from Banjul. It has been protected as a water catchment area since 1916 and was officially declared a nature reserve in 1968. With a current size of 106 ha, Abuko Nature Reserve is home to a wide diversity of mammals, birds and invertebrates.
Rectangular in shape, the reserve is surrounded by a 300 m wide buffer zone and it is centered on the Lamin village stream which surfaces within the lower half of the reserve, thereby providing a fairly humid microclimate in the heart of the area. The transect locations are shown in Figure 2.
For most of the year, the central part of the reserve is very humid due to the presence of a dense gallery forest, which surrounds a chain of three (3) pools. Soils are sandy in the periphery of the reserve and sandy/muddy towards the center where the tree canopy forms a continuous shade over the lower vegetation particularly during the wet season. The Termites were sampled from the Abuko Nature Reserve, Tanji Bird Reserve and the Nyambai Forest Park, which are protected areas in the coastal region ( Figure 1).

Abuko Nature Reserve
The Abuko Nature Reserve is located outside the village of Lamin (13 • 23 00.45 N, 16 • 38 37.9 W) in the Kombo North District, about 25 km away from Banjul. It has been protected as a water catchment area since 1916 and was officially declared a nature reserve in 1968. With a current size of 106 ha, Abuko Nature Reserve is home to a wide diversity of mammals, birds and invertebrates.
Rectangular in shape, the reserve is surrounded by a 300 m wide buffer zone and it is centered on the Lamin village stream which surfaces within the lower half of the reserve, thereby providing a fairly humid microclimate in the heart of the area. The transect locations are shown in Figure 2.
For most of the year, the central part of the reserve is very humid due to the presence of a dense gallery forest, which surrounds a chain of three (3) pools. Soils are sandy in the periphery of the reserve and sandy/muddy towards the center where the tree canopy forms a continuous shade over the lower vegetation particularly during the wet season.  Abuko Nature Reserve is among the least disturbed sites of The Gambia where numerous animal species as well plant species continue to be under strong conservation measures.

Tanji Bird Reserve
The Tanji River Bird Reserve is located along the Atlantic Coast in the Western Division, Kombo North. It is a few kilometers away from the fishing village of Ghana town (13°23′06.67″ N, 16°46′05.04′' W). The reserve was established in 1993 and covers a surface area of 612 ha (6.12 km 2 ). The three transect locations are shown in Figure 3. It encompasses the Tanji River and estuary and includes a mangrove ecosystem, coastal dune scrub woodland, and dry woodland savannah. The climate is greatly influenced by the ocean wind.
The northern strip is denser and has a lower canopy height due to previous clearance (transect 1 and transect 2). The southern strip is more open with isolated mature trees as a result of long-term grazing patterns (transect 3). The dominant plant species found are the Ginger Bread Plum, Parinari macrophylla, the Rhun Palm, Borassus aethiopium, and the Baobab, Adansonia digitata. The understorey is generally grass-dominated by the feathery flowered, Perotis indica, the stiff leafed Sporobolus spicatus and the spiny fruited Cenchrus biflorus. A variety of invertebrates populates the reserve, with arthropods being the most abundant. Abuko Nature Reserve is among the least disturbed sites of The Gambia where numerous animal species as well plant species continue to be under strong conservation measures.

Tanji Bird Reserve
The Tanji River Bird Reserve is located along the Atlantic Coast in the Western Division, Kombo North. It is a few kilometers away from the fishing village of Ghana town (13 • 23 06.67 N, 16 • 46 05.04 W). The reserve was established in 1993 and covers a surface area of 612 ha (6.12 km 2 ). The three transect locations are shown in Figure 3.  Abuko Nature Reserve is among the least disturbed sites of The Gambia where numerous animal species as well plant species continue to be under strong conservation measures.

Tanji Bird Reserve
The Tanji River Bird Reserve is located along the Atlantic Coast in the Western Division, Kombo North. It is a few kilometers away from the fishing village of Ghana town (13°23′06.67″ N, 16°46′05.04′' W). The reserve was established in 1993 and covers a surface area of 612 ha (6.12 km 2 ). The three transect locations are shown in Figure 3. It encompasses the Tanji River and estuary and includes a mangrove ecosystem, coastal dune scrub woodland, and dry woodland savannah. The climate is greatly influenced by the ocean wind.
The northern strip is denser and has a lower canopy height due to previous clearance (transect 1 and transect 2). The southern strip is more open with isolated mature trees as a result of long-term grazing patterns (transect 3). The dominant plant species found are the Ginger Bread Plum, Parinari macrophylla, the Rhun Palm, Borassus aethiopium, and the Baobab, Adansonia digitata. The understorey is generally grass-dominated by the feathery flowered, Perotis indica, the stiff leafed Sporobolus spicatus and the spiny fruited Cenchrus biflorus. A variety of invertebrates populates the reserve, with arthropods being the most abundant. It encompasses the Tanji River and estuary and includes a mangrove ecosystem, coastal dune scrub woodland, and dry woodland savannah. The climate is greatly influenced by the ocean wind.
The northern strip is denser and has a lower canopy height due to previous clearance (transect 1 and transect 2). The southern strip is more open with isolated mature trees as a result of long-term grazing patterns (transect 3). The dominant plant species found are the Ginger Bread Plum, Parinari macrophylla, the Rhun Palm, Borassus aethiopium, and the Baobab, Adansonia digitata. The understorey is generally grass-dominated by the feathery flowered, Perotis indica, the stiff leafed Sporobolus spicatus and the spiny fruited Cenchrus biflorus. A variety of invertebrates populates the reserve, with arthropods being the most abundant.

The Nyambai Forest
The Nyambai Forest Park is an artificial forest established in 1964. The park was enriched with the Gmelina arborea and Phyllostachys edullus species. It is located at midway between Farato village and Brikama (13 •

The Nyambai Forest
The Nyambai Forest Park is an artificial forest established in 1964. The park was enriched with the Gmelina arborea and Phyllostachys edullus species. It is located at midway between Farato village and Brikama (13°16′29.26″ N, 16°38′27.31″ W) about 35 km from Banjul. The transect locations are shown in Figure 4. The vegetation of the forest park is essentially composed of three different species: a spiny shrub vegetation, a tall but thin Gmelina arborea canopy, and a narrow strip of Phyllostachys sp. on the northern side.
The soil is completely covered with a thick layer of litter; a few thriving kinds of grasses grow here and there on the finely sandy to muddy soil. The relative humidity is high in the morning and late in the evening. Monthly average of temperatures range between 17-24 °C for the minima and 31-33 °C for the maxima.

Sampling Methods
To standardize sampling effort in the tropical forest areas, Jones & Eggleton [10] developed a protocol based on a 10 m × 2 m transect divided into 20 contiguous sections of 5 m × 2 m. Two experienced people sampled each section for 30 min.
In the studied sites, the sampling method, a derivative of the Jones & Eggleton sampling method, was carried out using a transect (3 transects/site) of 100 m long and 2 m wide. The transect is not subdivided into sections. The duration of the sampling is not limited but depends on the time required to cover the entire transect. In each transect, the termites are sampled by 3 experienced collectors searching for termites in the soil, litter, dead wood, the stump of trees, beneath the bark of trees, and termite arboreal nests.
The distance between transects ranges from 350 to 700 m at Abuko, from 360 to 1150 m at the Nyambai Forest and from 60 to 325 m at Tanji.
The encountered termite soldiers, workers, swarming individuals, kings, and queens are collected and kept in ethanol 70% within labeled containers bearing the name of the site, the date, and the micro-habitat.
The voucher specimens are conserved in the entomological collection of IFAN (University of Cheikh Anta Diop University, Dakar, Senegal). The duplicates of the Cubitermes were given to Prof. G. Josens (Université Libre de Bruxelle, Brussels, Belgium) and those of the soldierless termites to Prof. Y. Roisin (Université Libre de Bruxelle, Brussels, Belgium). The vegetation of the forest park is essentially composed of three different species: a spiny shrub vegetation, a tall but thin Gmelina arborea canopy, and a narrow strip of Phyllostachys sp. on the northern side.
The soil is completely covered with a thick layer of litter; a few thriving kinds of grasses grow here and there on the finely sandy to muddy soil. The relative humidity is high in the morning and late in the evening. Monthly average of temperatures range between 17-24 • C for the minima and 31-33 • C for the maxima.

Sampling Methods
To standardize sampling effort in the tropical forest areas, Jones & Eggleton [10] developed a protocol based on a 10 m × 2 m transect divided into 20 contiguous sections of 5 m × 2 m. Two experienced people sampled each section for 30 min.
In the studied sites, the sampling method, a derivative of the Jones & Eggleton sampling method, was carried out using a transect (3 transects/site) of 100 m long and 2 m wide. The transect is not subdivided into sections. The duration of the sampling is not limited but depends on the time required to cover the entire transect. In each transect, the termites are sampled by 3 experienced collectors searching for termites in the soil, litter, dead wood, the stump of trees, beneath the bark of trees, and termite arboreal nests.
The distance between transects ranges from 350 to 700 m at Abuko, from 360 to 1150 m at the Nyambai Forest and from 60 to 325 m at Tanji.
The encountered termite soldiers, workers, swarming individuals, kings, and queens are collected and kept in ethanol 70% within labeled containers bearing the name of the site, the date, and the micro-habitat.
The voucher specimens are conserved in the entomological collection of IFAN (University of Cheikh Anta Diop University, Dakar, Senegal). The duplicates of the Cubitermes were given to Prof. G. Josens (Université Libre de Bruxelle, Brussels, Belgium) and those of the soldierless termites to Prof. Y. Roisin (Université Libre de Bruxelle, Brussels, Belgium).

Species Identification
Specimens were observed and photographed using a stereomicroscope (Leica M80) equipped with a camera (Leica IC80 HD) connected to a computer. Leica suite application (Las version 4.2.0) is used for image acquisition and mensuration.
Specimens are compared with reference specimens from the IFAN (Institut fondamental d'Afrique noire) collection identified by W. A. Sands. The reference works by Silvestri [11,12], Sjöstedt [3], Emerson [13], Grassé [14,15], Bouillon & Mathot [16] and Roy-Noël [17] are used. The works of Sands focusing more on Nasutitermitinae [18] and on the genus Amitermes [19] are also used. Identification of the soldierless species of Apicotermitinae has been made after sands [5,7] on the basis of the morphology of the digestive tube: mesenteron-proctodeum junction and dissected enteric valves are observed under the stereomicroscope. Cubitermes species identification is based on the combination of the morphological characters of soldiers [3,[11][12][13]17] and the shape of the cushions of workers' enteric valves [20]. Enteric valves are dissected and mounted between lamellas, then observed under steromicroscope. Cubitermes species identenfication has been confirmed by Professor G. Josens (ULB, Belgium) who is working on the revision of the genus.
Measurement procedure of head and mandible. The head width corresponding to the maximum width in the dorsal view. The head length is measured in the dorsal view from the occiput to the base of the labrum (soldier) or the anterior of the clypeus (worker).
The length of the left mandible is measured in the dorsal view, from the lateral most proximal visible point to the apical point.

Termite Diversity in the Three Sites
Thirty-one (31) termite species have been recorded in the three sites. They belong to the following two families, six subfamilies and nineteen genera ( Table 2).

New Termite Species Recorded in The Gambia
Among the 31 termite species recorded in Abuko Nature Reserve, Nyambai Forest Park and in Tanji Bird Reserve, 19 termite species are recorded newly from The Gambia.

Termite Diversity in Abuko Nature Reserve
At the Abuko Nature Reserve, 27 species of termites belonging to 2 families and 5 subfamilies were recorded (Table 3). The variable number of the collected species between transects suggests a certain heterogeneity of the termite distribution in the site.
In terms of functional diversity, there is a predominance of the humivorous termites with 11 species followed by the fungus-growing Macrotermitinae which are represented by 9 species. The xylophagous (6 species) and the haverster termites (1 species) are the least diverse. This type of termite assemblage in Abuko is characteristic of a forestry profile.

Termite Diversity in Nyambai Forest Park
The species richness of termites in Nyambai Forest Park is of 20 species (Table 4). At the functional level, there is still greater diversity of the humivorous termites represented with 12 species followed by the fungus-growing termite (8 species). The harvester termites and the xylophagous termites are represented each by 1 species.
The spatial distribution of the termite species is rather heterogeneous: 12 species are recorded in transect 1, 10 species in transect 2 and 16 species in transect 3. The species richness and spatial distribution heterogeneity in Nyambai Forest are less important than in Abuko and could be associated with the relatively low botanical diversity in this artificial site.

Termite Diversity in Tanji Bird Reserve
At the Tanji Bird Reserve, with 20 species, the species richness is less important than in the other two sites ( Table 5). The spatial distribution is also heterogeneous in this site as 15 species are recorded in transect 1, 12 species in transect 2 and 4 species in transect 3.
In terms of functional diversity, the fungus-growing termites (11 species) largely dominate the humivorous (5 species) and the xylophagous (1 species).

Additional Information on Some Species
Based on the frequent confusion and misidentification in the West African Odontotermes and Cubitermes, we give some descriptive information on Odontotermes erraticus, Cubitermes severus and Cubitermes near proximatus. Euchilotermes tensus arcuata, a subspecies described by Silvestri, should be elevated to the rank of species, taking into account the distinctive features used in the description of the species of the genus. Finally, some information is given on Basidentitermes sp. and Noditermes cristifrons.    Grassé, 1944 The head of the soldier ( Figure 5) is yellow-orange in color or dark-brown.  Grassé, 1944 The head of the soldier ( Figure 5) is yellow-orange in color or dark-brown. The antennae are with 16 antennal segments. The left mandible shows a marginal tooth. The two soldier head measurements are as follows: head length 1.61 mm and 1.64 mm, head width 1.27 mm and 1.28 mm, left mandible length 1.10 mm and 1.15 mm, hind tibia length 1.09 mm. A large worker has 17 antennal segments in their antennae whereas a small worker individual has 16 antennal segments. Head measurements are shown in Table 6 and Table 7.

Cubitermes severus Silvestri, 1914
This is a species characterized by the shape (Figure 6) and the size (Table 8) of its soldier. Table  9 shows the dimensions of workers. It is the largest size Cubitermes in the collection.  A large worker has 17 antennal segments in their antennae whereas a small worker individual has 16 antennal segments. Head measurements are shown in Tables 6 and 7. This is a species characterized by the shape (Figure 6) and the size (Table 8) of its soldier. Table 9 shows the dimensions of workers. It is the largest size Cubitermes in the collection.
Cubitermes severus has been collected both in nests without caps (Figure 7a) and in typical mushroom nests (Figure 7b). The column of the nest is much higher than that of Cubitermes near proximatus. This mound builder species occupies his nest alone or shares it with the inquilines Promirotermes holmgreni, Noditermes cristifrons and Pericapritermes urgens. www.mdpi.com/journal/insects Cubitermes severus has been collected both in nests without caps (Figure 7a) and in typical mushroom nests (Figure 7b). The column of the nest is much higher than that of Cubitermes near proximatus. This mound builder species occupies his nest alone or shares it with the inquilines Promirotermes holmgreni, Noditermes cristifrons and Pericapritermes urgens. The observation of the enteric valves of the workers of these Cubitermes shows their proximity to C. proximatus. However, based on the morphology, the color and the dimensions of the soldier's head, we divided them into two morphotypes.

Morphotype 1 of Cubitermes Near proximatus
This is a species recognizable by the shape and the ochraceus color of the head of its soldiers (Figure 8). Table 10 shows the dimensions of the soldier and Table 11 shows those of the worker.

15
Cubitermes severus has been collected both in nests without caps (Figure 7a) and in typical mushroom nests (Figure 7b). The column of the nest is much higher than that of Cubitermes near proximatus. This mound builder species occupies his nest alone or shares it with the inquilines Promirotermes holmgreni, Noditermes cristifrons and Pericapritermes urgens. The observation of the enteric valves of the workers of these Cubitermes shows their proximity to C. proximatus. However, based on the morphology, the color and the dimensions of the soldier's head, we divided them into two morphotypes. The observation of the enteric valves of the workers of these Cubitermes shows their proximity to C. proximatus. However, based on the morphology, the color and the dimensions of the soldier's head, we divided them into two morphotypes.

Morphotype 1 of Cubitermes Near proximatus
This is a species recognizable by the shape and the ochraceus color of the head of its soldiers (Figure 8). Table 10 shows the dimensions of the soldier and Table 11 shows those of the worker.

Morphotype 2 of Cubitermes Near proximatus
The soldier of morphotype 2 ( Figure 9) is clearly larger (Table 12). Morphologically, differences are noted on the lateral margin of the head, which is less convergent, and the mandibles that are less curved in C. proximatus. The indentations at the base of the mandibles (ventral view of Figure 8 and Figure 9) are also distinctive features between the two morphotypes.

Morphotype 2 of Cubitermes Near proximatus
The soldier of morphotype 2 ( Figure 9) is clearly larger (Table 12). Morphologically, differences are noted on the lateral margin of the head, which is less convergent, and the mandibles that are less curved in C. proximatus. The indentations at the base of the mandibles (ventral view of Figures 8 and 9) are also distinctive features between the two morphotypes.   The measurements of the morphotype 2 workers are shown in Table 13. The mushroom nests of morphotype 2 are small in size ( Figure 10). The column is often sufficiently developed to allow a clear distinction with the cap. The nests are occupied solely by the builder or shared with inquilines such as Allognathotermes hypogeus, Euchilotermes tensus arcuata, Microtermes grassei and/or Promirotermes holmgreni infera.   The measurements of the morphotype 2 workers are shown in Table 13. The mushroom nests of morphotype 2 are small in size ( Figure 10). The column is often sufficiently developed to allow a clear distinction with the cap. The nests are occupied solely by the builder or shared with inquilines such as Allognathotermes hypogeus, Euchilotermes tensus arcuata, Microtermes grassei and/or Promirotermes holmgreni infera.

Euchilotermes tensus arcuata Silvestri, 1914
The head of the Euchilotermes tensus arcuata soldier (Figure 11) is distinctly rectangular in shape and yellowish in color with light brown mandibles. The mandibles are strongly curved. The labrum is long and wide with two apical large and rounded lobes. The measurements of the soldiers are noted in Table 14 and those of the workers in Table 15. The mushroom nests of morphotype 2 are small in size ( Figure 10). The column is often sufficiently developed to allow a clear distinction with the cap. The nests are occupied solely by the builder or shared with inquilines such as Allognathotermes hypogeus, Euchilotermes tensus arcuata, Microtermes grassei and/or Promirotermes holmgreni infera.   The head of the Euchilotermes tensus arcuata soldier (Figure 11) is distinctly rectangular in shape and yellowish in color with light brown mandibles. The mandibles are strongly curved. The labrum is long and wide with two apical large and rounded lobes. The measurements of the soldiers are noted in Table 14 and those of the workers in Table 15.  The specimens so designated seem different from all known species of the genus. However, more specimens, particularly of soldiers, are needed before the description of a new species.
3.6.6. Noditermes cristifrons (Wasmann, 1911) The measurements of the soldiers of Noditermes cristifrons are recorded in Table 16.   The specimens so designated seem different from all known species of the genus. However, more specimens, particularly of soldiers, are needed before the description of a new species.
3.6.6. Noditermes cristifrons (Wasmann, 1911) The measurements of the soldiers of Noditermes cristifrons are recorded in Table 16. The nests of Noditermes cristifrons (Figure 12) are free standing or backed to a tree which affects, in this case, the shape. However, in both cases, the nest displays a scaly appearance. Noditermes cristifrons occupies its nest alone or shares it with Pericapritermes urgens.

Discussion
The compilation of the references on the termites of The Gambia gives 30 species for this country. The present study has extended the number of termite species recorded from The Gambia to forty-six (46). Among the thirty-one (31) species that have been newly collected, nineteen (19) species are new for The Gambia and one species among the set is probably new with this field in science.
In Benin, Attignon et al. [21], using the Jones et al. sampling protocol [10], recorded 17 termite species in semi-deciduous forests and 10 species in teak plantations. In a savannah in northern Togo, with the same sampling method, 19 termite species were identified [22].
The protection of sites in The Gambia would explain the greater diversity of their termite fauna. However, in Senegal, in the Kolda region [23] (bordering inner Gambia in the south-east), except for Apicotermitinae, two species of Basidentitermes, Euchilotermes tensus arcuata and Amitermes spinifer, all of the other species recorded in Abuko, Nyambai and Tanji are found.
Of the thirty-one (31) species recorded during this study, only morphotype 2 of Cubitermes sp. near proximatus and Euchilotermes arcuata are not known in Senegal. Morphotype 1 of Cubitermes sp. near proximatus recorded in Senegal [24,25] was identified as C. bilobatodes. Cubitermes severus occurs exists in Casamance, Senegal, but has been cited by misidentification as C. fungifaber [25].
Odontotermes erraticus, described from Niger by Grassé [17], was indeed supposed to be restricted to Niger [4]. Ndiaye [25] points out for the first time its occurrence in Senegal. As one of the newly added species to Gambia's termite, its presence is seemingly throughout West Africa. O. erraticus would be widespread in the Sudano-Sahelian zones of West Africa. Its presence was probably hidden by numerous misidentifications, particularly confusions with the species O. vulgaris and O. latericius of southern Africa. As Ruelle [26] pointed out, the genus Odontotermes is the most complex of the Macrotermitinae.

Discussion
The compilation of the references on the termites of The Gambia gives 30 species for this country. The present study has extended the number of termite species recorded from The Gambia to forty-six (46). Among the thirty-one (31) species that have been newly collected, nineteen (19) species are new for The Gambia and one species among the set is probably new with this field in science.
In Benin, Attignon et al. [21], using the Jones et al. sampling protocol [10], recorded 17 termite species in semi-deciduous forests and 10 species in teak plantations. In a savannah in northern Togo, with the same sampling method, 19 termite species were identified [22].
The protection of sites in The Gambia would explain the greater diversity of their termite fauna. However, in Senegal, in the Kolda region [23] (bordering inner Gambia in the south-east), except for Apicotermitinae, two species of Basidentitermes, Euchilotermes tensus arcuata and Amitermes spinifer, all of the other species recorded in Abuko, Nyambai and Tanji are found.
Of the thirty-one (31) species recorded during this study, only morphotype 2 of Cubitermes sp. near proximatus and Euchilotermes arcuata are not known in Senegal. Morphotype 1 of Cubitermes sp. near proximatus recorded in Senegal [24,25] was identified as C. bilobatodes. Cubitermes severus occurs exists in Casamance, Senegal, but has been cited by misidentification as C. fungifaber [25].
Odontotermes erraticus, described from Niger by Grassé [17], was indeed supposed to be restricted to Niger [4]. Ndiaye [25] points out for the first time its occurrence in Senegal. As one of the newly added species to Gambia's termite, its presence is seemingly throughout West Africa. O. erraticus would be widespread in the Sudano-Sahelian zones of West Africa. Its presence was probably hidden