3urn:lsid:arphahub.com:pub:F7FCE910-8E78-573F-9C77-7788555F8AADPhytoKeysPK1314-20111314-2003Pensoft Publishers10.3897/phytokeys.159.5434154341Research ArticleCampanulaceaeBiodiversity & ConservationEast AfricaDistribution pattern and habitat preference for Lobelia species (Campanulaceae) in five countries of East AfricaMuchukuJohn K.123GichiraAndrew W.13ZhaoShu-Ying4ChenJin-Ming13ChenLing-Yunlychen83@qq.comhttps://orcid.org/0000-0003-3159-683115WangQing-Feng13Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, ChinaWuhan Botanical Garden, Chinese Academy of SciencesWuhanChinaDepartment of Botany, Jomo Kenyatta University of Agriculture and Technology, Nairobi 62000-00200, KenyaJomo Kenyatta University of Agriculture and TechnologyNairobiKenyaSino-Africa Joint Research Center, Chinese Academy of Sciences, Wuhan 430074, ChinaSino-Africa Joint Research Center, Chinese Academy of SciencesWuhanChinaSchool of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, ChinaSouth-Central University for NationalitiesWuhanChinaDepartment of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, ChinaChina Pharmaceutical UniversityNanjingChina
2020040920201594560968A5AE8-22F5-5424-A7A7-8B71D563FC2E40256032705202010082020John K. Muchuku, Andrew W. Gichira, Shu-Ying Zhao, Jin-Ming Chen, Ling-Yun Chen, Qing-Feng WangThis is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
East Africa is one of the centres of distribution and diversity for Lobelia L. (Campanulaceae, sub-family Lobelioideae). Lobelia habitats in East Africa have been facing habitat fragmentation and loss, which are recognised as a major threat to biodiversity. However, previous plant conservation studies in East Africa only focused on protected areas and ignored unprotected areas. Future conservation strategies of plants, such as Lobelia, will depend on knowledge of their distribution patterns and habitat preference in East Africa. To understand the distribution pattern and the habitat preference of Lobelia in five countries (Kenya, Uganda, Tanzania, Rwanda and Burundi) of East Africa, we conducted a literature review in the seven major vegetation regions (afro-alpine, afro-montane forest, drier savannah, grasslands, wetter savannah, Zambezian woodland and semi-desert and desert). We also employed meander and patterned searches, which allowed greater opportunities for recording Lobelia species. Our results showed that the genus is distributed in all of the seven regions of the five countries with 54 taxa. The afro-montane forest region, with 41 taxa, is the richest in species diversity, followed by the Zambezian woodland region with 18 taxa. The semi-desert and desert region has the lowest number with only four taxa. The afro-alpine region has 15 taxa, although the region is the smallest by area. The herbaceous type was found in all regions, while the giant type has a clear preference for the afro-alpine and afro-montane forest regions. Future conservation for Lobelia should consider its habitat preference by, for example, focusing on the afro-alpine and afro-montane forest regions. This study will facilitate the setting of future conservation strategies for Lobelia.
East AfricaFlora of Tropical East Africahabitat preferencesLobeliavegetation regionCitation
Muchuku JK, Gichira AW, Zhao S-Y, Chen J-M, Chen L-Y, Wang Q-F (2020) Distribution pattern and habitat preference for Lobelia species (Campanulaceae) in five countries of East Africa. PhytoKeys 159: 45–60. https://doi.org/10.3897/phytokeys.159.54341
Introduction
Understanding species richness, habitat preferences and geographical distribution patterns is imperative in formulating conservation strategies. Assessment of species habitat and distribution patterns dates back to the late 18th century (Forster et al. 1778). Johann Reinhold Forster, a naturalist, observed that there were species diversity and distribution gradients from the Equator to the Pole (Forster et al. 1778). Later, in 1805, Alexander von Humboldt (Humboldt 2005) suggested that there may be drivers that influenced the localisation, distribution and migration of plant species on Earth. Plants may demonstrate habitat preferences due to lower survival rates outside their preferred habitats (Comita et al. 2007). Consequently, plants are not uniformly distributed in a region (Brown 2014).
East Africa (EA) includes Kenya, Uganda, Tanzania, Rwanda, Burundi, Ethiopia, Somalia and South Sudan (Kalisa et al. 2019) and is a crucial biodiversity hotspot that is characterised by elevated plateaus and isolated mountains (Wang et al. 2020). The biomes in these EA countries were divided into altitudinal zones (Hedberg 1970), which have individual species microhabitats. The biomes were also divided into different regions including afro-alpine, afro-montane forest, drier savannah, grasslands, wetter savannah, zambezian woodland and semi-desert and desert regions (Kiage and Liu 2006). The distribution pattern for the EA species mainly depended on several factors, including geological events, elevation, edaphic factors (Stuart et al. 1990; Herron 2006), distance from the Equator, presence or absence of gene flow barriers, recent quaternary epoch, habitat preferences and anthropogenic activities (Hedberg 1954; Abdi 2013). For example, Arabisalpina L. (Brassicaceae) and Turritisglabra L. (Brassicaceae) have different habitat preferences. Arabisalpina has a preference for stream-banks and cliffs in an altitude of 2800–4800 m, while T.glabra has a preference for grasslands in an altitude of 920–2650 m (Agnew and Agnew 1994).
Lobelia L. (Campanulaceae, sub-family Lobelioideae) includes about 437 species. The genus is cosmopolitan, distributed in both temperate and tropical regions of Africa, America, Australia, New Zealand, Hawaii, Asia and other regions (Ruas et al. 2001; Lammers 2011; Antonelli 2008; Kokubugata et al. 2012). Africa is a species diversity centre for Lobelia species (lobelias), with 37% of all lobelias distributed in Africa (Kokubugata et al. 2012). Lobelia is well represented in EA, particularly in the early administrative divisions of Kenya (K1–7), Tanzania (T1–8), Uganda (U1–4), Rwanda and Burundi (Thulin 1984), where it inhabits most of the mountains and surrounding lowlands. The giant lobelias that are native to the higher altitude zones of the mountain groups in the EA form a conspicuous element of the flora.
Habitat loss and fragmentation are the major causes of biodiversity loss worldwide (Sukumaran and Jeeva 2008; Laurance 2010). Lobelia habitats in East Africa have been facing habitat fragmentation and loss (Kebede et al. 2007). Future conservation strategies of Lobelia in EA will depend on knowledge of their distribution patterns, habitat threats and habitat preferences. However, plant conservation studies in the EA only focused on protected areas and ignored unprotected areas (Eilu et al. 2007).
The distribution pattern of lobelias across different vegetations in the EA and the habitat preference remain unknown. As far as we know, lobelias are non-uniformly distributed in EA (Knox 1993; Kebede et al. 2007). For example, Lobeliatelekii Schweinf. was only found on three mountains, Mt. Elgon, Aberdare Ranges and Mt. Kenya. Lobeliadeckeniisubsp.burtii (E.A.Bruce) Mabb., Lobeliaburtiisubsp.telmaticola E.B.Knox and Lobeliaburtiisubsp.meruensis E.B.Knox were only found in areas within the T2 region, specifically on Mt. Meru, Mt. Hanang and Mt. Loolmalassin in Tanzania (Thulin 1984). Lobeliaaberdarica R.E.Fr. & T.C.E.Fr. inhabits the Cherangani Hills, Mau Ranges, Aberdare Ranges, Mt Elgon and Mt. Kenya. The upland afro-montane forest species Lobeliagiberroa Hemsl. is widely spread within an altitude of 1200–3000 m in ten African countries including Kenya, Uganda, Tanzania, Sudan, Ethiopia, DR Congo, Rwanda, Burundi, Malawi and Zambia. The growth forms in this genus include annual or perennial herbs, shrubs or sub-shrub rosettes and small trees (Thulin 1984; Ruas et al. 2001). Amongst these growth forms, the most conspicuous are the branched inflorescence vs. unbranched inflorescence forms and giant vs. herbaceous forms (Fig. 1). Several studies have investigated the adaptation to afro-alpine environments, systematics and biogeography of lobelias (Knox and Palmer 1998; Kebede et al. 2007; Chen et al. 2016). For example, phylogeographic analyses indicated that L.giberroa could have migrated throughout different afro-mountains via the afro-montane forest bridge in previous interglacial periods (Kebede et al. 2007).
In this study, we reviewed previous literature and extracted data from our field survey. We aimed to identify the distribution pattern and habitat preference of Lobelia in five countries in the EA region (Fig. 1). This knowledge will facilitate the setting of future conservation strategies of the genus in EA.
Materials and methodsStudy area
This study covered five of the eight East African countries, i.e. within and amongst the early administrative divisions of Kenya (K1–7), Uganda (U1–4), Tanzania (T1–8), Rwanda and Burundi. The other three countries (Ethiopia, Somalia and South Sudan) in EA have limited data from both herbaria and the Flora of Tropical East Africa (FTEA) on the distribution of the lobelias. Therefore, they were not included in this study. The study area ranged from coastal regions to the alpine zones of high mountains with changes in the elevation gradient. To obtain a clear understanding of the Lobelia habitats and distribution patterns, seven vegetation regions (afro-alpine, afro-montane forest, drier savannah, grasslands, wetter savannah, Zambezian woodland and semi-desert and desert) were used (Fig. 1; Kiage and Liu 2006). The vegetation regions in Rwanda and Burundi were not shown in the map of Fig. 1 (Kiage and Liu 2006). However, we recorded the distribution pattern of lobelias in the two countries by checking specimens and literature. Each lobelia in the two countries was assigned to the vegetation region, which is similar to the species’ habitat(s).
The major vegetation regions in East Africa, modified from Kiage and Liu (2006). Two pictures were used as examples of giant lobelias and herbaceous lobelias. The left picture is the giant Lobeliadeckenii Hemsl. from Mt Kenya, while the right picture is the herbaceous Lobelialindblomii Mildbr. from Mt Elgon (pictures by Ling-Yun Chen).
https://binary.pensoft.net/fig/449502Methods
All lobelias described in the Flora of Tropical East Africa (Thulin 1984), Knox and Pócs (1992) and Knox and Palmer (1998) were included in this study. The distribution and habitat for each species were explored using data from previous studies (Mabberley 1975; Thulin 1984; Knox and Pócs 1992; Agnew and Agnew 1994; Beentje et al. 1994; Knox and Palmer 1998; Knox et al. 2004; Zhou et al. 2017; Zhou et al. 2018), voucher specimens in the East African Herbarium of the National Museum of Kenya (NMK) and voucher specimens in the herbarium of Wuhan Botanical Garden (HIB) that had been collected from 2009 to 2019.
To maximise recording lobelias in traversed habitats, meander and patterned searches (Lancaster 2000) were used. The meander search was employed on difficult terrains, such as in mountains, deep river valleys and rocky hills. On the other hand, the systematic transect was employed on flat grounds, such as grassland and shrub-lands. Lobelias were identified to species or subspecies level.
Results
The lobelias in the seven regions of the five countries are represented by 54 taxa including herbs, shrubs and sub-shrubs (Table 1).
Lobelias diversity and distribution in Kenya, Uganda, Tanzania, Rwanda and Burundi of East Africa.
A-ar = Afro-alpine region, Amfr = Afro-montane forest region, Dsr = Drier savannah region, Gr = Grassland region, Wsr = Wetter savannah region, Zwr = Zambezian woodland region and S-ddr = Semi-desert and desert region.
FTEA =
Flora of Tropical East Africa, SR = Sight record, HS = Herbarium specimen, LR = Literature review; only if a species were not described in
FTEA, literature was used to check the habitat and distribution.
(1) Afro-alpine region. In this study, the afro-alpine region includes the sub-alpine ericaceous zone and the afro-alpine zone. The sub-alpine ericaceous zone ranges from about 3000 m to 3800 m (Wesche et al. 2000) and is dominated by Helichrysum Mill., Hypericum L. and Erica Boehm. The afro-alpine region extends to over 4900 m and is dominated by giant species of Dendrosenecio (Hauman ex Hedberg) B.Nord. and Lobelia. The giant lobelias include Lobeliastuhlmannii Schweinf. & E.A.Bruce, Lobeliadeckenii Hemsl., Lobeliagregoriana Baker f., Lobeliagregorianasubsp.satimae (R.E.Fr. & T.C.E.Fr.) E.B.Knox, Lobeliaburtii E.A.Bruce, L.burtiisubsp.telmaticola E.B.Knox, L.burtiisubsp.meruensis E.B.Knox, Lobeliabequaertii (De Wild.) Mabb., Lobeliawollastonii Baker f. and L.telekii. These species are mainly distributed in the upper alpine zone (Tables 1, 2). Besides these, a few herbaceous species, including Lobeliaminutula Engl., Lobeliacheranganiensis Thulin, Lobeliaholstii Engl. and Lobelialindblomii Mildbr. (Table 1; Thulin 1984), inhabit altitudes above 3000 m. Amongst the herbaceous species, L.lindblomii grows at the highest elevation (3000–4300 m), particularly in the upland grassland and moorland on Mt. Elgon (Kenya/Uganda), Aberdare Ranges and Mt. Kenya. Recurring fires on the ericaceous belt created a buffer zone between the lower afro-alpine and the upper afro-montane forest regions. This buffer zone was observed to provide regeneration habitats for the herbaceous species L.minutula, L.lindblomii and L.holstii (see Suppl. material 1: Table S1 for species details).
Summary for the distribution of lobelias in the seven vegetation regions.
Vegetation region
Altitude (m)
Number of taxa
Number of giant taxa
Number of herbaceous taxa
Afro-alpine
3000–4900
15
11
4
Afro-montane forest
0–3000
41
13
28
Lowland montane forest
0–1500
12
3
9
Upland montane forest
1500–3000
29
10
19
Drier savannah
10–1000
9
0
9
Grassland
1200–3000
9
0
9
Wetter savannah
0–1250
11
0
11
Zambezian woodland
700–1500
18
1
17
Semi-desert and desert
400–1500
4
0
4
(2) Afro-montane forest region. The afro-montane forest region currently occurs in anthropogenically-fragmented patches in East Africa and has an altitudinal range of 0–3000 m (Thulin 1984). The lowlands of the montane (< 1500 m) include deciduous trees and shrubs species, such as Celtisafricana Burm.f., Senegalia Raf. spps., Vachellia (wight & Arn.) Kuntze spps., Ilex L. spps., Haplocoelumfoliolosum (Hiern) Bullock and Ficus L. spp., amongst others. These lowlands were well inhabited by nine herbaceous lobelias, which include Lobeliaerinus L., Lobeliatrullifoliasubsp.minor Thulin, Lobeliawelwitschii Engl. & Diels ex Diels, Lobeliasapinii De Wild., Lobeliafervenssubsp.recurvata (E.Wimm.) Thulin, Lobeliachireensis A.Rich., Lobeliainconspicua A.Rich, Lobeliaadnexa E.Wimm. and Lobeliahartlaubi Buchenau. The giant lobelias distributed in this vegetation include Lobeliamorogoroensis E. B. Knox & Pócs, Lobelialongisepala Engl. and L.giberroa (Tables 1, 2) at altitudes ranging from 1200–1500 m (Thulin 1984). An interesting exception in this category is L.giberroa, which is widespread in Africa and has a distribution range that extends to about 3000 m (Table 1). This species inhabits a transition zone between the lowland and upland giant species. Interestingly, the lowland range of L.giberroa is found in understoreys of closed forest and riparian ecosystems, a similar habitat to its upland range. This provides insight into understanding the habitat preference of the species.
The highlands of the afro-montane forest region extend from 1500 m to 3000 m. These forests have recently been highly fragmented. They are similar in species composition across the East African countries. Dominant native species from other families found in this region include Oleaeuropaeasubsp.africana (Mill.) P.S. Green., Juniperusprocera Hockst ex Endl., Prunusafricana (Hook.) Kalkman., Oldeaniaalpina (K. Schum.) Stapleton and Hageniaabyssinica (Faber-Langendoen) J.F.Gmel. However, non-native species have become fully naturalised in disturbed areas for timber production. The species include Grevillearobusta A.Cunn. ex R.Br., Casuarinaequisetifolia L., Cupressuslusitanica Lindl. Ex Parl., Pinuspatula Schiede & Deppe ex Schltdl., Eucalyptusglobulus Labill., Eucalyptussaligna Sm., Corymbiacitriodora (Hook.) K.D.Hill & Johnson, Corymbiamaculata (Hook.) K.D.Hill & Johnson, Fraxinuspennsylvanica f.colorata B.Boivin, Araucariacunninghamii Sweet ex Courtois and Acrocarpusfraxinifolius Arn.
The afro-montane forest region above 1600 m is rich in lobelias. Most species at this altitude are herbaceous and include Lobeliagilgii Engl., Lobeliagraniticola E.Wimm., Lobeliatrullifolia Hemsl., Lobeliauliginosa E.Wimm., Lobeliadissecta M.B.Moss, Lobelianeumannii T.C.E.Fr., Lobeliaflaccidasubsp.granvikii (T.C.E.Fr.) Thulin, Lobeliamolleri Henriques., Lobeliarubescens De Wild., Lobeliaheyniana Spreng., L.minutula, Lobeliacymbalarioides Engl., Lobeliaduriprati T.C.E.Fr., L.holstii, Lobeliagoetzei Diels, Lobeliaovina E.Wimm., Lobeliabaumannii Engl., Lobeliafervens Thunb. and Lobeliaangolensis Engl. & Diels (Table 1).
The giant lobelias in this zone include Lobeliamildbraedii Engl., Lobeliasancta Thulin, Lobeliastricklandae Gilliland, Lobelialukwangulensis Engl., Lobeliaritabeaniana E.B.Knox, Lobeliadeckeniisubsp.incipiens E.B.Knox, Lobeliapetiolata Hauman, Lobeliaudzungwensis Thulin, L.aberdarica and L.bambuseti (Thulin 1984; see Suppl. materials 1: Table S2 for species details).
(3) Drier savannah region. The drier savannah region is found in Kenya, Ethiopia and Somalia, where Senegalia Raf. spp., Vachellia Wight & Arn. spp. and Commiphora Jacq. spp. dominate the area. The region ranges from 10 m to 1000 m (or up to 1500 m in some habitats; Thulin 1984). Herbaceous lobelias are found in muddy ditches, river or marshy edges and seasonally-flooding grasslands. These species include L.fervenssubsp.recurvata, L.goetzei, L.duriprati, L.inconspicua, L.flaccidasubsp.granvikii, L.trullifoliasubsp.minor, L.chireensis, L.holstii and L.welwitschii (Table 1). No giant lobelias were found in this region (see Suppl. material 1: Table S3 for species details).
(4) Grassland region. Grassland region is the most common habitat in the EA, and is dominated by alternating grasses with thorny bush-land and thicket. Although habitats in this region are different from others, some lobelias in this region are the same as in the areas of highland, wet and dry savannah and some even from the woodland. However, lobelias in this region are mostly restricted to the wet ground after rainfall (waterlogged grassland and seasonal river banks) and at the edges of wetlands in the marshy areas, streams and river banks, as well as tops of grass hills. The species include L.fervens, L.molleri, L.holstii, L.flaccidasubsp.granvikii, L.baumannii, L.goetzei, L.erinus and L.welwitschii (Table 1). No giant lobelias were found in this region (see Suppl. material 1: Table S4 for species details).
(5) Wetter savannah region. This region is widely distributed in Kenya, Tanzania and Uganda with altitudes from 0 m to 1250 m. Both Combretaceae R.Br., and Fabaceae Lindl. families dominate this region. Lobelias in this region include the herbaceous L.fervenssubsp.fervens, L.baumannii, L.goetzei, L.inconspicua, L.molleri, L.holstii, L.flaccidasubsp.granvikii, L.sapinii, L.chireensis, L.erinus and L.welwitschii (Table 1). No giant lobelias were found in this region (see Suppl. material 1: Table S5 for species details).
(6) Zambezian woodland region. This region occurs in the southern part of Tanzania at altitudes ranging from 700 m to 1500 m. It is dominated by members of the family Fabaceae, such as species of the genera Brachystegia Benth., Julbernardia Pellegr., Isoberlinia Craib & Stapf ex Holland and Uapaca Baill. Lobelia inhabits wet deciduous woodland habitats in this region. Herbaceous lobelias include L.fervenssubsp.fervens, L.chireensis, L.trullifoliasubsp.trullifolia, L.gilgii, L.sapinii, L.duriprati, L.goetzei, L.inconspicua, L.uliginosa, L.rubescens, Lobeliaheyneana Schult., L.adnexa, L.cymbalarioides, L.baumannii, L.erinus, L.angolensis and L.welwitschii (Table 1). The only giant lobelia is L.morogoroensis (Knox and Pócs 1992), which is distributed near Morogoro, Tanzania at altitudes from 725–1400 m and may extend up to 2000 m (see Suppl. material 1: Table S6 for species details).
(7) Semi-desert and desert region. The hostile climate of this region forms semi-desert and desert vegetations in northern Kenya and southern Ethiopia. This region is characterised by thorny scattered trees and shrubs. Lobelias are distributed in muddy ditches edges and seasonal river banks. However, they are exceedingly rare and only appear in the seasonally-flooded ground or marshy edges of the freshwater wetlands. Species that are distributed in this region include L.fervenssubsp.recurvata, L.trullifoliasubsp.minor, L.welwitschii and L.chireensis (Table 1) (see Suppl. material 1: Table S7 for species details).
DiscussionDistribution patterns for lobelias in five countries of East Africa
We employed a map (Fig. 1) with seven vegetation regions to cover the distribution of lobelias in Kenya, Uganda, Tanzania, Rwanda and Burundi (Kiage and Liu 2006). The seven regions are mainly dominated by stepped plateaus, flat land savannah, highlands, mountains and wetland ecosystems. The lobelias in the seven regions are represented by 47 species and seven subspecies including herbs, shrubs and sub-shrubs (Table 1). The most elevated habitat was inhabited by a giant species L.telekii on Mt. Kenya, while the lowest habitat was inhabited by herbaceous species, such as L.fervens and L.erinus. The altitudinal distribution of lobelias could have been shaped by their habitat preferences and by the adaptive evolution (Hedberg 1964; Chen et al. 2015). For example, L.telekii was confined to the afro-alpine belt characterised by an extreme climate with “summer every day and winter every night” (Hedberg 1964).
The EA Mountains form altitudinal island-like habitats. Most of these mountains, which are known as sky-islands, are of volcanic origin (Hedberg 1969) and lie within the Latitudes 2°N and 4°S. The mountain vegetation is completely different from that of the surrounding lowland. For example, the savannah and the highland forest are different from those of the upper alpine in both species richness and growth habits (Tables 1, 2). Amongst the five sub-floras of EA, Tanzania with 38 taxa is the richest in lobelias followed by Kenya (21), Uganda (19), Burundi (9) and Rwanda (8) (Suppl. material 1: Tables S8–S12).
East African Mountains are a centre of endemism for giant lobelias
The East African Mountains embrace a wide range of altitudinal habitats and ecosystems, from surrounding environs at the foot of the mountains to the alpine zone (Zhou et al. 2018). The diversity and richness of lobelias can thus seem to be dependent on existing diverse habitats. In general, the diversity of giant lobelias varies greatly within habitats. The diversity is higher in the afro-montane forest region (13 taxa, Table 2), followed by the afro-alpine region (11 taxa). The giant lobelias demonstrated a clear preference for afro-montane forest and afro-alpine regions. On the other hand, the number of herbaceous lobelias is higher in the afro-montane forest (28 taxa) and Zambezian woodland regions (17 taxa). The herbaceous type demonstrates a clear preference for a habitat characterised by trees in both afro-montane forest and Zambezian woodland regions.
East African Mountain biomes were differentiated into two major categories, the mountains that reach the alpine (upland) and those without the alpine regions (lowlands and Eastern Arc Mountains). The upland giant lobelias, except L.petiolata, normally have a single aerial stem that is unbranched. The branched L.petiolata inhabits Nyungwe in Rwanda and extends its range to Kahuzi in DR Congo in very wet afro-montane forest region. These species have a clear preference for a wet forest habitat (Knox and Palmer 1998).
The Eastern Arc Mountains (lowlands) form the easternmost blocks of East Africa (Burgess et al. 2007). Although they do not extend to the afro-alpine region, their location creates a Massenerbung effect, therefore generating variable and unique habitats (Knox and Palmer 1998). The lowland biomes form habitats characterised by the branched lobelias (Knox and Palmer 1998). These species include L.undzungwensis, L.morogoroensis, L.stricklandiae, L.ritabeaniana, L.sancta, L.lukwangulensis and L.longisepala. The Arc Mountains have evolved their distinctive lobelias, which are different from those of the upland mountains. The Arc Mountain biome, therefore, is a hotspot for the East Africa branched lobelias. The regions inhabited by lobelias have moist and warm habitats somewhat differentiated from the regions occupied by the inland giant lobelias. The Arc Mountain giant lobelias demonstrated a clear preference for moist and warm conditions within the mountains along the East Africa Coast, which is known as one of the world’s biodiversity hotspots (Stuart et al. 1990).
The Eastern Arc Mountains are separated from each other by lowland woodlands and savannah (Conte 2010). The Arc Mountain lobelias are distributed from open sites in seasonally-dry, semi-deciduous woodland (L.morogoroensis) to the sub-montane rainforests openings (L.longisepala) and also extend further to the cloud-forest summits (L.ritabeaniana, L.stricklandiae, L.undzungwensis, L.sancta and L.lukwangulensis (Table 1; Knox and Palmer 1998). Surprisingly, L.giberroa, which is found in the inland afro-montane forest, also grows on these Arc Mountains. Lobeliagiberroa in the Arc Mountains occupies habitats with similar physiognomic characteristics and similar associated plant species found elsewhere in the highland afro-montane forests (Knox and Palmer 1998). The Eastern Arc and other East African mountains demonstrated an extraordinary pattern of lobelias’ endemism and community preferences.
Major identified threats to afro-mountain lobelias’ habitat and its lowlands environments
Land-use changes associated with deforestation and land degradation are major causes of biodiversity loss in East Africa (Maitima et al. 2009). Currently, the afro-montane forest is fragmented and remains isolated around the EA Mountains. Without the present anthropogenic activities, the afro-montane forest would probably have existed as a single connected habitat (Hedberg 1969). The habitat fragmentation threatens the distribution patterns of some native species, for example, L.giberroa (Kebede et al. 2007). Therefore, habitat loss and fragmentation could threaten the forest-dependent lobelias. For example, L.bambuseti has been reported as being under threat (Kipkoech et al. 2019).
Moreover, the afro-montane forest and its environment are also threatened by invasive plants (Obiri 2011; Hulme et al. 2013). Most of the mountains in the EA have become centres for ecotourism. To facilitate tourist activities, roads and paths within the mountain have been built. The invasive species could follow the roadsides to reach different altitudes (Pauchard et al. 2009). According to our observation, the disturbed roadsides created opportunities for disturbed habitat lobelias to dominate the roadsides. For example, L.holstii has expanded its range to almost 3900+ m on Mt. Kenya and dominated the roadsides in rocky disturbed places. Additionally, non-native tree species established in the forest plantation for timber production may pose a considerable threat (Pauchard et al. 2009) to native forest lobelias’ ecosystems.
Mountain forests are major water towers, biodiversity hotspots, species evolution refugia, eco-tourism locations, sources of wild foods and centres of plant genetics (Viviroli and Weingartner 2008; Moelg et al. 2013; Kanui et al. 2016; Immerzeel et al. 2020). For example, they serve as a source of clean water for the drier lowlands, which are inhabited by lobelias, as observed in our extensive field survey. The afro-montane forest also provides places of cultural practices, such as religion for the native communities. Although lobelias are widely distributed in the seven vegetation regions, habitat loss is a challenge that calls for action. For example, the increasing human population has threatened the EA Mountain biomes. The habitat preference of lobelias’ hotspots is also facing the risk of both anthropogenic and climate change (Chala et al. 2016). Habitat destruction and fragmentation are recognised as a major threat to biodiversity (Liao et al. 2013). Therefore, the afro-montane forest and its environs are especially in need of protection (Immerzeel et al. 2020).
Conclusions
Our results showed that lobelias are distributed in all of the seven vegetation regions in five countries of East Africa. The afro-montane forest region is the richest in species diversity, although it is not the largest by area. The herbaceous type has a preference for the lowland regions, while the giant type has a clear preference for the afro-alpine and afro-montane forest. Future conservation for the genus should consider the habitat preferences of lobelias.
Acknowledgements
We thank Edwin Kadiori, Josephat Mbogo, Elizabeth Kamande and Ceaser Gitari for fieldwork assistance. This work was supported by the National Natural Science Foundation of China (grant number 31670226) and the Sino-Africa Joint Research Center.
ReferencesAbdiAA (2013) Diversity and distribution of the afro-alpine flora of Eastern Africa with special reference to the taxonomy of the genus Pentaschistis (Poaceae). Thesis, Kenyatta University, Nairobi, Kenya.AgnewADQAgnewS (1994) Upland Kenya wild flowers-a flora of the ferns and herbaceous flowering plants of Upland Kenya. East Africa Natural History Society, Nairobi, Kenya.AntonelliA (2008) Higher level phylogeny and evolutionary trends in Campanulaceae subfam. Lobelioideae: Molecular signal overshadows morphology.46(1): 1–18. https://doi.org/10.1016/j.ympev.2007.06.015BeentjeHAdamsonJBhanderiD (1994) Kenya trees, shrubs, and lianas. National Museums of Kenya, Nairobi, Kenya.BrownJH (2014) Why are there so many species in the tropics? Journal of Biogeography 41(1): 8–22. https://doi.org/10.1111/jbi.12228BurgessNButynskiTCordeiroNDoggartNFjeldsaJHowellKKilahamaFLoaderSLovettJCMbilinyiBMenegonMMoyerDCNashandaEPerkinARoveroFStanleyWTStuartSN (2007) The biological importance of the Eastern Arc Mountains of Tanzania and Kenya.134(2): 209–231. https://doi.org/10.1016/j.biocon.2006.08.015ChalaDBrochmannCPsomasAEhrichDGizawAMasaoCABakkestuenVZimmermannNE (2016) Goodbye to tropical alpine plant giants under warmer climates? Loss of range and genetic diversity in Lobeliarhynchopetalum. Ecology and Evolution 6(24): 8931–8941. https://doi.org/10.1002/ece3.2603ChenLYMuchukuJKYanXHuGWWangQF (2015) Phylogeography of Haplocarpharueppelii (Asteraceae) suggests a potential geographic barrier for plant dispersal and gene flow in East Africa.60(13): 1184–1192. https://doi.org/10.1007/s11434-015-0832-xChenLYRennerSSWangQF (2016) East Asian Lobelioideae and ancient divergence of a giant rosette Lobelia in Himalayan Bhutan.65(2): 293–304. https://doi.org/10.12705/652.6ComitaLSConditRHubbellSP (2007) Developmental changes in habitat associations of tropical trees.95(3): 482–492. https://doi.org/10.1111/j.1365-2745.2007.01229.xConteCA (2010) Forest history in East Africa’s Eastern Arc Mountains: Biological science and the uses of history.60(4): 309–313. https://doi.org/10.1525/bio.2010.60.4.9EiluGOriekotJTushabeH (2007) Conservation of indigenous plants outside protected areas in Tororo District, eastern Uganda. African Journal of Ecology 45(s3): 73–78. https://doi.org/10.1111/j.1365-2028.2007.00861.xForsterJRThomasNGuestH (1778) Observations made during a voyage round the world. University of Hawaii Press.HedbergO (1954) A pollen-analytical reconnaissance in tropical East Africa.5(2): 137–166. https://doi.org/10.2307/3565157HedbergO (1964) Features of Afroalpine Plant Ecology. Acta Phytogeographica Suecica: 1–49.HedbergO (1969) Evolution and speciation in a tropical high mountain flora. Biological Journal of the Linnean Society.1(1–2): 135–148. https://doi.org/10.1111/j.1095-8312.1969.tb01816.xHedbergO (1970) Evolution of the afro-alpine flora.2(1): 16–23. https://doi.org/10.2307/2989783HerronM (2006) Phylogenetic studies in the genus Jamesbrittenia tribe Manuleae, family Scrophulariaceae. Master Thesis, University of Cape Town, Cape Town.HulmePEBurslemDFDawsonWEdwardERichardJTrevelyanR (2013) Aliens in the Arc: Are invasive trees a threat to the montane forests of East Africa? Plant invasions in protected areas. Springer, 145–165. https://doi.org/10.1007/978-94-007-7750-7_8HumboldtAv (2005) Alexander von Humboldt. In: Moreno Yánez, Segundo E (Eds) Diarios de viaje en la Audiencia de Quito, Translated by Borchardt de Moreno, Christiana OXY, Quito.ImmerzeelWWLutzAFAndradeMBahlABiemansHBolchTHydeSBrumbySDaviesBJElmoreACEmmerAFengMFernándezAHaritashyaUKargelJSKoppesMKraaijenbrinkPDAKulkarniAVMayewskiPANepalSPachecoPPainterTHPellicciottiFRajaramHRupperSSinisaloAShresthaABViviroliDWadaYXiaoCYaoTBaillieJEM (2020) Importance and vulnerability of the world’s water towers.577(7790): 364–369. https://doi.org/10.1038/s41586-019-1822-yKalisaWIgbawuaTHenchiriMAliSZhangSBaiYZhangJ (2019) Assessment of climate impact on vegetation dynamics over East Africa from 1982 to 2015. Scientific Reports 9(1): e16865. https://doi.org/10.1038/s41598-019-53150-0KanuiTKibwageJMurangiriM (2016) Water tower ecosystems services and diversification of livelihood activities to neighbouring communities; a case study of Chyulu Hills Water Tower in Kenya. Journal of Geography.6(4): 1–12. https://doi.org/10.9734/JGEESI/2016/26620KebedeMEhrichDTaberletPNemomissaSBrochmannC (2007) Phylogeography and conservation genetics of a giant lobelia (Lobeliagiberroa) in Ethiopian and Tropical East African mountains.16(6): 1233–1243. https://doi.org/10.1111/j.1365-294X.2007.03232.xKiageLMLiuK (2006) Late Quaternary paleoenvironmental changes in East Africa: A review of multiproxy evidence from palynology, lake sediments, and associated records.30(5): 633–658. https://doi.org/10.1177/0309133306071146KipkoechSMellyDKMwemaBWMwachalaGMusiliPMHuGWangQ (2019) Conservation priorities and distribution patterns of vascular plant species along environmental gradients in Aberdare Ranges Forest.131: 91–113. https://doi.org/10.3897/phytokeys.131.38124KnoxEB (1993) The species of giant senecio (Compositae) and giant lobelia (Lobeliaceae) in eastern Africa.19: 241–257.KnoxELukeQThulinM (2004) A new giant Lobelia from the Eastern Arc Mts, Tanzania.59(2): 189–194. https://doi.org/10.2307/4115849KnoxEBPalmerJD (1998) Chloroplast DNA evidence on the origin and radiation of the giant lobelias in eastern Africa.23(2): 109–149. https://doi.org/10.2307/2419583KnoxEPócsT (1992) Lobeliamorogoroensis: Another Tanzanian giant.47(3): 503–508. https://doi.org/10.2307/4110577KokubugataGNakamuraKForsterPIHirayamaYYokotaM (2012) Antitropical distribution of Lobelia species (Campanulaceae) between the Ryukyu Archipelago of Japan and Oceania as indicated by molecular data.60(5): 417–428. https://doi.org/10.1071/BT11316LammersTG (2011) Revision of the infrageneric classification of Lobelia L. (Campanulaceae: Lobelioideae).98(1): 37–62. https://doi.org/10.3417/2007150LancasterJ (2000) ANPC guidelines for rare plant surveys in Alberta. Alberta Native Plant Council. Edmonton, AB. http://www.anpc.ab.ca/assets/rareplant.pdfLauranceWF (2010) Habitat destruction: death by a thousand cuts. In: Sodhi NS, Ehrlich, Paul R (Eds) Conservation Biology for All, 73–87. https://doi.org/10.1093/acprof:oso/9780199554232.003.0005LiaoJLiZHiebelerDEEl-BanaMDeckmynGNijsI (2013) Modelling plant population size and extinction thresholds from habitat loss and habitat fragmentation: Effects of neighbouring competition and dispersal strategy.268(24): 9–17. https://doi.org/10.1016/j.ecolmodel.2013.07.021MabberleyDJ (1975) The giant lobelias: Pachycauly, biogeography, ornithophily and continental drift.74(2): 365–374. https://doi.org/10.1111/j.1469-8137.1975.tb02623.xMaitimaJMMugathaSMReidRSGachimbiLNMajuleALyaruuHPomeryDMathaiSMugishaS (2009) The linkages between land use change, land degradation and biodiversity across East Africa.3(10): 1–51.MoelgTCullenNJHardyDRKaserGNicholsonLPrinzRWinklerM (2013) East African glacier loss and climate change: Corrections to the UNEP article “Africa without ice and snow”.6(1): 1–6. https://doi.org/10.1016/j.envdev.2013.02.001ObiriJF (2011) Invasive plant species and their disaster-effects in dry tropical forests and rangelands of Kenya and Tanzania. Jàmbá.3(2): 417–428. https://doi.org/10.4102/jamba.v3i2.39PauchardAKuefferCDietzHDaehlerCCAlexanderJEdwardsPJArévaloJRCavieresLAGuisanAHaiderSJakobsGMcDougallKMillarCINaylorBJParksCGRewLJSeipelT (2009) Ain’t no mountain high enough: Plant invasions reaching new elevations.7(9): 479–486. https://doi.org/10.1890/080072RuasPMVVanzelaALLVieiraAOSBerniniCRuasCF (2001) Karyotype studies in Brazilian species of LobeliaL.,subgenusTupa (Campanulaceae).24(3): 249–254. https://doi.org/10.1590/S0100-84042001000300002StuartSNAdamsRJJenkinsM (1990) Biodiversity in sub-Saharan Africa and its islands: conservation, management, and sustainable use. IUCN. https://portals.iucn.org/library/sites/library/files/documents/SSC-OP-006.pdfSukumaranSJeevaS (2008) A floristic study on miniature sacred forests at Agastheeshwaram, southern peninsular India.2: 66–72.ThulinM (1984) Rotterdam, Balkema, 59 pp.ViviroliDWeingartnerR (2008) “Water towers” – A Global View of the Hydrological Importance of Mountains. In: WiegandtE (Ed.) Sources of Water, Sources of Knowledge., 15–20. https://doi.org/10.1007/978-1-4020-6748-8_2WangSWZhouYDMusiliPMMwachalaGHuGWWangQF (2020) Inventory incompleteness and collecting priority on the plant diversity in tropical East Africa. Biological Conservation 241: 108313. https://doi.org/10.1016/j.biocon.2019.108313WescheKMieheGKaeppeliM (2000) The significance of fire for afro-alpine ericaceous vegetation. Mountain Research and Development 20(4): 340–347. https://doi.org/10.1659/0276-4741(2000)020[0340:TSOFFA]2.0.CO;2ZhouYChenSHuGMwachalaGYanXWangQ (2018) Species richness and phylogenetic diversity of seed plants across vegetation zones of Mount Kenya, East Africa.8(17): 8930–8939. https://doi.org/10.1002/ece3.4428ZhouYDLiuBMbuniYYanXMwachalaGHuGWWangQF (2017) Vascular flora of Kenya, based on the Flora of Tropical East Africa.90: 113–126.Supplementary materials10.3897/phytokeys.159.54341.suppl1402560998B8C089-774C-50D1-A257-CCC885DA9741
Tables S1–S12
data statistics
Data statistics for each species.
https://binary.pensoft.net/file/449503This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.John K. Muchuku, Andrew W. Gichira, Shu-Ying Zhao, Jin-Ming Chen, Ling-Yun Chen, Qing-Feng Wang