Research Article
Research Article
The Maghreb – one more important biodiversity hot spot for tiger beetle fauna (Coleoptera, Carabidae, Cicindelinae) in the Mediterranean region
expand article infoRadomir Jaskula
‡ Deartment of Invertebrate Zoology & Hydrobiology, University of Lodz, Lodz, Lodz, Poland
Open Access


The tiger beetle fauna of the Maghreb region is one of the richest in the Palaearctic, including 22 species and 5 subspecies and 19% of all Palaearctic species of Cicindelinae. Assembled to their chorotypes, the Maghreb tiger beetles fall into eight different groups that include Maghreb endemics (26% of fauna), Mediterranean (7%), West Mediterranean (40%), North African (4%), Mediterranean-Westturanian (4%), West Palaearctic (4%), Afrotropico-Indo-Mediterranean (4%), and Saharian (11%) species. The Mediterranean Sclerophyl and Atlas Steppe are the Maghreb biogeographical provinces with the highest species richness, while the Sahara Desert has the lowest Cicindelinae diversity. Twenty-five cicindelid species and subspecies (93% of Maghreb fauna) are restricted to only one or two habitat types in lowland areas. Only Calomera littoralis littoralis and Lophyra flexuosa flexuosa are recognized as eurytopic species and occur in three types of habitat. The highest tiger beetle diversity characterizes salt marshes and river banks (in both cases 11 species and subspecies or 41% of Maghreb fauna). Approximately 85% of all Maghreb tiger beetle species and subspecies are found in habitats potentially endangered by human activity.


Coleoptera , Cicindelinae , tiger beetles, zoogeography, biodiversity, species richness, habitat preferences, Mediterranean region, North Africa, Morocco, Algeria, Tunisia


Tiger beetles (Carabidae: Cicindelinae) include approximately 2600 species of small to medium-sized beetles (Pearson and Cassola 2005). They are predatory with word-wide distributions, excepting some oof the ceanic islands and polar regions (Cassola and Pearson 2000; Pearson and Vogler 2001). Most prefer various sandy habitats where both larvae and adult beetles live. Many recent studies from different continents show that most cicindelid taxa have very narrow habitat specialization and can be found only in one or at most in few very similar types of macrohabitats. As a consequence, tiger beetles have become a very important global flagship group for beetle and insect conservation, often used as biological indicators for determining both regional and global patterns of biodiversity (Knisley and Hill 1992; Pearson and Cassola 1992, 2005; Kitching 1996; Carroll and Pearson 1998a, 1998b; Andriamampianina et al. 2000; Pearson and Vogler 2001; Arndt et al. 2005; Jaskuła 2011). Moreover, as both adults and larvae of cicindelid beetles are predators that prey on different small invertebrates, they can be used for biological control of pests causing important economic destruction (Rodriquez et al. 1988).

The Maghreb is a part of the Mediterranean region, which is known as one of the 25 most important word biodiversity hot spots (Myers et al. 2000; Cuttelod et al. 2008). Concluding from the recent studies upon different plant and animal groups it is also a very important terrestrial Pleistocene glacial refugium, both on the local scale (Husemann et al. 2014) and for the whole Western Palaearctic (Hewitt 1996, 1999; Thomson 2005; Blondel et al. 2010; Habel et al. 2010). High levels of biodiversity in the Maghreb region can be explained by the mosaic heterogeneous landscapes occurring in this area as well as by relatively high climatic stabilization of this region (Blondel et al. 2010). Moreover, Maghreb served as an important natural bridge for historical and present dispersal between Africa and Europe, mainly via the Gibraltar and Sicily sea straits which are known as important biogeographical links between both continents at different times (Habel et al. 2010).

The first data on tiger beetle fauna of the Maghreb region were published in the second half of 18th and at the beginning of 19th centuries (e.g. Linnaeus 1758; Fabricius 1781, 1787, 1801; Vigors 1825; Dejean 1831). Since then, more than 80 papers have been published on this topic. Unfortunately, in most cases they include only single faunistic records or data on a single species. Till recently the knowledge on diversity and distribution of tiger beetle fauna was summarized for Tunisia by Korell and Cassola (1987) and Jaskuła and Rewicz (in prep.) and for Morocco by Cassola (1973) and Jaskuła et al. (in prep.).

The paper is the second part of wider studies concerning biodiversity and zoogeography of tiger beetle fauna of the Mediterranean region (Jaskuła 2011). Its aim is to summarize the knowledge on diversity of tiger beetles in the Maghreb region with particular emphasis on the group diversity, distribution, zoogeographical composition as well as the macrohabitat preferences of cicindelid taxa.

Study area

Here, the Maghreb region is defined as a part of northwestern Africa with its northern boundary made up of the Mediterranean Sea, the western boundary at Atlantic coast, the southern at Sahara Desert, and the eastern at the political border of Tunisia and Libya (Michard et al. 2008, Fig. 1). Politically the area includes four countries, three of them completely confined to the Maghreb region (Tunisia, Algeria, and Morocco) as well as the two small enclaves (Ceuta and Melilla) belonging to Spain. The region has a total area of 2,991,933 km2, which is nearly 10% of the entire African continent and some 5.5% of the Palaearctic ecozone.

Figure 1. 

Geographical and administrative divisions of the Maghreb region: I – Rif, II – Central Massif, III – Middle Atlas, IV – High Atlas, V – Anti-Atlas, VI – High Plateaus, VII – Tell Kabyllas, VIII – Saharan Atlas, IX – Tunisian Atlas, X – Ougarta, XI – Saharan Platform, MO – Morocco, AG – Algeria, TU – Tunisia, SP – Spain (Ceuta and Melilla), AO – Atlantic Ocean, MS – Mediterranean Sea.

The largest surface of the Maghreb region is montane. Lowlands extend only along the lower reaches of rivers that are grouped into two drainages of the Mediterranean Sea and of the Atlantic Ocean (Woodward 2009). Geographically the Maghreb is divided into the following main regions: Rif, Central Massif, Anti-Atlas, Middle Atlas, Tell Kabyllas, High Plateaus, Tunisian Atlas, Saharan Atlas, High Atlas, Ougarta, and Saharan Platform (Michard et al. 2008; Fig. 1).

According to biogeographical divisions by Udvardy (1975) the Maghreb region belongs to three provinces (Fig. 2): Mediterranean Sclerophyl – which includes Mediterranean coasts of Tunisia, Algeria, and Morocco as well as entire areas of Spanish enclaves, Ceuta and Melilla; the Atlas Steppe – with the highest montane areas of Tunisia, Algeria, and Morocco; and the Sahara Desert – the biggest area of Maghreb with the southernmost parts of Algeria and Tunisia.

Figure 2. 

Tiger beetle faunas in the biogeographical provinces of the Maghreb region (division after Udvardy 1975): light grey – Mediterranean Sclerophyl, black – Atlas Steppe, dark grey – Sahara Desert. Numbers in the circles indicate the number of cicindelid taxa for the separate regions and the squares give the number of taxa common to the provinces shared (large – species, small in brackets – subspecies).

Material and methods

The basis for the analysis of tiger beetle fauna of the Maghreb region comes from published literature data, museum collections (Museum and Institute of Zoology, Polish Academy of Science, Warsaw, Poland; Museum of Natural History, Vienna, Austria; Royal Belgium Institute of Natural Sciences, Brussels, Belgium), and the author's collections gathered during two scientific trips covering almost entire areas of Morocco and Tunisia (2nd and 4th TB-Quest Expeditions) in 2009 and 2010. Additionally, single specimens were studied thanks to Dr. J. Ch. Habel (Germany). Recently all these faunistic data were summarized in two papers on tiger beetle species of Tunisia and Morocco (Jaskuła and Rewicz in prep., Jaskuła et al. in prep.).

All the statistical analyses used in this paper follow my previous work on tiger beetles occurring in the Mediterranean region (Jaskuła 2011) to enable proper comparison. The tiger beetle species richness and distribution of taxa were analyzed based on squares of 1° longitude and latitude. In each square the total number of all species recorded was summarized. Similarities among tiger beetle fauna between geographical divisions of the Maghreb region were measured using the Bray-Curtis index for presence/absence data (Primer v. 5.0) as well as Jaccard’s (1902) index was used to present the degree of dissimilarity between zoogeographic regions proposed by Udvardy (1975):

R = 100c/a+b-c

where: a – number of species in the richest fauna, b – number of species in the poorest fauna, c – number of species common to both faunas.

Chorotype definition follows Vigna Taglianti et al. (1999).


Diversity of tiger beetles in Maghreb region

According to Werner (1991, 1992), Putchkov and Matalin (2003), Lopéz et al. (2006), Cassola and Wiesner (2009), and Deuve (2011, 2012) approximately 110 tiger beetle species occur in Palaearctic (species recorded by Putchkov and Matalin (2003) in the oriental part of China and in Taiwan were excluded). Out of that, 22 species and 5 subspecies have been found in the area of Maghreb region (Table 1) which is approximately 19% of all the Palaearctic tiger beetle species.

Table 1.

Chorotypes of Maghreb tiger beetles (based on Vigna Taglianti et al. 1999).

Region Species
Maghreb endemics Platydela coquerelii coquerelii, Platydela coquerelii theryi, Platydela segonzaci, Neolaphyra leucosticta leucosticta, Neolaphyra leucosticta simulans, Neolaphyra peletieri, Neolaphya truquii
West Mediterranean Calomera littoralis littoralis, Calomera lunulata, Cassolaia maura maura, Cassolaia maura cupreothoracica, Cephalota circumdata imperialis, Cephalota littorea goudotii, Cephalota luctuosa, Cicindela campestris atlantis, Cicindela maroccana maroccana, Cylindera trisignata trisignata, Cylindera trisignata siciliensis
North African Cephalota tibialis lyonii
Mediterranean Calomera aulica aulica, Lophyra flexuosa flexuosa
Mediterranean-Westturanian Grammognatha euphratica euphratica
West Palaearctic Cicindela campestris campestris
Afrotropico Indo-Mediterranean Myriochila melancholica melancholica
Saharian Habrodera leucoptera leucoptera, Myriochila dorsata, Myriochila mirei

The Maghreb cicindelid species belong to eleven genera (92% of the Mediterranean or 61% of the Palaearctic fauna) including: Grammognatha (1 species, 100% of both Mediterranean and Palaearctic), Myriochila (3 species, 75% of Mediterranean and 27% of the Palaearctic), Habrodera (1 species, 50% of both Mediterranean and Palaearctic), Calomera (3 species, 50% of Mediterranean and 19% of Palaearctic), Lophyra (1 species, 50% Mediterranean and 8% of Palaearctic), Cephalota (4 species, 40% Mediterranean of and 21% of Palaearctic), Cassolaia (1 species, 50% of both Mediterranean and Palaearctic), Neolaphyra (3 species, 75% of both Mediterranean and Palaearctic), Platydela (2 species, 100% of both Mediterranean and Palaearctic), Cylindera (1 species, 8% of Mediterranean and 3% of Palaearctic), and Cicindela (1 species, 17% of Mediterranean and 2% of Palaearctic). Comparing to the total list of tiger beetle genera occurring in the Mediterranean region, only the genus Homodela (distributed in Syria and the southern part of Turkey) is not present in Maghreb.

Seven tiger beetle taxa belonging to five species (Platydela coquerelii coquerelii, P. c. theryi, P. segonzaci, Neolaphyra leucosticta leucosticta, Neolaphyra l. simulans, N. peletieri, and N. truquii) are endemic to the Maghreb region. Additionally, for three taxa (Habrodera leucoptera leucoptera, Myriochila dorsata, and M. mirei) Maghreb is the only place of occurrence in the Palaearctic ecozone (distributed also south of Sahara) and for four others, this area is the only one in the African part of the Palaearctic (they are known from south-western Europe and/or from south-western Asia).

Based on the chorotypes, tiger beetles of the Maghreb region can be included into eight different groups (Vigna Taglianti et al. 1999; Table 1). Except Maghreb endemics, which constitute 26% of all tiger beetle taxa (species and subspecies) noted from this area, representatives of West Mediterranean (40%), North-African (4%), Mediterranean (7%), Mediterranean-Westturanian (4%), West Palaearctic (4%), Afrotropico Indo-Mediterranean (4%), and Saharian (11%) taxa can be found in this region.

The number of Maghreb tiger beetle species is high if compared with the number noted from other regions of the West Palaearctic with other areas of similar size (Table 2), especially when the large part of Algerian Sahara is excluded (a great part of the Sahara desert is so dry that there are no habitats which would be attractive for Cicindelinae). In this case, the diversity and species richness of the Maghreb tiger beetle fauna is similar not only to the faunas of all the other most important glacial refugia in Europe (Iberian, Balkan, and Italian Peninsula) and in south-western Asia (Turkey), but even to the fauna known from the entire territory of the European part of Russia.

Table 2.

Comparison of area and tiger beetle species richness of Maghreb and some other regions from Western Palaearctic (data compiled from different sources).

Region Area (km2) Number of species
Maghreb 2 991 933 22
Maghreb (excluding biogeographical province – Sahara Desert) ca. 714 500 21
Iberian Peninsula 580 000 19
Balkan Peninsula 550 000 19
Italian Peninsula 150 000 13
France (mainland) 675 000 14
Scandinavian Peninsula 800 000 5
Ukraine 603 700 19
Turkey 783 562 26
Russia (European part) 4 268 850 28

Distribution of tiger beetles in the Maghreb region

Records from the literature and from my own observations within squares of 1° latitude and longitude show that the species richness of particular regions within the Maghreb differs both in species composition and in number of taxa. The highest number of tiger beetle taxa is found along the sea coasts of the Mediterranean Sea and of the Atlantic Ocean, both according to the geographical divisions and biogeographic regions defined by Udvardy (1975, Figs 23). The greatest Cicindelinae species richness in the Maghreb can be found in two biogeographic provinces which are similar in their surface area: the Mediterranean Sclerophyl (18 species or 22 species and subspecies, 82% of the Maghreb fauna) and the Atlas Steppe (13 species or 15 species and subspecies, 56% of fauna). The lowest species richness characterizes the Sahara Desert, where only two species (7% of fauna) have been noted, despite the fact that the Sahara Desert covers a part of Maghreb that is larger than both previous provinces combined.

Figure 3. 

Species richness of tiger beetles within the Maghreb region. The colour gradient indicates an enhanced diversity from zero species (white square) to seven (black square).

The Bray-Curtis analysis of similarities among the tiger beetle faunas from different Maghreb geographical regions shows the presence of four main groups (Fig. 4). One of them includes the Saharan Platform, Anti-Atlas, and Ougarta regions belonging to the southernmost part of Maghreb and covering a great part of Udvardy’s (1975) Sahara Desert and a small part of the Atlas Steppe. The second group composes of the Middle Atlas and the High Atlas regions which include the highest mountains within Maghreb, mentioned in biogeographic studies as the western part of the Atlas Steppe. The third group includes four regions located mainly in lowlands and highlands along the Mediterranean and Atlantic coasts: Rif, Central Massif, Tell Kabyllas and Tunisian Atlas. All these geographical regions belong to Udvardy’s (1975) Mediterranean Sclerophyl. The last region is composed of the High Plateaus and of the Saharan Atlas (both being part of the central part of the Atlas Steppe) and covers the greater part of mountain areas in northern Algeria. The Jaccard’s similarity index for Mediterranean Sclerophyl – Atlas Steppe was 42%, for Mediterranean Sclerophyl – Sahara Desert was 4%, and for Atlas Steppe – Sahara Desert was null.

Figure 4. 

Similarities among tiger beetle faunas inhabiting regions of the Maghreb (Bray-Curtis similarity index for presence/absence data).

Ecotypes of Maghreb tiger beetles

In the tiger beetle fauna of Maghreb the most eurytopic taxa are Calomera littoralis littoralis and Lophyra flexuosa flexuosa (Table 3), both of them occurring in three types of macrohabitats. Five other species/subspecies have been found to occupy two types of habitats, including Calomera aulica aulica, Cassolaia maura maura, Cicindela campestris atlantis, Cylindera trisignata trisignata, and C. t. siciliensis. Twenty other taxa (74% of Maghreb fauna) are known only from one type of habitat, including Habrodera leucoptera leucoptera, Grammognatha euphratica euphratica, Myriochila myriochila myriochila and all four Cephalota species from salt marshes, seven taxa restricted to river banks (Cicindela maroccana maroccana, Myriochila dorsata, M. mirei, and all Neolaphyra), four found exclusively in mountain and highland pastures and meadows (Cicindela campestris campestris, and all Platydela), and one taxon known only from sandy sea beaches (Calomera aulica aulica). Among all these tiger beetles, 23 species and subspecies (85%) can be classified as coastal and riverine taxa, occupying habitats close to water, such as salt marshes, banks of rivers and lakes, and sea coasts, while four other taxa (19%) are typical mountain beetles occurring in sandy areas in meadows and pastures at higher elevations.

Table 3.

Tiger beetles of the Maghreb region and their ecological distribution: 1 – salt marshes, 2 – sandy sea beaches, 3 – sandy-rocky sea beaches, 4 – banks of rivers, 5 – banks of lakes, 6 – oases, 7 – mountain and highland pastures and meadows.

No. Taxon Macrohabitat type
1 2 3 4 5 6 7
1. Calomera aulica aulica (Dejean, 1831) + +
2. Calomera littoralis littoralis (Fabricius, 1787) + + +
3. Calomera lunulata (Fabricius, 1781) +
4. Cassolaia maura cupreothoracica Korell & Cassola, 1987 +
5. Cassolaia maura maura (Linnaeus, 1758) + +
6. Cephalota circumdata imperialis (Klug, 1834) +
7. Cephalota littorea goudotii (Dejean, 1829) +
8. Cephalota luctuosa (Dejean, 1831) +
9. Cephalota tibialis lyonii (Vigors, 1825) +
10. Cicindela campestris atlantis Mandl, 1944 + +
11. Cicindela campestris campestris Linnaeus, 1758 +
12. Cicindela maroccana maroccana Fabricius, 1801 +
13. Cylindera trisignata trisignata (Dejean, 1822) + +
14. Cylindera trisignata siciliensis (W. Horn, 1891) + +
15. Grammognatha euphratica euphratica Latreille & Dejean, 1822 +
16. Habrodera leucoptera leucoptera (Dejean, 1831) +
17. Lophyra flexuosa flexuosa (Fabricius, 1787) + + +
18. Myriochila dorsata (Brullé, 1834) +
19. Myriochila melancholica melancholica (Fabricius, 1798) +
20. Myriochila mirei Rivalier, 1961 +
21. Neolaphyra leucosticta leucosticta (Fairmaire, 1859) +
22. Neolaphyra leucosticta simulans (Bedel, 1895) +
23. Neolaphyra peletieri (Lucas, 1848) +
24. Neolaphya truquii (Guérin-Méneville, 1855) +
25. Platydela coquerelii coquerelii (Fairmaire, 1867) +
26. Platydela coquerelii theryi (Alluad, 1930) +
27. Platydela segonzaci (Bedel, 1903) +
Total 11 5 1 11 2 1 5

Discussion and conclusions

Diversity and distribution of tiger beetles in the Maghreb region

Compared to the surface area of other regions of the Palaearctic, the diversity of tiger beetles of the Maghreb region is high and constitutes about 19% of all Cicindelinaespecies known from this biogeographic realm (Putchkov and Matalin 2003; Lopéz et al. 2006; Cassola and Wiesner 2009; Deuve 2011, 2012). This clearly proves an important role of Maghreb as diversity hot spot for tiger beetles, noted earlier for many other different taxonomic groups, including plants, terrestrial and freshwater invertebrates, and vertebrates (eg. Schleich et al. 1996; Beauchard et al. 2003; Omodeo et al. 2003; Thompson 2005; Delforge 2006; Blondel and Médail 2009; Blondel et al. 2010). The high diversity of tiger beetle fauna in this area can be explained by two main factors. First is the topographic position of Maghreb within the West Palaearctic realm as the area was (and still is, mainly because of Gibraltar and Sicily sea straits) an important natural bridge between European and African faunas (eg. Harris et al. 2002; Paulo et al. 2002; Carranza et al. 2004, 2006; Veith et al. 2004; Fritz et al. 2006; Weingartner et al. 2006; Recuero et al. 2007; Habel et al. 2008, 2010; Skog et al. 2009). As a result of these biogeographical links between both continents at different times, presently Maghreb region is inhabited by a mixed tiger beetle fauna with representatives of 22 species belonging to eight different groups according to their chorotypes (Table 1). Some of these taxa presently occur both in Northern Africa and in southern Europe (eg. all Maghreb species of Calomera, Cephalota, Cylindera, and Grammognatha) (Putchkov and Matalin 2003; Serrano 2013). Similar patterns in faunal elements have been noted also among other groups of invertebrates, including some groups of insects (Weingartner et al. 2006; Riservato et al. 2009; Habel et al. 2008), scorpions (Gantenbein and Largiadèr 2003), amphibians and reptiles (Busack 1986; Schleich et al. 1996; Alvarez et al. 2000; Cox et al. 2006), mammals (Dobson 1998; Cosson et al. 2005; Temple and Cuttelod 2008; Skog et al. 2009) and plants (Thompson 2005).

The second reason of high level species richness of Maghreb tiger beetle fauna is the high diversity of habitats preferred by this beetle group, including sandy sea beaches, salt marshes, river banks, as well as oases and sandy areas in the mountains.

A relatively high level of landscape mosaic and heterogeneity may also explain the general distribution patters of tiger beetle species within the Maghreb region with higher diversity and species richness in the lowlands. The reason is that sandy habitats preferred both by larvae and adult cicindelid beetles are much more diverse at the sea coasts than in the montane areas. This patterns appears to be typical for this beetle group and it is very similar in other regions of the Mediterranean area (Cassola 1970, 1973; Lisa 2002; Jaskuła 2011; Jaskuła and Rewicz 2014) and also in other regions of the world, including western and northern Australia, and the Indian subcontinent (Pearson and Cassola 1992). In contrast, at higher elevations, the percentage of habitat opportunists can be much higher, as was shown by Bhargav et al. (2008) in studies on tiger beetles of Shivalik in Himachal Pradesh in north western India. In these studies, habitat specialists were found only in few of the studied habitats. Probably it can be explained by much higher homogeneity of that landscape when compared with lowland areas.

Ecological preferences in Maghreb tiger beetles

The analysis of macrohabitat preferences of Maghreb tiger beetles show that most species have very narrow habitat specialization and occur only in one or at most in two very similar types of habitat. Only two of all the 27 taxa known from this region occupy three different habitats – Calomera littoralis littoralis and Lophyra flexuosa flexuosa (Table 3). Similar observations were made also in other areas of the Mediterranean region, as well as in some other regions of the world. For example, of 19 tiger beetle species and subspecies noted in the Balkans, only two – Calomera littoralis nemoralis and Calomera aulica aulica – were recorded respectively from four and three different habitat types (Jaskuła 2011). In Australia, among 29 studied species only two (Myriochila mastersi and M. semicincta) were found as occurring in several habitat types (Freitag 1979). In the Sulphur Springs Valley (Arizona, USA) only Cicindelidia nigrocoerulea, one of 20 species noted during studies, was recorded from more than one habitat type (Knisley and Pearson 1984) and in the Colfax County (New Mexico, USA) only four of 19 species (Cicindela fulgida, C. tranquebarica, Cicindelidia punctulata, and C. nigrocoerulea,) were noted as habitat generalists occurring in seven different macrohabitat types (Knisley 1984). Similar results were provided also by Acciavatti and Pearson (1989) from the Indian subcontinent where among 151 tiger beetle species only Calochroa flavomaculata was noted from several different habitat types. Pearson (1984) noted Odontocheila annulicornis as the only one cicindelid taxon (of 29 species) inhabiting more than one forest habitat type in the Tambopata Reserve Zone in Peru. Also data from Japan by Satoh et al. (2006) show that usually only single tiger beetle species are eurytopic. In their studies on riparian Cicindelinae in the Tedori River System only Cicindela transbaicalica was distributed widely along the river while two other taxa were restricted to only one habitat type. Moreover, the habitat specialization can be so narrow that species occurrence can be restricted to only a small part of a particular habitat. Sometimes, a different type of habitat/microhabitat is occupied by adult beetles and by the larvae. Ganeshaiah and Belavadi (1986), during their studies of four Asian riverine Cicindelinae species, showed that tiger beetles were segregated distinctly along the river beds according to separate habitats. Similar observations were made also in the USA by Schultz and Hadley (1987) who noted that Cicindela tranquebarica preffered dry areas while Cicindela oregona occupied mainly stream edges, and by Jaskuła (2011) who observed in the different parts of the Balkans that Calomera littoralis nemoralis preferred mainly wet sand on edges of water reservoirs while the drier salt marsh substrate was inhabited by Cephalota chiloleuca, C. c. circumdata and Cylindera trisignata hellenica. Interesting results were also provided by Satoh and Hori (2005) who found spatial segregation during the larval stage of six Japanese tiger beetles. Each of the studied taxa preferred specific type of microhabitat. Moreover, in most of the species the habitat type was different for larvae and for adult beetles.

Many authors explain such narrow cicindelid specialization to habitat/microhabitat type by morphological (Pearson and Murry 1979; Schultz and Hadley 1987; Satoh et al. 2003; Satoh and Hori 2005; Dangalle et al. 2013), physiological (Schultz and Hadley 1987; Hadley et al. 1990), or behavioural (Knisley and Pearson 1981; Pearson and Lederhouse 1987) adaptations of adults and larvae. Moreover, at least in some cases, the opportunistic feeding behaviour can play an important role in colonization of different habitat types by some eurytopic tiger beetle species. A good example comes from the Balkan Peninsula, where a species previously known as typical predatory beetle and habitat generalist, Calomera littoralis nemoralis, was observed on sandy sea beach feeding on plant material (Jaskuła 2013). As the same species (but another subspecies – C. l. littoralis) is also one of the only two habitat generalists known from the Maghreb region, it cannot be excluded that similar feeding behaviour may occur also in the North African population of this species.

Underwood et al. (2009a, 2009b) noted that Mediterranean type of habitats are among the rarest globally and are restricted to only 2% of the Earth's land surface. Most of these areas are endangered by human activity. Within the Mediterranean region, including Maghreb, less than 1% of the land surface is legally protected. Moreover, presently almost all habitat types occupied by the Maghreb tiger beetles (eg. salt marshes, sandy sea beaches, and banks of freshwater reservoirs) are significantly altered and are recognised as globally threatened (eg. Silliman et al. 2009). According to the ecological distribution of Maghreb Cicindelinae (Table 3), at least 85% of the recorded taxa occur in these threatened environments and, as a result, are potentially threatened. Additionally, three other taxa (all belonging to Platydela) have very restricted world distributions as they are endemics occurring only in small parts of the Moroccan Atlas mountains. All the above, as well as the fact that the Maghreb is a very important transition zone between Africa and Western Europe where faunal elements of various origin meet, clearly prove the unique character of this region as an important biodiversity hot spot for tiger beetle fauna both in the Mediterranean region and in the Western Palaearctic.


I would like to express my thanks to Dr. Piotr Jóźwiak who prepared the maps in this paper (University of Łódź, Łódź, Poland). Tomasz Rewicz, Jacek Hikisz, Anna Kleszcz, and Jakub Szymański (Łódź, Poland) helped in collecting tiger beetle material during two “TB-Quest Expeditions” to North Africa and Dr. Jan Christian Habel (Freising-Weihenstephan, Germany) made some cicindelid specimens collected by him in Morocco accessible for this study. The research was partly financially supported by SYNTHESYS Project AT-TAF-418.


  • Acciavatti RE, Pearson DL (1989) The tiger beetle genus Cicindela (Coleoptera, Insecta) from the Indian subcontinent. Annals of Carnegie Museum 58: 77–353.
  • Alvarez Y, Mateo JA, Andreu AC, Diaz-Paniagua C, Diez A, Bautista JM (2000) Mitochondrial DNA haplotyping of Testudo graeca on both continental sides of the straits of Gibraltar. Journal of Heredity 91: 39–41. doi: 10.1093/jhered/91.1.39
  • Arndt E, Aydin N, Aydin G (2005) Tourism impairs tiger beetle (Cicindelidae) populations – a case study in a Mediterranean beach habitat. Journal of Insect Conservation 9: 201–206. doi: 10.1007/s10841-005-6609-9
  • Andriamampianina L, Kremen C, Vane-Wright D, Lees D, Razafimahatratra V (2000) Taxic richness patterns and conservation of Madagascar tiger beetles (Coleoptera: Cicindelidae). Journal of Insect Conservation 4: 109–128. doi: 10.1023/A:1009667712512
  • Beauchard O, Gagneur J, Brosse S (2003) Macroinvertebrate richness patterns in North African streams. Journal of Biogeography 30: 1821–1833. doi: 10.1111/j.1365-2699.2003.00954.x
  • Bhargav V, Uniyal VP, Sivakumar K (2009) Distinctive patterns in habitat association and distribution of tiger beetles in the Shivalik landscape of North Western India. Journal of Insect Conservation 13: 459–473. doi: 10.1007/s10841-008-9193-y
  • Blondel J, Aronson J, Bodiou J-Y, Boeuf G (2010) The Mediterranean Region: Biological Diversity through Space and Time. 2nd Edition. Oxford University Press, Oxford, 328 pp.
  • Blondel J, Médail F (2009) Biodiversity and conservation. In: Woodward C (Ed.) The Physical Geography of the Mediterranean basin. Oxford University Press, Oxford, 604–638.
  • Busack SD (1986) Biogeographic analysis of the herpetofauna separated by the formation of the Strait of Gibraltar. National Geographic Research 2: 17–36.
  • Carranza S, Arnold EN, Wade E, Fahd S (2004) Phylogeography of the false smooth snakes, Macroprotodon (Serpentes, Colubridae): mitochondrial DNA sequences show European populations arrived recently from Northwest Africa. Molecular Phylogenetics and Evolution 33: 523–532. doi: 10.1016/j.ympev.2004.07.009
  • Carranza S, Harris DJ, Arnold EN, Batista V, de la Vega JPG (2006) Phylogeography of the lacertid lizard, Psammodromus algirus, in Iberia and across the Strait of Gibraltar. Journal of Biogeography 33: 1279–1288. doi: 10.1111/j.1365-2699.2006.01491.x
  • Carroll SS, Pearson DL (1998b) The effectc of scale and sample size on the accuracy of spatial predictions of tiger beetle (Cicindelidae) species richness. Ecography 21: 401–414. doi: 10.1111/j.1600-0587.1998.tb00405.x
  • Cassola F (1970) The Cicindelidae of Italy. Cicindela 2(4): 1–20.
  • Cassola F (1973) Contribution à la connaissance des Cicindèles du Maroc. Bulletin de la Société de Sciences Naturelles et Physiques du Maroc 53(1): 253–268.
  • Cassola F, Pearson DL (2000) Global patterns of tiger beetle species richness (Coleoptera: Cicindelidae): their use in conservation planning. Biological Conservation 95: 197–208. doi: 10.1016/S0006-3207(00)00034-3
  • Cassola F, Wiesner J (2009) A new Myriochila (subgenus Monelica) from Baluchistan, Pakistan. Mitteilungen des Internationalen Entomologischen Vereins 33(3/4): 81–87.
  • Cosson JF, Hutterer R, Libois R, Sarà M, Taberlet P, Vogler P (2005) Phylogeographic footprints of the Strait if Gibraltar and Quaternary climatic fluctuations in the Western Mediterranean: a case study with the greater white-toothed skrew, Crocidura russula (Mammalia: Soricidae). Molecular Ecology 14: 1151–1162. doi: 10.1111/j.1365-294X.2005.02476.x
  • Cox N, Chanson J, Stuart S (2006) The Status and Distribution of Reptiles and Amphibians of the Mediterranean Basin. IUCN, Gland-Cambridge, 42 pp. doi: 10.2305/IUCN.CH.2006.MRA.2.en
  • Cuttelod A, Garcia N, Abdul Malak D, Temple H, Katariya V (2008) The Mediterranean: a biodiversity hot spot under threat. In: Vie J-C, Hilton-Taylor C, Stuart SN (Eds) The 2008 Review of The IUCN Red List of Threatened Species. IUCN, Gland.
  • Dangalle CD, Pallewatta N, Vogler AP (2013) The association between body-size and habitat-type in tiger beetles (Coleoptera, Cicindelidae) of Sri Lanka. Ceylon Journal of Science 42(1): 41–53.
  • Dejean PMFA (1831) Spécies général des Coléoptères V. Mequignon-Marvis, Paris, 883 pp.
  • Delforge P (2006) Orchids of Europe, North Africa and the Middle East. A&C Black, 640 pp.
  • Deuve T (2011) Esquisse pour l’étude des Cicindela proches de campestris, desertorum, herbacea et javeti au Proche-Orient (ColeopteraCaraboidea). L’Entomologiste 67: 125–138.
  • Deuve T (2012) Esquisse pour l’étude des populations est-méditerranéennes du groupe de Cicindela campestris (ColeopteraCaraboidea). L’ Entomologiste 68: 3–16.
  • Dobson M (1998) Mammal distributions in the Western Mediterranean: the role of human invention. Mammal Review 28(2): 77–88. doi: 10.1046/j.1365-2907.1998.00027.x
  • Fabricius JC (1781a) Species Insectorum enhibentes eorum differenties specificas, synonyma, auctorum, loca natalia, metamorphosim adiectis observationibus, descriptionibus. Tomus I. C.E. Bohn, Hamburg et Kilonii, 552 pp.
  • Fabricius JC (1787) Mantissa insectorum, sistens eorum species nuper detectas adiectis characteribus genericis, differentiis specificis, emendationibus, observationibus (Tom. I). CG Proft, Hafhiae, 348 pp.
  • Fabricius JC (1801) Systema Eleutheratorum secundum ordines, genera, species; adiectis synonymu, locis, observationibus, descriptionibus. Bibliopolii Academici Novi, Kiliae, 506 pp (Tomus I), 687 pp (Tomus II).
  • Freitag R (1979) Reclassification, phylogeny and zoogeography of the Australian species of Cicindela (Coleoptera: Cicindelidae). Australian Journal of Zoology (Supplementary Series) 66: 1–99. doi: 10.1071/AJZS066
  • Fritz U, Barata M, Busack SD, Fritsch G, Castilho R (2006) Impact if mountain chains, sea straits and peripheral populations on genetic and taxonomic structure of freshwater turtle, Mauremys leprosa (Reptilia, Testudines, Geoemydidae). Zoologica Scripta 35: 97–108. doi: 10.1111/j.1463-6409.2005.00218.x
  • Ganeshaiah KM, Belavadi VV (1986) Habitat segregation in four species of adult tiger beetles (Coleoptera; Cicindelidae). Ecological Entomology 11: 147–154. doi: 10.1111/j.1365-2311.1986.tb00289.x
  • Gantenbein B, Largiadèr CR (2003) The phylogeographic importance of the Strait of Gibraltar as a gene flow barier in terrestrial arthropods: a case study with the scorpion Buthus occitanus as model organism. Molecular Phylogenetics and Evolution 28: 119–130. doi: 10.1016/S1055-7903(03)00031-9
  • Habel JC, Drees C, Schmitt T, Assmann T (2010) Review: Refugial Areas and Postglacial Colonizations in the Western Palearctic. In: Habel JC, Assmann T (Eds) Relict Species: Phylogeography and Conservation Biology. Springer-Verlag, Berlin Heidelberg, 189–197.
  • Habel JC, Meyer M, El Mousadik A, Schmitt T (2008) Africa goes Europe: the complete phylogeography of the Marbled White butterfly species complex Melanargia galatea/M. lachesis (Lepidoptera: Satyridae). Organisms Diversity and Evolution 8: 121–129. doi: 10.1016/j.ode.2007.04.002
  • Hadley NF, Knisley CB, Schultz TD, Pearson DL (1990) Water relations of tiger beetle larvae (Cicindela marutha): correlations with habitat microclimate and burrowing activity. Journal of Arid Environment 19: 189–197.
  • Harris DJ, Carranza S, Arnold EN, Pinho C, Ferrand N (2002) Complex biogeographical distribution of genetic variation within Podarcis Wall lizard cross the Strait of Gibraltar. Journal of Biogeography 29: 1–6. doi: 10.1046/j.1365-2699.2002.00744.x
  • Husemann M, Schmitt T, Zachos FE, Ulrich W, Habel C (2014) Palaearctic biogeography revised: evidence for the existence of a North African refugium for Western Palaearctic biota. Journal of Biogeography 41: 81–94.
  • Hewitt GM (1996) Some genetic consequences of ice ages, and their role in divergence and speciation. Biological Journal of the Linnean Society 58: 247–276. doi: 10.1111/j.1095-8312.1996.tb01434.x
  • Jaccard P (1902) Lois de distribution florale dans la zone alpine. Bulletin de la Société Vaudoise des Sciences Naturelles 38: 69–130.
  • Jaskuła R (2011) How unique is the tiger beetle fauna (Coleoptera, Cicindelidae) of the Balkan Peninsula? ZooKeys 100: 487–502. doi: 10.3897/zookeys.100.1542
  • Jaskuła R (2013) Unexpected vegetarian feeding behaviour of a predatory tiger beetle Calomera littoralis nemoralis (Olivier, 1790) (Coleoptera: Cicindelidae). Journal of the Entomologcal Research Society 15(1): 01–06.
  • Jaskuła R, Rewicz T (2014) Tiger beetle fauna (Coleoptera: Cicindelidae) of Syria: distribution, geographical origin, taxa list and new records. Baltic Journal of Coleopterology 14(2): 191–198.
  • Jaskuła R, Rewicz T (in prep.) Tiger beetle fauna (Coleoptera: Carabidae: Cicindelinae) of Tunisia: distribution, phenology taxa list and new records.
  • Jaskuła R, Rewicz T, Kwiatkowski K (in prep.) Tiger beetle fauna (Coleoptera: Carabidae: Cicindelinae) of Morocco: distribution, taxa list and new records.
  • Kitching IJ (1996) Identifying complementary areas for conservation in Thailand: and example using owls, hawkmoths and tiger beetles. Biodiversity Conservation 5(7): 841–858. doi: 10.1007/BF00054738
  • Knisley CB (1984) Ecological distribution of tiger beetles (Coleoptera: Cicindelidae) in Colfax County, New Mexico. Southwestern Naturalist 29(1): 93–104. doi: 10.2307/3670774
  • Knisley CB, Hill JM (1992) Effects of habitat change from ecological succession and human impact on tiger beetles. Virginian Journal of Science 43: 134–142.
  • Knisley CB, Pearson DL (1981) The function of turret building behaviour in the larval tiger beetle, Cicindela willistoni (Coleoptera: Cicindelidae). Ecological Entomology 6: 401–410. doi: 10.1111/j.1365-2311.1981.tb00631.x
  • Knisley CB, Pearson DL (1984) Biosystematics of larval tiger beetles of the Sulphur Springs Valley, Arizona. Transactions of the American Entomological Society 110: 465–551.
  • Korell A, Cassola F (1987) Über die Sandlaufkäfer Tunesiens. Mitteilungen der Münchner Entomologischen Gesselschaft 77: 85–101.
  • Linnaeus C (1758) Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis (Tomus I). Editio decima, reformata. [Salvius], Holmiæ, 824 pp.
  • Lisa T (2002) Le Cicindela d’Italia. Revue de l’Association Roussillonnaise d’Entomologie (Supl. ) 1: 1–55.
  • Lopéz MA, de la Rosa JJ, Baena M (2006) Descripcion de Cephalota (Taenidia) dulcinea sp. n. de la Peninsula Iberica (Coleoptera, Cicindelidae). Boletin Sociedad Entomólogica Aragonesa 39: 165–170.
  • Michard A, Frizon de Lamotte D, Saddiqi O, Chalouan A (2008) An Outline of the Geology of Morocco. In: Michard A, Saddiqi O, Chalouan A, Frizon de Lamotte D (Eds) Continental evolution: The Geology of Morocco. Structure, stratigraphy, and tectonics of the Africa-Atlantic-Mediterranean triple junction. Springer-Verlag, Berlin Heidelberg, 1–32.
  • Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Jennifer K (2000) Biodiversity hotspots for conservation priorities. Nature 403: 853–858. doi: 10.1038/35002501
  • Omodeo P, Rota E, Baha M (2003) The megadrile fauna (Annelida: Oligochaeta) of Maghreb: a biogeographical and ecological characterization. Pedobiologia 47(5/6): 458–465.
  • Paulo OS, Pinto I, Bruford MW, Jordan WC, Nichols RA (2002) The double origin of Iberian peninsular chameleons. Biological Journal of the Linnean Society 75: 1535–1551. doi: 10.1046/j.1095-8312.2002.00002.x
  • Pearson DL (1984) The tiger beetles (Coleoptera: Cicindelidae) of the Tambopata Reserved Zone, Madre e Dios, Peru. Revista Peruviana de Entomologia 27: 15–24.
  • Pearson DL, Cassola F (1992) World-wide species richness patterns of tiger beetles (Coleoptera: Cicindelidae): indicator taxon for biodiversity and conservation studies. Conservation Biology 6: 376–391. doi: 10.1046/j.1523-1739.1992.06030376.x
  • Pearson DL, Cassola F (2005) A quantitative analysis of species descriptions of tiger beetles (Coleoptera: Cicindelidae), from 1758 to 2004, and notes about related developments in biodiversity studies. The Coleopterologist Bulletin 59(2): 184–193. doi: 10.1649/739
  • Pearson DL, Lederhouse RC (1987) Thermal ecology and the structure of an assemblage of adult tiger beetles (Cicindelidae). Oikos 50: 247–255. doi: 10.2307/3566008
  • Pearson DL, Mury EJ (1979) Character divergence and convergence among tiger beetles (Coleoptera: Cicindelidae). Ecology 60: 557–566. doi: 10.2307/1936076
  • Pearson DL, Vogler AP (2001) Tiger beetles: the evolution, ecology, and diversity of the cicindelids. Cornell University Press, Ithaca and London, 333 pp.
  • Putchkov AV, Matalin AV (2003) Subfamily Cicindelinae Latreille, 1802. In: Löbl L, Smetana A (Eds) Catalogue of Palaearctic Coleoptera. V.1. Archostemata – Myxophaga – Adephaga. Apollo Books, Strenstrup, 99–118.
  • Recuero E, Iraola A, Rubio X, Machordom A, Garcia-Paris M (2007) Mitochondrial differentiation and biogeography of Hyla meridionalis (Anura: Hylidae): an unusual phylogeographical pattern. Journal of Biogeography 34: 1207–1219. doi: 10.1111/j.1365-2699.2007.01688.x
  • Riservato E, Boudot JP, Ferreira S, Jović M, Kalkman VJ, Schneider W, Samraoui B, Cuttelod A (2009) The status and distribution of dragonflies of the Mediterranean Basin. IUCN, Gland-Malaga, 33 pp. doi: 10.2305/IUCN.CH.2009.18.en
  • Rodriguez JP, Pearson DL, Barrera RR (1998) A test for adequacy of bioindicator taxa: are tiger beetles (Coleoptera: Cicindelidae) appropriate indicators for monitoring the degradation of tropical forests in Venezuela? Biological Conservation 83(1): 69–76. doi: 10.1016/S0006-3207(97)00017-7
  • Satoh A, Hori M (2005) Microhabitat segregation in larvae of six species of coastal tiger beetles in Japan. Ecological Research 20(2): 143–149. doi: 10.1007/s11284-004-0028-3
  • Satoh A, Uéda T, Enokido Y, Hori M (2003) Patterns of species assemblages and geographical distribution associated with mandible size differences in coastal beetles in Japan. Population Ecology 45(2): 67–74. doi: 10.1007/s10144-003-0141-0
  • Satoh A, Uéda T, Ichion E, Hori M (2006) Distribution and habitat of three species of riparian tiger beetle in the Tedori River System in Japan. Environmental Entomology 35(2): 320–325. doi: 10.1603/0046-225X-35.2.320
  • Schleich HH, Werner Kästle W, Kabisch K (1996) Amphibians and Reptiles of North Africa: biology, systematics, field guide. Koeltz Scientific Books, 630 pp.
  • Schultz TD, Hadley NF (1987) Microhabitat segregation and physiological differences in co-occurring tiger beetle species, Cicindela oregona and Cicindela tranquebarica. Oecologia 73: 363–370. doi: 10.1007/BF00385252
  • Serrano J (2013) New catalogue of the family Carabidae of the Iberian Peninsula (Coleoptera). Universidad de Mercia, Servicio de Publicaciones, 192 pp.
  • Silliman BR, Bertness MD, Grosholz ED (Eds) (2009) Human impact on salt marshes – a global perspective. University of California Press, Berkeley-Los Angeles-London, 311–336.
  • Skog A, Zachos FE, Rueness EK, Feulner PGD, Mysterud A, Langvatn R, Lorenzini R, Hmwe SS, Lehoczky I, Hartl GB, Stenseth NC, Jakobsen KS (2009) Phylogeography of red reed (Cervus elaphus) in Europe. Journal of Biogeography 36: 66–77. doi: 10.1111/j.1365-2699.2008.01986.x
  • Temple HJ, Cuttelod A (Eds) (2009) The status and distribution of Mediterranean mammals. IUCN, Gland-Cambridge, 32 pp. doi: 10.2305/IUCN.CH.2009.19.en
  • Udvardy MDF (1975) A classification of the biogeographical provinces of the world. IUCN Occasional PaperNo.18. International Union for Conservation of Nature and Natural Resources, 49 pp.
  • Underwood EC, Klausmeyer KR, Cox RL, Busby SM, Morrison SA, Shaw MR (2009a) Expanding the global network of protected areas to save the imperiled mediterranean biome. Conservation Biology 23(1): 43–52. doi: 10.1111/j.1523-1739.2008.01072.x
  • Underwood EC, Viers JH, Klausmeyer KR, Cox RL, Shaw MR (2009b) Threats and biodiversity in the mediterranean biome. Diversity and Distribution 15: 188–197. doi: 10.1111/j.1472-4642.2008.00518.x
  • Veith M, Mayer C, Samraoui B, Barroso DD, Bogaerts S (2004) From Europe to Africa and vice versa: evidence for multiple intercontinental dispersal in ribbed salamanders (genus Pleurodeles). Journal of Biogeography 31: 159–171. doi: 10.1111/j.1365-2699.2004.00957.x
  • Vigna Taglianti A, Audisio PA, Biondi M, Bologna MA, Carpaneto GM, De Biase A, Fattorini S, Piattella E, Sindaco R, Venchi A, Zapparoli M (1999) A proposal for a chorotype classification of the Near East fauna, in the framework of the Western Palaearctic region. Biogeographia 20: 31–59.
  • Vigors NA (1825) Descriptions of some rare, interesting, or hitherto uncharacterized subjects of zoology. Zoological Journal of London 1: 409–418.
  • Weingartner E, Wahlberg N, Nylind S (2006) Speciation in Pararge (Satyrinae: Nymphalidae) butterflies – North Africa is the source of ancestral populations of all Pararge species. Systematic Entomology 31: 621–632. doi: 10.1111/j.1365-3113.2006.00333.x
  • Werner K (1991) Cicindelidae Regionis Palaearcticae. Megacephalini: Megacephala, Cicindelini 1: CicindelaLophyridia. The Beetles of the World 13. Sciences Nat., 74 pp.
  • Werner K (1992) Cicindelidae Regionis Palaearcticae. Cicindelini 2: CosmodelaPlatydelaLophyraHabroderaChaetoderaNeolaphyraCephalotaCassolaiaHomodelaCylinderaEugraphaMyriochileSalpingophoraHyphaetaAbroscelisCallytron. The Beetles of the World 15. Sciences Nat., 94 pp.
  • Woodward J (Ed.) (2009) The Physical Geography of the Mediterranean. Oxford University Press, 663 pp.
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