Journal of Ornithology

, Volume 149, Issue 3, pp 423–430

Distinct taxonomic position of the Madagascar stonechat (Saxicola torquatus sibilla) revealed by nucleotide sequences of mitochondrial DNA

  • Friederike Woog
  • Michael Wink
  • Eskandar Rastegar-Pouyani
  • Javier Gonzalez
  • Barbara Helm
Open AccessOriginal Article

DOI: 10.1007/s10336-008-0290-1

Cite this article as:
Woog, F., Wink, M., Rastegar-Pouyani, E. et al. J Ornithol (2008) 149: 423. doi:10.1007/s10336-008-0290-1

Abstract

Stonechats (genus Saxicola) are passerine birds with an extraordinarily large breeding distribution. Recent studies provide strong evidence that the taxon shows far greater geographic differentiation than originally suspected, with African, Siberian and European stonechats forming distinct, monophyletic groups that have been suggested to be species in their own right. Here, we present additional data on the geographic differentiation among African stonechats, Saxicola torquatus. Nucleotide sequences of the mitochondrial NADH dehydrogenase subunit 2 and cytochrome b genes indicate that the stonechats from Eastern Madagascar (Saxicola t. sibilla) form a distinct clade and that they constitute a monophyletic group with stonechats from mainland eastern Africa (Saxicola t. axillaris) and La Réunion (Saxicola tectes). The genetic and morphological data suggest that the Madagascar stonechat is very likely to be a distinct species, Saxicola sibilla (Linnaeus 1766). However, further studies are needed to verify this. A detailed description of the plumage and various external body measurements is given.

Keywords

Mitochondrial DNAMorphometricsPhylogenySaxicolaTaxonomy

Introduction

According to recent genetic analyses, several of the stonechats belonging to the palaeotropic species complex “Saxicola torquatus” form species in their own right. The two allospecies S. rubicola and S. maurus, for example, can be clearly differentiated based on nucleotide sequences of mitochondrial (mt)DNA (Wittmann et al. 1995; Wink et al. 2002a, b; Urquhart 2002), and these two taxa are in turn distinct from the African stonechat S.torquatus. African stonechat groups belonging to the species complex of S. torquatus should probably be considered sister taxa of the European stonechat groups S. rubicola, S. maurus and S. dacotiae (the latter is found on Fuerteventura in the Canary Islands and lacks a black throat). For the at least 12 African subspecies, species status is still being discussed and subject to debate, paralleling the situation within the European and Asian Stonechat groups. However, data are still scarce.

On Madagascar, only one subspecies, Saxicola torquatus sibilla (L.) 1766, is currently recognised by most researchers, although two other forms have been described: Saxicola torquatus ankaratrae (Salomonsen 1934) and S. torquatus tsaratananae (Milon 1950).

To investigate the systematic position of S. t. sibilla from Madagascar, we used S. torquatus axillaris (Shelley 1885) as representative of mainland Africa and S. tectes (Gmelin, 1789) from the island of La Réunion (Fig. 1). Saxicola tectes is largely accepted as a separate species. Similar to S. dacotiae, it lacks a black throat and its plumage is quite distinct.
https://static-content.springer.com/image/art%3A10.1007%2Fs10336-008-0290-1/MediaObjects/10336_2008_290_Fig1_HTML.gif
Fig. 1

Distribution map for Saxicola torquatus sibilla, S. tectes and S. t. axillaris, modified from Urquhart (2002). Samples from the other taxa indicated by shading were not available

Here, we present new results pertaining to the systematic position and status of S. t. sibilla based on nucleotide sequences of mitochondrial cytochrome b (cytb) and NADH dehydrogenase subunit 2 (nd2) genes and give a detailed description of the plumage and the external morphology of the taxon.

Distribution, habitat and breeding season of stonechats studied

Stonechats (S. t. sibilla) are widespread on Madagascar. They are found in a variety of habitats, including montane heathland and scrub, the open areas nearby, forest clearings and also in secondary growth, at elevations from sea level to 2500 m a.s.l. (Morris and Hawkins 1998, own observations). Nesting has been observed between July and January, peaking in October (Langrand 1990, own observations).

Saxicola tectes is endemic to the island of La Réunion (elevation 800 to over 3000 m a.s.l.), thrives in a variety of habitats, including tree heather, and breeds between mid-October to the end of January (Urquhart 2002). It is not known to migrate large distances.

Saxicola t. axillaris ranges throughout the highlands of Kenya, northern and western Tanzania, including the Lake Victoria basin, western and southern Uganda, Rwanda, Burundi and eastern Zaire (Keith et al. 1992, Urquhart 2002). It occurs in alpine heathlands, moorlands, grassy hillsides but also in bush and forest habitats at elevations ranging from 1200 to 3200 m a.s.l. (Britton 1980). These stonechats are paired year round, defend all-purpose territories (Keith et al. 1992), are seasonal breeders and do not exhibit migratory behaviour.

Methods

Samples

The origins of the samples examined are listed in Table 1. The origins of Eurasian stonechats are described in Wink et al. (2002a, b). The Malagasy samples were taken at Maromizaha (Andasibe, eastern Madagascar), located approximately 150 km east of the capital Antananarivo (elevation approximately 1200 m a.s.l.). Blood samples of stonechats from mainland Africa (S. t. axillaris) originated from the Lake Nakuru region, Kenya (0°14′S, 36°0′E; Fig. 1, region K) and from the Arusha region near Mount Meru, Tanzania (3°10′S, 36°40′E; Fig. 1, region T) from birds caught in the wild at approximately 2000 m a.s.l. (Scheuerlein and Gwinner 2006). Samples of other stonechat taxa from mainland Africa were not available.
Table 1

Origin, collection codes and accession numbers of taxa sequenced in this study

Species

IPMB codea

GenBank accession numbers

cytb

nd2

Origin

Luscinia luscinia

4385

EU190893

EU190929

Biebrza, Poland

Luscinia luscinia

4386

EU190894

EU190930

Biebrza, Poland

Saxicola rubetra

4384

EU190895

EU190931

Biebrza, Poland

Saxicola rubetra

4383

EU190896

EU190932

Biebrza, Poland

Saxicola r. hibernans

10475

EU190897

EU190933

Waterford, Ireland

Saxicola rubicola

4412

EU190898

EU190934

Évora, Portugal

Saxicola rubicola

4387

EU190899

EU190935

Scotland

Saxicola rubicola

4418

EU190900

EU190936

Turkey, Ulu Dag

Saxicola rubicola

4419

EU190901

EU190937

Turkey, Ulu Dag

Saxicola rubicola

4420

EU190902

EU190938

Turkey, Ulu Dag

Saxicola rubicola

4421

EU190903

EU190939

Turkey, Ulu Dag

Saxicola rubicola

10467

EU190904

EU190940

Lake Neusiedl, Austria

Saxicola dacotiae

15403

EU190905

EU190941

Fuerteventura, Canary Islands

Saxicola dacotiae

15402

EU190906

EU190942

Fuerteventura, Canary Islands

Saxicola caprata

10462

EU190907

EU190943

Southeast Asia (commercially obtained)

Saxicola caprata

10463

EU190908

EU190944

Southeast Asia (commercially obtained)

Saxicola tectes

10502

EU190909

EU190945

Takamaka, La Réunion

Saxicola tectes

10503

EU190910

EU190946

Takamaka, La Réunion

Saxicola tectes

10504

EU190911

EU190947

Takamaka, La Réunion

Saxicola tectes

10505

EU190912

EU190948

Takamaka, La Réunion

Saxicola torquatus sibilla

32114

EU190913

EU190949

Eastern Madagascar, Maromizaha

Saxicola t. sibilla

32115

EU190914

EU190950

Eastern Madagascar, Maromizaha

Saxicola t. sibilla

32116

EU190915

EU190951

Eastern Madagascar, Maromizaha

Saxicola t. sibilla

32117

EU190916

EU190952

Eastern Madagascar, Maromizaha

Saxicola maurus

4413

EU190917

EU190953

Near Dokutschaewka, Kazakhstan

Saxicola maurus

4414

EU190918

EU190954

Near Dokutschaewka, Kazakhstan

Saxicola maurus

4415

EU190919

EU190955

Near Dokutschaewka, Kazakhstan

Saxicola maurus

4417

EU190920

EU190956

Near Dokutschaewka, Kazakhstan

Saxicola torquatus axillaris

10461

EU190921

EU190957

Tanzania, Arusha region near Mt Meru

Saxicola t. axillaris

11696

EU190922

EU190958

Tanzania, Arusha region near Mt Meru

Saxicola t. axillaris

11697

EU190923

EU190959

Tanzania, Arusha region near Mt Meru

Saxicola t. axillaris

11699

EU190924

EU190960

Tanzania, Arusha region near Mt Meru

Saxicola t. axillaris

11605

EU190925

EU190961

Kenya, Lake Nakuru/Naivasha Region

Saxicola t. axillaris

11606

EU190926

EU190962

Kenya, Lake Nakuru/Naivasha Region

Saxicola t. axillaris

11607

EU190927

EU190963

Kenya, Lake Nakuru/Naivasha Region

Saxicola t. axillaris

11608

EU190928

EU190964

Kenya, Lake Nakuru/Naivasha Region

aIPMB, Institut für Pharmazie und Molekulare Biotechnologie, Heidelberg University; nd2, NADH dehydrogenase subunit 2 gene; cytb, mitochondrial cytochrome b gene

On La Réunion, blood samples were taken from nestlings (Wink et al. 2002b).

The blood samples (200–300 μl) were obtained from the brachial vein and preserved in storage buffer containing 10% EDTA, 1% sodium dodecyl sulphate, 0.5% NaF, 0.5% thymol and 100 mM Tris, pH 7.4 (Wink 2006). For some taxa, tissue was used as outlined in Wink et al. (2002a, b).

DNA extraction, PCR amplification and sequencing

DNA was extracted from blood/tissue samples using the proteinase K protocol (Wink 2000). The mitochondrial cytb gene was amplified by PCR and sequenced directly according to Wink et al. (2002a, b). The mitochondrial nd2 gene was amplified by PCR using the primers metl and asn (Zink et al. 2006). The PCR amplifications were performed in 50-μl reaction volumes containing 2.5 mM MgCl2, 10 mM Tris (pH 8.5), 50 mM KCl, 100 μM dNTPs, 0.8 U DFS Taq DNA polymerase (Bioron, Ludwigshafen, Germany), 300 ng DNA and 5 pmol of primers.

The cycling protocol consisted of an initial denaturation at 95°C for 5 min, followed by 35 cycles of 95°C for 45 s (denaturation), 49°C for 50 s (annealing) and 72°C for 2 min (extension) and terminated with a final extension at 72°C for 10 min. Before sequencing, PCR products were precipitated in 4 M NH4Ac and ethanol (1:1:6), then centrifuged for 25 min at 13,000 rpm, washed in 70% ethanol and resolved in 20 μl of distilled water.

A cycling sequencing reaction (total volume 5 μl) contained 1 μl of reaction mix (according to the premix terminator protocol; Amersham Biosciences, Piscataway, NJ), 5 pmol of one of the forward primers (metl or L347; Zink et al. 2006) and 1–2 μl of the template. The cycling sequencing protocol consisted of 28 cycles of 20 s at 96°C, 15 s at 49°C and 2.5 min at 60°C. The sequencing products were diluted in 15 μl distilled water and purified by Sephadex G-50 columns (Amersham Biosciences) and MultiScreen filter plates (Millipore Corp, Bedford, MA) following the manufacturer’s instructions. The sequences were analysed by capillary electrophoresis using an automated sequencer MegaBACE 1000 (Molecular Dynamics, Amersham Pharmacia) and deposited at GenBank under the accession numbers listed in Table 1.

Sequence analysis and phylogenetic reconstruction

The sequences were aligned by BioEdit ver. 7.0.5 (Hall 1999). Basic statistics and P-distances were calculated with MEGA ver. 4.0 (Tamura et al. 2007). Phylogenetic trees were reconstructed using maximum likelihood (ML), maximum parsimony (MP) and neighbour-joining [NJ, using the Kimura-2-parameter model (Kimura 1980)] in PAUP* ver. 4.0b10a (Swofford 2001). The phylogenetic analyses were performed for both genes separately and concatenated. The MP and ML heuristic searches were performed with ten random stepwise additions, tree-bisection-reconnection branch-swapping and “multrees” option. We explored the model of sequence evolution that fits the data best using Modeltest ver. 3.7 (Posada and Crandall 1998). The best model was then used with the ML analyses. The robustness of the nodes was assessed by 1000 bootstrap replicates. Finally, the Thrush Nightingale Luscinia luscinia was used as an outgroup.

Morphometrics and plumage

We examined and measured 66 individuals of S. t. sibilla from the following museums: Muséum d’Histoire Naturelle Paris (MHNH, n = 43), Naturkundemuseum Berlin (ZMB, n = 11), Museum Alexander Koenig, Bonn (ZFMK, n = 6), Staatliches Museum für Naturkunde Stuttgart (SMNS, n = 6). We also examined wild samples (n = 24). The following measurements were taken (for methods, see Redfern and Clark 2001): wing length (maximum chord), tarsus length (minimum), bill width, bill depth, bill length (from the tip of the bill to the distal end of the nostril), bill length from bill tip to skull, distance of tip of outermost secondary to wing tip (Kipp), tail and weight (only for wild birds). The Kipp index was calculated as Kipp × 100/wing-length (Kipp 1959). A high Kipp value indicates a more pointed wing, a low value a more rounded wing.

Measurements taken from study skins were not pooled with those of living birds because some measurements change when the skins dry. All measurements were exact to 0.5 mm. All measurements (wing, tail, tarsus, skull, beak measurements and Kipp index of males and females from Madagascar) were analysed using t tests in Minitab (Minitab 2005). Significance levels were set at P < 0.05. The plumage of all taxa studied has been described by Urquhart (2002) in much detail. Therefore, we provide only additional observations within the framework of those given by Urquhart.

Results

Phylogenetic relationships

We obtained 915- and 1041-bp fragments of the cytb and nd2 genes, respectively. Different tree-building methods (ML, MP, and NJ) all produced trees with a congruent topology (Fig. 2), therefore, only the ML tree obtained from the combined data set is shown in this communication. Saxicola rubicola, S. dacotiae and S. maurus form a clade (94% bootstrap support) representing stonechats from Europe and Asia. The African stonechats S. torquatus axillaris, S. tectes and S. torquatus sibilla form a separate clade (92% bootstrap support). Saxicola tectes and S. t. sibilla are both monophyletic (100% bootstrap support) and cluster as sibling species. Saxicola t. sibilla forms a distinct clade in all tree reconstructions, indicating a separate evolutionary lineage, while S. caprata and S. rubetra take basal positions (100 and 95% bootstrap support) in the stonechat tree.
https://static-content.springer.com/image/art%3A10.1007%2Fs10336-008-0290-1/MediaObjects/10336_2008_290_Fig2_HTML.gif
Fig. 2

Maximum likelihood (ML) tree based on a combined data set of the mitochondrial cytochrome b gene (cytb) and the NADH dehydrogenase subunit 2 (nd2) gene. ML bootstrap values ≥50% (1000 replicates) are indicated for each node. The ML model selected was GTR + I = 0.443 + Γ = 0.989. ML tree −lnL = 8665.02

Genetic distances

Genetic distances (P-distances) were obtained from the combined data set (cytb + nd2; see Table 2). The genetic distance between the African S. t. axillaris and S. tectes from La Réunion was 5.3%. The Malagasy S. t. sibilla is separated from S. t. axillaris by 4.9% and from S. tectes by 4.3%. Within the Eurasian stonechat taxa (Siberian and European) inter-specific distances are in the same range (4.5–4.9%). The variation within each taxon studied was low (P-distances <1%), and most of the birds from the same region presented identical sequences (except for S. t. axillaris from Kenya and Tanzania, which differed by 2.1% and are therefore less related than expected). Since the genetic distances between S. t. sibilla and other stonechats from mainland Africa and from La Réunion range from 4 to 5% and taking into account that these distances were far larger than those within individual species, S. t. sibilla can be considered to form a separate and distinct genetic lineage. If we assume the 2% rule for a molecular clock of protein-coding mitochondrial genes (Wilson et al. 1987; Tarr and Fleischer 1993), then S. t. sibilla, S. tectes and S. t. axillaris may have diverged from their common ancestor about 2–2.5 million years ago.
Table 2

Matrix of P-distances (mean values) for cytb and nd2 genes

Taxon

1

2

3

4

5

6

7

8

1. S. rubetra

9.9

9.9

10.6

12.3

10.5

9.8

11.1

2. S. rubicola

 

4.5

4.7

11.6

6.0

5.4

6.1

3. S. maurus

  

4.9

11.3

5.3

5.4

5.9

4. S. dacotiae

   

11.4

6.3

5.7

6.6

5. S. caprata

    

10.9

11.0

11.2

6. S. tectes

     

4.3

5.3

7. S. t. sibilla

      

4.9

8. S. t. axillaris

       

Plumage and morphometrics

The plumage of stonechats is difficult to describe because it gradually changes with feather wear, which may in turn obscure factual differences in colouration. In addition, individual variation between stonechats is large.

The outermost primary (P10) is 19–22 mm long and, when the wing is folded, the tip of P9 falls opposite to P3 and P4 or falls between them (on rare occasions it may fall between P2 and P3). The wing tip (n = 38) is formed by P7 (68%), by P6 and P7 (13%), by P6 (16%) and very rarely by P8 (3%). The primary projection is similar to that of S. rubicola, relatively short and rounded, with the wing point extending over about half the length of the overlying tertials (see Urquhart 2002, p 182).

Male stonechats S. t. sibilla have a black bill; their legs, upper parts, entire head, chin and throat are also black, and the chest, upper breast and occasionally the flanks are chestnut. The extent of black on the throat and chestnut on the breast has been used to describe subspecies by some authors. However, in some cases, the extent of chestnut seems to vary more between individuals than between taxa. For example, in contrast to the illustrations in Urquhart (2002), the chestnut of S. t. sibilla captured in the field and of those photographed in the collections was very rarely restricted to a small crescent; even in very worn plumage it varied from small to large, extending well onto the flanks. This variation was only partly explained by feather wear, and there was no geographic pattern (Fig. 3). This large individual variation is also known from other Saxicola taxa, such as captive S. t. axillaris from Kenya (B Helm, personal observation).
https://static-content.springer.com/image/art%3A10.1007%2Fs10336-008-0290-1/MediaObjects/10336_2008_290_Fig3_HTML.jpg
Fig. 3

Individual variation in the extent of the chestnut chest, upper belly and black throat in S. t. sibilla. C Central Madagascar, N north, S south, E east, W west, f fresh plumage, w worn plumage, m intermediate plumage. The numbers indicate collection numbers of the Muséum d’Histoire Naturelle Paris

The black tail feathers have—very rarely—some white at their bases; their cream-coloured edges can be up to 3 mm wide in fresh S. t. sibilla (best seen from below). In worn plumage, these tips disappear entirely. The rump is pale, and individual feather tips are chestnut in fresh plumage, but appear white when abraded. The warm chestnut edges on the mantle, scapulars and tertials become an increasingly duller brown with age, possibly due to bleaching by the sun. In fresh plumage, the black throat feathers sometimes have white tips up to 1 mm long, but in some individuals these tips are missing even when the plumage is fresh. They have broad, white- to cream-coloured fringes on the remiges (best visible when checked from below; see also Urquhart 2002). In fresh plumage, the underwing coverts of male S. t. sibilla have black bases with white tips often appearing as a mix of white and black (white in 17%, mixed in 71% and black in 12% of the birds, n = 42). In worn plumage, the axillaries may appear as an almost pure black.

Female S. t. sibilla differ from males by their less contrasting plumage. Their heads are brown and their upper parts dark brown to lighter brown when bleached out. Their rump is chestnut to light brown and occasionally shows some white in the centre of individual rump feathers. Only in very worn plumage does the rump appear predominantly white. Because females were underrepresented in the collections and rarely caught, we are not able to provide more accurate information about them.

As in many passerines, male stonechats from Madagascar are larger than females. Differences in wing length, tarsus, most beak measurements and Kipp index were significant (Table 3). There was no difference in tail length or weight.
Table 3

Measurements (mm) of male and female stonechats from Madagascar taken from museum skins and weight (g) of live birds from Maromizaha

Variable (mm)

Males

Females

Difference between males and females

n

Mean ± SE (range)

n

Mean ± SE (range)

t, P, df

Wing

40

69.3 ± 0.4 (65.0–73.0)

13

67.3 ± 0.4 (65.0–69.5)

3,42, 0.002*, 32

Tail

39

50.8 ± 0.4 (46.0–54.0)

13

49.9 ± 0.5 (47–53)

1.52, 0.14, 30

Tarsus

37

24.4 ± 0.2 (22.5–27.0)

11

23.8 ± 0.2 (23.0–25.0)

2.2, 0.04*, 28

Skull

37

16.2 ± 0.1 (15.2–17.1)

13

15.7 ± 0.1 (15–16.5)

3.49, 0.002*, 26

Bill length

36

8.1 ± 0.1 (7.2–8.7)

13

7.8 ± 0.1 (7.2–8.4)

2.17, 0.04*, 20

Bill width

36

4.1 ± 0.0 (3.5–4.5)

13

3.9 ± 0.1 (3.5–4.3)

2.30, 0.03*, 21

Bill depth

36

3.8 ± 0.1 (3.4–4.5)

13

3.8 ± 0.1 (3.4–4.1)

0.25, 0.81, 25

Kipp index

29

17.4 ± 0.2 (14.7–19.6)

12

16.4 ± 0.4 (14.0–18.4)

2.21, 0.04*, 16

Weight

18

15.6 ± 0.25 (13.3–17.4)

6

16.5 ± 0.59 (14–18.1)

1.38, 0.21, 6

* Significant at P < 0.05

t Tests were carried out to test for differences between males and females

Discussion

Our results based on mtDNA indicate that the Saxicola populations we have investigated here are genetically distinct and that stonechats from Eastern Madagascar differ from their geographic neighbours S. t. axillaris and S. tectes by a considerable sequence divergence (4.3–5.3%). As taxon sampling on Madagascar was limited to one site, we do not know how genetically divergent stonechats are within Madagascar. Furthermore, the status of S. torquatus ankaratrae (Salomonsen 1934) and S. torquatus tsaratananae (Milon 1950) still needs to be clarified. Nevertheless, based on our results, it is very likely that Malagasy stonechats, Saxicola torquatus sibilla (Linnaeus 1766), can be assigned species rank: Saxicolasibilla (Linnaeus 1766).

Our molecular data do not allow a complete reconstruction of the phylogenetic relationships, radiation, and evolution of stonechats (Wink et al. 2002a, b) and because some crucial regions in Africa were not sampled, the African sister group of the Malagasy/Réunion clade could not be identified with certainty. Additional taxa of the Saxicola-complex from Madagascar, Africa and Asia need to be included in the analysis to further clarify the systematic position and the biogeographical background of this assemblage. A more complete phylogenetic picture could inspire evolutionary scenarios of stonechat radiation and guide the interpretation of geographically distinct behavioural characteristics that have been described in this taxonomic group (Gwinner et al. 1983; Dittami and Gwinner 1985; Helm et al. 2005; Helm and Gwinner 2006).

Zusammenfassung

Die taxonomische Stellung des Madagaskarschwarzkehlchens (Saxicola torquatus sibilla) anhand von Nukleotidsequenzen mitochondrialer DNA

Schwarzkehlchen (Gattung Saxicola) sind Singvögel mit einer außergewöhnlich weitläufigen Brutverbreitung in der Alten Welt. Neuere Studien belegen, dass dieses Taxon eine weit stärkere geografische Differenzierung aufweist, als ursprünglich angenommen: So sind Afrikanische, Sibirische und Europäische Schwarzkehlchen deutlich verschiedenen monophyletischen Gruppen zuzuordnen und werden von manchen Autoren als eigene Arten angesehen. In der vorliegenden Arbeit stellen wir neue Untersuchungen zur geografischen Differenzierung innerhalb des Afrikanischen Schwarzkehlchens, Saxicola torquatus, vor. Die Analyse von Nukleotidsequenzen mitochondrialer NADH Dehydrogenase Untereinheit 2 und Cytochrome b Gene ergaben, dass Schwarzkehlchen aus dem Osten Madagaskars (Saxicola t. sibilla) eine eigene Gruppe darstellen. Gemeinsam mit Schwarzkehlchen des ostafrikanischen Festlandes (Saxicola t. axillaris) und dem Réunionschwarzkehlchen (Saxicola tectes) bilden sie eine monophyletische Gruppe.

Genetische und morphologische Daten legen nahe, dass das Madagaskarschwarzkehlchen sehr wahrscheinlich als eigene Art anzusehen ist: Saxicola sibilla (Linnaeus 1766). Eine genaue Beschreibung des Gefieders und verschiedener äußerer Körpermaße wird gegeben. Weitere vergleichende genetische, morphologische und bioakustische Untersuchungen von Taxa aus dem afrikanischen Saxicola-Komplex sind erforderlich, um die phylogenetische Stellung sowie die biogeografische Entwicklung der madagassischen Schwarzkehlchen abschließend zu klären.

Acknowledgments

We are indebted to the Malagasy Government for the permission to carry out parts of this research. Furthermore, our appreciation goes to the “NAT”-foundation for inviting us to work at Maromizaha. We thank our Malagasy colleagues at the University of Antananarivo, at ANGAP, the Ministère de l’Environnement, des Eaux et Forêts, Frank Hawkins from Conservation International and all the people that helped us in the field. The “Gesellschaft zur Förderung des Naturkundemuseums Stuttgart” funded part of this research. Hedi Sauer-Gürth (IPMB. Heidelberg) kindly sequenced the cytochrome b gene. We thank Heidrun and Jochen Albrecht, Hans-Heinrich Witt, Alexander Scheuerlein and Ingrid Schwabl for collecting samples. We also thank Eric Pasquet (Muséum National d’Histoire Naturelle, Paris), Sylke Frahnert (Museum für Naturkunde, Berlin) and Renate v.d. Elzen (Museum Alexander Koenig, Bonn) for kindly granting access to their bird collections. We thank Prof. Dr. H. Bock (Managing Director of IWR) and S. Friedel for access to parallel computing facilities at the Interdisciplinary Centre for Scientific Computing (IWR, Heidelberg University). T.C.H. Cole made valuable comments that improved this manuscript. We also thank two anonymous reviewers. All observations, field work and sampling complied with the regulations of the countries in which the study was carried out.

Copyright information

© Dt. Ornithologen-Gesellschaft e.V. 2008

Authors and Affiliations

  • Friederike Woog
    • 1
  • Michael Wink
    • 2
  • Eskandar Rastegar-Pouyani
    • 2
  • Javier Gonzalez
    • 2
  • Barbara Helm
    • 3
  1. 1.Staatliches Museum für Naturkunde StuttgartStuttgartGermany
  2. 2.Institut für Pharmazie und Molekulare BiotechnologieRuprecht-Karls-Universität HeidelbergHeidelbergGermany
  3. 3.Max Planck Institute for OrnithologyAndechsGermany