- Research article
- Open Access
Inter-familial relationships of the shorebirds (Aves: Charadriiformes) based on nuclear DNA sequence data
© Ericson et al; licensee BioMed Central Ltd. 2003
- Received: 23 May 2003
- Accepted: 23 July 2003
- Published: 23 July 2003
Phylogenetic hypotheses of higher-level relationships in the order Charadriiformes based on morphological data, partly disagree with those based on DNA-DNA hybridisation data. So far, these relationships have not been tested by analysis of DNA sequence data. Herein we utilize 1692 bp of aligned, nuclear DNA sequences obtained from 23 charadriiform species, representing 15 families. We also test earlier suggestions that bustards and sandgrouses may be nested with the charadriiforms. The data is analysed with methods based on the parsimony and maximum-likelihood criteria.
Several novel phylogenetic relationships were recovered and strongly supported by the data, regardless of which method of analysis was employed. These include placing the gulls and allied groups as a sistergroup to the sandpiper-like birds, and not to the plover-like birds. The auks clearly belong to the clade with the gulls and allies, and are not basal to most other charadriiform birds as suggested in analyses of morphological data. Pluvialis, which has been supposed to belong to the plover family (Charadriidae), represents a basal branch that constitutes the sister taxon to a clade with plovers, oystercatchers and avocets. The thick-knees and sheathbills unexpectedly cluster together.
The DNA sequence data contains a strong phylogenetic signal that results in a well-resolved phylogenetic tree with many strongly supported internodes. Taxonomically it is the most inclusive study of shorebird families that relies on nucleotide sequences. The presented phylogenetic hypothesis provides a solid framework for analyses of macroevolution of ecological, morphological and behavioural adaptations observed within the order Charadriiformes.
- Maximum Parsimony
- Nuclear Intron
- True Evolutionary History
- Myoglobin Gene
- Charadriiform Bird
Family-names for charadriiform birds The families included in the order Charadriiformes (sensu del Hoyo et al. 1996). Asterisks mark taxa that are not included in this study.
Lapwings and plovers
Coursers and pratincoles
Avocets and stilts
Sandpipers, snipes and phalaropes
Skuas and jaegers
While in broad agreement with the studies of Strauch  and Chu  the DNA-DNA hybridisation data of Sibley and Ahlquist  did not identify auks (Alcidae) as a separate lineage instead placing them as the sister taxon to gulls, terns, skimmers and skuas. Moreover, alternative relationships were recovered from the data when different tree-building algorithms were applied. This resulted in the gulls and their allies being placed as the sister group to the sandpiper-like birds rather than to the plover-like birds (op. cit. fig. 337). Several other differences occur between the results produced by the various datasets. For example, the Scolopacidae was found to be monophyletic in the analyses of Strauch  and Sibley and Ahlquist , while Chu  and Mickevich and Parenti  found the scolopacids to be paraphyletic. Obviously, the higher-level phylogeny of the shorebirds is still ambiguous. In this paper we investigate if DNA sequence data can be used to produce a more robust hypothesis of charadriiform relationships.
The choice of molecular markers becomes critical when old divergences are studied. Although the times of divergences among the extant charadriiform lineages are largely unknown, fossils of extinct groups commonly referred to the order Charadriiformes occur already in deposits dated to the Late Cretaceous . The oldest fossils assigned to modern families of charadriiforms date from the late Tertiary [11, 12]. It can thus be safely assumed that some branches in the phylogenetic tree for these taxa date back to the early Tertiary, if not longer. This is in agreement with the assumption, based on biogeography and molecular-clock models, that the evolution and diversification of several orders and families of extant birds have occurred in the late Cretaceous or Early Tertiary, some 100 to 50 mya [13–17]. It should be noted, however, that estimates of divergence times based on the fossil record are generally lower than those based on molecular data .
The old age of many bird taxa presents one explanation of why their higher-level systematic relationships have been difficult to resolve using mitochondrial sequence data [16, 19, 20]. The mitochondrial genes most commonly used in these studies (cytochrome b and 12S) are normally assumed to evolve at a rate of ~1% per million years . It has been argued that the cytochrome b gene gives reliable information in birds only for divergences younger than 9 million years , i.e. evolutionary events considerably younger than the evolution of most modern orders and families. Thus, to use DNA sequence data to resolve higher-level branching patterns among birds requires molecular markers that evolve considerably slower than the mitochondrial genome.
In recent years nuclear genes have been utilized for this purpose. The most commonly used nuclear markers are the protein-encoding c-myc, RAG-1, and c-mos genes with the former two evolving at rates 4 to 12 times slower than the mitochondrial cytochrome b gene in the same taxa (Ericson pers. obs.). The evolutionary rates of these genes may, however, be too slow for many studies as the number of mutations observed to accumulate between evolutionary branching events can be very low. This results in short internodes with poor statistical support in the phylogenetic tree, which in turn makes the phylogenetic hypotheses weak. To enhance studies of medium-old (ca 20–60 my) divergences in birds it is desirable to find molecular markers with slightly faster evolutionary rates than the protein-encoding nuclear genes used so far, and introns in nuclear genes may provide such markers.
Herein we use an intron positioned in the myoglobin gene, which has proven especially useful to resolve relationships among passerine birds [23–25], in addition to the protein-encoding RAG-1 gene. By using two independent molecular markers we can also compare the phylogenetic signal produced by each genic region. While a tree based on a single gene or region may be misleading purely because of stochastic factors [26, 27], observed congruence between individual gene trees increases the probability that they represent the true evolutionary history of the group.
Molecular variation and base compositions
A segment of 930 homologous base pairs from RAG-1 was obtained from all taxa with no indels detected. Sequences for the myoglobin intron II ranged from 693 base pairs (Alca torda, Larus fuscus) to 734 base pairs (Afrotis atra). The intron exhibited several indels, of which two were phylogenetically informative (one between positions 38 and 48, and the other between positions 532 and 544).
Despite sequencing in both directions with several primers, certain nucleotide positions could not be determined unambiguously. This relates to 24 positions in the RAG-1 sequences (0.1%), and 48 positions in the myoglobin sequences (0.3%). The observed polymorphisms may be due to true heterozygosity in the individual, but also to PCR or sequencing artefacts.
After alignment the data matrix consisted of 1692 base pairs, of which 930 base pairs derive from RAG-1 and 762 base pairs from myoglobin intron II. In RAG-1, 644 positions (69%) were constant, 164 (18%) were variable but not phylogenetically informative, while 122 (13%) were potentially informative. In myoglobin intron II 395 positions (52%) were constant, 207 (27%) variable but not phylogenetically informative, and 160 (21%) were potentially informative.
Sequence distances and patterns of substitutions
In RAG-1 the uncorrected sequence divergences between charadriiform taxa ranged from 0.1% (Catharacta vs. Stercorarius) to 7.1% (Chionis vs.Thinocorus) (Table 2, see Additional file 1). Divergences between charadriiform taxa and the columbiforms (dove and sandgrouse) and gruiforms (bustard and crane), ranged from 2.4% to 7.1%. Generally, larger distances were observed in comparisons involving the outgroup megapod and screamer (5.5% to 9.7%). The corresponding ranges in sequence divergences for myoglobin intron II were from less than 0.1% (Catharacta vs. Stercorarius) to 10.3% (Cursorius vs.Jacana) within the charadriiforms, from 6.1% to 14.6% between the charadriiforms and the columbiforms and gruiforms, and from 9.5% to 17.1% in comparisons involving the outgroups (Table 2, see Additional file 1). The pairwise sequence divergences were higher, on average, in myoglobin intron II than in RAG-1.
Monophyly of the Charadriiformes (sensu ) is strongly supported by the combined data set, with a bootstrap value of 94% in the maximum parsimony (MP) tree (Fig. 8), and a 100% Bayesian support in the maximum-likelihood (ML) tree (Fig. 7). Neither the sandgrouse (Pteroclididae) nor bustard (Otididae) clustered within the Charadriiformes, nor does either taxon unambiguously form the sister-group.
There is strong bootstrap support in both the parsimony and maximum-likelihood analyses for a division of the order into two major clades. The first consists of sandpiper-like birds (representing the families Scolopacidae, Jacanidae, Rostratulidae, Thinocoridae) along with gulls and their allies (Laridae, Sternidae, Rynchopidae, Stercorariidae), auks (Alcidae) and the coursers (Glareolidae). The second consists of plover-like birds (representing Charadriidae, Haematopodidae, Recurvirostridae) along with the sheathbill (Chionidae) and thick-knee (Burhinidae).
Within the first clade, two subclades are evident. One, comprising Alcidae, Stercorariidae, Laridae, Sternidae, Rynchopidae, and Glareolidae is strongly supported (MP: 100%, Bayesian: 100%) and defined by a synapomorphic indel between positions 532 and 544 in the myoglobin intron II. Relationships within this clade cannot be determined with certainty, but there is support (MP: 61%, Bayesian: 100%) for a dichotomy between Glareolidae and the rest. This dichotomy is also supported by a synapomorphic indel, between positions 38 and 48 of the myoglobin intron II. The second subclade comprises the family Scolopacidae (Arenaria, Calidris, Tringa, Phalaropus, Gallinago) that is sistergroup to a clade consisting of Jacanidae, Thinocoridae and Rostratulidae. The relationships within Scolopacidae are more difficult to determine although Gallinago is identified as the sister to all the others, in both trees. The relationships between Jacanidae, Thinocoridae and Rostratulidae cannot be established, although they appear to constitute a monophyletic group.
Within the second major clade a relationship between Burhinidae and Chionidae was strongly supported (MP: 99%, Bayesian: 100%), and a lineage including Charadriidae, Vanellidae, Recurvirostridae and Haematopodidae (MP: 94%, Bayesian: 100%) constitutes their sistergroup. The family Charadriidae is not recovered as monophyletic. Instead, Charadrius (Charadriidae) and Vanellus (Vanellidae) group together, with Recurvirostra (Recurvirostridae) and Haematopus (Haematopodidae) as their sister. Pluvialis (considered as belonging to Charadriidae) falls outside these four taxa.
There are two contradictions between the trees based on RAG-1 and myoglobin intron II, respectively (Fig. 9). According to the myoglobin intron II tree, Jacanidae and Thinocoridae constitute one group, and this group is the sister to Rostratulidae. In the RAG-1 tree, Jacanidae and Rostratulidae group together, with Thinocoridae as their sister. The low nodal support values indicate that the relationships between these three taxa are effectively unresolved in the present analyses. Furthermore, Alcidae is the sister to Glareolidae in the myoglobin tree, and to Stercorariidae in the RAG-1 tree, but neither suggestion receives bootstrap support.
Utility of the RAG-1 and myoglobin intron II sequences
Both nuclear DNA regions examined here were suitable for phylogenetic analyses at this taxonomic level as neither showed any sign of saturation in the present data set. This was expected for RAG-1 based on previous results obtained for analyses of avian data sets [24, 28–30] but was unexpected for the non-coding myoglobin intron II. Slade et al.  and Lessa  have previously advocated the use of nuclear introns as markers for resolving patterns of intra-specific differentiation in vertebrates and this approach has been adopted in population genetic studies of birds [33, 34]. More recently, nuclear introns have been used to reconstruct species-level phylogenies [35–41]. Their application at this taxonomic level is supported by comparative studies, which suggest that beta-fibrinogen intron 7 contains similar phylogenetic signal to the mitochondrial cytochrome b gene in birds . Based on these limited findings, saturation of nuclear intron sequences and poor phylogenetic resolution might logically be expected to occur at higher taxonomic levels. This was not observed for myoglobin intron II in the present data set, which examined intra-ordinal relationships. Despite its non-coding function myoglobin intron II appeared to evolve at a rate only about 60% faster than that of the RAG-1 gene.
The analysis of the concatenated nuclear DNA sequences strongly supports monophyly of the charadriiform order, albeit that the two genes provide markedly less support when analysed individually. Contrary to certain previous suggestions [11, 42, 43] there is no support for the placement of the sandgrouse or bustard within the charadriiforms. Neither do the data provide strong support for a link between the Columbiformes and Charadriiformes with the two columbiform outgroups (Pterocles and Scardafella) occurring basal in the maximum-likelihood tree and as part of an unsupported basal polytomy in the maximum-parsimony analysis.
The charadriiform families clearly divide into three clades consistent with DNA-DNA hybridisation data although the relationships among these clades differ from those reported by . One of the best-supported groupings of charadriiform families in the present analysis consists of the Lari (gulls, terns, skimmers and jaegers) along with the Alcae (auks, puffins, murrelets and allies) and glareolids (coursers and pratincoles). This group constitutes the Laroidea of  and has never been suggested as forming a monophyletic group on the basis of morphology. The auks and their allies, considered basal in morphological analyses [4–6], are clearly nested within the Lari and form the sister group to the Stercorariidae (skuas and jaegers) in most analyses. The Glareolidae are basal in this group. Although the taxonomic boundaries of the Glareolidae have been disputed it is most often considered to include six genera Glareola, Cursorius, Rhinoptilus, Smutsornis, Stiltia and Pluvianus, of which only two were studied herein. Given the uncertainty about the monophyly of Glareolidae, it is worth noting that the DNA-DNA hybridization study included two other glareolid genera (Glareola and Stiltia) than those used herein (Cursorius and Rhinoptilus).
Relationships within the Lari are not firmly resolved by the present data, although the relationships suggested, with the skimmers (Rynchopidae) as sister to gulls and terns (Laridae and Sternidae) and skuas (Stercorariidae) basal are identical to the results based on DNA-DNA hybridization and consistent with the morphological analyses of Schnell [44, 45]. In comparing 51 measurements from skeletal elements among 93 species of jaegers, skuas, gulls, terns, and skimmers, Schnell concluded that skimmers are most similar to terns, and that the differences between jaegers and gulls are greater than those between gulls and terns.
The remaining Charadrii families included in this study divide into two clades, one comprising the sandpiper-like birds (Scolopacidae, Jacanidae and Thinocoridae), and the other the plover-like birds (Charadiidae, Recurvirostridae, Haemtopodidae) along with sheathbills (Chionidae) and thick-knees (Burhinidae). The sandpiper-like birds unambiguously form the sistergroup to the Lari-Alcae-glareolid clade with strong bootstrap support in both methods of analysis (MP: 81%, Bayesian: 100%). This systematic arrangement is rather unusual. Based on morphology, the gulls and allies have traditionally been placed together with the plover-like birds [3, 6], a relationship also suggested by UPGMA analysis of DNA-DNA hybridization data . However, the application of an alternative clustering algorithm (FITCH) to the DNA-DNA hybridization data groups the gull and allies with the sandpiper-like birds [: fig. 337], in accordance with the results of the present study.
The clade containing the sandpiper-like birds includes a well-supported, monophyletic group of scolopacid taxa, and a likewise well-supported group consisting of the jacana, painted snipe and seedsnipe. Relationships among the latter three taxa are unresolved although maximum-likelihood analysis, skeletal morphology  and the down patterns of the young  suggest a closer relationship between jacanas and painted-snipes. Their sister clade includes all scolopacid representatives included in the study with the snipe (Gallinago) as the basal taxon and a sister-relationship between the turnstone (Arenaria) and sandpiper (Calidris) recovered in all analyses. These scolopacid relationships agree well with the results based on DNA-DNA hybridization data. Neither the low (60%) support for this clade in the maximum-likelihood analysis, nor the likewise low (0.3) delta-T50 value in the study of the DNA-DNA hybridization data, allow strong hypotheses about the evolutionary relationships between phalaropes, shanks, and other scolopacids to be formulated.
The remaining clade containing the plover-like birds (plover, lapwing, avocet and oystercatcher), sheathbill and thick-knee is basal in the phylogeny. The intra-relationships of this clade match closely those suggested by DNA-DNA hybridization data, and only the position of the plover Pluvialis differs. In the DNA-DNA hybridization study Pluvialis groups adjacent to a clade containing the plover (Charadrius) and lapwing, while the present data places it basal to all other plover-like birds including the oystercatcher and avocet. The distinctiveness of Pluvialis and its basal position relative to other plover-like birds is also supported by the allozyme data of . It is highly unexpected that the oystercatchers and avocets should be nested within the Charadriidae, as suggested by the present data, and this issue needs further investigation.
The analysis of the sequence data places a clade with the thick-knee and sheathbill as the sistergroup to the plover-lapwing-oystercatcher-avocet group, but the branch leading to this larger clade is short and receives no statistical support. The relationship between the thick-knee (Burhinus) and sheathbill (Chionis) is well supported, however. As with many other systematic relationships supported by the DNA sequence data analysed herein, the grouping of the thick-knee with the sheathbill is unexpected when morphology and general behaviour are taken into consideration. However, the same relationship is strongly suggested by Paton et al.  who analyzed DNA sequences obtained from the complete RAG-1 gene.
The DNA sequence data obtained from two segments of the nuclear genome provides independent estimates of the phylogenetic relationships of the charadriiform birds. The great similarity between the two resulting phylogenies suggests that the concatenated data set can be used to infer the true evolutionary history of the group. Parsimony and maximum-likelihood analyses of the combined sequences resulted in a well-resolved phylogenetic tree with many strongly supported internodes. The DNA sequence data suggests that the order Charadriiformes is monophyletic, and that the sandgrouses and bustards are not part of it. It is also suggested that the order be divided into two major groups. In the first, a clade of gulls, terns, skimmers, auks and jaegers forms the sistergroup of the coursers and pratincoles, while another clade, consisting of scolopacids (sandpipers and allied groups), jacanas, painted-snipes and seedsnipes, constitutes the sistergroup of them. The second major group of charadriiform birds consists of, on one hand, the plovers, lapwings, oystercatchers and avocets, and the thick-knees and sheathbills on the other. The presented phylogenetic hypothesis provides a solid framework for analyses of macroevolution of ecological and behavioural adaptations observed within the order Charadriiformes.
23 individuals representing 15 of the 18 families of the order Charadriiformes were selected for study (Table 3). As monophyly of Charadriiformes has not been unequivocally demonstrated by morphology, we also included representatives of two taxa that have been proposed to be close to the shorebirds, or nested within them [cf. [11, 42, 43]]. These are a sandgrouse (Pterocles gutturalis, Pteroclididae) and a bustard (Afrotis atra, Otididae). As the alternative systematic positions of these two taxa are with the pigeons and the gruiform birds, respectively, two representatives of these were also included (Scardafella squammata, Columbidae, and Grus canadensis, Gruidae). As outgroups, we include a screamer (Chauna torquata, Anhimidae) and a megapod (Alectura lathami, Megapodiidae) which are members of the Galloanserae, the presumed sistergroup to Neoaves (sensu ) to which the shorebirds belong.
Samples used in the study Acronyms: FMNH: Field Museum of Natural History; LSUZM: Museum of Natural Science, Lousiana State University; NMWM: National Museum of Namibia; NRM: Swedish Museum of Natural History; PFIAO: Percy FitzPatrick Institute of African Ornithology, University of Cape Town; TJP: Thomas J. Parsons.
Lesser Black-backed Gull
South Polar Skua
Extraction, amplification, and sequencing
DNA was extracted from tissue or blood specimens using the QIAamp® DNA Mini Kit (QIAGEN®) following the manufacturer's recommendations, or by standard techniques of Proteinase K/SDS digestion followed by phenol chloroform extraction and ethanol precipitation, as described in . Polymerase chain reaction (PCR) amplifications were carried out with Ready-To-Go® PCR Beads (Amersham Pharmacia Biotech, Uppsala, Sweden), with 1 μl of each primer, 22 μl distilled water, and 1 μl template. Different combinations of four primers: R17, R22, R50, and R51 were used for the amplification of RAG-1 [28, 29] using a step-down PCR protocol. This involved an initial soak at 94°C for 5 min, followed by four cycles of 94°C for 40 s, 63°C for 60 s, and 72°C for 60 s, followed by four cycles at 60°C annealing and 32 cycles at an annealing temperature of 55°C with the same temperatures and intervals. There was a final soak; 72°C for 5 min. Myoglobin intron II was amplified using the primer Myo2 in combination with Myo3F or Myo3 [31, 49]. For some taxa nested PCR was used, whereby the Myo2/Myo3 amplicon was re-amplified with Myo2/Myo3F. Thermocycling procedures for the myoglobin intron began with a soak at 94°C for 5 min, followed by 40 cycles of 94°C for 40 s, 59°C for 40 s and 72°C for 5 min and completed with a final soak at 72°C for 5 min.
The products from the PCR were purified using QIAquick™ PCR purification Kit (QIAGEN®), and then sequenced with Perkin Elmer Applied BioSystems 377 automated fluorescent sequencing instruments, and Perkin Elmer Applied BioSystems PRISM terminator cycle sequencing kits, with AmpliTaq FS polymerase with BigDye terminators. Both strands were sequenced. Sequencing of myoglobin intron II was performed using the primers Myo2, Myo3F, Myoint.c and Myoint.nc [25, 31, 49]. The segment corresponds to the region between positions 303 (exon 2) and 400 (exon 3) in humans (GenBank XM009949) and includes the complete intron II, as well as 13 and 10 base pairs of the flanking exons 2 and 3, respectively . RAG-1 was sequenced using the primers R50, R51, R52, and R53 . The fragment obtained corresponds to positions 1054–1983 in the published chicken sequence .
The multiple segments obtained by sequencing with different primers were assembled to complete sequences using SEQ MAN II™ (DNASTAR®). When nucleotides could not be unambiguously determined the IUB coding system  was used. The combined sequences were then aligned by eye with MEG ALIGN™ (DNASTAR®). The sequences are deposited in GenBank (accession numbers AY339073-AY339126).
MEGA 2.0  was used to determine nucleotide variation and divergence values. To investigate the extent of saturation in RAG-1 and the myoglobin intron the number of transitions and transversions were plotted against uncorrected sequence divergence (p-distance). This was done to determine whether RAG-1 should be partitioned in order to down-weight saturated positions and to assess the phylogenetic usefulness of the non-coding myoglobin intron at these taxonomic levels. In addition, the pairwise uncorrected sequence divergences for the two genic regions were plotted against each other to compare their evolutionary properties.
Parsimony and maximum-likelihood analyses were performed using PAUP* 4.0b10 , designating Chauna torquata and Alectura lathami as outgroups. Parsimony analyses were performed for the two genic regions separately, and for both genic regions combined. Searches for most parsimonious trees were done under the heuristic search option, with random additions of taxa and tree bisection-reconnection (TBR) branch-swapping. Ten random additions were performed to reduce the risk of finding local optima only. Data were unweighted and coded as unordered. Gaps were treated as missing values. Strict consensus trees were generated and nodal supports estimated with 1000 bootstrap replicates with a 50% majority rule applied.
MODELTEST 3.06  was used to choose the model of substitutions for the maximum-likelihood analysis of the combined data set. This program determines the simplest model of evolution that cannot be rejected in favour of a more complex one that gives a significantly better tree. The model chosen for the analysis was the GTR + Γ + I time-reversible model for nucleotide substitutions, with six types of substitutions and the proportions of invariable sites and shape parameter alpha estimated (I = 0.212 and α = 1.105). These estimates were used in a heuristic search with TBR branch-swapping. Ten random additions of taxa were performed. A Bayesian inference analysis was performed using MR BAYES 2.01 , with the Markov chain Monte Carlo method. 400,000 generations were run and every hundredth tree after stabilisation was saved. The remaining 3000 trees were imported into PAUP* 4.0b10 , and posterior probabilities were obtained from the 50% majority-rule consensus tree calculated from these.
An analysis of DNA sequences of the entire RAG-1 gene (c. 2.9 kb) obtained from representatives of a similar set of taxa as studied herein will shortly be published by Paton et al. . The two studies are entirely independent but arrive at very similar conclusions about phylogenetic relationships within the Charadriiformes. The studies complement each other despite having analyzed partly overlapping DNA sequences obtained from the RAG-1 gene. Although we studied a shorter stretch (930 bp) of the RAG-1 gene than did Paton et al., we also included information from a second nuclear marker (myoglobin intron II). The low degree of conflicts observed between the RAG-1 and myoglobin gene trees, along with the general agreement between the studies of Paton et al. and ourselves, lend confidence to the hypothesis that the observed phylogenetic patterns accurately reflect the evolutionary history of the shorebirds.
We thank the Field Museum of Natural History, Chicago; Museum of Natural Science, Louisiana State University; National Museum of Namibia, Windhoek; Percy FitzPatrick Institute of African Ornithology, University of Cape Town; Swedish Museum of Natural History; and Thomas J. Parsons for providing tissue. We are also thankful to Ulf S. Johansson, Pia Eldenäs and Mari Källersjö for help and advice in the laboratory. Thanks also to Les Christidis, Christer Erseus, Niklas Janz, Ulf S. Johansson and two anonymous reviewers for commenting on the manuscript. This work has been funded by the Swedish Research Council (grant no. 621-2001-2773 to P.E.) and the Swedish Museum of Natural History.
- del Hoyo J, Elliott A, Sargatal J, Eds: Handbook of the Birds of the World, volume 3. Hoatzin to Auks. 1996, Barcelona: Lynx editionsGoogle Scholar
- Peters JL: Check-list of Birds of the World. 1934, Cambridge: Harvard University Press, 2:Google Scholar
- Strauch JG: The phylogeny of the Charadriiformes (Aves): A new estimate using the method of character compatibility analysis. Transactions of the Zoological Society of Lond. 1978, 34: 263-345.View ArticleGoogle Scholar
- Mickevich MF, Parenti LR: Review of, "The phylogeny of the Charadriiformes (Aves): a new estimate using the method of character compatibility analysis.". Systematic Zoology. 1980, 29: 108-113.View ArticleGoogle Scholar
- Björklund M: Phylogenetic relationships among Charadriformes: reanalysis of previous data. Auk. 1994, 111: 825-832.View ArticleGoogle Scholar
- Chu PC: Phylogenetic reanalysis of Strauch's osteological data set for the Charadriiformes. Condor. 1995, 97: 174-196.View ArticleGoogle Scholar
- Jehl JR: Relationships in the Charadrii (shorebirds): a taxonomic study based on color patterns of the downy young. San Diego Soc Nat Hist Memoir. 1968, 3: 1-54.Google Scholar
- Sibley CG, Ahlquist JE: Phylogeny and classification of Birds. A study in molecular evolution. 1990, New Haven: Yale University PressGoogle Scholar
- Christian PD, Christidis L, Schodde R: Biochemical systematics of the Charadriiformes (shorebirds): relationships between the Charadrii, Scolopaci and Lari. Australian Journal of Zoology. 1992, 40: 291-302.View ArticleGoogle Scholar
- Hope S: The Mesozoic radiation of Neornithes. In Mesozoic Birds: Above the Heads of Dinosaurs. Edited by: Chiappe LM, Witmer L. 2002, Berkeley: University of California Press, 339-388.Google Scholar
- Olson SL: The fossil record of birds. In Avian Biology 8. Edited by: Farner DS, King JR, Parkes KC. 1985, New York: Academic Press, 79-238.View ArticleGoogle Scholar
- Hou L, Ericson PGP: A Middle Eocene shorebird from China. Condor. 2002, 104: 896-899.View ArticleGoogle Scholar
- Cooper A, Penny D: Mass survival of birds across the Cretaceous-Tertiary boundary: molecular evidence. Science. 1997, 275: 1109-1113. 10.1126/science.275.5303.1109.View ArticlePubMedGoogle Scholar
- van Tuinen M, Hedges SB: Calibration of avian molecular clocks. Molecular Biology and Evolution. 2001, 18: 206-213.View ArticlePubMedGoogle Scholar
- Cracraft J: Avian evolution, Gondwana biogeography and the Cretaceous-Tertiary mass extinction event. Proceedings of the Royal Society of London Ser B. 2001, 268: 459-469. 10.1098/rspb.2000.1368.View ArticleGoogle Scholar
- Ericson PGP, Christidis L, Cooper A, Irestedt M, Jackson J, Johansson US, Norman JA: A Gondwanan origin of passerine birds supported by DNA sequences of the endemic New Zealand wrens. Proceedings of the Royal Society of London Ser B. 2002, 269: 235-241. 10.1098/rspb.2001.1877.View ArticleGoogle Scholar
- Paton T, Haddrath O, Baker AJ: Complete mitochondrial DNA genome sequences show that modern are not descended from transitional shorebirds. Proceedings of the Royal Society of London Ser B. 2002, 269: 839-846. 10.1098/rspb.2002.1961.View ArticleGoogle Scholar
- Feduccia A: The Origin and Evolution of Birds. 1996, New Haven: Yale University PressGoogle Scholar
- van Tuinen M, Sibley CG, Hedges SB: The early history of modern birds inferred from DNA sequences of nuclear and mitochondrial ribosomal genes. Molecular Biology and Evolution. 2000, 17: 451-457.View ArticlePubMedGoogle Scholar
- García-Moreno J, Mindell DP: Rooting a phylogeny with homologous genes on opposite sex chromosomes (gametologs): a case study using avian CHD. Molecular Biology and Evolution. 2000, 17: 1826-1832.View ArticlePubMedGoogle Scholar
- Fleischer RC, McIntosh CE, Tarr CE: Evolution in a volcanic conveyor belt: using phylogeographic reconstructions and KAr-based ages of the Hawaiian Islands to estimate molecular evolutionary rates. Molecular Ecology. 1998, 7: 533-545. 10.1046/j.1365-294x.1998.00364.x.View ArticlePubMedGoogle Scholar
- Moore WJ, DeFillippis VR: The window of taxonomic resolution for phylogenies based on mitochondrial cytochrome b. In Avian Molecular Evolution and Systematics. Edited by: Mindell DP. 1997, San Diego: Academic Press, 84-119.Google Scholar
- Hunt JS, Bermingham E, Ricklefs RE: The molecular systematics and biogeography of antillean thrashers, tremblers, and mockingbirds (Aves: Mimidae). Auk. 2001, 118: 35-55.View ArticleGoogle Scholar
- Ericson PGP, Christidis L, Irestedt M, Norman JA: Systematic affinities of the lyrebirds (Passeriformes: Menura), with a novel classification of the major groups of passerine birds. Molecular Phylogenetics and Evolution. 2002, 25: 53-62. 10.1016/S1055-7903(02)00215-4.View ArticlePubMedGoogle Scholar
- Irestedt M, Fjeldså J, Johansson US, Ericson PGP: Systematic relationships and biogeography of the tracheophone suboscines (Aves: Passeriformes). Molecular Phylogenetics and Evolution. 2002, 23: 499-512. 10.1016/S1055-7903(02)00034-9.View ArticlePubMedGoogle Scholar
- Pamilo P, Nei M: Relationships between gene trees and species trees. Molecular Biology and Evolution. 1988, 5: 568-583.PubMedGoogle Scholar
- Avise JC: Gene trees and organismal histories: a phylogenetic approach to population biology. Evolution. 1989, 43: 1192-1208.View ArticleGoogle Scholar
- Groth JG, Barrowclough GF: Basal divergences in birds and the phylogenetic utility of the nuclear RAG-1 gene. Molecular Phylogenetics and Evolution. 1999, 12: 115-123. 10.1006/mpev.1998.0603.View ArticlePubMedGoogle Scholar
- Irestedt M, Johansson US, Parsons TJ, Ericson PGP: Phylogeny of major lineages of suboscines (Passeriformes) analysed by nuclear DNA sequence data. Journal of Avian Biology. 2001, 32: 15-25. 10.1034/j.1600-048X.2001.320103.x.View ArticleGoogle Scholar
- Johansson US, Parsons TJ, Irestedt M, Ericson PGP: Clades within "higher land birds", evaluated by nuclear DNA sequences. Journal of Zoological Systematics and Evolutionary Research. 2001, 39: 37-51. 10.1046/j.1439-0469.2001.00153.x.View ArticleGoogle Scholar
- Slade RW, Moritz C, Heideman A, Hale PT: Rapid assessment of single-copy nuclear DNA variation in diverse species. Molecular Ecol. 1993, 2: 359-373.View ArticleGoogle Scholar
- Lessa EP: Rapid surveying of DNA sequence variation in natural populations. Molecular Biology and Evolution. 1992, 9: 323-330.PubMedGoogle Scholar
- Friesen VL, Congdon BC, Walsh HE, Birt TP: Intron variation in marbled murrelets detected using analyses of single-stranded conformational polymorphisms. Molecular Ecology. 1997, 6: 1047-1058. 10.1046/j.1365-294X.1997.00277.x.View ArticlePubMedGoogle Scholar
- Congdon BC: Mechanisms of population differentiation in marbled murrelets: historical versus contemporary processes. Evolution. 2000, 54: 974-986.View ArticlePubMedGoogle Scholar
- Johnson KP, Clayton DH: A molecular phylogeny of the dove genus Zenaida: Mitochondrial and nuclear DNA sequences. Condor. 2000, 102: 864-870.View ArticleGoogle Scholar
- Johnson KP, Clayton DH: Nuclear and mitochondrial genes contain similar phylogenetic signal for pigeons and doves (Aves: Columbiformes). Molecular Phylogenetics and Evolution. 2000, 14: 141-151. 10.1006/mpev.1999.0682.View ArticlePubMedGoogle Scholar
- Prychitko TM, Moore WS: Comparative evolution of the mitochondrial cytochrome b gene and nuclear beta-fibrinogen intron 7 in woodpeckers. Molecular Biology and Evolution. 2000, 17: 1101-1111.View ArticlePubMedGoogle Scholar
- Johnson KP, de Kort S, Dinwoodey K, Mateman AC, ten Cate C, Lessells CM, Clayton DH: A molecular phylogeny of the dove genera Streptopelia and Columba. Auk. 2001, 118: 874-887.View ArticleGoogle Scholar
- Nicholls JA: Molecular systematics of the thornbills, Acanthiza. Emu. 2001, 101: 33-37. 10.1071/MU00064.View ArticleGoogle Scholar
- Weibel AC, Moore WS: A test of a mitochondrial gene-based phylogeny of woodpeckers (genus Picoides) using an independent nuclear gene, beta-fibrinogen intron 7. Molecular Phylogenetics and Evolution. 2002, 22: 247-257. 10.1006/mpev.2001.1062.View ArticlePubMedGoogle Scholar
- Saetre GP, Borge T, Lindroos K, Haavie J, Sheldon BC, Primmer CR, Syvanen AC: Sex chromosome evolution and speciation in Ficedula flycatchers. Proceedings of the Royal Society of London. Ser. B. 2003, 270: 53-59. 10.1098/rspb.2002.2204.View ArticleGoogle Scholar
- Maclean GL: Die systematische Stellung der Flughühner (Pteroclididae). Journal für Ornithologie. 1967, 108: 203-217.View ArticleGoogle Scholar
- Hendrickson HT: A comparative study of egg white proteins of some species of the avian order Gruiformes. Ibis. 1969, 111: 80-91.View ArticleGoogle Scholar
- Schnell GD: A phenetic study of the suborder Lari (Aves) I: Methods and results of principal component analyses. Systematic Zoology. 1970, 19: 35-57.View ArticleGoogle Scholar
- Schnell GD: A phenetic study of the suborder Lari (Aves) II. Phenograms, discussion, and conclusions. Systematic Zoology. 1970, 19: 264-302.View ArticlePubMedGoogle Scholar
- Paton TA, Baker AJ, Groth JG, Barrowclough GF: RAG-1 sequences resolve phylogenetic relationships within Charadriiform birds. Molecular Phylogenetics and Evolution.Google Scholar
- Sibley CG, Monroe BL: Distribution and taxonomy of birds of the world. 1990, New Haven: Yale University PressGoogle Scholar
- Norman JA, Christidis L, Westerman M, Hill AR: Molecular analysis confirms the species status of the Christmas Island Hawk-Owl (Ninox natalis). Emu. 1998, 98: 197-208.View ArticleGoogle Scholar
- Heslewood MM, Elphinstne MS, Tidemann SC, Baverstock PR: Myoglobin intron variation in the Gouldian Finch Erythura gouldiae assessed by temperature gradient gel electrophoresis. Electrophoresis. 1998, 19: 142-151.View ArticlePubMedGoogle Scholar
- Carlson LM, Oettinger MA, Schatz DG, Masteller EL, Hurley EA, McCormack WT, Baltimore D, Thompson CB: Selective expression of RAG-2 in chicken b cells undergoing immunoglobulin gene conversion. Cell. 1991, 64: 201-208.View ArticlePubMedGoogle Scholar
- Johansson US, Ericson PGP: Molecular support for a sister group relationship between Pici and Galbulae (Piciformes sensu Wetmore 1960). Journal of Avian Biology. 2003, 34: 185-197. 10.1034/j.1600-048X.2003.03103.x.View ArticleGoogle Scholar
- IUB Nomenclature Committee: European Journal of Biochemistry. 1985, 150: 1-5.View ArticleGoogle Scholar
- Kumar S, Tamura K, Jakobsen IB, Nei M: MEGA2: molecular evolutionary genetics analysis software. Bioinformatics. 2001, 17: 1244-1245. 10.1093/bioinformatics/17.12.1244.View ArticlePubMedGoogle Scholar
- Swofford DL: PAUP*: Phylogenetic analysis using parsimony (* and other methods), version 4.0. 1998, Sunderland: SinauerGoogle Scholar
- Posada D, Crandall KA: MODELTEST: testing the model of DNA substitution. Bioinformatics. 1998, 14: 817-818. 10.1093/bioinformatics/14.9.817.View ArticlePubMedGoogle Scholar
- Huelsenbeck JP, Ronquist F, Hall B: MrBayes: Bayesian inference of phylogeny. Bioinformatics. 2001, 17: 754-55. 10.1093/bioinformatics/17.8.754.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.