Comparative morphology of the radial carpal bone of neornithine birds and the phylogenetic significance of character variation

The morphology of the radial carpal bone (os carpi radiale) of neornithine birds is for the first time evaluated in a comparative context. An unexpected morphological variation of this bone is documented, and characteristic derived morphologies are identified. One of these characterizes a subclade of Accipitridae, which includes the taxa Harpiinae, Circinae, Melieraxinae, Accipitrinae, Milvinae, Haliaeetinae, Buteoninae, and Aquilinae. Another derived morphology of the radial carpal is found in the Picocoraciae, the clade including Coraciiformes sensu stricto, Alcediniformes, Bucerotes, and Piciformes. This latter morphology is absent in Leptosomidae and Trogonidae and constitutes the first morphological apomorphy of Picocoraciae. A distinctive morphology of the radial carpal is further present in passeriform birds. Character variation of the radial carpal provides new data for the evaluation of conflicting phylogenetic hypotheses, and it is detailed that the morphology of this bone further contributes to a phylogenetic placement of controversial avian taxa in the fossil record.     

Metaves,Mirandornithes, Strisores and other novelties – a critical review of the higher‐level phylogeny of neornithine birds

Recent hypotheses on the higher‐level phylogeny of modern birds are reviewed, and areas of agreement and major conflict are detailed, with emphasis being put on congruence among independent molecular and morphological data sets. Although molecular data significantly contributed to a better understanding of avian phylogeny, they do not seem to be free of homoplasy and caution is warranted in the interpretation of some results. The recently proposed ‘Metaves’ clade is likely to be an artefact of the β‐fibrinogen gene, and current molecular data do not yield well‐supported phylogenies for some groups whose interrelationships can be resolved with morphological evidence. There exists, however, congruent and strong molecular evidence for several novel clades that were not recognized by morphologists before, and to ease future discussions the terms Picocoraciae (non‐leptosomid ‘Coraciiformes’ and Piciformes) and Aequornithes (‘waterbird assemblage’) are introduced. Molecular studies further congruently recover some clades, which have not yet been adequately appreciated and are outlined in the present review.     

Evolutionary relationships among copies of feather beta ({beta}) keratin genes from several avian orders

The feather beta (β) keratins of the white leghorn chicken (order Galliformes, Gallus gallus domesticus) are the products of a multigene family that includes claw, feather, feather-like, and scale genes (Presland et al. 1989a). Here we characterize the feather β-keratin genes in additional bird species. We designed primers for polymerase chain reactions (PCR) using sequences available from chicken, cloned the resulting amplicons to isolate individual copies, and sequenced multiple clones from each PCR reaction for which we obtained amplicons of the expected size. Feather β-keratins of 18 species from eight avian orders demonstrate DNA sequence variation within and among taxa, even in the protein-coding regions of the genes. Phylogenies of these data suggest that Galliformes (fowl-like birds), Psittaciformes (parrots), and possibly Falconiformes (birds of prey) existed as separate lineages before duplication of the feather β-keratin gene began in Ciconiiformes (herons, storks, and allies), Gruiformes (cranes, rails, and allies), and Piciformes (woodpeckers and allies). Sequences from single species of Coraciiformes (kingfishers) and Columbiformes (pigeons) are monophyletic and strikingly divergent, suggesting feather β-keratin genes in these birds also diverged after these species last shared a common ancestor with the other taxa investigated. Overall, these data demonstrate considerable variation in this structural protein in the relatively recent history of birds, and raise questions concerning the origin and homology of claw, feather-like, and scale β-keratins of birds and the reptilian β-keratins.     

XLIV.—Some Observations on the Base: Pennulum Ratio and Angular Ratio of the Barbules of the Primaries in various Groups of Birds.

The base: pennulum ratio and the angular ratio generally vary according to the affinities of the bird, and appear sometimes to be correlated; but in Strigiformes, (Caprimulgi, and possibly some Falconiformes the base: pennulum ratio has probably been modified by special adaptation.
The base is relatively longer and the distal angle relatively more acute in most Coraciomorphæ, especially the orders Passeriformes, Piciformes, and Coraciiformes, than in Alectoromorphæ, Pelargomorphæ, and Colymbomorphæ.
In the Galli the base: pennulum ratio is distinctly and uniformly higher, and the angular ratio is usually lower, than in other Alectoromorphæ.
In base: pennulum and angular ratios the Crypturiformes seem to agree fairly closely with the Galli.
The arrangement of the barbules in Dromœus is essentially similar to that found in the Carinatæ.
Finally, it must be emphasized that these observations are of a preliminary nature.     

Higher-order phylogeny of modern birds (Theropoda, Aves: Neornithes) based on comparative anatomy. II. Analysis and discussion

In recent years, avian systematics has been characterized by a diminished reliance on morphological cladistics of modern taxa, intensive palaeornithogical research stimulated by new discoveries and an inundation by analyses based on DNA sequences. Unfortunately, in contrast to significant insights into basal origins, the broad picture of neornithine phylogeny remains largely unresolved. Morphological studies have emphasized characters of use in palaeontological contexts. Molecular studies, following disillusionment with the pioneering, but non-cladistic, work of Sibley and Ahlquist, have differed markedly from each other and from morphological works in both methods and findings. Consequently, at the turn of the millennium, points of robust agreement among schools concerning higher-order neornithine phylogeny have been limited to the two basalmost and several mid-level, primary groups. This paper describes a phylogenetic (cladistic) analysis of 150 taxa of Neornithes, including exemplars from all non-passeriform families, and subordinal representatives of Passeriformes. Thirty-five outgroup taxa encompassing Crocodylia, predominately theropod Dinosauria, and selected Mesozoic birds were used to root the trees. Based on study of specimens and the literature, 2954 morphological characters were defined; these characters have been described in a companion work, approximately one-third of which were multistate (i.e. comprised at least three states), and states within more than one-half of these multistate characters were ordered for analysis. Complete heuristic searches using 10 000 random-addition replicates recovered a total solution set of 97 well-resolved, most-parsimonious trees (MPTs). The set of MPTs was confirmed by an expanded heuristic search based on 10 000 random-addition replicates and a full ratchet-augmented exploration to ascertain global optima. A strict consensus tree of MPTs included only six trichotomies, i.e. nodes differing topologically among MPTs. Bootstrapping (based on 10 000 replicates) percentages and ratchet-minimized support (Bremer) indices indicated most nodes to be robust. Several fossil Neornithes (e.g. Dinornithiformes, Aepyornithiformes) were placed within the ingroup a posteriori either through unconstrained, heursitic searches based on the complete matrix augmented by these taxa separately or using backbone-constraints. Analysis confirmed the topology among outgroup Theropoda and achieved robust resolution at virtually all levels of the Neornithes. Findings included monophyly of the palaeognathous birds, comprising the sister taxa Tinamiformes and ratites, respectively, and the Anseriformes and Galliformes as monophyletic sister-groups, together forming the sister-group to other Neornithes exclusive of the Palaeognathae (Neoaves). Noteworthy inferences include: (i) the sister-group to remaining Neoaves comprises a diversity of marine and wading birds; (ii) Podicipedidae are the sister-group of Gaviidae, and not closely related to the Phoenicopteridae, as recently suggested; (iii) the traditional Pelecaniformes, including the shoebill (Balaeniceps rex) as sister-taxon to other members, are monophyletic; (iv) traditional Ciconiiformes are monophyletic; (v) Strigiformes and Falconiformes are sister-groups; (vi) Cathartidae is the sister-group of the remaining Falconiformes; (vii) Ralliformes (Rallidae and Heliornithidae) are the sister-group to the monophyletic Charadriiformes, with the traditionally composed Gruiformes and Turniciformes (Turnicidae and Mesitornithidae) sequentially paraphyletic to the entire foregoing clade; (viii) Opisthocomus hoazin is the sister-taxon to the Cuculiformes (including the Musophagidae); (ix) traditional Caprimulgiformes are monophyletic and the sister-group of the Apodiformes; (x) Trogoniformes are the sister-group of Coliiformes; (xi) Coraciiformes, Piciformes and Passeriformes are mutually monophyletic and closely related; and (xii) the Galbulae are retained within the Piciformes. Unresolved portions of the Neornithes (nodes having more than one most-parsimonious solution) comprised three parts of the tree: (a) several interfamilial nodes within the Charadriiformes; (b) a trichotomy comprising the (i) Psittaciformes, (ii) Columbiformes and (iii) Trogonomorphae (Trogoniformes, Coliiformes) + Passerimorphae (Coraciiformes, Piciformes, Passeriformes); and (c) a trichotomy comprising the Coraciiformes, Piciformes and Passeriformes. The remaining polytomies were among outgroups, although several of the highest-order nodes were only marginally supported; however, the majority of nodes were resolved and met or surpassed conventional standards of support. Quantitative comparisons with alternative hypotheses, examination of highly supportive and diagnostic characters for higher taxa, correspondences with prior studies, complementarity and philosophical differences with palaeontological phylogenetics, promises and challenges of palaeogeography and calibration of evolutionary rates of birds, and classes of promising evidence and future directions of study are reviewed. Homology, as applied to avian examples of apparent homologues, is considered in terms of recent theory, and a revised annotated classification of higher-order taxa of Neornithes and other closely related Theropoda is proposed. (c) 2007 The Linnean Society of London, Zoological Journal of the Linnean Society, 2007, 149, 1-95.     

Phylogenetic relationships in the louse genus Penenirmus based on nuclear (EF-1α) and mitochondrial (COI) DNA sequences

Abstract. Ischnoceran lice in genus Penenirmus are parasites of birds in orders Piciformes and Passeriformes. No comprehensive revision of this genus has been published, but a few host-based revisions have been done. Here we present a phylogenetic analysis of Penenirmus based on nuclear (elongation factor-1 alpha) and mitochondrial (cytochrome oxidase I) gene sequences. Sequences from portions of both these genes provide a well resolved tree that is relatively stable across methods of analysis and to bootstrap resampling. Some aspects of the Penenirmus phylogeny reflect the phylogeny of their avian hosts. We identified monophyly of a group of Penenirmus species occurring on Passeriformes as well as monophyly of a group containing species sometimes placed in a genus Picophilopterus . Species of Penenirmus occurring on Old World barbets fall in several positions at the base of the tree, suggesting that other lineages of Penenirmus may be derived from those occurring on Old World barbets.     

Alignment and phylogenetic analysis of beta-fibrinogen intron 7 sequences among avian orders reveal conserved regions within the intron

We sequenced beta-fibrinogen intron 7 (beta-fibint 7) from 28 species of birds, representing 18 families in nine orders. Although the antiquity of the avian orders is estimated to be 55 to 90 Myr, and numerous indels have accrued among diverging lineages, the intron sequences were not difficult to align. However, alignment of avian sequences with mammal or snake sequences was difficult, and the residual phylogenetic signal was weak. beta-fibint 7 is an AT-rich intron, and its base composition varies little over the diversity of birds represented by our sample. Alignment of these anciently diverged sequences reveals at least five clusters of conserved nucleotides; at least two clusters appear to be in excess of the minimal set usually associated with intron excision, but their functions are unknown. Two equally most-parsimonious (MP) trees were found when indels were not included in the phylogenetic analysis, and six such trees were found when indels were included. The Neighbor-Joining and maximum-likelihood trees were identical to each other and to one of the MP trees in each MP analysis. Indels, as well as nucleotide substitutions, are phylogenetically informative, and bootstrap support exceeded 90% for 21 of 24 inferred nodes when indels were included in the MP analysis. All traditional orders represented by two or more species appear monophyletic. Relationships among avian orders are strongly supported with the exception of an inferred sister-group relationship between Caprimulgiformes and Columbiformes. A relatively close relationship between Piciformes and Passeriformes is inferred, at odds with earlier DNA-DNA hybridization studies but consistent with traditional classifications. Among Passeriformes, the traditional perspective of a sister-group relationship of suboscines and oscines is supported, as is the subsequent split of the oscines into a lineage representative of the Corvida before the diversification of the Passerida. The four species of owls divide into two strongly supported clades, corresponding to the widely accepted bifurcation of owls into two families, Tytonidae and Strigidae. A sister-group relationship between gallinaceous birds and waterfowl, the Galloanserae, is also strongly supported.     

Cestodes d'oiseaux de Côte-d'Ivoire. II. Parasites de Coraciiformes et Piciformes

Résumé Les cestodes récoltés en Côte d'Ivoire chez deux ordres d'oiseaux, les Coraciiformes et les Piciformes, sont présentés. Un nouveau genre, Thaumasiolepis (Hymenolepididae, Hymenolepidinae), est créé et discuté. Il comprend des cestodes récoltés chez différentes espèces de Capitonidae et caractérisés par des crochets rostraux spiniformes tout à fait originaux. L'espèce T. microarmata est créée pour ce matériel. D'autre part deux nouveaux Raillietina de Picidae, R. (S.) campetherae et R. (P.) yapoensis sont décrits. R. (S.) campetherae est la première espèce de ce sous genre trouvée chez les Piciformes. Biuterina meropina macrancistrota est trouvé chez Merops albicollis. Ce taxon est élevé au rang d'espèce et devient par conséquent B. macrancistrota Fuhrmann, 1908. Skrjabinoporus merops (Woodland, 1928) Spassky & Borgarenko, 1960 est retrouvé. Cette espèce peu commune est redécrite et sa position parmi les Metadilepididae confirmée. Enfin, Raillietina cf (P.) bargetzii Mahon, 1954 est signalé chez Gymnobucco calvus.

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Cestodes collected in the two bird orders, the Coraciiformes and the Piciformes, in the Ivory Coast are presented. The new genus Thaumasiolepis (Hymenolepididae, Hymenolepidinae) is created and discussed. It includes cestodes collected in two species of the Capitonidae. Its main characteristic is the presence of very unusual spiniform hooks. The species T. microarmata is created for this material. We also describe two new species of Raillietina parasitising the Picidae, R. (P.) yapoensis and R. (S.) campetherae, the latter being the first species of this subgenus recorded from the Piciformes. In addition, Biuterina meropina macrancistrota has been found in Merops albicollis. We recognize a full specific status for this taxon which becomes B. macrancistrota Fuhrmann, 1908. Skrjabinoporus merops (Woodland, 1928) Spassky & Borgarenko, 1960 has been rediscovered. This rare species is redescribed and its position among the Metadilepididae is confirmed. Finally, Raillietina cf (P.) bargetzii Mahon, 1954 is recorded from Gymnobucco calvus.

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Ce travail fait partie de la thèse du premier auteur.     

Clades within the ‘higher land birds’, evaluated by nuclear DNA sequences

In this study we investigated the phylogenetic relationships within the ‘higher land birds’ by parsimony analysis of nucleotide DNA sequences obtained from the two nuclear, protein-coding genes, c- myc and RAG-1. Nuclear genes have not previously been used to address this phylogenetic question. The results include high jackknife support for a monophyletic Apodiformes (including the Trochilidae). This arrangement was further supported by the observation of an insertion of four amino acids in the c- myc gene in all apodiform taxa. Monophyly was also inferred for each of the two piciform groups Galbulae and Pici. Within Pici, the Capitonidae was found to be paraphyletic, with the New World barbets more closely related to the Ramphastidae than to the Old World barbets. Another clade with high jackknife support consists of the Upupidae, Phoeniculidae and Bucerotidae. The families Momotidae and Todidae, and Coraciidae and Brachypteraciidae, respectively, also form well supported monophyletic clades. The results are inconclusive regarding the monophyly of the orders Coraciiformes and Piciformes, respectively.     

ON THE FORAGING METHOD OF THE BANDED GYMNOGENE

Bennett, G. F., Earlé, R. A. &; Peirce, M. A. 1993. The Leucocytozoidae of South African birds: Musophagiformes, Cuculiformes and Piciformes. Ostrich 64:73-78.

The leucocytozoids of the avian orders Musophagiformes, Cuculiformes and Piciformes are reviewed. Leucocytozoon dinizi Tendeiro, 1947 of the Musophagidae is re-described and a neohapantotype designated. Leucocytozoon centropi Fantham, 1921 is re-described and L. coccyzus Coatney &; West, 1938 is synonymized with it and a neohapantotype designated. Leucocytozoon squamatus Nandi, 1986 of the Pi-cidae is re-described and compared with Leucocytozoon capitonis n. sp. of the piciform family Capitonidae.     

Molecular support for a sister group relationship between Pici and Galbulae (Piciformes sensu Wetmore 1960)

Woodpeckers, honeyguides, barbets, and toucans form a well-supported clade with approximately 355 species. This clade, commonly referred to as Pici, share with the South American clade Galbulae (puffbirds and jacamars) a zygodactyls foot with a unique arrangement of the deep flexor tendons (Gadow's Type VI). Based on these characters, Pici and Galbulae are often considered sister taxa, and have in traditional classification been placed in the order Piciformes. There are, however, a wealth of other morphological characters that contradicts this association, and indicates that Pici is closer related to the Passeriformes (passerines) than to Galbulae. Galbulae, in turn, is considered more closely related to the rollers and ground-rollers (Coracii). In this study, we evaluate these two hypotheses by using DNA sequence data from exons of the nuclear RAG-1 and c- myc genes, and an intron of the nuclear myoglobin gene, totally including 3400 basepairs of aligned sequences. The results indicate a sister group relationship between Pici and Galbulae, i.e. monophyly of the Piciformes, and this association has high statistical support in terms of bootstrap values and posterior probabilities. This study also supports several associations within the traditional order Coraciiformes, including a sister group relationship between the kingfishers (Alcedinidae) and a clade with todies (Todidae) and motmots (Momotidae), and with the bee-eaters (Meropidae) placed basal relative to these three groups.     

Size and structure of the bird genome--I. DNA content of 48 species of Neognathae

The nuclear DNA content was evaluated in 48 species of Neognathae birds belonging to 13 orders, namely Anseriformes, Charadriiformes, Columbiformes, Ciconiiformes, Falconiformes, Galliformes, Gruiformes, Passeriformes, Pelicaniformes, Phoenicopteriformes, Piciformes, Psittaciformes and Strigiformes. The DNA content, expressed in pg/nucleus, ranges from 2.81 to 4.97. The genome size variability within and among families is discussed on the basis of the Hinegardner's (1976) model of genome evolution.     

Epizootiology, development, and pathology of Geopetitia aspiculata Webster, 1971 (Nematoda: Habronematoidea) in tropical birds at the Assiniboine Park Zoo, Winnipeg, Canada

Geopetitia aspiculata was found in 12 species of Passeriformes, one species of Coraciiformes, and one species of Charadriiformes which died in a free-flight area in the Tropical House at the Assiniboine Park Zoo, Winnipeg, Canada. The nematodes occurred in chronic inflammatory cysts attached to the serosa of the posterior end of the esophagus, proventriculus, and the anterior part of the gizzard. Posterior ends of worms were observed to extend from the cyst into the lumen of the proventriculus. Birds hatched and raised in the Tropical House acquired infections, probably through the agency of feral crickets. Experimental studies showed that G. aspiculata developed to the infective third stage in the fat body of Acheta domesticus (L.). This is the first transmission cycle of Geopetitia spp. to be elucidated and the egg, first, third, and early fifth stages of the parasite are described. The absence of spicules in males of G. aspiculata is confirmed. Geopetitia aspiculata was probably introduced to the Zoo by infected tropical birds obtained from dealers or other zoos. The wild source of the parasite is not known since G. aspiculata has never been reported in wild birds; the report of G. aspiculata in wild Piciformes in Cuba by Barus (1971) is in error.     

The global distribution of frugivory in birds

Aim To examine patterns of avian frugivory across clades, geography and environments. Location Global, including all six major biogeographical realms (Afrotropics, Australasia, Indo‐Malaya, Nearctic, Neotropics and Palaearctic). Methods First, we examine the taxonomic distribution of avian frugivory within orders and families. Second we evaluate, with traditional and spatial regression approaches, the geographical patterns of frugivore species richness and proportion. Third, we test the potential of contemporary climate (water–energy, productivity, seasonality), habitat heterogeneity (topography, habitat diversity) and biogeographical history (captured by realm membership) to explain geographical patterns of avian frugivory. Results Most frugivorous birds (50%) are found within the perching birds (Passeriformes), but the woodpeckers and allies (Piciformes), parrots (Psittaciformes) and pigeons (Columbiformes) also contain a significant number of frugivorous species (9–15%). Frugivore richness is highest in the Neotropics, but peaks in overall bird diversity in the Himalayan foothills, the East African mountains and in some areas of Brazil and Bolivia are not reflected by frugivores. Current climate explains more variance in species richness and proportion of frugivores than of non‐frugivores whereas it is the opposite for habitat heterogeneity. Actual evapotranspiration (AET) emerges as the best single climatic predictor variable of avian frugivory. Significant differences in frugivore richness and proportion between select biogeographical regions remain after differences in environment (i.e. AET) are accounted for. Main conclusions We present evidence that both environmental and historical constraints influence global patterns of avian frugivory. Whereas water–energy dynamics possibly constrain frugivore distribution via indirect effects on food plants, regional differences in avian frugivory most likely reflect historical contingencies related to the evolutionary history of fleshy fruited plant taxa, niche conservatism and past climate change. Overall our results support an important role of co‐diversification and environmental constraints on regional assembly over macroevolutionary time‐scales.     

The haemoproteids of the avian families Eurylaimidae (broadbills) and Pittidae (pittas)

The haemoproteids of the avian suboscine families Eurylaimidae and Pittidae are reviewed. Haemoproteus eurylaimus n. sp. and H. pittae n. sp. are described.     

The phylogenetic relationships of the early Tertiary Primoscenidae and Sylphornithidae and the sister taxon of crown group piciform birds

The phylogenetic relationships of the early Tertiary Primoscenidae and Sylphornithidae are, for the first time, evaluated in a cladistic context. Both taxa include small arboreal birds with a permanently (Primoscenidae) or facultatively (Sylphornithidae) retroverted fourth toe. Primoscenidae were hitherto considered to be most closely related to either woodpeckers and allies (Piciformes) or to songbirds (Passeriformes), whereas the Sylphornithidae were classified into the roller-kingfisher-hornbill assemblage (Coraciiformes). Analysis of 56 morphological characters supports monophyly of a clade including Sylphornithidae and crown group Piciformes and results in sister group relationship between Passeriformes and a clade including Primoscenidae and the early Miocene Zygodactylidae. However, an analysis in which the search was constrained to trees supporting piciform affinities of the Primoscenidae resulted in trees that were only five steps longer than those from the primary analysis. The character evidence for each hypothesis is discussed. The systematic position of the Primoscenidae appears to be connected to the identity of the sister taxon of crown group Piciformes, as the primary search indicated Upupiformes (hoopoes and wood-hoopoes) and Bucerotiformes (hornbills) as sister taxa of Piciformes, whereas the constrained search resulted in sister group relationship between Coliiformes (mousebirds) and Piciformes. Songbirds do not show the slightest indication of a zygodactyl foot but in these birds the hindtoe is greatly elongated, an alternative strategy to increase the grasping capabilities of the foot. If Passeriformes are indeed the sister group of the clade (Primoscenidae + Zygodactylidae), these birds would be an example that, in closely related taxa, selection towards the same functional demands can result in entirely different morphological specializations.Communicated by F. Bairlein     

A miscellaneous collection of bird karyotypes

In the framework of a project on bird sexing for zoos, orcein stained karyotypes were studied of 16 species belonging to 7 avian orders, viz.Tinamus solitarius (Tinamiformes),Scopus umbretta, Jabiru mycteria, Mycteria cinerea, Ciconia (=Dissoura) (episcopus) stormi andC. (=D.) e. episcopus (Ciconiiformes),Aburria pipile cumanensis, A. p. grayi, Penelope purpurascens, Lagopus lagopus andArborophila orientalis (Galliformes),Phalcoboenus megalopterus (Falconiformes),Burhinus magnirostris (Charadriiformes),Carpococcyx renauldi (Cuculiformes), andCeratogymna (=Bycanistes) subcylindricus andC.(=B.) bucinator (Coraciiformes). With the exception ofCiconia (=Dissoura) e. episcopus, all these karyotypes are new to cytology. They are briefly described and compared to karyotypes of the respective families and orders known from the literature. Cytotaxonomic implications are briefly discussed. The karyotypes ofBurhinus magnirostris (2n=42),Ceratogymna subcylindricus (2n=44) andC. bucinator (2n=40) exhibit the lowest diploid chromosome numbers hitherto found in birds. Of these, the twoCeratogymna species almost completely lack microchromosomes.     

Two new species of Haemoproteus Kruse, 1890 (Haemosporida,Haemoproteidae) from European birds,with emphasis on DNA barcoding for detection of haemosporidians in wildlife

Two new species of Haemoproteus Kruse, 1890 (Haemosporida, Haemoproteidae) are described: Haemoproteus (Parahaemoproteus) homovelans n. sp. from Grey-faced Woodpecker, Picus canus Gmelin, and Haemoproteus (Parahaemoproteus) concavocentralis n. sp. recorded in Hawfinch, Coccothraustes coccothraustes (Linnaeus), both sampled in Bulgaria. The morphology of the gametocytes and their host-cells are described and mitochondrial cytochrome b (cyt b) gene sequences are generated. Haemoproteus homovelans possesses circumnuclear gametocytes lacking volutin granules. This parasite is particularly similar to Haemoproteus velans Coatney & Roudabush, 1937 also possessing circumnuclear gametocytes that are, however, overfilled with volutin. Haemoproteus concavocentralis can be readily distinguished from all described avian haemoproteids due to the presence of an unfilled concave space between the central part of advanced gametocytes and erythrocyte nucleus. Bayesian phylogenetic analyses of 40 haemosporidian cyt b lineages showed close relationships of H. concavocentralis (hHAWF2) with a group of Haemoproteus spp. possessing gametocytes that are pale-stained with Giemsa. The lineage hPICAN02 of H. homovelans clustered with parasites infecting non-passerine birds. Phylogenetic analyses support the current subgeneric classification of the avian haemoproteids and suggest that cyt b lineage hPIPUB01 (GenBank EU254552) has been incorrectly assigned to Haemoproteus picae Coatney & Roudabush, 1937, a common parasite of corvid birds (Passeriformes). This study emphasises the importance of combining molecular techniques and light microscopy in the identification and field studies of avian haemosporidian parasites. Future development of barcodes for molecular identification of haemoproteids will allow better diagnostics of these infections, particularly in veterinary studies addressing insufficiently investigated tissue pathology caused by these parasites.     

Risks to Birds Traded for African Traditional Medicine: A Quantitative Assessment

Few regional or continent-wide assessments of bird use for traditional medicine have been attempted anywhere in the world. Africa has the highest known diversity of bird species used for this purpose. This study assesses the vulnerability of 354 bird species used for traditional medicine in 25 African countries, from 205 genera, 70 families, and 25 orders. The orders most represented were Passeriformes (107 species), Falconiformes (45 species), and Coraciiformes (24 species), and the families Accipitridae (37 species), Ardeidae (15 species), and Bucerotidae (12 species). The Barn owl (Tyto alba) was the most widely sold species (seven countries). The similarity of avifaunal orders traded is high (analogous to “morphospecies”, and using Sørensen''s index), which suggests opportunities for a common understanding of cultural factors driving demand. The highest similarity was between bird orders sold in markets of Benin vs. Burkina Faso (90%), but even bird orders sold in two geographically separated countries (Benin vs. South Africa and Nigeria vs. South Africa) were 87% and 81% similar, respectively. Rabinowitz''s “7 forms of rarity” model, used to group species according to commonness or rarity, indicated that 24% of traded bird species are very common, locally abundant in several habitats, and occur over a large geographical area, but 10% are rare, occur in low numbers in specific habitats, and over a small geographical area. The order with the highest proportion of rare species was the Musophagiformes. An analysis of species mass (as a proxy for size) indicated that large and/or conspicuous species tend to be targeted by harvesters for the traditional medicine trade. Furthermore, based on cluster analyses for species groups of similar risk, vultures, hornbills, and other large avifauna, such as bustards, are most threatened by selective harvesting and should be prioritised for conservation action.