100,510 research outputs found
The Effect of a Doctor of Physical Therapy Program Curriculum on Cultural Competence Among Students at a Public, Midsize, Midwestern University
No full textDoctor of Physical Therapy (DPT) and other healthcare professional education programs have been charged with developing a culturally competent healthcare workforce in order to better meet the needs of diverse communities and reduce health inequities. The purpose of this quantitative, longitudinal, quasi-experimental educational intervention dissertation-in-practice (DIP) study was to examine the effects of an integrated DPT program curriculum on student cultural competence at a public, midsize, midwestern university. The Intercultural Development Inventory (IDI) was administered to three separate student cohorts across four different timepoints, including upon entry into the program (baseline) and at the end of the first, second, and third year. Developmental Orientation (DO) and Orientation Gap (OG) scores from the IDI were utilized. Data analysis was performed using descriptive statistics, independent and dependent samples t-tests, and one-way ANOVA with pairwise comparison. Results showed statistically significant improvements in both DO and OG scores from baseline to the end of the DPT didactic curriculum; however, significant change only occurred during Year 1 (p < 0.001) with a medium effect size (d = 0.63 for DO, d = 0.68 for OG). With greater understanding and visibility, the study findings were analyzed, leveraged, and incorporated into recommendations for curricular revision and program reform targeting cultural competence development among DPT students.ProQuest Traditional Publishing Optio
Geocerthia Chesser and Claramunt
No full textGeocerthia Chesser and Claramunt, genus nov. Type species. Upucerthia serrana Taczanowski, 1875. Included species. Geocerthia serrana (Taczanowski, 1875) comb. nov., Striated Earthcreeper. Diagnosis, morphology. Large earthcreeper (19–20 cm, 44–52 g, Remsen 2003). Bill longish, decurved; face grizzled brown and whitish; whitish superciliary; crown medium-dark brown with pale streaking, especially on forehead; back medium brown with faint pale streaking; wings, tail, and uppertail coverts rufous; throat whitish; underparts dull gray-brown with prominent pale streaking. Geocerthia differs from true Upucerthia earthcreepers, which have long, thin, highly decurved bills, by its comparatively shorter and stouter decurved bill and its overall darker plumage. Distinguished from all Cinclodes and Upucerthia species by its rufous wings, uppertail coverts, and tail. Lacks the wingband typical of Cinclodes species. Etymology. From the Greek geo (earth) and certhia (treecreeper), referring to the terrestrial habits of G. serrana and to its bill, which resembles those of the treecreepers. The construction of the name is a direct parallel to the English name earthcreeper. The name is feminine. Molecular analyses. A molecular analysis of furnariid species revealed that Geocerthia is sister to a clade composed of all species of Cinclodes and all species of Upucerthia sensu stricto, which in turn are sister taxa. To demonstrate that Geocerthia and Upucerthia are not sister genera, we present an analysis of a subset of taxa from the larger study. Taxon sampling for this subset (Table 1) included representatives of U. serrana, all other species of the traditional genus Upucerthia (Upucerthia, Tarphonomus, Ochetorhynchus), two species of Cinclodes, and single species of the genera Furnarius, Leptasthenura, Synallaxis, Certhiaxis, Pseudocolaptes, Philydor, Thripadectes, Automolus, and Lochmias. We used as outgroups the dendrocolaptines Dendrocincla fuliginosa, Drymornis bridgesii, and Xiphorhynchus fuscus, as well as the basal furnariid Geositta isabellina. As a simple test of its monophyly and phylogenetic relationships, a second individual of Geocerthia serrana (ZMUC [Zoological Museum, University of Copenhagen] S 444; GenBank Accession #s: EF 635339, EF 635358, EF 635319) was sequenced. This individual differed from the first by only one nucleotide substitution and grouped with it in all analyses in which it was included (results not shown). Table 1. Tissues used in the phylogenetic analysis. Taxon Museum Tissue ID Locality Geositta isabellina AMNH 12181 CHILE: Region Metropolitana, 15 km ENE Embalse El Yeso, ca. 3400m Upucerthia dumetaria AMNH 10396 ARGENTINA: Prov. Neuquén, Sierra Auca Mahuida . albigula LSUMNS B 61491 PERU: Depto. Arequipa, 14 km E Pancarpata, 3222m . jelskii LSUMNS B 103886 PERU: Depto. Tacna, Tacna-Ilave Road, ca 25 km NE Tarata, 4050m. validirostris LSUMNS B 17160 ARGENTINA: Prov. Tucumán, 12 km N, 4 km W Tafi de Valle, 3060 m. serrana LSUMNS B 49662 PERU: Depto. Lima, Santa Eulalia road, ca 86 km NE Lima Tarphonomus certhioides LSUMNS B 18872 BOLIVIA: Depto. Santa Cruz, Estancia Perforación, ca 130 km E Charagua, 520 m harterti LSUMNS B 34573 BOLIVIA: Depto. Santa Cruz, Tambo, 14 km SE Camarapa Ochetorhynchus andaecola LSUMNS B 1199 BOLIVIA: Depto. La Paz;, 2.5 km by road S Mecapaca, ca 26 km by road S Calacoto, 3050m . ruficaudus LSUMNS B 103908 PERU: Depto. Arequipa, km 60 on Div. Arequipa-Juliaca road, ca 10 road km W Chaguata . phoenicurus AMNH 9943 ARGENTINA: Prov. Río Negro, 20 km E Ñorquinco, 1000 m. melanura AMNH 12148 CHILE: Region Metropolitana, ca 4 km SSW by road from peak of Cerro de El Roble, ca 1600 m Cinclodes fuscus AMNH 12169 CHILE: Region Metropolitana, 2 km ENE Embalse El Yeso, ca. 2500 m Taxon Museum Tissue ID Locality . nigrofumosus AMNH 12164 CHILE: Region Valparaíso, Roca Brava, ca. 2 km N Zapallar Furnarius figulus FMNH 392828 BRAZIL: Estado Alagoas, Piranhas, Fazenda Bela Vista . rufus AMNH 10431 ARGENTINA: Prov. Neuquén, Centenario Leptasthenura aegithaloides AMNH 10306 ARGENTINA: Prov. Neuquén, Sierra Auca Mahuida Synallaxis albescens AMNH 2295 BOLIVIA: Depto. Santa Cruz, 300 m N of Rio Mercedes, 600 m Certhiaxis cinnamomeus AMNH 6190 BOLIVIA: Depto. Santa Cruz, 300 m N of Rio Mercedes, 600 m Pseudocolaptes lawrencii AMNH 3694 COSTA RICA: Prov. Herodia, 3 km N Porrosati, 2200 m Philydor pyrrhodes AMNH 8864 VENEZUELA: Estado Amazonas, Mrakapiwie Thripadectes rufobrunneus AMNH 3651 COSTA RICA: Prov. San Jose, Cerro de la Muerte, 3350 m Automolus rufipileatus LSUMNS B 1074 BOLIVIA: Depto. La Paz, Río Beni, ca 20 km by river N Puerto Linares, 600 m Lochmias nematura AMNH 12074 ARGENTINA: Prov. Misiones, Parque Provincal Urugua-i, ca. 1 km W park headquarters, Ruta Provincial 19, ca 400 m Dendrocincla fuliginosa AMNH 12706 VENEZUELA: Estado Amazonas; Río Baria, Cerro de la Neblina Base Camp Drymornis bridgesii LSUMNS B 25799 PARAGUAY: Depto. Alto Paraguay, Madrejón Xiphorhynchus fuscus LSUMNS B 35576 BRAZIL: Estado Bahia, ca 16 km W Porto Seguro RPPN Vera Cruz Tissue collections: LSUMNS – Louisiana State University Museum of Natural Science, Baton Rouge; AMNH – American Museum of Natural History, New York; FMNH – Field Museum of Natural History, Chicago. Total DNA was extracted from 25 mg of pectoral muscle using the DNeasy kit (Qiagen) and the standard protocol. Following methods described in Chesser et al. (2007), we amplified and sequenced the mitochondrial genes ND 3 and CO 2, and the autosomal nuclear gene beta-fibrinogen intron 7. Following the same methods, we amplified and sequenced an additional mitochondrial gene (ND 2) using the primers H 6313 (Johnson and Sorenson 1998) and L 5215 (Hackett 1996). Two additional nuclear protein-coding genes (RAG 1 and RAG 2) were included for one individual from each genus. These RAG sequences were taken from Moyle et al. (2009) except for those of Geocerthia serrana, which we amplified and sequenced following the methods in Moyle et al. (2009). The six-gene concatenated dataset included 6,970 base pairs after alignment issues and unique inserts were excluded from BF 7, the nuclear intron. An exception to a complete dataset was a partial BF 7 sequence for the individual representing Ochetorhynchus andaecola. In addition, the ND 2 gene could not be amplified for the selected individuals of Philydor pyrrhodes or Lochmias nematura; ND 2 sequence from a second individual of these same species (amplified for a separate analysis) was used instead. Because the dataset included protein-coding mitochondrial genes, a nuclear intron and protein-coding nuclear genes, it was unlikely that a single nucleotide substitution model would provide the best fit to the data. To determine the best partition of the dataset, we evaluated six different partitioning regimes ranging from unpartitioned to the maximum of sixteen partitions. Partitions were examined by performing maximum likelihood (ML) analyses using RAxML 7.0. 4 on the Cipres Portal V 1.5 (http://www.phylo.org/sub_sections/portal/). RAxML implements the GTR+Γ model and this was applied in each partition regime. We used the Akaike Information Criterion (AIC) to choose the best partitioning strategy, which was the GTR+ Γ+I model and fully partitioned dataset. We then used RAxML to evaluate nodal support by performing 150 bootstrap replicates (Stamatakis et al. 2008). The analysis resulted in a single maximum-likelihood tree (-log L = 28529.0) with high bootstrap support for most relationships (Fig. 1). Individuals of Upucerthia sensu stricto formed a strongly supported clade (100 % bootstrap) that was sister to Cinclodes. The Upucerthia - Cinclodes clade was well supported (100 %), and the single species G. serrana received strong support as sister to this clade (92 %). These results clearly demonstrate that G. serrana is not a member of the Upucerthia clade.Published as part of Chesser, Terry, Claramunt, Santiago, Derryberry, Elizabeth & Brumfield, Robb T., 2009, Geocerthia, a new genus of terrestrial ovenbird (Aves: Passeriformes: Furnariidae), pp. 64-68 in Zootaxa 2213 on pages 64-67, DOI: 10.5281/zenodo.18990
Geocerthia, a new genus of terrestrial ovenbird (Aves: Passeriformes: Furnariidae)
No full textChesser, Terry, Claramunt, Santiago, Derryberry, Elizabeth, Brumfield, Robb T. (2009): Geocerthia, a new genus of terrestrial ovenbird (Aves: Passeriformes: Furnariidae). Zootaxa 2213: 64-68, DOI: 10.5281/zenodo.18990
Pseudasthenes Aleixo, Chesser, Jr & Brumfield, 2010, genus nov.
No full textPseudasthenes, genus nov. Type species. Synallaxis patagonica d’Orbigny, 1839 Included species. Asthenes patagonica (d’Orbigny 1839), Asthenes cactorum Koepcke 1959, Asthenes humicola (Kittlitz 1830), Asthenes steinbachi (Hartert 1909). Diagnosis. We were unable to identify a synapomorphic phenotypic character for the genus, but the four species share the following features: small furnariids (15–22 g), with predominantly gray and brown plumage and no streaks on dorsal parts; gular patch feathers black and white, or dull orange (P. cactorum) but never a combination of black and orange; tail slightly longer than wing (tail/wing ratio 1.1–1.3), graduated (rectrix 6 / rectrix 1 ratio 0.55–0.70), and composed of 12 blunt rectrices with well-integrated barbs (except for the tip in some species). Phylogenetic diagnosis: the most inclusive crown clade that includes Asthenes patagonica and A. humicola but not Pseudoseisura lophotes or Spartonoica maluroides (d'Orbigny & Lafresnaye) (Baycapped Wren-Spinetail). Etymology. The generic name, from the Greek pseudo (false) and asthenes (insignificant, strengthless), denotes the outward resemblance of species of this genus to species of Asthenes but highlights the fact that they are not closely related. The name is feminine in gender. Genetic analyses. A preliminary genetic analysis of our data from all furnariid species found that Pseudasthenes was sister to a clade composed of Pseudoseisura and Spartonoica. This preliminary analysis also indicated that Asthenes, as currently recognized, is not monophyletic because Schizoeaca and Oreophylax are nested within it. To demonstrate that Asthenes is not monophyletic, and to propose a new hypothesis for phylogenetic relationships among Asthenes, Schizoeaca, and Oreophylax, we present an analysis of a subset of taxa from this larger study. This restricted analysis includes all species of Asthenes except A. heterura (Berlepsch) (Maquis Canastero) and A. berlepschi (Hellmayr) (Berlepsch’s Canastero), all species of Schizoeaca except S. coryi (Berlepsch) (Ochre-browed Thistletail), and Oreophylax moreirae (Ribeiro) (Itatiaia Spinetail). We also included in the analysis the furnariids Furnarius rufus (Gmelin) (Rufous Hornero), Leptasthenura aegithaloides (Kittlitz) (Plain-mantled Tit-Spinetail), Cranioleuca erythrops (Sclater) (Redfaced Spinetail), Thripophaga fusciceps Sclater (Plain Softtail), Phacellodomus rufifrons (Wied-Neuwied) (Rufous-fronted Thornbird), Spartonoica maluroides, Xenerpestes singularis (Taczanowski & Berlepsch) (Equatorial Graytail), Pseudoseisura lophotes, Philydor pyrrhodes (Cabanis) (Cinnamon-rumped Foliagegleaner), Automolus infuscatus (Sclater) (Olive-backed Foliage-gleaner), and Xenops minutus (Sparrman) (Plain Xenops) (Table 1). We used the dendrocolaptid species Dendrocolaptes sanctithomae (Lafresnaye) (Northern Barred Woodcreeper) to root the tree. Tissue collections: AMNH—American Museum of Natural History, New York City, USA; DZUFMG—Coleção Ornitológica do Departamento de Zoologia da Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil; FMNH—Field Museum of Natural History, Chicago, USA; ICN—Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Bogotá, Columbia; LSUMNS— Louisiana State University Museum of Natural Science, Baton Rouge, USA; UFMG—Laboratório de Biodiversidade e Evolução Molecular da Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil; USNM—National Museum of Natural History, Smithsonian Institution, Washington, D.C, USA. Using the Qiagen DNeasy kit, genomic DNA was extracted from 25 mg of pectoral muscle following the manufacturer's protocol. We amplified and sequenced three mitochondrial genes (ND 3, CO 2, and ND 2), as well as the autosomal nuclear gene beta-fibrinogen intron 7 (Bf 7), following methods described in Chesser et al. (2007). For at least one individual per genus, two additional nuclear protein-coding genes (RAG 1 and RAG 2) were sequenced. Most of the RAG sequences from were taken from Moyle et al. (2009); samples of Xenerpestes singularis, Pseudoseisura lophotes, and Oreophylax moreirae were amplified and sequenced for this study, according to methods described in Moyle et al. (2009). Following alignment and the exclusion of unique inserts from Bf 7, the six-gene concatenated dataset included 6,972 base pairs. In model-based phylogenetic inference, there is a trade-off between modeling the evolutionary process as closely as possible and the risk of over parameterization (Sullivan & Joyce 2005; McGuire et al. 2007). In preliminary analyses using the Akaike Information Criterion (Sullivan & Joyce 2005) we identified the General Time Reversible model of nucleotide substitution with gamma distributed rate variation across sites (GTR + Γ) and a fully partitioned dataset (a different model for each position of each coding gene [15] and the nuclear intron) as the best model and partitioning regime. We then performed a Bayesian analysis as implemented in MRBAYES 3.1 (Altekar et al. 2004; Huelsenbeck & Ronquist 2001; Ronquist & Huelsenbeck 2003) on CIPRES Portal v1.15 (Miller et al. 2009). The Bayesian posterior probability density was estimated by Metropolis-coupled Markov chain Monte Carlo in two independent runs. Each run consisted of four incrementally heated chains, continued for 25 million generations, and was sampled every 2500 generations. All chains reached stationarity, the independent runs converged (split frequencies 200) as evaluated in Tracer v1.4.1 (Drummond & Rambaut 2007). After discarding the first 5 million generations as burn-in, we computed a majority-rule consensus tree. Following methods in Chesser et al. (2009), we also performed a Maximum Likelihood (ML) analysis. The best tree from this analysis was identical to the majority-rule consensus tree; therefore, we do not include the ML results here. All individuals of Pseudasthenes formed a strongly supported clade (posterior probability = 1.0) sister to the Pseudoseisura-Spartonoica clade (Fig. 1). All other Asthenes species (hereafter Asthenes sensu stricto), together with Oreophylax moreirae and all sampled species of Schizoeaca, formed a monophyletic group. These results demonstrate that Pseudasthenes and Asthenes sensu stricto do not form a clade. Although several authors have suggested that Asthenes is not monophyletic (Pacheco et al. 1996; Zyskowski & Prum 1999; Remsen 2003; Vasconcelos et al. 2008), the pattern of relationships that we found had not been predicted. Asthenes is usually subdivided into at least two informal subgroups based on differences in plumage pattern, habitat, and nest architecture: a group of plain-plumaged species that inhabit deserts and dry forests and make nests of sticks, and a group of streaked species that inhabit grassy areas and make nests of grasses (Pacheco et al. 1996; Collias 1997; Remsen 2003). We recovered a strongly supported clade that corresponds to the streaked group of canasteros. Members of this lineage include A. humilis, A. wyatti (Sclater & Salvin) (Streak-backed Canastero), A. sclateri (Cabanis) (Puno Canastero), A. anthoides (King) (Austral Canastero), A. hudsoni (Sclater) (Hudson’s Canastero), A. urubambensis, A. flammulata (Jardine) (Many-striped Canastero), A. virgata (Sclater) (Junin Canastero), and A. maculicauda (Berlepsch) (Scribble-tailed Canastero). In addition, we found that A. modesta (Eyton) (Cordilleran Canastero), a plain-looking species that constructs stick nests, is part of this clade. On the other hand, the plain-plumaged, stick-nesting canasteros, considered by many to be a natural group, consist of at least two major clades (in addition to A. humicola, discussed above). Four belong to the newly described genus Pseudasthenes. Two other species, A. dorbignyi (Reichenbach) (Rusty-vented Canastero) and A. baeri, form a clade sister to the remaining species of Asthenes sensu stricto (Fig. 1). There is a resemblance in morphology and habits between these two Asthenes species and Pseudasthenes. Further, they show a pattern of geographic replacement similar to that found in a species complex or even a superspecies (Remsen 2003). After careful examination of specimens of these species, mostly study skins but also some skeletons, we were unable to find diagnostic characters that unequivocally separate A. dorbignyi and A. baeri from all species of Pseudasthenes, especially because of plumage similarities of the former with P. c a c t o r u m and P. steinbachi. After transferring the corresponding species to Pseudasthenes, Asthenes remains paraphyletic because Oreophylax moreirae and all species of Schizoeaca are nested within it. We found a well-supported clade (posterior probability = 1.0) that includes all species of Schizoeaca and Oreophylax as well as three longtailed species of Asthenes: A. pudibunda (Sclater) (Canyon Canastero), A. ottonis (Berlepsch) (Rusty-fronted Canastero), and A. pyrrholeuca. The close relationship of the Schizoeaca thistletails and the monotypic genus Oreophylax is not surprising given their similarities in morphology, nesting behavior, habitat, and voice (Vaurie 1980; Remsen 2003; B. Whitney, pers. comm.), and a close relationship between Asthenes and Schizoeaca was previously suspected on the basis of similar throat patch configurations (Remsen 2003). However, the polyphyly of Schizoeaca with respect to the three long-tailed Asthenes listed above is surprising given the phenotypic distinctness of Schizoeaca, especially in tail morphology. Moreover, Schizoeaca species were considered homogeneous to the point of being treated as a single species in the past (Vaurie 1980). The position of A. luizae Vielliard (Cipo Canastero) within Asthenes sensu stricto was unresolved; this species formed a trichotomy with the two main Asthenes clades. Pearman (1990) proposed, on the basis of voice and plumage, that its closest relative might be A. dorbignyi or A. patagonica. Vas c on c el o s et al. (2008), summarizing this and additional evidence, noted that all traits that it shared with other Asthenes were potentially plesiomorphic and concluded that its sister species could not be determined from the phenotypic data available. In fact, our data indicate this species is not closely related to any of the other Asthenes, including the species mentioned by Pearman (1990) and Vasconcelos et al. (2008), and forms a separate lineage within Asthenes sensu stricto. The relationships of the three species not included in this study can be inferred tentatively from phenotypic characters. Asthenes berlepschi is almost certainly closely related to A. dorbignyi and may be a subspecies of A. dorbignyi (Cory & Hellmayr 1925; Bond & Meyer de Schauensee 1942; Fjeldså & Krabbe 1990). The second missing species, A. heterura, has been considered closely related to (Cory & Hellmayr 1925; Bond 1945), sister species to (Vaurie 1980), or conspecific with (Meyer de Schauensee 1966) A. pudibunda. Pearman (2001), however, noted that A. heterura is sufficiently similar to A. pyrrholeuca in plumage that they can easily be confused in the field and even in the hand. Because A. pudibunda and A. pyrrholeuca are not sister species the specific placement of A. heterura is better regarded as uncertain, although it probably belongs to the long-tailed Asthenes / Schizoeaca / Oreophylax clade. Schizoeaca coryi is similar to other Schizoeaca thistletails in plumage, tail structure, and habitat (Remsen 1981, 2003), and it presumably forms part of the same clade. We recommend the following provisional classification of Asthenes and Pseudasthenes, based on our phylogeny and the rationale provided above for the missing species:Published as part of Aleixo, Alexandre, Chesser, Terry, Jr, Remsen & Brumfield, Robb T., 2010, Pseudasthenes, a new genus of ovenbird (Aves: Passeriformes: Furnariidae), pp. 61-68 in Zootaxa 2416 on pages 62-66, DOI: 10.5281/zenodo.29404
FIGURE 2. 50 in Isleria, a new genus of antwren (Aves: Passeriformes: Thamnophilidae)
No full textFIGURE 2. 50% Majority-rule Bayesian consensus tree of a subset of the Thamnophilidae showing that Isleria is not closely related to Myrmotherula or Epinecrophylla. Numbers at each node indicate posterior probability values.Published as part of Bravo, Gustavo A., Chesser, Terry & Brumfield, Robb T., 2012, Isleria, a new genus of antwren (Aves: Passeriformes: Thamnophilidae), pp. 61-67 in Zootaxa 3195 on page 65, DOI: 10.5281/zenodo.20886
The maritime portion of South Australia [cartographic material] : from Captn. Flinders & from more recent surveys made by the Survr. Genl. of the Colonies /
No full textInsets: Sketch of Encounter Bay / by Col. Light & B. T. Finniss esqr. 1838 -- Sketch of Nepean Bay and Kingscote Harbour/ by Wm. Chesser -- the city of Adelaide with the acre allotments numbered / Surveyed by Col. Light -- [Gulf of St. Vincent].; Map with notes on vegetation and topography. Relief shown by hachures, and bathymetric soundings
FIGURE 1. A in Pseudasthenes, a new genus of ovenbird (Aves: Passeriformes: Furnariidae)
No full textFIGURE 1. A simplified majority-rule Bayesian consensus tree of the Furnariidae (see text) that highlights the lack of a sister relationship between Pseudasthenes and Asthenes as well as the paraphyly of Asthenes, Schizoeaca, and Oreophylax. Asterisks represent nodes with a posterior probability of 1.0.Published as part of Aleixo, Alexandre, Chesser, Terry, Jr, Remsen & Brumfield, Robb T., 2010, Pseudasthenes, a new genus of ovenbird (Aves: Passeriformes: Furnariidae), pp. 61-68 in Zootaxa 2416 on page 65, DOI: 10.5281/zenodo.29404
FIGURE 2 in Certhiasomus, a new genus of woodcreeper (Aves: Passeriformes: Dendrocolaptidae)
No full textFIGURE 2. Majority-rule Bayesian consensus tree of the Dendrocolaptidae that highlights the lack of a sister relationship between Certhiasomus and Deconychura. Numbers above the branches indicate posterior probability values.Published as part of Derryberry, Elizabeth, Claramunt, Santiago, Chesser, Terry, Aleixo, Alexandre, Cracraft, Joel, Moyle, Robert G. & Brumfield, Robb T., 2010, Certhiasomus, a new genus of woodcreeper (Aves: Passeriformes: Dendrocolaptidae), pp. 44-50 in Zootaxa 2416 on page 48, DOI: 10.5281/zenodo.29391
The maritime portion of South Australia [cartographic material] : from the surveys of Captn. Flinders & of Col. Light, Survr. Genl. /
No full textImprint statement partly obliterated by partially removed label.; Insets: Sketch of Encounter Bay / by Col. Light & B. T. Finniss esqr. 1838 -- Sketch of Nepean Bay and Kingscote Harbour / by Wm. Chesser -- The City of Adelaide, with the acre allotments numbered /surveyed by Col. Light -- [Gulf of St. Vincent].; Map with notes on vegetation and topography. Relief shown by hachures and bathymetric soundings.; Ms. notes and colouring.; Tooley 108.; Also available in an electronic version via the Internet at: http://nla.gov.au/nla.map-t108
FIGURE 1. A in Geocerthia, a new genus of terrestrial ovenbird (Aves: Passeriformes: Furnariidae)
No full textFIGURE 1. A maximum-likelihood phylogeny highlighting the lack of a sister relationship between Upucerthia serrana and other species of Upucerthia sensu stricto. Numbers above the branches indicate bootstrap support based on 150 maximum-likelihood replicates.Published as part of Chesser, Terry, Claramunt, Santiago, Derryberry, Elizabeth & Brumfield, Robb T., 2009, Geocerthia, a new genus of terrestrial ovenbird (Aves: Passeriformes: Furnariidae), pp. 64-68 in Zootaxa 2213 on page 67, DOI: 10.5281/zenodo.18990
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