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306 results for “Alberta”
Fig. 2 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 2. Stacked frequency distribution of adult D. dendriticum in calf, juvenile, and adult elk collected between 1997 and 2011 from Cypress Hills Park, Alberta.
Fig. 4. Relationship between liver weight and host age for elk sampled from 2009 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 4. Relationship between liver weight and host age for elk sampled from 2009 to 2011 from Cypress Hills Park, Alberta. Regression lines are maximum likelihood estimates.
Fig. 3 in Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada
Fig. 3. Age–abundance profile of infection for the invasive trematode, D. dendriticum in beef cattle sampled from 2003 to 2013 from Cypress Hills Park, Alberta. The solid line represents the negative binomial distribution model fit using maximum likelihood; the dashed lines represent the 95% confidence interval.
Fig. 1 in Detecting co-infections of Echinococcus multilocularis and Echinococcus canadensis in coyotes and red foxes in Alberta, Canada using real-time PCR
Fig. 1. Standard curve for qPCR assays to detect E. canadensis and E. multilocularis using Cox143 and Nad234 primers/probes, respectively.
EXPLANATION OF PLATE I Left lateral aspect of skull of Stephanosaurus marginatus; one- fifth the natural size. Abbreviations.-D, lateral temporal fossa; DN, dentary; J, jugal; L, lachrymal; MX, maxilla; N, nasal; NO, nasal opening; OR, orbit; PD, predentary; PF, prefrontal; PM, premaxilla; Q, quadrate; QJ, quadrato-jugal; S, squamosal; SA, surangular. in On a new genus and species of carnivorous dinosaur from the Belly River Formation of Alberta, with a description of the skull of Stephanosaurus marginatus from the same horizon
EXPLANATION OF PLATE I Left lateral aspect of skull of Stephanosaurus marginatus; one- fifth the natural size. Abbreviations.-D, lateral temporal fossa; DN, dentary; J, jugal; L, lachrymal; MX, maxilla; N, nasal; NO, nasal opening; OR, orbit; PD, predentary; PF, prefrontal; PM, premaxilla; Q, quadrate; QJ, quadrato-jugal; S, squamosal; SA, surangular.
Text-fig. 2. Map showing the distribution of localities included in the treatment of Brown (1962), based on the coordinates presented in Appendix Table 1. Localities are distributed across New Mexico (NM), Colorado (CO), Wyoming (WY), Montana (MT), South Dakota (SD) and North Dakota (ND). Also plotted are cited Canadian localities: Joffre Bridge, in Alberta (AB), and Ravenscrag, in Saskatchewan (SK). Map generated with Map-It (2014) website. in Revisions To Roland Brown'S North American Paleocene Flora
Text-fig. 2. Map showing the distribution of localities included in the treatment of Brown (1962), based on the coordinates presented in Appendix Table 1. Localities are distributed across New Mexico (NM), Colorado (CO), Wyoming (WY), Montana (MT), South Dakota (SD) and North Dakota (ND). Also plotted are cited Canadian localities: Joffre Bridge, in Alberta (AB), and Ravenscrag, in Saskatchewan (SK). Map generated with Map-It (2014) website.
Fig. 1 in Environmental and ecological factors driving trematode parasite community assembly in central Alberta lakes
Fig. 1. Host-Parasite diversity correlations. Spearman rank correlations of A) snail and trematode richness, pooled by site, B) non-pooled, sample-based, snail and trematode richness, C) snail and trematode effective species based on Shannon index (exp(H)) for all lakes, and D) effective species by each site at Buffalo Lake. PP = Pelican Point, RS = Rochon Sands, TN = The Narrows.
Fig. 3 in Environmental and ecological factors driving trematode parasite community assembly in central Alberta lakes
Fig. 3. Canonical correspondence analysis (CCA) of trematode component communities. Relative abundances of trematode species by sample are constrained by environmental variables from the best-fit model (community \lake trophic status \+ ecoregion \+ latitude). Trematode species abbreviations are shown in grey. CCA results are in red as eigenvectors. Ecoregions are identified with a blue dotted line. The trophic status of each lake is identified with an ellipse.
Fig. 2 in Environmental and ecological factors driving trematode parasite community assembly in central Alberta lakes
Fig. 2. Multivariate Homogeneity of Group Dispersion for Trematode Communities. Bray-Curtis dissimilarities were used to examine the homogeneity of variance among samples (trematode species counts) when grouped by different geographical or anthropogenic-use distinctions. The left panels show the twodimensional visualizations of the data by Principal Coordinate Analysis (PCA) plots. Each grouping is labeled in the center, and ellipses represent 95% confidence intervals. The right panels provide a boxplot of the distance to centroid for each group in the multivariate analysis. A) samples grouped by site, B) grouped by river basin, C) grouped by ecoregion, D) group by site-type or anthropogenic use (beach or boat launch). Statistical significance for differences between groups is indicated by an asterisk.
Fig. 2 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 2. Reconstruction of the skull of Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta, in right lateral view. Preserved elements are stippled; missing portions are dotted and modeled after Centrosaurus apertus.
Fig. 6 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 6. Phylogenetic hypotheses for relationships within Ceratopsidae, focusing on Centrosaurinae. A. Strict reduced consensus tree using "traditional" codings for the epiparietal homologies in selected centrosaurines (see text), with Sinoceratops zhuchengensis and Rubeosaurus ovatus removed. B. Strict consensus tree using "new" codings for epiparietal homologies, following a posteriori deletion of Sinoceratops zhuchengensis and Centrosaurus brinkmani. At selected nodes, the top number indicates Bremer support and the bottom number indicates bootstrap support values above 50%.
Fig. 5 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 5. Schematized parietals of centrosaurine ceratopsids in dorsal view, showing possible homologies for the first four epiparietal loci. A. Albertaceratops nesmoi Ryan, 2007. B. Spinops sternbergorum gen. et sp. nov. C. Centrosaurus apertus Lambe, 1902. D. Styracosaurus albertensis Lambe, 1913. E. Rubeosaurus ovatus Gilmore, 1930. F. Einiosaurus procurvicornus Sampson, 1995. Numbers indicate locus positions. For A and B, the numbers on the right side of the parietal indicate numbering under the "traditional" scheme; numbers on the left side indicate numbering under the revised scheme proposed here. Locus numbering is the same in both the traditional and revised schemes for C, D, E, and F, and are thus presented only on the left side of the parietal for those taxa. Not to scale.
Fig. 4 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 4. Partial skull of the centrosaurine ceratopsid Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta, NHMUK R16306; in right lateral (A), rostral (B), and dorsal (C) views.
Fig. 3 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 3. Centrosaurine ceratopsid Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta. A. Partial right squamosal in lateral view, NHMUK R16309. B. Partial parietal with adherent bone fragments in dorsal view, NHMUK R16308. C. Partial parietal in dorsal (C1), rostral (C2), and left lateral (C3) views, holotype NHMUK R16307.
Fig. 1 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 1. Map showing the presumed location of the Spinops sternbergorum gen. et sp. nov. type locality within the area informally called the "Steveville badlands," Dinosaur Provincial Park, Alberta Canada. Charles Sternberg (unpublished data in NHMUK archives) indicated that the bone bed was one mile below the mouth of Berry Creek, and the estimated area that this covers is indicated by the grey semi−circle. Intense prospecting on the east side of the river has failed to relocate the quarry, and badlands on the west side are outside of the Park boundary and currently inaccessible for prospecting. The indicated southeast Park boundary does not include the margins of two major coulees in this region that are also within the Park. Note that the quarry for the holotype of Styracosaurus albertensis Lambe, 1913 (CMN 344) is in the southeast part of the Park. The inset photograph, courtesy of David Eberth, shows a typical view of the contact between the Dinosaur Park Formation (DPF) and Oldman Formation (OF) near the Steveville badlands.
Fig.3. A–C in New earliest Tiffanian (late Paleocene) mammals from Cochrane 2, southwestern Alberta, Canada
Fig.3. A–C. Pararyctes rutherfordi sp.nov., Cochrane 2 locality, Alberta. A.Holotype, incomplete right maxilla with P4, M2–3, UALVP 45094 in occlusal view (A1, A2). B.Left M2, UALVP 25180 in occlusal view. C.Left m1 or m2, UALVP 45095 in labial (C 1), lingual (C2), and occlusal (C3) views. D–I. Bessoecetor septentrionalis comb.nov., Cochrane 2 locality, Alberta. D.Right P4, UALVP 25119 in occlusal view. E.Left M1, UALVP 28423 in occlusal view. F.Left M2, UALVP 28412 in occlusal view. G.Right p4, UALVP 28438 in labial (G 1), lingual (G2), and occlusal (G3) views. H. Left m2, UALVP 28414 in labial (H1), lingual (H2), and occlusal (H3) views. I.Holotype, left m3, UALVP 126 in labial (I 1), lingual (I2), and occlusal (I3) views.Scale bars 1 mm.
Fig.1. A–C in New earliest Tiffanian (late Paleocene) mammals from Cochrane 2, southwestern Alberta, Canada
Fig.1. A–C. Ptilodus gnomus sp.nov., Cochrane 2 locality, Alberta. A.Holotype, right P4, UALVP 45145 in labial (A 1), lingual (A2), and occlusal (A3) views. B.Left p4, UALVP 45148 in labial (B 1), lingual (B2), and anterior (B3) views. C.Incomplete left dentary having i1, p3–4, UALVP 18670 in labial (C1) and lingual (C2) views. D. Baiotomeusrusselli sp.nov., Cochrane 2 locality, Alberta.Holotype, left P4, UALVP 18787 in labial (D 1), lingual (D2), and occlusal (D3) views. E–H. Thryptacodonorthogonius, comb.nov., Cochrane 2 locality, Alberta. E.Left M1, UALVP 45099 in occlusal view. F.Holotype, left M2, UALVP 124 in occlusal view. G.Left M3, UALVP 24993 in occlusal view. H.Right m1, UALVP 42872 in labial (H 1), lingual (H2), and occlusal (H3) views. Scale bars 1 mm.
Fig. 7 in Description, life cycle, and development of the myxozoan Myxobolus rasmusseni n. sp. in fathead minnows, Pimephales promelas: A possible emerging pathogen in southern Alberta, Canada
Fig. 7. Coronal histological section of the anterior head region of a Myxobolus rasmusseni n. sp. infected fathead minnow. Approximately 8 myxospore-filled plasmodia are located between the two optic lobes in the anterior-dorsal region of the head cavity. Plasmodia demarcated from adjacent host tissue by a thin fibrocytic membrane that also encircles Ornithodiplostomum ptychocheilus metacercariae. 100X magnification. Op = Ornithodiplostomum ptychocheilus metacercariae, Olb: Optic lobe of the minnow brain, Ps: Plasmodia of Myxobolus rasmusseni n. sp. Inset demonstrates distribution of numerous stained and unstained myxospores located within plasmodia.
Fig. 8 in Description, life cycle, and development of the myxozoan Myxobolus rasmusseni n. sp. in fathead minnows, Pimephales promelas: A possible emerging pathogen in southern Alberta, Canada
Fig. 8. Size-frequency distributions of fathead minnows collected from two wetlands in southern Alberta. The left-hand triplet of graphs (A, B, C) indicates size distributions of the 2020 cohort of fathead minnows assessed in Sept. 2020, June 2021, and Sept. 2021 at McQuillan Reservoir. The right-hand triplet (D, E, F) indicates size distributions assessed at the same times for Coalhurst Stormwater Pond. Dark bars indicate minnows with M. rasmusseni n. sp. lesions.
Fig. 6 in Description, life cycle, and development of the myxozoan Myxobolus rasmusseni n. sp. in fathead minnows, Pimephales promelas: A possible emerging pathogen in southern Alberta, Canada
Fig. 6. Coronal histological section through the dorsal head region along the frontal plane of a fathead minnow that contained multiple, various-sized plasmodia of Myxobolus rasmusseni n. sp. 1.25X magnification. Rt - Retina of the eye, Ps - Plasmodia, Br - Brain, Ls - Lens of the eye, Ns - Nares, Of – Opercular flap.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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