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24 results for “Eudyptula minor”

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zenodo40/100

Fig. 3 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 3. Agarose gel electrophoresis of amplification products obtained through nested PCR tests targeting the 18S rRNA gene of Babesia (primers Bab5.1/BabB followed by RLBF/RLBR) or the mitochondrial cytochrome b gene of Haemoproteus/Plasmodium (primers HaemNFI/HaemNR3 followed by HaemF/HaemR2). The following samples are represented: (a) captive-born little penguin chick, negative blood smear; (b) adult wild little penguin, negative blood smear; (c) Babesia-infected adult wild little penguin, as confirmed through blood smear; (d) Haemoproteus-infected adult tropical screech owl, as confirmed through blood smear; (e) Plasmodium-inoculated chicken, raised in arthropod-free environment; (f) blood parasite-free chicken, raised in arthropodfree environment.

opencc-by-4.0Aug 2015View details →
zenodo40/100

Fig. 1 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 1. Geographic distribution of sampling locations, southeast Australia. Site details are given in Table 1. The geographic distribution of little penguins (black area) is shown in the top right map (adapted from Marchant and Higgins, 1990).

opencc-by-4.0Aug 2015View details →
zenodo40/100

Fig. 4 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 4. Maximum likelihood phylogenetic tree of the 18S rRNA gene of the studied Babesia lineages. Lineages identified in this study are emphasized in red, and other avianinfecting lineages are emphasized in blue. For each lineage, the following information is provided: morphospecies (Genbank ascension number) host species. For avianinfecting lineages, the geographic location is also provided. Branch lengths are drawn proportionally to evolutionary distance (scale bar is shown). For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.

opencc-by-4.0Aug 2015View details →
zenodo40/100

Fig. 2 in Epidemiology and molecular phylogeny of Babesia sp. in Little Penguins Eudyptula minor in Australia

Fig. 2. Babesia sp. in the blood smear of a little penguin. Individual details: TAS- 124, male, adult, moulting, sampled at "Darlington Foreshore" (Maria Island, Tasmania) in 21/02/2013, Genbank ascension number KP144323, Giemsa stain.

opencc-by-4.0Aug 2015View details →
zenodo40/100

Fig. 9 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 9. Similarity of Toxoplasma gondii from Little Penguins with representative strains from Archetypals I, II, and III in the B1 gene. A: shows polymorphisms at the 366 nucleotide. B: shows polymorphisms at the 504 nucleotide. Declaration of competing interest

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 6 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 6. (And detail) – four parasites in a cyst within the cytoplasm of a host cell, spleen (x3810, bar = 2 μm) Image left: E - erythrocyte, Ph - phagocyte, P - protozoa; image right (detail): N - nucleus.

opencc-by-4.0Apr 2022View details →
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Fig. 5 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 5. Splenic impression smear, erythrocytes (E), splenic stromal cells (S) and numerous protozoa (arrows) (Wright's Giemsa stain, 1000x).

opencc-by-4.0Apr 2022View details →
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Fig. 4 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 4. Liver, intact and necrotic hepatocytes and numerous protozoa (arrows), free and within cysts (5 μm section, Martius Scarlet Blue stain, 400x). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 11 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 11. Liver, staining of protozoan antigen in intact and necrotic hepatocytes (x400 Toxoplasma polyclonal antibody IHC).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Fig. 3 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 3. Liver, necrotic focus (the area of relative pallor, within which numerous organisms were identifiable) (5 μm section, Haematoxylin and Eosin stain, 100x).

opencc-by-4.0Apr 2022View details →
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Fig. 10 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 10. Liver, several foci of brown staining indicate Toxoplasma antigen within a necrotic focus (x100, Toxoplasma polyclonal antibody IHC). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Apr 2022View details →
zenodo36/100

Fig. 8 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 8. Dividing protozoan forming merozoites (x15000, bar = 1 μm).

opencc-by-4.0Apr 2022View details →
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Fig. 7 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 7. Protozoan with apical complex (x15000, bar = 1 μm).

opencc-by-4.0Apr 2022View details →
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Fig. 2 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 2. Enlarged spleen with speckled tan areas of discolouration.

opencc-by-4.0Apr 2022View details →
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Fig. 1 in Fatal toxoplasmosis in Little Penguins (Eudyptula minor) from Penguin Island, Western Australia

Fig. 1. Enlarged liver with multiple, pinpoint cream to white spots.

opencc-by-4.0Apr 2022View details →
dryad36/100

Data for: Energetic consequences of prey type in little penguins (Eudyptula minor)

<p>Investigation of foraging decisions can help understand how animals efficiently gather and exploit food. Prey chase and handling times are important aspects of foraging efficiency, influencing the net energy gain derived from a prey item. However, these metrics are often overlooked in studies of foraging behaviour due to the difficulty in observing them. The present study used animal-borne cameras to investigate the type, duration and energetic consequences of predator-prey interactions in little penguins (<em>Eudyptula minor</em>) (n = 32) from two colonies in Bass Strait, south-eastern Australia. A total of 7 main prey items were observed and consumed by little penguins. Penguins were observed to consume prey types and use strategies that have not been previously documented. These included consumption of bellowsfish (<em>Macroramphosus scolopax</em>) and other fish species captured sheltering around jellyfish or extracted dead from the tentacles. Chase and handling time varied with prey type and lasted ~2 s for most prey. Profitability varied amongst prey types, with a greater amount of low profitable prey being consumed, suggesting a trade-off between minimising energetic costs, and increasing capture rates. These results highlight the use of animal-borne video data loggers to further understand the foraging adaptations of important predators in the marine environment.</p>

opencc-zeroAug 2023View details →
dryad36/100

Data for: Energetic consequences of prey type in little penguins (Eudyptula minor)

Open the record for dataset details and reuse information.

publicAug 2023View details →
dryad36/100

Finite element modelling of hearing capabilities in the Little Penguin (Eudyptula minor)

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publicAug 2024View details →
dryad32/100

Data from: Non-equilibrium conditions explain spatial variability in genetic structuring of little penguin (Eudyptula minor)

Factors responsible for spatial structuring of population genetic variation are varied, and in many instances there may be no obvious explanations for genetic structuring observed, or those invoked may reflect spurious correlations. A study of little penguins (Eudyptula minor) in southeast Australia documented low spatial structuring of genetic variation with the exception of colonies at the western limit of sampling, and this distinction was attributed to an intervening oceanographic feature (Bonney Upwelling), differences in breeding phenology, or sea level change. Here, we conducted sampling across the entire Australian range, employing additional markers (12 microsatellites and mitochondrial DNA, 697 individuals, 17 colonies). The zone of elevated genetic structuring previously observed actually represents the eastern half of a genetic cline, within which structuring exists over much shorter spatial scales than elsewhere. Colonies separated by as little as 27 km in the zone are genetically distinguishable, while outside the zone, homogeneity cannot be rejected at scales of up to 1400 km. Given a lack of additional physical or environmental barriers to gene flow, the zone of elevated genetic structuring may reflect secondary contact of lineages (with or without selection against interbreeding), or recent colonization and expansion from this region. This study highlights the importance of sampling scale to reveal the cause of genetic structuring.

opencc-zeroDec 2014View details →
dryad32/100

Temperatures inside Little Penguin (Eudyptula minor) artificial nest habitats exceed upper thermal limits in a range-edge population

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publicAug 2025View details →

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