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55 results for “Melanoleuca”
Fig. 5 in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Fig. 5. Population dynamics in 100 years when changing range of dispersal ages, assuming only males to disperse
Fig. 4 in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Fig. 4. Population size of different sexes dispersing with 90% survival of dispersers in 100 years. M90%, F90% and F&M90% indicate dispersal of only males, only females, or both sexes, respectively
Fig. 1 in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Fig. 1. The distribution of each subpopulation and the suggested "corridor belts" within the Minshan metapopulation. ZZWG sub-pop, BH sub-pop, MS sub-pop, BCH sub-pop, QFS sub-pop and GGS sub-pop are abbreviations for Zezhawagou subpopulation, Baihe subpopulation, Minshan subpopulation, Baicaohe subpopulation, Qianfoshan subpopulation, and Guangguangshan subpopulation,
Fig. 3 in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Fig. 3. Minshan metapopulation size in 100 years, assuming different dispersal rates and probabilities of disperser survival. Different curves correspond to different dispersal rates, as shown in the legend
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Figures represent five groups respectively. In group, when the dispersal rate is equal to 1% values of the probability of disperser survival are 1, 0.9, 0.8, 0.7, 0.6, 0.5 respectively as in groups and
Fig. 2. Stoch-r in The Influence Of Dispersal On The Metapopulation Viability Of Giant Panda (Aliuropoda Melanoleuca) In The Minshan Mountains
Fig. 2. Stoch-r of Baihe subpopulation with different dispersal rate and probability of disperser survival. Curves 1%, 2%, 4%, 8%, 16% represent different dispersal rates
Fig. 1 in Review on parasites of wild and captive giant pandas (Ailuropoda melanoleuca): Diversity, disease and conservation impact
Fig. 1. Distribution of wild giant pandas in six mountain regions (Qinling, Minshan, Qionglai, Liangshan, Daxiangling and Xiaoxiangling) in three Provinces (Gansu, Shaanxi, and Sichuan) of China. Adapted from Wang et al. (2018).
Fig. 1 in Comparison of a commercial ELISA and indirect hemagglutination assay with the modified agglutination test for detection of Toxoplasma gondii antibodies in giant panda (Ailuropoda melanoleuca)
Fig. 1. Receiver operating characteristics (ROC) analysis of the ELISA. ROC analysis shows an area under the curve (AUC) of 0.861 (95% CI: 0.712–1.000) for ELISA (a), 0.894 (95% CI: 0.791–0.997) for ELISA (b), and 0.902 (95% CI: 0.799–1.000) for ELISA (c).
Magnetic Resonance Imaging Scan of the Brain of a Giant panda (Ailuropoda melanoleuca)
<p>Magnetic Resonance Imaging Scan of the Brain of a Giant panda (<i>Ailuropoda melanoleuca</i>) from http://braincatalogue.org/Giant_panda</p>
Data from: Transcriptome-derived tetranucleotide microsatellites and their associated genes from the giant panda (Ailuropoda melanoleuca)
Recently, an increasing number of microsatellites or Simple Sequence Repeats (SSRs) have been found and characterized from transcriptome. Such SSRs can be employed as putative functional markers to easily tag corresponding genes, which play an important role in biomedical studies and genetic analysis. However, the transcriptome-derived SSRs for giant panda (Ailuropoda melanoleuca) are not yet available. In the present work, we identified and characterized 20 tetranucleotide microsatellite loci from a transcript database generated from the blood of giant panda. Furthermore, we assigned their predicted transcriptome locations: 16 loci were assigned to untranslated regions (UTRs) and 4 loci were assigned to coding regions (CDSs). Gene identities of 14 transcripts contained corresponding microsatellites were determined, which provide useful information to study the potential contribution of SSRs to gene regulation in giant panda. The polymorphic information content (PIC) values ranged from 0.293 to 0.789 with an average of 0.603 for the 16 UTRs-derived SSRs. Interestingly, four CDS-derived microsatellites developed in our study were also polymorphic, and the instability of these four CDS-derived SSRs was further validated by re-genotyping and sequencing. The genes contained these four CDS-derived SSRs were embedded with various types of repeat motifs. The interaction of all the length-changing SSRs might provide a way against coding region frameshift caused by microsatellite instability. We hope these newly gene-associated biomarkers would pave the way for genetic and biomedical studies for giant panda in the future. In sum, this set of transcriptome-derived markers complements the genetic resources available for giant panda.
FIGURES 32–35 in Taxonomy of Fulgoraecia melanoleuca (Fletcher, 1939), (Lepidoptera: Epipyropidae) in India, a biological control agent of Pyrilla perpusilla (Walker) (Hemiptera: Lophopidae)
FIGURES 32–35. Genitalia of F. melanoleuca. 32. Ventral view of male genitalia with aedeagus in situ; 33. Dorsal view of male genitalia with aedeagus in situ; 34. Aedeagus; 35. Dorsal view of female genitalia.
FIGURES 9–13 in Taxonomy of Fulgoraecia melanoleuca (Fletcher, 1939), (Lepidoptera: Epipyropidae) in India, a biological control agent of Pyrilla perpusilla (Walker) (Hemiptera: Lophopidae)
FIGURES 9–13. Larvae of F. melanoleuca. 9. Larva removed from the abdomen of P. perpusilla; 10. After removing waxy material from the body of the larva; 11. Proboscis for sucking fluids from the body of the host P. perpusilla; 12. Uniserial crochets on abdominal prolegs; 13. Uniserial crochets on anal prolegs.
FIGURES 1–8 in Taxonomy of Fulgoraecia melanoleuca (Fletcher, 1939), (Lepidoptera: Epipyropidae) in India, a biological control agent of Pyrilla perpusilla (Walker) (Hemiptera: Lophopidae)
FIGURES 1–8. Life stages of F. melanoleuca. 1. Male and female emerged from pupae; 2.Eggs; 3. Larva parasitizing on nymph of Pyrilla perpusilla; 4. Larva parasitizing on adult's abdomen of P. perpusilla; 6. Pupa of F. melanoleuca; 7. F. melanoleuca adult male; 8. F. melanoleuca adult male.
FIGURES 14–21 in Taxonomy of Fulgoraecia melanoleuca (Fletcher, 1939), (Lepidoptera: Epipyropidae) in India, a biological control agent of Pyrilla perpusilla (Walker) (Hemiptera: Lophopidae)
FIGURES 14–21. Pupae of F. melanoleuca. 14. Dorsal view of male pupa;15.Ventral view of male pupa; 16. Lateral view of male pupa; 17. Dorsal view of female pupa; 18. Ventral view of female pupa; 19. Lateral view of male pupa; 20. Male genital scar; 21. Female genital ostium scar.
FIGURES 22–31 in Taxonomy of Fulgoraecia melanoleuca (Fletcher, 1939), (Lepidoptera: Epipyropidae) in India, a biological control agent of Pyrilla perpusilla (Walker) (Hemiptera: Lophopidae)
FIGURES 22–31. Adult structures of F. melanoleuca. 22. Habitus of female; 23. Habitus of male; 24. Lateral view of head; 25.Male antenna; 26. Female antenna; 27. Foreleg; 28. Midleg; 29. Hindleg; 30. Forewing venation; 31. Hindwing venation.
Fig. 7. Derancistrachroma melanoleuca, female holotype. a in The Prioninae (Coleoptera: Cerambycidae) of Hispaniola, with Diagnoses, Descriptions of New Species, Distribution Records, and a Key for Identification
Fig. 7. Derancistrachroma melanoleuca, female holotype. a) Dorsal habitus, b) Ventral habitus, c) Lateral habitus.
Fig. 8. Derancistrachroma melanoleuca, female holotype. a in The Prioninae (Coleoptera: Cerambycidae) of Hispaniola, with Diagnoses, Descriptions of New Species, Distribution Records, and a Key for Identification
Fig. 8. Derancistrachroma melanoleuca, female holotype. a) Pronotum and head, dorsal view, b) Prosternum, mesosternum, and head, ventral view, c) Head, anterior view, d) Head, lateral view, e) Lateral pronotal margin, f) Prothorax and prosternum, lateral view.
Fig. 9. Derancistrachroma melanoleuca, female holotype. a in The Prioninae (Coleoptera: Cerambycidae) of Hispaniola, with Diagnoses, Descriptions of New Species, Distribution Records, and a Key for Identification
Fig. 9. Derancistrachroma melanoleuca, female holotype. a) Scutellum, b) Elytral apex, c) Elytral integument,
FIGURE 6 in Integration of nuclear and mitochondrial gene sequences and morphology reveals unexpected diversity in the forest cobra (Naja melanoleuca) species complex in Central and West Africa (Serpentes: Elapidae)
FIGURE 6. Distribution of the five species of the N. melanoleuca complex. A full list of voucher specimens beyond those included in multivariate analyses and Appendix 2 is available on request from the first author.
FIGURE 1 in Integration of nuclear and mitochondrial gene sequences and morphology reveals unexpected diversity in the forest cobra (Naja melanoleuca) species complex in Central and West Africa (Serpentes: Elapidae)
FIGURE 1. Maximum likelihood mitochondrial phylogeny of the Naja melanoleuca complex. Node support values indicate % bootstrap support; support values for the most distal nodes not shown. Country abbreviations: CAR = Central African Republic, DRC = Democratic Republic of Congo, KZN = KwaZulu-Natal Province, South Africa, RoC = Republic of Congo. Mitochondrial candidate species (CS) are shown in the same colours as in Figures 2–4. For specimen information see Appendix 1.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.