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7 results for “Mastomys natalensis”
Impacts of black rat invasion on the primary rodent host of Lassa virus, Mastomys natalensis
<p>Shared here is code and data supporting the manuscript, "Reservoir displacement by an invasive rodent reduces Lassa virus zoonotic spillover risk."</p> <p>The project directory, which contains numerous large raster data files, was stored as a split zip archive to facilitate upload to Zenodo and consists of the files "rat_invasion.z01", "rat_invasion.z02", "rat_invasion.z03", and "rat_invasion.zip". Following download, these files may need to be decompressed using dedicated archiver software (such as The Unarchiver [https://theunarchiver.com/] on macOS). Note that the entire project repository is ~7 GB when uncompressed. The files shared here mirror the GitHub project repository (https://github.com/eveskew/rat_invasion) with the addition of the large environmental raster data in the "data/environmental" subdirectory.</p>
Fig. 1 in Host competence of African rodents Arvicanthis neumanni, A. niloticus and Mastomys natalensis for Leishmania major
Fig. 1. Xenodiagnosis and external manifestation of L. major in rodents. Direct xenodiagnosis with P. duboscqi in plastic tubes covered with fine mesh held on the ear of the anaesthetized A. niloticus (A) and external manifestation of L. major LV109 in ear pinnae (site of inoculation) of A. neumanni by week 10 p.i., (B); A. niloticus by week 30 p.i. (C, D) and M. natalensis by week 19 p.i. (E).
FIG. 2. — Neoheligmonella lamaensis n in Two new species of Nippostrongylinae (Nematoda, Trichostrongylina, Heligmonellidae), coparasites of Mastomys natalensis (Muridae, Murinae) from Benin
FIG. 2. — Neoheligmonella lamaensis n. sp.; A, male, anterior extremity, ventral view; B, C, transverse sections at mid-body; B, male; C, female; D, female, posterior extremity, left lateral view; E, male, caudal bursa, ventral view; F, female, posterior extremity, disappearance of the ridges, right lateral view; G, female, transverse section anterior to vulvar opening; H, female, posterior extremity, disappearance of the ridges, left lateral view. Abbreviations: r, right; v, ventral side.
FIG. 1. — Heligmonina kotoensis n in Two new species of Nippostrongylinae (Nematoda, Trichostrongylina, Heligmonellidae), coparasites of Mastomys natalensis (Muridae, Murinae) from Benin
FIG. 1. — Heligmonina kotoensis n. sp.; A, male, anterior extremity, ventral view; B, C, transverse sections at mid-body; B, male; C, female; D, female, posterior part, left lateral view; E, male, genital cone, ventral view; F, male, caudal bursa, ventral view; G, female, transverse section of body anterior to vulvar opening. Abbreviations: r, right; v, ventral side. Scale bars: A-D, G, 50 μm;
On following pages: 578. African Smoky Mouse (Heimyscus fumosus); 579. Baer's Wood Mouse (Hylomyscus baer); 580. Mount Oku Wood Mouse (Hylomyscus grandis); 581. Dahomey Gap Wood Mouse (Hylomyscus pamfi), 582. West African Wood Mouse (Hylomyscus simus); 583. Beaded Wood Mouse (Hylomyscus aeta); 584. Allen's Wood Mouse (Hylomyscus alleni); 585. Ansell's Wood Mouse (Hylomyscus ansell); 586. Lesser Wood Mouse (Hylomyscus parvus); 587. Walter Verheyen's Wood Mouse (Hylomyscus walterverheyeni); 588. Stella Wood Mouse (Hylomyscus stella); 589. Albertine Rift Wood Mouse (Hylomyscus vulcanorum); 590. Eastern Arc Wood Mouse (Hylomyscus arcimontensis); 591. Montane Wood Mouse (Hylomyscus denniae); 592. Mount Kenya Wood Mouse (Hylomyscus endorobae); 593. Tanzanian Wood Mouse (Hylomyscus kaimosae), 594. Kerbis-Peterhans''s Wood Mouse (Hylomyscus kerbispeterhansi); 595. Angolan Wood Mouse (Hylomyscus carillus); 596. Heinrich's Wood Mouse (Hylomyscus heinrichorum); 597. Awash Multimammate Mouse (Mastomys awashensis), 598. Natal Multimammate Mouse (Mastomys natalensis); 599. Reddish-white Multimammate Mouse (Mastomys erythroleucus); 600. Hubert's Multimammate Mouse (Mastomys hubert)); 601. Kollmannsperger's Multimammate Mouse (Mastomys kollmannspergeri); 602. Dwarf Multimammate Mouse (Mastomys pernanus); 603. Southern African Multimammate Mouse (Mastomys coucha); 604. Shortridge's Multimammate Mouse (Mastomys shortridge). in Muridae
On following pages: 578. African Smoky Mouse (Heimyscus fumosus); 579. Baer's Wood Mouse (Hylomyscus baer); 580. Mount Oku Wood Mouse (Hylomyscus grandis); 581. Dahomey Gap Wood Mouse (Hylomyscus pamfi), 582. West African Wood Mouse (Hylomyscus simus); 583. Beaded Wood Mouse (Hylomyscus aeta); 584. Allen's Wood Mouse (Hylomyscus alleni); 585. Ansell's Wood Mouse (Hylomyscus ansell); 586. Lesser Wood Mouse (Hylomyscus parvus); 587. Walter Verheyen's Wood Mouse (Hylomyscus walterverheyeni); 588. Stella Wood Mouse (Hylomyscus stella); 589. Albertine Rift Wood Mouse (Hylomyscus vulcanorum); 590. Eastern Arc Wood Mouse (Hylomyscus arcimontensis); 591. Montane Wood Mouse (Hylomyscus denniae); 592. Mount Kenya Wood Mouse (Hylomyscus endorobae); 593. Tanzanian Wood Mouse (Hylomyscus kaimosae), 594. Kerbis-Peterhans''s Wood Mouse (Hylomyscus kerbispeterhansi); 595. Angolan Wood Mouse (Hylomyscus carillus); 596. Heinrich's Wood Mouse (Hylomyscus heinrichorum); 597. Awash Multimammate Mouse (Mastomys awashensis), 598. Natal Multimammate Mouse (Mastomys natalensis); 599. Reddish-white Multimammate Mouse (Mastomys erythroleucus); 600. Hubert's Multimammate Mouse (Mastomys hubert)); 601. Kollmannsperger's Multimammate Mouse (Mastomys kollmannspergeri); 602. Dwarf Multimammate Mouse (Mastomys pernanus); 603. Southern African Multimammate Mouse (Mastomys coucha); 604. Shortridge's Multimammate Mouse (Mastomys shortridge).
Data from: No relationship between canalization and developmental stability in the skull of a natural population of Mastomys natalensis (Rodentia: Muridae)
The aim of the present work was to investigate the relationship between canalization and developmental stability under varying environmental conditions. Three different cohorts of Mastomys natalensis (Rodentia, Muridae), displaying different growth trajectories, were analyzed by means of Geometric morphometrics. A set of 23 landmarks was digitalized on the dorsal skull of 292 specimens from Morogoro (Tanzania). Patterns of among- and within-individual (measured as fluctuating asymmetry) variation were assessed and compared among and within the three groups in order to test for the presence of a common mechanism between canalization and developmental stability. Results showed that there was no congruence between canalization and developmental stability: 1) levels of FA and among-individual variation varied in a discordant fashion, 2) no correspondence between variance-covariance matrix of among- and within individual variation was found, 3) environmental effects were able to alter the covariance structure of among- individual variation living patterns associated with fluctuating asymmetry unaffected. These findings support the view of multiple mechanisms underlying developmental buffering of shape variation.
Data from: No relationship between canalization and developmental stability in the skull of a natural population of Mastomys natalensis (Rodentia: Muridae)
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