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9 results for “Herpestes javanicus”
Fig. 3 in Javan mongoose (Herpestes javanicus) abundance and spatial ecology in a degraded dry dipterocarp forest
Fig. 3. Map of Sakaerat Biosphere Reserve with radio tracked (December 2019 to January 2021) Javan mongoose (Herpestes javanicus) home ranges and prey grids (PG). 95% utilisation contours (U.C) for male (M6, M1) and female (F1) mongooses are labelled in the legend. 50% U.C are solid line circles within each individual's home range. Prey grids collected ground-dwelling invertebrate mass as well as rodent biomass within the DDF (October to December 2020). Stars indicate where only ground-dwelling invertebrates were collected. Triangles indicate areas where sweep netting for invertebrates occurred in addition to sampling for rodent biomass and ground-dwelling invertebrates.
Fig. 1 in Javan mongoose (Herpestes javanicus) abundance and spatial ecology in a degraded dry dipterocarp forest
Fig. 1. Map and location of Sakaerat Biosphere Reserve with camera trap stations used to estimate Javan mongoose (Herpestes javanicus) abundance in 2017. Prey grid stations were used to calculate yearly averaged rodent biomass from January 2017 to November 2017.
Figure 3 in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan
Figure 3. Light microscopic (hematoxylin and eosin stained) sections (40×) of the ovaries of female small Indian mongoose (Herpestes javanicus) from the Potohar Plateau, Pakistan: A) showing 3 Graafian follicles indicative of the state of preovulation during February 2013; B) events of early gestation period during March 2013, corpus luteum of moderate size and reddish yellow, antrum being a bit convoluted in structure rather than being complete; C) events of late gestation period during April 2013, whereby corpora lutea are seen as the most prominent structures; D) showing lactation phase of the species with no corpora lutea or ripe follicles during June 2013. (*P.F.: primary follicle; S.F.: secondary follicle; C.L.: corpus luteum; G.F.: Graafian follicle; Pr. F.: primordial follicle).
Figure 4. A in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan
Figure 4. A) Foot prints of small Indian mongoose established around its burrow, B) Especially designed mesh trap for live capturing of the species, C) Placental Scars, D) Developing embryos inside the uteri of female mongoose exposed after dissection, E) A vigilant mongoose, F) Small Indian mongoose and her pups caught in a live trap
Figure 2 in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan
Figure 2. Levels (mIU/mL) of follicle stimulating hormone (FSH) and luteinizing hormone (LH) in plasma samples of small Indian mongoose females (Herpestes javanicus) trapped on the Potohar Plateau. LH levels show 2 peaks (1 in September 2012 and 1 in March 2013).
Fig. 1 in Conservation Status Of Small Asian Mongoose Herpestes Javanicus (É. Geoffroy Saint-Hilaire, 1818) (Mammalia: Carnivora: Herpestidae) In Lao Pdr
Fig. 1. Lao PDR, with locations of post-1990 Small Asian Mongoose records, survey areas, and sites mentioned in the text. Filled stars: confirmed records; open stars: provisional records. Increasing altitude is represented by increasing darkness: areas of level terrain are therefore areas of uniform shading. Dotted outlines indicate national protected areas (all surveyed to at least some extent). Survey areas outside NPA system: A, Phongsali town and surrounds; B, Upper Lao Mekong and Bokeo plain; C, Xiangkhouang plateau, Phou (= Mount) Gnouan and Phou San; D, Muang (= District) Sangthong, Vientiane municipality; E, Nam Theun Extension proposed NPA (= former Nam Chat–Nam Phan provincial protected area); F, Pakxan wetlands; G, Nakai plateau; H, Muang Vilabouli, Savannakhet province; I, western Savannakhet lowlands and Mekong; J, central Savannakhet lowlands; K, Phou Ahyon; L, Dakchung plateau; M, Salavan town and surrounds; N, Phou Kathong proposed NPA; O, Xe (= River) Namnoy catchment and Bolaven Southwest proposed NPA; P, Muang Pathoumphon, Champasak province; Q, Nam Ghong provincial protected area; R, Dong Khanthung proposed NPA. In addition various sites around Vientiane received at least moderate coverage.
On following pages: 3. Small Indian Mongoose (Herpestes auropunctatus); 4. Short-tailed Mongoose (Herpestes brachyurus); 5. Indian Gray Mongoose (Herpestes edwardsii); 6 Indian Brown Mongoose (Herpestes fuscus); 7. Egyptian Mongoose (Herpestes ichneumon); 8. Javan Mongoose (Herpestes javanicus); 9. Collared Mongoose (Herpestes semitorquatus); 10. Ruddy Mongoose (Herpestes smithii); 11. Crab-eating Mongoose (Herpestes urva); 12. Stripe-necked Mongoose (Herpestes vitticollis). in Herpestidae
On following pages: 3. Small Indian Mongoose (Herpestes auropunctatus); 4. Short-tailed Mongoose (Herpestes brachyurus); 5. Indian Gray Mongoose (Herpestes edwardsii); 6 Indian Brown Mongoose (Herpestes fuscus); 7. Egyptian Mongoose (Herpestes ichneumon); 8. Javan Mongoose (Herpestes javanicus); 9. Collared Mongoose (Herpestes semitorquatus); 10. Ruddy Mongoose (Herpestes smithii); 11. Crab-eating Mongoose (Herpestes urva); 12. Stripe-necked Mongoose (Herpestes vitticollis).
Data from: Convergence analysis of a finite element skull model of Herpestes javanicus (Carnivora, Mammalia): implications for robust comparative inferences of biomechanical function
Predictions of skull biomechanical capability based on virtual models constitute a valuable data source for testing hypotheses about craniodental form and feeding behavior. Such comparative analyses also inform dietary reconstruction in extinct species. 3D modeling using Finite Element (FE) methods is a common technique applied to the comparative analysis of craniodental function in extinct and extant vertebrates. However, taxonomically diverse skull models in the literature often are not directly comparable to each other, in part because of distinctions in how boundary conditions are defined, but also because of substantial differences in the number of FEs composing the models. In this study, we test whether a conventional convergence test is adequate in identifying the minimum number of FEs needed to achieve internally stable results for a single species. We constructed a series of skull models of Herpestes javanicus, and simulated unilateral biting across the dentition; the models differed in the number of FEs, degrees of freedom at the joint and bite point constraints, and type of tetrahedral FEs used. We found that convergence patterns differed across constraint types, FE quantities, and bite position simulated. Four-noded tetrahedral (tet-4) FE models with relaxed constraints produced the most stable measurements compared to over-constrained tet-4 models and to relaxed tet-10 models. In absence of an optimal FE quantity from convergence testing, we propose a broadly applicable sub-sampling protocol, whereby average measurement values across multiple models per specimen are used for among-species comparisons. A regime of sampling three low FE quantity models produced the closest estimates of mean measurement values relative to larger model sets, being within the 95% bootstrap estimated confidence intervals. Future studies should focus on identifying sources of variation associated with other FE modeling protocols, so that they can be accounted for before biomechanical attributes from these simulations are used to infer form–function linkage.
Data from: Convergence analysis of a finite element skull model of Herpestes javanicus (Carnivora, Mammalia): implications for robust comparative inferences of biomechanical function
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