5 research outputs found
Higher Himalayan Crystalline (HHC) Belt: its shear sense indicators and their implications on its tectonic evolution
Identifying realistic recovery targets and conservation actions for tigers in a human dominated landscape using spatially-explicit densities of wild prey and their determinants
Aim
Setting realistic population targets and identifying actions for site and landscape-level recovery plans are critical for achieving the global target of doubling wild tiger numbers by 2022. Here, we estimate the spatially explicit densities of wild ungulate prey across a gradient of disturbances in two disjunct tiger habitat blocks (THBs) covering 5212 km2, to evaluate landscape-wide conditions for tigers and identify opportunities and specific actions for recovery.
Location
Western Terai Arc Landscape, India.
Methods
Data generated from 96 line transects in 15 systematically selected geographical cells (166.5 km2) were used to estimate spatially explicit densities of six wild ungulate prey species at a fine scale (1 km2). Employing distance-based density surface models, we derived species-specific estimates within three major forest land management categories (inviolate protected areas (PA), PAs with settlements and multiple-use forests). By scaling estimated prey densities using an established relationship, we predicted the carrying capacity for tigers within each THB.
Results
Species-specific responses of the six wild ungulates to natural-habitat and anthropogenic covariates indicated the need for targeted prey recovery strategies. Inviolate PAs supported the highest prey densities compared with PAs with settlements and multiple-use forests, and specifically benefited the principal tiger prey species (chital Axis axis and sambar Rusa unicolor). The estimated mean prey density of 35.16 (±5.67) individuals per km2 can potentially support 82 (62–106) and 299 (225–377) tigers across THB I and THB II, which currently support 2 (2–7) and 225 (199–256) tigers, respectively. This suggests a potential c. 68% increase in population size given existing prey abundances. Finally, while THB I represents a potential tiger recovery site given adequate prey, PAs where resettlement of pastoralists is underway represent potential prey recovery sites in THB II.
Main conclusions
This systematic approach of setting realistic population targets and prioritizing spatially explicit recovery strategies should aid in developing effective landscape conservation plans towards achieving global tiger conservation targets
Glucocrinology of Modern Sulfonylureas: Clinical Evidence and Practice-Based Opinion from an International Expert Group
Provide enhanced digital features for this article
If you are an author of this publication and would like to provide additional
enhanced digital features for your article then please contact [email protected].
The journal offers a range of additional features designed to increase
visibility and readership. All features will be thoroughly peer reviewed to
ensure the content is of the highest scientific standard and all features are
marked as ‘peer reviewed’ to ensure readers are aware that the content has been
reviewed to the same level as the articles they are being presented alongside.
Moreover, all sponsorship and disclosure information is included to provide
complete transparency and adherence to good publication practices. This ensures
that however the content is reached the reader has a full understanding of its
origin. No fees are charged for hosting additional open access content.
Other enhanced features include, but are not limited to:
• Slide decks
• Videos and animations
• Audio abstracts
</p
Euthymia in Diabetes: Clinical Evidence and Practice-Based Opinion from an International Expert Group
Full copyright for enhanced digital
features is owned by the authors.
Article full
text
The full text of this article can be found here.
Provide enhanced digital features for this article
If you are an author of this publication and would like to provide additional
enhanced digital features for your article then please contact [email protected].
The journal offers a range of additional features designed to increase
visibility and readership. All features will be thoroughly peer reviewed to
ensure the content is of the highest scientific standard and all features are
marked as ‘peer reviewed’ to ensure readers are aware that the content has been
reviewed to the same level as the articles they are being presented alongside.
Moreover, all sponsorship and disclosure information is included to provide
complete transparency and adherence to good publication practices. This ensures
that however the content is reached the reader has a full understanding of its
origin. No fees are charged for hosting additional open access content.
Other enhanced features include, but are not limited to:
• Slide decks
• Videos and animations
• Audio abstracts
• Audio slides</p
A kinome-wide screen identifies a CDKL5-SOX9 regulatory axis in epithelial cell death and kidney injury
© 2020, The Author(s). Renal tubular epithelial cells (RTECs) perform the essential function of maintaining the constancy of body fluid composition and volume. Toxic, inflammatory, or hypoxic-insults to RTECs can cause systemic fluid imbalance, electrolyte abnormalities and metabolic waste accumulation- manifesting as acute kidney injury (AKI), a common disorder associated with adverse long-term sequelae and high mortality. Here we report the results of a kinome-wide RNAi screen for cellular pathways involved in AKI-associated RTEC-dysfunction and cell death. Our screen and validation studies reveal an essential role of Cdkl5-kinase in RTEC cell death. In mouse models, genetic or pharmacological Cdkl5 inhibition mitigates nephrotoxic and ischemia-associated AKI. We propose that Cdkl5 is a stress-responsive kinase that promotes renal injury in part through phosphorylation-dependent suppression of pro-survival transcription regulator Sox9. These findings reveal a surprising non-neuronal function of Cdkl5, identify a pathogenic Cdkl5-Sox9 axis in epithelial cell-death, and support CDKL5 antagonism as a therapeutic approach for AKI
