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Kent, E.

Publications and source records attributed to Kent, E..

2 recordsLinked to original sources

Simplifying complexity: the reliability of lidar-derived forest structural complexity metrics for conservation management

Abstract 1. Forest structural complexity is regarded as a driver of biodiversity. The restructuring of forests to increase structural complexity is now a common objective of forest restoration and conservation projects. Lidar provides an efficient means of monitoring forest structure; however, the reliability of lidar-derived structural complexity metrics remains uncertain. Most metrics require a choice of resolution (such as pixel or voxel size), and whilst metric outcomes are sensitive to this choice, an understanding of how this impacts subsequent ecological interpretations of forest restoration monitoring is missing. 2. We assess how metric resolution choices impact FSC estimates using terrestrial laser scanning data from 32 single-species forest plots in Cairngorms National Park, Scotland. These plots represent four contrasting structural categories: ancient woodland (AW), old plantation (OP), old plantation with restructuring management (OPM) and natural restoration (NR); with a hypothesised order of complexity: AW, OPM, OP, NR (from highest complexity to lowest). We computed 21 FSC metrics and calculated how each metric ranked our forest structural categories across a resolution gradient (0.02-1.5m). We evaluated the stability of metric rankings across resolution values, their ability to discriminate forest categories, and the consistency of ecological interpretation of forest management targets. 3. Nine metrics produced unstable rankings, indicating that ecological conclusions were sensitive to resolution selection. Stable metrics discriminated well between categories with obvious structural differences but failed to discriminate between categories with subtle differences, particularly OP and OPM. 4. AW did not consistently exhibit the highest structural complexity, instead occupying an intermediate position characterised by a combination of canopy occupancy, openness and height inequality, not captured by any single metric. 5. We conclude that methodological choices can influence FSC estimates and ecological conclusions drawn from them. 6. Synthesis and applications: Reliable assessment of forest restoration depends not only on the choice of metric but also on how that metric is parameterised. We recommend transparent reporting and justification of resolution parameter selection together with the use of stable metrics that capture structural characteristics relevant to management objectives being monitored, to improve reliability and comparability of lidar-based forest monitoring.

ecology↗

A robust evaluation of TDP-43, poly GP, cellular pathology, and behavior in a AAV-C9ORF72 (G4C2)66 mouse model

The G4C2 hexanucleotide repeat expansion in C9ORF72 is the major genetic cause of both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) (C9-ALS/FTD). Despite considerable efforts, the development of mouse models of C9-ALS/FTD useful for therapeutic development has proven challenging due to the intricate interplay of genetic and molecular factors underlying this neurodegenerative disorder, in addition to species differences. This study presents a robust investigation of the cellular pathophysiology and behavioral outcomes in a previously described AAV mouse model of C9-ALS expressing 66 G4C2 hexanucleotide repeats. Despite displaying key molecular ALS pathological markers including RNA foci, dipeptide repeat (DPR) protein aggregation, p62 positive stress granule formation as well as mild gliosis, the AAV-(G4C2)66 mouse model in this study exhibits negligible neuronal loss, no motor deficits, and functionally unimpaired TAR DNA-binding protein-43 (TDP-43). While our findings indicate and support that this is a robust and pharmacologically tractable model for investigating the molecular mechanisms and cellular consequences of (G4C2) repeat driven DPR pathology, it is not suitable for investigating the development of disease associated neurodegeneration, TDP-43 dysfunction, gliosis, and motor performance. Our findings underscore the complexity of ALS pathogenesis involving genetic mutations and protein dysregulation and highlight the need for more comprehensive model systems that reliably replicate the multifaceted cellular and behavioral aspects of C9-ALS.

neuroscience↗