Search bioRxiv⌕ Search

Biology subjects

Arnold, H.

Publications and source records attributed to Arnold, H..

3 recordsLinked to original sources

Application of Machine Learning Tools for Waterbird Colony Monitoring Provides Gains in Precision and Temporal Efficiency

Waterbirds serve as important indicators of both aquatic and terrestrial ecosystem health, making effective monitoring essential for tracking population health and identifying potential causes of decline. Drones have provided opportunities to overcome historic waterbird monitoring challenges, but the expertise and time required for manual image analysis creates a major bottleneck. Recent advances in deep learning-based object detection have enabled rapid, automatic detection of features in complex ecological imagery, though applications have largely been limited to single-species colonies, and practitioners lack quantitative comparisons of annotation time and accuracy across different levels of automation. We systematically compared four waterbird monitoring approaches using identical survey areas from Chester Island, a mixed-species colony in Matagorda Bay, Texas, in 2025: (1) traditional ground-based counts, (2) manual drone imagery-based counts, (3) computer-assisted counts using pre-annotations from an object detector with manual human verification (Human+ML), and (4) fully automated counts using object detector annotations (ML-only). We trained a YOLOv10 object detection model on manually annotated imagery of Chester Island in 2021 and applied it to the 2025 imagery. Manual drone annotation detected 6,530 birds in 40.5 hr and served as the primary reference standard. Human+ML detected 5,826 birds (89% of manual) in 7.7 hr, an 81% reduction in annotation time. ML-only detected 5,679 birds (87% of manual) in approximately 46 min, a 98% reduction. Ground counts recorded 5,868 birds (90% of manual). Detection generalized well across species while classification depended heavily on training data and morphological distinctiveness. The Human+ML workflow emerged as a practical middle ground, providing practitioners with empirical data to evaluate partial versus full automation strategies based on monitoring objectives. LAY SUMMARYO_LIConservation programs need accurate counts of nesting waterbirds, but analyzing drone images by hand has become a major bottleneck, slowing the availability of monitoring data for use. C_LIO_LIWe compared four ways to count waterbirds at a large nesting colony in coastal Texas where many species nest together: traditional ground-based counts, manual annotation of drone imagery, computer-assisted annotation, and fully automated annotation using a trained object detection model. C_LIO_LIDetection generalized well across species while classification depended on training data availability and morphological distinctiveness. C_LIO_LIPairing automated detection with site-specific or human classification offers a practical path forward for monitoring mixed-species colonies. C_LI

ecology↗

Distinct topologically associated domains underlie the regulatory logic in lymphatic endothelial cells contributing to proper cell differentiation

The activation and repression of genes is a fundamental part of proper embryonic development and functional tissue formation, ensuring that unique molecular codes are set up to orchestrate cell differentiation. Changes in chromatin organisation dictate accessibility to gene regulatory elements and control gene expression. Several molecular factors regulating lymphatic endothelial cell (LEC) specification and differentiation have been identified. However, it remains to be defined how chromatin is organised in lymphatic endothelium and how it orchestrates lymphatic vessel network formation. In this study, we combined Hi-C and ATAC-sequencing to characterise 3D chromatin architecture and accessibility in LECs and blood endothelial cells (BECs). We have identified cell type-specific topologically associated domains (TADs) in LECs and BECs. Specifically, our data revealed changes in the TAD boundaries and differentially segregating enhancers regions in lymphatic-associated loci, such as prox1a and tbx1. This multi-omic approach also defined the regulatory logic for nine genes whose expression is enriched in LECs. In vivo validation of their short- and long-range enhancers confirmed their LEC-confined activity. Leveraging these datasets, we reconstructed mafba tissue-specific regulatory networks and identified a genetic interaction with tfe3a in vivo necessary to limit ectopic vessel formation. Overall, our work provides a powerful resource of multi-omic datasets that can be used to systematically determine the regulatory networks governing LEC identity and genes linked to lymphatic disease.

developmental biology↗

Opposing lineage specifiers induce a pro-tumor hybrid-identity state in lung adenocarcinoma

The ability of cancer cells to alter their identity, known as lineage plasticity, is crucial for tumor progression and therapy resistance. In lung adenocarcinoma (LUAD), tumor progression is characterized by a gradual loss of lineage fidelity and the emergence of non-pulmonary identity programs. This can lead to hybrid-identity (hybrid-ID) states in which developmentally incompatible identity programs are co-activated within individual cells. However, the molecular mechanisms underlying these identity shifts remain incompletely understood. Here, we identify the gastrointestinal (GI) transcriptional regulator HNF4 as a critical driver of tumor growth and proliferation in KRAS-driven LUAD. In LUAD cells that express the lung lineage specifier NKX2-1, HNF4 can induce a GI/liver-like state by directly binding and activating its canonical targets. HNF4 also forms an aberrant protein complex with NKX2-1, which disrupts NKX2-1 localization and dampens pulmonary identity within hybrid-ID LUAD. Sustained signaling through the RAS/MEK pathway is critical for maintaining the hybrid-ID state. Moreover, RAS/MEK inhibition augments NKX2-1 chromatin binding at pulmonary-specific genes and induces resistance-associated pulmonary signatures. Finally, we demonstrate that HNF4 depletion enhances sensitivity to pharmacologic KRASG12D inhibition. Collectively, our data show that co-expression of opposing lineage specifiers leads to a hybrid identity state that can drive tumor progression and dictate response to targeted therapy in LUAD.

cancer biology↗