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Biology subjects

Jones, A. K.

Publications and source records attributed to Jones, A. K..

5 recordsLinked to original sources

MetaBeeAI: an AI pipeline for full-text systematic reviews in biology

The volume and complexity of scientific literature are expanding rapidly, making it increasingly difficult to extract and synthesise information across studies. This challenge is particularly acute in the biological sciences, where evidence spans multiple levels of organisation and heterogeneous experimental designs. Large Language Model (LLM) pipelines offer a scalable route to evidence synthesis, but many existing approaches lack transparency, modularity, and effective mechanisms for human oversight. We present MetaBeeAI, an open-source, modular pipeline that integrates established LLM techniques into a coherent, auditable workflow for structured data extraction in biology. MetaBeeAI combines modular prompting, multi-pass extraction, and expert-in-the-loop validation within an interface that presents model outputs alongside source text, enabling inspection, correction, and iterative refinement. The pipeline produces machine-readable records of prompts, configurations, and expert annotations, supporting reproducibility and continuous improvement. We apply MetaBeeAI to 924 research papers on bees and pesticides, extracting structured information on species, compounds, exposure designs, and experimental context. Evaluation demonstrates improved consistency, convergence with expert judgement, and robustness across heterogeneous biological studies, highlighting the value of expert-guided refinement. MetaBeeAI provides a transparent and extensible framework for scalable evidence synthesis, supporting reliable integration of LLMs into biological research workflows.

ecology↗

Syntrichia ruralis: Emerging model moss genome reveals a conserved and previously unknown regulator of desiccation in flowering plants

Water scarcity poses a significant threat to ecosystems in the face of global climate change. Syntrichia ruralis, a dryland moss known for its desiccation tolerance, provides valuable insights into surviving water-limited conditions. In this study, the genome of S. ruralis was sequenced and assembled into 12 chromosomes encompassing 21,169 protein-coding genes. Additionally, 3,199 unplaced scaffolds were identified as non-nuclear and symbiont DNA. Transposable elements (TEs) constitute 51.24% of the genome. Notably, chromosome 12, the largest in size due to its high TE load, was identified as the putative sex chromosome. Comparative analysis with the closely related Syntrichia caninervis genome reveals significant large-scale synteny yet some rearrangements, as well as the occurrence of older duplication events that are shared by both. Desiccation and drought tolerance associated gene families, such as early light-inducible proteins (ELIPs) and late embryogenesis abundant (LEA) proteins, were characterized. In addition to a subset of LEA genes being species-specific, a comparative transcriptomic analysis revealed that some shared LEA genes respond differently to dehydration in these two species. Many ELIPs (9 out of 30) are the product of tandem duplication events. As expected, our analyses revealed the importance of the phytohormone abscisic acid (ABA) in the desiccation response of S. ruralis. A significant number of ABA responsive genes were found to be regulated by S. ruralis orthologs of ABA insensitive 3 (ABI3) and abscisic acid responsive element binding factor 2 (AREB2). Markedly, an uncharacterized, but deeply conserved MYB transcription factor, appears to act as a negative regulator of AREB2 in S. ruralis. Interestingly, we determined that the orthologous MYB TF is also involved in an ABA-dependent stress response in the model flowering plant A. thaliana. In sum, the new genomic resources from this emerging model moss offer new insights into the evolution of desiccation tolerance in land plants.

genomics↗

Boundary effects of expectation in human pain perception

Perception of sensory stimulation is influenced by numerous psychological variables. One example is placebo analgesia, where expecting low pain causes a painful stimulus to feel less painful. Yet, because pain evolved to signal threats to survival, it should be maladaptive for highly-erroneous expectations to yield unrealistic pain experiences. Therefore, we hypothesised that a cue followed by a highly discrepant stimulus intensity, which generates a large prediction error, will have a weaker influence on the perception of that stimulus. To test this hypothesis we collected two independent pain-cueing datasets. The second dataset and the analysis plan were preregistered (osf.io/5r6z7). Regression modelling revealed that reported pain intensities were best explained by a quartic polynomial model of the prediction error. The results indicated that the influence of cues on perceived pain decreased when stimulus intensity was very different from expectations, suggesting that prediction error size has an immediate functional role in pain perception.

neuroscience↗

Neural representations of aversive value encoding in pain catastrophizers

Chronic pain is exacerbated by maladaptive cognition such as pain catastrophizing (PC). Biomarkers of PC mechanisms may aid precision medicine for chronic pain. Here, we investigate EEG biomarkers using mass univariate and multivariate (machine learning) approaches. We test theoretical notions that PC results from a combination of augmented aversive-value encoding (\"magnification\") and persistent expectations of pain (\"rumination\"). Healthy individuals with high or low levels of PC underwent an experimental pain model involving nociceptive laser stimuli preceded by cues predicting forthcoming pain intensity. Analysis of EEG acquired during the cue and laser stimulation provided event-related potentials (ERPs) identifying spatially and temporally-extended neural representations associated with pain catastrophizing. Specifically, differential neural responses to cues predicting high vs. low intensity pain (i.e. aversive value encoding) were larger in the high PC group, largely originating from mid-cingulate and superior parietal cortex. Multivariate spatiotemporal EEG patterns evoked from cues with high aversive value selectively and significantly differentiated the high PC from low PC group (64.6% classification accuracy). Regression analyses revealed that neural patterns classifying groups could be partially predicted (R2 = 28%) from those neural patterns classifying the aversive value of cues. In contrast, behavioural and EEG analyses did not provide evidence that PC modifies more persistent effects of prior expectation on pain perception and nociceptive responses. These findings support the hypothesis of magnification of aversive value encoding but not persistent expression of expectation in pain catastrophizers. Multivariate patterns of aversive value encoding provide promising biomarkers of maladaptive cognitive responses to chronic pain that have future potential for psychological treatment development and clinical stratification.

neuroscience↗

Improved Aedes aegypti mosquito reference genome assembly enables biological discovery and vector control

Female Aedes aegypti mosquitoes infect hundreds of millions of people each year with dangerous viral pathogens including dengue, yellow fever, Zika, and chikungunya. Progress in understanding the biology of this insect, and developing tools to fight it, has been slowed by the lack of a high-quality genome assembly. Here we combine diverse genome technologies to produce AaegL5, a dramatically improved and annotated assembly, and demonstrate how it accelerates mosquito science and control. We anchored the physical and cytogenetic maps, resolved the size and composition of the elusive sex-determining \"M locus\", significantly increased the known members of the glutathione-S-transferase genes important for insecticide resistance, and doubled the number of chemosensory ionotropic receptors that guide mosquitoes to human hosts and egg-laying sites. Using high-resolution QTL and population genomic analyses, we mapped new candidates for dengue vector competence and insecticide resistance. We predict that AaegL5 will catalyse new biological insights and intervention strategies to fight this deadly arboviral vector.

genomics↗