Search bioRxiv⌕ Search

Biology subjects

Barlow, J.

Publications and source records attributed to Barlow, J..

At least 19 recordsLinked to original sources

Unsupervised source separation and clustering of soundscape recordings predicts avian richness in hyperdiverse systems

1: Passive Acoustic Monitoring (PAM) has emerged as a leading approach for biodiversity research, but analysing the vast quantities of data produced by this method remains challenging. Acoustic indices are often employed to estimate species richness in soundscape recordings, but their generalisability and overall efficacy in speciose regions has increasingly been challenged. An alternative, multi-species classification models, still suffer from performance limitations, particularly in the tropics. 2: We introduce an unsupervised approach that estimates avian species richness using an integrated source separation model trained on birds (BirdMixIT), a leading bird vocalization embedding model (Perch 2.0), and hierarchical agglomerative clustering. We count the clusters of embeddings generated from separated channels to estimate the species richness in recordings at differing timescales. 3: We test the generalisability and predictive performance of our approach, "source-clustering", using a large combined dataset featuring 103 total hours of manually-annotated soundscape recordings from the Amazon rainforest in Peru and Brazil. To compare the performance of source-clustering to existing approaches, we estimated species richness in the same recordings with both traditional acoustic indices and Perch classifications at various confidence thresholds. 4: Our source-clustering method performed consistently well between our separate datasets. Source-clustering performed better for predicting avian species richness than traditional acoustic indices at all levels, and was complementary with Perch, performing similarly overall to its best settings combinations, though it was more robust for short recordings, and should be more resilient in locations with less training data. Source-clustering generally predicted species richness better than the best-performing Perch settings at the 15-second, 1-minute, and 15-minute temporal resolutions, while most settings of Perch performed better at the 1-hour resolution. 5: Source-clustering can complement or exceed the performance of presently established methods for estimating avian species richness from soundscape recordings, namely traditional acoustic indices and the out-of-box versions of leading automated identification modes. This is particularly true at narrow temporal resolutions, in systems where training data is scarce, and where species density is high enough to generate significant overlapping vocalisations, rendering it especially useful in hyperdiverse tropical ecosystems where other methods for interpreting soundscape recordings face persistent challenges.

bioinformatics↗

Senataxin loss induces cGAS–STING-mediated mitochondrial dysfunction

Ataxia with oculomotor apraxia type 2 (AOA2) is a rare neurodegenerative disease caused by loss-of-function mutations in Senataxin, which encodes an RNA:DNA helicase. Many studies on Senataxin loss focus on its putative roles in regulating transcription and RNA transcript localization. However, several phenotypes remain underexplored, including metabolic dysregulation associated with ataxias. Using Senataxin-deficient mouse cells, we observed increased nuclear and genomic instability, as well as innate immune activation via the cGAS-STING axis. We also observed elevated ROS levels, decreased mitochondrial function, and hyperfused mitochondria. Importantly, mitochondrial dysfunction depends on cGAS/STING activity, indicating that the two phenotypes are functionally connected. Senataxin-deficient mice and AOA2 patient cells similarly exhibit spontaneous innate immune activation, and AOA2 patient cells also show decreased mitochondrial function. Our work identifies a previously unseen phenotype for AOA2 in which loss of Senataxin results in mitochondrial dysfunction promoted by cGAS and STING. SummaryThis study demonstrates a previously unidentified phenotype in AOA2 and Senataxin research in which cGAS-STING promotes mitochondrial dysregulation in Setx-/- MEFs. Further, these innate immune activation and mitochondrial dysregulated phenotypes are recapitulated in AOA2 patient cells.

Cell Biology↗

Anthropogenic disturbance inverts microclimate stratification in tropical forests

Tropical rainforests generate and maintain their own microclimate regimes and the resultant cooler, more humid and stable environments foster the hyperdiversity typical of these ecosystems. Although the temporal and spatial (horizontal) distributions of microclimates have been relatively well studied, the vertical dimension has received less attention, and little is known about how forest disturbance affects the vertical stratification of microclimates in tropical forests. In this study, we examine how the vertical distribution of temperatures varies between undisturbed and burned Amazonian forests. We installed five vertical transects with temperature dataloggers distributed at 7 different heights to collect data over multiple days during the end of the dry season. We investigated how anthropogenic disturbance (fire) mediates the vertical stratification of microclimate and whether microclimate buffering (i.e, the difference between understorey and canopy temperatures) varies according to the forest structure. We showed that anthropogenic disturbance can cause an inversion in the vertical stratification of microclimates, with burned forests having hotter temperatures (up to 2 {degrees}C) in the understorey than in the canopy during the day - the opposite of what is found in undisturbed forests (typically 3 {degrees}C cooler). During the night, while understorey and canopy temperatures are similar in undisturbed forests, we found that, in burned forests, understorey temperatures were up to 2 {degrees}C cooler than in the canopy. Microclimate buffering by day was best explained by aboveground carbon stocks, with higher temperature buffering in more carbon rich forests. Our study shows that anthropogenic disturbance alters the vertical stratification of temperatures in Amazonian forests, leading to significant temporal changes along the diel cycle. Future research should focus on understanding these changes across a wider range of disturbance regimes, and explore the consequences for biodiversity and ecosystem functions from the canopy to the forest floor.

ecology↗

Golgi-localised Guanylate-binding protein 5 enhances glycolysis in macrophages

Guanylate-binding proteins (GBPs) are part of a family of large interferon gamma (IFN{psi})-inducible GTPases, with ascribed roles in infection control and induction of programmed cell death. While pathogen-specific functions of GBPs have been studied in detail, their broader regulation of frontline immune defences remain unexplored. Here, we analysed the global contribution of human GBP1-5 to cellular metabolism in IFN{psi}-stimulated macrophages. We found a robust role of GBP2 and GBP5 in macrophage glycolysis. Only GBP5, and not GBP2 deficiency impaired surface expression and cytokine production of classically IFN{psi}/LPS-activated macrophages. The GTPase activity of GBP5 was required for the regulation of glycolysis and cytokine production. We found that GBP5 deficiency impaired cellular glucose uptake and lactate production specifically. Isotopic tracing with [U-13C6]-Glucose confirmed a decrease in several glycolytic intermediates, including glucose 6-phosphate, pyruvate, and lactate, but stable levels of traced tricarboxylic acid cycle (TCA) intermediates. Elevated ribose-5-phosphate and glycerol levels suggest an altered cytosolic redox balance and enhanced breakdown of fatty acids. GBP5 localised predominantly to the cis-Golgi and in the absence of GBP5 we observed increased Golgi fragmentation, however the total Golgi size remained unchanged. Our results underscore the fundamental role of GBP5 in glycolytic fluxes and Golgi integrity in IFN{psi}-stimulated macrophages, highlighting its significance in immune function in general and immunometabolism specifically.

immunology↗

The reliability of acoustic classification models for determining avian vocalisation patterns

Automated detection and classification of species vocalisations offers the potential to utilise acoustic datasets across unprecedented spatial and temporal scales. However, classification algorithms inevitably generate errors, and error rates vary with context. While methods for quantifying error rates in ecoacoustics are well established, there is limited research on what level of model performance is sufficient to reliably determine avian vocalisation patterns. Using an extensive fully expert-labelled acoustic dataset from Peru (18 hours, 6 sites), we examined changes in the probability of detecting target bird vocalisations in the first hour after dawn to address three key questions: (1) How sensitive are models predicting detection probability over time to reductions in classification accuracy? (2) To what extent does aggregating detections over longer time periods impact classification accuracy? Additionally, we used the labelled dataset to assess how the creation and composition of a test dataset for assessing classifier performance can impact the reliability of accuracy metrics: (3) Are estimates of classification precision robust when test and deployment datasets are not independent and identically distributed? Our results indicate that poor classification performance--especially low precision--can lead to misleading inferences about temporal patterns of vocalisations. Aggregating classifier predictions over longer time periods improved recall but often resulted in misleading patterns of vocal behaviour by reducing precision and temporal resolution. We also demonstrate that precision can be substantially overestimated when species presences are rarer in the deployment dataset than in test data. These findings highlight the importance of cautious application of automated classification in acoustic ecology and the need for accuracy assessment methods tailored to the intended ecological analysis.

ecology↗

Hyperdominance and rarity in Amazonian secondary forests

Recent studies have shown that a few tree species dominate abundance and carbon storage in undisturbed Amazonian forests. However, this pattern remains poorly understood in forests regrowing after deforestation. Understanding dominance patterns in secondary forests is important as it could improve insights into their functioning and guide management and restoration efforts. We used unweighted and novel plot-weighted approaches to assess hyperdominance in abundance and carbon storage of trees and palms during secondary forest recovery, using data from 102 plots across four regions in the eastern Amazon, separated by an average distance of 600 km (range: 150-1,000 km). Secondary forests show extreme hyperdominance in all approaches, with just 16-25 species ([~]3.6-5.6%) accounting for over 50% of abundance and carbon storage. A small subset of species ([~]9%) were found across all regions and successional stages, highlighting their key role in ecosystem structure and function during forest regrowth. Annona exsucca, Cecropia palmata, Tapirira guianensis, Inga alba, Attalea maripa, Amphiodon effusus, Banara guianensis, and Vismia guianensis consistently emerged as hyperdominant across stem size classes, approaches, and metrics, jointly accounting for roughly 16-27% of total abundance and carbon in Amazonian secondary forests. For larger stems >10cm DBH, hyperdominant species exhibited lower wood density compared to non-hyperdominant species across all successional stages, suggesting these specialist pioneers have distinct ecological strategies from the rest of the community. Our findings indicate that secondary forest functioning can be largely predicted by a relatively limited set of species, providing a framework for future research ranging from ecophysiology to remote sensing of canopy traits and restoration planning.

ecology↗

Combined interventions are required to reverse biodiversity and carbon losses in tropical forest frontiers

Halting deforestation and promoting restoration are at the core of biodiversity and climate strategies in tropical forest regions. Avoiding forest disturbances is also critically important but has received far less attention, and there is a lack of clarity about the cost-effectiveness of these three different interventions. We provide the first comparison of the biodiversity and carbon benefits and costs associated with each intervention, comparing observed and counterfactual outcomes based on in-depth field assessments and high-resolution remote sensing in Amazonian Brazil. Avoiding forest disturbances delivered the greatest benefits and was more cost-effective than either avoiding deforestation or restoration, with results being robust to a range of benefit and cost assumptions. However, combined interventions delivered the greatest gains and were essential to reverse biodiversity and carbon losses.

ecology↗

G-quadruplex stabilization induces DNA breaks in pericentromericrepetitive DNA sequences in B lymphocytes

DNA secondary G-quadruplex (G4) structures can impair and even obstruct the DNA replication. Defects in processing G4 structures are associated with replication stress, a common property of both B cell cancers and hyperproliferative premalignant cells. Genome instability arising from replication stress is a hallmark of cancer and strongly contributes to the chromosome rearrangements in B cell cancers. Here, we define the impact of G4-stabilizing ligands on generating genome instability in primary and malignant B cells. Treatment with the G4-stabilizing compound pyridostatin (PDS) causes breaks and chromosome rearrangements at ribosomal DNA and pericentromeric major satellite regions in both mouse primary B cell culture and CH12 lymphoma cells. PDS also causes extensive pericentromeric DNA damage in immortalized human B cell lines. Remarkably, PDS causes high level of tetraploid metaphase cells correlated with high level of dicentric chromosomes specifically in primary but not in CH12 B cells. Unlike primary B cells, CH12 cells undergo checkpoint activation and strong G2/M arrest in response to PDS treatment thus preventing tetraploid appearance. Altogether, these results highlight the difference between primary and malignant B cells in response to PDS, revealing the therapeutic potential of G4-stabilizing drugs to selectively suppress tumor cell growth and proliferation. Significance StatementG-quadruplexes are guanine-rich DNA secondary structures, abundantly found in most eukaryotic genomes. Stabilization of G-quadruplexes creates an obstacle for DNA replication, particularly in DNA repair-deficient cells. We show that G-quadruplex stabilization by the small molecule pyridostatin leads to recurrent DNA breaks and aberrant chromosomal fusions in the repetitive DNA sequences found at major satellite pericentromeric repeats and ribosomal DNA arrays in mouse primary B cells. Pyridostatin also causes extensive pericentromeric DNA damage and pathogenic rearrangements in mouse and human B cell lymphoma cell lines. Thus we have found a role for G-quadruplexes in inciting damage driving the formation of recurrent rearrangements observed in lymphoid cancers.

molecular biology↗

DNA replication stress-induced transcriptome of Human Burkitt lymphoma identifies MBD1 as a novel suppressor of BCL6 rearrangements in germinal center derived B-lymphomagenesis

BCL6 is a master transcriptional regulator of germinal center (GC) B cells. BCL6 is frequently translocated at the major translocation cluster (MTC) within intron 1 of the BCL6 locus, a hotspot commonly rearranged in diffuse large B cell lymphomas (DLBCLs). BCL6 amplifications are associated with therapeutic resistance and poor survival outcomes in hematological and solid cancers. However the mechanisms suppressing genome instability at the BCL6-MTC preventing BCL6 rearragements remain unclear. Here, transcriptome analysis and genome-wide mapping of histone H3 lysine 4 trimethylation (H3K4me3) in hydroxyurea (HU)-treated Raji cells (a Burkitts lymphoma model) revealed the induced expression of MBD1, encoding the DNA CpG methylation-binding protein. Functional studies using shRNA silencing and ectopic overexpression demonstrated that MBD1 suppresses BCL6 transcription whose promoter harbours conserved CpG methylation sites, suggesting a DNA methylation-dependent regulation of BCL6 trasncription by MBD1. Conversely, BCL6 repressed MBD1 expression by binding to its promoter. MBD1-depleted Raji cells exhibited increased genomic instability at the BCL6-MTC upon HU treatment, heightened sensitivity to DNA replication inhibitors (HU, gemcitabine, and etoposide), and reduced tumorigenicity in xenograft mouse models. We propose that MBD1 prevents genomic instability at the BCL6-MTC to suppress DLBCL formation. Moreover, MBD1 promotes genomic stability and cell viability during DNA replication stress. MBD1 thus represents a potential therapeutic target for cancers exhibiting resistance to chemotherapies targeting DNA replication. Key PointsO_LIMBD1 suppresses BCL6 expression under the DNA replication stress C_LIO_LIMBD1 suppresses genomic instability at BCL6 translocation hotspots C_LIO_LIMBD1 depletion is associated with reduced tumorigenicity in mouse xenograft and sensitivity to DNA replication inhibitors. C_LI

cancer biology↗

Distal super-enhancer drives aberrant CXCL13 in Cancer cells driving growth and p53 dysregulation via CXCR5-CXCL13 axis

The CXCL13 chemokine plays a crucial role in guiding B cell migration to the light zones (LZs) during the germinal center (GC) reaction. While CXCL13 expression is absent in most cell types, aberrant amplification of the CXCR5-CXCL13 signaling is observed in various cancers, including germinal center-derived B-lymphomas (GCDBL), colorectal adenocarcinoma (COAD), and liver hepatocellular carcinoma (LIHC). However, the molecular mechanisms underlying abnormal CXCL13 transcription in cancer cells and its functional consequences remain elusive. We identify DNA-CpG methylation binding protein 1 (MBD1) as a suppressor of CXCL13 expression. Chromosomal conformation capture (3C) analysis reveals a distal super-enhancer located near CCNG2 that interacts with the CXCL13 promoter in GCDBL, suggesting that enhancer-hijacking drives the aberrant expression. Our functional validation demonstrates that CXCR5-CXCL13 signaling suppresses p53 and its target genes in GCDBLs, COAD, and LIHC. Notably, CXCL13 in the GCDBL cell line Raji disrupts CXCR5-mediated migration, a mechanism essential for (light zone) LZ-entry and affinity maturation of GC B cells. These findings highlight the dual role of the CXCR5-CXCL13 axis in immune response and cancer proliferation. Key PointsO_LISuper-enhancer near CCNG2 region interacts with CXCL13-TSS driving CXCL13 in cancers. C_LIO_LIAberrant CXCL13 prevents CXCR5-mediated migration of B-lymphomas and promotes growth and p53 dysregulation in CXCR5+ cells C_LIO_LICXCR5-CXCL13 axis impairs p53 target gene expression and promotes tumor growth C_LI O_FIG O_LINKSMALLFIG WIDTH=171 HEIGHT=200 SRC="FIGDIR/small/609994v2_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@abf94corg.highwire.dtl.DTLVardef@7bfd55org.highwire.dtl.DTLVardef@351645org.highwire.dtl.DTLVardef@1493e62_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIAberrant CXCL13 expression in hematological and solid cancers C_LIO_LIChemotherapeutic treatment of cancer cells promotes CXCL13 and CXCR5 expression C_LIO_LIDistal super-enhancer on CCNG2 interacts with CXCL13 promoter C_LIO_LICXCL13 expression in B-lymphomas prevents CXCR5-dependent migration C_LIO_LICXCR5-CXCL13 axis encounters p53 function in hematological and solid cancer cells C_LI

cancer biology↗

Constraints on avian seed dispersal reduce potential for resilience in degraded tropical forests

1. Seed dispersal - one of the many services supplied by biodiversity - is a critical process underpinning the resilience of tropical forests. Forest loss or degradation typically leads to defaunation, altering seed transfer dynamics and impairing the ability of forested habitats to regenerate or recover from perturbation. However, the extent of defaunation, and its likely impacts on the seed dispersers needed to restore highly degraded or clear-felled areas, remains poorly understood, particularly in human-modified tropical forest landscapes. 2. To quantify defaunation of seed-dispersing birds, we used field survey data from more than 400 transects in three regions of Brazil, first comparing the recorded assemblages with those predicted by geographic range maps, and then assessing frugivore habitat associations across gradients of land cover modification at local scales. 3. We found that current bird assemblages have lower functional trait diversity than predicted by species range maps in Amazonia (4-6%), with a greater reduction (28%) for the Atlantic Forest region, which has been more heavily deforested for a longer period. These reductions are probably caused by local extinctions of forest-dependent bird species following land-use change. 4. Direct measures of seed dispersal are difficult to obtain, so we instead focused on the potential for seed transfer inferred from shared species occurrence between land cover types. Of 83 predominantly frugivorous bird species recorded in relatively intact forests, we show that 10% were absent from degraded forest, and 57% absent from the surrounding matrix of agricultural land covers, including many of the large-beaked species. Of 112 frugivorous species using degraded forest, 47% were absent from matrix habitats. 5. Our findings suggest that degraded forest can supply seed dispersal services to adjacent cleared lands, and that direct transfer of seeds from intact forest to cleared areas may be limited, particularly for large-seeded trees. We conclude that resilience of tropical forest landscapes is best achieved by protecting a mosaic of forest types, including sufficient core areas of intact forest surrounded by buffer zones of degraded forest.

ecology↗

Listening to tropical forest soils

PAM has proven to be an effective tool for monitoring biotic soundscapes in the marine, terrestrial, and aquatic realms. Recently it has been suggested that it could also be an effective method for monitoring soil fauna, but has so far been used in only four studies in temperate and polar regions. We present the first study of soil soundscapes in tropical forests, using a novel analytical pipeline allowing for the use of in-situ recording of soundscapes with minimal soil disturbance. We found significant differences in soil soundscapes between burnt and unburnt forests and the first indications of a diel cycle in soil soundscapes. These promising results and methodological advances highlight the potential of PAM for large-scale and long-term monitoring of soil biodiversity. We use the results to discuss research priorities, including relating soil biophony to biodiversity, community structure and ecosystem functioning, and the use of appropriate hardware and analytical techniques.

ecology↗

Replicative ageing perturbs the metabolic signature of murine C2C12 skeletal myotubes

IntroductionChronological ageing is associated with mitochondrial dysfunction and increased reactive oxygen species (ROS) production in skeletal muscle. However, the effects of replicative ageing on skeletal muscle cellular metabolism are not well known. Using an established myoblast model of cellular (replicative) ageing, we investigated the impact of ageing on energy metabolism in murine C2C12 myotubes. MethodsControl (P7-11) and replicatively aged (P48-51) C2C12 myoblasts were differentiated over 72-120 h. Mitochondrial bioenergetics were investigated by respirometry and mitochondrial superoxide and cellular ROS were measured in the absence and presence of antimycin A (AA). Genes related to mitochondrial remodelling and the antioxidant response were quantified by RT-qPCR. Intracellular metabolites were quantified using an untargeted 1H-NMR metabolomics pipeline. ResultsMitochondrial coupling efficiency (Control: 79.5 vs. Aged: 70.3%, P=0.006) and relative oxidative ATP synthesis (Control: 48.6 vs. Aged: 31.7%, P=0.022) were higher in control vs. aged myotubes, but rates of mitochondrial superoxide production were lower (Control: 2.4x10-5 {+/-} 0.4 x 10-5 vs. Aged: 9.7x10-5 {+/-} 1.6x10-5 RFU/sec/cell; P=0.035). Replicatively aged myotubes had greater mRNA expression of mfn2 and Tfam compared to control. Yet, Nrf2 and PGC-1 expression were 2.8-fold and 3.0-fold higher in control versus aged myotubes over 24 h and 48 h (P<0.05), respectively. Branched chain amino acids L-leucine, L-isoleucine and L-valine, and L-carnitine were less abundant in aged versus control myotubes. Conclusion(s)Replicative ageing is associated with bioenergetic uncoupling, increased ROS production and impaired amino acid metabolism. Our findings suggest that cellular mitochondrial dysfunction and altered energy metabolism may exacerbate the age-related decline in skeletal muscle mass and function.

cell biology↗

GATA4 regionalizes intestinal metabolism and barrier function to prevent immunopathology

Different regions of the gastrointestinal tract have distinct digestive and absorptive functions, which may be locally disrupted by infection or autoimmune disease. Yet, the mechanisms underlying intestinal regionalization and its dysregulation in disease are not well understood. Here, we used mouse models, transcriptomics, and immune profiling to show that regional epithelial expression of the transcription factor GATA4 prevented adherent bacterial colonization and inflammation in the proximal small intestine by regulating retinol metabolism and luminal IgA. Loss of epithelial GATA4 expression increased mortality in mice infected with Citrobacter rodentium. In active celiac patients with villous atrophy, low GATA4 expression was associated with metabolic alterations, mucosal Actinobacillus, and increased IL-17 immunity. This study reveals broad impacts of GATA4-regulated intestinal regionalization and highlights an elaborate interdependence of intestinal metabolism, immunity, and microbiota in homeostasis and disease. One-sentence summaryEpithelial GATA4 regulates intestinal regionalization of bacterial colonization, metabolic pathways, and tissue immunity.

immunology↗

Senataxin and RNase H2 act redundantly to suppress genome instability during class switch recombination

Class switch recombination generates antibody distinct isotypes critical to a robust adaptive immune system and defects are associated with auto-immune disorders and lymphomagenesis. Transcription is required during class switch to recruit the cytidine deaminase AID--an essential step for the formation of DNA double-strand breaks--and strongly induces the formation of R loops within the immunoglobulin heavy chain locus. However, the impact of R loops on double-strand break formation and repair during class switch recombination remains unclear. Here we report that cells lacking two enzymes involved in R loop removal-- Senataxin and RNase H2--exhibit increased R loop formation and genome instability at the immunoglobulin heavy chain locus without impacting class switch recombination efficiency, transcriptional activity, or AID recruitment. Senataxin and RNase H2-deficient cells also exhibit increased insertion mutations at switch junctions, a hallmark of alternative end joining. Importantly, these phenotypes were not observed in cells lacking Senataxin or RNase H2B alone. We propose that Senataxin acts redundantly with RNase H2 to mediate timely R loop removal, promoting efficient repair while suppressing AID-dependent genome instability and insertional mutagenesis.

immunology↗

Optimising tropical forest bird surveys using passive acoustic monitoring and repeated short-duration point counts

Estimation of avian biodiversity is a cornerstone measure of ecosystem condition, with turnover in avian community composition underpinning many studies of land-use change in tropical forests. Surveys conducted using autonomous recorders have been frequently found to be more efficient than traditional point-count surveys. However, there has been limited research into optimal survey duration, despite autonomous recordings allowing for many more repeats of short-duration surveys with relative ease in comparison to traditional survey methods. We use an acoustic dataset collected from a region of very high avian biodiversity - the eastern Brazilian Amazon - to test the effect of using short-duration surveys to increase temporal coverage without increasing total survey duration. We use this dataset to assess whether a survey protocol consisting of 240 15-second surveys at 29 locations, short-duration surveys, has an influence on resulting alpha and gamma diversity, and detection frequency, than standard-duration surveys of four 15-minute surveys per location. We find that repeated short-duration surveys outperform longer duration surveys in every metric considered herein, with short-duration surveys predicted to detect approximately 50% higher alpha diversity, and 10% higher gamma diversity. Short-duration surveys also detect species more often, at more survey locations. Conversely, standard-duration surveys are almost four times more likely to produce false negatives (i.e. to fail to detect species presence). Whilst there is no difference between the proportion of uncommon species detected by the two methods, when considering species detected multiple times at multiple locations, short-duration surveys detected three times more uncommon species than standard-duration surveys. We conclude that short-duration recorded surveys should be considered the primary method for sampling the species richness of bird communities in tropical forests and is likely to be preferable to longer duration or traditional surveys in most environments.

ecology↗

Resistome metagenomics from plate to farm: the resistome and microbial composition during food waste feeding and composting on a Vermont poultry farm

Food waste diversion and composting, either mandated or voluntary, are growing alternatives to traditional waste disposal. An acceptable source of agricultural feed and composting material, methane-emitting food residuals, including post-consumer food scraps, are diverted from landfills allowing recapture of nutrients that would otherwise be lost. However, risk associated with the transfer of antimicrobial resistant bacteria (ARB), antibiotic resistance genes (ARGs), or pathogens from food waste is not well characterized. Using shotgun metagenomic sequencing, ARGs, microbial content, and associated virulence factors were successfully identified across samples from an integrated poultry farm that feeds post-consumer food waste. A total of 495 distinct bacterial species or sub-species, 50 ARGs, and 54 virulence gene sequences were found. ARG sequences related to aminoglycoside, tetracycline, and macrolide resistance were most prominent, while most virulence gene sequences were related to transposon or integron activity. Microbiome content was distinct between on-farm samples and off-farm food waste collection sites, with a reduction in pathogens throughout the composting process. While most samples contained some level of resistance, only 3 resistance gene sequences occurred in both on- and off-farm samples and no multidrug resistance (MDR) gene sequences persisted once on the farm. The risk of incorporating novel or multi-drug resistance from human sources appears to be minimal and the practice of utilizing post-consumer food scraps as feed for poultry and composting material may not present a significant risk for human or animal health. Pearson correlation and co-inertia analysis identified a significant interaction between resistance and virulence genes (P = 0.05, RV = 0.67), indicating that ability to undergo gene transfer may be a better marker for ARG risk than presence of specific bacterial species. This work expands the knowledge of ARG fate during food scrap animal feeding and composting and provides a methodology for reproducible analysis.

microbiology↗

Killer whale genomes reveal a complex history of recurrent admixture and vicariance

Reconstruction of the demographic and evolutionary history of populations assuming a consensus tree-like relationship can mask more complex scenarios, which are prevalent in nature. An emerging genomic toolset, which has been most comprehensively harnessed in the reconstruction of human evolutionary history, enables molecular ecologists to elucidate complex population histories. Killer whales have limited extrinsic barriers to dispersal and have radiated globally, and are therefore a good candidate model for the application of such tools. Here, we analyse a global dataset of killer whale genomes in a rare attempt to elucidate global population structure in a non-human species. We identify a pattern of genetic homogenisation at lower latitudes and the greatest differentiation at high latitudes, even between currently sympatric lineages. The processes underlying the major axis of structure include high drift at the edge of species range, likely associated with founder effects and allelic surfing during post-glacial range expansion. Divergence between Antarctic and non-Antarctic lineages is further driven by ancestry segments with up to four-fold older coalescence time than the genome-wide average; relicts of a previous vicariance during an earlier glacial cycle. Our study further underpins that episodic gene flow is ubiquitous in natural populations, and can occur across great distances and after substantial periods of isolation between populations. Thus, understanding the evolutionary history of a species requires comprehensive geographic sampling and genome-wide data to sample the variation in ancestry within individuals.

evolutionary biology↗