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Baker, D. J.

Publications and source records attributed to Baker, D. J..

2 recordsLinked to original sources

Microclimates can be accurately predicted across ecologically important remote ecosystems

Microclimate information is often crucial for understanding ecological patterns and processes, including under climate change, but is typically absent from ecological and biogeographic studies owing to difficulties in obtaining microclimate data. Recent advances in microclimate modelling, however, suggest that microclimate conditions can now be predicted anywhere at any time using hybrid physically- and empirically-based models. Here, for the first time, we test the utility of this approach across a remote, inaccessible, and climate change threatened polar island ecosystem at ecologically relevant scales. Microclimate predictions were generated at a 100 x 100 m grain (at a height of 4 cm) across the island, with models parameterised using either meteorological observations from the islands weather station (AWS) or climate reanalysis data (CRA). AWS models had low error rates and were highly correlated with observed seasonal and daily temperatures (root mean squared error of predicted seasonal average Tmean [≤] 0.6 {degrees}C; Pearsons correlation coefficient (r) for the daily Tmean [≥] 0.86). By comparison, CRA models had a slight warm bias in all seasons and a smaller diurnal range in the late summer period than in situ observations. Despite these differences, the modelled relationship between the percentage cover of the threatened endemic cushion plant Azorella macquariensis and microclimate varied little with the source of microclimate data (r = 0.97), suggesting that both model parameterisations capture similar patterns of spatial variation in microclimate conditions across the island ecosystem. Here, we have shown that the accurate prediction of microclimate conditions at ecologically relevant spatial and temporal scales is now possible using hybrid physically- and empirically-based models across even the most remote and climatically extreme environments. These advances will help add the microclimate dimension to ecological and biogeographic studies, which could be critical for delivering climate change-resilient conservation planning in climate-change exposed ecosystems.

ecology

CoronaHiT: large scale multiplexing of SARS-CoV-2 genomes using Nanopore sequencing

The COVID-19 pandemic has spread to almost every country in the world since it started in China in late 2019. Controlling the pandemic requires a multifaceted approach including whole genome sequencing to support public health interventions at local and national levels. One of the most widely used methods for sequencing is the ARTIC protocol, a tiling PCR approach followed by Oxford Nanopore sequencing (ONT) of up to 96 samples at a time. There is a need, however, for a flexible, platform agnostic, method that can provide multiple throughput options depending on changing requirements as the pandemic peaks and troughs. Here we present CoronaHiT, a method capable of multiplexing up to 96 small genomes on a single MinION flowcell or >384 genomes on Illumina NextSeq, using transposase mediated addition of adapters and PCR based addition of barcodes to ARTIC PCR products. We demonstrate the method by sequencing 95 and 59 SARS-CoV-2 genomes for routine and rapid outbreak response runs, respectively, on Nanopore and Illumina platforms and compare to the standard ARTIC LoCost nanopore method. Of the 154 samples sequenced using the three approaches, genomes with [≥] 90% coverage (GISAID criteria) were generated for 64.3% of samples for ARTIC LoCost, 71.4% for CoronaHiT-ONT, and 76.6% for CoronaHiT-Illumina and have almost identical clustering on a maximum likelihood tree. In conclusion, we demonstrate that CoronaHiT can multiplex up to 96 SARS-CoV-2 genomes per MinION flowcell and that Illumina sequencing can be performed on the same libraries, which will allow significantly higher throughput. CoronaHiT provides increased coverage for higher Ct samples, thereby increasing the number of high quality genomes that pass the GISAID QC threshold. This protocol will aid the rapid expansion of SARS-CoV-2 genome sequencing globally, to help control the pandemic.

genomics