The genome sequence of the Large Sharp-tail Bee, Coelioxys conoideus (Illiger,1806)

We present a genome assembly from an individual female Coelioxys conoideus (the Large Sharp-tail Bee; Arthropoda; Insecta; Hymenoptera; Megachilidae). The genome sequence is 417.6 megabases in span. Most of the assembly is scaffolded into 12 chromosomal pseudomolecules. The mitochondrial genome has also been assembled and is 20.8 kilobases in length.


Background
Coelioxys conoidea (Illiger, 1806) is a medium-sized bee (11-15 mm), the largest of the six UK species of sharp-tailed bees (Tribe: Megachilini), with a forewing length of 7-9 mm (Falk & Lewington, 2019).Both sexes have bright white hairs on the sides of the tergites and sternites, with interrupted hair bands present on tergites T2-T5 and sternites S2-S4.White hairs are present also on the face and sides of the thorax.The female has a cone-shaped abdomen, typical of the sharp tailed bees, with the final (6th) sternite being distinctly boat-shaped.The male has a broader abdomen, the final sternite bearing a pair of prominent, blunt teeth.For identification purposes, pictorial comparisons of UK Coelioxys spp.can be found in (Rowson & Pavett, 2008).
Sharp-tailed bees are kleptoparasites (cuckoos) of leaf-cutter bees (Megachile spp.) or flower bees (Anthophora spp.), and C. conoidea are specifically kleptoparasites of Megachile maritima (Kirby, 1802).A female uses her pointed abdomen to pierce and oviposit into the cell of the host.The larva then hatches before that of the host, whereupon it consumes the food stores collected for the latter, while destroying the host egg or newly-hatched larva (Bohart, 1970;Rowson & Pavett, 2008).In Europe, C. conoidea is known to be a kleptoparasite of M. lagopoda, which does not occur in the UK.
Coelioxys conoidea is a univoltine species, flying from June to August.The distribution in the UK follows the distribution of Megachile maritima, being mainly coastal, especially where sand dunes are present, while inland, it can be found on sandy heaths and occasionally on chalk.Adults are known to visit a wide range of flowering plants, including sea holly (Eryngium maritimum, brambles (Rubus spp.), knapweeds (Centaurea spp.) and ragworts (Jacobaea and Senecio spp.) (BWARS, 2023;Falk & Lewington, 2019).In the UK, C. conoidea is mainly restricted to southern England and Wales, including the Channel Islands (BWARS, 2023;Else et al., 2016;Falk & Lewington, 2019;NBN Atlas Partnership, 2023), although recent records from Nottinghamshire, Yorkshire and South Lancashire (BWARS, 2023;Falk & Lewington, 2019;NBN Atlas Partnership, 2023) suggest a possible range expansion.It is not regarded as scarce and can be locally common (Falk & Lewington, 2019).
On the continent C. conoidea is found throughout much of Europe and the Middle East (GBIF Secretariat, 2022).While it is listed as a species of Least Concern on the IUCN Red List Category (Europe) (Nieto et al., 2014;Ortiz Sánchez, 2014), in a more recent assessment, the Swedish Red List 2020 now lists C. conoidea as Critically Endangered (SLU Artdatabanken, 2020) due to a declining population.
The genome of Coelioxys conoidea was sequenced as part of the Darwin Tree of Life Project, a collaborative effort to sequence all named eukaryotic species in the Atlantic Archipelago of Britain and Ireland.Here we present a chromosomally complete genome sequence for Coelioxys conoidea, based on one female specimen from Penhale Dunes, Cornwall.

Genome sequence report
The genome was sequenced from one female Coelioxys conoideus (Figure 1) collected from Penhale Dunes,Cornwall (50.37,.A total of 41-fold coverage in Pacific Biosciences single-molecule HiFi long reads was generated.Primary assembly contigs were scaffolded with chromosome conformation Hi-C data.Manual assembly curation corrected 13 missing joins or mis-joins, reducing the scaffold number by 9.38%, and increasing the scaffold N50 by 11.35%. The final assembly has a total length of 417.6 Mb in 58 sequence scaffolds with a scaffold N50 of 25.9 Mb (Table 1).Most (82.24%) of the assembly sequence was assigned to 12 chromosomal-level scaffolds.Chromosome-scale scaffolds confirmed by the Hi-C data are named in order of size (Figure 2-Figure 5; Table 2).While not fully phased, the assembly deposited is of one haplotype.Contigs corresponding to the second haplotype have also been deposited.The mitochondrial genome was also assembled and can be found as a contig within the multifasta file of the genome submission.
Metadata for specimens, spectral estimates, sequencing runs, contaminants and pre-curation assembly statistics can be found at https://links.tol.sanger.ac.uk/species/2922063.

Sample acquisition and nucleic acid extraction
A female Coelioxys conoideus (iyCoeConi1) was collected from Penhale Dunes, Cornwall, UK (latitude 50.17, longitude -5.12) on 2021-06-30.The specimen was collected by Sue Taylor (Dipterists' Forum) and Sally Luker (University of Exeter), using an aerial net.The specimen was identified by Will Hawkes (University of Exeter) and Sue Taylor, and was snap-frozen on dry ice.
DNA was extracted at the Tree of Life laboratory, Wellcome Sanger Institute (WSI).The iyCoeConi1 sample was weighed and dissected on dry ice with tissue set aside for Hi-C sequencing.Abdomen tissue was disrupted using a Nippi Powermasher fitted with a BioMasher pestle.High molecular weight (HMW) DNA was extracted using the Qiagen MagAttract HMW DNA extraction kit.HMW DNA was sheared into an average fragment size of 12-20 kb in a Megaruptor 3 system with speed setting 30.Sheared DNA was purified by solid-phase reversible immobilisation using AMPure PB beads with a 1.8X ratio of beads to sample to remove the shorter fragments and concentrate the DNA sample.The concentration of the sheared and purified DNA was assessed using a Nanodrop spectrophotometer and Qubit Fluorometer and Qubit dsDNA High Sensitivity Assay kit.Fragment size distribution was evaluated by running the sample on the FemtoPulse system.

Sequencing
Pacific Biosciences HiFi circular consensus DNA sequencing libraries were constructed according to the manufacturers' instructions.DNA sequencing was performed by the Scientific Operations core at the WSI on Pacific Biosciences SEQUEL II (HiFi) instrument.Hi-C data were also generated from head and thorax tissue of iyCoeConi1 using the Arimav2 kit and sequenced on the Illumina NovaSeq 6000 instrument.

Genome assembly, curation and evaluation
Assembly was carried out with Hifiasm (Cheng et al., 2021) and haplotypic duplication was identified and removed with purge_dups (Guan et al., 2020).The assembly was then scaffolded with Hi-C data (Rao et al., 2014) using YaHS (Zhou et al., 2023).The assembly was checked for as described previously (Howe et al., 2021).Manual curation was performed using HiGlass (Kerpedjiev et al., 2018) and Pretext (Harry, 2022).The mitochondrial genome was assembled using MitoHiFi (Uliano-Silva et al., 2022), which runs MitoFinder (Allio et al., 2020) or MITOS (Bernt et al., 2013) and uses these annotations to select the final mitochondrial contig and to ensure the general quality of the sequence.
A Hi-C map for the final assembly was produced using bwa-mem2 (Vasimuddin et al., 2019) in the Cooler file format (Abdennur & Mirny, 2020).To assess the assembly metrics, the k-mer completeness and QV consensus quality values were calculated in Merqury (Rhie et al., 2020).This work was done Table 3 contains a list of relevant software tool versions and sources.

Wellcome Sanger Institute -Legal and Governance
The materials that have contributed to this genome note have been supplied by a Darwin Tree of Life Partner.
The submission of materials by a Darwin Tree of Life Partner is subject to the 'Darwin Tree of Life Project Sampling Code of Practice', which can be found in full on the Darwin Tree of Life website here.By agreeing with and signing up to the Sampling Code of Practice, the Darwin Tree  of Life Partner agrees they will meet the legal and ethical requirements and standards set out within this document in respect of all samples acquired for, and supplied to, the Darwin Tree of Life Project.
Further, the Wellcome Sanger Institute employs a process whereby due diligence is carried out proportionate to the nature of the materials themselves, and the circumstances under which they have been/are to be collected and provided for use.The purpose of this is to address and mitigate any potential legal and/or ethical implications of receipt and use of the materials as part of the research project, and to ensure that in doing so we align with best practice wherever possible.
The overarching areas of consideration are:

Software tool Version
This data note titled "The genome sequence of the large sharp-tail bee, Coelioxys conideus (Illiger, 1806)" is in line with the objectives proposed by the Darwin Tree of Life Consortium and consequently by the Earth Biogenome Project, which is to improve conservation strategies, preserve biodiversity and maintain ecosystem services vital to human well-being.
For the biological facts, we wonder if the authors can add the info on how long the female bee can live, and what type of social status this species has if the info is available.
The identification and sequencing of the samples were carried out according to the specifications of this project.
An important information that would be welcome in the study is confirmation or evidence that the number of chromosomes of the species matches that described.
Do reference genomes exist for other species in the genus?How many chromosomes did they have?Is synteny analysis possible?
The figures could be improved by editing the x-axis of fig 5 if it is possible.So readers have some idea about this graph.

Is the rationale for creating the dataset(s) clearly described? Yes
Are the protocols appropriate and is the work technically sound?Yes The paper is well-written and the methods are easy to follow.I have a couple very minor comments for the authors to consider: The justification for sequencing this organism in the text was limited to the project being part of the Darwin Tree of Life project, but what makes this genome exciting is its potential contribution to research in brood parasitism, which has evolved multiple times in Apoidea.I would encourage the authors to mention this in the last paragraph of the background. 1.
Please specify lat-lon when reporting the coordinates in the beginning of the genome sequence report section.

2.
Is the rationale for creating the dataset(s) clearly described?Yes

Are the protocols appropriate and is the work technically sound? Yes
Are sufficient details of methods and materials provided to allow replication by others?

Yes
Are the datasets clearly presented in a useable and accessible format?Yes Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Ecological genomics; parasitology; entomology; phylogenetics; population genetics I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

Figure 2 .
Figure 2. Genome assembly of Coelioxys conoideus, iyCoeConi1.1:metrics.The BlobToolKit Snailplot shows N50 metrics and BUSCO gene completeness.The main plot is divided into 1,000 size-ordered bins around the circumference with each bin representing 0.1% of the 417,592,752 bp assembly.The distribution of scaffold lengths is shown in dark grey with the plot radius scaled to the longest scaffold present in the assembly (41,884,646 bp, shown in red).Orange and pale-orange arcs show the N50 and N90 scaffold lengths (25,869,242 and 4,259,916 bp), respectively.The pale grey spiral shows the cumulative scaffold count on a log scale with white scale lines showing successive orders of magnitude.The blue and pale-blue area around the outside of the plot shows the distribution of GC, AT and N percentages in the same bins as the inner plot.A summary of complete, fragmented, duplicated and missing BUSCO genes in the hymenoptera_odb10 set is shown in the top right.An interactive version of this figure is available at https://blobtoolkit.genomehubs.org/view/iyCoeConi1.1/dataset/ CANQJN01/snail.

Figure 5 .
Figure 5. Genome assembly of Coelioxys conoideus, iyCoeConi1.1:Hi-C contact map of the iyCoeConi1.1 assembly, visualised using HiGlass.Chromosomes are shown in order of size from left to right and top to bottom.An interactive version of this figure may be viewed at https://genome-note-higlass.tol.sanger.ac.uk/l/?d=HpLT1q_ASdqw_NYwF8ARig.