Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

Whole plastid genome-based phylogenomics supports an inner placement of the O. insectifera group rather than a basal position in the rapidly diversifying Ophrys genus (Orchidaceae)

View ORCID ProfileJoris A. M. Bertrand, View ORCID ProfileAnaïs Gibert, Christel Llauro, View ORCID ProfileOlivier Panaud
doi: https://doi.org/10.1101/2020.12.16.423003
Joris A. M. Bertrand
aLaboratoire Génome & Développement des Plantes (UMR 5096 UPVD/CNRS), Université de Perpignan Via Domitia, Perpignan, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Joris A. M. Bertrand
  • For correspondence: joris.bertrand@univ-perp.fr
Anaïs Gibert
bPSL Université Paris, EPHE-UPVD-CNRS, USR 3278 CRIOBE, Université de Perpignan Via Domitia, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Anaïs Gibert
Christel Llauro
aLaboratoire Génome & Développement des Plantes (UMR 5096 UPVD/CNRS), Université de Perpignan Via Domitia, Perpignan, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Olivier Panaud
aLaboratoire Génome & Développement des Plantes (UMR 5096 UPVD/CNRS), Université de Perpignan Via Domitia, Perpignan, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Olivier Panaud
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Supplementary material
  • Preview PDF
Loading

Abstract

Some lineages of the Orchid genus Ophrys exhibit among the highest diversification rates reported so far. As a consequence of a such intense and rapid evolution, the systematics and the taxonomy of this genus remains unclear. A hybrid assembly approach based-on long- and short-read genomic data allowed us to outperform classical methods to successfully assemble whole plastid genomes for two new Ophrys species: O. aymoninii and O. lutea. Along with three other previously Ophrys plastid genome sequences, we then reconstructed the first whole plastome-based molecular phylogeny including representatives of the three mains recognized Ophrys lineages. Our results support the placement of the O. insectifera clade as sister group of ‘non-basal Ophrys’ rather than a basal position. Our findings corroborate recent results obtained from genomic data (RAD-seq and transcriptomes) but contrast with previous ones. These results therefore confirm that molecular phylogenetic hypotheses based on a limited number of loci (e.g. nrITS, matK, rbcL) may have provided a biased picture of phylogenetic relationships within Ophrys and possibly other plant taxa.

1. Introduction

Among the most speciose family of flowering plants that orchids (Orchidaceae) form, some lineages of the genus Ophrys display among the highest diversification rates ever reported (Givnish et al. 2015; Breitkopf et al. 2015). The adaptive radiation that Ophrys experience is likely to be due to their unusual pollination strategy (by sexual swindle) that leads to high levels of specialisation of these plants to their insect pollinators and favour evolutionary divergence (see Baguette et al. 2020 for a recent review). The systematic relationships of such fast and importantly diversifying groups are difficult to infer for two reasons. Firstly, because recent divergent times often renders molecular signal of lineage delineation undetectable or at least ambiguous (incomplete lineage sorting) and because emerging species are still particularly prone to introgressive hybridization and reticulate evolution.

The systematics and the taxonomy is particularly problematic in Ophrys for which different authors recognize a number of species ranging from 9 to 354 (see Bateman et al. 2018; Bateman 2018, Bertrand et al., 2021). In particular, contrasting results still make the phylogenetic position of the (three) main lineages (sometimes considered as subgenera) debated. Several molecular phylogenetic studies show that the genus Ophrys is basically subdivided in three main sub-lineages (sometimes considered as subgenera): a first clade formed by the Ophrys insectifera group (also defined as group A since the study of Devey et al. 2008), a second clade consisting of the groups B to E (O. tenthredinifera (B), O. speculum (C), O. bombyliflora (D), called ‘archaic Euophrys’ by Tyteca and Baguette (2017), plus the so-called Pseudophrys group (E) and a third clade to which belong the groups F to J (O. apifera (F), O. sphegodes (G), O. fuciflora (H), O. scolopax (I) and O. umbilicata (J), also called ‘recent Euophrys’). The terms Euophrys and Pseudophrys classify Ophrys according to the part of the pollinator insect’s body on which the pollinia are glued during pseudocopulation. Pseudophrys corresponds to Ophrys in which the pollinia are deposited on the abdominal region of the insect, while Euophrys corresponds to species in which the pollinia are deposited on its cephalic region (see Bertrand et al. 2021). As Euophrys is a taxonomically incorrect term to refer to Ophrys groups, ‘section Ophrys’ should be used as a contrast to section Pseudophrys. However, because the section Ophrys forms a paraphyletic group, we propose to use ‘basal Ophrys’ and ‘non-basal Ophrys’ instead of ‘archaic Euophrys’ and ‘recent Euophrys’ for clarity purpose.

Out of the studies that could not unambiguously resolve tree topology for the three main Ophrys lineages (e.g. Soliva et al. 2001; Tyteca and Baguette 2017) two contrasting hypothesis can be considered concerning the phylogenetic position of the O. insectifera (A) group. Most of the molecular phylogenetic hypotheses have (historically) rather supported a basal position (Tbasal) for the O. insectifera (A) group (Devey et al. 2008; Breitkopf et al. 2015, Zitoun et al. in prep). However, recent findings based on genomic data: SNPs derived from RAD-seq approaches (Bateman et al. 2018) or transcriptomes (Piñeiro Fernández et al. 2019) rather support that the group insectifera (A) is directly related to ‘non-basal Ophrys’ (groups F to H) both of which being sister to the clade comprising ‘basal Ophrys’ + Pseudophrys (groups B to E) (Tinner).

In this study, we aim to reconstruct a phylogenomic hypothesis to test whether whole plastid genomic data rather support the inner placement of the O. insectifera (A) group or alternatively, its basal position in the Ophrys genus. So far, three Ophrys plastid genomes have been published: O. iricolor Desf. (or O. fusca subsp. iricolor (Desf.) K.Richt) and O. sphegodes Mill. (Roma et al., 2018) and O. aveyronensis (J.J.Wood) P.Delforge (or O. sphegodes subsp. aveyronensis J.J.Wood) (Bertrand et al., 2019), none of which are members of the O. insectifera (A) group. To fill this knowledge gap, we generated genomic data for Ophrys aymoninii (Breistr.) Buttler (or O. insectifera subsp. aymoninii, Breistr.) a representative of the O. insectifera clade, endemic to a spatially restricted geographic area in the South of the Massif Central (France). We also provide similar data for O. lutea Cav., 1793, a widespread Western Mediterranean Pseudophrys species.

We relied on a hybrid approach to assemble the whole plastid genomes of the two Ophrys taxa mentioned above. In brief, this consists in a combination of long reads (here, Oxford Nanopore Technologies reads that can span repeated DNA regions known to be difficult to assemble) with the low error rate of short (paired-end) reads (here, Illumina reads). Although relatively recent, such hybrid strategy was found to outperform classical approaches (as recently supported by Wang et al. 2018 and Scheunert et al. 2020). To do so, we used the Unicyler pipeline (Wick et al. 2017) which is able to analyse reads from both platforms simultaneously. Gene annotation and basic downstream analyses were then carried out as described in our former study (Bertrand et al. 2019, see also Appendix1).

2. Materials and Methods

2.1 Field sampling and sample processing

We collected fresh leaves from an individual of O. aymoninii and an individual of O. lutea near Causse-Begon, France (N 44.05252°; E 3.35898°) and Versols-Et-Lapeyre, France (N 43.898677°; E 2.933099°), respectively on 12-05-2018. As O. aymoninii is a nationally protected species in France, sampling was carried out under permit ‘Arrêté préfectoral n°2018-s-20’ issued by the ‘Direction Régionale de l’Environnement de L’Aménagement et du Logement (DREAL)’ from the ‘Région Occitanie’ on 11-06-2018. Back in the lab, samples were frozen and stored at −20°C until DNA extraction. We used a CTAB2X protocol to extract genomic DNA from the two specimens sampled (see Appendix 1 for details).

2.2 DNA sequencing, plastid genome reconstruction and gene annotation

2.2.1 Long-read (Nanopore) sequencing

Four Nanopore sequencing libraries (two for each individual) were prepared with the SQK-LSK108 kit following the ONT “1D genomic DNA by ligation protocol” or the “1D gDNA long reads without BluePippin protocol” from 2730/3632 ng and 2964/2500 ng of unfragmented DNA for O. aymoninii and O. lutea, respectively (see Appendix 1 for detail). Long read sequencing was carried out from four FLO-MIN106D R9 flowcells (two for each individual) on a MinION (Oxford Nanopore Technologies, Oxford, UK) in the lab using MinKNOW v.1.15.1. FAST5 files were base-called with Albacore v.2.3.1 (see Appendix 1 for detail).

Adapters were removed with Porechop v.0.2.4 (https://github.com/rrwick/Porechop) with the –discard_middle option turned on. We then used Nanofilt v.2.7.1 (https://pypi.python.org/pypi/NanoFilt) to filter out reads shorter than 5 kb and bases with quality < 9 on both sides of reads. To facilitate assembly, we then extracted plastid reads by mapping short-reads onto a multi-fasta file comprising the three whole plastid genome sequences published for Ophrys species. As in Wang et al. (2018), we duplicated and concatenated each of the three sequences and included them in the reference set to avoid losing reads corresponding to the region where genomes were circularized. We then extracted reads that mapped onto this dataset with Minimap2 v.2.17 (Li, 2018).

2.2.2 Short-read (Illumina) sequencing

Whole genomic libraries were prepared and sequenced in paired-end mode (2×150 bp, insert size: 350 bp) by Novogene Co., Ltd (HK) from 1.92 and 1.97 pg of DNA for O. aymoninii and O. lutea, respectively. Genomic DNA was extracted with the same protocol than the one used for long reads. Raw reads were trimmed with Trimmomatic v.039 (Bolger et al. 2014) and the resulting read quality was checked with FastQC v0.11.8 (Andrews et al. 2010). Plastid read extraction was carried out by mapping short-reads onto the Ophrys plastome dataset, as mentioned above, this time with bowtie2 v.2.3.4 (Langmead and Salzberg, 2012). As too high coverage is prone to disturb the assembly process, we subsampled the resulting read set to an expected coverage of 100X (i.e. by keeping 500,000 of both R1 and R2 reads assuming a plastid genome size of around 150 kb) before the assembly step.

2.2.3 Plastid genome reconstruction and gene annotation

Hybrid de novo assembly was performed with both long- and short-reads simultaneously using default settings in Unicycler v0.4.9b (Wick et al. 2017). Gene annotation and alignments were performed as in our previous study (Bertrand et al. 2019). Some genes (ndhA to ndhK) exhibited significant differences in length and similarity, even between the closely related Ophyrs species considered here, probably as a result of pseudogenisation and were removed from the alignments for further analyses. In particular, O. sphegodes, O. aveyronensis and O. aymoninii presented truncation of most ndh genes and shared the loss of the partially duplicated gene of ycf1 and a truncation of ndhF gene as already reported by Roma et al. (2018), see also Appendix 4.

2.3 Phylogenetic reconstruction, concordance factors and tree topology tests

We used the Maximum Likelihood approach implemented in IQ-TREE v2.0.6 (Minh et al., 2020a) to reconstruct gene trees and species tree with 1,000 replicates (-B 1000) of Ultrafast Bootstrap Approximation (UFBoot) to assess nodes support. Species tree was constructed based on three data set: i) whole plastome, ii) genes and iii) CDS alignments. The genealogical concordance in the dataset was also quantified with gene concordance factor (gCF) and site concordance factor (sCF) (Minh et al., 2020b). In addition, tree topology tests implemented in IQ-TREE were performed to test whether the inferred species tree was rather consistent with the inner placement (Tinner) or the basal (Tbasal) position of O. aymoninii. To further investigate which loci specifically supports one or the other topology and to what extent (by evaluating its phylogenetic signal), we then computed the difference in gene-wise Log-likelihood scores (ΔGLS, see Shen et al. 2017). For all phylogenetic analyses the plastid genome of another Orchidoideae species, Platanthera japonica (GenBank Accession no.: MG925368) was used as outgroup.

3. Characterization of the plastid genomes of O. aymoninii and O. lutea and comparison with previously published Ophrys plastid genomes

Following the approach described in our previous study (i.e. using short-reads (Illumina) and NOVOPlasty (Dierckxens et al. 2017, Bertrand et al. 2019)) we failed to infer a complete plastid genome sequence for O. aymoninii. For the two remaining species: O. aveyronensis and O. lutea we could obtain a single contig, only when providing a closely related reference sequence of O. sphegodes and O. iricolor, respectively (Table 1). The hybrid assembly implemented in Unicycler thus seems to outperform the short-read based approach as we obtained a single contig of expected length for all three species (without reference sequence). The two new O. aymoninii and O. lutea genomes were found to be very similar in size and structure as well as compared to the three previously published Ophrys plastome sequences. The plastid genomes of O. aymoninii and O. lutea are described in Appendix 2 and have been deposited on GenBank with accession numbers MW309825 and MW309826, respectively. Raw reads are also available from the European Nucleotide Archive (Study Primary Accession PRJEB42431/Secondary Accession ERP12689, see Appendix 1 for details).

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 1.

Comparative summary of the assembly of the plastid genomes of Ophrys aveyronensis, O. aymoninii and O. lutea based on the short-read approach (NOVOPlasty) and the hybrid approach (Unicycler).

4. Phylogenetic relationships within the genus Ophrys

We found an overwhelming support for an inner placement (Tinner) of the O. insectifera (A) group within the Ophrys genus. Whatever the alignment considered: whole-plastome, concatenation of gene/CDS loci, bootstrap values fully support (UFBoot = 100) a topology according to which the representative of the O. insectifera group: O. aymoninii is sister to the ‘non-basal Ophrys’ representatives: O. sphegodes/O. aveyronensis; the Pseudophrys: O. lutea and O. iricolor occupying a basal position (Figure 1). The gene and site concordant factor metrics (gCF and sCF) do not contradict bootstrap values even though they were found to be lower (especially gCF). This may be explained by very short branch lengths and the very limited amount of information contained in each gene/CDS sequence. All the tree topology tests also reject the topology consistent with the basal placement of O. aymoninii when compared to the one consistent with its inner placement (Table 2). The distribution of ΔGLS values (Figure 2 and Appendix 3) confirms that most of the genes also support this topology and when they do not, they only weakly support the alternative one.

Figure 1.
  • Download figure
  • Open in new tab
Figure 1.

Maximum likelihood phylogenetic tree (as inferred with IQtree) from whole plastid genome sequence alignment. UFBoot (Ultrafast Bootstrap Approximation) values were 100 at each node whatever the alignment considered (whole plastome, genes, CDS). Values next to the bootstrap indicate gene Concordance Factor (gCF) and site Concordance factor (sCF) inferred from gene-(up) and CDS-based (down) ‘gene’ trees. Platanthera japonica (GenBank Accession no.: MG925368) is used as outgroup.

Figure 2.
  • Download figure
  • Open in new tab
Figure 2.

Genewise phylogenetic signal (ΔGLS) for Tinner versus Tbasal, the two alternative tree topologies for each gene (A) and CDS (B) along the plastid genome. Positive ΔGLS values support an inner placement of O. aymoninii whereas negative values rather support its basal placement.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 2.

Summary of the tree topology test statistics performed to compare the inner placement hypothesis of the O. insectifera group (Tinner) to the one supporting its basal position (Tbasal)

Altogether, our results are therefore congruent with the genomic-based findings recently reported by Bateman et al. (2018) and Piñeiro Fernandez et al. (2019) and contrast with several previous studies. Although being located in a single molecule, plastid regions have been shown to not necessarily behave as a single locus and experience certain forms of intra- and inter-molecular recombination (see Gonçalves et al., 2019; Walker et al., 2019). As most of the plastid genes are also known to encode important biological functions, they may display a sequence evolution patterns that deviate from the species tree topology, and even from non-coding plastid sequences, because of positive selection. Phenomena such as Incomplete Lineage Sorting (ILS), hybridization and introgression, gene duplication of loss as well as horizontal transfers may also affect gene tree topology. Finally, plastids are generally assumed to be maternally inherited in angiosperms but evidences of biparental inheritance have been documented in angiosperms. In spite of all these possible biases potentially affecting plastid gene trees in angiosperms, we did not find any gene strongly supporting the basal position of the O. insectifera group in Ophrys. We found that particular structural variation also supports the relative phylogenetic proximity of the O. insectifera lineage (here O. aymoninii) with the O. sphegodes relatives (O. sphegodes and O. aveyronensis). However, Ophrys aymoninii shows singular characteristics that further confirms that the O. insectifera forms a clearly distinct Ophrys lineage. As suggested by other authors for angiosperms, GLS show that the phylogenetic signal of genes such as matK slightly outperform rbcL but that other loci such as ycf1 (but also ycf2), rpoC2 (see Walker et al., 2019), rpoB and rpoC1 may be considered as good candidates for plastid-based phylogenetic analyses in Ophrys. Although our plastid-based findings are congruent with published genome-scale nuclear ones (RADseq- and transcriptome-based) they confirm the necessity of relying on an important number of loci to properly infer the evolutionary history of such rapidly evolving groups.

Disclosure statement

The authors declare no conflict of interest.

Acknowledgements

This study is set within the framework of the “Laboratoires d’Excellences (LABEX)” TULIP [ANR-10-LABX-41] and was supported by a ‘Bonus Qualité Recherche’ grant from the Université de Perpignan Via Domitia. We thank Marie-Christine Carpentier, Moaine El Baidouri, Panpan Zhang and the Mechanisms of AdaptatioN and GenOmics (MANGO) team for the support they provided with bioinformatic analyses.

Footnotes

  • Joris Bertrand conducted fieldwork, analyzed the data and wrote the manuscript.

  • Anaïs Gibert contributed to fieldwork and manuscript writing.

  • Christel Llauro generated the long-read data set.

  • Olivier Panaud contributed to research funding and manuscript writing.

References

  1. ↵
    Andrews, S., Lindenbaum, P., Howard, B. and Ewels, P. 2010. “FastQC: a quality control tool for high throughput sequence data”. http://www.bioinformatics.babraham.ac.uk/projects/fastqc
  2. ↵
    Baguette, M., Bertrand, J.A.M., Stevens, V., Schatz, B. and Noûs C. 2020. “Why are there so many Bee-orchids? Adaptive radiation by intraspecific competition for mnemonic pollinators”. Biological Reviews 95: 1630–1663.
    OpenUrl
  3. ↵
    Bateman, R.M. 2018. Two bees or not two bees? An overview of Ophrys systematics. Berichte Aus Den Arbeitkreisen Heimische Orchideen 35: 5–46.
    OpenUrl
  4. ↵
    Bateman, R.M., Sramkó, G. and Paun, O. 2018. “Integrating restriction site-associated DNA sequencing (RAD-seq) with morphological cladistics analysis clarifies evolutionary relationships among major species groups of bee orchids”. Annals of Botany 121: 85–105.
    OpenUrl
  5. ↵
    Bertrand, J.A.M., Gibert, A., Llauro, C. and Panaud O. 2019. “Characterization of the complete plastome of Ophrys aveyronensis, Euro-Mediterranean orchid with an intriguing disjunct geographic distribution”. Mitochondrial DNA Part B 4: 3256–3257.
    OpenUrl
  6. ↵
    1. M.C. Maugin and
    2. P. Grandcolas
    Bertrand, J.A.M. Baguette, M., Joffard, N. and Schatz, B. 2021. “Challenges inherent in the systematics and taxonomy of genera that have recently experienced explosive radiation: the case of orchids of the genus Ophrys”. In Systematics and Exploration of Life (eds. M.C. Maugin and P. Grandcolas). ISTE, Paris.
  7. ↵
    Bolger, A.M., Lohse M. and Usadel, B. 2014. “Trimmomatic: a flexible trimmer for Illumina sequence data”. Bioinformatics 30: 2114–2120.
    OpenUrlCrossRefPubMedWeb of Science
  8. ↵
    Breitkopf, H., Onstein, R.E., Cafasso, D., Schlüter, P.M. and Cozzolino, S. 2015. “Multiple shifts between different pollinators fueled rapid diversification in sexually deceptive Ophrys orchids”. New Phytologist 207: 377–386.
    OpenUrlCrossRefPubMed
  9. ↵
    Devey, D.S., Bateman, R.M., Fay, M.F. and Hawkins, J.A. 2008. “Friends or realtives? Phylogenetics and species delimitation in the controversial European orchid genus Ophrys”. Annals of Botany 101: 385–402.
    OpenUrlCrossRefPubMed
  10. Dierckxsens, N. Mardulyn, P. and Smits, G. 2017. “NOVOPlasty: De novo assembly of organelle genomes from whole genome data”. Nucleic Acids Research 45 e18.
    OpenUrlCrossRef
  11. ↵
    Givnish, T.J., Spalink D., Ames, M., Lyon, S. P., Hunter, S.J., Zuluaga, A., Iles, W.J.D., Clements, M.A., Arroyo, M.T.K., Leebens-Mack, J., Endara, L., Kriebel, R., Neubig, K.M., Whitten, W.M., Williams, N.H. and Cameron, K.M. 2015. “Orchid phylogenomics and multiple drivers of their extraordinary diversification”. Proceedings of the Royal Society B 282: 20151553.
    OpenUrlCrossRefPubMed
  12. ↵
    Gonçalves, D.J.P., Simpson, B.B., Ortiz, E.M., Shimizu, G.H. and Jansen R.K. 2019. “Incongruence between gene trees and species trees and phylogenetic signal variation in plastid genes”. Molecular Phylogenetics and Evolution, 138: 219–232.
    OpenUrlCrossRef
  13. Langmead, B. and Salzberg, S.L. 2014. “Fast gapped-read alignment with bowtie 2”. Nature Methods 9: 357–359.
    OpenUrl
  14. ↵
    Li, H. 2018. “Minimap2: pairwise alignment for nucleotide sequences”. Bioinformatics, 34: 3094–3100.
    OpenUrlCrossRefPubMed
  15. Minh, B.Q., Schmidt, H.A., Chernomor, O., Schrempf, M.D., Woodhams, A., von Haeseler, A. and Lanfear, R. 2020 “IQ-TREE 2: New models and efficient methods for phylogenetic inference in the genomic era”. Molecular Biology and Evolution, 37: 1510–1534.
    OpenUrl
  16. Minh, B.Q., Hahn, M.W. and Lanfear, R. 2020. “New methods to calculate concordance factoes for phylogenomic datasets. Molecular Biology and Evolution, 37: 2727–2733.
    OpenUrl
  17. ↵
    Piñeiro Fernández, L., Byers, K.J.R.P, Cai, J., Seedeek, K.M.E., Kellenberger, R.T., Russo, A., Qi, W., Aquino Fournier, C. and Schlüter, P.M. 2019. “A phylogenomic analysis of the floral transcriptomes of sexually deceptive and rewarding European orchids, Ophrys and Gymnadenia” Frontiers in Plant Science 10: 1553.
    OpenUrl
  18. ↵
    Roma, L., Cozzolino, S., Schlüter, P.M., Scopece, G. and Cafasso, D. 2018. “The complete plastid genomes of Ophrys iricolor and O. sphegodes (Orchidaceae) and comparative analyses with other orchids” PLoS One 13: e0204174.
    OpenUrl
  19. ↵
    Scheunert, A., Dorfner, M., Lingl, T., Oberprieler C. 2020. “Can we use it? On the utility of de novo and reference-based assembly of Nanopore data for plant plastome sequencing”. PLoS One 15: e0226234.
    OpenUrl
  20. ↵
    Shen, X.-X., Hittinger, C.T. and Rokas, A. 2017. “Contentions relationships in phylogenomic studies can be driven by a handful of genes”. Nature in Ecology and Evolution, 1: 0126.
    OpenUrl
  21. ↵
    Soliva, M., Kocyan, A. and Widmer, A. 2001. “Molecular phylogenetics of the sexually deceptive orchid genus Ophrys (Orchidaceae) based on nuclear and chloroplast DNA sequences”. Molecular Phylogenetics and Evolution 20: 78–88.
    OpenUrlCrossRefPubMedWeb of Science
  22. ↵
    Tyteca, D. and Baguette, M. 2017. “Ophrys (Orchidaceae) systematics – When molecular phylogenetics, morphology and biology reconcile” Berichte Aus Den Arbeitkreisen Heimische Orchideen 34: 37–103.
    OpenUrl
  23. ↵
    Walker, J.F., Walker-Hale, N., Vargas, O.M., Larson, D.A. and Stull, G.W. 2019. “Characterizing gene tree conflict in plastome-inferred phylogenies”. PeerJ 7:e7747.
    OpenUrlCrossRef
  24. ↵
    Wang, W., Schalamun, M., Morales-Suarez, A., Kainer, D. Schwessinger, B. and Lanfear, R. 2018. “Assembly of chloroplast genomes with long- and short read data: a comparison of approaches using Eucalyptus pauciflora as a test”. BMC Genomics 19: 977.
    OpenUrl
  25. ↵
    Wick, R.R., Judd, L.M., Gorrie, C.L. and Holt, K.E. 2017. “Unicycler: resolving bacterial genome assemblies from short and long sequencing reads”. PLoS Computational Biology 13: e1005595.
    OpenUrl
Back to top
PreviousNext
Posted February 16, 2021.
Download PDF

Supplementary Material

Email

Thank you for your interest in spreading the word about bioRxiv.

NOTE: Your email address is requested solely to identify you as the sender of this article.

Enter multiple addresses on separate lines or separate them with commas.
Whole plastid genome-based phylogenomics supports an inner placement of the O. insectifera group rather than a basal position in the rapidly diversifying Ophrys genus (Orchidaceae)
(Your Name) has forwarded a page to you from bioRxiv
(Your Name) thought you would like to see this page from the bioRxiv website.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Whole plastid genome-based phylogenomics supports an inner placement of the O. insectifera group rather than a basal position in the rapidly diversifying Ophrys genus (Orchidaceae)
Joris A. M. Bertrand, Anaïs Gibert, Christel Llauro, Olivier Panaud
bioRxiv 2020.12.16.423003; doi: https://doi.org/10.1101/2020.12.16.423003
Digg logo Reddit logo Twitter logo Facebook logo Google logo LinkedIn logo Mendeley logo
Citation Tools
Whole plastid genome-based phylogenomics supports an inner placement of the O. insectifera group rather than a basal position in the rapidly diversifying Ophrys genus (Orchidaceae)
Joris A. M. Bertrand, Anaïs Gibert, Christel Llauro, Olivier Panaud
bioRxiv 2020.12.16.423003; doi: https://doi.org/10.1101/2020.12.16.423003

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Subject Area

  • Evolutionary Biology
Subject Areas
All Articles
  • Animal Behavior and Cognition (3492)
  • Biochemistry (7341)
  • Bioengineering (5312)
  • Bioinformatics (20239)
  • Biophysics (9996)
  • Cancer Biology (7729)
  • Cell Biology (11288)
  • Clinical Trials (138)
  • Developmental Biology (6427)
  • Ecology (9936)
  • Epidemiology (2065)
  • Evolutionary Biology (13308)
  • Genetics (9357)
  • Genomics (12573)
  • Immunology (7694)
  • Microbiology (18997)
  • Molecular Biology (7432)
  • Neuroscience (40961)
  • Paleontology (300)
  • Pathology (1227)
  • Pharmacology and Toxicology (2133)
  • Physiology (3153)
  • Plant Biology (6855)
  • Scientific Communication and Education (1272)
  • Synthetic Biology (1894)
  • Systems Biology (5308)
  • Zoology (1087)