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Orchis patens Desf., Fl. Atlant. 2: 318 (1799) subsp. patens Type:— ALGERIA. Habitat in Atlante, donated by Desfontaines (lectotype: P-00307111!, designated by Hautzinger 1978; isolectotype B-W 16818-01 0!. Plate 248 in Desfontaines (1799) is also original material). Homotypic synonyms: Barlia patens (Desf.) Szlach., Polish Bot. J. 46: 127 (2001); Androrchis patens (Desf.) D.Tyteca & E.Klein, J. Eur. Orch. 40: 543 (2008). Heterotypic synonym: Orchis patens var. fontanesii Rchb.f. in H. G. L.Reichenbach, Icon. Fl. Germ. Helv. 13–14: 38 (1851), nom. inval., pro syn. Distribution:— Northern Algeria., Published as part of Calevo, Jacopo, Christenhusz, Maarten J. M. & Fay, Michael F., 2023, A taxonomic overview of Orchis sect. Robustocalcare (Orchidaceae), pp. 157-162 in Phytotaxa 592 (2) on page 159, DOI: 10.11646/phytotaxa.592.2.10, http://zenodo.org/record/7840332, {"references":["Hautzinger, L. (1978) Genus \" Orchis \" L. (Orchidaceae): Sectio \" Robustocalcare \" Hautzinger. Annalen des Naturhistorischen Museums in Wien 81: 31 - 73.","Desfontaines, R. L. (1799) Flora Atlantica, sive Historia plantarum, quae in Atlante, agro Tunetano et Algeriensi crescunt. Desgranges, Paris. https: // doi. org / 10.5962 / bhl. title. 6364"]}

Orchis patens subsp. brevicornis (Viv.) Asch. & Graeb., Syn. d. Mitteleurop. Fl.; 3: 697 (1907) Type:— ITALY. Liguria: In collibus Oreginae, Feritoris intra moenia Genuae, Viviani s.n., (lectotype: FI002791!, designated by Hautzinger 1978). Basionym: Orchis brevicornis Viv., Ann. Bot. (Genoa) 1(2): 184 (1804). Homotypic synonyms: Orchis patens var. brevicornis (Viv.) Rchb.f. in H. G. L.Reichenbach, Icon. Fl. Germ. Helv. 13–14: 39 (1851); Orchis patens ‘b’ brevicornis (Viv.) K.Richt., Pl. Eur. 1: 268 (1890). Heterotypic synonym: Orchis brevicornis var. minor Viv., Ann. Bot. (Genoa) 1(2): 184 (1804). Type:— ITALY. Liguria: Monte Fasce, Lando s.n. (FI?, not seen). Distribution:— North-western Italy (Liguria). Notes:— Richter (1890) already treated this as a subtaxon under O. patens, but rank was not specified. Viviani (1808) renamed it Orchis brevicornu, but this is an invalid ‘correction’, and therefore the epithet is brevicornis (Fig. 1b)., Published as part of Calevo, Jacopo, Christenhusz, Maarten J. M. & Fay, Michael F., 2023, A taxonomic overview of Orchis sect. Robustocalcare (Orchidaceae), pp. 157-162 in Phytotaxa 592 (2) on pages 158-159, DOI: 10.11646/phytotaxa.592.2.10, http://zenodo.org/record/7840332, {"references":["Hautzinger, L. (1978) Genus \" Orchis \" L. (Orchidaceae): Sectio \" Robustocalcare \" Hautzinger. Annalen des Naturhistorischen Museums in Wien 81: 31 - 73.","Viviani, D. (1808) Florae Italicae fragmenta. Giossi, Genoa, 184 pp."]}

Characterizing genetic diversity and structure of populations is essential for the effective conservation of threatened species.Orchis patenssensu lato is a narrowly distributed tetraploid species with a disjunct distribution (i.e., Northern Italy, North Africa and the Canary Islands), which is facing a severe decline. In this study, we evaluated levels of genetic diversity and population structuring using 12 new nuclear microsatellite markers. Our analyses of genetic differentiation based on multiple approaches (Structure analysis, PCA analysis, andF-statistics using the ploidy-independentRho-index) showed that gene flow is low across the range ofO. patens s.l., particularly in the Canary Islands. Clear differences in allele frequencies between Italy, Algeria and the Canary Islands underlie the genetic differentiation retrieved. Our study provides support for the recognition ofO. canariensisas a sister species toO. patensand the separation of the Italian populations as a new subspecies ofO. patens. Despite the high heterozygosity values found in all populations (ranging from 0.4 to 0.7), compatible with the tetraploid status of the species, small population sizes and reduced gene flow will be likely detrimental for the different populations in the long term, and we recommend immediate conservation actions to counteract further fragmentation and population decline.

Hybridization can often lead to the formation of novel taxa which can have traits that resemble either or both parental species. Determining the similarity of hybrid traits to parental taxa is particularly important in plant conservation, as hybrids that form between rare and common taxa may more closely resemble a rare parental species, thereby putting the rare parental taxon at further risk of extinction via increased backcrossing and introgression. We investigated the floral (morphological and chemical) traits and orchid mycorrhizal (OrM) fungal associations of the endangered orchid Orchis patens, its more common sister species O. provincialis, and their natural hybrid O. × fallax in natural sympatric populations. We found that both morphological and chemical floral traits of O. × fallax are shared by the parents but are more similar to O. patens than O. provincialis. OrM fungi were shared among all three taxa, indicating that the availability of OrM fungi should not represent a barrier to establishment of individuals of any of these taxa. These results suggest that O. × fallax may be able to expand its distribution within a similar niche to O. patens. This highlights the importance of quantifying differences between hybrids and parental taxon in species conservation planning.

The loss of orchid habitats has increased the investment on orchid conservation efforts to reduce the risk of extinction of rare species. In northwestern Italy, orchids are among the most threatene...

As orchids rely on their mycorrhizal fungi for nutrient supply, their spatial range is dependent on the distribution of orchid mycorrhizal (OM) fungi. We addressed possible correlations between mycorrhizal specificity and the geographic distribution of orchids and OM fungi in three populations of the rare sister species Orchis patens and O. canariensis. Metabarcoding of the fungal ITS2 region indicated that, although adult plants of either species were colonized by several ceratobasidioid, tulasnelloid, sebacinoid and serendipitoid fungi, the mycobiont spectra were dominated by Tulasnella helicospora (which occurred in 100% of examined plants with high read numbers), which is a globally distributed fungus. In vitro assays with a T. helicospora isolate obtained from O. patens indicated the effectiveness of this OM fungus at germinating seeds of its native host. At a local scale, higher read numbers for T. helicospora were found in soil samples collected underneath O. patens roots than at locations unoccupied by the orchid. Although these findings suggest that the geographical pattern of the main fungal symbiont does not limit the distribution of O. patens and O. canariensis at this scale, the actual causal link between orchid and OM fungal occurrence/abundance still needs to be better understood.

16. O. patens Desf., FI. Atl. 2: 318 (1799) (O. brevicornis Viv.). Tubers ovoid. Stem 25-70 cm, erect, with a basal rosette or cluster of 3-5 leaves and with sheaths above. Leaves oblong- ovate to lanceolate. Spike long-cylindrical. Bracts linear- lanceolate, 5- to 7-veined, c. i as long to as long as ovary. Flowers purple. Outer perianth-segments 8-10 mm, oblong, obtuse, greenish towards the base, the 2 lateral patent-deflexed, the median curved forward or erecto-patent; inner lanceolateoblong. Labellum 9-10 mm, ovate, spotted, 3-lobed; lateral lobes obliquely oblong, truncate; middle lobe broadly obcordate, emarginate, with 2 truncate, crenulate lobules; base of labellum with 2 inconspicuous ridges. Spur saccate, directed downwards, shorter than labellum, c. 4 as long as ovary. W. Mediterranean region. Bl Hs It Si., Published as part of D. M. Moore (ed.), 1980, CCIII Orchidaceae, pp. 325-350 in Flora Europaea, Vol 5: Alismataceae to Orchidaceae, Camebridge :Cambridge University Press on page 340, DOI: 10.5281/zenodo.215522