Published December 8, 2025 | Version v1
Journal article Open

From the Brazilian lowlands to the Andes: specialist fungus gnat pollination and self-incompatibility in two Malaxis species (Malaxidinae: Orchidaceae)

  • 1. Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil
  • 2. Universidad Nacional de San Cristóbal de Huamanga, Ayacucho, Peru

Description

Background and aims – Malaxis is a cosmopolitan genus comprising approximately 300 species and is one of the most diverse within the subtribe Malaxidinae. However, to date, no detailed studies have addressed its reproductive biology in the Neotropics. This study aimed to document the floral traits, pollination mechanisms, breeding system, and fruiting success of two native Neotropical species.

Material and methods – Plants of Malaxis parthoni were studied in Porto Alegre, southern Brazil (79 m a.s.l.), while individuals of M. excavata were examined at 3,500 m a.s.l. in Ayacucho, in the Peruvian Andes. To evaluate the breeding system, we tested for autonomous pollination and self-compatibility using flowers isolated from pollinators through bagging. Nectar production was assessed through qualitative tests to detect the presence of sugars in floral secretions. The pollination process, under natural conditions, was recorded in the field through video and photographs, and pollination efficiency and natural fruiting success were documented.

Key results – Both Malaxis species possess nectar-producing flowers and were found to be pollinator-dependent and self-incompatible. Fungus gnats of the genus Mycomya (Mycetophilidae) acted as pollinators. In both species, pollinia were attached to the ventral part of the prothorax. In both species, a high percentage of flowers with pollinia removed was observed, indicating high pollination efficiency. On average, fruiting success was 11.24% in M. parthoni and 36.01% in M. excavata, the latter showing a statistically higher percentage.

Conclusion – Our findings reveal that both species require cross-pollination to achieve fruit set, with fungus gnats acting as effective pollinators. The relatively high fruiting success compared to other congeners and self-incompatible orchids may result from a combination of factors, including the presence of floral rewards and high pollinator efficiency. This study provides the first comprehensive account of the reproductive biology of Neotropical Malaxis species.

Files

plecevo_article_164210.pdf

Files (11.2 MB)

Name Size Download all
md5:8794da0bf3d8be032ec6368503c1f1b6
11.2 MB Preview Download

System files (221.6 kB)

Name Size Download all
md5:80950ad8238d7fa3a88c4c0baaf0ec0c
221.6 kB Download

Linked records

Additional details

References

  • Ackerman JD, Mesler MR (1979) Pollination biology of Listera cordata (Orchidaceae). American Journal of Botany 66(7): 820–824. https://doi.org/10.1002/j.1537-2197.1979.tb06288.x
  • Ackerman JD, Phillips RD, Tremblay RL, Karremans A, Reiter N, Peter CI, Bogarín D, Pérez-Escobar OA, Liu H (2023) Beyond the various contrivances by which orchids are pollinated: global patterns in orchid pollination biology. Botanical Journal of the Linnean Society 202(3): 295–324. https://doi.org/10.1093/botlinnean/boac082
  • Adams PB, Lawson SD (1993) Pollination in Australian orchids: A critical assessment of the literature 1882–1992. Australian Journal of Botany 41(5): 553–575. https://doi.org/10.1071/BT9930553
  • Aragon S, Ackerman JD (2001) Density effects on the reproductive success and herbivory of Malaxis massonii. Lindleyana 16(1): 3–12.
  • Argue CL (2012) Tribe Malaxideae. In: Argue CL (Ed.) The Pollination Biology of North American Orchids: Volume 2. Springer, New York, 91–104. https://doi.org/10.1007/978-1-4614-0622-8_5
  • Argue CL (2014) The pollination biology of Malaxis paludosa (L.) Swartz (bog adder's-mouth) (=Hammarbya paludosa (L.) Kuntze). The Native Orchid Conference Journal 11(2): 1–7.
  • Ashman TL, Schoen DJ (1994) How long should flowers live? Nature 371(6500): 788–791. https://doi.org/10.1038/371788a0
  • Assis LC (2023) Pollination syndromes and the origins of floral traits. Annals of Botany 132(6): 1055–1072. https://doi.org/10.1093/aob/mcad147
  • Barbosa AR, de Melo MC, Borba EL (2009) Self-incompatibility and myophily in Octomeria (Orchidaceae, Pleurothallidinae) species. Plant Systematics and Evolution 283: 1–8. https://doi.org/10.1007/s00606-009-0212-6
  • Basith N, Richard PSS (2025) Fly pollination in Impatiens orchioides Bedd. (Balsaminaceae): possible role of fungus gnats and phorid flies as pollinators. Plant Species Biology 40(4): 366–377. https://doi.org/10.1111/1442-1984.70006
  • Blanco MA, Barboza G (2005) Pseudocopulatory pollination in Lepanthes (Orchidaceae: Pleurothallidinae) by fungus gnats. Annals of Botany 95(5): 763–772. https://doi.org/10.1093/aob/mci090
  • Bogarín D, Fernández M, Borkent A, Heemskerk A, Pupulin F, Ramírez S, Smets EF, Gravendeel B (2018) Pollination of Trichosalpinx (Orchidaceae: Pleurothallidinae) by biting midges (Diptera: Ceratopogonidae). Botanical Journal of the Linnean Society 186(4): 510–543. https://doi.org/10.1093/botlinnean/box087
  • Borba EL, Semir J (2001) Pollinator specificity and convergence in fly-pollinated Pleurothallis (Orchidaceae) species: a multiple population approach. Annals of Botany 88(1): 75–88. https://doi.org/10.1006/anbo.2001.1434
  • Borba EL, Barbosa AR, de Melo MC, Gontijo SL, de Oliveira HO (2011) Mating systems in the Pleurothallidinae (Orchidaceae): evolutionary and systematic implications. Lankesteriana 11(3): 207–221. https://doi.org/10.15517/lank.v11i3.18275
  • Burdíková N, Kaspřák D, Kjærandsen J, Tóthová AŠ, Ševčík J (2024) Molecular phylogeny of the fungus gnat subfamilies Sciophilinae and Leiinae (Mycetophilidae), with notes on Sciaroidea incertae sedis (Diptera: Bibionomorpha). Zoological Journal of the Linnean Society 202(1): 1–11. https://doi.org/10.1093/zoolinnean/zlad176
  • Buzatto CR, Nervo MH, Sanguinetti A, Van Den Berg C, Singer RB (2022) Efficient pollination and high reproductive success in two Brazilian Spiranthinae orchids: insights on the evolutionary history of pollination within the Pelexia clade. Plant Species Biology 37(2): 182–196. https://doi.org/10.1111/1442-1984.12366
  • Calderon‐Quispe FH, Singer BR (2024) Reproductive biology in Gomphichis valida Rchb. f. (Orchidaceae: Orchidoideae, Cranichidinae): generalist pollination in a high‐Andean terrestrial orchid with long‐lived flowers. Plant Species Biology 39(3): 153–166. https://doi.org/10.1111/1442-1984.12453
  • Cameron KM (2005) Leave it to the leaves: a molecular phylogenetic study of Malaxideae (Epidendroideae, Orchidaceae). American Journal of Botany 92(6): 1025–1032. https://doi.org/10.3732/ajb.92.6.1025
  • Castro JB, Perdomo O, Singer RB (2022) Pollination biology and reproductive success in four Brazilian species of Gomesa (Orchidaceae: Oncidiinae): specific pollinators, but high pollen loss and low fruit set. Plant Species Biology 37(1): 132–147. https://doi.org/10.1111/1442-1984.12361
  • Catling PM (1980) Rain-assisted autogamy in Liparis loeselii (L.) LC Rich. (Orchidaceae). Bulletin of the Torrey Botanical Club 107(4): 525–529. https://doi.org/10.2307/2484083
  • Chinchilla IF, Karremans AP, Blanco MA (2022) A new species and a new record of Malaxis (Malaxidinae) from Costa Rica. Lankesteriana 22(1): 37–51. https://doi.org/10.15517/lank.v22i1.50848
  • Claessens J, Kleynen J (2011) The Flower of the European Orchid: Form and Function. Published by the authors, Voerendaal 1–439.
  • Darwin C (1862) On the Various Contrivances by which British and Foreign Orchids are Fertilised by Insects. John Murray, London, 1–366.
  • Dressler RL (1981) The Orchids: Natural History and Classification. Harvard University Press, Cambridge, 1–344.
  • Duque Buitrago CA, Alzate Quintero NF, Otero JT (2014) Nocturnal pollination by fungus gnats of the Colombian endemic species, Pleurothallis marthae (Orchidaceae: Pleurothallidinae). Lankesteriana 13(3): 407–417. https://doi.org/10.15517/lank.v13i3.14429
  • Endara L, Grimaldi D, Roy B (2010) Lord of the Flies: pollination of Dracula orchids. Lankesteriana 10(1): 1–11. https://doi.org/10.15517/lank.v10i1.18318
  • Feigs JT, Holzhauer SI, Huang S, Brunet J, Diekmann M, Hedwall PO, Kramp K, Naaf T (2022) Pollinator movement activity influences genetic diversity and differentiation of spatially isolated populations of clonal forest herbs. Frontiers in Ecology and Evolution 10: 908258. https://doi.org/10.3389/fevo.2022.908258
  • Fick SE, Hijmans RJ (2017) WorldClim 2: new 1‐km spatial resolution climate surfaces for global land areas. International Journal of Climatology 37(12): 4302–4315. https://doi.org/10.1002/joc.5086
  • Fonseca RS, Santos FAD, Vieira MF (2015) Is the pollination efficiency of long-lived orchid flowers affected by age? Revista Ceres 62: 347–350. https://doi.org/10.1590/0034-737X201562040003
  • Goldblatt P, Bernhardt P, Vogan P, Manning JC (2004) Pollination by fungus gnats (Diptera: Mycetophilidae) and self-recognition sites in Tolmiea menziesii (Saxifragaceae). Plant Systematics and Evolution 244: 55–67. https://doi.org/10.1007/s00606-003-0067-1
  • Han ZD, Wu Y, Bernhardt P, Wang H, Ren ZX (2022) Observations on the pollination and breeding systems of two Corybas species (Diurideae; Orchidaceae) by fungus gnats (Mycetophilidae) in southwestern Yunnan, China. BMC Plant Biology 22(1): 426. https://doi.org/10.1186/s12870-022-03816-1
  • Hayashi T, Reiter N, Phillips RD, Peakall R (2022) Sexual deception of male Bradysia (Diptera: Sciaridae) by floral odour and morphological cues in Pterostylis (Orchidaceae). Botanical Journal of the Linnean Society 200(3): 433–449. https://doi.org/10.1093/botlinnean/boac015
  • Hayashi T, Reiter N, Phillips RD, Peakall R (2025) How widespread is pollination by sexual deception of fungus gnats in Pterostylis (Orchidaceae)? Botanical Journal of the Linnean Society 209(1): 1–19. https://doi.org/10.1093/botlinnean/boae088
  • INRENA (1995) Mapa Ecológico del Perú: Guía Explicativa. Ministerio de Agricultura, Lima, Peru, 1–146.
  • Jacquemyn H, Micheneau C, Roberts DL, Pailler T (2005) Elevational gradients of species diversity, breeding system and floral traits of orchid species on Réunion Island. Journal of Biogeography 32(10): 1751–1761. https://doi.org/10.1111/j.1365-2699.2005.01307.x
  • Jakovlev J (2012) Fungal hosts of mycetophilids (Diptera: Sciaroidea excluding Sciaridae): a review. Mycology 3(1): 11–23. https://doi.org/10.1080/21501203.2012.662533
  • Jermakowicz E, Ostrowiecka B, Tałałaj I, Pliszko A, Kostro-Ambroziak A (2015) Male and female reproductive success in natural and anthropogenic populations of Malaxis monophyllos (L.) Sw. (Orchidaceae). Biodiversity: Research and Conservation 39: 37–44. https://doi.org/10.1515/biorc-2015-0024
  • Jermakowicz E, Leśniewska J, Stocki M, Naczk AM, Kostro-Ambroziak A, Pliszko A (2022) The floral signals of the inconspicuous orchid Malaxis monophyllos: how to lure small pollinators in an abundant environment. Biology 11(5): 640. https://doi.org/10.3390/biology11050640
  • Kaiser R (1993) The scent of Orchids – Olfactory and Chemical Investigations. Editiones Roche, Basel, 1–259.
  • Katsuhara KR, Kitamura S, Ushimaru A (2017) Functional significance of petals as landing sites in fungus‐gnat pollinated flowers of Mitella pauciflora (Saxifragaceae). Functional Ecology 31(6): 1193–1200. https://doi.org/10.1111/1365-2435.12842
  • Kelly MM, Toft RJ, Gaskett AC (2013) Pollination and insect visitors to the putatively brood-site deceptive endemic spurred helmet orchid, Corybas cheesemanii. New Zealand Journal of Botany 51(3): 155–167. https://doi.org/10.1080/0028825X.2013.795905
  • Kite GC, Salazar GA (2008) Chemical composition of the inflorescence odor of Malaxis rzedowskiana (Orchidaceae). Revista Mexicana de Biodiversidad 79(1): 153–157. https://doi.org/10.22201/ib.20078706e.2008.001.524
  • Kolomeitseva GL, Ryabchenko AS, Babosha AV, Koval VA (2024) Homoplasy in the embryonic development of terrestrial and epiphytic orchids from the subtribe Malaxidinae (Orchidaceae). Planta 260(6): 143. https://doi.org/10.1007/s00425-024-04569-x
  • Kuiter RH (2020) Pollination by sexual deception of different fungus-gnat species, two (Mycetophilidae) in Pterostylis grandiflora and two (Sciaridae) in P. nana (Orchidaceae). The Victorian Naturalist 137(2): 41–47. https://www.biodiversitylibrary.org/page/62023736 [accessed 30.09.2025]
  • Kunin WE (1997) Population size and density effects in pollination: pollinator foraging and plant reproductive success in experimental arrays of Brassica kaber. Journal of Ecology 85(2): 225–234. https://doi.org/10.2307/2960653
  • Margońska HB, Kozieradzka-Kiszkurno M, Brzezicka E, Haliński ŁP, Davies KL, Lipińska MM (2021) Crepidium sect. Crepidium (Orchidaceae, Malaxidinae)—Chemical and morphological study of flower structures in the context of pollination processes. Plants 10(11): 2373. https://doi.org/10.3390/plants10112373
  • Margońska HB, Kozieradzka-Kiszkurno M, Brzezicka E, Haliński ŁP, Davies KL (2025) Floral morphological and chemical analyses of Dienia flowers (Orchidaceae, Malaxidinae) relative to pollination processes. Scientific Reports 15(1): 723. https://doi.org/10.1038/s41598-024-84538-2
  • Meléndez-Ackerman EJ, Ackerman JD (2001) Density-dependent variation in reproductive success in a terrestrial orchid. Plant Systematics and Evolution 227: 27–36. https://doi.org/10.1007/s006060170054
  • Mesler MR, Ackerman JD, Lu KL (1980) The effectiveness of fungus gnats as pollinators. American Journal of Botany 67(4): 564–567. https://doi.org/10.2307/2442297
  • Metcalfe DB, Kunin WE (2006) The effects of plant density upon pollination success, reproductive effort, and fruit parasitism in Cistus ladanifer L. (Cistaceae). Plant Ecology 185: 41–47. https://doi.org/10.1007/s11258-005-9082-3
  • Mochizuki K, Kawakita A (2018) Pollination by fungus gnats and associated floral characteristics in five families of the Japanese flora. Annals of Botany 121(4): 651–663. https://doi.org/10.1093/aob/mcx196
  • Mochizuki K, Okamoto T, Chen KH, Wang CN, Evans M, Kramer AT, Kawakita A (2023) Adaptation to pollination by fungus gnats underlies the evolution of pollination syndrome in the genus Euonymus. Annals of Botany 132(2): 319–333. https://doi.org/10.1093/aob/mcad081
  • Neiland MRM, Wilcock CC (1998) Fruit set, nectar reward, and rarity in the Orchidaceae. American Journal of Botany 85: 1657–1671. https://doi.org/10.2307/2446499
  • Nilsson LA, Rabakonandrianina E, Razananaivo R, Randriamanindry JJ (1992) Long pollinia on eyes: hawk-moth pollination of Cynorkis uniflora Lindley (Orchidaceae) in Madagascar. Botanical Journal of the Linnean Society 109(1): 145–160. https://doi.org/10.1111/j.1095-8339.1992.tb00263.x
  • Nuammee A (2018) Taxonomic revision and pollination biology of orchid genera Crepidium Blume and Dienia Lindl. (Malaxidinae, Orchidaceae) in Thailand. PhD Thesis, Chulalongkorn University, Thailand. https://doi.org/10.58837/CHULA.THE.2018.42
  • Okamoto T, Okuyama Y, Goto R, Tokoro M, Kato M (2015) Parallel chemical switches underlying pollinator isolation in Asian Mitella. Journal of Evolutionary Biology 28(3): 590–600. https://doi.org/10.1111/jeb.12591
  • Okuyama Y, Kato M, Murakami N (2004) Pollination by fungus gnats in four species of the genus Mitella (Saxifragaceae). Botanical Journal of the Linnean Society 144(4): 449–460. https://doi.org/10.1111/j.1095-8339.2003.00259.x
  • Okuyama Y, Pellmyr O, Kato M (2008) Parallel floral adaptations to pollination by fungus gnats within the genus Mitella (Saxifragaceae). Molecular Phylogenetics and Evolution 46(2): 560–575. https://doi.org/10.1016/j.ympev.2007.09.020
  • Orford KA, Vaughan IP, Memmott J (2015) The forgotten flies: the importance of non-syrphid Diptera as pollinators. Proceedings of the Royal Society B: Biological Sciences 282: 20142934. https://doi.org/10.1098/rspb.2014.2934
  • Overbeck GE, Müller SC, Pillar VD, Pfadenhauer J (2005) Fine‐scale post‐fire dynamics in southern Brazilian subtropical grassland. Journal of Vegetation Science 16(6): 655–664. https://doi.org/10.1111/j.1654-1103.2005.tb02408.x
  • Phillips RD, Scaccabarozzi D, Retter BA, Hayes C, Brown GR, Dixon KW, Peakall R (2014) Caught in the act: pollination of sexually deceptive trap-flowers by fungus gnats in Pterostylis (Orchidaceae). Annals of Botany 113(4): 629–641. https://doi.org/10.1093/aob/mct295
  • Potts SG, Biesmeijer JC, Kremen C, Neumann P, Schweiger O, Kunin WE (2010) Global pollinator declines: trends, impacts and drivers. Trends in Ecology & Evolution 25(6): 345–353. https://doi.org/10.1016/j.tree.2010.01.007
  • Power EF, Stabler D, Borland AM, Barnes J, Wright GA (2018) Analysis of nectar from low‐volume flowers: a comparison of collection methods for free amino acids. Methods in Ecology and Evolution 9(3): 734–743. https://doi.org/10.1111/2041-210X.12928
  • POWO (2025a) Malaxis excavata (Lindl.) Kuntze. Plants of the World Online. Facilitated by the Royal Botanic Gardens, Kew. https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:149789-2 [accessed 01.07.2025]
  • POWO (2025b) Malaxis parthoni C.Morren. Plants of the World Online. Facilitated by the Royal Botanic Gardens, Kew. https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:642411-1 [accessed 01.07.2025]
  • Primack RB (1985) Longevity of individual flowers. Annual Review of Ecology and Systematics 16: 15–37.
  • Qi X, Zhang Z, Luo Q, Hu S, Cui X, Liu S, Deng Z, Huang C, Deng J, Dong S, Cheng J (2024) Flowering phenology and pollination process of Liparis gigantea (Orchidaceae) in Guangxi, China. Biology Bulletin 51: 1515–1523. https://doi.org/10.1134/S1062359023606341
  • R Core Team (2024) R: a Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/ [accessed 30.09.2025]
  • Raguso RA (2020) Don't forget the flies: dipteran diversity and its consequences for floral ecology and evolution. Applied Entomology and Zoology 55(1): 1–7. https://doi.org/10.1007/s13355-020-00668-9
  • Ratto F, Simmons BI, Spake R, Zamora‐Gutierrez V, MacDonald MA, Merriman JC, Tremlett CJ, Poppy GM, Peh KS-H, Dicks LV (2018) Global importance of vertebrate pollinators for plant reproductive success: a meta‐analysis. Frontiers in Ecology and the Environment 16(2): 82–90. https://doi.org/10.1002/fee.1763
  • Reeves LM, Reeves T (1984) Life history and reproduction of Malaxis paludosa in Minnesota. American Orchid Society Bulletin 53: 1280–1291.
  • Reiter N, Freestone M, Brown G, Peakall R (2019) Pollination by sexual deception of fungus gnats (Keroplatidae and Mycetophilidae) in two clades of Pterostylis (Orchidaceae). Botanical Journal of the Linnean Society 190(1): 101–116. https://doi.org/10.1093/botlinnean/boz009
  • Sagili RR, Chakrabarti P, Melathopoulos A, Delaplane KS, Dag A, Danka RG, Freitas BM, Garibaldi LA, Hormaza JI, Steinhauer N (2025) Standard methods for pollination research with Apis mellifera 2.0. Journal of Apicultural Research 64(2): 612–646. https://doi.org/10.1080/00218839.2024.2369284
  • Sanguinetti A, Singer RB (2014) Invasive bees promote high reproductive success in Andean orchids. Biological Conservation 175: 10–20. https://doi.org/10.1016/j.biocon.2014.04.011
  • Santos TF, Smidt EC (2023) A new Malaxis (Orchidaceae: Malaxidinae) from the Campos de Altitude of the Atlantic Rainforest in southern Brazil. Nordic Journal of Botany 2023(12): e04164. https://doi.org/10.1111/njb.04164
  • Schmitt J (1983) Flowering plant density and pollinator visitation in Senecio. Oecologia 60: 97–102. https://doi.org/10.1007/BF00379326
  • Song B, Chen G, Stöcklin J, Peng DL, Niu Y, Li ZM, Sun H (2014) A new pollinating seed‐consuming mutualism between Rheum nobile and a fly fungus gnat, Bradysia sp., involving pollinator attraction by a specific floral compound. New Phytologist 203(4): 1109–1118. https://doi.org/10.1111/nph.12856
  • Steinacher G, Wagner J (2010) Flower longevity and duration of pistil receptivity in high mountain plants. Flora 205(6): 376–387. https://doi.org/10.1016/j.flora.2009.12.012
  • Suetsugu K (2019) Rain-triggered self-pollination in Liparis kumokiri, an orchid that blooms during the rainy season. Ecology 100(7): 1–4. https://doi.org/10.1002/ecy.2683
  • Sunakawa Y, Mochizuki K, Kawakita A (2024) Pollination of Oberonia japonica (Orchidaceae) by gall midges (Cecidomyiidae). Ecology 105(5): e4293. https://doi.org/10.1002/ecy.4293
  • Tan KH, Nishida R, Toong YC (2002) Floral synomone of a wild orchid, Bulbophyllum cheiri, lures Bactrocera fruit flies for pollination. Journal of Chemical Ecology 28(6): 1161–1172. https://doi.org/10.1023/A:1016277500007
  • Tremblay RL, Ackerman JD, Zimmerman JK, Calvo RN (2005) Variation in sexual reproduction in orchids and its evolutionary consequences: a spasmodic journey to diversification. Biological Journal of the Linnean Society 84: 1–54. https://doi.org/10.1111/j.1095-8312.2004.00400.x
  • Ulloa Ulloa C, Acevedo-Rodríguez P, Beck S, Belgrano MJ, Bernal R, Berry PE, Brako L, Celis M, Davidse G, Forzza RC, Gradstein SR, Hokche O, León B, León-Yánez S, Magill RE, Neill DA, Nee M, Raven PH, Stimmel H, Strong MT, Villaseñor JL, Zarucchi JL, Zuloaga FO, Jørgensen PM (2017) An integrated assessment of the vascular plant species of the Americas. Science 358(6370): 1614–1617. https://doi.org/10.1126/science.aao0398
  • Wickham H (2016) ggplot2: Elegant Graphics for Data Analysis. Springer International Publishing, Cham, 1–260. https://doi.org/10.1007/978-3-319-24277-4
  • Woodcock TS, Larson BM, Kevan PG, Inouye DW, Lunau K (2014) Flies and flowers II: floral attractants and rewards. Journal of Pollination Ecology 12: 63–94. https://doi.org/10.26786/1920-7603(2014)5
  • Zeng MY, Li MH, Lan S, Yin WL, Liu ZJ (2024) Comparative phylogenomic study of Malaxidinae (Orchidaceae) sheds light on plastome evolution and gene divergence. International Journal of Molecular Sciences 25(20): 11181. https://doi.org/10.3390/ijms252011181
  • Zhang S, Wu SM, Gao JY (2024) Floral mechanisms promote pollination success and reduce the incidence of self‐pollination in a fly‐pollinated self‐incompatible orchid. Ecology and Evolution 14(4): e11295. https://doi.org/10.1002/ece3.11295