GENERAL LITERATURE

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Articles or books by two or more authors are cited as follows. When there are two authors, citation is alphabetical after the second author's name. When there are three or more authors, references are cited in the body of the text as (e.g.) Chase et al. 2000a, 2000b, 2000c, and are listed following these sometimes alphabetically qualified dates of publication immediately after all the single- or two-authored articles by the first author.

Ma, F. [et al. 2024], Fu, Y., Wei, W., Li, Z., Liu, J., Bi, B., & Liu, W. 2024. Zygotic quiescence prolongs the reproductive cycle in Berchemia sinica (Rhamnaceae). Flora 314:152493. https://doi.org/10.1016/j.flora.2024.152493

Ma, G. [et al. 2012], Zhang, X., Bunn, E., & Dixon, K. 2012. Megasporogenesis and embryogenesis in three sympatric Posidonia seagrass species. Aquat. Bot. 100: 1-7.

Ma, H. [Haozhi] [et al. 2023], Crowther, T. W., Mo, L., Maynard, D. S., Renner, S. S., van den Hoogen, J., Zou, Y., Liang, J., de-Miguel, S., Nabuurs, G.-J., Reich, P. B., Niinemets, Ü, Abegg, M., Adou Yao, Y. C., Alberti, G., Almeyda Zambrano, A. M., Alvarado, B. V., Alvarez-Dávila, E., Alvarez-Loayza, P., Alves, L. F., Ammer, C., Antón-Fernández, C., Araujo-Murakami, A., Arroyo, L., Avitabile, V., Aymard, G. A., Baker, T. R., Balazy, R., Banki, O., Barroso, J. G., Bastian, M. L., Bastin, J.-F., Birigazzi, L., Birnbaum, P., Bitariho, R., Boeckx, P., Bongers, F., Bouriaud, O., Brancalion, P. H. S., Brandl, S., Brearley, F. Q., Brienen, R., Broadbent, E. N., Bruelheide, H., Bussotti, F., Gatti, R. C., César, R. G., Cesljar, G., Chazdon, R., Chen, H. Y. H., Chisholm, C., Cho, H., Cienciala, E., Clark, C., Clark, D., Colletta, G. D., Coomes, D. A., Cornejo Valverde, F., Corral-Rivas, J. J., Crim, P. M., Cumming, J. R., Dayanandan, S., de Gasper, A. L., Decuyper, M., Derroire, G., DeVries, B., Djordjevic, I., Dolezal, J., Dourdain, A., Engone Obiang, N. L., Enquist, B. J., Eyre, T. J., Fandohan, A. B., Fayle, T. M., Feldpausch, T. R., Ferreira, L. V., Finér, L., Fischer, M., Fletcher, C., Fridman, J., Frizzera, L., Gamarra, J. G. P., Gianelle, D., Glick, H. B., Harris, D. J., Hector, A., Hemp, A., Hengeveld, G., Hérault, B., Herbohn, J. L., Herold, M., Hillers, A., Honorio Coronado, E. N., Hui, C., Ibanez, T. T., Amaral, I., Imai, N., Jagodzinski, A. M., Jaroszewicz, B., Johannsen, V. K., Joly, C. A., Jucker, T., Jung, I., Karminov, V., Kartawinata, K., Kearsley, E., Kenfack, D., Kennard, D. K., Kepfer-Rojas, S., Keppel, G., Khan, M. L., Killeen, T. J., Kim, H. S., Kitayama, K., Köhl, M., Korjus, H., Kraxner, F., Kucher, D., Laarmann, D., Lang, M., Lewis, S. L., Lu, H., Lukina, N. V., Maitner, B. S., Malhi, Y., Marcon, E., Marimon, B. S., Marimon-Junior, B. H., Marshall, A. R., Martin, E. H., Meave, J. A., Melo-Cruz, O., Mendoza, C., Merow, C., Mendoza, A. M., Moreno, V. S., Mukul, S. A., Mundhenk, P., Nava-Miranda, M. G., Neill, D., Neldner, V. J., Nevenic, R. V., Ngugi, M. R., Niklaus, P. A., Oleksyn, J., Ontikov, P., Ortiz-Malavasi, E., Pan, Y., Paquette, A., Parada-Gutierrez, A., Parfenova, E. I., Park, M., Parren, M., Parthasarathy, N., Peri, P. L., Pfautsch, S., Phillips, O. L., Picard, N., Piedade, M. T. F., Piotto, D., Pitman, N. C. A., Mendoza-Polo, I., Poulsen, A. D., Poulsen, J. R., Pretzsch, H., Ramirez Arevalo, F., Restrepo-Correa, Z., Rodeghiero, M., Rolim, S. G., Roopsind, A., Rovero, F., Rutishauser, E., Saikia, P., Salas-Eljatib, C., Saner, P., Schall, P., Schelhaas, M.-J., Schepaschenko, D., Scherer-Lorenzen, M., Schmid, B., Schöngart, J., Searle, E. B., Seben, V., Serra-Diaz, J. M., Sheil, D., Shvidenko, A. Z., Silva-Espejo, J. E., Silveira, M., Singh, J., Sist, P., Slik, F., Sonké, B., Souza, A. F., Miscicki, S., Stereczak, K. J., Svenning, J.-C., Svoboda, M., Swanepoel, B., Targhetta, N., Tchebakova, N., ter Steege, H., Thomas, R., Tikhonova, E., Umunay, P. M., Usoltsev, V. A., Valencia, R., Valladares, F., van der Plas, F., Van Do, T., van Nuland, M. E., Vasquez, R. M., Verbeeck, H., Viana, H., Vibrans, A. C., Vieira, S., von Gadow, K., Wang, H.-F., Watson, J. V., Werner, G. D. A., Westerlund, B., Wiser, S. K., Wittmann, F., Woell, H., Wortel, V., Zagt, R., Zawila-Niedzwiecki, T., Zhang, C., Zhao, X., Zhou, M., Zhu, Z. X., Zo-Bi, I. C., & Zohner, C. M. 2023. The global biogeography of tree leaf form and habit. Nature Plants 9: 1795-1809. https://doi.org/10.1038/s41477-023-01543-5

Ma, H. [Hui] [et al. 2015], Lu, J., Liu, B.-B., He, X.-D., & Liu, J.-Q. 2015. Phylotranscriptomic analyses in plants using Betulaceae as an example. J. Syst. Evol. 53: 403-410.

Ma, J. [Ji] [et al. 2013], Yang, B., Zhu, W., Sun, L., Tian, J., & Wang, X. 2013. The complete chloroplast genome sequence of Mahonia bealei reveals a significant expansion of the inverted repeat and phylogenetic relationship with other angiosperms. Gene 528: 120-131.

Ma, J. [Jianchow] [et al. 2022], Wang, S., Zhu, X., Sun, G., Chang, G., Li, L., Huy, X., Zhang, S., Zhou, Y., Song, C.-P., & Huang J. 2022. Major episodes of horizontal gene transfer drove the evolution of land plants. Molec. Plant 15: 857–871.

Ma, J. F., & Takahashi, E. 2002. Soil, Fertilizer, and Plant Silicon Research in Japan. Elsevier, Amsterdam.

Ma, J. [et al. 2021], Sun, P., Wang, D., Wang, Z., Yang, J., Li, Y., Mu, W., Xu, R., Wu, Y., Dong, C., Shrestha, N., Liu, J., & Yang, Y. 2021. The Chloranthus sessilifolius genome provides insight into early diversification of angiosperms. Nature Communic. 12:6929.

Ma, J.-H. [et al. 2023], Chen, X., Hou, W.-X., Geng, L.-Y., & Tang, C.-Q. 2023. Plastome phylogenomics of Micromeles (Rosaceae). Phytotaxa 589: 179-190.

Ma, L. [et al. 2015], Hatlen, A., Kelly, L. J., Wang, W., Kovarik, A., Leitch, I. J., & Leitch, A. R. 2015. Angiosperms are unique among land plant lineages in the occurrence of key genes in the RNA-directed DNA methylation (RdDM) pathway. Genome Biol. Evol. 7: 2648-2662.

Ma, O. S. W., & Saunders, R. M. K. 2003. Comparative floral ontogeny of Maesa (Maesaceae), Aegiceras (Myrsinaceae) and Embelia (Myrsinaceae): Taxonomic and phylogenetic implications. Plant Syst. Evol. 243: 39-58.

Ma, P.-F. [et al. 2014], Zhang, Y.-X., Zeng, C.-X., Guo, Z.-H., & Li, D.-Z. 2014. Chloroplast phylogenomic analyses resolve deep-level relationships of an intractable bamboo tribe Arundinarieae (Poaceae). Syst. Biol. 63: 933-950.

Ma, P.-F. [et al. 2021], Liu, Y.-L., Jin, G.-H., Liu, J.-X., Wu, H., He, J., Guo, Z.-H., & Li, D.-Z. 2021. The Pharus latifolius genome bridges the gap of early grass evolution. Plant Cell 33: 846-864.

Ma, Q. [et al. 2017a], Liu, X., Franks, R. G., & Xiang, Q.-Y. (J.) 2017. Alterations of CorTFL1 and CorAP1 expression correlate with major evolutionary shifts of inflorescence architecture in Cornus (Cornaceae) — a proposed model for variation of closed inflorescence forms. New Phytol. 216: 519-535. doi: 10.1111/nph.14197

Ma, Q. [et al. 2017b], Zhang, W., & Xiang, Q.-Y. (J.) 2017. Evolution and genetics of floral display — a review of progress. J. Syst. Evol. 55: 487-515.

Ma, Q. [et al. 2024], Liu, H.-S., Li, H.-J., Bai, W.-P., Gao, Q.-F., Wu, S.-D., Yin, X.-X., Chen, Q.-Q., Shi, Y.-Q., Gao, T.-G., Bao, A.-K., Yin, H.-J., Li, L., Rowland, O., Hepworth, S. R., Luan, S., & Wang, S.-M. 2024. Genomic analysis reveals phylogeny of Zygophyllales and mechanism for water retention of a succulent xerophyte. Plant Physiol. 195: 617-639. https://doi.org/10.1093/plphys/kiae040

Ma, Q.-W. [et al. 2009], Ferguson, D. K., Li, F.-L., & Li, C.-S. 2009. Leaf epidermal structures of extant plants of Cunninghamia and Taiwania (Cupressaceae sensu lato) and their taxonomic application. Rev. Palaeobot. Palynol. 155: 15-24.

Ma, Y. [et al. 2022], Mao, X., Wang, J., Zhang, L., Jiang, Y., Geng, Y., Ma, T., Cai, L., Huang, S., Hollingsworth, P., Mao, K., Kang, M., Li, Y., Yang, W., Wu, H., Chen, Y., Davis, C. C., Shrestha, N., Ree, R. H., Xi, Z., Hu, Q., Milne, R. I., & Liu, J. 2022. Pervasive hybridization during evolutionary radiation of Rhododendron subgenus Hymenanthes in mountains of southwest China. National Sci. Review 9:nwac276. https://doi.org/10.1093/nsr/nwac276

Ma, Y.-P. [et al. 2008], Fang, X.-H., Chen, F., & Dai, S.-L. 2008. DFL a FLORICAULA/LEAFY homologue gene from Dendranthema lavandulifolium is expressed both in the vegetative and reproductive tissues. Plant Cell Reports 27: 647-654.

Ma, X. [et al. 2023/2024], Vanneste, S., Chang, J., Chang, J., Ambrosino, L., Barry, K., Bayer, T., Bobrov, A., Boston, L.-B., Campbell, J., Chen, H., Chiusano, M. L., Dattolo, E., Grimwood, J., He, G., Jenkins, J., Khachaturyan, M., Marín-Guirao, L., Mesterházy, A., Muhd, D.-D., Pazzaglia, J., Plott, C., Rajasekar, S., Rombauts, S., Ruocco, M., Scott, A., Tan Min, P., Van de Velde, J., Vanholme, B., Webber, J., Wong, L. L., Yan, M., Yeong, Y. S., Novikova, P., Schmutz, J., Reusch, T., Procaccini, G., Olsen, J., & Van de Peer, Y. 2023. Seagrass genomes reveal a hexaploid ancestry facilitating adaptation to the marine environment. bioRχiv doi: https://doi.org/10.1101/2023.03.05.531170 = Ma, X. [et al. 2024], Vanneste, S., Chang, J., Chang, J., Ambrosino, L., Barry, K., Bayer, T., Bobrov, A., Boston, L.-B., Campbell, J., Chen, H., Chiusano, M. L., Dattolo, E., Grimwood, J., He, G., Jenkins, J., Khachaturyan, M., Marín-Guirao, L., Mesterházy, A., Muhd, D.-D., Pazzaglia, J., Plott, C., Rajasekar, S., Rombauts, S., Ruocco, M., Scott, A., Tan Min, P., Van de Velde, J., Vanholme, B., Webber, J., Wong, L. L., Yan, M., Yeong, Y. S., Novikova, P., Schmutz, J., Reusch, T., Procaccini, G., Olsen, J., & Van de Peer, Y. 2024. Seagrass genomes reveal ancient polyploidy and adaptations to the marine environment. Nature Plants 10: 240-255. https://doi.org/10.1038/s41477-023-01608-5

Ma, Z. [et al. 2001], Bielenberg, D. G., Brown, K. M., & Lynch, J. P. 2001. Regulation of root hair density by phosphorus availability in Arabidopsis thaliana. Plant Cell Environ. 24: 459-467.

Ma, Z. [et al. 2018], Guo, D., Xu, X., Lu, M., Bardgett, R. D., Eissenstat, D. M., McCormack, M. L., & Hedin, L. O. 2018. Evolutionary history resolves global organization of root functional traits. Nature 555: 94-97.

Ma, Z.-Y. [ert al. 2020], Nie, Z.-L., Ren, C., Liu, X.-Q., Zimmer, E. A., & Wen, J. 2021 [= 2020]. Phylogenomic relationships and character evolution in the grape family (Vitaceae). Molec. Phyl. Evol. 154:106948. https://doi.org/1016/j.ympev.2020.106948

Maad, J., & Nilsson, L. A. 2004. On the mechanism of floral shifts in speciation: Gained pollination efficiency from tongue- to eye-attachment of pollinia in Platanthera (Orchidaceae). Biol. J. Linnean Soc. 83: 481-495.

Maas, P. J. M. 1972. Flora Neotropica Monograph No. 8. Costoideae (Zingiberaceae). Hafner, New York.

Maas, P. J. M. 1977. Flora Neotropica Monograph No. 18 Renealmia (Zingiberaceae - Zingiberoideae), Costoideae (Additions) (Zingiberaceae). New York Botanical Garden, New York.

Maas, P. J. M., & Maas-van der Kamer, H. 1993. Flora Neotropica Monograph 61. Haemodoraceae. New York Botanical Garden, New York.

Maas, P. J. M., & Rübsamen, T. 1986. Flora Neotropica Monograph Number 40. Triuridaceae. New York Botanical Garden, New York.

Maas, P. J. M., & Ruyters, P. 1986. Flora Neotropica Monograph Number 41. Voyria and Voyriella (Saprophytic Gentianaceae). New York Botanical Garden, New York.

Maas, P. J. M., & Westra, L. Y. T. 1984. Studies in Annonaceae. II A monograph of the genus Anaxagorea A. St. Hil. Part 1. Bot. Jahrb. Syst. Pflanzenges. Pflanzengeog. 105: 73-134.

Maas, P. J. M., & Westra, L. Y. T. 1984. Studies in Annonaceae. II A monograph of the genus Anaxagorea A. St. Hil. Part 2. Bot. Jahrb. Syst. Pflanzenges. Pflanzengeog. 105: 145-204.

Maas, P. J. M., & Westra, L. Y. T. 1993. Neotropical Plant Families. Koeltz, Koenigstein.

Maas, P. J. M. [et al. 1986], Maas-van der Kamer, H., van Benthem, J., Snelders, H. C. M., & Rübsamen, T. 1986. Flora Neotropica Monograph Number 42. Burmanniaceae. New York Botanical Garden, New York.

Maas, P. J. M. [et al. 1992], Baas, P., Boesewinkel, F. D., Hiepko, P., Lobreau-Callen, D., van den Oever, L., & ter Welle, B. J. H. 1992. The identity of "Unknown Z": Maburea Maas, a new genus of Olacaceae in Guyana. Bot. Jahrb. Syst. Pflanzenges. Pflanzengeog. 114: 275-291.

Maas, P. J. M. [et al. 2003], Westra, L. Y. T., Chatrou, L. W., & collaborators. 2003. Flora Neotropica Monograph 18 Duguetia (Annonaceae). New York Botanical Garden, New York.

Maas, P. J. M. [et al. 2011], Westra, L. Y. T., Reiner, H., Lobão, A. Q., & Erkens, R. H. J. 2011. An updated index to genera, species, and infraspecific taxa of Neotropical Annonaceae. Nordic J. Bot. 29: 257-356.

Maas, P. J. M. [et al. 2015], Westra, L. Y. T., Guerrero, S. A., Lobão, A. Q., Scharf, U., Zamora, N. A., & Erkens, R. H. J. 2015. Confronting a morphological nightmare: Revision of the Neotropical genus Guatteria (Annonaceae). Blumea 60: 1-219.

Maas, P. J. M. [et al. 2019], Baas, P., Christenhusz, M. J. M., Clarkson, J. J., Koek-Noorman, J., Mennega, A. M. W., Tokuoka, T., van der Bank, M., van der Ham, R. W. J. M., van Marle, E.-J., Westra, L. Y. T., & Chase, M. W. 2019. 'Unknown yellow': Pibiria, a new genus of Passifloraceae with a mixture of features found in Passifloroideae and Turneroideae. Bot. J. Linnean Soc. 189: 397-407.

Maassoumi, A. [et al. 2016], Kazempour Osaloo, S., & Sotoodeh, A. 2016. A new infrageneric grouping of Astragalus (Fabaceae). Iranian J. Bot. 22: 88-100.

Maas-van de Kamer, H. 1995. Triuridiflorae - Gardner's delight? Pp. 287-301, in Rudall, P. J., Cribb, P. J., Cutler, D. F., & Humphries, C. J. (eds), Monocotyledons: Systematics and Evolution. Royal Botanic Gardens, Kew.

Maas-van de Kamer, H. 1998. Burmanniaceae. Pp. 154-163, in Kubitzki, K. (ed.), The Families and Genera of Vascular Plants. III. Flowering Plants: Monocotyledons. Lilianae (except Orchidaceae). Springer, Berlin.

Maas-van de Kamer, H. 2003. Afrothismia gesnerioides, another new species of Afrothismia (Burmanniaceae) from tropical Africa. Blumea 48: 475-478.

Maas-van de Kamer, H., & Maas, P. J. M. 2008. The Cannaceae of the world. Blumea 53: 247-318.

Maas-van de Kamer, H., & Weustenfeld, T. 1998. Triuridaceae. Pp. 452-458, in Kubitzki, K. (ed.), The Families and Genera of Vascular Plants. III. Flowering Plants: Monocotyledons. Lilianae (except Orchidaceae). Springer, Berlin.

Maas-van de Kamer, H. [et al. 2016], Maas, P. J. M., Wieringa, J. J., & Specht, C. D. 2016. Monograph of African Costaceae. Blumea 61: 280-318.

Mabberley, D. J. 1997. The Plant Book. Ed. 2. Cambridge University Press, Cambridge.

Mabberley, D. J. 2008. Mabberley's Plant Book: A Portable Dictionary of Plants, their Classifications, and Uses. Ed. 3. Cambridge University Press, Cambridge.

Mabberley, D. J. 2011. Meliaceae. Pp. 185-211, in Kubitzki, K. (ed.), The Families and Genera of Flowering Plants. X. Flowering Plants: Eudicots. Sapindales, Cucurbitales, Myrtaceae. Springer, Berlin.

Mabberley, D. J. 2017. Mabberley's Plant Book: A Portable Dictionary of Plants, their Classifications, and Uses. Ed. 4. Cambridge University Press, Cambridge.

Mabberley, D. J. [et al. 1995], Pannell, C. M., & Sing, A. M. 1995. Meliaceae. Pp. 1-407, in Kalkman, C. et al. (eds), Flora malesiana. Vol. 12. Rijksherbarium, Leiden.

Mabry, M. E., & Simpson, M. G. 2018. Evaluating the monophyly and biogeography of Cryptantha (Boraginaceae). Syst. Bot. 43: 53-76.

Mabry, M. E. [et al. 2020], Brose, J. M., Blischak, P. D., Sutherland, B., Dismukes, W. T., Bottoms, C. A., Edger, P. P., Washburn, J. D., An, H., Hall, J. C., McKain, M. R., Al-Shehbaz, I., Barker, M. S., Schranz, M. E., Conant, G. C., & Pires, J. C. 2020. Phylogeny and multiple independent whole-genome duplication events in Brassicales. American J. Bot. 107: 1148-1164.

Mabry, M. E. [et al. 2021], Turner-Hissong, S. D., Gallagher, E. Y., McAlvay, A. C., An, H., Edger, P. P., Moore, J. D., Pink, D. A. C., Teakle, G. R., Stevens, C. J., Barker, G., Labate, J., Fuller, D. Q., Allaby, R. G., Beissinger, T., Decker, J. E., Gore, M. A., & Pires, J. C. 2021. The evolutionary history of wild, domesticated, and feral Brassica oleracea (Brassicaceae). Molec. Biol. Evol. 38: 4419-4434. https://doi.org/10.1093/molbev/msab183

Mc... and Mac... go together.

McAbee, J. M. [et al. 2005], Kuzoff, R. K., & Gasser, C. S. 2005. Mechanisms of derived unitegmy among Impatiens species. Plant Cell 17: 1674-1684.

McAbee, J. M. [et al. 2006], Hill, T. A., Skinner, D. J., Izhaki, A., Hauser, B. A., Meister, R. J., Reddy, G. V., Meyerowitz, E. M., Bowman, J. L., & Gasser, C. S. 2006. ABERRANT TESTA SHAPE encodes a KANADI family member, linking polarity determination to separation and growth of Arabidopsis ovule integuments. Plant J. 46: 522-531. https://doi.org/10.1111/j.1365-313X.2006.02717.x

McAdam, S. A. M., & Brodribb, T. J. 2012a. Fern and lycophyte guard cells do not respond to endogenous abscisic acid. Plant Cell 24: 1510-1521.

McAdam, S. A. M., & Brodribb, T. J. 2012b. Stomatal innovation and the rise of seed plants. Ecology Lett. 15: 1-8.

McAdam, S. A. M., & Brodribb, T. J. 2013. Ancestral stomatal control results in a canalization of fern and lycophyte adaptation to drought. New Phytol. 198: 429-441.

McAdam, S. A. M., & Brodribb, T. J. 2014. Separating active and passive influences on stomatal control of transpiration. Plant Physiol. 164: 1578-1586.

McAdam, S. A. M., & Brodribb, T. J. 2016. Linking turgor with ABA biosynthesis: Implications for stomatal responses to vapor pressure deficit across land plants. Plant Physiol. 171: 2008-2016.

McAdam, S. A. [et al. 2016], Brodribb, T. J., Banks, J. A., Hedrich, R., Atallah, N. M., Cai, C., Geringer, M. A., Lind, C., Nichols, D. S., Stachowski, K., Geiger, D., & Sussmilch, F. C. 2016. Abscisic acid controlled sex before transpiration in vascular plants. Proc. National Acad. Sci. 113: 12862-12867,

McAdam, S. A. M. [et al. 2021], Duckett, J. G., Sussmilch, F. C., Pressel, S., Renzaglia, K. S., Hedrich, R., Brodribb, T. J., & Merced, A. 2021. Stomata: The holey grail of plant evolution. American J. Bot. 108: 366-371.

McAllister, C. A. [et al. 2018], McKain, M. R., Li, M., Bookout, B., & Kellogg, E. A. 2018. Specimen-based analysis of morphology and the environment in ecologically dominant grasses: The power of the herbarium. Phil. Trans. Royal Soc. B, 2017:0403. http://dx.doi.org/10.1098/rstb.2017.0403

McArt, S. H. [et al. 2016], Miles, T. D., Rodriguez-Saona, C., Schilder, A., Adler, L. S., & Grieshop, M. J. 2016. Floral scent mimicry and vector-pathogen associations in a pseudoflower-inducing plant pathogen system. PLoS ONE 11(11):e0165761. https://doi.org/10.1371/journal.pone.0165761

McBride, C. S. [et al. 2009], van Velzen, R., & Larsen, T. B. 2009. Allopatric origin of cryptic butterfly species that were discovered feeding on distinct host plants in sympatry. Molec. Ecol. 18: 3639-3651.

McCall, A. C., & Fordyce, J. A. 2010. Can optimal defence theory be used to predict the distribution of plant chemical defences? J. Ecol. 98: 985-992.

McCarren, S. [et al. 2021], Coetzee, A., & Midgley, J. 2021. Corolla stickiness prevents nectar robbing in Erica. J. Plant Res. 134: 963-970.

McCarren, S. [et al. 2024], Midgley, J. J., Coetzee, A., & Johnson, S. D. 2024. Pollen transfer efficiency in Erica depends on type of pollinator. PhytoKeys 244: 237-248. https://doi.org/10.3897/phytokeys.244.107288

McCartha, G. L. [et al. 2019], Taylor, C. M., van der Ent, A., Echevarria, G., Navarrete Gutiérrez, D. M., & Pollard, A. J. 2019. Phylogenetic and geographic distribution of nickel hyperaccumulation in Neotropical Psychotria. American J. Bot. 106: 1377-1385.

McCarthy, J. K. [et al. 2020], McGlone, M. S., & Heenan, P. B. 2021 [= 2020]. Lineage through time analyses have their limitations: The case of the New Zealand flora. New Zealand J. Bot. 59: 157-174.

McCarthy, P. M. (ed.). 1995. Flora of Australia. Volume 16. Elaeagnaceae, Proteaceae 1. A.B.R.S/C.S.I.R.O., Melbourne.

Machado, M. C. 2008. What is the role of hybridization in the evolution of Cactaceae? Bradleya 26: 1-18.

Machado, S. R. [et al. 2014], Teixeira, S. D. P., & Rodrigues, T. M. 2014. Bacterial leaf glands in Styrax camporum (Styracaceae): First report for the family. Botany 92: 403-411.

Machado, S. R. [et al. 2016], Canaveze, Y., & Rodrigues, T. M. 2017 [= 2016]. Structure and functioning of oil cavities in the shoot apex of Metrodorea nigra A. St.-Hil. (Rutaceae). Protoplasma 254: 1661-1674. https://doi.org/10.1007/s00709-016-1056-x

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Martínez, C. [et al. 2013], Madriñan, S., Zavada, M., Jaramillo, C. A. 2013. Tracing the fossil pollen record of Hedyosmum (Chloranthaceae), an old lineage with recent Neotropical diversification. Grana 52: 161-180.

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Martínez-Alberola, F. [et al. 2013], del Campo, E. M., Lázaro-Gimeno, D., Mezquita-Claramonte, S., Molins, A., Mateu-Andrés, I., Pedrola-Monfort, J., Casano, L. M., & Barreno, E. 2013. Balanced gene losses, duplications and intensive rearrangements led to an unusual regularly sized genome in Arbutus unedo chloroplasts. PLoS ONE 8(11):e79685. doi:10.1371/journal.pone.0079685

Martínez-Azorín, M. [et al. 2011], Crespo, M. B., Juan, A., & Fay, M. F. 2011. Molecular phylogenetics of subfamily Ornithogaloideae (Hyacinthaceae) based on nuclear and plastid DNA regions, including a new taxonomic arrangement. Ann. Bot. 107: 1-37.

Martínez-Azorín, M. [et al. 2015], Pinter, M., & Wetschnig, W. 2015. Desertia, a new genus in Massonieae (Asparagaceae, Scilloideae), including the description of Desertia luteovirens and the taxonomic revisions of Whiteheadia and Namophila. Phytotaxa 221: 201-225.

Martínez-Azorín, M. [et al. 2019], Crespo, M. B., Alonso-Vargas, M. Á., Dold, A. P., Crouch, N. R., Pfosser, M., Mucina, L., Pinter, M., & Wetschnig, W. 2019. New combinations in the tribe Urgineeae (Asparagaceae subfam. Scilloideae) with comments on contrasting taxonomic treatments. Phytotaxa 397: 291-299.

Martínez-Azorín, M. [et al. 2022], Crespo, M. B., Alonso-Vargas, M. Á., Pinter, M., Crouch, N. R., Dold, A. P., Mucina, L., Pfosser, M., & Wetschnig, W. 2023 [= 2022]. Molecular phylogenetics of subfamily Urgineoideae (Hyacinthaceae): Toward a coherent generic circumscription informed by molecular, morphological, and distributional data. J. Syst. Evol. 61: 42-63.

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Martínez-Domínguez, L. [et al. 2022], Nicolalde-Morejón, F., Vergara-Silva, F., & Stevenson, D. W. 2022. Monograph of Ceratozamia (Zamiaceae, Cycadales): an endangered genus. PhytoKeys 208: 1-102. https://doi.org/10.3897/phytokeys.208.80382

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Martínez-Gómez, J. [et al. 2022], Atluri, T. A. M., Rose, I. J., Holliday, A. J., Strock, C. F., Lynch, J. P., Miller, W. B., Stevenson, D. W., & Specht, C. D. 2022. Developmental morphology and anatomy shed light on both parallel and convergent evolution of the umbellate inflorescence in monocots, underlain by a new variant of metatopy. Front. Plant Sci. 13:873505. doi: 10.3389/fpls.2022.873505

Martínez-Gómez, J. [et al. 2023], Park, S., Hartogs, S. R., Soza, V. L., Park, S. J., & Di Stilio, V. S. 2023. Flower morphology as a predictor of pollination mode in a biotic to abiotic pollination continuum. Ann. Bot. 132: 61-76. https://doi.org/10.1093/aob/mcad069

Martínez-Habibe, M. C. 2022. Fruit anatomy of the Canarieae (Burseraceae). Plants (Basel) 11(3):253. doi: 10.3390/plants11030253

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Martínez-Quezada, D. M. [et al. 2020], Arias, S., Korotkova, N., & Terrazas, T. 2020. The phylogenetic significance of the stem morpho-anatomy in the Hylocereeae (Cactoideae, Cactaceae). Plant Syst. Evol. 306:8. https://doi.org/10.1007/s00606-020-01639-x

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Moonlight, P. W. [et al. 2019], Ardi, W. H., Padilla, L. A., Chung, K.-F., Fuller, D., Girmansyah, D., Hollands, R., Jara-Muñoz, A.,, Kiew, R., Leong, W.-C., Liu, Y., Mahardika, A.,, Marasinghe, L. D. K., O'Connor, M., Peng, C.-I, Pérez, Á J., Phutthai, T., Pullan, M., Rajbhandary, S., Reynel, C., Rubite, R. R., Sang, J., Scherberich, D., Shui, Y.-M., Tebbitt, M. C., Thomas, D. C., Wilson, H. P., Zaini, N. H., & Hughes, M. 2018. Dividing and conquering the fastest-growing genus: Towards a natural sectional classification of the mega-diverse genus Begonia (Begoniaceae). Taxon 67: 267-323.

Moonlight, P. W. [et al. 2024], Baldaszti, L., Cardoso, D., Elliott, A., Särkinen, T., & Knapp, S. 2024. Twenty years of big plant genera. Proc. Royal Soc. B, 291:20240702. https://doi.org/10.1098/rspb.2024.0702

Moore, A. J. [et al. 2012], Bartoli, A., Tortosa, R. D., & Baldwin, B. G. 2012. Phylogeny, biogeography, and chromosome evolution of the amphitropical genus Grindelia inferred from nuclear ribosomal and chloroplast sequence data. Taxon 61: 211-230.

Moore, A. J. [et al. 2017], de Vos, J. M., Hancock, L. P., Goolsby, E., & Edwards, E. J. 2018 [= 2017]. Targeted enrichment of large gene families for phylogenetic inference: Phylogeny and molecular evolution of photosynthesis genes in the Portullugo clade (Caryophyllales). Syst. Biol. 67: 367-383.

Moore, B. D. [et al. 2004], Wallis, I. R., Palá-Paúl, J., Brophy, J. J., Willis, R. H., & Foley, W. J. 2004. Antiherbivore chemistry of Eucalyptus - cues and deterrents for marsupial folivores. J. Chem. Ecol. 30: 1743-1769.

Moore, B. R., & Donoghue, M. J. 2007. Correlates of diversification in the plant clade Dipsacales: Geographic movement and evolutionary innovations. American Naturalist 170: S28-S55.

Moore, B. R., & Donoghue, M. J. 2009. A Bayesian approach for evaluating the impact of historical events on rates of diversification. Proc. National Acad. Sci. 106: 4307-4312.

Moore, C. D. [et al. 2024], Farman, D. I., Särkinen, T., Stevenson, P. C., & Vallejo-Marín, M. 2024. Floral scent changes in response to pollen removal are rare in buzz-pollinated Solanum. Planta 260:15. https://doi.org/10.1007/s00425-024-04403-4

Moore, D. M., & Chater, A. O. 1971. Studies of bipolar disjunct species I Carex. Bot. Notis. 124: 317-334.

Moore, H. E. Jr. 1953. The genus Milla (Amaryllidaceae-Allieae) and its allies. Gentes Herb. 8: 262-296.

Moore, H. E. Jr. 1973. The major groups of palms and their distributions. Gentes Herb. 11: 27-141.

Moore, J. P. [et al. 2007], Lindsey, G. G., Farrant, J. M., & Brandt, W. F. 2007. An overview of the dessication-tolerant resurrection plant Myrothamnus flabellifer Ann. Bot. 99: 211-217.

Moore, K. A., & Short, F. T. 2006. Zostera: Biology, ecology, and management. Pp. 361-386, in Larkum, A. W. D., Orth, R. J., & Duarte, C. M. (eds), Seagrasses: Biology, Ecology and Conservation. Springer, Dordrecht.

Moore, M. J., & Jansen, R. K. 2006. Molecular evidence for the age, origin, and evolutionary history of the American desert plant Tiquilia (Boraginaceae). Molec. Phyl. Evol. 39: 668-687.

Moore, M. J. [et al. 2006], Tye, A., & Jansen, R. K. 2006. Patterns of long-distance dispersal in Tiquilia subg. Tiquilia (Boraginaceae): Implications for the origins of amphitropical disjuncts and Galápogas Islands endemics. American J. Bot. 93: 1163-1177.

Moore, M. J. [et al. 2007], Bell, C. D., Soltis, P. S., & Soltis, D. E. 2007. Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms. Proc. National Acad. Sci. 104: 19363-19368.

Moore, M. J. [et al. 2008], Bell, C. D., Soltis, P. S., & Soltis, D. E. 2008. Analysis of an 83-gene, 86-taxon plastid genome data set resolves relationships among several deep-level eudicot lineages. P. 97, in Botany 2008. Botany without Borders. [Botanical Society of America, etc. Abstracts.]

Moore, M. J. [et al. 2010], Soltis, P. S., Bell, C. D., Burleigh, J. G., & Soltis, D. E. 2010. Phylogenetic analysis of 83 plastid genomes further resolves the early diversification of eudicots. Proc. National Acad. Sci. 107: 4623-4628.

Moore, M. J. [et al. 2011], Hassan, N, Gitzendanner, M. A., Bruenn, R. A., Croley, M., Vandeventer, A., Horn, J. W., Dhingra, A., Brockington, S. F., Latvis, M., Ramdial, J., Alexandre, R., Piedrahita, A., Xi, Z., Davis, C. C., Soltis, P. S., & Soltis, D. E. 2011. Phylogenetic analysis of the plastid inverted repeat for 244 species: Insights into deeper-level angiosperm relationships from a long, slowly evolving sequence region. Internat. J. Plant Sci. 172: 541-558.

Moore, M. J. [et al. 2016], Mota, J. F., Douglas, N. A., Flores Olvera, H., & Ochoterena, H. 2016. The ecology, assembly and evolution of gypsophile floras. Pp. 97-128, in Rajakaruna, N., Boyd, R. S., & Harris, T. B. (eds), Plant Ecology and Evolution in Harsh Environments. Nova Science, Hauppauge, New York.

Moore, M. R., & Jameson, M. L. 2013. Floral associations of cyclocephaline scarab beetles. J. Insect Sci. 13(100): 1-43. See http://digitalcommons.unl.edu/entomologypapers/151

Moore, M. R. [et al. 2015], Beza-Beza, C. F., Wickell, D. A., Beck, J. B., & Jameson, M. L. 2015. Molecules, morphology and Mimeoma scarabs: Evolutionary and taxonomic implications for a palm-associated scarab group. Syst. Entomol. 40: 891-900.

Moore, R. J. 1948. Cytological studies in the Loganiaceae. II. Embryology of Polypremum procumbens. American J. Bot. 35: 404-410.

Moore, S. [et al. 2013], Evans, C. D., Page, S. E., Garnett, M. H., Jones, T. G., Freeman, C., Hooijer, A., Wiltshire, A. J., Limin, S. H., & Gauci, V. 2013. Deep instability of deforested tropical peatlands revealed by fluvial organic carbon fluxes. Nature 493: 660-3. doi: 10.1038/nature11818

Moore, T. E. [et al. 2010], Verboom, G. A., & Forest, F. 2010. Phylogenetics and biogeography of the parasitic genus Thesium (Santalaceae), with an emphasis on the Cape of South Africa. Bot. J. Linnean Soc. 162: 435-452.

Moore, T. R. 1996. The carbon budget of boreal forests: Reducing the uncertainty. Pp. 17-40, in Breymeyer, A. I., Hall, D. O., Melillo, J. M., & Ågren, G. I. (eds), Global Change: Effects on Coniferous Forests and Grasslands. John Wiley, Chichester.

Moquet, L., [et al. 2017a], Vanderplanck, M., Moerman, R., Quinet, M., Roger, N., Michez, D., & Jacquemart, A.-L. 2017a. Bumblebees depend on ericaceous species to survive in temperate heathlands. Insect Conserv. Divers. 10: 78-93.

Moquet, L. [et al. 2017b], Bruyère, L., Pirard, B., & Jacquemart, A.-L. 2017b. Nectar foragers contribute to the pollination of buzz-pollinated plant species. American J. Bot. 104: 1451-1463. doi:10.3732/ajb.1700090

Mora, M. M., & Clark, J. L. 2016. Molecular phylogeny of the Neotropical genus Paradrymonia (Gesneriaceae), reexamination of generic concepts and the resurrection of Trichodrymonia and Centrosolenia. Syst. Bot. 41: 82-104.

Moraes, A. P. [et al. 2015], Souza-Chies, T. T., Stiehl-Alves, E. M., Burchardt, P., Eggers, L., Siljak-Yakovlev, S., Brown, S. C., Chauveau, O., Nadot, S., Bourge, M., Viccini, L. F., & Kaltchuk-Santos, E. 2015. Evolutionary trends in Iridaceae: New cytogenetic findings from the New World. Bot. J. Linnean Soc. 177: 27-49. doi: 10.1111/boj.12232

Moraes, A. P. [et al. 2017], Koehler, S., Cabral, J. S., Gomes, S. S. L., Viccini, L. F., Barros, F., Felix, L. P., Guerra, M., & Forni-Martins, E. R. 2017. Karyotype diversity and genome size variation in Neotropical Maxillariinae orchids. Plant Biol. 19: 298-308.

Moraes, A. P. [et al. 2020], Vatanparast, M., Polido, C., Marques, A., Souza, G., Fortuna-Perez, A. P., & Forni-Martins, E. R. 2020. Chromosome number evolution in dalbergioid legumes (Papilionoideae, Leguminosae). Brazilian J. Bot. 43: 575-587.

Moraes, A. P. [et al. 2022], Engel, T. B. J., Forni-Martins, E. R., de Barros, F., Felix, L. P., & Cabral, J. S. 2022. Are chromosome number and genome size associated with habit and environmental niche variables? Insights from the Neotropical orchids. Ann. Bot. 130: 11-25.

Morais, E. B. [et al. 2019], Schönenberger, J., Conti, E., Antonelli, A., & Szövényi, P. 2019. Orthologous nuclear markers and new transcriptomes that broadly cover the phylogenetic diversity of Acanthaceae. Appl. Plant Sci. 7(9):e11290. doi: 10.1002/aps3.11290

Morales, C. L., & Aizen, M. A. 2006. Invasive mutualisms and the structure of plant-pollinator interactions in the temperate forests of north-west Patagonia, Argentina. J. Ecol. 94: 171-180.

Morales, J. F. [et al. 2017a], Endress, M. E., & Liede-Schumann, S. 2017a. Sex, drugs and pupusas: Disentangling relationships in Echiteae (Apocynaceae). Taxon 66: 623-644.

Morales, J. F. [et al. 2017b], Endress, M. E., & Liede-Schumann, S. 2017b. Systematics of Prestonia (Apocynaceae: apocynoids: Echiteae) 80 years after Woodson. Ann. Missouri Bot. Gard. 102: 520-541.

Morales-Briones, D. F. [et al. 2018a], Romoleroux, K., Kolár, F., & Tank, D. C. 2018a. Phylogeny and evolution of the Neotropical radiation of Lachemilla Rosaceae: Uncovering a history of reticulate evolution and implications for infrageneric classification. Syst. Bot. 43: 17-34.

Morales-Briones, D. F. [et al. 2018b], Liston, A., & Tank, D. C. 2018b. Phylogenomic analyses reveal a deep history of hybridization and polyploidy in the Neotropical genus Lachemilla (Rosaceae). New Phytol. 218: 1668-1684.

Morales-Briones, D. F. [et al. 2019/2020], Kadereit, G., Tefarikis, D. T., Moore, M. J., Smith, S. A., Brockington, S. F., Timoneda, A., Yim, W. C., Cushman, J. C., & Yang, Y. 2019. Disentangling sources of gene tree discordance in phylogenomic datasets: A case study from Amaranthaceae s.l.. bioRχiv doi: https://doi.org/10.1101/794370 = Morales-Briones, D. F. [et al. 2020], Kadereit, G., Tefarikis, D. T., Moore, M. J., Smith, S. A., Brockington, S. F., Timoneda, A., Yim, W. C., Cushman, J. C., & Yang, Y. 2021 [= 2020]. Disentangling sources of gene tree discordance in phylogenomic datasets: Testing ancient hybridizations in Amaranthaceae s.l.. Syst. Biol. 70: 219-235.

Morales-Briones, D. F. [et al. 2020/2021], Gehrke, B., Hsuang, C.-H., Liston, A., Ma, H., Marx, H. E., Tank, D. C., & Yang, Y. 2020. Analysis of paralogs in target enrichment data pinpoints multiple ancient polyploidy events in Alchemilla s.l. (Rosaceae). bioRχiv doi: https://doi.org/10.1101/2020.08.21.261925 = Morales-Briones, D. F. [et al. 2021], Gehrke, B., Hsuang, C.-H., Liston, A., Ma, H., Marx, H. E., Tank, D. C., & Yang, Y. 2022 [= 2021]. Analysis of paralogs in target enrichment data pinpoints multiple ancient polyploidy events in Alchemilla s.l. (Rosaceae). Syst. Biol. 71: 190-207.

Morales-Briones, D. F. [et al. 2022], Lin, N., Huang, E. Y., Grossenbacher, D. L., Sobel, J. M., Gilmore, C. D., Tank, D. C., & Yang, Y. 2022. Phylogenomic analyses in Phrymaceae reveal extensive gene tree discordance in relationships among major clades. American J. Bot. 109: 1035-1046.

Morales-Fierro, V. [et al. 2020], Muñoz-Schick, M., & Moreira-Muñoz, A. 2020. Synopsis of Schizanthus Ruiz & Pav. (Solanaceae), a genus endemic to the southern Andes. PhytoKeys 154: 57-102.

Morales-Linares, J. [et al. 2018], García-Franco, J. G., Flores-Palacios, A., Valenzuela-González, J. E., Mata-Rosas, M., & Díz-Castelazo, C. 2018. Orchid seed removal by ants in Neotropical ant-gardens. Plant Biol. 20: 525-530.

Moran, B. M. [et al. 2021], Payne, C., Langdon, Q., Powell, D., Brandvain, Y., & Schumer, M. 2021. The genomic consequences of hybridization. eLife 10:e69016.

Moran, J. A. [et al. 2013], Gray, L. K., Clarke, C., & Chin, L. 2013. Capture mechanisms in paleotropical pitcher plants (Nepenthaceae) is constrained by climate. Ann. Bot. 112: 1279-1291.

Moran, J. A. [et al. 2018], Anderson, B., Chin, L., Greenwood, M., & Clarke, C. 2018. Nutritional mutualisms of Nepenthes and Roridula. Pp. 359-371, in Ellison, A. M., & Adamec, L. (eds), Carnivorous Plants. Physiology, Ecology, and Evolution. Oxford University Press, Oxford.

Moran, R. C. 2022. Remarks on aerophores and the relationship between sterome and stomata in ferns. Brittonia 74: 123-147.

Moran, R. C., & Smith, A. R. 2001. Phytogeographic relationships between Neotropical and African-Madagascan pteridophytes. Brittonia 53: 304-351.

Moran, R. C. [et al. 2007], Hanks, J. G., & Rouhan, G. 2007. Spore morphology in relation to phylogeny in the fern genus Elaphoglossum (Dryopteridaceae). Internat. J. Plant Sci. 168: 905-929.

Moran, R. C. [et al. 2010a], Labiak, P. H., & Sundue, M. 2010a. Phylogeny and character evolution of the bolbitoid ferns (Dryopteridaceae). Internat. J. Plant Sci. 171: 547-559.

Moran, R. C. [et al. 2010b], Hanks, J. G., Labiak, P. H., & Sundue, M. 2010b. Perispore morphology of bolbitoid ferns (Dryopteridaceae) in relation to phylogeny. Internat. J. Plant Sci. 171: 872-881.

Moran, R. C. [et al. 2018], Hanks, J. G., & Labiak, P. H. 2018. Evolution of spore morphology in the Blechnaceae. Internat. J. Plant Sci. 179: 712-729.

Moran, R. C. [et al. 2019], Hanks, J. G., & Sundue, M. 2019. Phylogenetic relationships of Neotropical lady ferns (Athyriaceae), with a description of Ephemeropteris, gen. nov.. Taxon 68: 425-441.

Morant, A. V. [et al. 2008], Bjarnholt, N., Kragh, M. E., Kjærgaard, C. H., Jørgensen, K., Paquette, S. M., Piotrowski, P., Imberty, A., Olsen, C. E., Møller, B. L., & Back, S., 2008. The ß-glucosidases responsible for bioactivation of hydroxynitrile glucosides in Lotus japonicus. Plant Physiol. 147: 1072-1091.

Mora-Osejo, L. E. [et al. 2011], Pabón-Mora, N., & González, F. 2011. Gunneraceae. New York Botanical Garden, Bronx, New York. [Flora Neotropica Monograph 109.]

Morawetz, J. J., & Randle, C. P. 2009. Progress and pitfalls: Towards a phylogeny of the tropical broomrapes (Orobanchaceae). Pp. 10-11, in Botany and Mycology 2009. Snowbird, Utah July 25-29. Abstract Book.

Morawetz, J. J., & Riina, R. 2011. Euphorbia subgenus Rhizanthium: An entirely Old World lineage with surprisingly low sequence diversity despite great morphological diversity. Pp. 231-232, in XVIII International Botanical Congress 2011, Melbourne. [Abstracts.]

Morawetz, J. J., & Wolfe, A. D. 2009. Assessing the monophyly of Alectra and its relationships to Melasma (Orobanchaceae). Syst. Bot. 34: 561-569.

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Morawetz, J. [et al. 2014], Barrett, C., & Randle, C. 2014. Divergent photosynthetic pathway degradation in holoparasitic sister genera Harveya and Hyobanche (Orobanaceae): Evidence from plastid genomes. Pp. 303-304, in Botany 2014. New Frontiers in Botany. Abstract Book.

Morawetz, W. 1986a. Remarks on karyological differentiation patterns in tropical woody plants. Plant Syst. Evol. 152: 49-100.

Morawetz, W. 1986b. Systematics and karyoevolution in Magnoliidae: Tetrameranthus as compared with other Annonaceae genera of the same chtomosome number. Plant Syst. Evol. 154: 147-173.

Morawetz, W. 1988. Karyosystematics and evolution of Australian Annonaceae as compared with Eupomatiaceae, Himantandraceae, and Austrobaileyaceae. Plant Syst. Evol. 159: 49-79.

Morawetz, W. [et al. 1992], Henzl, M., & Wallnoefer, B. 1992. Tree killing by herbicide producing ants for the establishment of pure Tococa occidentalis [= T. guianensis] populations in the Peruvian Amazon. Biodivers. Conserv. 1: 19-33.

Moray, C. [et al. 2015], Hua, X., & Bromham, L. 2015. Salt tolerances is evolutionarily labile in a diverse setof angiosperm families. BMC Evol. Biol. 15: 90 doi 10.1186/s12862-015-0379-0

Moré, M. [et al. 2013], Cocucci, A. A., & Raguso, R. A. 2013. The importance of oligosulfides in the attraction of fly pollinators to the brood-site deceptive species Jaborosa rotacea (Solanaceae). Internat. J. Plant Sci. 174: 863-876.

Moreau, C. S., & Bell, C. D. 2013. Testing the museum versus cradle tropical biological diversity hypothesis: Phylogeny, diversification, and ancestral biogeographic range evolution of the ants. Evolution 67: 2240-2257.

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Moreira, A. S. F. P., & Isaias, R. M. dos S. 2008. Comparative anatomy of the absorption roots of terrestrial and epiphytic orchids. Brazilian Arch. Biol. Technol. 51. http://dx.doi.org/10.1590/S1516-89132008000100011

Moreira, X. [et al. 2013], Lundborg, L., Zas, R., Carrillo-Gavilán, A., Borg-Karlson, A.-K., & Sampedro, L. 2013. Inducibility of chemical defences by two chewing insect herbivores in pine trees is specific to targeted plant tissue, particular herbivore and defensive trait. Phytochem. 94: 113-122.

Moreira, X. [et al. 2022], Abdala-Roberts, L., Castagneyrol, B., Caujapé-Castells, J., Cruz-Guedes, J., Lago-Núñez, B., Vicens-Fornés, M., & García-Verdugo, C. 2022. A phylogenetically controlled test does not support the prediction of lower putative anti-herbivore leaf traits for insular woody species. J. Biogeog. 49: 274-285.

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Morf, E. 1950. Vergleichende-morphologische Untersuchungen an Gynoeceum der Saxifragaceen. Bull. Soc. Bot. Suisse 60: 516-590.

Morgan, D. R., & Soltis, D. E. 1993. Phylogenetic relationships among members of the Saxifragaceae sensu lato based on rbcL sequence data. Ann. Missouri Bot. Gard. 80: 631-660.

Morgan, D. R. [et al. 1994], Soltis, D. E., & Robertson, K. R. 1994. rbcL sequence variation in Rosaceae. American J. Bot. 81: 890-903.

Morgan, D. R. [et al. 2009], Korn, R.-L., & Mugleston, S. L. 2009. Insights into reticulate evolution in Machaerantherinae (Asteraceae: Astereae): 5S ribosomal RNA spacer variation, estimating supoport for incongruence, and constructing reticulate phylogenies. American J. Bot. 96: 920-932.

Morgan, J. A. [et al. 2011], LeCain, D. R., Pendall, E., Blumenthal, D. M., Kimball, B. A., Carrillo, Y., Williams, D. G., Heisler-White, J., Dijkstra, F. A., & West, M. 2011. C4 grasses prosper as carbon dioxide eliminates desiccation in warmed semi-arid grassland. Nature 476: 202-205.

Mori, G. M. [et al. 2015], Zucchi, M. I., Sampaio, I., & Souza, A. P. 2015. Species distribution and ibntrogressive hybridization of two Avicennia species from the Western Hemisphere unveiled by phylogeographic patterns. BMC Evol. Biol. 15:01. doi: 10.1186/s12862-015-0343-z

Mori, S. A. 2007-onwards. The Lecythidaceae Pages. http://sweetgum.nybg.org/lp/index.html

Mori, S. A., & Boeke, J. D. 1987. [The Lecythidaceae of a lowland Neotropical forest: La Fumeé mountain, French Guiana.] Chapter XII. Pollination. Mem. New York Bot. Gard. 44: 137-155.

Mori, S. A., & Kallunki, J. A. 1977. A revision of the genus Phyllonoma (Grossulariaceae). Brittonia 29: 69-84.

Mori, S. A., & Prance, G. T. 1990a. Flora Neotropica Monograph 21 (II). Lecythidaceae - Part II. The Zygomorphic-Flowered New World Genera (Couroupita, Corythophora, Bertholletia, Couratari, Eschweilera, & Lecythis). New York Botanical Garden, New York.

Mori, S. A., & Prance, G. T. 1990b. Taxonomy, ecology and economic botany of the Brazil nut (Bertholletia excelsa Humb. & Bonpl.: Lecythidaceae). Adv. Econ. Bot. 8: 130-150.

Mori, S. A. [et al. 2007], Tsou, C.-H., Wu, C.-C., Cronholm, B., & Anderberg, A. A. 2007. Evolution of Lecythidaceae with an emphasis on the circumscription of Neotropical genera: Information from combined ndhF and trnL-F sequence data. American J. Bot. 94: 289-301.

Mori, S. A. [et al. 2015a], Carollo Matos, C., Huang, Y.-Y., Smith, N. P., & de Moraes Potascheff, C. 2015a. The utility of placentation in the circumscription of genera of new world Lecythidaceae (Brazil nut family). Phytoneuron 2015-13: 1-46.

Mori, S. A. [et al. 2015b], Smith, N. P., Huang, Y.-Y., Prance, G. T., Kelley, L. M., & Matos, C. C. 2015b. Towards a phylogenetic-based generic classification of Neotropical Lecythidaceae - II. Status of Allantoma, Cariniana, Couratari, Coroupita, Grias and Gustavia. Phytotaxa 203: 122-137.

Mori, S. A. [et al. 2017], Kiernan, E. A., Smith, N. P., Kelley, L. M., Huang, Y.-Y., Prance, G. T., & Thiers, B. 2016. Observations on the phytogeography of the Lecythidaceae clade (Brazil nut family). Phytoneuron 2017-30: 1-85.

Morin, E. [et al. 2019], Miyauchi, S., San Clemente, H., Chen, E. C., Pelin, A., de la Providencia, I., Ndikumana, S., Beaudet, D., Hainaut, M., Drula, E., Kuo, A., Tang, N., Roy, S., Viala, J., Henrissat, B., Grigoriev, I. V., Corradi, N., Roux, C., & Martin, F. M. 2019. Comparative genomics of Rhizophagus irregularis, R. cerebriforme, R. diaphanus and Gigaspora rosea highlights specific genetic features in Glomeromycotina. New Phytol. 222: 1584-1598.

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Peterson, P. M. [et al. 2010a], Romaschenko, K., & Johnson, G. 2010a. A classification of the Chloridoideae (Poaceae) based on multi-gene phylogenetic trees. Molec. Phyl. Evol. 55: 580-598.

Peterson, P. M. [et al. 2010b], Romaschenko, K., & Johnson, G. 2010b. A phylogeny and classification of the Muhlenbergiinae (Poaceae: Chloridoideae: Cynodonteae) based on plastid and nuclear DNA sequences. American J. Bot. 97: 1532-1554.

Peterson, P. M. [et al. 2011a], Romaschenko, K., & Johnson, G. 2011a. Phylogeny of the Chloridoideae (Poaceae) based on analysis of 11 DNA loci. Pp. 270-271, in XVIII International Botanical Congress 2011, Melbourne. [Abstracts.]

Peterson, P. M. [et al. 2011b], Romaschenko, K., Barker, N. P., & Linder, H. P. 2011b. Centropodieae and Ellisochloa, a new tribe and genus in Chloridoideae (Poaceae). Taxon 60: 1113-1122.

Peterson, P. M. [et al. 2012], Romaschenko, K., Snow, N., & Johnson, G. 2012. A molecular phylogeny and classification of Leptochloa (Poaceae: Chloridoideae: Chlorideae) sensu lato and related genera. Ann. Bot. 109: 1317-1329.

Peterson, P. M. [et al. 2014a], Romaschenko, K., & Herrera Arrieta, Y. 2014a. A molecular phylogeny and classification of the Cteniinae, Farragininae, Gouiniinae, Gymnopogoninae, Perotidinae, and Trichoneurinae (Poaceae: Chloridoideae: Cynodonteae). Taxon 63: 275-286. doi:10.12705/632.35

Peterson, P. M. [et al. 2014b], Romaschenko, K., Arrieta, Y. H., & Saarela, J. M. 2014b. A molecular phylogeny and a new subgeneric classification of Sporobolus (Poaceae: Chloridoideae: Sporobolinae). Taxon 63: 1212-1243.

Peterson, P. M. [et al. 2015a], Romaschenko, K., & Herrera Arrieta, Y. 2015a. A molecular phylogeny and classification of the Eleusininae with a new genus, Micrachne (Poaceae: Chloridoideae: Cynodonteae). Taxon 64: 445-467.

Peterson, P. M. [et al. 2015b], Romaschenko, K., & Herrera Arrieta, Y. 2015b. Phylogeny and subgeneric classification of Bouteloua with a new species, B. herrera-arrietae (Poaceae: Chloridoideae: Cynodonteae: Boutelouinae). J. Syst. Evol. 53: 351-366.

Peterson, P. M. [et al. 2016a], Romaschenko, K., & Herrera Arrieta, Y. 2016a. A molecular phylogeny of the Cynodonteae (Poaceae: Chloridoideae). P. 185, in Botany 2016. Celebrating our History, Conserving our Future. Savannah, Georgia. [Abstracts.]

Peterson, P. M. [et al. 2016b], Romaschenko, K., & Herrera Arrieta, Y. 2016. A molecular phylogeny and classification of the Cynodonteae (Poaceae: Chloridoideae) with four new genera: Orthacanthus, Triplasiella, Tripogonella, and Zaqiqah; three new subtribes: Dactylocteniinae, Orininae, and Zaqiqahinae; and a subgeneric classification of Distichlis. Taxon 65: 1263-1287. doi:https://doi.org/10.12705/656.4

Peterson, P. M. [et al. 2017], Romaschenko, K., Herrera Arrieta, Y., & Saarela, J. M. 2017. A molecular phylogeny of the subtribe Sporobolinae and a classification of the subfamily Chloridoideae (Poaceae). Pp. 127-151, in Campbell, L. M., Davis, J. I., Meerow, A. W., Naczi, R. F. C., Stevenson, D. M., & Thomas, W. W. (eds), Diversity and Phylogeny of the Monocotyledons. Contributions from Monocots V. New York Botanical Garden, Bronx, NY. [Mem. New York Bot. Gard. 118.]

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Peterson, P. M. [et al. 2021b], Roquet, C., Romaschenko, K., Arrieta, Y. H., & Susanna, A. 2022 [= 2021b]. A biogeographical analysis of Muhlenbergia (Poaceae: Chloridoideae: Cynodonteae: Muhlenbergiinae). J. Syst. Evol. 60: 621-629. https://doi.org/10.1111/jse.12805

Peterson, P. M. [et al. 2021c], Soreng, R. J., Romaschenko, K., Barberá, P., Quintanar, A., Aedo, C., & Saarela, J. H. 2022 [ = 2021c]. Phylogeny and biogeography of Calamagrostis (Poaceae: Pooideae: Poeae: Agrostidinae), description of a new genus, Condilorachia (Calothecinae), and expansion of Greeneochloa and Pentapogon (Echinopogoninae). J. Syst. Evol. 60: 570-590. https://doi.org/10.1111/jse.12819

Peterson, P. M. [et al. 2022a], Romaschenko, K., & Arrieta, Y. H. 2022a. A phylogeny of the Triraphideae including Habrochloa and Nematopoa (Poaceae, Chloridoideae). PhytoKeys 194: 123-133.

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Peterson, P. M. [et al. 2023], Arrieta, Y. H., Cabezas, S. L., & Romaschenko, K. 2023. Taxonomic revision of Muhlenbergia (Poaceae, Chloridoideae, Cynodonteae, Muhlenbergiinae) in Central America: Phylogeny and classification. Phytokeys 230: 1-106.

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