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.

Aagard, J. A. [et al. 2005], Olmstead, R. G., Willis, J. H., & Phillips, P. C. 2005. Duplication of floral regulatory genes in Lamiales. American J. Bot. 92: 1284-1293.

Aagesen, L. 1999. Phylogeny of the tribe Colletieae, Rhamnaceae. Bot. J. Linnean Soc. 131: 1-43.

Aagesen, L., & Sanso, A. M. 2003. The phylogeny of the Alstroemeriaceae, based on morphology, rps16 intron, and rbcL sequence data. Syst. Bot. 28: 47-69.

Aagesen, L. [et al. 2005], Medan, D., Kellermann, J., & Hilger, H. H. 2005. Phylogeny of the tribe Colletieae (Rhamnaceae) - a sensitivity analysis of the plastid region trnL-trnF combined with morphology. Plant Syst. Evol. 250: 197-214.

Aagesen, L. [et al. 2016], Biganzoli, F., Bena, J., Godoy-Bürki, A. C., Reinheimer, R., & Zuloaga, F. O. 2016. Macro-climatic distribution limits show both niche expansion and niche specialization among C4 panicoids. PLoS ONE 11(3):e0151075. https://doi.org/10.1371/journal.pone.0151075

Aanen, D. K. [et al. 2002], Eggleton, P., Rouland-LeFèvre, C., Guldberg-Frøslev, T., Rosendahl, S., & Boomsma, J. J. 2002. The evolution of fungus-growing termites and their mutualistic fungal symbionts. Proc. National Acad. Sci. 23: 14887-14892.

Aanen, D. K. [et al. 2007], Ros, V. I. D., Licht, H. H. de F., Mitchell, J., de Beer, Z. W., Slippers, B., Rouland-LeFèvre, C., & Boomsma, J. J. 2007. Patterns of interaction specificty of fungus-growing termites and Termitomyces symbionts in South Africa. BMC Evol. Biol. 7:115. doi:10.1186/1471-2i48-7-115

Aase, H. C. 1915. Vascular anatomy of the megasporophyll of conifers. Bot. Gaz. 60: 277-313.

Abbasi, M. [et al. 2005], Goodwin, S. B., & Scholler, M. 2005. Taxonomy, phylogeny, and distribution of Puccinia graminis, the black stem rust: New insights based on rDNA sequence data. Mycoscience 46: 241-247.

Abbe, E. C. 1935. Studies in the phylogeny of the Betulaceae. I. Floral and inflorescence anatomy and morphology. Bot. Gaz. 97: 1-67.

Abbe, E. C. 1974. Flowers and inflorescences of the "Amentiferae". Bot. Review 40: 159-261.

Abbott, J. R. 2011. Notes on the disintegration of Polygala (Polygalaceae), with four new genera for the Flora of North America. J. Bot. Res. Inst. Texas 5: 125-137.

Abbott, J. R. [et al. 2013], Neubig, K., & Carlsward, B. 2013. Further insight into the disintegration of the polyphyletic mess that was Polygala s.l. (Polygalaceae). P. 254, in Botany 2013. Celebrating Diversity! July 27-31 - New Orleans. Abstracts.

Abdallah, J. M., & Monela, G. G. 2007. Overview of the Miombo woodlands in Tanzania. Finnish Forest. Res. Inst. 50: 9-23.

Abdallah, M. S. 1967. The Resedaceae: A taxonomical revision of the family. Meded. Landbouwhoog. Wageningen 67(8): 1-98, fig. 2-17. [Reprint: Belmontia N.S. 8, 1978.]

Abdallah, M. S., & de Wit, H. C. D. 1978. The Resedaceae: A taxonomical revision of the family (final instalment). Meded. Landbouwhoog. Wageningen 78(14): 96-416, fig. 1, 18-91. [Reprint: Belmontia N.S. 8, 1978.]

Abdelaziz, M. [et al. 2019], Bakkali, M., Gómez, M., Olivieri, E., & Perfectti, F. 2019. Anther rubbing, a new mechanism that actively promotes selfing in plants. American Naturalist 193: 140-147.

Abdelgaleil, S. A. M., & Hashinaga, F. 2007. Allelopathic potential of two sequiterpene lactones from Magnolia grandiflora L. Biochem. Syst. Ecol. 35: 737-742.

Abdel Khalik, K. [et al. 2008], Abd El-Ghani, M., & El Kordy, A. 2008. Fruit and seed morphology in Galium (Rubiaceae) and its importance for taxonomic identification. Act. Bot. Croatica 67: 1-20.

Abdel-Massih, R. M. [et al. 2023], Debst, E., Othman, L., Attieh, J., & Cabrerizo, F. M. 2023. Glucosinolates, a natural chemical arsenal: More to tell than the myrosinase story. Front. Microbiol. 14:1130208. doi: 10.3389/fmicb.2023.1130208

Abdelrhaman, M. A. 2016. Modeling water clarity and light quality in oceans. J. Marine Sci. Engin. 4:80. https://doi.org/10.3390/jmse4040080.

Abdillahi, H. S. [et al. 2010], Stafford, G. I., Finnie, J. F., & van Stade, J. 2010. Ethnobotany, phytochemistry and pharmacology of Podocarpus sensu latissimo. South African J. Bot. 76: 1-24.

Abdullah [et al. 2020a], Henriquez, C. L., Mehmood, F., Carlsen, M. M., Islam, M., Waheed, M. T., Poczai, P., Croat, T. B., & Ahmed, I. 2020a. Complete chloroplast genomes of Anthurium huixtlense and Pothos scandens (Pothoideae, Araceae): Unique inverted repeat expansion and contraction affect rate of evolution. J. Molec. Evol. 88: 562-574.

Abdullah [et al. 2020b], Henriquez, C. L., Mehmood, F., Shahzadi, I., Ali, Z., Waheed, M. T., Croat, T. B., Poczai, P., & Ahmed, I. 2020b. Comparison of chloroplast genomes among species of unisexual and bisexual clades of the monocot family Araceae. Plants 9:737.

Abe, J. P. 2005. An arbuscular mycorrhizal genus in the Ericaceae. Inoculum 56(4): 6.

Abe, K. 1972a. Contribution to the embryology of the family Orchidaceae. VI. Development of the embryo sac in 15 species of orchids. Sci. Reports Tôhoko Univ. Ser. IV Biol., 36: 135-178.

Abe, K. 1972b. Contribution to the embryology of the family Orchidaceae. VII. A comparative study of the orchid embryo sac. Sci. Reports Tôhoko Univ. Ser. IV Biol., 36: 179-201.

Abele, D. [et al. 2005], Rudolph, B., Thiede, J., & Schirarend, C. 2005. Phylogeny of the genus Masdevallia Ruiz & Pav. based on morphological and molecular data. Pp. 111-116, in Raynal-Roques, A., Roguenant, A., & Prat, D. (eds), Proceedings of the 18th World Orchid Conferemnce. Naturalia Publications, Turriers, France.

Abercrombie, J. M. [et al. 2011], O'Meara, B. C., Moffatt, A. R., & Williams, J. H. 2011. Developmental evolution of flowering plant pollen tube cell walls: Callose synthase (CalS) gene expression pattern. EvoDevo 2011, 2:14. doi: 10.1186/2041-9139-2-14

Aberhan, M., & Kiessling, W. 2015. Persistent ecological shifts in marine molluscan assemblages across the end-Cretaceous mass extinction. Proc. National Acad. Sci. 112: 7207-7212.

Abraham, Y., & Elbaum, R. 2013. Hygroscopic movements in Geraniaceae: The structural variations that are responsible for coiling or bending. New Phytol. 199: 584-594.

Abrahamczyk, S., & Renner, S. S. 2015. The temporal build-up of hummingbird/plant mutualisms in North America and temperate South America. BMC Evol. Biol. 15:104.

Abrahamczyk, S., & Steudel, B. 2022. Why are some hummingbird-pollinated plant clades so species-rich? American J. Bot. 109: 1059-1062.

Abrahamczyk, S. [et al. 2014], Souto-Vilarós, D., & Renner, S. S. 2014. Escape from extreme specialization: Passionflowers, bats and the sword-billed hummingbird. Proc. R. Soc. B 281:20140888. http://dx.doi.org/10.1098/rspb.2014.0888

Abrahamczyk, S. [et al. 2015], Souto-Vilarós, D., McGuire, J. A., & Renner, S. S. 2015. Diversity and clade ages of West Indian hummingbirds and the largest plant clades dependent on them: A 5-9 Myr young mutualistic system. Biol. J. Linnean Soc. 114: 848-859.

Abrahamczyk, S. [et al. 2016], Kessler, M., Hanley, D., Karger, D. N., Müller, M. P. J., Knauer, A. C., Keller, F., Schwerdtfeger, M., & Humphreys, A. M. 2016. Pollinator adaptation and the evolution of floral nectar sugar concentration. J. Evol. Biol. 30: 112-127.

Abrahamczyk, S. [et al. 2017a], Poretschkin, C., & Renner, S. S. 2017a. Evolutionary flexibility in five hummingbird/plant mutualistic systems: Testing temporal and geographic matching. J. Biogeog. 44: 1847-1855.

Abrahamczyk, S. [et al. 2017b], Lozada-Gobilard, S., Ackermann, M., Fischer, E., Krieger, V., Redling, A., & Weigend, M. 2017b. A question of data quality - testing pollination syndromes in Balsaminaceae. PLoS ONE 12(10):e0186125. https://doi.org/10.1371/journal.pone.0186125

Abrahamczyk, S. [et al. 2021], Humphreys, A. M., Trabert, F. Droppelmann, F., Gleichmann, M., Krieger, V., Linnartz, M., Lozada-Gobilard, S., Rahelivololona, M. E., Schubert, M., Janssens, S. B., Weigend, M., & Fischer, E. 2021. Evolution of brood-site mimicry in Madagascan Impatiens (Balsaminaceae). Persp. Plant Ecol. Evol. Syst. 49:125590. https://doi.org/10.1016/j.ppees.2021.125590

Abrahamson W. G., & Weis A. E. 1997. Evolutionary Ecology Across Three Trophic levels: Goldenrods, Gallmakers, and Natural Enemies. Princeton University Press, Princeton.

Abrahamson, W. G. [et al. 1998], Melika, G., Scrafford, R., & Csóka, G. 1998. Gall-inducing insects provide insights into plant systematic relationships. American J. Bot. 85: 1159-1165.

Abrams, M. 1895. Bau und Entwicklungsgeschichte der Wandverdickungen in den Samenoberhautzellen einiger Cruciferen. Jahrb. Wissens. Bot. 16: 599-637.

Abrams, M. D. 1992. Fire and the development of oak forests. BioScience 42: 346-353.

Abrams, M. D. 1996. Distribution, historical development and ecophysiological attributes of oak species in the eastern United States. Ann. Sci. Forest. 53: 487-512.

Abrams, M. D. 2003. Where has all the white oak gone? BioScience 53: 927-939.

Abril, A. 2011. The leaf cutting ant-plant interaction from a microbial ecology perspective. Pp. 39-63, in Seckbach, J., & Dubinsky, Z. (eds), All Flesh is Grass: Plant-Animal Interrelationships. Springer, Dordrecht.

Abrouk, M. [et al. 2010], Murat, F., Pont, C., Messing, J., Jackson, S., Faraut, T., Tannier, F., Plomion, C., Cooke, R., Feuillet, C., & Salse, J. 2010. Palaeogenomics of plants: Synteny-based models of extinct ancestors. Trends Plant Sci. 15: 479-487.

Accorsi, W. R. A. 1949. Características morfólogicas, anatómicas e citológicas da epiderme inferior da folha das Rubiaceae. Lilloa 16: 5-59.

Acevedo-Rodríguez, P. [et al. 2011], van Welzen, P. C., Adema, F., & van der Ham, R. W. J. M. 2011. Sapindaceae. Pp. 357-407, in Kubitzki, K. (ed.), The Families and Genera of Flowering Plants. X. Flowering Plants: Eudicots. Sapindales, Cucurbitales, Myrtaceae. Springer, Berlin.

Acevedo-Rodríguez, P. [et al. 2017], Wurdack, K. J., Ferrucci, M. S., Johnson, G., Dias, P., Coelho, R. G., Somner, G. V., Steinmann, V. W., Zimmer, E. A., & Strong, M. T. 2017. Genetic relationships and classification of tribe Paullinieae (Sapindaceae) with a new concept of supertribe Paulliniodae. Syst. Bot. 42: 96-114.

Acevedo-Rosas, R. [et al. 2004], Cameron, K., Sosa, V., & Pell, S. 2004. A molecular phylogenetic study of Graptopetalum (Crassulaceae) based on ETS, ITS, rpl16 and trnL-F nucleotide sequences. American J. Bot. 91: 1099-1104.

Acha, S. [et al. 2021], Linan, A., MacDougal, J., & Edwards, C. 2021. The evolutionary history of vines in a Neotropical biodiversity hotspot: Phylogenomics and biogeography of a large passion flower clade (Passiflora section Decaloba). Molec. Phyl. Evol. 164:107260.

Achille, F. [et al. 2006], Motley, T. J., Lowry, P. P. II, & Jérémie, J. 2006. Polyphyly in Guettarda L. (Rubiaceae, Guettardeae) based on nrDNA ITS sequence data. Ann. Missouri Bot. Gard. 93: 103-121.

Ackerfield, J. [et al. 2020], Susanna, A., Funk, V., Kelch, D., Park, D. S., Thornhill, A. H., Yildiz, B., Arabaci, T., & Dirmenci, T. 2020. A prickly puzzle: Generic delimitations in the Carduus-Cirsium group (Compositae: Cardueae: Carduini). Taxon 69: 715-738.

Ackerley, D. 2009. Conservatism and diversification of plant functional traits: Evolutionary rates versus phylogenetic signal. Proc. National Acad. Sci. 106, suppl. 2: 19699-19706.

Ackerman, J. D. 1983. Specificity and mutual dependency of the orchid-euglossine bee interaction. Biol. J. Linnean Soc. 20: 301-314.

Ackerman, J. D. 1985. Euglossine bees and their nectar hosts. Pp. 225-233, in D'Arcy, W. G., & Correa, M. D. (eds), The Botany and Natural History of Panama. Missouri Botanical Garden, St Louis.

Ackerman, J. D. 1986. Mechanisms and evolution of food-deceptive pollination systems in orchids. Lindleyana 1: 108-113.

Ackerman, J. D. 1993. Pollen germination and pollen tube growth in the marine angiosperm Zostera marina L.. Aquat. Bot. 46: 189-202.

Ackerman, J. D. 1995. Convergence of filiform pollen morphologies in seagrasses: Functional mechanisms. Evol. Ecol. 9: 139-153.

Ackerman, J. D. 2000. Abiotic pollen and pollination: Ecological, functional, and evolutionary perspectives. Plant Syst. Evol. 222: 167–185.

Ackerman, J. D. 2006. Sexual reproduction in seagrasses: Pollination in the marine context. Pp. 89-109, in Larkum, A. W. D., Orth, R. J., & Duarte, C. M. (eds), Seagrasses: Biology, Ecology and Conservation. Springer, Dordrecht.

Ackerman, J. D., & Roubik, D. W. 2012. Can extinction risk help explain plant-pollinator specificity among euglossine bee pollinated plants? Oikos 121: 1821-1827.

Ackerman, J. D., & Williams, N. H. 1980. Pollen morphology of the tribe Neottieae and its impact on the classification of the Orchidaceae. Grana 19: 7-18.

Ackermann, M., & Weigend, M. 2006. Nectar, floral morphology and pollination syndrome in Loasaceae subfamily Loasoideae (Cornales). Ann. Bot. 98: 503-514.

Ackery, P. R. 1988. Hostplants and classification: A review of nymphalid butterflies. Biol. J. Linnean Soc. 33: 95-203.

Ackery, P. R. 1991. Hostplant utilization by African and Australian butterflies. Biol. J. Linnean Soc. 44: 335-351.

Ackery, P. R., & Vane-Wright, R. I. 1984. Milkweed Butterflies: Their Cladistics and Biology. Cornell University Press, Ithaca, NY.

Acosta, K. [et al. 2021], Appenroth, K. J., Borisjuk, L., Edelman, M., Heinig, U., Jansen, M. A. K., Oyama, T., Pasaribu, B., Schubert, I., Sorrels, S., Sree, K. S., Xu, S., Michael, T. P., & Lam, E. 2021. Return of the Lemnaceae: Duckweed as a model plant system in the genomics and postgenomics era. Plant Cell 33: 3207-3234.

Acosta, M. C. [et al. 2006], Ordóñez, A. del V., Cocucci, A. A., & Moscone, E. A. 2006. Chromosome reports in South American Nicotianeae (Solanaceae), with particular reference to Nierembergia. Ann. Missouri Bot. Gard. 93: 634-646.

Acosta, J. M. [et al. 2009], Perreta, M., Amsler, A., & Vegetti, A. C. 2009. The flowering unit in the synflorescences of Amaranthaceae. Bot. Review 75: 365-376.

Acosta, J. M. [et al. 2019], Zuloaga, F. O., & Reinheimer, R. 2019 Nuclear phylogeny and hypothesized allopolyploidization events in the subtribe Otachyriinae (Paspaleae, Poaceae). Syst. Biodiv. 17: 277-294.

Ács, Z. [et al. 2009], Challis, R. J., Bihari, P., Blaxter, M., Hayward, A., Melika, G., Csóka, G., Pénzes, Z., Pujade-Villar, J., Nieves-Aldrey, J.-L., Schönrogge, K., & Stone, G. N. 2010 [= 2009]. Phylogeny and DNA barcoding of inquiline oak gallwasps (Hymenoptera: Cynipidae) of the Western Palaearctic. Molec. Phyl. Evol. 55: 210-225.

Acuña, R. [et al. 2017], Fließwasser, S., Ackermann, M., Henning, T., Luebert, F., & Weigend, M. 2017. Phylogenetic relationships and generic re-arrangements in "South Andean loasas" (Loasaceae). Taxon 66: 385-378.

Acuña Castillo, R. [et al. 2019], Luebert, F., Henning, T., & Weigend, M. 2019. Major lineages of Loasaceae subfam. Loasoideae diversified during the Andean uplift. Molec. Phyl. Evol. 141:106616. https://doi.org/10.1016/j.ympev.2019.106616

Acuña-Castillo, R. [et al. 2021], Romolereux, K., Luebert, F., Henning, T., & Weigend, M. 2021. Morphological, ecological and geographical evolution of the Neotropical genus Nasa (Loasaceae subfamily Loasoideae). Bot. J. Linnean Soc. 196: 480-505.

Adachi, J. [et al. 1995], Kosuge, K., Denda, T., & Watanabe, K. 1995. Phylogenetic relationships of the Berberidaceae based on partial sequences of the gapA gene. Pp. 351-353, in Jensen, U., & Kadereit, J. W. (eds.), Systematics and Evolution of the Ranunculiflorae. Springer, Vienna. [Plant Syst. Evol. Suppl. 9.]

Adachi, S. A. [et al. 2015], Machado, S. R., & Guimarães, E. 2015. Structural and ultrastructural characterization of the floral lip in Gongora bufonia (Orchidaceae): Understanding the slip-and-fall pollination mechanism. Botany 93: 759-768.

Adam, H. [et al. 2007], Jouannic, S., Morcillo, F., Verdeil, J.-L., Duval, Y., & Tregear, J. W. 2007. Determination of flower structure in Elaeis guineensis: Do palms use the same homeotic genes as other species? Ann. Bot. 100: 1-12.

Adamczyk, B. [et al. 2010], Smolander, A., Kitunen, V., & Godlewski, M. 2010. Proteins as nitrogen source for plants. A short story about exudation of proteases by plant roots. Plant Signall. Behav. 5: 817-819.

Adamec, L. 2009. Ecophysiological investigation on Drosophyllum lusitanicum: Why doesn't the plant dry out? Carniv. Plant Newsl. 38: 71-74.

Adamec, L. 2011a. Functional characteristics of traps of aquatic carnivorous Utricularia species. Aquatic Bot. 95: 226-233.

Adamec, L. 2011b. Ecophysiological look at plant carnivory. Why are plants carnivorous? Pp. 457-489, in Seckbach, J., & Dubinsky, Z. (eds), All Flesh is Grass: Plant-Animal Interrelationships. Springer, Dordrecht.

Adamec, L. 2012. News in ecophysiological research on aquatic Utricularia traps. Carniv. Plants Newsl. 41: 92-104.

Adamec, L., & Poppinga, S. 2016. Measurement of critical negative pressure inside traps of aquatic carnivorous Utricularia species. Aquatic Bot. 133: 10-16.

Adamec, L. [et al. 2006], Kohout, P., & Benes, K. 2006. Root anatomy of three carnivorous plant species. Carniv. Plant Newsl. 35: 19-22.

Adamec, L. [et al. 2021], Matusíková, I., & Pavolic, A. 2021. Recent ecophysiological, biochemical and evolutional insights into plant carnivory. Ann. Bot. 128: 241-259.

Adams, D. G. 2002. Cyanobacteria in symbiosis with hornworts and liverworts. Pp. 117-135, in Rai, A. N., Bergman, B., & Rasmussen, U. (eds), Cyanobacteria in Symbiosis. Kluwer, Dordrecht.

Adams, D. G., & Duggan, P. S. 2008. Cyanobacteria-bryophyte symbioses. J. Experim. Bot. 59: 1047-1058.

Adams, D. G. [et al. 2006], Bergman, B., Nierzwicki-Bauer, S. A., Rai, A. N., & Schubler, A. 2006. Cyanobacterial-plant symbioses. Pp. 331-363, in Dworkin, M., Falkow, S., Rosenberg, E., Schleifer, K.-H., & Stackebrandt, E. (eds), The Prokaryotes, Vol. 1. Springer, New York.

Adams, F. [et al. 2006], Reddell, P., Webb, M. J., & Shipton, W. A. 2006. Arbuscular mycorrhizas and ectomycorrhizas on Eucalyptus grandis (Myrtaceae) trees and seedlings in native forests of tropical north-eastern Australia. Australian J. Bot. 54: 271-281.

Adams, K. L., & Palmer, J. D. 2003. Evolution of mitochondrial gene content: Gene loss and transfer to the nucleus. Molec. Phyl. Evol. 29: 380-395.

Adams, K. L., & Wendel, J. F. 2005. Polyploidy and genome evolution in plants. Curr. Opin. Plant Biol. 8: 135-141.

Adams, K. L. [et al. 2001], Rosenblueth, M., Qiu, Y.-L., & Palmer, J. D. 2001. Multiple losses and transfers to the nucleus of two mitochondrial succinate dehydrogenase genes during angiosperm evolution. Genetics 158: 1289-1300.

Adams, K. L. [et al. 2002a], Daly, D. O, Whelan, J., & Palmer, J. D. 2002a. Genes for two mitochondrial ribosomal proteins in flowering plants are derived from their chloroplast or cytosolic counterparts. Plant Cell 14: 931-943.

Adams, K. L. [et al. 2002b], Qiu, Y.-L., Stoutemyer, M., & Palmer, J. D. 2002b. Punctuated evolution of mitochondrial gene content: High and variable rates of mitochondrial gene loss and transfer to the nucleus during angiosperm evolution. Proc. National Acad. Sci. 99: 9905-9912.

Adams, J. E. 1949. Studies in the comparative anatomy of the Cornaceae. J. Elisha Mitchell Sci. Soc. 65: 219-244.

Adams, J. M. [et al. 2011], Ahn, S., Ainuddin, N., & Lee, M.-L. 2011. A further test of a palaeoecological thermometer: Tropical rainforests have more herbivore damage than temperate forests. Review Palaeobot. Palynol. 164: 60-66.

Adams, L. G. 1987. Philydraceae. Pp. 40-45, in George, A. S. (ed.), Flora of Australia. Volume 35. Hydatellaceae to Liliaceae. Australian Government, Canberra.

Adams, M. A. [et al. 2016], Turnbull, T. N., Sprent, J. I., & Buchmann, N. 2016. Legumes are different: Leaf nitrogen, photosynthesis, and water use efficiency. Proc. National Acad. Sci. 113: 4098-4103.

Adams, N. F. [et al. 2016], Collinson, M. E., Smith, S. Y., Bamford, M. K., Forest, F., Malakasi, P., Marone, F., & Sykes, D. 2016. X-rays and virtual taphonomy resolve the first Cissus (Vitaceae) macrofossils from Africa as early-diverging members of the genus. American J. Bot.

Adams, P. [et al. 1998], Nelson, D. E., Yamada, S. Chmara, W., Jensen, R. G., Bohnert, H. J. ,& Griffiths, H. 1998. Growth and development of Mesembryanthemum crystallinum (Aizoaceae). New Phytol. 138: 171-190.

Adams, P. B. 2011. Systematics of Dendrobiinae (Orchidaceae) with special reference to Australian taxa. Bot. J. Linnean Soc. 166: 105-126.

Adams, R. P. 2010. Junipers of the World: The Genus Juniperus. Ed. 3. Trafford, Bloomington, IN.

Adams, R. P. 2019. Inheritance of chloroplasts and mitochondria in conifers: A review of paternal, maternal, leakage and facultative inheritance. Phytologia 101: 134-138.

Adams, R. P., & Schwarzbach, A. 2013. Phylogeny of Juniperus using nrDNA and four cpDNA regions. Phytologia 95: 179-187.

Adams, S. P. [et al. 2001], Hartman, T. P. V., Lim, K. Y., Chase, M. W., Bennett, M. D., Leitch, I. J., & Leitch, A. R. 2001. Loss and recovery of Arabidopsis-type telomere repeat sequences 5'-(TTTAGGG)n-3' in the evolution of a major radiation of flowering plants. Proc. Royal Soc. B, 268: 1541-1546.

Adamson, R. S. 1958a. The South African species of Aizoaceae. IV. Mollugo, Pharnaceum, Coelanthum and Hypertelis. J. South African Bot. 24: 11-65.

Adamson, R. S. 1958b. The South African species of Aizoaceae. V. Corbichonia. J. South African Bot. 24: 67-69.

Adamson, R. S. 1959. The South African species of Aizoaceae. VI. Acrosanthes. J. South African Bot. 25: 23-28.

Adatia, R. D., & Gavde, S. G. 1962. Embryology of the Celastraceae. Pp. 1-11, in Maheshwari, P. (ed.), Plant Embryology - a Symposium. CSIR, New Delhi.

Addo-Fordjour, P., & Rahmad, Z. B. 2015. Liana assemblages in tropical forests of Africa and Southeast Asia: Diversity, abundance and management. Pp. 81-98, in Parthasaranthy, N. (ed.), Biodiversity of Lianas. Springer, Heidelberg.

Adhikari, B. [et al. 2015], Milne, R., Pennington, R. T., Särkinen, T., & Pendry, C. A. 2015. Systematics and biogeography of Berberis s.l. inferred from nuclear ITS and chloroplast ndhF gene sequences. Taxon 64: 39-48.

Adie, H., & Lawes, M. J. 2011. Podocarps in Africa: Temperate zone relicts or rainforest survivors? Smithsonian Contrib. Bot. 45: 79-100.

Adjoud-Sadadou, D., & Halli-Hargas, R. 2000. Occurrence of arbuscular mycorrhiza on aged Eucalyptus. Mycorrhiza 9: 287-290.

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Carlquist, S. 2003a. Wood anatomy of Polygonaceae: Analysis of a family with exceptional wood diversity. Bot. J. Linnean Soc. 141: 25-51.

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Carlquist, S. 2003c. Wood and stem anatomy of woody Amaranthaceae s.s.: Ecology, systematics and the problem of defining rays in dicotyledons. Bot. J. Linnean Soc. 143: 1-19.

Carlquist, S. 2004. Lateral meristems, successive cambia and their products: A reinterpretation based on roots and stems of Nyctaginaceae. Bot. J. Linnean Soc. 146: 129-143.

Carlquist, S. 2005a. Wood and bark anatomy of Muntingiaceae: A phylogenetic comparison within Malvales s.l. Brittonia 57: 59-67.

Carlquist, S. 2005b. Wood anatomy of Krameriaceae with comparisons with Zygophyllaceae: Phylesis, ecology and systematics. Bot. J. Linnean Soc. 149: 257-270.

Carlquist, S. 2006. Asteropeia and Physena (Caryophyllales): A case study in comparative wood anatomy. Brittonia 58: 301-313.

Carlquist, S. 2007a. Successive cambia in Aizoaceae: Products and process. Bot. J. Linnean Soc. 153: 141-155.

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Carlquist, S. 2007c. Wood anatomy of Crossosomatales: Patterns of wood evolution with relation to phylogeny and ecology. Aliso 24: 1-18.

Carlquist, S. 2009. Xylem heterochrony: An unappreciated key to angiosperm origin and diversifications. Bot. J. Linnean Soc. 161: 26-65.

Carlquist, S. 2010. Caryophyllales: A key group for understanding wood anatomy character states and their evolution. Bot. J. Linnean Soc. 164: 342-393.

Carlquist, S. 2012a. Monocot xylem revisited: New information, new paradigms. Bot. Review 78: 87-150.

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Carlquist, S. 2012c. How wood evolves: A new synthesis. Botany 90: 901-940.

Carlquist, S. 2013a. Interxylary phloem: Diversity and functions. Brittonia 65: 477-495.

Carlquist, S. 2013b. More woodiness/less woodiness: Evolutionary avenues, ontogenetic mechanisms. Internat. J. Plant Sci. 174: 964-991.

Carlquist, S. 2015a. Living cells in wood. 1. Absence, scarcity, and histology of axial parenchyma as keys to function. Bot. J. Linnean Soc. 177: 291-321.

Carlquist, S. 2015b. Living cells in wood. 2. Raylessness: Histology and evolutionary significance. Bot. J. Linnean Soc. 178: 529-555.

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