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Journal articles on the topic 'Alismatales'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Charlton, W. A. "Studies in the Alismataceae. IX. Development of the flower in Ranalisma humile." Canadian Journal of Botany 69, no. 12 (1991): 2790–96. http://dx.doi.org/10.1139/b91-349.

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The solitary flower of Ranalisma humile has three sepals, three petals, 8–12 stamens, and numerous carpels. The first six stamens appear to arise in pairs associated with the petal primordia. With respect to the perianth and the first six stamens, the flower conforms to the basic trimerous pattern detected in other Alismatalean flowers, but it differs in other aspects of development. Organogenesis is unidirectional during the period of sepal and petal initiation, since both sepal and petal initiation occur first on the same side of the flower bud. After the initiation of the first six stamens

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2

SANDULESCU, Emilia Brinduşa, and Mala Maria STAVRESCU-BEDIVAN. "CONSIDERATIONS UPON THE MORPHOANATOMICAL FEATURES OF DECORATIVE AQUATIC PLANTS Hydrocharis laevigata AND Lagenandra meeboldii." AgroLife Scientific Journal 12, no. 1 (2023): 202–6. http://dx.doi.org/10.17930/agl2023123.

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Two aquatic plant species were subjected to this study: Hydrocharis laevigata synonym Limnobium laevigatum (Alismatales: Hydrocharitaceae) and Lagenandra meeboldii (Alismatales: Araceae). The paper presents first insight into the microscopic aspects of cross-sections made through root, petiole and leaves of in-vitro plant L. laevigatum and Lagenandra meeboldii ‘Red’ form, biological material purchased from the Romanian market of ornamental aquarium plants. Considering the invasive potential of South American spongeplant, already well documented for other European countries, this short survey d

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3

Forni-Martins, Eliana Regina, and Karine Pablos Calligaris. "Chromosomal studies on Neotropical Limnocharitaceae (Alismatales)." Aquatic Botany 74, no. 1 (2002): 33–41. http://dx.doi.org/10.1016/s0304-3770(02)00038-4.

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4

Zidorn, Christian. "Secondary metabolites of seagrasses (Alismatales and Potamogetonales; Alismatidae): Chemical diversity, bioactivity, and ecological function." Phytochemistry 124 (February 12, 2016): 5–28. https://doi.org/10.1016/j.phytochem.2016.02.004.

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Zidorn, Christian (2016): Secondary metabolites of seagrasses (Alismatales and Potamogetonales; Alismatidae): Chemical diversity, bioactivity, and ecological function. Phytochemistry 124: 5-28, DOI: 10.1016/j.phytochem.2016.02.004, URL: http://dx.doi.org/10.1016/j.phytochem.2016.02.004

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5

Ross, T. Gregory, Craig F. Barrett, Marybel Soto Gomez, et al. "Plastid phylogenomics and molecular evolution of Alismatales." Cladistics 32, no. 2 (2015): 160–78. http://dx.doi.org/10.1111/cla.12133.

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6

Pott, Vali Joana, Suzana Neves Moreira, Ana Carolina Vitório Arantes, and Arnildo Pott. "Lista de Alismatales do estado de Mato Grosso do Sul, Brasil." Iheringia, Série Botânica 73 (March 31, 2018): 117–22. https://doi.org/10.21826/2446-8231201873s117.

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Pott, Vali Joana, Moreira, Suzana Neves, Arantes, Ana Carolina Vitório, Pott, Arnildo (2018): Lista de Alismatales do estado de Mato Grosso do Sul, Brasil. Iheringia, Série Botânica 73: 117-122, DOI: 10.21826/2446-8231201873s117, URL: http://dx.doi.org/10.21826/2446-8231201873s117

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Macfarlane, Terry D., Dmitry D. Sokoloff, and Margarita V. Remizowa. "Filling a morphological gap between Australasian and Eurasian/African members of Althenia (Potamogetonaceae, Alismatales): A. hearnii sp. nov. from SW Western Australia." Phytotaxa 317, no. 1 (2017): 53–60. https://doi.org/10.11646/phytotaxa.317.1.5.

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Macfarlane, Terry D., Sokoloff, Dmitry D., Remizowa, Margarita V. (2017): Filling a morphological gap between Australasian and Eurasian/African members of Althenia (Potamogetonaceae, Alismatales): A. hearnii sp. nov. from SW Western Australia. Phytotaxa 317 (1): 53-60, DOI: 10.11646/phytotaxa.317.1.5, URL: http://dx.doi.org/10.11646/phytotaxa.317.1.5

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8

Remizowa, Margarita V., Dmitry D. Sokoloff, Sebastiano Calvo, Agostino Tomasello, and Paula J. Rudall. "Flowers and inflorescences of the seagrassPosidonia(Posidoniaceae, Alismatales)." American Journal of Botany 99, no. 10 (2012): 1592–608. http://dx.doi.org/10.3732/ajb.1200227.

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9

Christenhusz, Maarten J. M., Sahr Mian, and Ilia J. Leitch. "The genome sequence of the common water plantain, Alisma plantago-aquatica L. (Alismataceae)." Wellcome Open Research 10 (April 23, 2025): 209. https://doi.org/10.12688/wellcomeopenres.24005.1.

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We present a genome assembly from a specimen of Alisma plantago-aquatica (common water plantain; Streptophyta; Magnoliopsida; Alismatales; Alismataceae). The genome sequence has a total length of 9,377.97 megabases. Most of the assembly (99.53%) is scaffolded into 7 chromosomal pseudomolecules. The mitochondrial and plastid genome assemblies have lengths of 250.4 kilobases and 159.88 kilobases, respectively.

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10

Wong, Sin Yeng, and Jyloerica Joling. "Checklist of aroids (Alismatales, Araceae) from Sabah (Malaysian Borneo)." Check List 17, no. 3 (2021): 931–74. http://dx.doi.org/10.15560/17.3.931.

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One hundred and fourteen species belonging to 29 genera of Araceae are recorded from Sabah: Aglaonema Schott, Alocasia (Schott) G.Don, Amorphophallus Blume ex Decne., Amydrium Schott, Anadendrum Schott, Arisaema Mart., Bucephalandra Schott, Colobogynium Schott, Colocasia Schott, Cryptocoryne Fisch. ex Wydler, Cyrtosperma Griff., Epipremnum Schott, Gamogyne N.E.Br., Homalomena Schott, Lasia Lour., Lemna L., Nabalu S.Y.Wong &amp; P.C.Boyce, Ooia S.Y.Wong &amp; P.C.Boyce, Phymatarum M.Hotta, Pistia L., Pothos L., Rhaphidophora Hassk., Pursegloveia S.Y.Wong, S.L.Low &amp; P.C.Boyce, Rh

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11

Coiffard, Clément, and Barbara A. R. Mohr. "Cretaceous tropical Alismatales in Africa: diversity, climate and evolution." Botanical Journal of the Linnean Society 188, no. 2 (2018): 117–31. http://dx.doi.org/10.1093/botlinnean/boy045.

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12

Furness, Carol A., and Hannah Banks. "Pollen Evolution in the Early‐Divergent Monocot Order Alismatales." International Journal of Plant Sciences 171, no. 7 (2010): 713–39. http://dx.doi.org/10.1086/654848.

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13

Nunes, Elaine Lopes Pereira, Mariana Cortes de Lima, Alessandra Ike Coan, and Maria Cecília de Chiara Moço. "Contribution to the embryology of Potamogeton L. (Alismatales: Potamogetonaceae)." Aquatic Botany 93, no. 1 (2010): 32–38. http://dx.doi.org/10.1016/j.aquabot.2010.03.006.

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14

Feitoza, L. L., L. P. Felix, A. A. J. F. Castro, and R. Carvalho. "Cytogenetics of Alismatales s.s.: chromosomal evolution and C-banding." Plant Systematics and Evolution 280, no. 1-2 (2009): 119–31. http://dx.doi.org/10.1007/s00606-009-0169-5.

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15

Wong, Sin Yeng, and Jyloerica Joling. "Checklist of aroids (Alismatales, Araceae) from Sabah (Malaysian Borneo)." Check List 17, no. (3) (2021): 931–74. https://doi.org/10.15560/17.3.931.

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One hundred and fourteen species belonging to 29 genera of Araceae are recorded from Sabah: <em>Aglaonema </em>Schott, <em>Alocasia </em>(Schott) G.Don, <em>Amorphophallus </em>Blume ex Decne., <em>Amydrium </em>Schott, <em>Anadendrum </em>Schott, <em>Arisaema </em>Mart., <em>Bucephalandra </em>Schott, <em>Colobogynium </em>Schott, <em>Colocasia </em>Schott, <em>Cryptocoryne </em>Fisch. ex Wydler, <em>Cyrtosperma </em>Griff., <em>Epipremnum </em>Schott, <em>Gamogyne </em>N.E.Br., <em>Homalomena </em>Schott, <em>Lasia </em>Lour., <em>Lemna </em>L., <em>Nabalu </em>S.Y.Wong & P.C.Boyce, <em>

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16

Choi, KyoungSu, Yong Hwang, Jeong-Ki Hong, and Jong-Soo Kang. "Comparative Plastid Genome and Phylogenomic Analyses of Potamogeton Species." Genes 14, no. 10 (2023): 1914. http://dx.doi.org/10.3390/genes14101914.

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Potamogetonaceae are aquatic plants divided into six genera. The largest genus in the family is Potamogeton, which is morphologically diverse with many hybrids and polyploids. Potamogetonaceae plastomes were conserved in genome size (155,863 bp–156,669 bp), gene contents (113 genes in total, comprising 79 protein-coding genes and 30 tRNA and 4 rRNA genes), and GC content (36.5%). However, we detected a duplication of the trnH gene in the IR region of the Potamogeton crispus and P. maakianus plastomes. A comparative analysis of Alismatales indicated that the plastomes of Potamogetonaceae, Cymod

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17

Campbell, Lisa, and Laurence J. Dorr. "A synopsis of Harperocallis (Tofieldiaceae, Alismatales) with ten new combinations." PhytoKeys 21 (May 9, 2013): 37–52. http://dx.doi.org/10.3897/phytokeys.21.4859.

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18

Petersen, Gitte, Ole Seberg, Argelia Cuenca, et al. "Phylogeny of the Alismatales (Monocotyledons) and the relationship ofAcorus(Acorales?)." Cladistics 32, no. 2 (2015): 141–59. http://dx.doi.org/10.1111/cla.12120.

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19

Chanda, Sunirmal, Siwert Nilsson, and Stephen Blackmore. "Phylogenetic trends in the Alismatales with reference to pollen grains." Grana 27, no. 4 (1988): 257–72. http://dx.doi.org/10.1080/00173138809429948.

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20

Campbell, Lisa, and Laurence J. Dorr. "A synopsis of Harperocallis (Tofieldiaceae, Alismatales) with ten new combinations." PhytoKeys 21 (May 9, 2013): 37–52. https://doi.org/10.3897/phytokeys.21.4859.

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Ten new combinations from <i>Asagraea</i>, <i>Isidrogaliva</i>, and <i>Tofieldia</i> are proposed in the previously monospecific genus <i>Harperocallis </i>(Tofieldiaceae, Alismatales). As circumscribed here, the genus is restricted to the Americas. The majority of species occur in the Andes or the Guayana region of northern South America; more than half have restricted distributions, and <i>H. flava</i> is narrowly endemic in the Coastal Plain of the southeastern United States. A key to species, synonymies, distributions, representative specimens, and salient notes are presented. Populations

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21

Amorim, J. A., I. L. R. Sa, M. V. R. Rojas, et al. "Aquatic Macrophytes Hosting Immature Mansonia (Mansonia) Blanchard, 1901 (Diptera, Culicidae) in Porto Velho, Rondonia State, Brazil." Journal of Medical Entomology 59, no. 2 (2022): 631–37. http://dx.doi.org/10.1093/jme/tjab223.

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Abstract High abundance of hematophagous mosquitoes of the genus Mansonia Blanchard, 1901 (Diptera: Culicidae) threatens human and domestic animal health and well-being. Knowledge of the biology of nuisance mosquito species is necessary to understand specific ecological and biological factors to enable rapid and effective monitoring measures for sustainable control programs. The establishment and dispersion of Mansonia species are associated with the occurrence of aquatic macrophytes species, which are indispensable for the development of larvae and pupae. To increase knowledge of the host pla

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22

Poli, Letícia P., Lívia G. Temponi, and Alessandra I. Coan. "Floral vasculature and its variation for carpellary supply inAnthurium(Araceae, Alismatales)." PeerJ 5 (January 26, 2017): e2929. http://dx.doi.org/10.7717/peerj.2929.

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Introduction and AimsAnthuriumis the largest genus of Araceae, with 950 species distributed in the neotropics. Despite the great diversity of the genus, the knowledge of its floral vasculature is based on observations in only two species, viz.A. denudatumandA. lhotzkyanum, with remarkable variation in vascular carpellary supply: carpels are either vascularized by ventral bundles alone or by reduced dorsal bundles in addition to the ventral ones. Our main objective is to test this peculiar variation through a detailed anatomical study of the floral vasculature in taxa belonging to some sections

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23

Pott, Vali Joana, Suzana Neves Moreira, Ana Carolina Vitório Arantes, and Arnildo Pott. "LISTA DE ALISMATALES DO ESTADO DE MATO GROSSO DO SUL, BRASIL." Iheringia, Série Botânica 73, Suppl (2018): 117–22. http://dx.doi.org/10.21826/2446-8231201873s117.

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24

Azuma, Hiroshi, and Hiroshi Tobe. "Molecular phylogenetic analyses of Tofieldiaceae (Alismatales): family circumscription and intergeneric relationships." Journal of Plant Research 124, no. 3 (2010): 349–57. http://dx.doi.org/10.1007/s10265-010-0387-5.

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25

Nunes, Elaine Lopes Pereira, Mariana Cortes de Lima, Maria Cecília de Chiara Moço, and Alessandra Ike Coan. "Floral development in Potamogeton (Potamogetonaceae, Alismatales) with emphasis on gynoecial features." Aquatic Botany 100 (July 2012): 56–61. http://dx.doi.org/10.1016/j.aquabot.2012.02.006.

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26

Ortiz, Orlando Oriel, Stapf María Sánchez de, Riccardo Maria Baldini, and Thomas Bernard Croat. "Synopsis of aroids (Alismatales, Araceae) from Cerro Pirre (Darién Province, Panama)." Check List 15, no. (4) (2019): 651–89. https://doi.org/10.15560/15.4.651.

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Ninety-four species belonging to 12 genera of Araceae are recorded on Cerro Pirre (Darién Province): <em>Adelonema</em> Schott (two); <em>Anthurium </em>Schott (39), <em>Chlorospatha </em>Engl. (2), <em>Dieffenbachia </em>Schott (3); <em>Heteropsis </em>Kunth (1); <em>Monstera </em>Adans. (6); <em>Philodendron </em>Schott (28), <em>Rhodospatha </em>Poepp. (2); <em>Spathiphyllum </em>Schott (2); <em>Stenospermation </em>Schott (3); <em>Syngonium </em>Schott (4) and <em>Xanthosoma </em>Schott (2). Taxonomic notes, identification key and comments on habitat and ecology of the species are p

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27

De Castro, Olga, Anna Geraci, Anna Maria Mannino, Nicolina Mormile, Annalisa Santangelo, and Angelo Troia. "A Contribution to the Characterization of Ruppia drepanensis (Ruppiaceae), a Key Species of Threatened Mediterranean Wetlands." Annals of the Missouri Botanical Garden 106 (January 28, 2021): 1–9. http://dx.doi.org/10.3417/2020520.

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To elucidate the taxonomic status of Ruppia drepanensis Tineo ex Guss. (Alismatales, Ruppiaceae), we performed morphological analysis and DNA barcoding of historical materials (including the lectotype) and fresh samples (including those from a recently discovered population near the locus classicus in Sicily, Italy). We conclude that R. drepanensis is a separate species, closely related to R. spiralis L. ex Dumort., that occurs in temporary inland waters from the western to central sectors of the Mediterranean region. We also highlight the importance of vouchers and the need to link molecular

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28

Remizova, Margarita, and Dmitry Sokoloff. "Inflorescence and floral morphology in Tofieldia (Tofieldiaceae) compared with Araceae, Acoraceae and Alismatales s.str." Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 124, no. 3 (2003): 255–71. http://dx.doi.org/10.1127/0006-8152/2003/0124-0255.

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29

Wang, Binghan, Shanshan Huang, Liangmao Zhang, et al. "Diversity of NC10 bacteria associated with sediments of submergedPotamogeton crispus(Alismatales: Potmogetonaceae)." PeerJ 6 (December 4, 2018): e6041. http://dx.doi.org/10.7717/peerj.6041.

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BackgroundThe nitrite-dependent anaerobic methane oxidation (N-DAMO) pathway, which plays an important role in carbon and nitrogen cycling in aquatic ecosystems, is mediated by “CandidatusMethylomirabilis oxyfera” (M. oxyfera) of the NC10 phylum.M. oxyfera-like bacteria are widespread in nature, however, the presence, spatial heterogeneity and genetic diversity ofM. oxyferain the rhizosphere of aquatic plants has not been widely reported.MethodIn order to simulate the rhizosphere microenvironment of submerged plants,Potamogeton crispuswas cultivated using the rhizobox approach. Sediments from

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30

Poli, Letícia Peres, Lívia Godinho Temponi, and Alessandra Ike Coan. "Gynoecial ontogeny of Anthurium: contributions for floral developmental studies in Araceae (Alismatales)." Botany 93, no. 1 (2015): 47–56. http://dx.doi.org/10.1139/cjb-2014-0136.

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Studies on floral development have widened the knowledge on the floral morphology of Araceae, particularly in genera delimited through classical taxonomic treatments. In Pothoideae, floral ontogenetic studies are limited to some representatives of Pothoidium Schott and Pothos L. and only one species of Anthurium Schott, with no focus on gynoecium. This background reveals a lack of ontogenetic data on the largest genus in the clade. This paper presents gynoecial ontogeny of species circumscribed in different sections of Anthurium, describes gynoecial developmental patterns, and evaluates the re

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31

Chen, Ling-Yun, Guido W. Grimm, Qing-Feng Wang, and Susanne S. Renner. "A phylogeny and biogeographic analysis for the Cape-Pondweed family Aponogetonaceae (Alismatales)." Molecular Phylogenetics and Evolution 82 (January 2015): 111–17. http://dx.doi.org/10.1016/j.ympev.2014.10.007.

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32

Li, Xiaoxian, and Zhekun Zhou. "Phylogenetic studies of the core Alismatales inferred from morphology and rbcL sequences." Progress in Natural Science 19, no. 8 (2009): 931–45. http://dx.doi.org/10.1016/j.pnsc.2008.09.008.

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33

Remizowa, Margarita V., Dmitry D. Sokoloff, Lisa M. Campbell, Dennis W. Stevenson, and Paula J. Rudall. "Harperocallis is congeneric with Isidrogalvia (Tofieldiaceae, Alismatales): Evidence from comparative floral morphology." TAXON 60, no. 4 (2011): 1076–94. http://dx.doi.org/10.1002/tax.604011.

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34

Liao, Lawrence Manzano, and Paul John Legaspi Geraldino. "Has Halophila beccarii Ascherson (Alismatales, Hydrocharitaceae) Been Locally Extirpated in the Philippines?" Tropical Natural History 20, no. 1 (2020): 104–10. https://doi.org/10.58837/tnh.20.1.206130.

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35

Lopes, Elisângela Novais, Élison Fabrício Bezerra Lima, Daniel Rodrigo Rodrigues Fernandes, and Carlos Roberto Sousa e. Silva. "PULGÕES (HEMIPTERA: APHIDIDAE) E SEUS INIMIGOS NATURAIS ASSOCIADOS À ORELHA-DE-ELEFANTE (Xanthosoma sagittifolium (L.) SCHOTT) (ALISMATALES: ARACEAE)." BRAZILIAN JOURNAL OF AGRICULTURE - Revista de Agricultura 87, no. 3 (2013): 181. http://dx.doi.org/10.37856/bja.v87i3.30.

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É relatada a ocorrência de Aphis spiraecola Patch, 1914 (Hemiptera: Aphididae: Aphidini) e Pentalonia nigronervosa Coquerel, 1859 (Hemiptera: Aphididae: Macrosiphini) atacando Xanthosoma sagittifolium (L.) Schott (Alismatales: Araceae) no Brasil. Devido ao ataque dos pulgões, as folhas da planta ornamental apresentaram áreas esbranquiçadas, principalmente ao redor da nervura central, e amplas áreas cobertas com secreção açucarada liberada pelos insetos. Junto com os pulgões foram identificados um predador, Cycloneda sanguinea (L., 1763) (Coleoptera: Coccinellidae), um parasitoide, Aphidius col

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36

Severova, Elena E., Olga A. Volkova, Olga N. Demina, Constantin I. Fomichev, Ingrid E. Lock, and Dmitry D. Sokoloff. "Diaperturate pollen in submerged aquatic monocots Althenia orientalis and Althenia filiformis (Potamogetonaceae: Alismatales)." Grana 59, no. 2-3 (2019): 194–202. http://dx.doi.org/10.1080/00173134.2019.1665707.

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37

Tobe, Hiroshi, and Tomoki Kadokawa. "Endosperm development in the Araceae (Alismatales) and evolution of developmental modes in monocots." Journal of Plant Research 123, no. 6 (2010): 731–39. http://dx.doi.org/10.1007/s10265-010-0327-4.

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38

Ortiz, Orlando Oriel, María Sánchez de Stapf, Riccardo Maria Baldini, and Thomas Bernard Croat. "Synopsis of aroids (Alismatales, Araceae) from Cerro Pirre (Darién Province, Panama)." Check List 15, no. 4 (2019): 651–89. http://dx.doi.org/10.15560/15.4.651.

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Ninety-four species belonging to 12 genera of Araceae are recorded on Cerro Pirre (Darién Province): Adelonema Schott (two); Anthurium Schott (39), Chlorospatha Engl. (2), Dieffenbachia Schott (3); Heteropsis Kunth (1); Monstera Adans. (6); Philodendron Schott (28), Rhodospatha Poepp. (2); Spathiphyllum Schott (2); Stenospermation Schott (3); Syngonium Schott (4) and Xanthosoma Schott (2). Taxonomic notes, identification key and comments on habitat and ecology of the species are presented.

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39

Sokoloff, Dmitry D., Sabine von Mering, Surrey W. L. Jacobs, and Margarita V. Remizowa. "Morphology ofMaundiasupports its isolated phylogenetic position in the early-divergent monocot order Alismatales." Botanical Journal of the Linnean Society 173, no. 1 (2013): 12–45. http://dx.doi.org/10.1111/boj.12068.

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40

Petersen, Gitte, Argelia Cuenca, Athanasios Zervas, et al. "Mitochondrial genome evolution in Alismatales: Size reduction and extensive loss of ribosomal protein genes." PLOS ONE 12, no. 5 (2017): e0177606. http://dx.doi.org/10.1371/journal.pone.0177606.

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41

Zidorn, Christian. "Secondary metabolites of seagrasses (Alismatales and Potamogetonales; Alismatidae): Chemical diversity, bioactivity, and ecological function." Phytochemistry 124 (April 2016): 5–28. http://dx.doi.org/10.1016/j.phytochem.2016.02.004.

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42

Poli, Letícia Peres, Lívia Godinho Temponi, and Alessandra Ike Coan. "Anatomical aspects of the gynoecium of species of Anthurium sect. Urospadix Engl. (Araceae, Alismatales)." Flora - Morphology, Distribution, Functional Ecology of Plants 207, no. 8 (2012): 615–21. http://dx.doi.org/10.1016/j.flora.2012.06.014.

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43

Volkova, Olga A., Margarita V. Remizowa, Dmitry D. Sokoloff, and Elena E. Severova. "A developmental study of pollen dyads and notes on floral development inScheuchzeria(Alismatales: Scheuchzeriaceae)." Botanical Journal of the Linnean Society 182, no. 4 (2016): 791–810. http://dx.doi.org/10.1111/boj.12482.

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44

Nah, Gyoungju, Ji Ran Jeong, Jae Hwan Lee, Soon Yil Soh, and Sang Yong Nam. "The complete chloroplast genome of Philodendron hederaceum (Jacq.) Schott 1829 (Alismatales: Araceae)." Mitochondrial DNA Part B 9, no. 2 (2024): 262–66. http://dx.doi.org/10.1080/23802359.2024.2311748.

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Barbosa, Tiago D. M., Suzana M. Costa, and Maria Do Carmo E. Do Amaral. "Aquatic and Palustrine Angiosperms of Viruá National Park, Brazilian Amazon—Nymphaeales, Alismatales, Dioscoreales, and Arecales." Harvard Papers in Botany 24, no. 2 (2019): 103. http://dx.doi.org/10.3100/hpib.v24iss2.2019.n4.

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Ortiz, Orlando O., María S. de Stapf, and Thomas B. Croat. "Diversity and distributional patterns of aroids (Alismatales: Araceae) along an elevational gradient in Darién, Panama." Webbia 74, no. 2 (2019): 339–52. http://dx.doi.org/10.1080/00837792.2019.1646465.

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Copeland, Robert S., Evariste Nkubaye, Benoit Nzigidahera, James P. Cuda, and William A. Overholt. "The African Burrowing Mayfly,Povilla adusta(Ephemeroptera: Polymitarcyidae), DamagesHydrilla verticillata(Alismatales: Hydrocharitaceae) in Lake Tanganyika." Florida Entomologist 94, no. 3 (2011): 669–76. http://dx.doi.org/10.1653/024.094.0332.

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Luo, Yang, Peng-Fei Ma, Hong-Tao Li, Jun-Bo Yang, Hong Wang, and De-Zhu Li. "Plastid Phylogenomic Analyses Resolve Tofieldiaceae as the Root of the Early Diverging Monocot Order Alismatales." Genome Biology and Evolution 8, no. 3 (2016): 932–45. http://dx.doi.org/10.1093/gbe/evv260.

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Lahay, Almira Fardani, and Muhammad Kholiqul Amiin. "Antibacterial Potential of Seagrass Cymodocea Rotundata (Alismatales: Cymodoceaceae) Extract on The Pathogenic Bacteria Staphylococcus Aureus." Jurnal Biologi Tropis 23, no. 2 (2023): 355–60. http://dx.doi.org/10.29303/jbt.v23i2.4884.

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Abstract:

Staphylococcus aureus is classified as a pathogenic bacterium in humans and animals. S. aureus infection in humans can cause skin infections, and produce toxins that result in shock syndrome, foodborne disease, bacteremia, endocarditis, metastatic infections, and sepsis, while in milk-producing animals it can cause mastitis infection. Initially, S. aureus can be overcome with penicillin antibiotics but often develops time S. aureus becomes resistant to penicillin to cause new infections, namely the Methicilin Resistant Staphylococcus aureus (MRSA) which was first reported in 1961. One of the n

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Liang, Jiye, Qing Ma, and Zhaoping Yang. "The first complete chloroplast genomes of two Alismataceae species, and the phylogenetic relationship under order Alismatales." Mitochondrial DNA Part B 4, no. 1 (2018): 122–23. http://dx.doi.org/10.1080/23802359.2018.1536486.

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