Difference between revisions of "Elatinaceae"
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--><p>The affinities of Elatinaceae have long been uncertain; relationships with <i>Caryophyllaceae</i> and Clusiaceae have been proposed (G. C. Tucker 1986). Recent molecular work, combined with a review of morphology, indicates a sister relationship with Malpighiaceae (C. C. Davis and M. W. Chase 2004; K. Wurdack and Davis 2009).</p> | --><p>The affinities of Elatinaceae have long been uncertain; relationships with <i>Caryophyllaceae</i> and Clusiaceae have been proposed (G. C. Tucker 1986). Recent molecular work, combined with a review of morphology, indicates a sister relationship with Malpighiaceae (C. C. Davis and M. W. Chase 2004; K. Wurdack and Davis 2009).</p> | ||
|tables= | |tables= | ||
| − | |references= | + | |references={{Treatment/Reference |
| + | |id=davis2004a | ||
| + | |text=Davis, C. C. and M. W. Chase. 2004. Elatinaceae are sister to Malpighiaceae; Peridiscaceae belong to Saxifragales. Amer. J. Bot. 91: 262–273. | ||
| + | }}{{Treatment/Reference | ||
| + | |id=tucker1986a | ||
| + | |text=Tucker, G. C. 1986. The genera of Elatinaceae in the southeastern United States. J. Arnold Arbor. 67: 471–483. | ||
| + | }} | ||
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|illustration copyright=Flora of North America Association | |illustration copyright=Flora of North America Association | ||
|distribution=Nearly worldwide in temperate and tropical regions. | |distribution=Nearly worldwide in temperate and tropical regions. | ||
| − | |reference= | + | |reference=davis2004a;tucker1986a |
|publication title= | |publication title= | ||
|publication year= | |publication year= | ||
|special status= | |special status= | ||
| − | |source xml=https://jpend@bitbucket.org/aafc-mbb/fna-data-curation.git/src/ | + | |source xml=https://jpend@bitbucket.org/aafc-mbb/fna-data-curation.git/src/f50eec43f223ca0e34566be0b046453a0960e173/coarse_grained_fna_xml/V12/V12_930.xml |
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Revision as of 19:57, 16 December 2019
Herbs [subshrubs], annual [short-lived perennial], synoecious [polygamous]. Leaves opposite [whorled], simple; stipules present; petiole present or absent; blade margins entire or serrulate; venation pinnate. Inflorescences axillary, usually cymes or flowers solitary, sometimes 2[–3]-flowered clusters. Flowers bisexual [pistillate]; perianth and androecium hypogynous; hypanthium absent; sepals 2–5, distinct or connate basally; petals (0 or) 2–5, distinct; nectary absent; stamens [0–]1–10, distinct, free; anthers dehiscing by longitudinal slits; pistil 1, 2–5-carpellate, ovary superior, 2–5-locular, placentation axile; ovules 2–33[–44] per locule, anatropous; styles 2–5, distinct; stigmas 2–5, capitate. Fruits capsules, dehiscence septicidal or irregular. Seeds 2–33[–44] per locule.
Distribution
Nearly worldwide in temperate and tropical regions.
Discussion
Genera 2, species ca. 50 (2 genera, 11 species in the flora).
The affinities of Elatinaceae have long been uncertain; relationships with Caryophyllaceae and Clusiaceae have been proposed (G. C. Tucker 1986). Recent molecular work, combined with a review of morphology, indicates a sister relationship with Malpighiaceae (C. C. Davis and M. W. Chase 2004; K. Wurdack and Davis 2009).
Selected References
Illustrations
Key
| 1 | Sepals 5, carinate; petals 5; inflorescences usually cymes, rarely solitary flowers, pedicels present; plants glandular-pubescent; stems solid or pithy. | Bergia |
| 1 | Sepals 2–4, not carinate; petals (0 or) 2–4; inflorescences solitary flowers, pedicels present or absent, or if flowers 2 per node (E. chilensis) then pedicels absent; plants glabrous; stems with longitudinal air spaces. | Elatine |