View source for Aizoaceae

{{Treatment/ID
|accepted_name=Aizoaceae
|accepted_authority=Martinov
|publications=
|common_names=Fig-marigold Family
|basionyms=
|synonyms=
|hierarchy=Aizoaceae
|hierarchy_nav=<div class="higher-taxa"><div class="higher-taxon"><small>family</small>[[Aizoaceae]]</div></div>
|volume=Volume 4
|mention_page=page 11, 76, 5
|treatment_page=page 75
}}<!--

--><span class="statement" id="st-d0_s0" data-properties="herb duration;herb duration;herb texture;herb relief;herb pubescence;herb pubescence;herb pubescence;herb pubescence;herb pubescence;shrub duration;shrub duration;shrub texture;shrub relief;shrub pubescence;shrub pubescence;shrub pubescence;shrub pubescence;shrub pubescence;subshrub duration;subshrub duration;subshrub texture;subshrub relief;subshrub pubescence;subshrub pubescence;subshrub pubescence;subshrub pubescence;subshrub pubescence"><b>Herbs,</b> shrubs, or subshrubs, annual or perennial, often succulent, papillate, glabrous, hairy, or scaly.</span> <span class="statement" id="st-d0_s1" data-properties="root texture;root architecture"><b>Roots </b>usually fibrous, sometimes tuberous.</span> <span class="statement" id="st-d0_s2" data-properties="stem location;stem growth form or orientation;stem growth form;stem orientation"><b>Stems </b>underground, or prostrate and mat-forming to erect.</span> <span class="statement" id="st-d0_s3" data-properties="leaf position;leaf position;leaf arrangement;leaf arrangement;leaf architecture;leaf architecture"><b>Leaves </b>cauline or basal, alternate or opposite, sessile or petiolate;</span> <span class="statement" id="st-d0_s4" data-properties="stipule count;stipule fusion;stipule fusion">stipules usually absent, or free from or adnate to petiole;</span> <span class="statement" id="st-d0_s5" data-properties="blade shape;blade shape;blade shape;blade shape;blade shape;blade shape">blade flat, terete, or triquetrous (3-angled), occasionally scalelike.</span> <span class="statement" id="st-d0_s6" data-properties="inflorescence position;inflorescence position;flower architecture or arrangement or growth form;flower architecture or arrangement or growth form"><b>Inflorescences </b>axillary or terminal, flowers solitary or in cymes;</span> <span class="statement" id="st-d0_s7" data-properties="bract count;bract count">bracts present or absent;</span> <span class="statement" id="st-d0_s8" data-properties="bracteole count">bracteoles usually absent (present in Trianthema, Cypselea);</span> <span class="statement" id="st-d0_s9" data-properties="pedicel count;pedicel count">pedicel present or absent.</span> <span class="statement" id="st-d0_s10" data-properties="flower reproduction;flower prominence;flower prominence;flower prominence;flower shape;flower shape"><b>Flowers </b>bisexual (sometimes unisexual in Tetragonia), inconspicuous to showy, tubular or campanulate;</span> <span class="statement" id="st-d0_s11" data-properties="hypanthium count">hypanthium present;</span> <span class="statement" id="st-d0_s12" data-properties="calyx lobe atypical count;calyx lobe atypical count;calyx lobe count;calyx lobe coloration;calyx lobe architecture;calyx lobe architecture;calyx lobe architecture;calyx lobe variability;calyx lobe size">calyx lobes (3–) 4–5 (–8), sometimes colored and petaloid, occasionally hooded and/or appendaged, equal or unequal;</span> <span class="statement" id="st-d0_s13" data-properties="nectary count;gland arrangement">nectary absent, a ring, or separate glands;</span> <span class="statement" id="st-d0_s14" data-properties="petal atypical count;petal count;petal fusion;petal fusion;petal architecture or arrangement;petal arrangement or course or shape">petals (including petaloid staminodia) 0–250 [–300], distinct or connate proximally, often 2–4-seriate, linear;</span> <span class="statement" id="st-d0_s15" data-properties="stamen atypical count;stamen count;stamen fusion;stamen fusion">stamens 1–500 (–700), distinct or connate in groups;</span> <span class="statement" id="st-d0_s16" data-properties="pistil count;pistil architecture">pistil 1, 1–25-carpellate;</span> <span class="statement" id="st-d0_s17" data-properties="">ovary superior, inferior, or half-inferior, 1–25-loculed;</span> <span class="statement" id="st-d0_s18" data-properties="ovary position;ovary position;ovary position;ovary position;ovary position;ovary architecture;ovary placentation;ovary arrangement;ovary position;free-central position">placentation usually parietal, infrequently axile, apical, free-central, or basal;</span> <span class="statement" id="st-d0_s19" data-properties="style count;style count;style fusion;style fusion">styles absent or 1–25, distinct or partly connate;</span> <span class="statement" id="st-d0_s20" data-properties="stigma count">stigmas 2–25.</span> <span class="statement" id="st-d0_s21" data-properties="fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit dehiscence;fruit architecture or shape;valve count"><b>Fruits </b>usually capsules, dehiscence loculicidal or septicidal, usually with multiple valves, with or without membranes covering seeds, or dehiscence circumscissile, or indehiscent berries, or nutlike.</span> <span class="statement" id="st-d0_s22" data-properties="seed atypical count;seed count;seed architecture;seed relief"><b>Seeds </b>1–500 (–1000), often arillate, usually papillose;</span> <span class="statement" id="st-d0_s23" data-properties="embryo architecture">embryo coiled around perisperm.</span><!--

-->{{Treatment/Body
|distribution=North America (especially Calif.);West Indies;Central America;South America;Europe;Asia;Africa;Australia;some species cultivated and introduced in temperate and tropical regions worldwide.
|discussion=<p>Genera 130, species ca. 2500 (12 genera, 18 species in the flora).</p><!--
--><p>Some California floras (e.g., P. A. Munz 1959, 1974) list Disphyma crassifolium (Linnaeus) L. Bolus as escaped from cultivation. That species is not well-enough established in the field to be considered naturalized. Many herbarium specimens labeled D. crassifolium are Malephora crocea (Jacquin) Schwantes (W. R. Ferren Jr. et al. 1981). Disphyma crassifolium has clavate leaves, long, terete peduncles, densely plumose stigmas, convex, minutely crenate ovary glands, five locules, and ovate, more or less smooth seeds.</p><!--
--><p>Lampranthus coccineus (Haworth) N. E. Brown also has been considered (e.g., P. A. Munz 1974) naturalized along the coast in California. V. Rattan (1896) made brief mention of the species. We were unable to locate any naturalized L. coccineus and believe that no continuing populations exist. R. M. Beauchamp (1986) cited populations on banks and dumps; he has stated subsequently (pers. comm.) that those populations no longer exist. Lampranthus coccineus has connate ovary glands, five locules, and pear-shaped, more or less black, rough seeds.</p><!--
--><p>Aizoaceae have been considered by some authors (e.g., F. A. Pax and K. Hoffmann 1960) to include the Molluginaceae. J. K. Small (1933) included the Molluginaceae and genera of the Aizoaceae (e.g., Cypselea, Galenia, Sesuvium, and Tetragonia) in Tetragoniaceae. In contrast, Mesembryanthemum in the broad sense has occasionally been treated as a separate family Mesembryanthemaceae (e.g., H. Herre 1971; H. Herre and O. H. Volk 1948). In our treatment, Mesembryanthemum and Tetragonia (Tetragoniaceae, e.g., J. C. Willis 1973) are included within the Aizoaceae (e.g., R. S. Adamson and L. Bolus 1950; H. Melchior 1964, vol. 2, pp. 87–90) and the Molluginaceae (including Glinus Linnaeus and Mollugo Linnaeus) is excluded (e.g., A. Cronquist 1981).</p><!--
--><p>Mesembryanthemum has been divided into segregate genera based largely on placentation and fruit structure. “The mesembs have characteristic fruit capsules with locules (chambers or cavities) containing the seed. With few exceptions they open and close repeatedly in response to moisture (hygrochastic). The capsules are closed when dry and open when wet, limiting the dispersal of seeds to wet conditions. This repetitious dehiscence mechanism, whereby the valves that form the lid of the capsule are opened and fold back, relies on the response of expanding keels to moisture. Seeds are liberated from the open capsules. This unique dispersal mechanism is particularly suited to dissemination and germination in habitats where rainfall is erratic” (G. F. Smith et al. 1998). For excellent illustrations of these complex fruit types, see Smith et al., pp. 22–23.</p><!--
--><p>Some genera of Aizoaceae have wide-ranging species (e.g., members of Trianthema and Sesuvium), which are thought to be bird- and water-dispersed and are associated with moist habitats. Other members of the family are more restricted in distribution. Those include many of the succulent species, which are dispersed locally by water drops splashing seeds out of the fruit (Mesembryanthemum crystallinum), by vegetative propagation (both by accident and for landscape purposes, i.e., Delosperma, and by flotation of various plant parts). Malephora crocea (W. R. Ferren Jr. et al. 1981) and Carpobrotus edulis are from South Africa and have been introduced in the flora and elsewhere through horticulture. The distributions of other species such as Mesembryanthemum crystallinum and M. nodiflorum of southern African origin are more difficult to explain. Their nineteenth-century distribution in the United States on ballast on the Atlantic coast and around bays and coastal headlands on the Pacific coast suggests a human vector. Collection by the earliest botanists suggests a long period of establishment. Considerable discussion and disagreement exist concerning the native status and mode of dispersal of a number of the coastal succulent members of the family (S. H. Bicknell and E. M. Mackey 1998). Perhaps the most controversial example has been Carpobrotus chilensis; opinions have ranged from introduced weed to rare and potentially endangered endemic.</p>
|tables=
|references={{Treatment/Reference
|id=adamson1950a
|text=Adamson, R. S. and H. M. L. Bolus. 1950. Aizoaceae. In: R. S. Adamson and T. M. Salter. 1950. Flora of the Cape Peninsula. Cape Town. Pp. 363–365.
}}{{Treatment/Reference
|id=boetsch2002a
|text=Boetsch, J. R. 2002. The Aizoaceae and Molluginaceae of the southeastern United States. Castanea 67: 42–53.
}}{{Treatment/Reference
|id=brown1931a
|text=Brown, N. E., A. Tischer, and M. C. Karsten. 1931. Mesembryanthema. Ashford.
}}{{Treatment/Reference
|id=herre1971a
|text=Herre, H. 1971. The Genera of the Mesembryanthemaceae. Cape Town.
}}{{Treatment/Reference
|id=jacobsen1976a
|text=Jacobsen, H. 1976. A Handbook of Succulent Plants…. 3 vols. Poole. Vol. 3.
}}{{Treatment/Reference
|id=jacobsen1977a
|text=Jacobsen, H. 1977. Lexicon of Succulent Plants…, ed. 2. Poole. Pp. 395–583.
}}{{Treatment/Reference
|id=pax1934a
|text=Pax, F. A. and K. Hoffmann. 1934. Aizoaceae. In: H. G. A. Engler et al., eds. 1924+. Die natürlichen Pflanzenfamilien…, ed. 2. 26+ vols. Leipzig and Berlin. Vol. 16c, pp. 179–233, 587.
}}{{Treatment/Reference
|id=schwantes1957a
|text=Schwantes, G. 1957. Flowering Stones and Mid-day Flowers. London.
}}{{Treatment/Reference
|id=smith1998a
|text=Smith, G. F. et al. 1998. Mesembs of the World. Pretoria.
}}
}}<!--

--><div class="treatment-key">
==Key==
<div class="treatment-key-group">
  
{| class="wikitable fna-keytable"
|-id=key-0-1
|1
|Petals (including petaloid staminodia) absent
|[[#key-0-2| > 2]]
|-id=key-0-1
|1
|Petals (including petaloid staminodia) present
|[[#key-0-6| > 6]]
|-id=key-0-2
|2
|Ovary inferior; placentation apical [subfam. Tetragonioideae]
|[[Tetragonia|Tetragonia]]
|-id=key-0-2
|2
|Ovary wholly or partly superior; placentation apical-axile, axile, free-central, or basal [subfam. Aizoideae]
|[[#key-0-3| > 3]]
|-id=key-0-3
|3
|Leaves alternate; placentation apical-axile
|[[Galenia|Galenia]]
|-id=key-0-3
|3
|Leaves opposite or subopposite
|[[#key-0-4| > 4]]
|-id=key-0-4
|4
|Styles 2-5; leaves of each pair equal; placentation axile
|[[Sesuvium|Sesuvium]]
|-id=key-0-4
|4
|Styles 1-2; leaves of each pair unequal; placentation free-central or basal
|[[#key-0-5| > 5]]
|-id=key-0-5
|5
|Stamens usually 3; stipules fringed; placentation free-central
|[[Cypselea|Cypselea]]
|-id=key-0-5
|5
|Stamens 5-10; stipules bidentate; placentation basal
|[[Trianthema|Trianthema]]
|-id=key-0-6
|6
|Placentation axile [subfam. Aptenioideae]
|[[#key-0-7| > 7]]
|-id=key-0-6
|6
|Placentation parietal [subfam. Ruschioideae]
|[[#key-0-8| > 8]]
|-id=key-0-7
|7
|Calyx lobes 4; ovary 4-loculed
|[[Aptenia|Aptenia]]
|-id=key-0-7
|7
|Calyx lobes (4-)5; ovary (4-)5-loculed
|[[Mesembryanthemum|Mesembryanthemum]]
|-id=key-0-8
|8
|Fruits fleshy, indehiscent berries [tribe Carpobroteae]
|[[Carpobrotus|Carpobrotus]]
|-id=key-0-8
|8
|Fruits dry, dehiscent capsules
|[[#key-0-9| > 9]]
|-id=key-0-9
|9
|Basal rosette present; cauline leaves usually alternate; capsules separating into segments; locules 10-25 [tribe Aptasieae]
|[[Conicosia|Conicosia]]
|-id=key-0-9
|9
|Basal rosette absent; cauline leaves opposite; capsules persistent, not separating into segments; locules 4-12 [tribe Ruschieae]
|[[#key-0-10| > 10]]
|-id=key-0-10
|10
|Ovary 8-12-loculed
|[[Malephora|Malephora]]
|-id=key-0-10
|10
|Ovary 4-6-loculed
|[[#key-0-11| > 11]]
|-id=key-0-11
|11
|Calyx lobes unequal; membrane covering seeds absent (vestigial); stig- mas not threadlike
|[[Delosperma|Delosperma]]
|-id=key-0-11
|11
|Calyx lobes equal; membrane covering seeds present; stigmas thread- like
|[[Drosanthemum|Drosanthemum]]
|}
</div></div><!--

-->{{#Taxon:
name=Aizoaceae
|author=Nancy J. Vivrette;John E. Bleck;Wayne R. Ferren Jr.
|authority=Martinov
|rank=family
|parent rank=
|synonyms=
|basionyms=
|family=Aizoaceae
|illustrator=Barbara Alongi
|distribution=North America (especially Calif.);West Indies;Central America;South America;Europe;Asia;Africa;Australia;some species cultivated and introduced in temperate and tropical regions worldwide.
|reference=adamson1950a;boetsch2002a;brown1931a;herre1971a;jacobsen1976a;jacobsen1977a;pax1934a;schwantes1957a;smith1998a
|publication title=
|publication year=
|special status=
|source xml=https://jpend@bitbucket.org/aafc-mbb/fna-fine-grained-xml.git/src/287ef3db526bd807d435a3c7423ef2df1e951227/V4/V4_157.xml
|blade shape=scalelike;triquetrous;terete;triquetrous;terete;flat
|bract count=absent;present
|bracteole count=absent
|calyx lobe architecture=appendaged;hooded;petaloid
|calyx lobe atypical count=5;8
|calyx lobe coloration=colored
|calyx lobe count=4;5
|calyx lobe size=unequal
|calyx lobe variability=equal
|embryo architecture=coiled
|flower architecture or arrangement or growth form=in cymes;solitary
|flower prominence=inconspicuous;showy
|flower reproduction=bisexual
|flower shape=campanulate;tubular
|free-central position=basal
|fruit architecture or shape=nutlike
|fruit dehiscence=indehiscent;circumscissile;indehiscent;circumscissile;dehiscence;septicidal;loculicidal;dehiscence
|gland arrangement=separate
|herb duration=perennial;annual
|herb pubescence=scaly;hairy;scaly;hairy;glabrous
|herb relief=papillate
|herb texture=succulent
|hypanthium count=present
|inflorescence position=terminal;axillary
|leaf architecture=petiolate;sessile
|leaf arrangement=opposite;alternate
|leaf position=basal;cauline
|nectary count=absent
|ovary architecture=1-25-loculed
|ovary arrangement=axile
|ovary placentation=parietal
|ovary position=apical;half-inferior;inferior;half-inferior;inferior;superior
|pedicel count=absent;present
|petal architecture or arrangement=2-4-seriate
|petal arrangement or course or shape=linear
|petal atypical count=250;300
|petal count=0;250
|petal fusion=connate;distinct
|pistil architecture=1-25-carpellate
|pistil count=1
|root architecture=tuberous
|root texture=fibrous
|seed architecture=arillate
|seed atypical count=500;1000
|seed count=1;500
|seed relief=papillose
|shrub duration=perennial;annual
|shrub pubescence=scaly;hairy;scaly;hairy;glabrous
|shrub relief=papillate
|shrub texture=succulent
|stamen atypical count=500;700
|stamen count=1;500
|stamen fusion=connate;distinct
|stem growth form=mat-forming
|stem growth form or orientation=prostrate
|stem location=underground
|stem orientation=erect
|stigma count=2;25
|stipule count=absent
|stipule fusion=adnate;free
|style count=1;25
|style fusion=connate;distinct
|subshrub duration=perennial;annual
|subshrub pubescence=scaly;hairy;scaly;hairy;glabrous
|subshrub relief=papillate
|subshrub texture=succulent
|valve count=multiple
}}<!--

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