SAPINDACEAE (Soapberry Family)
Plants mostly
monoecious or dioecious, often incompletely so, variously herbs, shrubs, or
trees, occasionally vining. Leaves alternate or opposite, petiolate, the
petiole bases usually noticeably swollen or expanded. Stipules mostly lacking
(often present in Cardiospermum, occasionally partly free from the
petiole base in Acer), but small tufts of purplish cobwebby hairs or
minute dark scales often present at the leaflet bases in Aesculus. Leaf
blades variously palmately, pinnately, or ternately compound or lobed, the
leaflets of various shapes, the margins usually toothed or lobed.
Inflorescences terminal or appearing lateral, panicles or clusters, usually
lacking bracts and bractlets. Flowers actinomorphic or zygomorphic, hypogynous
(the staminate ones often perigynous in Acer), mostly imperfect (a small
number of perfect flowers often present in some inflorescences. Calyces of 4 or
5(6) sepals, these sometimes fused, often colored, variously shaped, sometimes
persistent at fruiting. Corollas absent or of 4 or 5(6) free petals. Stamens
3–8 (reduced to tiny rudiments in pistillate flowers or appearing short but
fully formed in Koelreuteria), sometimes exserted, the filaments free,
usually attached to the inside of a sometimes inconspicuous nectar-ring, the
anthers usually more or less exserted, attached at the base. Pistil 1 per
flower (usually reduced to a peglike rudiment in staminate flowers), superior,
of 2 or 3 fused carpels. Ovary usually with 2 or 3 locules, sometimes strongly
lobed or flattened, the placentation axile. Styles 1 (then sometimes deeply
2-lobed) or 2 per flower, each (or each branch) with 1 stigma, this entire
(capitate to club-shaped) or deeply 3-lobed. Ovules 1 or 2 per locule. Fruits
samaras, drupelike berries, or capsules, if capsules then dehiscent
longitudinally, 1–3-seeded. Seeds various, often with arils. About 130 genera,
1,450–1,900 species, nearly worldwide, most diverse in tropical regions.
Recent
morphological and molecular studies have suggested that genera traditionally
classified in the families Aceraceae (2 genera, about 115 species) and
Hippocastanaceae (2 or 3 genera, 16–20 species) are better treated within an
expanded circumscription of the Sapindaceae (Judd et al., 1994; Harrington et
al., 2005; Buerki et al., 2009; Harris et al., 2009). Although the three
families have traditionally been thought to be closely related (Cronquist,
1981, 1991), their combination adds further variation to an already
morphologically variable family. Molecular phylogenetic research (Harrington et
al., 2005; Buerki et al., 2009) has supported the close relationship between
Aceraceae and Hippocastanaceae near the base of the lineage that includes the
remaining genera of Sapindaceae. However, these studies have agreed that at the
base of the entire lineage (below Aceraceae and Hippocastanaceae) is the odd,
monospecific, Chinese genus Xanthoceras Bunge, which traditionally has
always been classified in the Sapindaceae. The alternative approach of
segregating Xanthoceras into its own family and resplitting the
Aceraceae and Hippocastanaceae has also been proposed (Buerki et al., 2010),
but has not yet met with widespread acceptance by botanists. The family
Aceraceae was treated in Volume 2 of the present work (Yatskievych, 2006). The
Missouri treatment of the maples was completed before most of the compelling
molecular work on the group was published. Because of this, users of the
present work will have to consult Volume 2 for the treatment of the genus Acer,
which most botanists now agree should be included in a broadly circumscribed
Sapindaceae. For convenience, the family description above includes those
characters unique to Acer and the genus is included in the key to genera
of Sapindaceae below. Aesculus, which was treated in the
Hippocastanaceae by Steyermark (1963), is here included in the Sapindaceae.
The Sapindaceae
include a number of tropical timber trees. Many of the species produce saponins
and nonprotein amino acids that render them toxic to mammals, but surprisingly
a number of the tropical genera produce edible fruits, several of which are commercially
cultivated, including Blighia K.D. Koenig (ackee, akee), Dimocarpus
Lour. (longan), Litchi Sonn. (litchi, lychee), Nephelium L.
(rambutan), and Paullinia L. (guaraná). Often the edible portion is a
fleshy aril surrounding the seed. Some of the edible species also are sold as
juices. The hard seeds of some species are used as beads in handcrafts. The
saponins of some members of the family have been extracted to make soap.
However, in the United States, the main economic benefit from the family is in
the variety of horticulturally important species, including maples, buckeyes
(horse chestnuts), golden rain tree, and soapberry.
Steyermark
(1963) included another member of the order Sapindales, Melia azedarach
L. (Meliaceae; chinaberry tree, china tree, pride of India), in the flora
without any definite records, stating that because the species was commonly
cultivated in southeastern Missouri it likely would be discovered as an escape
along a railroad or in a waste area. Since that time, no specimens have been
collected in the state and the species is no longer very commonly grown as an
ornamental shade tree in the region. It has been recorded from adjacent
counties in northeastern Arkansas, but for the present must be excluded from
formal treatment in the Missouri flora. Melia azederach is a tree to 15
m tall with large leaves that are 2-times pinnately compound and similar in
appearance to those of Koelreuteria paniculata. The fruits (which
contain poisonous tetranorterpenes known as meliatoxins) are superficially
similar in size and appearance to those of Sapindus saponaria, but are
drupes with a 5-locular stone rather than 1-seeded berries. The flowers of Melia
differ from all members of the Sapindaceae in their unusual staminal structure:
the filaments form a slender, dark purple tube terminating in 20–24 sharply
pointed teeth, and the yellow anthers are attached inside the tube below the
apex. The flowers of Melia also differ from those of Missouri members of
the Sapindaceae in their 5(6) petals, which are 8–11 mm long, slender, stiffly
spreading, and lilac to pale pinkish purple.