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480 BURMANNIACEAE<br />

Tillandsia usneoides (L.) L., (like Usnea, old-man’s-beard, a lichen that hangs from trees)<br />

SPANISH-MOSS, OLD-MAN’S-BEARD, LONG-MOSS, BLACK-MOSS, PASTLE, FLORIDA-MOSS. Hanging<br />

strands <strong>to</strong> 3–4(–8) m long; roots nearly always absent; leaves � thread-like, 2–3(–6) cm long, ca.<br />

1–2 mm wide, densely scaly; inflorescence <strong>of</strong> a single flower; petals greenish or yellow-green.<br />

Epiphytic or on wires or o<strong>the</strong>r supports; e and s parts <strong>of</strong> East TX; also Gulf Prairies and Marshes<br />

and South TX Plains; se U.S. from VA s <strong>to</strong> FL w <strong>to</strong> TX. Feb–Jun. In moist areas in East TX, this<br />

species <strong>of</strong>ten hangs in large, extremely conspicuous fes<strong>to</strong>ons from trees. It occurs from <strong>the</strong> s U.S.<br />

s <strong>to</strong> Argentina, an incredible distribution stretching across 5,000 miles (8,047 km) <strong>of</strong> latitude. It<br />

is distributed by <strong>the</strong> wind and by birds using it as nest material. The dried <strong>plants</strong> have long<br />

been used in upholstery, as packing material (Kennedy 1841; Mabberley 1987), and in crafts and<br />

floral designs. This superficially lichen-like species is strikingly different morphologically<br />

from o<strong>the</strong>r members <strong>of</strong> <strong>the</strong> genus. However, mature <strong>plants</strong> <strong>of</strong> T. usneoides retain many characteristics<br />

commonly found in <strong>the</strong> seedling stage <strong>of</strong> o<strong>the</strong>r members <strong>of</strong> <strong>the</strong> genus, and T. usneoides<br />

is thus clearly linked <strong>to</strong> <strong>the</strong>se o<strong>the</strong>r species (Tomlinson 1995). m/303<br />

BURMANNIACEAE Blume<br />

BURMANNIA FAMILY<br />

Very small, delicate, apparently annual or possibly perennial herbs; leaves minute, bract-like;<br />

flowers perfect, in small, head-like, racemose, or cymose clusters (can be solitary); perianth<br />

segments 6, united, usually with free lobes; stamens 3; ovary inferior; fruit a capsule; seeds numerous,<br />

small.<br />

AA small (125–130 species in 13 or 14 genera, including Thismiaceae—Maas-van de Kamer<br />

1998; Caddick et al. 2002b; Lewis 2002) primarily pantropical and warm temperate family that<br />

occurs n <strong>to</strong> Japan and <strong>the</strong> e U.S. and s <strong>to</strong> New Zealand and Tasmania. The species are typically<br />

small forest herbs. Based on molecular studies, it is now generally agreed that <strong>the</strong> family is related<br />

<strong>to</strong> Thismiaceae (e.g., Caddick et al. 2002b; Neyland 2002), with some authorities combining<br />

<strong>the</strong> families (e.g., Caddick et al. 2002b) and o<strong>the</strong>rs recognizing two related families (e.g.,<br />

Neyland 2002). While traditionally <strong>of</strong>ten described as saprophytic, Burmanniaceae are<br />

mycophytic (= living symbiotically with fungi), and <strong>the</strong>ir manner <strong>of</strong> obtaining nutrition is<br />

more accurately described as mycotrophic or myco-heterotrophic (= obtaining nutrition via<br />

fungi) (Leake 1994). The family includes many mycotrophic species without chlorophyll,<br />

while green-leaved species are hemimycotrophic, constituting a transitional stage between au<strong>to</strong>trophy<br />

and heterotrophy. Fungi are located in special layers <strong>of</strong> cells in <strong>the</strong> roots (Maas-van de<br />

Kamer 1998). Relationships <strong>of</strong> this family have long been controversial. It was previously considered<br />

<strong>to</strong> be closely related <strong>to</strong> <strong>the</strong> Orchidaceae, based on <strong>the</strong> following shared characteristics:<br />

epigynous, bilaterally symmetrical flowers, numerous small seeds, and mycotrophy (Rasmussen<br />

1985). Subsequently, molecular and cladistic research suggests that <strong>the</strong> families are not related<br />

and <strong>the</strong> similarities are due <strong>to</strong> convergence (Rasmussen 1995; Chase et al. 2000; Soltis et al.<br />

2000). A number <strong>of</strong> molecular studies have suggested that Burmanniaceae is in <strong>the</strong><br />

Dioscoreales and thus more closely related <strong>to</strong> such families as Dioscoreaceae and Nar<strong>the</strong>ciaceae<br />

than <strong>to</strong> Orchidaceae (which is in order Asparagales) (Chase et al. 1995b; Caddick et al. 2000,<br />

2002b; Chase et al. 2000). In contrast, o<strong>the</strong>r recent molecular research including more genera<br />

than previously sampled indicates that <strong>the</strong> family (minus <strong>the</strong> superficially similar but unrelated<br />

genus Corsia now in <strong>the</strong> Corsiaceae) plus Thismiaceae is in a relatively isolated position<br />

“not closely aligned with ei<strong>the</strong>r <strong>the</strong> Dioscoreales or <strong>the</strong> Orchidaceae” (Neyland 2002). Additional<br />

research will be needed <strong>to</strong> clarify <strong>the</strong> relationships <strong>of</strong> this family. It has been suggested<br />

that <strong>the</strong> numerous tiny seeds are dispersed by water (Maas et al. 1986). (subclass Liliidae—<br />

Cronquist; order Dioscoreales—APG II)

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