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Orchid seeds are very small, extremely light and produced in great numbers. Most range in length from c. 0.05 to 6.0 mm, with the difference between the longest and shortest known seeds in the family being 120-fold. The ' widest ' seed at 0.9 mm is 90-fold wider than the ' thinnest ' one, which measures 0.01 mm (because orchid seeds are tubular or balloon-like, ' wide ' and ' thin ' actually refer to diameter). Known seed weights extend from 0.31 µg to 24 µg (a 78-fold difference). Recorded numbers of seeds per fruit are as high as 4 000 000 and as low as 20-50 (80 000-200 000-fold difference). Testae are usually transparent, with outer cell walls that may be smooth or reticulated. Ultrasonic treatments enhance germination, which suggests that the testae can be restrictive. Embryos are even smaller : their volume is substantially smaller than that of the testa. As a result, orchid seeds have large internal air spaces that render them balloon-like. They can float in the air for long periods, a property that facilitates long-distance dispersal. The difficult-to-wet outer surfaces of the testa and large internal air spaces enable the seeds to float on water for prolonged periods. This facilitates distribution through tree effluates and\or small run-off rivulets that may follow rains. Due to their size and characteristics, orchid seeds may also be transported in and on land animals and birds (in fur, feathers or hair, mud on feet, and perhaps also following ingestion).

In this review we provide a detailed description of Darwin's prediction of the coevolution of a long-spurred orchid, Angraecum sesquipedale, and a long-tongued moth, his correspondence on the subject, the history of the moth and the subsequent literature. On seeing the long spur of A. sesquipedale, Darwin predicted that its pollinator would be a moth with a long proboscis. For more than a century following Darwin's prediction this was assumed to be the case. The pollinator was taken to be Xanthopan morganii praedicta, despite the fact that it had not been observed to visit A. sesquipedale flowers. Direct observations, infra-red cinematography and photographs published between 1993 and 1997 and a video made in 2004, all of which show X. morganii praedicta visiting A. sesquipedale flowers and removing pollinia, proved that Darwin's prediction was accurate. Recent research suggests that selection pressure exerted by predators on the pollinators, resulted in the evolution of extreme tongue lengths and a special hovering flight.

Orchid seeds are nearly microscopic in size. Because of that, many fanciful theories were proposed for the origin of orchids. Almost 400 years separate the time when orchid seeds were seen for the first time and the development of a practical asymbiotic method for their germination. The seeds were first observed and drawn during the sixteenth century. Seedlings were first described and illustrated in 1804. The association between orchid and fungi was observed as early as 1824, while the requirement for mycorrhiza for seed germination was established in 1899. An asymbiotic method for orchid seed germination was developed in 1921. After Knudson's media B and C were formulated, orchids growing and hybridization became widespread. Hybrids which early growers may not have even imagined became possible.