Abstract

1. The flowers of Sarracenia purpurea are axillary, perfect, hypogynous, and radially symmetrical. The stamens are seventy to eighty in number and arise in ten groups. There are four microsporangia. There is a double layer of binucleate tapetal cells, derived from the primary archesporium. There are three to five parietal layers. The tetrad division is simultaneous; the microspore nucleus divides before the dehiscence of the anthers. The reduced number of chromosomes is twelve. 2. In the ovule there is a single archesporial cell, which is the megaspore mother cell. There is no tapetal cell. The ovule is anatropous and there is a single integument. The megaspore mother cell divides to a linear series of four megaspores, or after the first division the micropylar nucleus may fail to divide or may divide by a wall longitudinal to the ovule. 3. The chalazal megaspore is functional, and develops a typical eight-celled embryo sac. The polar nuclei fuse and the endosperm may become two to eight-celled before the complete fusion of male and female nuclei in fertilization. 4. The pollen tube grows through a definite conducting tissue in the upper expanded portion of the style, through schizogenic canals in the stalk of the style and between the placental outgrowths in the ovary. The generative nucleus divides before the tube has passed into the stalk of the ovary. Fertilization presents no peculiarities. 5. The embryo is elongated and straight, with cotyledons. The storage tissue is endosperm filled with aleurone. The seed coat is the external layer of the integument. The cotyledons function as haustoria in germination and survive as chlorophyl-bearing leaves. 6. The first epicotyledonary leaf is pitchered and arises from a finger-like primordium in which a cavity is developed by unequal growth.

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