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We conclude that expansigeny is the basic type of aerenchyma development in roots of flowering plants and that the presence of expansigenous honeycomb aerenchyma in root cortices was fundamental to the success of the earliest flowering plants found in wetland environments.

PERUMALLA, C. J., PETERSON, C. A. & ENSTONE, D. E., 1990. A survey of angiosperm species to detect hypodermal Casparian bands. I. Roots with a uniseriate hypodermis and epidermis. Roots of 181 species from 53 families were surveyed to determine the frequency of Casparian bands in hypodermal layers. For six species, inconclusive data were obtained. The roots of the remaining 175 species were divided into three categories on the basis of this survey. In the first, a hypodermis is absent (12 species): no wall modifications were observed in the outer cortex and this region was permeable to the apoplastic dye Cellufluor. In the second, a hypodermis is present, but a hypodermal Casparian band is absent (seven species). In roots of six species, no wall modifications were detected in the hypodermis; the one remaining species had lignified phi thickenings which were permeable to Cellufluor. In the third, both a hypodermis and a hypodermal Casparian band are present (156 species). These Casparian bands consisted of suberin deposits throughout the width of the anticlinal walls of the hypodermis. The tangential walls of the hypodermis were also suberized, indicating that suberin lamellae were probably also present. Hypodermal Casparian bands were found in roots of hydrophytic, mesophytic and xerophytic species and in members of primitive as well as advanced families. The widespread occurrence of these bands (in 89% of the species surveyed) suggests that they were present in the type ancestral to the flowering plants and that this feature has been retained by many species in this group. The epidermal cell walls of the majority of species examined were suberized but were permeable to Cellufluor.

Passage cells frequently occur in the endodermis and exodermis but are not ubiquitous in either layer. Passage cells occur in the form of short cells in the dimorphic type of exodermis. In both layers, Casparian bands are formed in all cells, but the subsequent development of suberin lamellae and thick, cellulosic walls are delayed or absent in the passage cells. Available evidence suggests that passage cells of the endodermis are important for the transfer of calcium and magnesium into the stele and thus into the transpiration stream. They become the only cells which present a plasmalemma surface to the soil solution (and are thus capable of ion uptake) when the epidermis and central cortex die. This occurs naturally in some herbaceous and woody species and is known to be promoted by drought. Most evidence indicates that the development of suberin lamellae in both the endodermis and exodermis increases the resistance of the root to the radial flow of water. Passage cells thus provide areas of low resistance for the movement of water, and the position of these cells in the endodermis (i.e., in close proximity to the xylem) is explained in terms of function. Exodermal passage cells have a cytoplasmic structure suggesting an active role in ion uptake. This may be related to the tendency of the epidermis to die, leaving the passage cells as the only ones with their membranes exposed to the soil solution. Passage cells in the exodermis attract endomycorrhizal fungi while those in the endodermis do not. It is clear that passage cells of the endodermis and exodermis play a variety of roles in the plant root system.