In modern plants, we tend to differentiate between vascular and non-vascular plants. In the fossil record, we observe several prevascular and early vascular plants with tracheids that differ from modern plants. As would be expected, there is a grade of plants and vascular cells that evolved during the Silurian Period.
Below is a listing of the grades of vascular tissues found in extinct and extant plants
The eophytes are a recently-described group of Paleozoic plants that possessed sugar-conducting cells (leptoids), but not water-conducting cells
Some modern bryophytes have conducting cells that lack secondary thickenings. These cells are referred to as hydroids. These cells can transport water, similar to xylem, but tend to provide little strengthening.
Plants such as Horneophyton have thick-walled H-type conducting cells, which would have moved water, minerals, and sugars from the rhizome to the aerial axes
These cells were involved in active solute transport versus passive water movement in tracheids (Kenrick & Long, 2025)
Along with eophytes, this evidence in Horneophyton may indicate that phloem-like cells evolved first, and xylem appeared secondarily to aid in passive water-flow
Some of the earliest vascular plants, such as rhyniophytes, had thickened conducting cells referred to as "S-type" tracheids.
These cells had annual or helical thickenings consisting of a spongy material. Prominent helical (possibly annular) thickenings show a spongy texture, which is also present in the underlying and intervening lateral walls of the elements. Both thickenings and intervening lateral walls are covered by a very thin layer with numerous closely spaced holes. Named after the plant Sennicaulis † (Kenrick et al., 1991)
e.g., cooksonioids and zosterophyllphytes
Secondary thickenings are annular, helical to occasionally approaching reticulate, and are connected by a sheet of resilient material that is fused to the presumed primary wall. The sheet is perforated by holes of varying size and usually rounded shape. Named after cells found in Gosslingia †, and found in many zosterophylls, as well as the ancestral clubmoss Asteroxylon †.
e.g., euphyllophytes and derived lycophytes
Metaxylem tracheids are long (< 3 mm) and markedly faceted (5–7 sides) compared with G-type. Pitting is essentially scalariform, and in superbly preserved specimens, there are pit-closing membranes present. Named after cells found in the Psilophyton †.