In a vascular plant, the stele is the central part of the root or stem containing the tissues derived from the procambium. These include vascular tissue, in some cases ground tissue (pith) and a pericycle, which, if present, defines the outermost boundary of the stele. Outside the stele lies the endodermis, which is the innermost cell layer of the cortex.
The concept of the stele was developed in the late 19th century by French botanists P. E. L. van Tieghem and H. Doultion as a model for understanding the relationship between the shoot and root, and for discussing the evolution of vascular plant morphology. Now, at the beginning of the 21st century, plant molecular biologists are coming to understand the genetics and developmental pathways that govern tissue patterns in the stele.
The earliest vascular plants had stems with a central core of vascular tissue. This consisted of a cylindrical strand of xylem, surrounded by a region of phloem. Around the vascular tissue there might have been an endodermis that regulated the flow of water into and out of the vascular system. Such an arrangement is termed a protostele.
There are three basic types of protostele:
Siphonosteles have a region of ground tissue called the pith internal to xylem. The vascular strand comprises a cylinder surrounding the pith. Siphonosteles often have interruptions in the vascular strand where leaves (typically megaphylls) originate (called leaf gaps).
Siphonosteles can be ectophloic (phloem present only external to the xylem) or they can be amphiphloic (with phloem both external and internal to the xylem). Among living plants, many ferns and some Asterid flowering plants have an amphiphloic stele.