Skip To Main Content (Press Enter).
CHAPTER 5 - CARTILAGE AND BONE
Histology Guide
application menu
  • HOME
  • SLIDE BOX
  • CHAPTER 5 - CARTILAGE AND BONE
  • INDEX
  • SEARCH
  • TERMS OF USE
  • HELP

MICROSCOPE SLIDE

SLIDE NAME
MH 045 Bone
TISSUE
Tibia (monkey)
Cross-Section
Longitudinal Section
PREPARATION
Decalcified Bone
STAIN
Hematoxylin & Eosin
FIXATIVE
10% Formaldehyde
Decalcified Bone
IMAGE SIZE
32,980 x 57,381 pixels
7 GB
FILE SIZE
195 MB
OBJECTIVE
40x
PIXEL SIZE
0.3171 µm
SOURCE
Department of Genetics, Cell Biology, and Development
School of Medicine
University of Minnesota
Minneapolis, MN

SETTINGS

Version 8.0


Display mode

Viewer options


Move Between WayPoints:



Description

Font size

CONTACT US

Questions or comments should be sent to
tcbrelje@gmail.com

This web site is owned and operated by:

T. Clark Brelje, Ph.D.

Faculty/Retired
University of Minnesota
Department of Genetics, Cell Biology and Development
6-160 Jackson Hall
321 Church St SE
Minneapolis, MN 55455

Robert L. Sorenson, Ph.D.

Professor Emeritus
University of Minnesota
Department of Genetics, Cell Biology and Development
6-160 Jackson Hall
321 Church St SE
Minneapolis, MN 55455

See Terms of Use for more information.

HELP

See HELP for more extensive information.

Get the User Guide v1.1 to discover new features that can enhance your use of this platform.

Each slide is shown with additional information to its right. The image can be changed using any combination of the following commands.

Sidebar

  • Links: Click to navigate to a specific region
  • Images: Click to show this view
  • Toolbar: Use controls to adjust magnification and pan the image

Mouse

  • Zoom In: Click left button
  • Zoom Out: Double-click left button
  • Pan/Move: Click and drag the image

Keyboard

  • Zoom In: ‘A’ key
  • Zoom Out: ‘Z’ key
  • Pan/Move: Arrow keys (Up, Down, Left, Right)
  • Reset View: ESC key (fit-to-screen view)

Touch

  • Tap: Zoom in on a specific area
  • Double-tap: Zoom out from the current view
  • Drag: Pan the image

SHARE

A link to a virtual slide can be saved for later viewing in different ways.

Clipboard

The address of this view has been copied to your clipboard. This link can be pasted in any other program.

Bookmark

A bookmark link can be created using the bookmark function (Ctrl-D for Windows or Cmd-D for Mac) of your browser. Choose a name for the bookmark and select the folder in which you want it saved.

MH 045 Bone

Osteon (or Haversian System)

Bones contain a high concentration of calcium salts, which makes them too hard to cut into thin tissue sections. It must be decalcified using acids or chelating agents to remove the mineral content, leaving behind the organic matrix, which can be sectioned and stained.

The osteon, or Haversian system, is the primary structural unit of compact bone. Each osteon is a cylindrical structure of concentric layers, called lamellae, arranged around a central Haversian canal. These cylinders run parallel to the long axis of the bone, contributing to its strength and nutrient delivery.

To properly analyze the structure of osteons, it is important to examine both cross-sectional and longitudinal sections.

    • - circular openings in the center of each osteon
      • - remnants of blood vessels and nerve fibers may be visible in some canals
      • - bone forming cells, sometimes visible lining the outer surface of the canals
    • - concentric rings of bone matrix surrounding each canal
    • - thin, darker staining (basophilic) boundary that marks the outer edge of an osteon
    • - found inside small spaces called lacunae between the lamellae (may appear shrunken or missing)
  • - this section was taken along the edge of the shaft, rather than across it, making it look thicker than the cross-section
    • - elongated channels running parallel to the length of the bone
      • - remnants of blood vessels and nerve fibers may be visible within some canals
      • - line the outer surface of the canals
    • - located in lacunae between the lamellae

An alternative method for studying bone is the preparation of ground bone sections. The bone is not demineralized; instead, it is sawed into thin wafers and polished using abrasives. This preserves the mineral content, improving the visualization of structures such as lamellae, canaliculi, and lacunae, which are less clear in decalcified sections (see MH 044 Ground Bone).

© 2005-2026. T. Clark Brelje and Robert L. Sorenson