ADDITIONAL INFORMATION:  Craig D. Byron

 

Title: Assistant Professor

                                                                    

 

Office Address:

225 Willet Science Building,

Department of Biology

 

Mailing Address:

1400 Coleman Ave.                  

Mercer University

Macon GA 31207

 

Phone:  478-301-2163

Fax:  478-301-2067

E-mail: byron_cd@mercer.edu

 

Joined Mercer Faculty: 2006

 

Specialty: Anatomy & Physiology, Histology, Functional Morphology, Skeletal Biology, Primate Evolution

 

Research Interest: My research seeks to elucidate mechanistic pathways that enable skeletal connective tissues to appropriately respond to mechanical stimuli leading to bone growth or bone resorption. By applying a mechanistic understanding to interpreting skeletal morphology, form and function relationships linking organismal behavior to functional anatomy may be clarified. Teaching courses in the anatomical and zoological sciences are of interest to me especially as they pertain to quantitative methods. A list of these courses includes anatomy and physiology, biostatistics, biological anthropology, and paleontology.

 

Degrees: B.A., Anthropology, Indiana University

                M.A., Biological Anthropology, Kent State University 

                Ph.D., Cell Biology and Anatomy, Medical College of Georgia

 

Publications:

1.   Hamrick MW, Pennington C, Byron C (2003): Bone architecture and disc degeneration in the lumbar spine of mice lacking GDF-8 (myostatin). Journal of Orthopaedic Research. 21:1025-1032.

2.   Byron CD, Covert HH (2004): Unexpected Locomotor Behavior: Brachiation by an Old World Monkey from Vietnam. Journal of Zoology. 263(1):101-106.

3.   Byron CD, Borke J, Yu J, Pashley D, Wingard C, Hamrick M (2004): The effects of increased muscle mass on mouse sagittal suture morphology and mechanics. The Anatomical Record Part A. 279A: 676-684.

  1. Covert HH, Workman C, Byron C (2004): The EPRC as an important research center: ontogeny of locomotor differences among Vietnamese colobines. In: Conservation of Primates in Vietnam, edited by Nadler T, Streicher U and Long HT. Hanoi: Frankfurt Zoological Society and Haki Publishing, p. 121-129.
  2. Byron CD, Hamrick M, Wingard C (2005): Alterations of temporalis muscle contractile force and histological content from the myostatin and Mdx deficient mouse. Archives of Oral Biology. 51(5): 396-405.
  3. Byron CD (2006): The role of the osteoclast in cranial suture waveform patterning. The Anatomical Record Part A. 288A:552–563.

 

Courses Taught:

Anatomy and Physiology, BIO 202 & BIO 203

2006-2007, Fall and Spring Semesters

Lecture MWF 11:00-11:50 AM

Lab T 1:40-4:30 PM

 

Introduction to Biology 1, BIO 210

2006, Fall Semester

Lecture MWF 9:00-9:50 AM

Recitation T 8:25-9:15 AM

Lab T 9:25-12:05 PM

 

Research Projects:

Cranial Suture Mechanobiology

My doctoral research mainly focused on the form and function of cranial sutures in the vertebrate skull. The cranial suture is a fibrous connective tissue joint composed of collagen bundles stretched between two perimeters of cranial bone (see figure on the right). This site represents the growth front of cranial bones and is commonly recognized as the “wavy”, zig- zag lines traversing the skull (see figure below). The shape of the line in a planar view and in cross-section relate to the functionality of this suture.

 

 

 

 

 

        

 

 

 

 

 

 

 

 

 

 

 

 

Recent work by me relating to cranial suture structure and function in primates reveals

that primates normally subsisting on diets with tougher material properties possess sutures with increased complexity. This is evidenced by comparing 4 species of Cebus primate to each other because C. apella is known to exploit very tough items such as palm nuts while C. albifrons, C. capucinus, and C. olivaceus do not exploit such foods.

 

Another finding of this research suggests that mechanical loading that results from chewing relates better to suture complexity than does brain size. This is significant because there has been some discussion in the literature concerning the role that encephalization (the process of braincase growth) plays in suture biology. These findings, that are currently in review, will help draw attention to the greater role diet plays in defining suture structure and overall cranial growth.

An immediate question is how increased mechanical loading induces differential growth responses in

 the suture connective tissue. Ongoing work in my lab seeks to understand mechanotransduction pathways

 in connective tissue by using mouse models with different strain distribution patterns that affect their cranial

 sutures. Preliminary data suggest that normal, in vivo, chewing forces cause fibroblast distortion and wounding

 (i.e., cell tearing and resealing) events. These events hypothetically induce downstream growth responses in

 osteoblasts and osteoclasts along the bone suture connective tissue interface. (See below right.)

 

    

 

 

Primate Locomotor Anatomy Studies

Also in my lab I am interested in the evolution of primate locomotor behaviors. Primate anatomy is

intricately related to locomotor and postural choices made in a natural habitat. This is demonstrated by

the figure found to the right. Different species show unique body segment composition and this relates

to the energetics of these postural decisions from an organismal perspective. My own contributions to

this field pertain to the leaf monkeys of southeast Asia, specifically those colobines found in Vietnam,

Cambodia, and Laos. Within this group of Asian colobines odd-nosed forms tend to utilize arm over

arm suspensory postures with much greater frequency than non-odd-nosed forms that tend to locomote

as arboreal quadrupeds. These differences are related to forelimb elongation and its role in facilitating

below-branch (suspensory) locomotion and foraging postures. The goal of these studies is to combine

anatomical and functional analyses to elucidate the ecological ramifications of evolutionary

modification in the primate skeleton.