The need of the hematologist for methods applicable to the study of the cells of the peripheral blood with the electron microscope has been pressing. Almost a decade ago Wolpers and Ruska studied thrombocyte structure in relation to fibrin deposition. Wolpers, separately, devised a technic for the direct electron micrography of red blood corpuscles and their membranes. Replica or indirect studies of the red blood corpuscular surfaces were reported later by Barnes, Burton and Scott and by Jones. More recent direct observations include those of Claude and Fullam who, with the electron microscope, studied mitochondria isolated from lymphosarcoma cells of the rat. They brought evidence for an enveloping membrane as well as for small elements within the body of certain mitochondria. Reed and Reed studied erythrocytes from dog's blood with reference to patterned aggregates of hemoglobin and other components which varied with the rapidity of drying of the erythrocyte in vacuo. Fine granules, rough, fibroblast-like forms, and massed aggregates arising from coalescence of the smaller structures were observed. Hovanitz studied resting chromosomes obtained from nuclei of erythrocytes of the chicken. A definite spiral structure was present which may have represented a thread imbedded in a matrix. Appendages were seen with their attachment threads. When the chromosomes were dissolved in M NaCl and precipitated, anastomosing strands composed of minute particles about 50 millimicrons in diameter were produced. Claude, Porter and Pickets were able to obtain macrophages from tissue cultures of centrifuged blood of normal chickens after explanting small fragments of the buffy coat. Their micrograph (their Fig. 1) depicted only the cytoplasm of such a macrophage. Golgi bodies, mitochondria and the particulate components (microsomes) of the ground substance were well portrayed. Bessis and Bursteinstudied the progression of structural changes occurring in thrombocytes in vitro. After addition of anticoagulant, the blood was centrifuged and a drop of the supernatant fluid rich in thrombocytes was utilized for electron microscopy. Their numerous excellent micrographs depict the succeeding stages, classified as circulating forms, dendritic forms, transitional forms, and ultimately, expanded forms. Expansion of the platelet is preceded by pseudopodia formation. In a later series of investigations, Bessis' employed the shadow-casting technic and demonstrated that thrombocyte protoplasm presented numerous radiate fibrils and rarer arcuate forms. The fibrils were composed of small spherules (50 to 200 millimicrons in diameter) separated from one