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This work has been selected by scholars as being culturally important, and is part of the knowledge base of civilization as we know it. This work was reproduced from the original artifact, and remains as true to the original work as possible. Therefore, you will see the original copyright references, library stamps (as most of these works have been housed in our most important libraries around the world), and other notations in the work. This work is in the public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work. As a reproduction of a historical artifact, this work may contain missing or blurred pages, poor pictures, errant marks, etc. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.
This historic book may have numerous typos and missing text. Purchasers can usually download a free scanned copy of the original book (without typos) from the publisher. Not indexed. Not illustrated. 1912 edition. Excerpt: ...beginning of the hepatic system of veins. It is difficult to determine where the capillaries from the portal vein cease and those of the he1: -atic vein begin. By searching the section you should be able to find where a vena centralis lobulae passes'into a sublobular vein. Sketch under low power. See Fig. 64. Fig. 66. Pig Liver x90. Shows a lobule, portal canals, central vein, and distinct perilobular con-nective tissue. Injected and Stained Liver. Portions of liver as injected above were stained in Delafield's hematoxylin, imbedded in celloidin, and sectioned. Remove the sections from the clearing oil and mount in balsam. Study as above, noting the relation of the hepatic cells to the capillaries, and sketch a small portion under high power. Stained Pig Liver. Small pieces of pig liver. were hardened in absolute alcohol and imbedded in paraffin. Fix the_section to, the slide, remove the paraffin, and stain in hematoxylin and eosin, clear in oil of cloves, and mount in balsam. Study the lobules and general structure under low power. The pig's liver is well adapted for the study of the general structure since the lobules are very distinct. Find a portal canal containing a bile duct, hepatic artery, and portal vein. V'hat is the position of the canal? Study the capsula fibrosa. Do you find lymphatic vessels in the canals? Draw a portal canal with portions of the adjacent lobules as seen under low power. See Fig. 66. Impregnated Liver. Oppel's Method. Pieces of liver were placed for three days in a solution consistigig of four parts 3% solution of potassium'liichromate and one part-fiof a 1% solution of osmic acid, and wengitlien placed in a;4 to.,1 %' solution of silver nitrate where they remained several...