The structure of a photoreceptor organelle in the eye of Pterotrachea mutica

Summary The photoreceptor cell of Pterotrachea consists of an elongated cell some 100 m long with recogniseable inner and outer segments. The photoreceptor membranes point towards the light. There are about 300 discs per photoreceptor, a small number of discs arising from a single ciliary base. There are bout 75–100 such bases on each receptor cell. The receptor cells themselves (the inner segments) have four recognisable regions. The vacuolated region, the region of mitochondria, the nuclear region, and the axonal region.The photoreceptor cells are organised in five roughly parallel rows, and separated from one another by pale supporting cells.My thanks are due to Professor J. Z. Young, F. R. S. for his enthusiastic support and help during this work. Dr. R. Bellairs kindly provided electron microscope facilities. Mr. R. Moss, Mrs. J. Hamilton and Mr. A. Aldridge provided excellent technical and photographic assistance.     

The nerve fibres in the basement membrane and related structures in Saccoglossus horsti (Enteropneusta)

Summary The structure of the basement membrane of Saccoglossus horsti has been examined with the electron microscope. The membrane consists of two lamellae each of two layers. An outer amorphous layer 150 nm across and an inner fibrillar layer 1–3 m across. The fibrils of the fibrillar layer are two sizes, the majority are 5–9 nm in diameter and at least 2 m long. The thicker 30 nm fibrils occur in small patches and have striations with a 30 nm period.Within the lamellae of the basement membrane are blood spaces. The only regularly found structures in these spaces are blood particles some 12–16 nm in diameter.Nerve fibres of varying diameters traverse all the layers of basement membrane. These fibres run longitudinally and obliquely through the basement membrane, and emerge amongst the muscle cells inserted into the coelomic side of the membrane. No motor end plates have been seen. Preliminary observations suggest that many of the nerve fibres have no sheath other than the cell membrane of the fibre itself.The muscle cells are attached to the basement membrane by structures that resemble hemidesmosomes. The blood vessels of Saccoglossus have a basement membrane on the lumenal side of the endothelial cell cytoplasm.I wish to thank Professor J. Z. Young, F. R. S. for continuous encouragement and advice. To Dr. R. Newell I am indebted for the collection and identification of the specimens. I am pleased to acknowledge my debt to Dr. R. Bellairs for the use of electron microscope facilities, and to Mrs. J. Hamilton and Mr. R. Moss for skillful technical assistance.     

The organization of the substantia gelatinosa rolandi in the cat lumbosacral spinal cord

Summary The organization of the substantia gelatinosa and adjacent lamina III in cat lumbo-sacral spinal cord has been studied by light and electron microscopical techniques in normal cord and following dorsal root section.The substantia gelatinosa (lamina II of Rexed) is characterized by bundles of small, non-myelinated axons, principally oriented longitudinally. The substantia gelatinosa cells are small, spindle shaped, with a cytoplasm generally devoid of Nissl substance. There are extensive axo-dendritic and axo-axonal contacts within the substantia gelatinosa and less frequent axo-somatic contacts.Larger marginal cells oriented horizontally on the surface of the substantia gelatinosa and containing Nissl substance are also seen.Lamina III is somewhat similar to the substantia gelatinosa, but lacks the complex bundles of non-myelinated axons.Following dorsal root section, heavy degeneration is seen by light and electron microscopy in lamina III, but is rarely seen in the substantia gelatinosa. It is concluded that the substantia gelatinosa and lamina III are distinct anatomically and therefore may differ functionally.The possible physiological role of the substantia gelatinosa is discussed.This work was supported by a Special Fellowship 2F11 NB 1140 02 NSRB from the National Institute of Neurological Diseases and Blindness, United States Public Health Service.The author is indebted to Dr. E. G.Gray for his excellent advice. I thank Dr. R. W. Guillery, Dr. L. E. Westeum and Dr. B. G. Cragg for their assistance, and Prof. J. Z. Young, F. R. S. for his kind suggestions. I also wish to thank Mr. S. Waterman for the photography.     

The fine structure of sensory receptor processes in the auricular epithelium of the planarian,Dugesia tigrina

Summary The marginal epithelium of the lateral auricles of the planarian, Dugesia tigrina, includes a cell type with surface cilia and microvilli, a basal nucleus, and dense cytoplasm containing secretory vacuoles, Golgi elements, mitochondria and ribosomes. Through channels within the epithelial cytoplasm, cellular processes, interpreted as extensions of neurosensory receptor cells located in the subepidermis, project to the surface. The receptor processes, containing microtubules, mitochondria, vesicles and an agranular tubular reticulum, project beyond the epithelial cell surface; one or two cilia each emerge from a basal body in the apex of the projection. Close to the point of emergence to the epithelial surface, each cylindrical receptor process is surrounded by a collar-like septate junction between adjacent plasma membranes. The cilia of the projections differ from those of the epithelial cells in diameter, density of matrix and in the banding patterns of the rootlets. A few projections appear with the apex and basal body retracted below the epithelial surface. The possible function of these ciliated processes in sensory reception is discussed.This work was supported by Grant No. SO 1 FR 5369 from the U.S. Public Health Service to the University of Illinois at the Medical Center.I thank Dr. J. P. Marbarger, Director of the Research Resources Laboratory, for use of the electron microscope facilities, Miss Irena Kairys for technical help, Miss Marie Jaeger for assistance with photography, and Mr. Robert Parshall for the drawing.To Professor Arthur Wagg Pollister, I respectfully dedicate this article on the occasion of his retirement from Columbia University.     

II. Ultrastructure of the type B sense organ of the specific lateral line system of Gymnarchus niloticus

Summary The type B cutaneous receptor represents one of the three kinds of specific organs of the lateral line system of Gymnarchus niloticus (Szabo and Barets, 1963). Electron microscopic observations reveal that the elementary unit (Fig. 18) of the type B organ consists of a well organized assembly of different epithelial elements grouped around each sensory cell. Several such units compose a type B organ innervated by a single myelinated nerve fiber.The cytoplasm of the sensory cell is characterised by a deep invagination lined by long and densely packed microvilli covered by a jelly-like substance. This jelly substance of allongated stylet form is situated in an intraepidermal cavity, overlaid by vacuolised epithelial cells oriented perpendicularly toward the external epidermal surface.Certain morphological characteristics of the organ B allows the conclusion that this organ is one of the possible electroreceptors of the Gymnarchus niloticus.This work was supported by grant No. 659535 of the Direction de Recherches et Moyens d'Essais (D.R.M.E.) to Dr. Szabo.This work was carried out on the electronmicroscope of the Service de Microscopie Electronique du Laboratoire de Médecine Experimentale (RCA) et du Laboratoire d'Histologie Normale et Pathologique du Système Nerveux (Siemens).With the technical assistance of Miss L. Seguin and Mr. C. Pennarun.     

Studies by negative staining on the structure of collagen fibrils in normal and lathyritic rats

Summary Electron microscope studies on collagen from rat-tail tendon using the negative staining technique indicate the presence of fine filaments 15–30 Å in diameter within the fibres. The banding of the fibrils was only slightly affected by aminoacetylnitrile bisulphate, but an increased amount of fine fibrous material was present in preparations from experimental animals. It is suggested that this material represents a soluble form of collagen which is known to predominate after administration of the drug. Despite the fact that this would be a chemically abnormal collagen, its structure by electron microscopy corresponds remarkably well with the form suggested from X-ray diffraction and physico-chemical studies on normal soluble collagen.The author would like to thank Mr. J. Clements for technical assistance and Mr. R. Thomas (Dental School, Bristol) for discussion on the effects of aminoacetylnitriles in rats.     

A possible correlation between ultrastructure and function in the thin descending and ascending limbs of the loop of Henle of rabbit kidney

Summary An ultrastructural study of the thin loops of Henle has been made in the renal papilla of the rabbit. Animals in different states of water balance were used but no morphological difference was observed in the loops obtained from animals in different experimental groupings. The cytoplasm of the squamous cells lining the limbs was characterised by a paucity of organelles. Descending and ascending limbs were distinguishable. A distinct morphological difference was seen in the junctional regions of cell processes of the descending and ascending thin limbs of the loop. The ascending limb processes were joined by continuous tight junctions whereas the descending limb junctional regions invariably showed a space of at least 70 Å between adjacent processes. It is suggested that there may be a correlation between the structure of these junctional regions and the different permeability characteristics of the two limbs. The thin ascending limb must, on physiological evidence, be relatively impermeable with reference to the thin descending limb.The author wishes to thank Professor F. R. Johnson for his advice and assistance, and Mr. R. F. Birchenough, Mr. P. L. Hyam and Mr. J. Manston for valuable technical assistance.     

An electron microscopical study of the ventral nerve cord of the leech

Summary Three types of fibrillar structure can be seen with the electron microscope in nerve cells of the vental nerve cord of the leech: the neurofibrillar bundles, the tubules and the tonofibrils. In neuroglial cells only the tonofibrils are present. The three types are structurally distinct, and, contrary to past suggestions, there is no evidence that neurofibrillar bundles may consist of tightly packed or badly fixed tubules.In vertebrates the electron microscope reveals bundles of discrete neurofilaments that form the basis for the argyrophilic neurofibrillae seen by light microscopy. Each neurofilamentous unit appears as a dot in cross section. In contrast, in the leech, the electron microscope shows compact fibrillar bundles that clearly correspond to the neurofibrils described by light microscopists. These bundles are made up of closely packed units rather than discrete filaments and where the units occur singly they are seen to have an angular or stellate outline in cross section. To make this distinction clear these have been termed neurofibrillar bundles rather than neurofilaments.Attachment plaques occur in both neurons and neuroglia. These plaques have tonofibrils attached, and the glial tonofibrils are far more numerous than the neuronal tonofibrils. The glial fibrils are identical with the tonofibrils in the glial cells.The attachment plaques are invariably related to an extracellular space that contains material identical with the basement membrane. This material is continuous, by a complex system of channels and diverticulae, with the outer basement membrane in the neuron packets, but forms isolated patches in the other parts of the nervous system.We are grateful to Prof. J. Z. Young, F. R. S., for his encouragement to Mrs. Astafiev for the drawings, to Miss B. Shirra and Mr. K. Watkins for technical assistance and to Mr. S. Waterman for photography.     

The fine structural localization of acid phosphatase in the gut epithelial cells of the slug,Avion ater (L.)

Summary Acid phosphatase, generally thought of as a lysosomal enzyme and indeed widely employed as a lysosomal marker, has been found associated with the Golgi complex of all cell types from the crop, intestine and digestive gland ofArion ater. Reaction product was also detected within the multivesicular bodies and cytoplasm of columnar cells from the crop and the multivesicular bodies of mucous cells from the intestine. A vacuolar localization was obtained in the digestive cells of the intestine and digestive gland. Secretory protein granules in the calcium cells of the same gland and apical vacuoles in the so-called thin cells also showed a positive reaction.This work was undertaken as part of a slug research project under the direction and co-ordination of Dr. D. K.Roach, supported by A.R.C. Assistance was given by Mr. T. R.Mainwaring in the preparation of tissue for electron microscopy.I would like to thank Professor J.Brough and Professor D.Bellamy for providing facilities and encouragement.     

Electron microscopic observations on the involution of the human corpus luteum of menstruation

Summary The involution of the granulosa lutein cell in the human corpus luteum is characterized by a dilatation of agranular endoplasmic reticulum vesicles and tubules. This process continues until the whole cell is filled with large vacuoles and the cytoplasm is reduced to thin strands between the vacuoles. The contents of the latter are of low electron density in contrast to the very electron dense lipid droplets in vascularization, bloom and early involution phase. Light microscopical evidence shows that the contents of the vacuoles must be lipid and the lower electron density might be explained by the relative decrease in phospholipids and increase in cholesterol and cholesterol esters during involution. Simultaneously processes of focal cytoplasmic degradation resulting in autophagic vacuoles occur in the cells. These lead in some cases to the formation of residual bodies which can be identified with lipofuscin granules. Finally, the degenerating cells disintegrate and part of the debris, including the lipofuscin granules are phagocytosed by macrophages, the so-called fluorocytes of Hamperl. During involution an amorphous substance with some protofilaments and collagen fibrils is deposited in the spaces between the shrinking lutein cells. This is the fibrohyalin material which will form the bulk of the corpus albicans.We are grateful for the assistance given by Dr. J. M. Moyes of the Women's Hospital, Crown Street, Sydney and the staff of King George V. Hospital at Sydney with the supply of the material.     

On the alleged presence of non-argyrophile argentaffin cells in the human gastro-intestinal tract

Summary The relationship between the argentaffin and argyrophile cells of the human gastrointestinal tract has been studied, in foetal and adult material, by a technique involving the staining of sections first by an argentaffin method (Gomori-hexamine silver, Schmorl, Diazonium) and subsequently by an argyrophile method (Bodian). A comparison of the cells staining by the two methods shows that all argentaffin cells of the human gastrointestinal tract are also argyrophile and that there is no evidence to support the claim of Hellweg (1952) and of HamPerl (1952) regarding the presence of non-argyrophile argentaffin cells.W. H. O. fellow from the Department of Anatomy, Medical College, Rohtak, India. — I am very grateful to Professor J. D. Boyd and to the World Health Organisation for having made it possible for me to carry out this research at the Anatomy School, Cambridge. I am indebted to Dr. G. A. Gresham and his staff for their very willing cooperation in providing material from surgical resections. My thanks are also due to Mr. J. F. Crane for the photographs and to Mr. J. W. Cash and Mr. R. Smith for helpful discussions on staining techniques.     

Some aspects of the fine structure of the statocysts of the molluscsPecten andPterotrachea

Summary The statocyst ofPecten is composed of hair cells and supporting cells. The hair cells bear kinocilia and microvilli at their distal ends and the supporting cells bear microvilli. The cilia have a 9+2 internal filament content, and arise from basal bodies that have roots, basal feet and microtubular connections. Two different ciliary arrangements are described, one with a small number of cilia arranged in a ring, and another with many more cilia arranged in rows. Below the hair cells are probable synapses. A ciliated duct connects to the lumen of the static sac and passes through the centre of the static nerve. The hair cells in the statocyst ofPterotrachea bear kinocilia and microvilli. The possible importance of cilia and microvilli in the transduction process is discussed.We would like to thank ProfessorJ. Z. Young for bringing specimens ofPterotrachea from Naples and also the staff of the Stazione Zoologica for the provision of specimens, Dr.M. Land for providing specimens ofPecten, the Science Research Council (U.K.) for providing the electron microscope used in much of the study and also for a grant to one of us (V.C.B.), and Mrs.J. Parkers and Mr.R. Moss and Mrs.J. Hamilton for much photographic and technical assistance.     

Staining of proteoglycans in mouse lung alveoli. I. Ultrastructural localization of anionic sites

Summary In order to contrast anionic sites, in mouse lung alveoli, two staining procedures were applied: (a) staining with Ruthenium Red and Alcian Blue and (b) staining with Cuprolinic Blue in a critical electrolyte concentration method. The Ruthenium Red-Alcian Blue staining procedure revealed electron-dense granules in the alveolar basement membrane. The granules were closely associated with the epithelial cell membrane and continued to stain even when the procedure was carried out at a low pH, indicating the presence of sulphate groups in the granules.After staining with Cuprolinic Blue, electron-dense filaments, also closely associated with the cell membrane, became visible in the basement membrane of type I epithelial cells. Their length depended on the MgCl₂ concentration used during staining. At 0.4m MgCl₂, the length was mostly within the range 100–180 nm. Using a modified Cuprolinic Blue method, the appearance of the filaments closely resembled that of spread proteoglycan monomers with their side-chains condensed. The basement membrane of type II epithelial cells also contained filaments positive towards Cuprolinic Blue; their length, however, was smaller in comparison with those of type I epithelial cells. The filaments lay in one plane and provided the whole alveolus with an almost continuous sheet of anionic sites. Cuprolinic Blue staining also revealed filaments in the basement membrane of the capillary endothelial cells. Furthermore, Cuprolinic Blue-positive filaments (average length about 40 nm) became apparent in close contact with collagen fibrils and separated from each other according to the main banding period of the collagen fibrils (about 60 nm), indicating a specific ultrastructural interaction between these two components. Filaments connecting collagen fibrils with each other were also detected.     

On the occurrence of twisted fibrillar structures in the cytoplasm of the red algaAlsidium helminthochorton (La Tourette) Kütz., ultrastructural and cytochemical observations

Summary The cytoplasm ofAlsidium cells contains unusual structures showing various fibrillar arrangements, either stacked rows of arcs or parallel fibrils in longitudinal view alternating with fibrils in cross-section. These regions, located exclusively in the cytoplasmic matrix, are highly proteinaceous and do not seem to be complexed with polysaccharides. Tilting observations under the electron microscope show that the appearance of arcs is an illusion and that the pattern fits the explanation given byBouligand and collaborators for various twisted biological structures.     

Immunohistochemical localization of D-aspartate oxidase in porcine peripheral tissues

d-Aspartate (d-Asp) is an endogenous substance in mammals. Degradation of d-Asp is carried out only by d-aspartate oxidase (DDO). We measured DDO activity in porcine tissues, and produced an anti-porcine DDO antibody to examine the cellular localization of DDO. All the tissues examined showed DDO activities, whereas the substrate d-Asp was not detected in kidney cortex, liver, heart, and gastric mucosa. In the kidney, intensive immunohistochemical staining for DDO was found in the epithelial cells of the proximal tubules. In the liver, the epithelial cells of interlobular bile ducts, liver sinusoid-lining cells with cytoplasmic processes, and the smooth muscle cells of arterioles were strongly stained for DDO. In the heart, cardiomyocytes and the smooth muscle cells of arterioles showed DDO-immunoreactivity. In the gastric mucosa, only the chief cells were DDO-positive. These newly identified DDO-positive cells seem to actively degrade d-Asp to prevent an excess of d-Asp from exerting harmful effects on the respective functions of porcine tissues.     

The occurrence of urediniospores of Cronartium ribicola within the petiole of Ribes petiolare

Urediniospores ofCronartium ribicola J. C. Fisch. exRabenh. were observed within the petiole ofRibes petiolare L. These spores occurred internal to xylem tissues within the region of undifferentiated parenchyma cells (pith). Fungal tissues were sparse and fully differentiated sori were absent.Research Plant Pathologist and Biological Laboratory Technician, USDA Forest Serv., Intermountain Forest and Range Exp. Sta., Ogden, Utah, stationed in Moscow, Idaho83843, at Forestry Sciences Laboratory, maintained in cooperation with the University of Idaho.     

Ultrastructure of transitional epithelium of man

Summary Blocks of human normal renal pelvis and ureter obtained at the time of surgery were fixed in glutaraldehyde and osmium with or without ruthenium red, for electron microscopic observations. The transitional epithelium is arranged in three cell layers: basal, intermediate and superficial. All epithelial cells show numerous microvilli and contain the characteristic vesicles of transitional epithelium, bundles of cytoplasmic filaments, microtubules and numerous free ribosomes. The epithelial extracellular compartment is notably large and appears as an intricate, tridimensional network of canaliculi and cisternae which are wider in the intermediate and superficial layers and in which microvilli and cytoplasmic folds of vicinal cells are often attached or interdigitated. At these sites there are desmosomes.The surface of all transitional epithelial cells is covered by a fibrillar mucous coat which is more developed at the plasmalemma of the free border of luminal cells in which microvilli are also seen. Ruthenium red stains selectively the plasmalemma and the mucous coat of the free surface of the epithelium, indicating the presence of an acid polysaccharide. With this technic (Luft, 1965), it is observed, radiating from the plasmalemma, branching filaments which measure 100 Å in diameter forming a zone of varying density which is about 400 m wide and which corresponds, at the light microscopic level, to the luminal border of the transitional epithelial cells in which a sialomucin has been identified. The slender filaments have a beaded appearance. At the free border, superficial cells are attached by functional complexes in which tight junctions seal the epithelial intercellular space, which is opened at the level of the basement membrane where only desmosomes are observed.The ultrastructure of human transitional epithelium of urinary tract resembles the duct cells of the salt gland of certain marine birds (Fawcett, 1962) and the amphibian epidermis (Farquhar and Palade, 1965) in which there are active processes of transport. The mucous surface coat, selectively stained by the ruthenium red, contains a sialomucin (Monis and Dorfman, 1965, 1967).The ultrastructure and histochemistry of the mucous fluffy coat of man transitional epithelium and the observations of Porter and Tamm (1955), on the ultrastructure of preparations of the Tamm and Horsfall mucoprotein (1952) are bases for suggesting that transitional epithelium of urinary tract of man is the site of biosynthesis of certain urinary mucoids. Present investigations are directed to obtain evidence to substantiate this hypothesis.General Abbreviations B basal cell - E exfoliating cell - I intermediate cell - L lumen - S superficial cell - SC surface coat - bm basement membrane - ci cell infolding - d desmosome (macula adhaerens) - f fibroblast - fi cytoplasmic filaments - is intercellular space - jc junctional complex - ly lysosome - lym lymphocyte - mt microtubules - m mitochondria - mv microvilli - n nucleus - r ribosomes - rv round vesicle - zo zonula occludens - za zonula adherens Dr. Monis wishes to thank Dr. E. De Robertis for the use of the electron microscope facilities of the Instituto de Anatomía General y Embriologia, Facultad de Medicina, Universidad de Buenos Aires. — Prof. E. Trabucco and Dr. R. J. Borzone (Cátedra de Clinica Genitourinaria de la Facultad de Medicina, Universidad de Buenos Aires) generously supplied the specimens which were the bases of this study. — Thanks are due to Mrs. A. M. Novara and Mrs. Defilippi-Novoa for efficient technical help and to Miss Rosa Gentile for secretarial assistance. Photomicrography by Mr. M. A. Saenz.Dr. Zambrano is investigator (CNICT).     

Changes in the fine structure of the human testicular interstitial cells after treatment with human gonadotrophins

Summary Study of the fine structure of the human interstitial cells after prolonged stimulation with human gonadotrophin reveals a striking increase in the quantity of the agranular endoplasmic reticulum. This is accompanied by an increase in the number of mitochondria which exhibit more extensive cristae, collections of intramitochondrial lipid and aggregations of electron-dense granular deposits. A rise is also evident in the number of lipofuscin pigment deposits and granular membrane-bounded bodies, both of which exhibit acid phosphatase activity. These changes after gonadotrophic stimulation are discussed in relation to steroid biosynthesis.In the pretreatment biopsies of these patients aged between 25–35 years, some interstitial cells contain intranuclear crystals which exhibit a hexagonal structure. The relationship of these intranuclear crystals to the cytoplasmic crystals of Reinke is discussed.The author is indebted to Dr. J. W. Johnstone and Dr. A. Long for the human material used in this study. Thanks are also due to Dr. H. P. Taft for helpful suggestions in the management of these patients, to Professor B. Hudson for the estimations of plasma testosterone and to Dr. J. B. Brown for the supply of human pituitary gonadotrophin and the estimations of urinary oestrogens. The technical help of Mr. T. Mezciems and the photographic assistance of Mr. J. S. Simmons F. R. P. S. and Miss S. Flett is gratefully acknowledged.     

The fine structure of the olfactory mucosa and nerve in the teleost Carassius carassius L.

Summary Morphological studies on teleost olfactory mucosa confirm the findings of previous authors regarding the general arrangement of conventional cell types, viz. receptor, sustentacular, mucous and basal, but teleosts show certain distinct differences. The receptor cells have the general mammalian bipolar shape but their peripheral dendrite does not project beyond the epithelial surface. In addition to numerous typical cilia, an exceptional ciliary formation was observed in which the filaments, instead of forming individual cilia, are grouped together in clusters and are enveloped in a single limiting membrane.At the junction between the finger-like process and the mucosal fold myelinated nerve fibres are observed within the subepithelial stroma.Within the postero-medial zone of the mucosa is a conspicuous well-differentiated new cell type. A thick rim of electron-dense cytoplasm, bounded by an outer trilaminar membrane, encloses prominent foliate (leaf-like) organelles, a basal nucleus, numerous mitochondria and vacuolar spaces. These foliaceous cells communicate with the external environment through a small stoma, their close association with epithelial components suggesting a possible secretory or absorptive function. Their intricate morphology, however, suggests that they may be receptors, but their role and neural connections still require definition.Supported by Grant 5 RO 5 TWOO 154-02 from the National Institutes of Health, United States Public Health Service.The authors are indebted to Dr. A. S. Wilson for his helpful criticism and gratefully acknowledge the photographic technical assistance of Mr. J. Simmons and Mr. S. Frank.     

Fluorescence studies on neural structures and endocrine cells in the pancreas of the cat

Summary With the use of the Falck-Hillarp histochemical technique for the detection of monoamines, nerve fibre fluorescence is observed throughout the tail of the pancreas of the cat and the arrangement and distribution of the nerve fibres can be studied in both the exocrine and endocrine tissue. In the exocrine pancreas, adrenergic nerve fibres innervate arterioles, larger veins and major pancreatic ducts. Adrenergic nerve fibres also appear to terminate on the non-adrenergic nerve cell bodies of the intrapancreatic ganglia. In the islets of Langerhans, adrenergic nerve fibres innervate both the endocrine cells and blood vessels. Some of the islet cells exhibit fluorescence with the Falck-Hillarp technique and these cells have been identified as alpha cells. In animals treated with reserpine, the fluorescence in nerve fibres and in alpha cells is absent.The author wishes to thank ProfessorG. C. Schofield and Dr.G. C. Smith for their encouragement and valuable criticism during the course of this study. The assistance of MissJ. Bennett and MissW. Kemp and the photographic help of Mr.J. S. Simmons, F.R.P.S., are gratefully acknowledged. The diagram was drawn by MissS. Flett.