Foregut morphology and ontogeny of the spider crab Maja brachydactyla (Brachyura,Majoidea, Majidae)

We describe the morphology of the foregut of the spider crab Maja brachydactyla Balss, 1922, from first larval stage to adult, with detailed stage‐specific documentation using light and scanning electron microscopy. A total of 40 ossicles have been identified in the foregut of adults of M. brachydactyla using Alizarin‐Red staining. The morphological pattern of the ossicles and gastric mill is very similar to other Majoidea species with only a few variations. The foregut of the zoeae stages appeared as a small and simple cavity, with a cardio‐pyloric valve that separates the stomach into cardiac and pyloric regions. The pyloric filter is present from the first zoea, in contrast to the brachyuran species which have an extended larval development. Calcified structures have been identified in the cardio‐pyloric valve and pyloric region of the zoeal stages. The most significant changes in foregut morphology take place after the metamorphosis from ZII to megalopa, including the occurrence of the gastric mill. In the megalopa stage, the foregut ossicles are recognizable by their organization and general morphology, but are different from the adult phase in shape and number. Moreover, the gastric teeth show important differences: the cusps of the lateral teeth are sharp (no molariform); the dorsal tooth have a small, dentate cusp (not a well‐developed quadrangular cusp); and the accessory teeth are composed of one sharp peak (instead of four sharp peaks). The gastric mill ontogeny from megalopa to adult reveals intermediate morphologies during the earlier juvenile stages. The relationship between gastric mill structures with food preferences and their contribution to the brachyuran phylogeny are briefly discussed. J. Morphol. 276:1109–1122, 2015. © 2015 Wiley Periodicals, Inc.     

Digestive anatomy of Halella azteca (Crustacea,Amphipoda)

The digestive tract of the freshwater amphipod Hyalella azteca is a straight but differentiated tube consisting of foregut, midgut, and hindgut divisions. The foregut is subdivided into a tubular esophagus, a cardiac stomach, and a pyloric stomach. The cuticular lining of the cardiac stomach is elaborated into a set of food-crushing plates and ossicles, the gastric mill, while the pyloric cuticle forms a complex straining and pressing mechanism. Nine caeca arise from the midgut, seven anteriorly and two posteriorly. Four of the anterior caeca, the hepatopancreatic caeca, are believed to be the primary sites of digestion and absorption. The remaining caeca may be absorptive, secretory, or both. The much-folded hindgut wall is capable of great distention by extrinsic muscle action for water intake to aid in flushing fecal material out of the anus; such action also may stimulate antiperistalsis by intrinsic rectal muscles.     

Foregut morphology and ontogeny of the mud crab Dyspanopeus sayi (Smith, 1869) (Decapoda,Brachyura, Panopeidae)

The morphology of the foregut of the Say's mud crab Dyspanopeus sayi was described in adults and larvae. The ossicle system was illustrated based on a staining method with Alizarin-Red. The gastric teeth and cardio-pyloric valve were dissected and examined using optical and scanning electron microscopy. In the adults, the morphology of ossicles and gastric teeth of D. sayi is very similar to the related species Rhithropanopeus harrisii. The foregut of first zoea (ZI) presented a functional cardio-pyloric valve while the filter press was lacking. The filter press was observed in the pyloric chamber from ZII. The most significant changes in morphology take place after metamorphosis from ZIV to megalopa, including the occurrence of the gastric mill. The organization and morphology of many megalopal foregut ossicles are recognizable in the adult phase, although the morphology of the gastric teeth differs from the morphology of adults. A correlation of gastric mill structures with food preferences and their contribution to the phylogeny are briefly discussed.     

Anatomy of the extrinsic gut musculature of Gammarus minus (Crustacea: Amphipoda)

Inserting on the buccal and esophageal foregut of Gammarus minus are numerous pairs of serially arranged dorsal dilator muscles, a single pair of lateral muscles, and two pairs of posterior muscles. Muscles of the cardiac stomach include three dorsal sets, a single pair associated with the pterocardiac ossicles, and two pairs inserting on the ventral aspect. A single pair of muscles inserts on the lateral aspect of the pyloric stomach. The extrinsic muscles of the foregut originate from exoskeletal apodemes of the cephalothoracic cuticle, sockets of the mandible, and a maxillary bridge that lies just ventral to the cardiac stomach. The extrinsic musculature of the hindgut is restricted to the rectal region and consists of paired dorsal and ventral series in an X-configuration. A single unpaired muscle inserts on the ventral midline. Extrinsic muscles of the hindgut originate from the integument of the last pleonic segment. The general arrangement of extrinsic gut muscles in G. minus is similar but not identical to that of other amphipods studied. However, the pattern is quite different from that of other malacostracans.     

Structure of the stomach cuticle in adult and larvae of the spider crab Maja brachydactyla (Brachyura,Decapoda)

The stomach of decapods is a complex organ with specialized structures that are delimited by a cuticle. The morphology and ontogeny of the stomach are largely described, but few studies have focused on the morphology of its cuticle. This study examined the morphology of the stomach cuticle of cardiac sacs, gastric mill ossicles, cardio-pyloric valve and pyloric filters, and during various stages (zoea I and II, megalopa, first juvenile, and adult) of the common spider crab Maja brachydactyla using dissection, histology and transmission electron microscopy. The results show that cuticle morphology varies among structures (e.g., cardiac sacs, urocardiac ossicle, cardio-pyloric valve, pyloric filters), within a single structure (e.g., different sides of the urocardiac ossicle) and among different life stages. The cuticle during the larval stages is very thin and the different layers (epicuticle, exocuticle, and endocuticle) are infrequently distinguishable by histology. Major changes during larval development regarding cuticle morphology are observed after the molt to megalopa, including the increment in thickness in the gastric mill ossicles and cardio-pyloric valve, and the disappearance of the long thickened setae of the cardio-pyloric valve. The cuticle of all the stomach structures in the adults is thicker than in larval and juvenile stages. The cuticle varies in thickness, differential staining affinity and morphology of the cuticle layers. The structure–function relationship of the cuticle morphology is discussed.     

Morphological changes in external and internal feeding structures during the transition phyllosoma-puerulus-juvenile in the Western Rock Lobster (Panulirus cygnus,Decapoda: Palinuridae)

External and internal feeding structures of the pelagic final phyllosoma, the transitional puerulus, and the benthic juvenile Western Rock Lobster, Panulirus cygnus, were studied by means of scanning electron microscopy. The study revealed that the external feeding structures of phyllosomata are well equipped for capture and mastication of food. The foregut, however, is not clearly divided into pyloric and cardiac regions and a gastric mill is absent, although a comb row and gland filter are present. Juveniles, on the other hand, have a well-developed gastric mill and gastric teeth, and a cardiopyloric valve separates the foregut into cardiac and pyloric regions. External mouthparts of juveniles are suitable for mastication of solid food particles and bear numerous setae. In contrast, external mouthparts of pueruli are largely non-setose. Furthermore, although the foregut is differentiated into pyloric and gastric regions and a gland filter and comb row are present, a functional gastric mill is absent during the puerulus stage. Absence of such structures indicates that the puerulus may be a non-feeding stage. It is postulated that absence of (or reduced) feeding may be a response to an increased risk of predation rather than a result of the considerable morphological changes taking place during the transition from a planktonic to a benthic lifestyle, as has been previously proposed. © 1994 Wiley-Liss, Inc.     

The functional anatomy of the foregut of Porcetlana platychetes and a comparison with Galathea squamifera and Upogebia deltaura (Crustacea: Decapoda)

Muscles, ossicles and internal structures of the foregut of Porcellana platycheles are described and figured. The function of the foregut is deduced from the distribution of food particle size within its chambers. The trough of the cardio-pyloric valve is considered to be the main site of digestion and the supra-ampullary valve to have an active role in the formation of the ventral cap of faecal pellets.
The structures and function of the foregut of Galathea squamifera are similar to those of P. platycheles. Certain differences found in the foregut of Upogebia deltaura may be related to the small size of food particles ingested and the absence of a ventral cap from faecal pellets may be due to the supra-ampullary valve having no action on surrounding particles.     

The anatomy and physiology of the stomatogastric nervous system ofSquilla

Summary The stomatogastric nervous system of a mantis shrimp,Squilla oratoria, is described. The motor nerves of the stomatogastric ganglion (STG) and their innervation of muscles of the posterior cardiac plate (pcp) and pyloric systems are detailed.The STG contains more than 25 neurons. It sends out one pair of major output nerves. The pcp-pyloric cycle recorded from the motor axons in this nerve consists of rhythmic bursts of several units which fire with a characteristic phase relationship to each other. The rhythm is intrinsic to the STG itself, but it is modifiable.Recordings from the peripheral nerves reveal that identifiable cardiac plate, pyloric dilator and pyloric neurons control sequential contractions of the pcp and pyloric muscles to constrict or dilate a number of their attached ossicles.Several modulatory input fibres in the stomatogastric nerve, activated via stimulation of the superior or inferior oesophageal nerve (son, ion), prime or trigger the cyclic motor outputs. The son inputs induce distinct effects on the cardiac and pcp-pyloric pattern generators, while the ion inputs, via the oesophageal ganglion, excite only the pcp-pyloric generator.On the basis of anatomical and physiological observations, the possible functions of motor neurons involved in the pcp-pyloric cycle are described with reference to opening of the pcp and pyloric channels.This stomatogastric nervous system inSquilla is compared to that in decapods which has been well analyzed.Abbreviations CG commissural ganglion - ion inferior oesophageal nerve - lvn lateral ventricular nerve - OG oesophageal ganglion - pep posterior cardiac plate - son superior oesophageal nerve - STG stomatogastric ganglion - stn stomatogastric nerve - ivn inferior ventricular nerve     

Mouthpart and foregut ontogeny in larval, postlarval, and juvenile spiny lobster, Panulirus argus Latreille (Decapoda, Palinuridae)

The spiny lobster Panulirus argus has a life cycle consisting of a long-term (～9-12 months) planktonic larval period with 11 larval stages (the phyllosoma), a short (<1 month?) planktonic-to-benthic transitional postlarval stage (the puerulus), and benthic juvenile and adult phases. The mouthparts and foregut during these stages were examined and described by means of scanning electron microscopy (SEM) in an investigation of the species' developmental morphology, diet, and ecology. The phyllosoma mouthparts close to the esophagus are the labrum, mandibles, paragnaths, and first maxillae. The second maxillae and first and second maxillipeds are increasingly distant from the esophagus as the larva develops. The pair of asymmetrical mandibles bear many teeth and spines, and the molar processes form what appears to be an intricate toothed shear. The mandibles remain similar throughout the phyllosoma stages. During the molt into the puerulus, the mouthparts are greatly changed, and the second maxilla and the three maxillipeds join the other mouthparts near the esophagus. However, the transformation appears incomplete, and many of the mouthparts are not fully formed until the molt to juvenile completes their development. The phyllosoma foregut lacks a gastric mill and has but one chamber. In addition, the first two stages lack a gland filter. During the molt to puerulus, the foregut is greatly changed and subsequently is similar to typical decapod foreguts in having an anterior cardiac and posterior pyloric chamber. Only rudimentary internal armature is present. Following the molt to juvenile, the foregut is quite similar to that of the adult, which exhibits a substantial gastric mill. The 11 phyllosoma stages were separated into two groups (group A = stages 1-5, group B = stages 6-11) on the basis of changes in both mouthpart and foregut morphology. The puerulus has never been observed to feed. Nothing was observed in our investigations that would prevent feeding, though both mouthpart and foregut development appeared incomplete. The mouthpart and foregut structures of larval, postlarval and juvenile P. argus differ widely, possibly reflecting the extreme modifications for different habitats found among these life phases.     

Activation of command fibres to the stomatogastric ganglion by input from a gastric mill proprioceptor in the crab,Cancer pagurus †

In semi‐intact preparations of the crab Cancer pagurus the normal output from the stomatogastric ganglion (StG) was a regular pyloric cycle (Figure 4). Repeated stimulation of the posterior stomach nerve (psn) of the posterior gastric mill proprioceptor (PSR) often induced series of spontaneous gastric cycles. We were therefore able to describe the normal gastric cycle as recorded in the output nerves from StG and to identify most of the relevant motor neurones by reference to the muscles that they innervate (Figure 10). The gastric cycle output was variable (Figures 5, 6), although in many preparations one complex type of output predominated (Figure 7). The basic feature of the gastric cycle was an alternation of activity between the single cardio‐pyloric neurone (CP) and a complex variable burst in the lateral cardiac (LC), the gastro‐pyloric (GP), the gastric (GM), and other associated neurones. During this normally occurring complex gastric burst significant changes occurred in the pyloric cycle, notably an increase in activity of the pacemaker pyloric dilator (PD) group and an inhibition of the lateral pyloric (LP), inferior cardiac (IC) and ventricular dilator (VD) neurones (Figures 6, 7, 8, 9). These changes are probably associated with an opening of the cardio‐pyloric valve and food passage into the pyloric filter. The gastric output was related to the normally observed movements of the dorsal ossicles of the gastric mill and thus to the operation of the teeth of the mill (Figure 11). Increased input from the PSR is associated with the grinding action of the teeth which is caused by the complex gastric burst (Figure 12).

Stimulation of the psn during an ongoing regular pyloric output caused changes in the cycle which mimicked those occurring during the spontaneous gastric cycle (Figure 13; Table 1). Stimulation of the psn during ongoing gastric activity also affected the gastric units (Figure 14). The input pathway from the PSR is shown to be through the stomatogastric nerve (sgn), the connection between the commissural ganglia and the stomatogastric ganglion (Figure 15). The commissural ganglia are known to receive most of the sensory input from the foregut and PSR input is probably processed there. Recordings from the sgn show that psn stimulation activates a small number of centrally originating units, and that the activity of these units coincides with the pyloric output changes (Figures 15, 16). We therefore label the units command interneurones. Their effects could be mediated by direct connections to only the PD pacemaker neurones of the pyloric cycle. Control experiments showed that PSR input is not necessary for the pyloric output changes to occur during gastric output but that similar output changes can be evoked by input resulting from induced gastric movements (Figure 15(E)). We think that the pyloric cycle output changes are normally controlled by a number of mechanisms at different levels (Figure 17). We cannot easily explain the effects of PSR input on the gastric cycle neurones.

These findings are important because they allow us to study a specific input to the StG without disrupting its normal input‐output pathways to the central nervous system. Further experiments on the system designed to test the assumption that the sgn units are in fact responsible for the pyloric output changes, and to investigate the processing of the PSR input are outlined.     

Motor pattern generation of the posterior cardiac plate-pyloric system in the stomatogastric ganglion of the mantis shrimp Squilla oratoria

Activity patterns of the constituent neurons of the posterior cardiac plate-pyloric system in the stomatogastric ganglion of the mantis shrimp Squilla oratoria were studied by recording spontaneous burst discharges intracellularly from neuronal somata. These neurons were identified electrophysiologically, and synaptic connections among them were qualitatively analysed. The posterior cardiac plate constrictor, pyloric constrictor, pyloric dilator and ventricular dilator motoneurons, and the pyloric interneuron were involved in the posterior cardiac plate-pyloric system. All the cell types could produce slow burst-forming potentials which led to repetitive spike discharges. These neurons generated sequentially patterned outputs. Most commonly, the posterior cardiac plate neuron activity was followed by the activity of pyloric constrictor neurons, and then by the activity of pyloric dilator/pyloric interneuron, and ventricular dilator neurons. The motoneurons and interneuron in the posterior cardiac plate-pyloric system were connected to each other either by electrical or by inhibitory chemical synapses, and thus constructed the neural circuit characterized by a wiring diagram which was structurally similar to the pyloric circuit of decapods. The circuitry in the stomatogastric ganglion was strongly conserved during evolution between stomatopods and decapods, despite significant changes in the peripheral structure of the foregut. There were more electrical synapses in stomatopods, and more reciprocal inhibitory synapses in decapods.Abbreviations EJP excitatory junctional potential - IPSP inhibitory postsynaptic potential - CoG commissural ganglion - CPG central pattern generator - ion inferior oesophageal nerve - OG oesophageal ganglion - pcp posterior cardiac plate - son superior oesophageal nerve - STG stomatogastric ganglion - stn stomatogastric nerve - PY pyloric constrictor - PD pyloric dilator - VD ventricular dilator - AB pyloric interneuron - lvn lateral ventricular nerves - tcpm transverse cardiac plate muscle     

Multiple motor patterns in the stomatogastric ganglion of the shrimp Penaeus japonicus

 Motor patterns of the cardiac sac, the gastric and the pyloric network in the stomatogastric nervous system of the shrimp Penaeus japonicus, the most primitive decapod species, were studied. Single neurons can switch from the gastric or the pyloric pattern to the cardiac sac pattern. Some of the pyloric neurons fire with the gastric pattern. All of the gastric neurons fire with the pyloric pattern, unlike those in reptantians. Proctolin activates and modulates the cardiac sac and the pyloric rhythm, and promotes reconfiguration of the networks. Neurons of the three networks have so many interconnections that they construct a multifunctional neural network like those in Cancer. This network may function in different configurations under the appropriate conditions. Several modes of interactions between the networks found in different reptantian species can apply to the penaeidean shrimp. Such interactions are general features of the stomatogastric nervous system in decapods. Phylogenetic differences among the decapod infraorders are seen in the number and orientation of muscles and the innervation pattern of muscles. The multifunctional networks have existed in the most primitive decapod species, and types of configurations of the networks would have evolved to produce a wide range of motor patterns as the foregut structure has become complex. Accepted: 26 October 1999     

Ontogeny of gut morphology in the white shrimp Penaeus setiferus (Decapoda,Penaeidae)

Ontogeny of the gut in Penaeus setiferus was investigated by reconstruction of serial sections examined by light microscopy. Development of the gut into the adult form is protracted over several weeks beyond metamorphosis in steps that may be directly related to the unique postlarval life history of Penaeus. The gastric mill is lacking in larval stages of P. setiferus. In protozoeal stages Z₁-Z₃, the pyloric ampullae are blind sacs that do not communicate with the midgut. The gland filter first appears in mysis stage M₂. The gastric mill in early postlarval (PL) stages consists of poorly chitinized lobes with flexible setae. By PL₂₁ the ossicles of the gastric mill are rigid and setae are replaced by spine-like denticles, but even by PL₃₅ the gastric mill is neither as massive nor heavily chitinized as in adults. During the mysis stages and early PL stages, the hepatopancreas communicates freely with both the foregut and the midgut trunk. By PL₃₅ the hepatopancreatic ducts are essentially isolated from the remainder of the midgut by foregut ossicles. The midgut in Z₁ consists of two pairs of simple caeca and the midgut trunk. During larval growth, each of the lateral midgut caeca develops into a number of lobes. After metamorphosis these lobes begin to ramify into small-diameter tubules, and by PL₃₅ have completely ramified into the hepatopancreas of adults. From M₁ to PL₄, the anterior midgut caeca decrease in absolute size and become a single anterior diverticulum. The posterior midgut diverticulum first appears in PL₂₁ as a simple sac and thereafter increases in size and complexity.     

Organization of protein digestion in adult Calosoma calidum (Coleoptera: Carabidae)

Organization of protein digestion was examined in adult male Calosoma calidum (Carabidae) fed either ground-beef or waxmoth larvae (Galleria mellonella). Although trypsin activities in the foregut are consistently higher than those in the midgut, the luminal contents of each region are in equilibrium. Movement of fluids between the midgut and foregut is brought about by muscular contractions of the proventriculus. A 42% fall in trypsin activity of the foregut after feeding on ground-beef is due largely to disgorged enzymes being left on the food. A far higher proportion of disgorged trypsin is recovered when C. calidum feed on waxmoth larvae; beetles ingest about 74% prey protein and yet avoid ingesting digestively refractory solids. The retention of undigested macromolecules in the midgut and foregut lumen was determined using [¹⁴C]inulin labelled waxmoth larvae. Nine per cent and 25% of the radiolabel was passed in the faeces in 2 and 4 days respectively, whilst 59 and 91% of the weight gained at feeding was lost in the same intervals. The role that the peritrophic membrane and pyloric valve play in this process, as well as its implications for enzyme conservation, is discussed.     

Gastric processing and evacuation during emersion in the red rock crab, Cancer productus

The passage of a radio-opaque meal was followed through the digestive system of the red rock crab, Cancer productus, using a fluoroscope. When the crabs were maintained in seawater, the food was apparent in the foregut as soon as the animals had fed. Release of food from the foregut was routinely slow and digesta appeared in the midgut only in small amounts at any one time. The foregut was emptied between 24 and 36 h, digesta was cleared from the midgut region at 36 h and by 48 h only a small amount of residual digesta was left in the posterior part of the hindgut. Contractions of the cardiac region of the foregut were somewhat sporadic and ranged between 6 and 11 min^-1. Contractions of the pyloric region were more stable, varying between 45-65 min^-1. In both cases, there was no change in rate during 18 h period in seawater. When crabs were subjected to both short- and long-term aerial exposure, release of food from the foregut was halted for the first 4-6 h of emersion. Although, small amounts of digesta appeared in the midgut and hindgut, there was no significant change in the amount in each region during emersion. There was a trend towards a depression of cardiac stomach contraction rates, but this was only significant in 3 h postprandial crabs during short-term emersion. A pronounced decrease in pyloric stomach contraction rate was maintained for the duration of the aerial exposure. When crabs were returned to seawater, contraction rates took 3-5 h to return to normal, but no significant change in gastric evacuation was observed during this period. During re-immersion, over 65% of the animals regurgitated the stomach contents. This regurgitation may act as a protective mechanism to avoid digestion and the subsequent specific dynamic action. The decrease in gastric processing in C. productus is probably part of an overall metabolic depression occurring during emersion.     

Observations on the morphology and histology of the foregut of Portunus sanguinolentus (Crustacea: Brachyura)

The morphological and histological characteristics of the foregut of the crab Portunus sanguinolentus (Herbst) are described, with special reference to the lining and glands of the oesophagus. The oesophagus is lined throughout with an outer keratin and an inner collagen layer. Glands secreting mucopolysaccharides are to be found embedded in the connective tissue of the oesophagus. Details of the armature of the pyloric stomach are given.     

Phylogeny of the Anomala (Crustacea, Decapoda, Reptantia) based on the ossicles of the foregut

We present a cladistic analysis of the Anomala based on 66 ingroup species and 5 outgroup representatives. Based on a comparative analysis of the morphology of the foregut we scored 124 characters related to size, shape, and fusion of foregut ossicles and other foregut structures. Our parsimony analysis resulted in 30 equally parsimonious trees which differ mainly at the lower hierarchical level. Our study reveals two large clades within Anomala. One large clade consists of Galatheoidea and Chirostyloidea. The internal relationships show a monophyletic Porcellanidae nested within a group comprising paraphyletic Galatheidae, and Munididae as well as Munidopsidae. The other large clade contains Aegla as sister group to a monophyletic group consisting of the Hippoidea and a clade formed by Lomis and the Paguroidea. Coenobitidae are nested within paraphyletic Diogenidae and Lithodidae are nested within paraphyletic Paguridae. The results are discussed in the context of other morphological and molecular analyses. Furthermore, some aspects of carcinization are touched upon; in particular, an anomalan stem species with a, at least to some extent, ventrally folded pleon is suggested.     

The histology and ultrastructure of a nuclear polyhedrosis virus of the webbing clothes moth, Tineola bisselliella

A histological and ultrastructural study of a nuclear polyhedrosis virus in the webbing clothes moth, Tineola bisselliella, was conducted. Polyhedral development was observed in nuclei of cells of the foregut, cardiac valve, midgut, pyloric valve, hindgut, Malpighian tubules, ganglia of the ventral nerve cord, muscle, tracheae, fat, and hypodermis. Observations made with the electron microscope suggest that virions from the gut lumen are transported in vesicles through the cytoplasm into the nuclei of the columnar cells. Here they are released, replicate, take on membrane, and ultimately become multiply occluded in polyhedral protein. Polyhedra observed in nuclei of other tissues appeared identical to those in the gut.     

Structure of Intestine, Pancreas, and Spleen of the Australian Lungfish, Neoceratodus forsteri (Krefft)

The structure of the intestine and its adnexa in the Australian lungfish Neoceratodus forsteri (Krefft), is described from four adult specimens and compared with that of other lungfish. In all lungfish genera the intestine is thick and straight and contains a complicated spiral valve; a pyloric fold separates the foregut from the midgut. In Neoceratodus the coiling of the intestinal lumen begins in the prepyloric or gastric region, unlike in other vertebrates with a spiral valve, where it begins behind the pylorus. The spiral valve of Neoceratodus begins as a deep groove on the right side of the foregut, just behind the glottis. Such a prepyloric groove is present but poorly developed also in the lungfishes Protopterus and Lepidosiren and contains a prepyloric spleen in all genera. A separate postpyloric spleen is situated in the free margin of the spiral valve, i.e. in the axis of the intestine. The spleen has a heavily pigmented cortex containing large amounts of iron. The pancreas, buried in the spiral valve in front of the pylorus in Neoceratodus , contains numerous islets of Langerhans, similar to those of tetrapods. This is unexpected because the islets of Protopterus , described by Gabe in 1969, are more like the large, encapsulated "Brockmann bodies" of teleosts.