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.     

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.     

Structure,molting, and mineralization of the dorsal ossicle complex in the gastric mill of the blue crab,Callinectes sapidus

This study examined the mesocardiac and urocardiac ossicles in the gastric mill of the blue crab to describe its structure, mineralization, and dynamics throughout the molt cycle, and to assess its possible utility in age determination. Morphologically, the mineralized ossicles are similar to the calcified dorsal carapace having a lamellate structure comprised of sheets of chitin/protein fibrils. Staining with acridine orange showed the same arrangement of an epicuticle, exocuticle, and endocuticle. In much of the mesocardiac and urocardiac ossicles, the endocuticle is very reduced, with the exocuticle predominating; the reverse of the dimensions of the exoskeleton. The lamellate structure of the ossicles was confirmed with scanning electron microscopy; however, elemental mapping by energy‐dispersive analysis of X‐rays revealed that the ossicles are mineralized with calcium phosphate, in contrast to the calcium carbonate biomineral of the exoskeleton. The medial tooth of the urocardiac ossicle is not calcified, but the epicuticle is highly elaborated and impregnated with silica. Histological examination of the ossicles demonstrated that they are molted during ecdysis, so despite the appearance of bands in the mesocardiac ossicle, it is difficult to hypothesize how the bands could represent a record of chronological age. J. Morphol. 276:1358–1367, 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.     

Development and functional morphology of the foreguts of larvae and postlarvae of three crustacean decapods

The development of the foregut structure and the digestive function of the decapods Litopenaeus vannamei, Sesarma rectum and Callichirus major larvae and post larvae were examined. The protozoeal foregut of L. vannamei is simple, lacking a cardiopyloric valve and bearing a rudimentary filter press. In mysis, the filter press is more developed. In the juvenile stage, grooves and a small lateral tooth arise. In S. rectum, the foregut has a functional cardiopyloric valve and a filter press. The megalopal and juvenile stages of this species have a gastric mill similar to those in adult crabs. In C. major, the foregut of the zoeae is specialized, with the appearance of some rigid structures, but no gastric mill was found. Calcified structures are observed in the megalopae and they become more developed in the juvenile stage. The results support suppositions, previously reported in other studies, that feeding behavior of each larval and postlarval stage is directly related to the morphological characteristics of the foreguts.     

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.     

Development and metamorphosis of the digestive system of larval lobsters,Homarus americanus (Decapoda: Nephropidae)

This study provides a detailed account of the development of the digestive system of larval lobsters (Homarus americanus H. Milne Edwards, 1837) and the morphological changes that occur at metamorphosis. The most dramatic of these changes involves the gastric mill of the cardiac stomach. First-and second-stage lobsters lack the medial and lateral teeth characteristic of the grinding stomach of adult lobsters. Clearly recognizable, heavily cuticularized teeth first appear in the third stage, and accessory lateral teeth do not appear until the fourth stage. In place of the teeth of the gastric mill, first- and second-stage stomachs have a series of pads and ridges which are the apparent rudiments of the teeth. The development of the gastric mill during the larval stages enables lobsters to deal successfully with the more substantial food they encounter in the benthic environment, and corresponds to the drastic change of habitat and diet which occurs at metamorphosis. Confusion about the extent of the midgut and hindgut in larval lobsters has been clarified. The results of this study have shown that the larvae have a long midgut, which lacks a cuticle, and a short hindgut with a cuticular lining, just as in adult lobsters. The junction between midgut and hindgut lies in the sixth abdominal segment in all of the first four stages, as well as in the adult.     

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.     

Skeletal morphology of the mud star,Ctenodiscus crispatus (Echinodermata: Asteroidea)

The morphology of the following eight major ossicle types is described and illustrated for the goniopectinid asteroid Ctenodiscus crispatus: terminal plates, superomarginal and inferomarginal ossicles, adambulacral and ambulacral ossicles, odontophores, oral intermediate plates, and superambulacral ossicles. Development, variation, and relationships with soft body-parts and with other ossicles are embphasized. Each ossicle type is distinguished by numerous structures related to its function and to articulation with adjoining skeletal elements. Because major structures (such as pustules, alveoli, and articulation surfaces) distinguishing ossicle types develop early during ontogeny, immature ossicles are readily identifiable. However, changes in form and orientation of these structures occur during ossicle growth. Ontogenetic changes are influenced by development of associated skeletal and soft parts. Ambulacral and adambulacral ossicles near the peristome are highly modified but retain the basic characteristics of structure and orientation which define these major types of skeletal elements.     

The foregut-ossicle system of Dromia wilsoni, Dromia personata and Lauridromia intermedia (Decapoda, Brachyura, Dromiidae), studied with a new staining method

The ossicles of the cardiac and pyloric foregut of three species of decapods: Dromia wilsoni [Fulton and Grant, 1902], Dromia personata [Linnè, 1758] and Lauridromia intermedia [Lauri, 1906] are described and illustrated in detail. Five new ossicles are recognized based on a specific staining-method with Alizarin-Red. The ossicle terminology of the brachyuran foregut is revised now to include 37 ossicles. All described ossicles are documented by drawings and photographs. The two new cardiac ossicles, the prepterocardiac and the postpterocardiac ossicles are narrow ossicles associated with the pterocardiac ossicles at the antero-dorsal margin of the cardiac foregut. The pyloric foregut includes the newly described lateral mesopyloric- and the posterior uropyloric ossicles. These pyloric ossicles are clearly recognizable only in the stained condition. Based on our data we provide new additional evidence for brachyuran monophyly and the paraphyletic status of the podotrematan crabs.     

The crustacean cuticle does not record chronological age: New evidence from the gastric mill ossicles

A proposed method to determine chronological age of crustaceans uses putative annual bands in the gastric mill ossicles of the foregut. The interpretation of cuticle bands as growth rings is based on the idea that ossicles are retained through the moult and could accumulate a continuous record of age. However, recent studies presented conflicting findings on the dynamics of gastric mill ossicles during ecdysis. We herein study cuticle bands in ossicles in four species of commercially important decapod crustaceans (Homarus gammarus, Nephrops norvegicus, Cancer pagurus and Necora puber) in different phases of the moult cycle using dissections, light microscopy, micro-computed tomography and cryo-scanning electron microscopy. Our results demonstrate that the gastric mill is moulted and ossicles are not retained but replaced during ecdysis. It is therefore not plausible to conclude that ossicles register a lifetime growth record as annual bands and thereby provide age information. Other mechanisms for the formation of cuticle bands and their correlation to size-based age estimates need to be considered and the effect of moulting on other cuticle structures where ‘annual growth bands’ have been reported should be investigated urgently. Based on our results, there is no evidence for a causative link between cuticle bands and chronological age, meaning it is unreliable for determining crustacean age.     

Development and metamorphosis of the feeding apparatus of the stone crab,Menippe mercenaria (brachyura,xanthidae)

Analysis of the feeding apparatus of the stone crab, Menippe mercenaria (Brachyura, Xanthidae), has demonstrated that substantial internal and external morphological alterations occur at metamorphosis and suggests that the mastication of food shifts from the mandibles to the gastric mill at that time. These changes correspond to the changes in environment and diet that take place at metamorphosis, when the previously planktotrophic larvae begin benthic life. A detailed account of the structure and development of the mandibles is presented. The mandibles of all zoeal stages are similar: The incisor process has a series of teeth and denticles and the prominent molar process appears to be well adapted for grinding food. Megalopal mandibles are transitional but have the form that is typical of all subsequent stages: The expanded incisor process is rounded and toothless and the molar process is less prominent and has lost its grinding denticles. The cardiac stomach of the zoeal stages has no gastric mill; the medial and lateral teeth of the mill first appear in the megalopa. A very simple procedure is described for preparing larval mandibles for scanning electron microscopy using the molted exoskeletons from larval rearing experiments.     

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.     

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.     

Arm joint articulations in the ophiuran brittlestars (Echinodermata: Ophiuroidea): a morphometric analysis of ontogenetic, serial, and interspecific variation

The ophiuroid arm contains a series of vertebral ossicles that form an articulated internal skeleton. Ontogenetic, serial, and interspecific variation in these skeletal elements are investigated using morphometric data from 35 species of brittle-stars (Order Ophiurae). Multiple ossicles were sampled from each individual and several individuals were sampled from each species to reconstruct serial and ontogenetic changes in vertebral morphology. Within species, ontogenetic and serial allometries are not statistically different. These data support 'Jackson's law of localized stages' (Jackson, 1899; Clark, 1914), which proposes that serial variation along the arm reflects ontogenetic stages of ossicle growth.
A multivariate analysis of interspecific variation shows two major vertebral forms: ossicles with a proximal depression and distal keel, and ossicles lacking these features. Variation within these groups is largely continuous, but individual species show distinct shape differences and unique allometric patterns of serial variation. These results suggest that vertebral ossicle variation among species can be described by: 1) variation in initial shape; and 2) variation in the allometric trajectory along the proximal-distal axis.
In all species, the most proximal ossicles within the disk show a non-keeled morphology. In species with keeled arm ossicles, however, there is an abrupt transition within the disk between non-keeled and keeled vertebral forms. A single ossicle, having features of both vertebral types, occurs at this site. The taxonomic distribution of the two vertebral forms and the anatomical transition between forms is discussed with reference to current classification systems and recent phylogenetic schemes for the Ophiuroidea.     

Morphology and ultrastructure of the esophagus during the ontogeny of the spider crab Maja brachydactyla (Decapoda,Brachyura, Majidae)

The esophagus of the eucrustaceans is known as a short tube that connects the mouth with the stomach but has generally received little attention by the carcinologists, especially during the larval stages. By this reason, the present study is focused on the morphology and ultrastructure of the esophagus in the brachyuran Maja brachydactyla during the larval development and adult stage. The esophagus shows internally four longitudinal folds. The simple columnar epithelium is covered by a thick cuticle. The epithelial cells of the adults are intensively interdigitated and show abundant apical mitochondria and bundles of filamentous structures. The cuticle surface has microspines and mutually exclusive pores. Three muscle layers surrounded by the connective tissue are reported: circular muscles forming a broad continuous band, longitudinal muscle bundles adjacent to the circular muscles, and dilator muscles crossing the connective tissue vertically toward the epithelium. The connective tissue has rosette glands. The esophagus of the larvae have epithelial cells with big vesicles but poorly developed interdigitations and filamentous structures, the cuticle is formed by a procuticle without differentiated exocuticle and endocuticle, the connective layer is thin and the rosette glands are absent. The observed features can be explained by his role in the swallowing of the food.     

Evolutionary relationships between the amphibian, avian, and mammalian stomachs

Although the gut is homologous among different vertebrates, morphological differences exist between different species. The most obvious variation in the guts of extant vertebrates appears in the stomach. To investigate the evolution of this structure, we compared the histology of the stomach and gastrointestinal tract in amphibian (Xenopus laevis), avian (Gallus gallus), and mammalian (Mus musculus) organisms, and defined the expression patterns of several genes within the developing guts of these lineages. In all three groups, we find that the anterior portion of the stomach has a similar glandular histology as well as a common embryonic expression of the secreted factors Wnt5a and BMP-4. Likewise, within the amniote lineages, the posterior nonglandular stomach and pyloric sphincter regions are also comparable in both histological and molecular phenotypes. The posterior stomach expresses Six2, BMPR1B, and Barx1, whereas the pyloric sphincter expresses Nkx2.5. Although the adult Xenopus stomach exhibits both glandular and aglandular regions and a distinct pyloric sphincter similar to that of the amniotic vertebrates, the histology of the Xenopus tadpole gut shows less distinct variation in differentiation in this region, which is most likely a derived condition. The molecular signature of the embryonic Xenopus gut correlates with the more derived morphology of the larval phase. We conclude that the global patterning of the gut is remarkably similar among the different vertebrate lineages. The distinct compartments of gene expression that we find in the gut be necessary for the unique morphological specializations that distinguish the stomachs from terrestrial vertebrates.     

Feeding and masticatory structures of selected Anomura (Crustacea)

Seven species representing the three superfamilies of the Anomura were studied regarding food, feeding mechanisms, and masticating ossicles of the gastric mill in order to determine whether the structure of the gastric mill was determined by diet or phylogeny. The hippid representative and both porcellanids examined feed on suspended detritus and plankton while the pagurids feed on a variety of substances ranging from detritus to motile prey. The morphology of the mouthparts and chela are related to feeding activity, especially the hippid and porcellanids, but general features of feeding requiring specific anatomical characters were not found in the paguridae. Feeding similarity was measured using the overlap measure of Horn.Among the species the masticating ossicles of the gastric mill differ in those species feeding primarily on detritus; it is finely toothed or setose with the masticating portions of the ossicles blunt. The gastric mill of the species feeding on macromaterial is strongly toothed and sparcely setose, with the masticating portions sharp and cutting. The structure of the gastric mill was found to be influenced by both diet and phylogeny, but the effect of diet appears to be more important.