The functional morphology of the abyssal Limopsis cristata (Arcoida: Limopsidae) with a discussion on the evolution of the more advanced bivalve foot

The bivalve Limopsis cristata pursues a semi‐endobenthic life in abyssal soft sediments. It attaches to particles by up to three byssal threads and filter feeds by inhaling water from posterior and anterior directions. Because of partial burial, however, only the latter is functionally significant. Complex ciliary currents in the mantle cavity concerned with the rejection of unwanted particles keep most material out of the simplified intestine. It is generally considered that the ligament is the constraining force in arcoid evolution. This may be true in part, but the lack of pallial fusions and the retention of anterior and posterior inhalant flows are more powerful limits to radiation in the Arcoida. In the deep sea, the Limopsidae has radiated into many micro‐niches through micro‐morphological adaptations. Loss of the arcoid ‘heel’ has resulted in the union of the separate rejectory currents of the visceral mass and foot, creating a single discharge point in more advanced bivalves. This greatly simplifies the rejectory roles of the visceral mass and foot and is thus of functional and selective advantage.     

Deposit feeding in Abra tenuis (Bivalvia: Tellinacea)

Deposit feeding in Abra tenuis is described in terms of the size of particles utilized.
Material is collected by the inhalant siphon performing a circular motion sucking in sediment from beneath and on the surface.
The size distribution of silica admitted into the mantle cavity is described and shown to be controlled by physical parameters. The density of a particle does not affect its uptake by the inhalant siphon. The size distribution of the sediment affects the size distribution of particles admitted to the mantle cavity.
No selection of material for ingestion in terms of size occurs after it has been taken into the mantle cavity. Thus the range of material ingested is ultimately controlled by a physical parameter, the inhalant opening.     

The biology and functional morphology of Arca noae (Bivalvia: Arcidae) from the Adriatic Sea, Croatia, with a discussion on the evolution of the bivalve mantle margin

In the Croatian Adriatic, Arca noae occurs from the low intertidal to a depth of 60 m; it can live for > 15 years and is either solitary or forms byssally attached clumps with Modiolus barbatus. The shell is anteriorly foreshortened and posteriorly elongate. The major inhalant flow is from the posterior although a remnant anterior stream is retained. There are no anterior but huge posterior byssal retractor muscles and both anterior and posterior pedal retractors. The ctenidia are of Type B(1a) and the ctenidial–labial palp junction is Category 3. The ctenidia collect, filter and undertake the primary sorting of potential food in the inhalant water. The labial palps are small with simple re‐sorting tracks on the ridges of their inner surfaces. The ciliary currents of the mantle cavity appear largely concerned with the rejection of particulate material. The mantle margin comprises an outer and an (either) inner or middle fold. The outer fold is divided into outer and inner components that secrete the shell and are photo‐sensory, respectively. The latter bears a large number of pallial eyes, especially posteriorly. The inner/middle mantle fold of A. noae, possibly representative of simpler, more primitive conditions, may have differentiated into distinct folds in other recent representatives of the Bivalvia.     

Xenochironomus canterburyensis (Diptera: Chironomidae), a commensal of Hyridella menziesi (Lamellibranchia) in Lake Taupo; features of pre-adult life history

Abstract

The larvae and pupae of the univoltine chironomid Xenochironomus canterburyensis (Freeman) are inquiline commensals of the freshwater mussel Hyridella menziesi (Gray). The 1st- and 2nd-instar larvae enter the mantle/valve cavity of the mussel in midsummer, and by early winter migrate as 3rd-instar larvae to the posterior end of the valve to lodge near its margin beside the inhalant siphon. During the spring, growth of the periostracum of the valve margin between the larva and the mantle of the mussel leaves the 4th-instar larva outside the mantle/valve cavity, where it pupates before leaving the mussel for the lake surface and adult emergence.     

The ecology and functional morphology of Trigonothracia jinxingae (Bivalvia: Anomalodesmata: Thracioidea) from Xiamen, China

All anomalodesmatans are 'rare' but Trigonothrucia jinxingae is relatively common in Xiamen Harbour, Fujian Province, China. This is because the species has a life span of approximately one year and is a simultaneous hermaphrodite, probably with either a short or absent planktonic larval stage. That is, success results from rapid maturation, self-fertilization, direct development and within-habitat recruitment over an extended period in early summer.
Trigonothracia jinxingae is interesting in another way, however. The Thraciidae is the Mesozoic stem group of the Thracioidea which also contains the more modern (Caenozoic) Laternulidae and Periplomatidae. Features of the anatomy of T. jinxingae , such as the method of hydraulically moving the foot by the pumping of blood into a capacious pallial haemocoel, and the structure of the stomach, are reminiscent of the earliest (Palaeozoic) anomalodesmaans, i.e. the Pholadomyoidea, represented today by Pholadomya candida. The thraciid Asthenothaerus sp. (Pelseneer, 1911) even has, like P. cundida , an opisthopodium on its visceral mass. P. candida , however, fed on sub-surface deposits using its foot. T. jinxingae is also a deposit feeder, but on surface deposits using the inhalant siphon.
Modern periplomatids resemble thraciids in their separate siphons, but both representatives of this family and the Laternulidae are suspension feeders with extensive sorting areas on the wall of the stomach to process such material. The Thraciidae thus form a link between the oldest, pedal feeding, pholadomyoidean anomalodesmatan and the most advanced, suspension feeding, laternulids and periplomatids.     

Life‐history strategy,with ctenidial and pallial larval brooding,of the troglodytic ‘living fossil’ Congeria kusceri (Bivalvia: Dreissenidae) from the subterranean Dinaric Alpine karst of Croatia

Among freshwater bivalves, the brooding of embryos and larvae within the maternal ctenidia is well known. Exceptions to this generalization are the non‐brooding freshwater and estuarine species of Dreissena and Mytilopsis, respectively. It was reported that the freshwater troglodytic cousin, Congeria kusceri Bole, 1962, of these dreissenids does not brood either. It is herein demonstrated that C. kusceri undergoes one reproductive cycle each year. Sexes are separate, with an early male and later female bias. A small percentage (2.14%) of individuals is hermaphroditic. The gonads mature over summer from May to November. Spawning commences in September, when females release mature oocytes into their ctenidia and inhale sperm from mature males. Here the oocytes are fertilized, and develop within interfilamentary marsupia. Ctenidial tissues glandularize, and may provide a source of maternal nutrition for the embryos. At the late prodissoconch‐1 or prodissoconch‐2 stage (PR2, ~220 μm), larvae are released into the infrabranchial chamber via a birth channel along the outer edge of the ventral marginal food groove of both inner demibranchs. Here, they are brooded further in mantle pouches located beneath the inhalant siphon. Subsequently, after the PR2 stage (nepioconch/dissoconch), they are released from the inhalant siphon and assume an independent life as crawling juveniles. Such juveniles may be found amongst clusters of adults. Not only is C. kusceri unique amongst the Dreissenidae in possessing the capacity to brood internally fertilized ova, but it is also exceptional amongst the Bivalvia in possessing the described methods of brooding and birth. Explanations for both lie in its troglodytic lifestyle, decadal length longevity and habitat: that of byssal attachment to the hard surfaces of underground freshwater rivers, caves, pits, and sinkholes in the Tethyan arc of the Dinaric karst. Internal fertilization of a few large yolky eggs, lecithotrophic larvae, ctenidial brooding, and secondary pallial parental care represent relatively recent, Late Miocene, evolutionary adaptations from a Tethyan lentic ancestor.     

Observations on the ciliary feeding mechanism of the brachiopod Crania anomala

In young Crania anomala with a trocholophe or an early schizolophe one inhalant current enters the anterior gape, filters past the single bell-shaped cirrous basket and spills out diffusely as exhalant current both anteriorly and laterally. Late schizolophe or early spirolophe forms two separate cirrous baskets which produce two separate inhalant currents: the exhalant current still diffuses out anteriorly and laterally. In later stages either one single exhalant current comes out at the anteromedial region, or three exhalant currents, including an additional one at each posterolateral region.
The roof of the visceral cavity is attached in five places to the dorsal valve of Crania to form a mantle recess, an anterior passage and two lateral passages. A hole bored through the dorsal valve into the mantle recess or the anterior passage lets out exhalant current. The palaeobiological significance of this lies in the possible use of the hole in the perforate shell valve of the siphonotretid fossil inarticulate Schizambon australis as an exhalant opening. In this species the hole leads into the mantle recess, which also communicates via a lateral passage with each posterolateral part of the mantle space.     

The nucleus of the posterior pallial commissure in Lacerta sicula (Rafinesque) and its ontogenetic connection to the thalamus]

The nucleus of the posterior pallial commissure of Lacerta sicula originates between the 11th and 18day of incubation. During this time, the developing nucleus shows a distinct and wellformed cellular connection with the rostral, dorsally lying ventral thalamus. The whole connecting nuclear mass lies close to the matrix of the diencephalic and telencephalic ventricle and the connecting foramen interventriculare. It is evident that cells which originate from the the ventral thalamus are possibly delivered to the telencephalic nucleus of the posterior pallial commissure. The cellular connection between thalamus and hemisphere ruptures between the 18th and 19th day of incubation as a result of growth displacement and is no longer visible in later stages.     

The pallial organ of Atrina pectinata (Bivalvia: Pinnidae): its structure and function

Hitherto, the unique pallial organ of the Pinnidae has been considered to fulfil a cleansing role, removing sediment and shell fragments from the mantle cavity. This study of the pallial organ of Atrina pectinata describes structure in greater detail than before but was unable to demonstrate a cleansing function. Rather, the organ is thigmotropic and massively secretory. Study of the pallial organ head demonstrates it to have a pH of between 2 and 4 and that tall, apparently empty cells in the head epithelium contain sulphuric acid which can be precipitated as barium sulphate crystals following irrigation with barium chloride.
Acid-secreting cells are recorded from a number of animal groups, notably opisthobranch gastropods, where they are concluded to possess a defensive function. Such a structure has not hitherto been recorded from the Bivalvia.     

The sorting of food particles by Abra sp. (bivalvia: tellinacea)

The selection of food particles by Abra tenuis (Montagu), A. alba (Wood) and A. nitida (Müller) has been investigated.Material for ingestion smaller than 30μm is not selected according to size by A. tenius. Particles smaller than 0.5 μm are retained by the palliai organs and ingested but only particles larger than 1 μm appear to be retained with an efficiency approaching 100 %. The mesh size of the gill filter is found to be ≈ 3.0 × 0.5 μm.A. tenuis does not appear able to discriminate between particles smaller than 20 μm by their food value; however, relatively large silica particles which are devoid of food are partially rejected by the labial palps in favour of particles of similar size but having a bacterial coating. To a lesser extent the physical nature of particles seems to influence their selection by A. tenuis; clean angular particles are rejected in favour of clean rounded ones.Small, light particles appear to be transported on the gills directly to the mouth without coming into contact with the palps. Larger, heavier particles tend to drop from the gill to be caught by the palps which extend posteriorly to cup the entire ventral margin of the inner demibranch when the animal is feeding.The material ingested by A. alba is significantly finer than that taken into the mantle cavity indicating that the pallial organs actively select food by size. Selection of material for ingestion by size in A. nitida appears to be optional since only some of the animals examined had stomach contents significantly finer than material from the mantle cavity.     

Recent bivalve molluscs of the genus Calyptogena (Vesicomyidae)

The genus Calyptogena (Bivalvia: Vesicomyidae) comprises highlyspecialized bivalves living in symbiosis with sulphur-oxidizingbacteria in reducing habitats. In this study, the genus is revisedusing shell and anatomical features. The work is based on typematerial, as well as on the extensive collection of vesicomyidsobtained during twelve expeditions to the Pacific and IndianOceans. Nine Recent species are ascribed to the genus Calyptogena,four of which are new: C. pacifica Dall, 1891, C. fausta Okutani,Fujikura & Hashimoto, 1993, C. rectimargo Scarlato, 1981,C. valdiviae (Thiele & Jaeckel, 1931), C. gallardoi Sellanes& Krylova, 2005, C. goffrediae n. sp., C. starobogatovin. sp., C. makranensis n. sp. and C. costaricana n. sp. Thecharacteristic features of Calyptogena are: shell up to 90 mmin length, elongate-elliptical or elongate; presence of escutcheon;presence of broad posterior ramus (3b) of right subumbonal cardinaltooth as well as right posterior nymphal ridge; absence of pallialsinus as a result of attachment of intersiphonal septal retractorimmediately adjacent to ventral surface of posterior adductor;absence of processes on inner vulva of inhalant siphon; presenceof inner demibranch only, with descending and ascending lamellaewith interlamellar septa not divided into separate tubes. Themost closely related taxa to Calyptogena are probably the genusIsorropodon Sturany, 1896, and the group of species representedby ‘Calyptogena’ phaseoliformis Métivier,Okutani & Ohta, 1986. These groups have several charactersin common, namely absence of pallial sinus, presence of singleinner pair of demibranchs and absence of processes on innervulva of inhalant siphon. The worldwide distribution of thegenus Calyptogena suggests that methane seeps at continentalmargins are the major dispersal routes and that speciation waspromoted by geographical isolation. Recent species diversityand fossil records indicate that the genus originated in thePacific Ocean. Sufficient data to discuss the distribution atspecies level exist only for C. pacifica, which has a remarkablynarrow bathymetric range. Published studies on the physiologyof C. pacifica suggest that adaptation to a specific geochemicalenvironment has led to coexisting vesicomyid genera. The bacteria-containinggill of C. pacifica and other Calyptogena species is one ofthe most specialized in the family Vesicomyidae and may reflectthese ecological adaptations. (Received 23 December 2005; accepted 3 April 2006)     

Influence of diet on pre-ingestive particle processing in bivalves: II. Residence time in the pallial cavity and handling time on the labial palps

Previous studies have demonstrated that bivalve molluscs respond to changing food conditions through processes such as preferential selection and ingestion of particulate matter. Little is known, however, about the underlying mechanisms accountable for these responses. To further explain feeding processes at the level of the pallial organs, we determined pallial cavity residence times, or the amount of time it took particles to travel from the inhalant aperture to the stomach, in two species of bivalves, Crassostrea virginica and Mytilus edulis, under conditions of differing particle quality, particle concentration, and temperature. From these residence times, particle-handling times on the labial palps were determined. Diets of three different qualities were tested, including Rhodomonas lens cells, particles prepared from ground Spartina sp. detritus, and a 50/50 mixture of both. Bivalves were delivered one of the three diets along with 10-μm fluorescent polystyrene beads (tracer), removed from feeding chambers at intervals from 30 s up to 20 min, and placed in liquid nitrogen to halt particle transport. Digestive systems of bivalves were then dissected and examined for the presence of tracer beads. Particle-residence times in the pallial cavity and handling times on the labial palps of C. virginica were significantly affected by changes in diet type. Particle-handling times on the palps decreased with increasing diet quality and ranged from 2.2 min (100% R. lens) to 22.8 min (100% ground Spartina sp.), accounting for 88% and 99%, respectively, of the total time particles spent in the pallial cavity. In contrast, diet quality had little effect on particle-residence times in the pallial cavity of M. edulis. However, residence times were affected by temperature and diet concentration. Temperature significantly affected residence times at particle concentrations of both 20 and 100 particles μl⁻¹, whereas particle concentration affected residence times at 20 °C, but not at 5 °C. Particle-handling times on the labial palps ranged from less than 1 to 5.5 min, depending on temperature and concentration, accounting for 50% to 82%, respectively, of the total time particles spent in the pallial cavity. We suggest that (1) observed interspecific differences in particle handling on the labial palps may be due to differences in palp morphology and function, and (2) particle sorting and selection on the labial palps is a rate-limiting step of pre-ingestive feeding processes in by bivalves.     

Morphology and biology of Polysaccus japonicus (Crustacea, Rhizocephala, Akentrogonida, Polysaccidae, fam. n.), a parasite of the ghost-shrimp Callianassa japonica

The morphology and biology of Polysaccus japonicus Høeg & Lützen, 1993 is described. Nearly all infected hosts are adults, the females of which become castrated. Each bears 4–50 (female) externae on the underside of the abdomen. The externae are interconnected via a root system within the host's perineural blood sinus. The externae pass through three moults. Cypris larvae inject spermatogonia into the immature externa's mantle cavity, which is where spermiogenesis occurs later. Multiplication of the male cells is probably supported by secretion from paired mantle cavity glands, presumably homologous to the receptacles of kentrogonid rhizocephalans. Late during the 2nd intermoult the visceral mass ruptures to release the ova into the mantle cavity where they become fertilized. The third moult results in opening of the mantle aperture which initiates a period of vigorous peristalsis of the muscular mantle. Following emission of the cypris larvae the externae perish leaving distinct scars. The root system always contains buds of various sizes and stage of development. When the scarred host moults, the most advanced buds emerge to give rise to a new generation of externae. This is thought to be repeated for the rest of the host's life.
The antennule of the cyprid has a relatively very long and slender 3rd segment, a unique construction among Akentrogonida. Because of this and the presence of special mantle cavity glands, a new family, Polysaccidae, is erected, which in some characters is intermediate between the Kentrogonida and the Akentrogonida.     

Interhemispheric connections through the pallial commissures in the brain of Podarcis hispanica and Gallotia stehlinii (Reptilia,Lacertidae)

The cells-of-origin and the mode and site of termination of the interhemispheric connections passing through the anterior and posterior pallial commissures in the telencephalon of two lizards (Podarcis hispanica and Gallotia stehlinii) were investigated by studying the anterograde and retrograde transport of unilaterally injected horseradish peroxidase. The commissural projections arise mainly from pyramidal cells in the medial, dorsomedial, and dorsal cortices (medial subfield). Additionally some non-pyramidal neurons in the medial and dorsal cortices contribute to the commissural system. Medial cortex neurons project to the contralateral anterior septum through the anterior pallial commissure. The dorsomedial cortex projects contralaterally via the anterior pallial commissure to the dorsolateral septum and to the medial, dorsomedial, and dorsal cortices. The projection to the medial cortex terminates in two bands at the inner and outer border, respectively, of the cell layer; the projection to the dorsomedial and dorsal cortex ends in a zone in layer 1 which previously has been described to be Timm-negative, and in a diffuse band in the inner half of layer 3. The medial subfield of the dorsal cortex projects through the anterior pallial commissure to the dorsomedial and dorsal cortices with a similar pattern of termination to that found for the dorsomedial cortex. The posterior pallial commissure contains only the projections from the ventral cortex to its contralateral counterpart and to the ventral part of the caudal medial cortex. The similarities found between this commissural system and the mammalian hippocampal interhemispheric connections are discussed.     

Stacking Increments: A New Model and Morphospace for the Analysis of Bivalve Shell Growth

A model employing stacking increments is introduced for the analysis of bivalve shell growth and form. The model is based on the components of shell growth that are potentially independent: the rate of mantle cell proliferation, the rate of precipitation of shell material, and the rate of translation of the pallial line, where the mantle is attached to the shell. This model is defined in terms of the following parameters: (1) the ratio of accretion of shell material at the shell margin to growth of the mantle by cell division, (2) the ratio of shell accretion at the pallial line to mantle growth, and (3) the ratio of the amount of pallial muscle translation, away from the umbo toward the shell margin, to mantle growth. In this model, the shape of a radial section through the shell is simulated by stacking of internal microgrowth increments. The mode of stacking of the increments is determined by the balance among the parameters defining growth. A theoretical morphospace defined on the basis of this model is largely consistent with the range of forms of naturally occurring bivalve shells. Analysis of the distribution of actual shell forms in relation to this morphospace suggests that the absolute rate of shell precipitation and the gradient in precipitation rate away from the shell margin along a radial cross-section are physiologically as well as geometrically constrained.     

Comparison of the mammalian and avian telencephalon from the perspective of gene expression data.

Pallial and subpallial morphological subdivisions of the mouse and chicken telencephalon were examined from the new perspective given by gene markers expressed in these territories during development. The rationale of this approach is that common gene expression patterns may underlie similar histogenetic specification and, consequently, comparable morphological nature. The nested expression domains of the genes Dlx-2 and Nkx-2.1 are characteristic for the subpallium (lateral and medial ganglionic eminences). Similar expression of these markers in parts of the mouse septum and amygdala suggests that such parts may be considered subpallial. The genes Pax-6, Tbr-1 and Emx-1 are expressed in the pallium. Complementary areas of the septum and amygdala shared expression of these genes, suggesting these are the pallial parts of these units. Differences in the relative topography of pallial marker genes also define different regions of the pallium, which can be partially traced into the amygdala. Importantly, there is evidence of a novel "ventral pallium" subdivision, which is a molecularly distinct pallial territory intercalated between the striatum and the lateral pallium. Its derivatives in the mouse apparently belong to the claustroamygdaloid complex. Chicken genes homologous sequence-wise to these mouse developmental genes are expressed in topologically comparable patterns during development. The avian subpallium -the paleostriatum- expresses Dlx-2 and Nkx-2.1; expression extends as well into the septum and anterior and medial parts of the archistriatum. The avian pallium expresses Pax-6, Tbr-1 and Emx-1 and also contains a distinct ventral pallium, formed by the neostriatum and ventral intermediate parts of the archistriatum. The lateral pallium comprises the hyperstriatum ventrale, overlying temporo-parieto-occipital corticoid layer and piriform cortex, plus dorsal intermediate and posterior archistriatum. The dorsal pallium includes the dorsal, intercalated and accessory hyperstriatum, plus the dorsolateral corticoid area. The medial pallium contains the hippocampus and parahippocampal area. A dorsal part of the septum shares pallial molecular markers. Gene markers thus suggest common sets of molecular developmental determinants in either pallial or subpallial domains of the mouse and chicken telencephalon, extending all the way from the posterior pole (amygdala) to the septum. Ventral pallial derivatives identified as claustroamygdaloid in the mouse correlate with avian neostriatum and parts of the archistriatum.     

SOME BEHAVIOURAL AND ELECTRICAL RESPONSES OF SCROBICULARIA PLANA (BIVALVIA:TELLINACEA) TO SIPHONAL WOUNDING

Water pumping, valve movements and heart rate have been recordedfrom Scrobicularia for short periods of normal behaviour andthen after siphonal wounding. Scrobicularia exhibits regularand repetitive pumping periods interrupted for only 2–3s after siphonal wounding, without the regularity of these periodsbeing affected. Wounding does not prevent animals from usingtheir inhalant siphons for deposit feeding. A preliminary investigationof neural responses to stimulation has shown that wounding thesiphon causes minimal disturbance to the animal, a brief (2s)burst of nerve activity occurs, the siphon is retracted, butvalve adduction does not occur. In contrast to this tactilestimulation of the mantle edge always elicits a large burstof impulses in the posterior adductor nerve, valve closure results,usually for 14–15 s. ¹Present address: Dept of Zoology, University of Cape Town,Rondebosch 7700, South Africa. (Received 2 February 1981;     

How the 'forceps' of Lithophaga aristata (Bivalvia: Mytiloidea) are formed

The calcareous substratum borer, Lithopaga aristata Dillwyn, 1817, secretes posterior incrustations that take the form of interlocking 'forceps'. These are secreted, initially, as asymmetrical ridges by similarly asymmetrical dorsal and ventral glands in the left and right middle folds of the posterior mantle lobes. In the adult, the secretions are more uniformly spread over the posterior shell margins, concealing the juvenile ridges.
Opening and closing of the valves smooths the outer surfaces of the 'forceps' against the burrow wall, which also comes to be lined with calcium carbonate that is reciprocally smoothed, so that they occlude the borehole more effectively. Extension and retraction of the siphons probably smooths the inner surfaces of the 'forceps' which are sharpened by abrasion, one against the other, during valve opening and closing. The pair of inequilateral spikes so produced, project from the burrow aperture, occluding it, but probably, more importantly, distancing aperturally attacking predators from the true posterior shell margin. Interlocking of the 'forceps' and their sharpness may further deter would-be predators.     

Discovery of ventrally directed spiralia in a Permian spiriferellid brachiopod and implications for its feeding system

Spiralia are lophophore‐supporting, coiled internal structures developed in some extinct brachiopods. In spite of considerable variations in their orientation, the spiralia of most spiriferide and spiriferinide taxa are known to be laterally directed. Recent studies have shown that these brachiopods consistently have a median inhalant and lateral exhalant feeding system. Here, we report a Permian spiriferellid brachiopod fossil (Spiriferella protodraschei) bearing ventrally directed spiralia in its interior. Using the serial sections of the specimen, we have reconstructed the detailed morphology and orientation of the spiralia. Each spiralium in the specimen does not show the apically tapering pattern supposedly universal in all the known types of spiralia: instead it maintains a similar diameter even at its last whorl. The spiralia appear to have directly developed from strong and anteriorly extended crura, consisting of ten whorls in one side and 13 whorls in the other side. As the morphology and orientation of spiralia are immediately associated with the arrangement of spirolophous lophophore within the mantle cavity, the extraordinary orientation and form of the spiralia indicate that this brachiopod likely had developed a considerably modified feeding pattern with respect to most other spirolophous brachiopods. It is postulated that the inhalant/exhalant current circulation of the species (and its descendants) would be considerably different from that of other spiriferide taxa. In particular, the combination of the vertically oriented life posture (free‐lying with thickened ventral apex bottom) and ventrally directed spiralia resembles both fossil atrypide and modern rhynchonellide brachiopods in the orientation of spirolophe, suggesting that some spiriferellid brachiopods may have developed a lateral inhalant/median exhalant feeding current system. A few spiriferide and spiriferinide brachiopod taxa with a weakly transverse but strongly convex ventral valve are noted to exhibit similar modifications in their spiralia, possibly due to the spatial limitation of their mantle cavities.