Mantle canals on brachiopod interareas and their significance in brachiopod classification

Wright, A.D. 1994 10 15: Mantle canals on brachiopod interareas and their significance in brachiopod classification.
Mantle canals have been located on the internal surface of the interareas in several clitambonitacean brachiopod genera. This indicates that, in contrast to the cardinal areas of Recent terebratulides and rhynchonellides, these surfaces were lined with mantle, with no fusion of the mantle lobes at the lateral ends of the hinge line, and the coelomic cavity confined to a median zone at the posterior of the shell. The discovery provides additional support for the view of Jaanusson (1971; Smiths. Contr. Paleobiol. 3 ) that the Beecher (1891) classification has considerable merit, and indicates that the calcareous brachiopods may be subdivided into the three subclasses Craniformea, Protremata and Telotremata. Brachiopoda, classification, Clitambonitacea, interareas, mantle canals, Protremata .     

RHYNCHONELLIFORMEAN BRACHIOPODS WITH SOFT-TISSUE PRESERVATION FROM THE EARLY CAMBRIAN CHENGJIANG LAGERSTÄTTE OF SOUTH CHINA

Abstract:  Cosmopolitan kutorginates, the most abundant Early Cambrian rhynchonelliformean brachiopods, became extinct at the end of the Middle Cambrian. Consequently, any information concerning the anatomy of this peculiar lineage of brachiopods has great phylogenetic significance with regard to their extant relatives for analogies with the stem-group clade. Such data have been supplied from fossils of which the soft parts have been preserved in exceptional detail. A new brachiopod, Kutorgina chengjiangensis sp. nov., from the Early Cambrian Chengjiang Lagerstätte of southern China, is described here. It is the first articulated brachiopod species collected from this deposit. The specimens preserve a set of soft-body parts, i.e. lophophore, digestive tract and pedicle, all previously poorly known in almost all Palaeozoic calcareous brachiopod taxa. The lophophore attains an early spirolophe stage, clearly homologous to that in the coeval lingulids. The digestive tract consists of a mouth, oesophagus, swollen stomach, intestine and a terminal anus. The pedicle protruding between the valves is stout and elongate, with annulated lamellae on the surface, and contains a putative cœlomic cavity. K. chengjiangensis displays the characteristics of the stem group of calcareous brachiopods, and illustrates anatomical similarities between Cambrian phosphatic- and calcareous-shelled brachiopods, thus corroborating that the Brachiopoda are a monophyletic group.     

The first occurrence of a lingulid brachiopod from the Cretaceous of Sergipe,Brazil, with a restudy of ‘<Emphasis Type="Italic">Lingula</Emphasis>’ <Emphasis Type="Italic">bagualensis</Emphasis> Wilckens, 1905 from southern Patagonia

The lingulid brachiopod Lingularia? notialis sp. nov. is described from the upper Turonian (Cretaceous) of the Sergipe Basin in northeastern Brazil. The rare but well-preserved new material shows morphological characters such as muscle scars, mantle canals and a baculate shell structure. In a preliminary note L.? notialis was referred to Lingularia? bagualensis (Wilckens, 1905) from the uppermost Cretaceous of southern Patagonia, a species restudied here and referred conditionally to Credolingula Smirnova in Smirnova and Ushatinskaya, 2001.     

Microborings in Recent brachiopods and the functions of caeca

Microborings in the primary shell layer of Recent brachiopods are clearly seen to avoid endopunctamicroscopic canals pervading the shell fabric and housing papillose extcnlions of the mantle (the caeca). This avoidance confirms the suggestion that the caecal contents inhibit boring organisms (Owen & Williams 1969; Proc. R. Soc. Loud. B, 172 ), and as such the caecum can be considered as an important instrument in protecting the brachiopod shell. A comparison of the relative fecundity of co-habitating impunctate and cndopunctate New Zealand brachiopods provides indirect evidence that the caecum may indeed also function in a nutrient storage capacity. Brachiopods, microborings, primary shell layer, endopuncta, defence, storage.     

The oldest Lingulids of the Siberian Platform: Microornamentation and shell structure

New brachiopod genus of the order Lingulida Sukharilingula with new type species S. luchininae is described from the Lower Botomian (Lower Cambrian) of northwestern Siberian Platform, basin of the Yenisei River, section on the Sukharikha River. The study of the microornamentation and shell structure of the new genus revealed that the initial shell structure of lingulid shells could transform in the course of early diagenesis. The importance of reconstruction of burial conditions of the valves for the reconstruction of posthumous transformations is discussed.     

A soft-bodied lophophorate from the Silurian of England

Soft-bodied taxa comprise an important component of the extant lophophorate fauna, but convincing fossils of soft-bodied lophophorates are extremely rare. A small fossil lophophorate, attached to a brachiopod dorsal valve, is described from the Silurian (Wenlock Series) Herefordshire Lagerstätte of England. This unmineralized organism was bilaterally symmetrical and comprised a subconical body attached basally to the host and partially enclosed by a broad ‘hood’; the body bore a small, coiled lophophore. Where the hood attached laterally, there is a series of transverse ridges and furrows. The affinities of this organism probably lie with Brachiopoda; the hood is interpreted as the homologue of a dorsal valve/mantle lobe, and the attachment as the homologue of the ventral valve and/or pedicle. The ridges are arranged in a manner that suggests constructional serial repetition, indicating that they are unlikely to represent mantle canals. Extant brachiopods are not serially structured, but morphological and molecular evidence suggests that their ancestors were. The new organism may belong to the brachiopod stem group, and might also represent a significant element of the Palaeozoic lophophorate fauna.     

The elkaniide brachiopodVolborthia from the lower ordovician of Baltoscandia

The rare, enigmatic brachiopodVolborthia recurva (Kutorga) is redescribed based on new, well preserved collections from the Lower Ordovician (lower Llanvirn; Oeland Series; Kunda Stage) of Ingria (St. Petersburg district); it is also recorded for the first time from Sweden, where it occurs in the Kunda Stage on the Island of Oland.V. recurva has usually been classified questionably within the order Paterinida, but the shell structure, micro-ornamentation, muscle scars, and presence of a lingulid-type pedicle groove now indicate that it is an aberrant member of the lingulid family Elkaniidae; it is the only known lingulid with a high conical dorsal valve characterised by mixoperipheral growth.     

Morpho-anatomical differences of the Early Cambrian Chengjiang and Recent lingulids and their implications

Since the publication of Darwin's theory of evolution in 1859, lingulids have probably been the most widely quoted examples of arrested evolution. This, to some degree, may be because few anatomical features are impressed either on or inside valves so these may not adequately reflect the extent of change incurred during lingulid evolution. Two lingulid brachiopods, Lingulella chengjiangensis and Lingulellotreta malongensis, from the Early Cambrian Chengjiang Lagerstätte (Yunnan, South China) show preservation of a series of soft parts, notably the lophophores, setae mantle canals and perfectly impressed visceral region, which are vital to understanding the evolution and lifestyle of brachiopods. Analysis of the valve interiors favours the claim that an epifaunal mode of life could be a plesiomorphic state in contrast to the infaunal one of modern lingulids. Based on these fossils, the three‐pseudosiphon formation of setae found in Recent lingulids is proposed to be an apomorphy derived as an adaptation to an infaunal lifestyle. Comparison between the interior of the fossils with that of modern lingulids does little to support the widespread notion that the morphology of this lineage has remained remarkably constant since at least the early Palaeozoic.     

Functional disposition of the lophophore in living Brachiopoda

Emig, C. C. 1992 07 15: Functional disposition of the lophophore in living Brachiopoda.
The shape and disposition of adult brachiopod lophophores relate to in- and excurrent apertures. to the internal water irrigation system, to shell orientation at substratum and to near-bottom currents. The arrangement of the mantle canals and gonads of different lophophores are induccd by water circulation. The trocholophe (2% of living species) is considered as a plesiomorphic character which represents the basic plan of the lophophore, shared by all Lophophorata. Three different types of schizolophe (10%) are represented in terebratuloids, thecidioids and discinids. The spirolophe (19%), characteristic of rhynchonellides and most inarticulate brachiopods, except the schizolophe Pelagodiscus , has evolved divergently into specific arrangements of the mantle canals and gonads. The zygo-plectolophe (67%) is characteristic of most Terebratulida. The ptycholophe (2%) probably evolved independently in Megathlris and the thecidioids. The mesolophe, known in the fossil chonetdceans, is considered to be a primitive zygo-plectolophe. The median brachiopod sulcus increases the efficiency of the excurrent system and is considered as an evolved character but a homoplasy within the brachiopods. The characteristics of Recent lophophore types have to be taken into account when reconstructing the lophophore in fossil forms. Brachiopoda, Lophophorata, lophophore, water system, orientation, evolution .     

Shell Structure And Inferred Growth, Functions And Affinities Of The Sclerites Of The Problematic Micrina

The stratiform laminae of Micrina sclerites originally consisted of rheomorphic successions of monolayers of micrometric–sized, apatitic tablets, presumably interleaved with chitin and glycosaminoglycans (GAGs). Paired laminae enclose slot–like chambers swelling into lobes distally that originally contained GAGs and deposits of spherulitic and prismatic apatite. The laminae are pervaded by apatitic tubes, apparently secreted by microvillous setoblasts and containing, at the surface, chitinous setae. Internal markings suggest that the triangular (sellate) sclerite supported a pair of muscles and the planospiral (mitral) sclerite, a medial muscle and gonadal sacs flanked by a pair of crescentic muscle bases. Both sclerites were secreted by a mantle with a circumferential fold. The sellate and mitral sclerites are homologized with the anterior and posterior shells of Halkieria and could have become the dorsal and ventral valves of the ancestral brachiopod by a sequence of transformations. These include: the folding of the halkieriid body axis; accelerated mixoperipheral growth of the anterior (dorsal) shell to enclose, with the posterior (ventral) shell, a mantle cavity lined with modified ciliated epithelium of the foot; reduction of sclerite–secreting epithelium to the locus of the brachiopod pedicle epithelium; and the anterior (dorsal) spread of gonadal lamellae.     

Blood cells and coelomocytes of the inarticulate brachiopod Lingula anatina

Three cell types are described from the coelomic cavity of the pedicle of the brachiopod Lingula anatina . Erythrocytes are abundant in the blood vessels of the mantle and also occur, in reduced numbers, in the pedicle. Phagocytic amoebocytes, characterized by a variable number of electrondense, homogeneous granules are common in the coelomic fluid of the pedicle. The enigmatic spindle bodies described by earlier authors constitute the most common cell type encountered in the pedicle coelom of aquarium-maintained specimens. The origin of spindle bodies from muscle cells is suggested.     

Development of the pedicle in the articulate brachiopod Terebratalia transversa (Brachiopoda,Terebratulida)

Summary The development of the pedicle in the articulate brachiopod Terebratalia transversa has been examined by electron microscopy. The posterior half of the free-swimming larva comprises a non-ciliated pedicle lobe that contains the primordium of the juvenile pedicle at its distal end. During settlement at five to six days post-fertilization, the pedicle lobe secretes a sticky sheet that attaches the larva to the substratum. As metamorphosis proceeds, the epithelium in the posterior half of the pedicle lobe produces a thin overlying cuticle, and the pedicle primordium develops into a stalk-like anchoring organ. The juvenile pedicle protrudes through the gape that occurs between the posterior margins of the shell valves. A cup-like canopy, called the pedicle capsule, lines the posterior end of the shell and surrounds the newly formed pedicle. The core of the juvenile pedicle is filled with a solid mass of connective tissue. Numerous tonofibrils occur in the pedicle epithelium, and the overlying cuticle consists of amorphous material covered by a thin granular fringe. By one year post-metamorphosis, a body cavity develops anterior to the pedicle. Two pairs of adjustor muscles extend from the posterior end of the shell and traverse the cavity to insert in the pedicle. The connective tissue core of the pedicle in sub-adult specimens lacks muscle cells but contains numerous fibroblasts and collagen fibers. Three regions are recognizable in the connective tissue compartment of the adult pedicle: a subepithelial layer of non-fibrous connective tissue, a central fibrous zone, and a proximal mass of tissue that resembles cartilage.List of abbreviations as adhesive sheet - bc body cavity - bv brachial valve of shell - cf collagen fibrils - ct connective tissue - cu cuticle - di diductor muscle - ec epithelial cell - f fibroblast - fz fibrous zone - g gut - gc granular cell - gd gastric diverticulum - ht hinge tooth - ia interarea of pedicle valve - icl inner cuticular layer - lo lophophore - lu lumen of gut - m mesenchyme - ma mantle - ml mantle lobe - ocl outer cuticular layer - p periostracum - pc pedicle capsule - pce pedicle capsule epithelium - pcl pedicle collar of shell - pcn pedicle connectives - pd pedicle - pe pedicle epithelium - pl pedicle lobe - pv pedicle valve of shell - pzc proximal zone of cartilage-like tissue - s substratum - sel subepithelial layer - t tendon - tf tonofibril - vam ventral adjustor muscle     

A new rhynchonelliform brachiopod Longtancunella with soft-part preservation from the Hongjingshao Formation (Cambrian Stage 3) in Yunnan,South China

Rhynchonelliform brachiopods made their first appearance in early Cambrian, and became a major group within the palaeozoic evolutionary fauna since late Cambrian. Exceptionally preserved fossils from the early Cambrian Lagerstätten provide valuable chances to investigate their phylogeny and ecology. Longtancunella is one of the most interesting early rhynchonelliforms, and has been mainly recovered from the Chengjiang Lagerstätte (Series 2, Stage 3). Here, we report a new rhynchonelliform Longtancunella xiazhuangensis n. sp. from the lower Hongjingshao Formation (upper Stage 3) in Yunnan Province, China. These specimens were well preserved with soft parts, including pinnate mantle canal system and a pedicle. It is identified as a new species based mainly on its difference in shell ornamentations, pinnate mantle canals and pedicle morphology from the type species. Its pedicle looks unusually stout with distinct annulated lamellae on the surface, and reveals crucial evidence in illustrating its ecology and settling strategy as an early marine epifauna. The ecological interaction between L. xiazhuangensis and other marine animals also provides insights into the food web structure in the early Cambrian.     

The development of growth lines on articulate brachiopods

Three types of growth lines are recognised on articulate brachiopod shells: (1) very fine diurnal growth lines formed by calcite increments at the shell margin, (2) seasonal growth lines, formed by inward reflection (doubling back) of the mantle edge, seen as concentric steps on the shell surface and marked by re-orientation of growth vectors evidenced by secondary shell fibres, (3) disturbance lines, formed by abrupt regression of the mantle edge, also seen as concentric steps on the shell surface, but indicated by a dislocation in the shell fabric. Lamellose and spinose ornaments of the sort seen in Tegulorhynchia are essentially genetically controlled. Periodic outgrowths from the outer mantle lobe secrete frills of primary shell that project from the shell surface and form short hollow spines where they cross the radial ornament. In longitudinal section spine formation is seen to involve gradual increase in the rate of secretion of primary shell followed by retraction, and often collapse, of the mantle outgrowth, accompanied by regression. Reflection of the mantle edge usually follows spine formation.     

Differentiation and Growth of the Brachiopod Mantle

Cell differentiation in the mantle edge of Notosaria, Thecidelhnaand Glottidia, representing respectively, the impunctate andpunctate calcareous articulate and chitinophosphatic inarticulatebrachiopods, is described. Comparison of electron micrographssuggests that outer epithelium which secretes periostracum andmineral shell, is separated from inner epithelium by a bandof "lobate" cells, of variable width, exuding an impersistentmucopolysaccharide film or pellicle. The lobate cells alwaysoccupy the same relative position on the inner surface of theouter mantle lobe; but the outer epithelium is commonly connectedwith the inner surface of the periostracum by papillae and protoplasmicstrands which persist during mineral deposition and ensure thatboth shell and attached mantle remain in situ relative to theoutwardly expanding inner surface of the outer mantle lobe.In the prototypic brachiopod, the lobate cells are likely atfirst to have occupied the hinge of the mantel fold but laterto have been displaced into their present position by the rigidoutward growing edge of the mineral shell.     

Intermediary metabolism and shell growth in the brachiopod Terebratalia transversa

Juvenile Terebratalia transversa (Brachiopoda) metabolize carbohydrates in the anterior-most marginal mantle at a rate of 0.46 μM glucose/g/hr (in vitro incubation of mantle in C¹⁴-glucose in a carrying medium of 10^-3 M non-radioactive glucose). The rate declines to 0.18μM glucose/g/hr in full-grown specimens. Carbohydrate metabolism in the marginal (anterior-most) mantle averages approximately 3.7 times greater than metabolism in (a portion of the ‘posterior’) mantle situated between the coelomic canals and the marginal mantle. This ratio remains constant in specimens of all sizes (i.e. an ontogenetic trend in the ratio is absent at p≤ 0.05). Organic acids are not detectable within the mantle (HPLC techniques) even after simulated anoxia (N₂ bubbling during mantle incubation). Glucose metabolism in vitro declines in both the marginal and ‘posterior’ mantles during anoxia and the metabolic ratio between marginal/‘posterior’ mantles becomes 1/1. We found no difference (at p≤ 0.05) in mean metabolic activity or in sue-related metabolic trends among populations from depths ranging between mean sea level and 70 m. However, the activity within the ‘posterior’ mantle was more variable in specimens from 70 m than in those from shallower habitats (10 m - mean sea level). The size of the specimens analyzed was most variable in the groups obtained from the shallowest habitats and least variable at 70 m depth. Our results may help define the energetics of fossil as well as living brachiopod shell growth. Brachiopod shell growth is known to be very slow relative to that of bivalves and our results indicate that this is a result of the animals' slow metabolism. The inflation of the valves in T. transversa is, in part, a function of the high ratio of intermediary metabolism in the marginal vs‘posterior’ mantle (i.e. parallels the relative growth rates at the shell margin vs‘posterior’ areas). We found that the bivalve, Chlamys hastata, which is commonly associated with T. transversa, has a lower ratio of metabolic activities in the ventral/dorsal mantle areas than the brachiopod has in the anterior/posterior. The difference produces a flatter shell in the bivalve in accord with allometric principles. The higher metabolic rate in the marginal vs‘posterior’ brachiopod mantle and its more pronounced decline with anaerobiosis is reflected in the greater definition of growth increments in the outer shell layer. Our results do not support recent generalizations that correlate shell thickness of a wide variety of invertebrates inversely with metabolic rate. Growth rate as determined from width of shell growth increments is a better index of metabolic rate. Although the genetic basis of glucose metabolism is unknown, the observed metabolic variability is consistent with suggestions that populations of marine organisms living in stable offshore environments are genetically more variable but morphologically more uniform than populations from shallow water. Furthermore, our results support suggestions that bivalved molluscs and brachiopods are very different metabolically, but the data are neutral with respect to theories of competitive exclusion of the two taxa throughout geologic history.     

Electron microscopic studies of growth margins of articulate brachiopods

Summary The brachiopod shell is secreted by the mantle epithelium lining the internal surfaces of its two valves. Growth lines, seen on their external surfaces, have been interpreted in terms of mantle regression and transgression from the valve margins. This scanning electron microscope study of the shell microstructure in recent brachiopods confirms these views and shows the skeletal evidence upon which such interpretations can be made. Electron micrographs reveal that from a growth line a plane dips posteriorly into the shell substance along which normal skeletal secretion was interrupted. Commonly a mosaic of secondary fibres, similar to that seen on the inside surface of the valve, is preserved upon this regression plane, most of the inside surface of which is covered by primary shell, usually extending posteriorly well into the secondary shell layer. The regression plane marks the area from which the mantle withdrew and the area over which shell secretion was interrupted. During mantle transgression primary shell was deposited over much of this surface, before the redevelopment of secondary fibres, so that the old internal surface of the valve was preserved as a false mosaic within the shell. In this way it is possible to recognise the extent of mantle regression and to note the position of the primary — secondary shell secreting junction of the mantle at the time when shell secretion was resumed.     

Chemico-structure of the organophosphatic shells of siphonotretide brachiopods

The organophosphatic shell of siphonotretide brachiopods is stratiform with orthodoxly secreted primary and secondary layers. The dominant apatitic constituents of the secondary layer are prismatic laths and rods arranged in monolayers (occasionally in cross-bladed successions), normally recrystallized as platy laminae. Sporadically distributed, interlaminar, lenticular chambers, containing apatitic meshes of laths and aggregates of plates and spherulites, probably represent degraded, localized exudations of glycosaminoglycans (GAGs) with dispersed apatite.
The shells of Helmersenia and Gorchakovia are perforated by canals with external depressions (antechambers) that possibly contained chitinous tubercles in vivo . The immature shell of Siphonotreta and most other siphonotretids is similarly perforated and pitted; but the mature part bears recumbent, rheomorphic, hollow spines that grew forward out of pits. Internally, spines pierce the shell as independent structures to terminate as pillars in GAGs chambers. Spines and pillars were probably secreted by collectives of specialized cells (acanthoblasts) within the mantle.
The shell of the oldest siphonotretide, Schizambon , is imperforate but the ventral valve has a pedicle foramen that lies forward of the posterior margin of the juvenile valve. This relationship characterizes all siphonotretides, suggesting that the pedicle, in vivo , originated within the ventral outer epithelium and not from the posterior body wall as in lingulides.     

Revision of the Lower Cambrian brachiopod Heliomedusa Sun & Hou, 1987

Jin Yugan & Wang Huayu 1992 01 15: Revision of the Lower Cambrian brachiopod Heliomedusa Sun & Hou, 1987. Lethaia , voi. 25. pp. 35–49. Oslo. ISSN 0024–1164.
Fossils referred to Heliomedusa , from the Chiungchussu Formation of Early Cambrian age in Yunnan. are extraordinarily preserved. They were previously considered to represent jellyfish. and have been suspected more recently of being an obolellid brachiopod. A study of the morphology of this genus indicates that it is related closely lo the non-pediculate craniopsids. which occurred from Early Ordovician to Carboniferous time. The soft parts of this brachiopod. such as setae and nerves, which usually are not preserved in fossils also are described. Brachiopoda, Inarticulata, Craniapsidue, anatomy, setae, nervous system, mantle canals, Early Cambrian .