The coeloms in a late brachiolaria larva of the asterinid sea star Parvulastra exigua: deriving an asteroid coelomic model

Morris, V.B., Selvakumaraswamy, P., Whan, R., and Byrne, M. 2011. The coeloms in a late brachiolaria larva of the asterinid sea star Parvulastra exigua: deriving an asteroid coelomic model. —Acta Zoologica (Stockholm) 92 : 266–275. The coeloms and their interconnexions in a late pre‐metamorphic brachiolaria larva of a sea star are described from the series of images in the frontal, transverse and sagittal planes obtained by confocal laser scanning microscopy. A larval, brachial coelom connects with the coeloms of the adult rudiment that lie posteriorly. The connexion is through the anterior coelom, which lies over the head of the archenteron, to the right anterior coelom and then to the left posterior coelom through the ventral horn of the left posterior coelom. The right posterior coelom is a separate coelom. The hydrocoele is on the larval left side separated from other coeloms except for a connexion to the anterior coelom. On the larval right side, the anterior coelom and right anterior coelom connect with the pore canal that opens to the exterior at the hydropore. From these coeloms, we derived an asteroid coelomic model comprising the larval left and right coeloms linked over the head of the archenteron by a common anterior coelom. The asymmetry of the hydrocoele and the left posterior coelom on the left side linked through the common anterior coelom to the right side, with the external opening, translates into the oral and aboral coeloms of the adult stage. The coelomic model has application in the search for morphological homology between the echinoderm classes and the deuterostome phyla.     

Early life history stages of peacock flounder Bothus lunatus (Bothidae) from the western and central tropical Atlantic

Previously unknown larvae and poorly studied metamorphic and postmetamorphic stages of development of peacock flounder Bothus lunatus (Bothidae) with a length of 5.4 to 39.5 mm from the western and central tropical waters of the Atlantic Ocean are described, and their identification is substantiated. Small-and medium-sized larvae of this species (with a length of nearly 10 mm) at stages of pre-and postflexion, like all larvae of the genus Bothus at the corresponding stages of development, have a strongly flattened from the sides, moderately deep, and almost pigment-free transparent body; bear a long anterior ray in the dorsal fin; and have single melanophores in the end part of the body. They differ from larvae of other Atlantic species of the genus known at early stages of development in the shape of the anterior head profile, namely in the presence of a deep notch in front of the eyes. With growth, their body assumes a rounded shape. During metamorphosis of larval B. lunatus, the right eye shifts to the left side of the head through a slit formed during the separation of the origin of dorsal fin base from the cranium. This specific feature distinguishes them from larvae of the remaining species of the genus in which, during metamorphosis, the right eye passes to the left side through the hole in the head.     

Morphology,Morphogenesis and Small Subunit rRNA Gene Sequence of a Soil Hypotrichous Ciliate,Perisincirra paucicirrata (Ciliophora,Kahliellidae), from the Shoreline of the Yellow River,North China

The morphology, morphogenesis, and 18S rRNA gene sequence of a soil hypotrichous ciliate Perisincirra paucicirrata, isolated from north China, were investigated. Perisincirra paucicirrata differs from its congeners in: (1) having a body length to width ratio in vivo of 4:1, (2) its adoral zone occupying between 15% and 25% of the total body length, and (3) the presence of two parabuccal cirri, three left (with 10–16 cirri each) and two right marginal rows (with 14–24 cirri each), and three dorsal kineties. Our study offers a first attempt to begin to map the morphogenetic processes of the genus, which are mainly characterised by the following: the formation of four frontal ventral transverse anlagens for each daughter cell, with the proter's anlage I originating from the reorganised anterior part of the parental paroral; the paroral and endoral anlage developed from the reorganised old endoral and do not contribute the first frontal cirrus; the frontoventral transverse anlage I contributing the left frontal cirrus; anlage II generating the middle frontal and the buccal cirri; anlage III developing the right frontal cirrus and the anterior parabuccal cirrus; and anlage IV contributing the posterior parabuccal cirrus. As an additional contribution, we judge that the inner one or the two right rows of P. kahli and P. longicirrata are marginal rows. Phylogenetic analysis based on SSU rDNA sequences suggests that Perisincirra is related to sporadotrichids, but provides no credible evidence for its taxonomic position.     

The embryonic value of the micromeres in Ilyanassa obsoleta,as determined by deletion experiments. II. The second quartet cells

Summary

Each of the second quartet micromeres of Ilyanassa obsoleta was removed and the effects on larval development analyzed. Structures most often affected by removal of 2a were the left velar lobe, the left eye and the left statolith. Removal of 2b resulted in no consistent pattern of defects. Removal of 2c resulted in atypical shell development, absence of the heart, and eversión of the stomodeum; additional effects noted in some individuals involved the right velar lobe, the right statolith and perhaps the right eye. Anomalous birefringent bodies appeared frequently in the anterior region of the larva, on the right side after removal of 2c, and on the left side after removal of 2a. After removal of 2d the external shell was usually absent or rudimentary, the stomodeum was often everted, and other effects were noted in some individuals. On the basis of the deletion experiments, each second quartet micromere is judged to have a different embryonic value.     

Two New Endozoic Ciliates,Clevelandella lynni sp. n. and Nyctotherus galerus sp. n., Isolated from the Hindgut of the Wood‐feeding Cockroach Panesthia angustipennis (Illiger, 1801)

Two new ciliate species, Clevelandella lynni sp. n. and Nyctotherus galerus sp. n., were discovered in the hindgut of wood‐feeding panesthiine cockroaches. Their morphology was studied using standard methods, and their phylogenetic positions within the order Clevelandellida were determined using the 18S rRNA gene sequences. Clevelandella lynni is characterized by a prominent peristomial projection, a notched left body margin, a tear‐shaped to broadly ovoidal macronucleus, a karyophore attached to the right body margin, and by an adoral zone composed of on average 48 membranelles and extending about 51% of body length. The diagnostic features of N. galerus include a short posterior body projection, a spherical to broadly ellipsoidal macronucleus, a karyophore attached to the right and left body margins, refractile bodies densely packed anterior to the macronucleus, and an adoral zone composed of on average 57 membranelles and extending about 70% body length. The order Clevelandellida was consistently depicted as monophyletic in 18S rRNA gene phylogenies. Nyctotherus galerus was placed in the paraphyletic family Nyctotheridae, as sister taxon to all other Nyctotherus and Clevelandella species isolated from cockroaches. Clevelandella lynni fell in the monophyletic family Clevelandellidae, as sister taxon to C. panesthiae KC139718 but with very poor statistical support.     

Larval development of the invasive charru mussel,Mytella strigata (Bivalvia: Mytilidae)

ABSTRACT

The South American charru mussel, Mytella strigata, was recently recorded in Singapore waters, possibly introduced into Southeast Asia through shipping. The mussels have rapidly spread across estuarine coastal mudflats. Adult mussels were collected, spawned in aquaria and larvae were successfully cultured to the juvenile stage in the laboratory. The larval morphology and development of M. strigata is described in this paper. D-shaped veligers were produced within 20 h of fertilization and were approximately 75 µm in shell length. These larvae were capable of settlement two weeks post fertilization. Given an adequate amount of food, they were able to grow up to 1 mm in shell length within 30 days. The larval shell of M. strigata possesses anterodorsal G2 hinge teeth as distinct wavy ledges, with a pitted resilial ridge clearly evident in the juvenile shell.     

Suttonema delta n. g., n. sp. (Nematoda: Trichostrongylina: Heligmosomoidea) from Oxymycterus rufus (Rodentia: Sigmodontinae) in Argentina

A new nippostrongyline, Suttonema delta n. g., n. sp., is described from the intestine of Oxymycterus rufus (Rodentia: Sigmodontinae) from Argentina, in a host from which trichostrongylid nematodes were hitherto unknown. The new genus is very similar to Stilestrongylus Freitas, Lent & Almeida, 1937 and Malvinema Digiani, Sutton & Durette-Desset, 2003, both parasites of Neotropical sigmodontines, in the features of the caudal bursa (with a pattern of type 1-4, asymmetrical with hypertophied right lobe) and the presence of cephalic structures resembling cuticular cordons. The larval synlophe is also identical to that of Stilestrongylus freitasi Durette-Desset, 1968. The new genus is differentiated by an adult synlophe with few ridges (9-12 at mid-body) of two different types: small, rounded ridges without cuticular support on the dorsal side, and pointed ridges of unequal size on the ventral side and in lateral fields. It is also characterised by the presence of comaretes on the left ventral and ventral fields of the synlophe.     

Loxocaudinae: A new subfamily in the ostracod family loxoconchidae

A new Ostracoda subfamily, Loxocaudinae subfam. nov., separated from the subfamily Loxoconchinae of the family Loxoconchidae with five genera (Loxocauda Schornikov, 1969, Glacioloxoconcha Hartmann, 1990, Phlyctocythere Keij, 1958, Pseudoloxoconcha Müller, 1894 and Sarmatina Stancheva, 1984) is described in the paper. The new subfamily differs from Loxoconchinae Sars, 1926 s. str. by the presence of a compact eye, the absence of an eye tubercle, an originally adont hinge with a tendency to formation of an anterior tooth on the left valve and a posterior one on the right valve, a pronounced caudal process and reduction of fossa-mural sculpture. The volume of the genera that are included in the subfamily is determined. A review of 55 various species and forms mentioned in the literature in open nomenclature, whose taxonomic position has not been determined yet is presented. A total of 45 species close to Loxocauda are attributed to the new subfamily, but proper morphological investigations are necessary for their classification. Ten species that were referred earlier to the genera included in Loxocaudinae are excluded from this subfamily. Issues of functional morphology of Loxocaudinae shells and morphological evolution of their sculpture are considered.     

Embryonic development and endosymbiont transmission mode in the symbiotic clam Lucinoma aequizonata (Bivalvia: Lucinidae)

Summary

Lucinoma aequizonata is a large lucinid clam which lives in reducing mud around 500 m deep. Adults harbor intracellular chemoautotrophic sulfur-oxidizing bacteria in specialized gill cells called bacteriocytes. The embryonic and early larval development of L. aequizonata is described by using light and scanning electron microscopy. Gametes were obtained by injection of 0.2ml of 4 mM serotonin solution in seawater into the posterior adductor muscle. The oocytes, 200 μm in diameter, are surrounded by a glycoprotein capsule which gives to the egg a total diameter of 500μm. The development which occurs at 10°C is slow. The first polar body is detected 2.5 h after contact between sperm and oocytes (T_o+2.5 h), and the first cleavage begins 10 h later (T_o+12.5 h). The following successive cleavages produce a nonciliated morula, then a ciliated gastrula which begins to rotate within the egg-capsule at T_o+4.5 days. At this stage, the first shell pellicle appears on the dorsal side of the embryo. At T₀+8 days, the trochophore larvae develop discrete ciliary bands which constitute the prototroch. Typical straight-hinge veligers, D-shaped larvae, hatch from the egg-capsule 12 days after fertilization. The newly hatched larvae are 240 μm in length and 200μm in height, and the straight hinge 150μm long. To elucidate the symbiont transmission mode, two symbiont-specific primers were designed and used in amplifications by PCR. This primer set was unsuccessful in amplifying symbiont DNA targets from mature gonads, spawned oocytes, eggs, and veligers whereas successful amplifications were obtained from symbiont-containing gill tissues. These data rule out the vertical transmission mode and strongly suggest that the symbionts are environmentally transmitted to the new host generation in L. aequizonata as for all tropical lucinids examined to date.     

Quantitative analysis strengthens qualitative assessment: a case study of Devonian brachiopod species

Species recognition attributed to the brachiopod family Atrypidae is evaluated based on qualitative and quantified morphological characters. I identified two brachiopod species—Pseudoatrypa lineata and Pseudoatrypa devoniana—from a rich assemblage of brachiopods recovered from the middle Devonian Genshaw Formation of the Traverse Group. Qualitative examination suggested that the former had fine-medium-sized ribbing, a narrow hinge line, widened anterior, moderately steep mid-anterior fold, domal shaped dorsal valve, and an inflated ventral valve in contrast to the coarse ribbing, widened hinge line, narrow anterior, gentle mid-anterior fold, arched-shape dorsal valve, and flat ventral valve of the latter. The shell outline appears rounded for P. lineata and elongated for P. devoniana. Quantitative assessment of the morphological characters on the dorsal, ventral, anterior, and posterior regions of the valves of the two species using geometric morphometric and statistical analyses suggests that the morphologies of the two species are considerably different (P  $ \ll $  0.01). Thus, qualitative differences between the two atrypid species were further corroborated by quantitative results. This emphasizes the fact that these two species of Pseudoatrypa were indeed different from each other. This study highlights the necessity of incorporating quantified morphological characters to successfully investigate the taxonomic distinctness of fossil invertebrates to the species level.     

Euplotes raikovi Agamaliev, 1966 (Ciliophora, Hypotrichida) From New Hampshire: Description and Morphogenesis

Euplotes raikovi, an interstitial hypotrich ciliate described once from the Caspian Sea, was isolated from intertidal sand at Rye Harbor, New Hampshire. Specimens were observed in life, and also stained by Corliss’ modification of the Chatton-Lwoff wet-silver technic and by 2 nigrosin methods. Living individuals and those fixed with Parducz's fluid are 43 × 30 (37-50 × 25–35) μm. The AZM has an average length of 27 μm and contains 24–32 membranelles. The anterior part of AZM lies on the ventral face of an apical channel, much as in E. bisulcatus. There are 7 fronto-ventral, 4 transverse, 1 left marginal, and 2 right caudal cirri. An additional small, rounded argentophilic area resembling a cirrus base is evident in silver-stained preparations, but it is barren in virtually 100% of the population. There are 7–8 (usually 7) dorsal ciliary rows with E. patella-type argyrome. The modal number of cilia in rows I-VII are 3-7-9-9-9-10-10. The unique fronto-ventral cirrus pattern is stable and predictable at the time of streak phase. Morphogenetic development indicates that the barren cirrus base is 2/V (Wallengren system), and that it apparently buds from 1/V. The left marginal cirrus and right caudal cirri have different origins.     

Structure and formation of the adventitious tube of the Japanese watering-pot shell Stirpulina ramosa (Bivalvia, Anomalodesmata, Clavagellidae) and a comparison with that of the Penicillidae

Abstract. Stirpulina ramosa is the only extant endobenthic representative of the Clavagellidae and is restricted to the waters of Japan. A single intact adventitious tube of this species has been obtained and its structure is described. The right valve is 16 mm long and located within the adventitious tube. It has an opisthodetic ligament located on resilifers. There are anterior and posterior adductor muscle scars, a thick pallial line, and pallial and pedal gape (right valve only) sinuses. The left shell valve is but 9 mm long and is united into the fabric of the adventitious tube via the intermediary of a shelly saddle. Internally, only the anterior adductor muscle scar and a small element of the pallial line scar are identifiable on the left valve. The posterior adductor and the rest of the pallial line scar (including a pallial sinus) are, remarkably, located on the adventitious tube beyond the shell valve margin. The adventitious tube of S. ramosa is formed in a manner wholly dissimilar from that of Brechites vaginiferus (Penicillidae). In B. vaginiferus, the tube is secreted as a single entity from the general outer mantle surface, including the siphons, covering the body. As a consequence, both shell valves are incorporated into the structure of the tube and the watering pot is bilaterally symmetrical. In S. ramosa, the tube and watering pot are secreted from the mantle margin and surface surrounding and extending from the left shell valve, so that only the left valve is incorporated into its structure. A dorsally derived mantle element is progressively extended over to the right side of the body, meeting a ventrally derived counterpart that passes beneath it, forming a pleat in the calcareous structure of the right side of the tube that they secrete. This pleat extends into the complex of watering‐pot tubules and forms the pedal gape. The watering pot is thus Ω shaped. The ventrally derived mantle element forms a sinusoidal crest on the right‐hand base of the watering pot, creating a pedal gape sinus scar on the right valve. The Clavagellidae radiated widely in the Mesozoic, leaving behind a rich fossil record for Stirpulina. Only S. ramosa, however, has survived until the present. In contrast, the Cenozoic Penicillidae has a poor fossil record, but there is a rich variety of extant endobenthic watering‐pot shells. It has been argued hitherto that the two families represent a remarkable example of convergent evolution. In view of the success of the Penicillidae and thus the endobenthic, tube‐dwelling lifestyle, however, it is hard to understand why Stirpulina has largely died out—even S. ramosa being known by but one or two specimens. A study of the anatomy of S. ramosa might one day answer this question.     

Post-larval and larval shells ofJuranomia Fürsich & Werner 1989, andAnomia Linnaeus 1758 (Anomüdae, Bivalvia)

Post-larval and larval shells ofJuranomia calcibyssata from the Bathonian to Callovian of Poland and RecentAnomia membranacea from the Mediterranean are described and compared to other fossil and Recent members of the family Anomüdae. The stratigraphic range of the monospecific genusJuranomia, which, up to now, was only known from the Kimmeridgian, can be extended to include the Lower Bathonian. The state of preservation of the fossil species allows recognition of an internal aragonitic, branching and complex cross-lamellar shell layer in the post-larval left valve, which previous studies could only assume to be present.Anomia membranacea is a member of theA. ephippium lineage as proved, among other characters, by the presence of an outer calcitic prismatic layer in its right valve. It possesses an anterior pedal retractor in the left valve, which, in the original discussion of the phylogenetic affinities ofJuranomia, was thought to be lacking in species ofAnomia. Consequently, the generaJuranomia andAnomia only differ in two important shell characters: closeness or distance between the three central muscles and thickness of the inner aragonitic shell layer of the left valve. Larval shells ofJuranomia are similar to those of Recent anomiids in shape, size, the presence of a byssal notch in the right valve, and an external sinus and internal shelly process in the left valve. The last three features are parts of a single character which is considered as an autapomorphy of the stem species of the Anomiiudae. The small P I size ofJuranomia calcibyssata suggests a purely planktic-planktotrophic development and thus, high potential of dispersal, just as its modern counterparts. Irrespective of the general similarity in shell size, the mean dimensions of the P II are likely species-specific.     

Biology and functional morphology of a new species of endolithic Bryopa (Bivalvia: Anomalodesmata: Clavagelloidea) from Japan and a comparison with fossil species of Stirpulina and other Clavagellidae

Abstract. A new species of Clavagellidae, Bryopa aligamenta, from Okinawa, Japan, is described. The species is endolithic in living corals, with the left valve cemented to the crypt wall, as in all clavagellids. The free right valve exhibits an unusual growth pattern, with commarginal lines seemingly arising from the posterior valve margin and extending towards the anterior. This results from: (i) progressive anterior erosion of the umbones, probably as a consequence of the boring process; (ii) the apparent migration posteriorly, as the umbones are eroded, of the dorso‐ventral growth axis of the shell; and (iii) enhanced posterior inter‐commarginal growth. Unlike other clavagellid genera and species, however, there is no discernible primary ligament, at least in the adult. It is possible, however, that if a juvenile ligament were present (as in B. lata), it too would be lost as a consequence of antero‐dorsal erosion during boring. To retain valve alignment in the absence of a primary ligament, and possibly upon reaching an adult size, the mantle lays down alternating layers of calcium carbonate and proteinaceous periostracum onto the interior surface of the shell to thicken it, most noticeably marginally and, especially, posteriorly. The two valves are united dorsally, therefore, by thin layers of periostracum that probably exert a minimal opening force. B. aligamenta is, however, further characterised by large adductor, pallial, and siphonal retractor muscles so that the entire animal is encased tightly within an internally strengthened shell within a crypt. Movement must be minimal, blood being pumped into pallial haemocoels to push open the valves and extend the siphons. Despite a suggestion to the contrary, Bryopa is retained in the Clavagellidae, its unusual growth processes resulting from an endolithic life style within living corals. The fossil clavagellid Stirpulina bacillus, from the Pliocene/Pleistocene of Palermo, Sicily, Italy, was, unlike Bryopa aligamenta and other clavagellids, endobenthic, with a long adventitious tube and anterior watering pot superficially similar to species of Penicillidae, another family of the Clavagelloidea. Furthermore, as in all clavagellids only the left valve is fused into the fabric of the tube, the right being free within it. In all penicillids, both valves are fused into the fabric of their tubes. The watering pots of the fossil S. coronata, S. vicentina, and S. bacillus, moreover, are formed in a different manner to that of penicillids, by progressive encasement of the right valve inside the tube. In penicillids, the tube is secreted in a single event from the general mantle surface and the incorporation of both valves into its fabric. The constituent genera of the Clavagellidae thus constitute an example of parallel evolution with members of the Penicillidae.     

Larval development of the shell and the shell gland inMytilus (Bivalvia)

Summary In the newly hatched larva ofMytilus galloprovincialis the larval shell field almost totally invaginates to form a shell gland. Only very few cells remain outside and they meet at one point. Only these cells secrete the pellicle, which in the beginning is protected by the glycocalyx and the microvilli of the surrounding cells. The invaginated cells do not participate in pellicle secretion. The secretion partly passes through infoldings of the apical cell membrane. Mineralization of each valve begins along the hinge line, continues to the valve margins and includes the valve centre.     

Development of the coelomic cavities in larvae of the living isocrinid sea lily Metacrinus rotundus

Coelomogenesis in the isocrinid sea lily, Metacrinus rotundus, is described through the swimming larval stages. After the late gastrula stage, the archenteron separates from the ectoderm to form an archenteral sac, which develops into a dumbbell shape consisting of anterior and posterior lobes, and a middle part connecting both lobes. The anterior and posterior lobes, and the middle part, become separated into an axo-hydrocoel, the left and right somatocoels and an enteric sac, respectively. The hydrocoel forms from the left lower edge of the axo-hydrocoel and becomes separated from the axocoel by the late dipleurula stage, when chambered organs and coelom X bud off from the anterior tip of the right and left somatocoels, respectively. Coelom X does not occur in comatulid crinoids (feather stars), and its fate is unclear. The pore canal extends from the axocoel. The hydrocoel differentiates into a crescent shape at the overtime semidoliolaria stage, a few days after the semidoliolaria becomes competent to settle. Coelomogenesis in M. rotundus is much simpler than in the comatulids and probably represents the ancestral mode of the crinoids. As each portion of the dumbbell sac differentiates almost in situ into each coelom, presumptive fates in the sac are easily followed in M. rotundus.     

Aspects of the biology of the big-handed crab,Heterozius rotundifrons (Decapoda: Brachyura), from Kaikoura,New Zealand

Abstract

From January 1975 to June 1976, samples of Heterozius rotundifrons A. Milne Edwards, 1867 were taken monthly from the intertidal zone at First Bay, Kaikoura Peninsula (42°25′S, 173°42′E). Small crabs (< 8 mm carapace width) were never common; they were either too cryptic to be collected in quantity, or have a different habitat from larger crabs. Ovigerous females were present in all months except February (in both 1975 and 1976), but generally formed less than 50% of the total sample of females each month. The number of newly deposited eggs (0.75×0.81 mm) carried by females increased with increase in carapace width according to the equation y = -1123.56+102.97x (r ² = 0.8213). Egg development lasted 3–5 months, and egg mortality during this period was almost 10%. The overall sex ratio for the 18-month sampling period was 1846 ♀ : 993 ♂, which suggests that females were approximately twice as numerous as males. However, when crabs were sorted into size classes it was evident that the sex ratio was not significantly different from 1:1 in crabs of 6–12 mm carapace width, whereas females significantly (P<0.001) outnumbered males in the 13–21 mm size range. The right and left chela were approximately equal in length in females of all sizes, but the right chela of large males was greatly enlarged compared with the left, and with the chelae of females of comparable carapace width. Increase in the growth rate of the males’ right chela commenced at a carapace width of approximately 11.0 mm. Since the smallest ovigerous female collected also had a carapace width of 11.0 mm, it is concluded that both males and females attain sexual maturity at this size.     

On the taxonomic position of Sciaromium lacustre Herz. & Rich. in Rich.

Abstract

Sciaromium lacustre Herz. & Rich. in Rich. from Peru is misplaced in Sciaromium and a new genus, Richardsiopsis, is erected to accommodate it. Richardsiopsis is considered most closely related to Donrichardsia macroneuron (Grout) Crum & Anderson from Texas on the basis of their similar gametophyte characters including the strong costa, oblong-rhomboidal to linear-flexuose, prorate lamina cells which are partly arranged in pluristratose strands and foliose, suborbicular, broadly rounded at the apex pseudoparaphyllia.     

Major differences in the larval anatomy of the digestive and excretory systems of three Oestridae species revealed by micro‐CT

Oestrid flies (Diptera: Oestridae) do not feed during the adult stage, so they depend on an efficient assimilation and storage of nutrients during their parasitic larval stage. We describe the general morphology and provide volumetric data for the digestive and excretory organs of the three larval instars of the nasal bot fly Oestrus ovis L., using micro‐computed tomography. The size of the digestive and excretory organs greatly increased across larval instars. In all instars, the two salivary glands were remarkably large and formed a ‘glandular band’ by coming together, but without lumina uniting, at their posterior ends. The distal region of the anterior Malpighian tubules was greatly enlarged and full of highly radio‐opaque concretions. Moreover, the anatomy of O. ovis third‐instar larva was compared to that of two species of, respectively, similar and different feeding habits: Cephenemyia stimulator (Clark) and Hypoderma actaeon Brauer. Whereas the general morphology and arrangement of the digestive and excretory systems of C. stimulator was similar to that of O. ovis, some differences were observed in H. actaeon: a swollen anterior region of the midgut, salivary glands shorter and not forming a ‘band’ and anterior Malpighian tubules narrowly uniform throughout their entire length.