Embryogenesis of a springtail,Tomocerus ishibashii (Collembola,tomoceridae): External morphology

The external features of the developing embryos of the springtail, Tomocerus ishibashii, are described. The clypeolabral anlage arises as a single, unpaired swelling. The entognathy is completed by the ventral growth of the tergal anlagen of mandibular, maxillary, and labial segments. These anlagen also form the posterior part of the cranium. The palpi of maxilla and labium are homologous with the telopodites, and proximal parts of these head appendages are homologous with the coxopodites. The sternal element of the labial segment does not participate in the postmentum formation. The anlagen of abdominal appendages appear in the first to the fourth abdominal segments. The first, third, and fourth appendage anlagen form the ventral tube, tenaculum, and furcula, respectively. The fused proximal parts of the first, third, and fourth appendage anlagen are homologous with the coxopodites, and the distal parts which do not fuse are homologous with the telopodites. The anlagen of the second abdominal appendages become flattened and spread over the ventral side of this segment. The ventral structures of the first four abdominal segments are appendicular in origin.     

Fine Structure of the Midgut and Hindgut in Lepidocampa weberi (Insecta,Diplura)

The fine structure of the alimentary canal, especially the midgut and hindgut of Lepidocampa weberi (Diplura: Campodeidae) is described. The general organization of the canal is similar to that of Campodea. The midgut epithelium is composed of columnar apical microvillated cells. Each nucleus contains a single intranuclear crystal. Close to the pyloric region, the posterior midgut cells are devoid of microvilli and intranuclear crystals. There is no special pyloric chamber as in Protura or pyloric cuticular ring as in Collembola but a morphological transformation from midgut to hindgut cells. Eight globular Malpighian papillae, consisting of distal microvillated cells and flat proximal cells, open into the gut lumen via ducts formed by hindgut cells. The structure of the hindgut is complicated and can be divided into three segments. The anterior hindgut cells have an irregular shape and compact cytoplasm. A striking interdigitation between the large bottle-shaped epithelial cells and longitudinal muscle cells occurs in the middle segment of the hindgut. The thick cuticle gives rise to long spikes projecting into the gut lumen. The posterior hindgut cells possess the morphological features for water reabsorption. Some hypotheses are advanced about the function of the different regions of the gut.     

The controversial origin of the abdominal appendage‐like processes in immature insects: Are they true segmental appendages or secondary outgrowths? (Arthropoda hexapoda)

In this article, I review the major characteristics of different types of appendage‐like processes that develop at the abdominal segments of many immature insects, and I discuss their controversial morphological value. The main question is whether the abdominal processes are derived from segmental appendages serially homologous to thoracic legs, or whether they are “secondary” outgrowths not homologous with true appendages. Morphological and embryological data, in particular, a comparison with the structure and development of the abdominal appendages in primitive apterygote hexapods, and data from developmental genetics, support the hypothesis of appendicular origin of many of the abdominal processes present in the juvenile stages of various pterygote orders. For example, the lateral processes, such as the tracheal gills in aquatic nymphs of exopterygote insects, are regarded as derived from lateral portions of appendage primordia, homologous with the abdominal styli of apterygotan insects; these processes correspond either to rudimentary telopodites or to coxal exites. The ventrolateral processes, such as the prolegs of different endopterygote insect larvae, appear to be derived from medial portions of the appendicular primordia; they correspond to coxal endites. These views lead to the rejection of Hinton's hypothesis (Hinton [1955] Trans R Entomol Soc Lond 106:455–545) according to which all the abdominal processes of insect larvae are secondary outgrowths not derived from true appendage anlagen. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.     

Embryonic development of the scorpionfly Panorpa emarginata Cheng with special reference to external morphology (Mecoptera: Panorpidae)

The Mecoptera are thought to be one of the most primitive groups in the Holometabola, but their embryology is rarely studied. By means of scanning electron microscopy, we studied the external features of the embryo of the scorpionfly Panorpa emarginata in middle and late development. The embryo remains in the superficial position until hatching. Embryonic development can be divided into 10 stages along with the first‐instar larva. The external features are described from the germ band to the first‐instar larva, with special reference to the components and segmentation of the head, the segmentation of abdomen and the formation of abdominal prolegs. Our results confirm that the head consists of an anterior‐most acron and six trunk segments: the labral, antennal, intercalary, mandibular, maxillary, and labial segments. The labrum is confirmed to derive from the paired appendages. Our observations also provide additional direct evidence that the abdominal prolegs are not serially homologous with the thoracic legs. The presence of the eleventh abdominal segment is clarified. J. Morphol. 2009. © 2009 Wiley‐Liss, Inc.     

Different requirements for l(1)giant in two embryonic domains of Drosophila melanogaster

L(1)giant is a zygotic lethal mutation which affects the embryonic development of both the labial/thoracic segments and a subset of posterior abdominal segments. Using antibodies specific for proteins encoded by several Drosophila genes to identify the compartmental origin of the defects, we show that the requirement of giant activity is different in these two embryonic domains. Anteriorly, the posterior compartment of the labial segment is missing at the blastoderm stage. Posteriorly, cells are specifically deleted by cell death within the anterior compartments of abdominal segments 5–7 during germ band elongation. In mature embryos, posterior compartment structures of the peripheral nervous system of A5–7 are fused. In addition to a different pattern of defect in the two parts of the embryo, the kind of action appears different. Anteriorly, giant resembles a gap mutation in that a particular region is missing from the blastoderm fate map, whereas in the abdominal domain, giant affects the development of anterior compartment-specific structures.     

Ultrastructure of germination and mucilage production inHalosphaeria appendiculata (Halosphaeriaceae)

The germination of ascospores of the marine fungusHalosphaeria appendiculata was investigated with transmission electron microscopy. Prior to germination, settled ascospores became surrounded by a fibro-granular layer. Small, membrane-bounded vesicles and larger electron-dense membrane-bounded vesicles aggregated at the site of germ tube formation where the plasmalemma adjacent to the aggregation was convoluted. The vesicles appeared to fuse with the plasmalemma, releasing their contents. Enzymatic digestion of the spore wall probably occurred at the time of germ tube emergence. After the nucleus had migrated into the newly formed germ tube, a septum was formed to delimit the germ tube from the ascospore. The growing germ tube can be divided into 3 morphological regions, namely the apical, sub-apical and vacuolated regions, and is typical of other fungi. A mucilaginous sheath was associated with the older mycelium. The germ tube displaced the polar appendage, and the ascospore, germ tube and appendage were enclosed in a mucilaginous sheath. In ascospores which subtended old germ tubes, the nucleus and lipid body became irregular in shape and the cytoplasm was more vacuolated. Microbody-like structures remained associated with the lipid throughout development, and were present in old ascospores.     

Embryonic development of a whirligig beetle,Dineutus mellyi,with special reference to external morphology (insecta: Coleoptera,Gyrinidae)

The egg morphology and successive changes of developing embryos of the whirligig beetle, Dineutus mellyi (Adephaga: Gyrinidae) are described from observations based on light and scanning electron microscopy. The egg surface is characterized by minute conical projections covering the entire egg surface, a stalk‐like micropylar projection at the anterior pole of the egg, and a longitudinal split line along which the chorion is cleaved during the middle embryonic stages. The germ band or embryo is formed on the ventral egg surface, and develops on the surface throughout the egg period; thus, the egg is a superficial type, as is the case in most coleopteran species. A pair of lateral tracheal gills (LTGs) of the first abdominal segment originates from appendage‐like projections arising at the lateral side of pleuropodia, and the LTGs of the second to ninth abdominal segments are arranged in a row with that of the first segment. Therefore, LTGs are structures with serial homology. The paired dorsal tracheal gills (DTGs) of the ninth abdominal segment are formed on the regions just latero‐dorsal to the LTGs of this segment. Regarding the pleuropodia as the structures being homologous with thoracic legs, neither the LTGs nor DTGs are homologous with thoracic legs, but originate in the more lateral region corresponding to the future pleura of the thoracic segments. The last (10th) abdominal segment in the larva is formed by the fusion of the embryonic 10th and 11th abdominal segments. Four terminal hooks at the end of the last abdominal segment originate from two pairs of swellings on the posterior end of the embryonic 11th abdominal segment. It is proposed that the terminal hooks possibly correspond to the claws of medially fused cerci of the embryonic 11th abdominal segment. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.     

Barbronia weberi (Clitellata,Hirudinida, Salifidae) has ovary cords of the Erpobdella type

The organization of the ovaries in representative of the Salifidae (Hirudinida, Erpobdelliformes) was studied at the ultrastructural level for the first time. Like in other leeches, the ovaries of Barbronia weberi are composed of an outer envelope (i.e., an ovisac made up of two coelomic epithelia, muscle cells, and connective tissue) and several internal units, which are broadly similar to the ovary cords found in representatives of the Erpobdellidae. There are usually 6–8 ovary cords that are twisted or cambered with a narrow apical part and a broader, irregularly shaped distal end in each ovisac of B. weberi. Each ovary cord is built from somatic and germ‐line cells and the latter tend to form multicellular cysts that are equipped with a central cytoplasmic core (cytophore). There are two morphologically different subpopulations of germ‐line cells: oocytes and more numerous nurse cells. Growing oocytes form protuberances on the ovary cord surface and eventually detach from the cord and float freely in the ovisac lumen, whereas the other components of germ‐line cysts (i.e., nurse cells and cytophore) degenerate. It should be pointed out that there is a prominent gradient of germ‐cell development along the long axis of the cord. The somatic cells form the ovary cord envelope (the so‐called spongiosa cells) and also penetrate the spaces between germ‐line cells. Both kinds of the somatic cells, that is, those forming the cord envelope and the somatic cells that are associated with oocytes (follicular cells) have a well‐developed system of intercellular channels. Additionally, one prominent somatic cell, the apical cell, was found at the apical tip of each ovary cord. Because the aforementioned features of ovary cords found in B. weberi are very similar (with a few minor exceptions) to the ovary cords that have been described in Erpobdella octoculata and E. johanssoni, we propose the term “ovary cords of the Erpobdella type” for them. Our results support a close phylogenetic relationship between Salifidae and Erpobdellidae. J. Morphol. 275:479–488, 2014. © 2013 Wiley Periodicals, Inc.     

The embryonic development of Stylops ovinae (Strepsiptera,Stylopidae) with emphasis on external morphology

External features of the embryonic development of Stylops ovinae (Strepsiptera) were examined. Eighteen distinct embryological stages are suggested. Many embryological traits are closely correlated to the parasitic life style of the first instar larvae or to vivipary. The high number of eggs, their small size, the characteristic egg membrane, and the lack of micropyles are derived groundplan features of Strepsiptera. The development with a semi-long germ embryo is shared with several other groups of Holometabola. The reduction of the labrum and antennae are autapomorphies of Strepsiptera. The cephalic ventral plate of the first instar larva of S. ovinae is formed by parts of the head capsule and the anlagen of the maxillae and labium. It is involved in the formation of the specific entognathous condition, and the entire character complex is autapomorphic for Stylopidae. The trochanter is recognizable in the anlagen of all three legs. Its fusion with the femur in the later stages is an autapomorphy of Stylopidia. The extreme spiralization and compression of the abdomen during blastokinesis is a derived feature, like the reduction of the anlagen of the anterior abdominal appendages. The caudal bristles on segment XI are possibly re-activated cerci. The same is likely in the case of segment XI.     

Sequence of mitochondrial DNA cytochrome oxidase II inCryptopygus nanjiensis and Phylogeny of Apterygota

The mitochondrial cytochrome oxidase II (Co II) from four different apterygotensCryptopygus nanjiensis (Collembola),Neanura latior (Collembola),Gracilentulus maijiawensis (Protura) andLepidocampa weberi (Diplura) were sequenced. Their A+T content, number of nucleotide substitutions, TV/TV ratio, and Tamura-Nei’s distance were calculated. A series of phylogenetic trees were constructed by parsimony and distance methods using a crustaceanArtemia franciscana as outgroup. Finally the evolutionary trend A+T content of CO II genetic divergence and phylogenetic relationship of apterygotan groups were discussed.     

A scanning electron microscopy study of the embryonic development of Pycnogonum litorale (Arthropoda,Pycnogonida)

The phylogenetic position of the enigmatic Pycnogonida (sea spiders) is still controversial. This is in part due to a lack of detailed data about the morphology and ontogenesis of this, in many aspects, aberrant group. In particular, studies on the embryonic development of pycnogonids are rare and in part contradictory. Here, we present the first embryological study of a pycnogonid species using scanning electron microscopy (SEM). We describe the late embryogenesis of Pycnogonum litorale from the first visible appendage anlagen to the hatchling in 11 embryonic stages. The three pairs of appendage anlagen gain in length by growth, as well as by extension of furrows into the embryo. The opening of the stomodaeum is located far in front of the anlagen of the chelifores and has a Y‐shaped lumen from the onset. During further embryogenesis, the position of the mouth shifts ventrally, until it is located between the chelifores. The proboscis anlage grows out as a circumoral wall‐like structure, which is initially more pronounced ventrally. Hypotheses about the evolution of the proboscis by fusion of originally separated components are critically discussed, because the proboscis anlage of P. litorale shows no indications of a composite nature. In particular, a participation of post‐cheliforal elements in proboscis formation is rejected by our data. Further, no preoral structure and no stage in proboscis formation was found, which could plausibly be homologized with the labrum of othereuarthropods. Thus, our study supports the assumption of a complete lack of a labrum in Pycnogonida. J. Morphol., 2010. © 2010 Wiley‐Liss, Inc.     

Abdominal segment formation in Spirorbis moerchi (Polychaeta)

Summary The development of abdominal segments in Spirorbis moerchi (Polychaeta: Annelida) was studied by light and electron microscopy. Abdominal segments develop in strict succession from anterior to posterior. Segmentation is initiated in the mesoderm and is followed by segmentation of the ectoderm. The mesoderm of the abdominal segments arises entirely from pygidial residual mesoderm; inward migration of cells from the pygidial ectoderm to give rise to mesoderm does not occur. The primordial germ cells remain distinct from the residual mesoderm of the pygidial growth region. After several abdominal segments have developed, the primordial germ cells migrate posteriorly from the achaetous region, invade the abdominal segments, and give rise to the retroperitoneal gonads. Abdominal segment formation is discussed in terms of heteronomy, primordial germ cell origin, gonad formation, and development of the circulatory system.     

External features of the developing embryo of the stonefly,Kamimuria tibialis (pictet) (plecoptera,perlidae)

External features of the egg, developing embryo, and first instar nymph of Kamimuria tibialis are described. The embryonic development from the germ disc to the full-grown embryo is divided into 12 stages. The saclike embryonic rudiment is formed by the bending and folding of the germ disc. The embryo first elongates at the egg surface and then sinks into the yolk due to caudal flexure. In the head, four paired protocerebral lobes differentiate and the fourth lobes are thought to be the rudiments of preantennal ganglia. The columnar serosal cells appear at the posterior pole of the egg and they disappear before katatrepsis. The coniform chloride cells occur at the hind margins of the first nine abdominal segments in the full-grown embryo and first instar nymph. Amnion formation in K. tibialis is very similar to that of Allonarcys proteus and the Isoptera. It is proposed that the immersed type of growth pattern of embryos is divided into two subtypes in hemimetabolous insects; one is in the Palaeoptera and Paraneoptera, and the other is in the Plecoptera, Orthoptera, Notoptera, Isoptera, Embioptera, and the blattarian, Periplaneta americana.     

Comparative morphology of the first instar of three species of Metopia Meigen (Diptera: Sarcophagidae, Miltogramminae)

The first instar larva is described for three species of the kleptoparasitic miltogrammine genus Metopia Meigen: M. campestris (Fallén), M. argentata Macquart and M. argyrocephala (Meigen). Using a combination of light microscopy and scanning electron microscopy, the morphology of the cephaloskeleton as well as the general external morphology are extensively documented, and the phylogenetic implications are discussed. Like other species of Miltogramminae, the first instar of species of Metopia possesses a strong labrum and well‐developed mouth‐hooks. Some other features found in Metopia spp. are rare in the Miltogramminae, such as a serrated ventral surface of the tip of the mouth‐hook and the lack of a posterior spiracular cavity. A few larval features apparently unique for species of Metopia have so far been documented: base of mouth‐hook with a lateral arm‐like extension and abdominal segments with transverse furrow ventrally. The body is equipped with longitudinal cuticular ridges on all segments, which may be a subfamily ground‐plan autapomorphy. Marked morphological and behavioural differences are documented between the first instar of M. argentata and that of M. argyrocephala, the adult females of which are otherwise difficult to separate.     

Early embryonic development of the head region of Gryllus assimilis Fabricius, 1775 (Orthoptera,Insecta)

We report our investigations on the embryonic development of Gryllus assimilis, with particular attention to the head. Significant findings revealed with scanning electron microscopy (SEM) images include: (1) the pre-antennal lobes represent the anterior-most segment that does not bear any appendages; (2) each of the lobes consists of central and marginal regions; (3) the central region thereof develops into the protocerebrum and the optic lobes, whereas the marginal region thereof becomes the anterior portion of the head capsule; (4) the initial position of the antennal segment is posterior to the mouth region; (5) appendage anlagen are transitorily present in the intercalary segment, and they later vanish together with the segment itself; (6) a bulged sternum appears to develop from the ventral surface of the mandibular, maxillary and labial segments. Embryonic features are then compared across the Insecta and further extended to the embryos of a spider (Araneae, Chelicerata). Striking similarities shared by the anterior-most region of the insect and spider embryos lead the authors to conclude that such comparison should be further undertaken to cover the entire Euarthropoda. This will help us to understand the embryology and evolution of the arthropod head.     

Die Bildung und Differenzierung des postnauplialen Keimstreifs vonDiastylis rathkei (Crustacea,Cumacea)

Zusammenfassung Die Differenzierung der hinter den Mandibeln gebildeten ektodermalen Querreihen des Keimstreifs vonDiastylis wird beschrieben. 4 dieser Querreihen von Zellen werden nicht durch Ektoteloblasten gebildet, sondern lagern sich direkt als Blastodermzellen aneinander. Dahinter werden 12 Reihen durch Ektoteloblasten gebildet. Die Ektoteloblasten teilen sich zum Schlu\ in die Reihen XIII und XIV. Alle Zellreihen treten in eine Folge von differentiellen Teilungen ein, so da\ die genaue Differenzierung und Musterbildung der Zellen bis zur Bildung von Ganglienanlagen und ExtremitÄtenknospen zellgenealogisch verfolgt werden kann. Die ersten 2 Reihen hinter den Mandibeln, die Reihen (0) und (1), tragen zur Bildung des vorderen und mittleren Teils des 1. Maxillensegments bei. Der hintere Teil des 1. Maxillensegments wird durch die vorderen Zellabkömmlinge der Reihe (2) gebildet. Die 1. Maxille ist aus Zellen von verschiedenen Zellklonen zusammengesetzt, die zur Reihe (1) und (2) gehören. Die 2. Maxille und die Thorakalbeine werden ebenfalls durch verschiedene Zellklone zusammengesetzt.Die Reihen (2) und (3) haben ein Ähnliches Differenzierungsmuster. Die Unterschiede betreffen hauptsÄchlich den extremitÄtenbildenden Bereich. Die Reihe (3) und die erste ektoteloblastisch gebildete Reihe I sowie die folgenden extremitÄtenbildenden Reihen sind in ihrer Differenzierung fast identisch. Die Ganglien bilden sich durch Neuroblasten, welche Ganglienmutterzellen ins Innere abgeben. Die Neuroblasten haben ein kompliziertes Teilungsmuster. Sie können sich auch nach Abgabe von Ganglienmutterzellen Äqual teilen. Die Intersegmentalfurchen laufen schrÄg durch die Abkömmlinge einer Reihe und markieren nicht die genealogischen Grenzen.Die Ergebnisse werden im Vergleich mit anderen Mandibulaten, besonders mit den Insekten diskutiert. Es ergeben sich interessante Ähnlichkeiten und Unterschiede in der Bildung eines morphologischen Differenzierungszentrums und in der Anlage von ExtremitÄtenknospen, von Ganglien und Intersegmentalfurchen.

---

Formation and differentiation of the post-naupliar germ bandm Diastylis rathkei (crustacea, cumacea)II. Differentiation and pattern formation of the ectoderm

Summary The differentiation of ectodermal cell rows arranged on the germ band ofDiastylis behind the presumptive mandibular segment is described. 4 of the cell rows are not budded off from ectoteloblasts, but are formed directly by blastoderm cells. Behind these 4 rows, 12 cell rows are budded off from ectoteloblasts. Eventually, the ectoteloblasts divide to form rows XIII and XIV. All of these cell rows have a fixed sequence of mitoses by which a detailed analysis of the cell-lineage up to the formation of ganglion anlagen and appendage buds is possible. The rows (0) and (1) form the anterior and middle parts of the maxillular segment. The posterior part of this segment is formed by derivatives of the subsequent cell row (2). Thus, the maxillulae are complex structures, composed by cells from different cell clones. The maxillae and the thoracic limbs are complex structures as well. Rows (2) and (3) have a similar differentiation pattern. The differences are mainly found in the appendage-forming parts. The differentiation of row (3) is nearly identical to row I, i.e. the first row budded off from ectoteloblasts, and to the subsequent rows II–VI.Ganglion cells are formed by the division of ganglion mother cells that are budded off from neuroblasts. The neuroblasts have a complicated pattern of divisions. There may be an alternation of unequal and equal mitoses. The intersegmental furrows run in a transverse and slightly oblique plane through the derivatives of one cell row. They do not indicate genealogical boundaries.The results are compared with similar developmental processes in other Mandibulata, especially Insecta. The similarities and differences in the existence of a morphological differentiation center and in the formation of appendage buds, ganglion anlagen, and intersegmental furrows are discussed.

     

The oral apparatus of tadpoles of Rana dalmatina, Bombina variegata, Bufo bufo, and Bufo viridis (Anura)

The morphology and development of the larval oral apparatus of Rana dalmatina, Bombina variegata, Bufo bufo, and Bufo viridis are described and compared using scanning electron microscopy. The species show different arrangements of the mouthparts. The small oral apparatus of R. dalmatina larvae has three labial tooth rows on the upper labium, while there are four tooth rows on the lower labium with a medial gap in row proximal to the mouth. The margins of the oral apparatus are defined by papillae that encircle the lower labium. B. variegata tadpoles have two upper labial tooth rows and three lower labial tooth rows that are uninterrupted, unlike the ones of R. dalmatina. The mouth is encircled by papillae that are larger than those of R. dalmatina. The oral discs of tadpoles of both B. bufo and B. viridis are similar. They are defined by two upper labial tooth rows (the second of which is interrupted by a medial gap) and by three lower tooth rows that differ in lengths in the two Bufo species. Both species develop papillae on the mouth angles and in two rows on the upper labium. Some morphological differences among the oral discs of R. dalmatina, B. variegata, B. bufo, and B. viridis tadpoles can be attributed to phylogenetic differences, but most can be related to their varying feeding habits and/or to their dietary specializations.     

Characterization of abdominal appendages in the sawfly, Athalia rosae (Hymenoptera), by morphological and gene expression analyses

Larvae of the sawfly, Athalia rosae, have remarkable abdominal prolegs. We analyzed the morphogenesis of appendages and the expression of decapentaplegic and Distal-less genes during embryonic development to characterize the origin of prolegs. Proleg primordia in abdominal segments A1–A9 appeared shortly after the inner lobes (endites) of gnathal appendages were formed. These were located on the ventral plates, medioventral to the appendages of the other segments in light of serial homology. Nothing was seen where the main axis of the appendage should develop in abdominal segments. The primordia in A1 and A9 disappeared before larval hatching. Anal prolegs appeared separate from cerci, the main axes of appendages, which were formed temporarily in A11. The expression of decapentaplegic, which reflects the primary determination of appendages, was detected in the lateral juxtaposition with the prolegs. Distal-less was expressed in the main axes of appendages, protruding endites and the cerci, but not in prolegs and anal prolegs or the gnathal endites which do not protrude. These findings suggest a possibility that the abdominal and anal prolegs of A. rosae are outgrowths of ventral plates which derived from coxopodal elements, but not main axes of appendages.     

Expression patterns of the homeotic genes Scr, Antp, Ubx, and abd-A during embryogenesis of the cricket Gryllus bimaculatus

We have studied embryogenesis of the two-spotted cricket Gryllus bimaculatus as an example of a hemimetabolous, intermediate germ insect, which is a phylogenetically basal insect and may retain primitive features. We observed expression patterns of the orthologs of the Drosophila homeotic genes, Sex combs reduced (Scr), Antennapedia (Antp), Ultrabithorax (Ubx) and abdominal-A (abd-A) during embryogenesis and compared the expression patterns of these genes with the more basal thysanuran insect, Thermobia domestica (the firebrat), and the derived higher dipteran insect, Drosophila melanogaster. Although Scr is expressed commonly in the presumptive posterior maxillary and labial segment in all three insects, the thoracic expression domains vary. Antp is expressed similarly in the three thoracic segments, the limbs, and the anterior abdominal region among these three insects. The early Antp expression in the firebrat and cricket obeys a segmental register in all three thoracic segments, while in Drosophila its initial expression appears in parasegments 4 and 6. Ubx is expressed in the metathoracic (T3) and abdominal segments similarly in the three insects, whereas the expression pattern in the T3 leg differs among them. abd-A is expressed in the posterior compartment of the first abdominal segment and the remaining abdominal segments in all three insects, although its posterior border varies among them.     

Embryogenesis of Heliconius erato (Lepidoptera,Nymphalidae): A contribution to the anatomical development of an evo‐devo model organism

This study reports on the embryogenesis of Heliconius erato phyllis between blastoderm formation and the prehatching larval stage. Syncytial blastoderm formation occurred approximately 2 h after egg laying (AEL) and at about 4 h, the cellular blastoderm was formed. The germ band arose from the entire length of the blastoderm, and rapidly became compacted occupying approximately two‐thirds of the egg length. At about 7 h AEL, protocephalon and protocorm differentiation occurred. Continued proliferation of the germ band was followed by penetration into the yolk mass, forming a C‐shaped embryo at about 10 h. Approximately 12 h AEL, the gnathal, thoracic and abdominal segments became visible. The primordium of the mouthparts and thoracic legs formed as paired evaginations, while the prolegs formed as paired lobes. At about 30 h, the embryo reversed dorsoventrally. Approximately 32 h AEL, the protocephalon and gnathal segments fused, shifting the relative position of the rudimentary appendages in this region. At about 52 h, the embryo was U‐shaped in lateral view and at approximately 56 h, the bristles began evagination from the larval cuticle. Larvae hatched at about 72 h. We found that H. erato phyllis followed an embryonic pattern consistent with long‐germ embryogenesis. Thus, we believe that H. erato phyllis should be classified as a long‐germ lepidopteran. The study of H. erato phyllis embryogenesis provided a structural glimpse into the morphogenetic events that occur in the Heliconius egg period. This study could help future molecular approaches to understanding the evolution of Heliconius development.