A morphometric comparison of dissimilar early development in sibling species of Platynereis (Annelida,Polychaeta)

Summary Early development of Platynereis massiliensis was studied in serial sections of fixed embryos and in living or fixed embryos whose nuclei had been made visible with a fluorescent label. The unfertilized egg is an ellipsoid with three axes of differing length. The longest axis corresponds to the dorsoventral axis of the developing embryo. Egg volume is ten times that in the sibling species, P. dumerilii, mainly due to increased yolk content. The timing and spatial pattern of cleavage were observed from first cleavage to the 62-cell stage. Volumes of the blastomeres, their nuclei, their yolk-free cytoplasm and their yolk were determined from serial sections up to the 29-cell stage. In the P. massiliensis embryo, cell cycles are on average 3.7 times longer than in P. dumerilii; volume proportions among the blastomeres also differ and the macromeres containing the bulk of yolk are particularly large, but otherwise the cleavage patterns, differential segregation of yolk and yolk-free cytoplasm, and the histogenetic fates of the blastomeres are the same as in P. dumerilii. This equivalence of cell lineage and of cytoplasmic segregation mechanisms in both species, maintained in spite of the different appearance of the embryos, suggests functional importance of and selective constraint on these developmental features. The relatively accelerated divisions of the 2d cell line in P. massiliensis may be interpreted as the precocious development of cell lines which give rise to adult structures. Several structures, obviously functional in developing P. dumerilii, have lost their function in P. massiliensis: the egg contains few cortical granules, giving rise to only a moderate egg jelly layer in the zygote; prototroch cells develop cilia, but the heavy embryo is unable to swim; the larva develops three pairs of parapodia but, unlike the corresponding stage in P. dumerilii, is not capable of coordinate locomotion. This loss of motility is related to the brooding habit of the species developing inside the parental tube and is explained as the result of a switch from pelagic to benthic, protected reproduction in P. massiliensis. Offprint requests to: A.W.C. Dorresteijn     

A correlative study of experimentally changed first cleavage and Janus development in the trunk of Platynereis dumerilii (Annelida,Polychaeta)

Summary Among zygotes of Platynereis dumerilii treated with cytochalasin B (CCB) prior to first cleavage, a wide variety of developmental effects were observed. One effect is a delay in the first cleavage. Treated embryos may skip the first or even more than one cleavage cycle and become multinucleated. Once these eggs start cleaving their cleavage plane takes the same position as in synchronously fertilized controls. Accordingly, the first cleavage in embryos having skipped the first normal cleavage cycle is meridional and equal, but their second cleavage is equatorial as in the third cleavage in controls. None of the embryos that were observed to skip early cleavages showed normal organogenesis, but developed into vesicle-shaped embryos with little cytological differentiation. Another effect of CCB treatment is altered blastomere size in those embryos which begin cleaving in synchrony with controls. While the majority of treated embryos followed a normal cleavage pattern, i.e. they cleaved at the right time and inequally, some of them cleaved equally or almost equally (adequally). Most of these embryos showed cleavage defects in subsequent cleavage cycles and became abnormal vesicle-shaped embryos. However, some of these embryos cleaving on schedule and equally or adequally developed into juvenile worms showing complete duplication of urites and parapodial rows (0.3% of all treated eggs) and are described as Janus duplicitates. This means that the occurrence of duplicitates and geometrically altered first cleavage patterns are correlated phenomena. The character and origin of the duplications and the consequences for dorsoventral polarity are discussed.     

Electron microscopical investigations of the intercellular contacts during the early cleavage stages ofLymnaea stagnalis (Mollusca,Gastropoda)

Summary In early cleavage stages ofLymnaea stagnalis, three kinds of intercellular junctions could be distinguished up to the sixth cleavage: intermediate, septate and gap junctions. The first two form junctional belts located on the cell border at the periphery of the embryo. For the purpose of our study we were most interested in gap junctions as they are alleged to be structures that allow cell-to-cell communication. Gap junctions first appear at the four cell stage. Up to the sixth cleavage no difference in the distribution pattern could be found between and within each of the four quadrants of the embryo. Some of the cell tiers along the animal-vegetal axis lack gap junctions either between the blastomeres within the tier or between the blastomeres from adjacent tiers. All gap junctions observed in freeze fracture replicas show plaques with an irregular IMP pattern. The average IMP diameter measures 12 nm (SD±2 nm). In stages fixed after the fifth cleavage, gap junctions are found between micromeres at the animal pole and the central 3D macromere. This is in agreement with the presumed interaction between these cells at this stage. The possibility of a transition of non-functional into functional gap junctions after the fifth cleavage is discussed.     

Chromatin condensation and acrosome development during spermiogenesis of Ensis ensis (Mollusca,Bivalvia)

We describe chromatin condensation and acrosome development during spermiogenesis of Ensis ensis. The overall shape of the mature spermatozoon corresponds to the primitive type. The nucleus is oval and on its superior pole there is an elongated acrosome; the middle piece contains four mitochondria around the centriolar complex. The condensation of the nuclei seems to occur in three steps: first the diameter of chromatin fibers increases slightly from 17 to 20 nm; second, in midspermatids fiber pairs coalesce; and third, the coalescence continues by addition of other fibers until the nuclei become highly compacted. Chromatin changes are related with nuclear protein composition. Small proacrosomal vesicles show two regions of different electron density. At a later stage they fuse to give a single, spherical vesicle in round spermatids, which migrates to the upper pole and transforms into a tapered acrosome (18 μm long) with a central channel filled with finely fibrous material. © 1994 Wiley-Liss, Inc.     

Occurrence of Conchophthirus acuminatus (Protista: Ciliophora) in Dreissena polymorpha (Mollusca: Bivalvia) along the River Shannon, Ireland

Samples of Dreissena polymorpha were collected at several sites along the River Shannon navigation in Ireland, to determine the occurrence and distribution of their obligate host-specific commensalistic ciliate, Conchophthirus acuminatus, in this newly invaded region. Mussels collected by various methods were fixed immediately in 75% ethanol, in which they were later dissected under a stereoscopic microscope, beginning with thorough flushing of the mantle cavity and removal of the gills. One ml of sediment flushed from the mantle cavity and dissection residue of each mussel was examined under a compound light microscope using brightfield, phase-contrast, and differential-interference-contrast optics. Of 180 mussels examined, 125 (69.44%) harbored C. acuminatus. The ciliates were invariably well fixed and easily identifiable in all preparations. Mean sampling intensity for infected mussels was 8.47 ciliates per ml of sediment. Both prevalence and sampling intensity varied between sites, but no pattern was discernible. The present results are consistent with other reports of C. acuminatus being the most widespread and abundant symbiont of D. polymorpha throughout Europe, often occurring where no other symbionts occur. Its occurrence in Ireland indicates introduction of the mussels as adults, since planktonic veliger larvae are not known to harbor ciliates. Following similar reasoning, it is possible that the earlier North American invasion by D. polymorpha included only veligers, since C. acuminatus has not been found on that continent. Using these simple and quick methods, the ciliates could be easily identified and counted to give general comparative data among sites regarding intensity and prevalence. Thus, this method has promise for future efforts to obtain basic information rapidly in newly invaded systems.     

Cleavage and gastrulation of the euphausiacean<Emphasis Type="Italic"> Meganyctiphanes norvegica</Emphasis> (Crustacea,Malacostraca)

According to the Articulata hypothesis the cleavage of arthropods must be derived from spiral cleavage. However, arthropods show a great variety of cleavage modes with a widespread occurrence of superficial cleavage. In the Malacostraca, holoblastic cleavage occurs in some taxa such as Amphipoda, Euphausiacea and Dendrobranchiata. In particular, the cleavage of euphausiaceans has been proposed to be a modified spiral cleavage. The cell lineage of early stages up to blastoderm formation of the euphausiacean Meganyctiphanes norvegica is reconstructed using recent methods of fluorescent staining. Only the oblique angle of the mitotic spindles during the transition from the 2- to the 4-cell stage resembles the spiral cleavage mode. At the 8-cell stage, four cells each form a pattern of two interlocking bands which is preserved until the 122-cell stage. One blastomere is delayed in division and shows an oblique division from the fourth cleavage on. It is the precursor cell of two enlarged and cleavage-arrested cells at the 32-cell stage. At the 62-cell stage, these two cells are surrounded by eight cells following a specific cell division pattern during the subsequent division cycles. The cleavage pattern of M. norvegica occurs in two mirror images. A comparative approach reveals distinct similarities between the early cleavage patterns of Euphausiacea and Dendrobranchiata which are suggested to be homologous. Furthermore, the relationships to non-malacostracan cleavage patterns are discussed. It is shown that the early cleavage pattern of M. norvegica does not offer an example of a spiral cleavage within arthropods.     

The presence of an extracellular matrix between cells involved in the determination of the mesoderm bands in embryos ofPatella vulgata (Mollusca,gastropoda)

Summary In 32-cell stage embryos ofPatella vulgata one of the macromeres contacts the animal micromeres, and as a result is induced to differentiate into the stem cell of the mesodermal cell line. In this study we show the presence of an extracellular matrix (ECM) between these two interacting cell types. The ECM appears to be formed by the micromeres during the 32-cell stage. Staining experiments with alcian blue and tannic acid indicate that in contains glycoconjugates, possibly in the form of proteoglycans. The characteristics of the ECM were examined further by fluorescein isothiocyanate (FITC)-lectin labelling. Of 17 lectins tested, concanavalin A (ConA), succinyl-ConA, LCH-B (Lens culinaris) and PEA (Pisum sativum) showed a positive labelling of the ECM. These results are in accordance with the electron microscopic data. The appearance of the ECM at this specific stage and place suggests that it might play an important role in the induction of the mesodermal cell line.     

Embryonic development in culture of two dasyurid marsupials,Sminthopsis crassicaudata (gould) and Sminthopsis macroura (spencer), during cleavage and blastocyst formation

Embryos of Sminthopsis crassicaudata and Sminthopsis macroura were cultured for up to 96 hours during cleavage and early expansion of the blastocyst in Dulbecco's modified Eagle's medium (DMEG), DMEG containing 2.76 gm/liter sodium lactate (DMEGL), DMEG containing 3.5 gm/liter galactose (DMEGAL), DMEG containing 15 ng/ml progesterone (DMEGP) or 150 ng/ml progesterone (DMEGP10), and DMEGL containing 15 ng/ml progesterone (DMEGLP). The disappearance of sperm was used to indicate the time of ovulation (day 0). Fertilized eggs were found in the uterus at the end of day 1, four-cell stages at the end of day 2, and embryos completing the fourth division by the end of day 3 in S. macroura and day 4 in S. crassicaudata. Estimated developmental times in culture were similar to those obtained in vivo. In both species, the first two divisions take about 24 hours, cleavage is arrested for 24 hours or longer at the rounded four-cell stage, and the third and fourth divisions take a further 24 hours. The blastocyst expands during the next 24 hours in which time the fifth and sixth divisions occur. It was possible to culture embryos from S. macroura but not S. crassicaudata over the four-cell stage to early expanding blastocysts. DMEGAL did not support cleavage in culture. DMEG, DMEGL, DMEGP, DMEGP10, and DMEGLP all supported culture during cleavage and early blastocyst expansion. Blastocyst expansion was slightly enhanced using media containing sodium lactate. More embryos completed the fifth division and formed expanding blastocysts in DMEG, DMEGL, and DMEGLP.     

The formation of the pronuclei and their associated perinuclear cytoplasm; the determination of the phases of the first cleavage cycles in Crepidula fornicata (Mollusca,Gastropoda)

Summary

The behaviour of the male and the female pronuclei in Crepidula fornicata is studied, beginning at the formation of the second polar body. Shortly after the extrusion of the second polar body the female pronucleus is formed, and then the male pronucleus enters the yolk-free cytoplasm near the animal pole. Both pronuclei are enveloped by a typical nuclear membrane, and increase in size until the prophase; a zygote nucleus is not formed (“Ascaris type” of fertilization). In the meantime, the chromatin of both pronuclei is arranged in a meshwork in the centre of the pronuclei.

Shortly after the formation of the second polar body a special cytoplasm, the “perinuclear cytoplasm”, is formed in the vicinity of each of the pronuclei. During the early stages of the first cleavage cycle this cytoplasm is composed of numerous Golgi complexes, small dense Golgi vesicles, smooth endoplasmic reticulum vesicles, mitochondria and rosettes of glycogen-like granules. At later stages, when the pronuclei have met and their plasms coalesced, the number of Golgi elements decreases; at the same time, the small dense Golgi vesicles increase in number and aggregate in clusters.

The phases of the first three cleavage cycles are determined by cytophotometry. The nuclear DNA of the male pronucleus and that in the nuclei of the blastomeres of the 2- and the 4-cell stage is reduplicated between 7 and 33% of the normalized cleavage cycles; the G₂-phase is between 33 and 57%, while the mitotic phase occupies the last part of each cleavage cycle and the first 7% of the next cleavage cycle. There is no G j-phase. Since the female pronucleus lies just beneath the polar bodies, its DNA content could not be measured separately.     

Fertilization,post-fertilization development and larval biology of the South African polychaete,Arenicola loveni loveni (Kinberg 1866)

Summary

Larval development in the South African polychaete Arenicola loveni loveni is described, and the effects of seawater temperature on fertilization success, post-fertilization development and early post-settlement survivorship are experimentally determined. Fertilization success was significantly effected by seawater temperature, with maximum fertilization success measured in the range 15–18°C, which is close to the ambient temperature range at the time of natural spawning. Poor fertilization success and abnormal cleavage were observed at the low temperature treatment of 7°C and the high temperature treatment of 23°C. A. loveni loveni exhibits spiral cleavage typical of polychaetes and has a short lecithotrophic swimming trochophore larval stage of 4–5 days. High mortality was noted during the transitional periods from gastrula-trochophore and during the settlement process. Settlement occurs just 4–5 days post-fertilization and the postsettlement stage begins feeding 1 week post-fertilization. Temperatures in the range 16.5–23°C were found to have a significant effect on larval and post-larval survivorship and growth rate increased with temperature within this range. The effects of manipulating spawning date on subsequent offspring survival and development rates were also investigated. Advancing or delaying spawning time caused reduced development rates, and delaying spawning for 3 months was found to significantly reduce offspring survivorship.     

Novel reproductive modes in freshwater clams: brooding and larval morphology in Southeast Asian taxa of Corbicula (Mollusca, Bivalvia, Corbiculidae)

While the majority of marine bivalves are oviparous, the two freshwater families among the order Veneroida, i.e. Corbiculidae and Sphaeriidae, comprise species with ovoviviparous and viviparous reproduction. Within the Corbiculidae, the genus Corbicula, which is well‐known for its invasive and, thus, ecologically important representatives, is characterized by (i) a wide range of limnic habitats, inhabiting both brackish water and freshwater environments, and (ii) contrasting modes of reproduction, including ‘planktonic’ development via a free‐swimming larva vs. intrabranchial incubation (brooding) of shelled juveniles. The present investigation of five species of Corbicula from the Indonesian islands Sumatra and Sulawesi, which were hitherto not studied anatomically, adds to the diversity in reproductive patterns in this genus. As a unique feature among Corbicula we here report on two newly observed modes of brooding in species endemic to Sulawesi, (i) tetragenous brooding (i.e. in both demibranchs) in Corbicula possoensis Sarasin & Sarasin, 1898 from Lake Poso, and (ii) prolonged incubation in the maternal gills, with juvenile shells reaching up to 1.3 mm in length and with a well‐developed hinge in C. linduensis Bollinger, 1914 from the Lindu River system. In contrast, a third method is seen in the following taxa that incubate their young in their inner demibranchs only until the stage of juveniles with straight‐hinged shells (D‐shaped): C. matannensis Sarasin & Sarasin, 1898 from Lake Matano and Lake Mahalona, C. loehensis Kruimel, 1913 from Lake Masapi (all on Sulawesi) and C. moltkiana Prime, 1878 from Lakes Maninjau and Singkarak (on Sumatra). Details of the anatomical and histological features of ctenidia are described for each type of brooding, and some trends in the evolution of reproductive strategies within the Corbiculidae are discussed, comparing them with those known from other limnic molluscs.     

Functional morphology of mouthparts and digestive system during larval development of the cleaner shrimp Lysmata amboinensis (de Man, 1888)

Mouthpart and alimentary canal development was examined in Lysmata amboinensis larvae using scanning electron microscopy and histology. The gross morphological features of external mouthparts and internal digestive tract structures of larvae at different developmental stages indicate that ingestive and digestive capabilities are well developed from early on. With increasing age of the larvae the mouthpart appendages increased in size, the hepatopancreas in tubular density and the midgut in length. The density of setae and robustness of teeth and spines of individual structures increased. The most pronounced changes from early to late stage larvae involved formation of pores on the paragnaths and labrum, transformation of the mandibular spine‐like teeth to molar cusps, development of the filter press in the proventriculus and of infoldings in the previously straight hindgut. The results suggest that early stage L. amboinensis larvae may benefit from soft, perhaps gelatinous prey, whereas later stages are better equipped to handle larger, muscular or more fibrous foods. J. Morphol. 2011. © 2011 Wiley‐Liss, Inc.     

The ontogeny of Pseudis platensis (Anura,Hylidae): Heterochrony and the effects of larval development on postmetamorphic life

Recent studies have described the giant tadpole, delayed metamorphic transformations, and absence of postmetamorphic growth of the skeleton of Pseudis Platensis. These features address questions about derived patterns of life cycles and the role of the heterochrony during the metamorphosis in anurans. Using anatomical methods, we provide new data on the development of reproductive, digestive and integument systems, and age inference obtained from ontogenetic series of Pseudis platensis. Our results indicate that at the end of metamorphosis, the adult skin is completely differentiated, including the calcified dermal layer; the testis has seminiferous tubules with spermatogonia, spermatocytes, and spermatids; ovarian sacs present previtellogenic ova; and the adult digestive tract is fully formed. The froglets differ from adults only in being unable to reproduce. The entire life cycle of P. platensis can occur in 4 years. In the first year, larval development, growth to adult size, and gonad differentiation are completed. Long larval development rather than size of the tadpoles seems to be involved in the absence of juvenile stages. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.     

Immunofluorescence and electron microscopic studies of microtubule organization during the cell cycle ofDictyota dichotoma (Phaeophyta,Dictyotales)

Summary Interphase cells ofDictyota dichotoma (Hudson) Lamour. lack cortical microtubules (Mts) but display an impressive network of cytoplasmic microtubules (c-Mts). These are focussed on two opposed perinuclear centriolar sites where centrin or a centrin-homologue is localized. Some of the Mts surround the nucleus, but the majority traverse the cytoplasm as bundles variously directed towards the plasmalemma. In apical cells, and to a lesser extent in the square or slightly elongated meristematic cells, Mts are more or less evenly arranged. In elongated cells they form thick bundles longitudinally traversing the cytoplasm; a pattern maintained in differentiated cells. In early prophase the non-perinuclear Mts disappear but by late prophase a bi-astral arrangement of short Mts is observed. They enter polar nuclear depressions and attach to differentiated regions of the nuclear envelope where polar gaps open. By metaphase the spindle Mts converge on the centrioles at the polar gaps. At anaphase, interzonal Mts are evident and the asters start to reassemble. After telophase disruption of the interzonal Mts, the daughter nuclei approach each other, but move apart again before cytokinesis. The latter movement keeps pace with the development of two interdigitating Mt systems, ensheathing both daughter nuclei. The partition membrane bisects this Mt cage. Between telophase and cytokinesis the centrosomes separate, finally occupying opposed perinuclear sites. New Mts arise at the new centrosomes, some terminating on the consolidating partition membrane. Our data show thatD. dichotoma vegetative cells display a prominent cytoplasmic Mt cytoskeleton, which undergoes continual, but definite, change in organization during the cell cycle.     

Histo-morphology of the thyroid gland during the larval development of Pleurodema borellii (Anura,Leptodactylidae)

The thyroid gland is essential in anurans, since thyroid hormones (TH) are the main regulators of larval development. Its absence or inactivity interrupts development and precludes metamorphosis. Histological changes are important diagnostic criteria for evaluating thyroid gland activity. However, there is a large larval diversity where the development of the thyroid gland development has not been studied. Pleurodema borellii is an anuran from northwest of Argentina with typical omnivorous pond tadpoles that can be easily raised in captivity. This study explores the histo-morphological changes of the thyroid gland architecture during larval development. Histological parameters indicate peak glandular activity in parallel with the intensity of the metamorphic transformations. These parameters regress towards the end of metamorphosis, indicating low TH release. P. borellii's thyroid gland does not appear to have relevant activity in post-metamorphic juvenile stages. This study is a first step towards understanding endocrine regulation during the development of Pleurodema borellii, and a reference to future studies in this species involving thyroid-dependent processes.     

Carbohydrate metabolism during embryonic and larval development of Odonthestes humensis(De Buen, 1953) (Pisces—Atherinidae)

Changes in glucose and glycogen concentrations during embryonic and larval development of Odonthestes humensis (De Buen, 1953) (Pisces—Atherinidae) were followed.
Glycogen decreased immediately after fertilization but remained constant throughout the embryonic period, suggesting that although present glycogenolisis may not be the most important energetic pathway during this period. Glucose levels only show a significant increase on the fifth day of development coincident with the beginning of heart activity.
In fed larvae glycogen utilization increases during development, resulting in an increase in glucose concentration. Such a pattern does not occur in starved animals, where glycogen and glucose are present respectively at high and low concentrations similar to embryos. The change of pattern seems to be associated with the first larval feeding.