Egg Envelope Research Articles

Structure of the egg envelope in rice-fish Oryzias sinensis Chen, Uwa & Chu, 1989, with comments on the relationship to Oryzias latipes

Structure of the egg envelope in rice-fish <i>Oryzias sinensis</i> Chen, Uwa &amp; Chu, 1989, with comments on the relationship to <i>Oryzias latipes</i>

Gonad morphology, gametogenesis, and reproductive modes in fishes of the tribe Starksiini (Teleostei, Blenniiformes)

A comparative study of the reproductive organs in 17 of the 30 species of the tribe Starksiini (Labrisomidae, Blenniiformes) and related labrisomids reveals the major traits of gamete form and production and likely reproductive modes. The testes are of the lobular type and have a testicular gland and sperm ducts. Isodiametric sperm (aquasperm) with a globular head or anisodiametric sperm (introsperm) with an elongate head, or both, were observed in the studied species. Both types have either one or two flagella in the sperm tail. Ovaries of the Starksiini are bilobed and exhibit synchronous or asynchronous egg production. Although viviparity or "ovoviviparity" reportedly characterizes the group, our study revealed evidence of both internal and external fertilization and three modes of reproduction. External fertilization or ovuliparity is suggested for the Starksia atlantica and S. lepicoelia species complexes by the presence in males of a short genital papilla that is not reinforced through adhesion with the first anal-fin spine and by the absence of sperm within the ovaries. Internal fertilization and zygoparity is indicated for most species by the presence of an intromittent papilla in males that is adhered to the first anal-fin spine, "nests" of sperm within the ovaries, absence of embryos within the ovarian lamellae and usually thick egg envelopes bearing dense covers of adhesive filaments. Internal fertilization and embryoparity is indicated for starksia fulva and Xenomedea rhodopyga by an intromittent papilla that is adhered to the first anal-fin spine of males, anisodiametric sperm in males, delicate egg envelopes without adhesive filaments and developing embryos within follicular envelopes or within the follicle in females. Although many of these features are seen in the internally fertilizing clinid blennies, starksiins differ in retaining the testicular gland typical of labrisomids and in lacking sperm packaging typical of other internally fertilizing teleosts.

Adaptive evolution of fish hatching enzyme: one amino acid substitution results in differential salt dependency of the enzyme

Embryos of medaka Oryzias latipes hatch in freshwater, while those of killifish Fundulus heteroclitus hatch in brackish water. Medaka and Fundulus possess two kinds of hatching enzymes, high choriolytic enzyme (HCE) and low choriolytic enzyme (LCE), which cooperatively digest their egg envelope at the time of hatching. Optimal salinity of medaka HCE was found in 0 mol l(-1) NaCl, and activity decreased with increasing salt concentrations. One of the two Fundulus HCEs, FHCE1, showed the highest activity in 0 mol l(-1) NaCl, and the other, FHCE2, showed the highest activity in 0.125 mol l(-1) NaCl. The results suggest that the salt dependencies of HCEs are well adapted to each salinity at the time of hatching. Different from HCE, LCEs of both species maintained the activity sufficient for egg envelope digestion in various salinities. The difference in amino acid sequence between FHCE1 and FHCE2 was found at only a single site at position 36 (Gly/Arg), suggesting that this single substitution causes the different salt dependency between the two enzymes. Superimposition of FHCE1 and FHCE2 with the 3-D structure model of medaka HCE revealed that position 36 was located on the surface of HCE molecule, far from its active site cleft. The results suggest a hypothesis that position 36 influences salt-dependent activity of HCE, not with recognition of primary structure around the cleavage site, but with recognition of higher ordered structure of egg envelope protein.

Egg ultrastructure of the amabiliid cestode Tatria biremis Kowalewski, 1904 (Cyclophyllidea, Amabiliidae), with an emphasis on the oncospheral envelopes

This is the first report on the ultrastructure of eggs in the cestode family Amabiliidae Braun, 1900. The gravid proglottides of Tatria biremis easily detach from the strobila. Their thick-walled saccate uterus contains numerous rounded or oval eggs measuring about 30-32 μm in diameter. In the early preoncospheral phase, three primary embryonic envelopes are formed around the developing and differentiating embryos, namely: (1) vitelline capsule originating from vitellocyte material; (2) outer envelope formed by two macromeres, and (3) inner envelope originating from a fusion of three mesomeres. Thus, both the outer and inner envelopes of T. biremis eggs are cellular in origin and syncytial in nature. During egg maturation, the three primary embryonic envelopes undergo differentiation into fully formed oncospheral or egg envelopes. Most significant changes were observed in the inner envelope which becomes progressively subdivided into 3 sub-layers: the extra-embryophoral sub-layer, the embryophore, and the intra-embryophoral sub-layer, containing mesomere nuclei. The mature hexacanth is covered by a thin layer of the oncospheral tegument. Within the infective hexacanth larva, five cell types were distinguished: (1) a binucleated subtegumental cell; (2) U-shaped penetration gland; (3) nerve cells; (4) somatic cells representing the myocytons of both somatic and hook musculature, and (5) large germinative cells. Ultrastructural characteristics of T. biremis eggs are compared with those described in representatives of other cestode taxa. Since the functional ultrastructure of cestode egg envelopes is defined by multiple factors such as the type of life cycles, habitats and behaviour of the intermediate hosts, mode of the intermediate host infection, etc., ultrastructural studies of the greater diversity of cestodes are needed to obtain comparative data for fruitful analysis of cyclophyllidean cestode adaptations to their diverse life cycles.

Developmental disorders and altered gene expression in the tropical clawed frog (Silurana tropicalis) exposed to 17α‐ethinylestradiol

Several endocrine-disrupting chemicals with estrogenic activity can affect sexual development and reproduction in aquatic wildlife. The occurrence of oocytes in the testis (testis-ova) is one reproductive disorder and can be used as a valid endpoint when studying disruptive effects of estrogenic chemicals. To elucidate the molecular basis of testis-ova induction, we conducted gene expression analysis in the gonads of Silurana tropicalis exposed to 0, 3, 10 and 30 ng l(-1) 17α-ethinylestradiol (EE2) from 2 days after fertilization to the juvenile stage (14 weeks after fertilization). The frequencies of testis-ova induction or male to female sex-reversal of the gonads increased in an EE2 dose-dependent manner. Microarray analysis showed that expressions of a large number of genes were significantly changed by EE2 exposure. Genes including egg envelope composition (zp4, zpax, zpc, zp3.2 and egg cortical granule lectin), 42S particle genes (42Sp50, 42Sp43 and 42Sp48) and regulation of female germ cells (figla) are associated with the testis-ova and sex-reversal situation in the gonads. Of those, expression of zpc and 42Sp50 genes is associated with testis-ova. Thus, we propose that these genes are useful biomarkers for toxicological research in amphibians developmentally exposed to estrogenic chemicals.

Gamete ultrastructure in some species of the family Mullidae from the South China Sea

In tropical representatives of the family Mullidae, the ultrastructure of oocyte envelopes (Parupeneus multifasciatus and Upeneus tragula) and spermatozoa (P. multifasciatus and P. barberinoides) is studied. The egg envelopes include the single-layered zona radiata and weakly expressed chorion. The spermatozoa are characterized by the presence of the oval head flattened on a side and deep nuclear fossa reaching approximately 90% of the head length. The centriolar complex and basal part of the flagellum are located inside the nuclear fossa.

An oocyte-specific astacin family protease, alveolin, is released from cortical granules to trigger egg envelope hardening during fertilization in medaka (Oryzias latipes)

It has long been hypothesized that in fishes the contents of cortical granules are involved in the hardening of egg envelope following fertilization. We previously purified the egg envelope hardening initiation factor from the exudates released from activated medaka (Oryzias latipes) eggs and tentatively termed this protein alveolin. Alveolin is a member of the astacin metalloprotease family and was proposed to be a protease which hydrolyzes ZPB at one restricted position to allow starting cross-linking with ZPC. Here, we investigated the complete pathway from biosynthesis and accumulation to secretion of alveolin. A single alveolin transcript was detected only in ovarian preparations, confirming the specific expression of alveolin in the ovary. In situ hybridization indicated that the alveolin mRNA is already expressed in the very early previtellogenic oocytes. However, immunocytochemical studies revealed that the appearance of alveolin protein was delayed until the beginning of the vitellogenic stage. The cortical granules isolated from unfertilized eggs contained a high molecular weight form of glycosylated alveolin with a 50kDa relative molecular mass. Hypotonic treatment burst isolated granules in vitro and transformed alveolin to a 21.5kDa form, which is the same size as that of natural alveolin released from eggs upon fertilization. This transformation was inhibited in the presence of leupeptin and 4-(2-aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF), suggesting that a serine protease is involved in alveolin activation upon fertilization. Furthermore, the phylogenetic relationship of alveolin with other vertebrate astacin family members was analyzed. The result shows that alveolin and its teleostean homologs make a new group which is separate from either the hatching enzyme, meprin and BMP1/tolloid groups.

Differentiation and function of the ovarian somatic cells in the pseudoscorpion, Chelifer cancroides (Linnaeus, 1761) (Chelicerata: Arachnida: Pseudoscorpionida)

Pseudoscorpion females carry fertilized eggs and embryos in specialized brood sacs, where embryos are fed with a nutritive fluid produced and secreted by somatic ovarian cells. We used various microscopic techniques to analyze the organization of the somatic cells in the ovary of a pseudoscorpion, Chelifer cancroides. In young specimens, the ovary is a cylindrical mass of internally located germline cells (oogonia and early previtellogenic oocytes) and two types of somatic cells: the epithelial cells of the ovarian wall and the internal interstitial cells. In subsequent stages of the ovary development, the oocytes grow and protrude from the ovary into the hemocoel (opisthosomal cavity). At the same time the interstitial cells differentiate into the follicular cells that directly cover the oocyte surface, whereas some epithelial cells of the ovarian wall form the oocyte stalks – tubular structures that connect the oocytes with the ovarian tube. The follicular cells do not seem to participate in oogenesis. In contrast, the cells of the stalk presumably have a dual function. During ovulation the stalk cells appear to contribute to the formation of the external egg envelope (chorion), while in the post-ovulatory phase of ovary function they cooperate with the other cells of the ovarian wall in the production of the nutritive fluid for the developing embryos.

Dose- and time-related changes in aerobic metabolism, chorionic disruption, and oxidative stress in embryonic medaka (Oryzias latipes): Underlying mechanisms for silver nanoparticle developmental toxicity

Silver nanoparticles (AgNPs) are widely employed in commercial products, and are thus inevitably released into the aquatic environment. Many studies have indicated that AgNPs could induce toxicological effects on embryonic fish. To understand the mechanism of AgNP developmental toxicity, we determined the effects of AgNPs on the egg membrane, aerobic metabolism, antioxidant system, lipid peroxidation, as well as reactive oxygen species (ROS) and singlet oxygen (1O2) generation in early-life medaka fish (Oryzias latipes). AgNP treatment at 62.5–1000μg/L caused significant increase in retarded development and abnormalities. Destruction of the surface ornamentation and egg envelope was observed at a higher AgNP concentration (≥125μg/L) using light microscopy and scanning electron microscopy. A dose-dependent increase in lactate dehydrogenase activity, an indicator of anaerobic metabolism, and superoxide dismutase activity was observed in the treated embryos. In contrast, the total reduced glutathione level decreased. A high thiobarbituric acid reactive substance concentration was generated upon AgNP exposure from day 1 to day 7 postfertilisation. The biochemical parameters suggested that oxidative stress was induced by the AgNPs. Unexpectedly, a dose-dependent reduction in ROS and 1O2 generation upon high AgNP exposure (≥250μg/L) was observed. Although the morphological damages induced by the AgNPs were irreversible, restorable antioxidant defenses were noted in the well-developed embryos. This finding supported the idea that the stage of morphogenesis and organogenesis is a critical window to chemical exposure or environmental stress. Overall, the results suggested that hypoxia, disturbed egg chorion, and oxidative stress are mechanistically associated with AgNP toxicity in embryonic fish.

Sperm proteasome degrades egg envelope glycoprotein ZP1 during fertilization of Japanese quail (Coturnix japonica)

At the time of fertilization, the extracellular matrix surrounding avian oocytes, termed the perivitelline membrane (pvm), is hydrolyzed by a sperm-borne protease, although the actual protease that is responsible for the digestion of the pvm remains to be identified. Here, we show evidence that the ubiquitin-proteasome system is functional in the fertilization of Japanese quail. The activities for the induction of the acrosome reaction and binding to ZP3 as revealed by ligand blotting of purified serum ZP1 are similar to those of pvm ZP1. Western blot analysis of purified ZP1 and ZP3 by the use of the anti-ubiquitin antibody showed that only pvm ZP1 was reactive to the antibody. In vitro penetration assay of the sperm on the pvm indicated that fragments of ZP1 and intact ZP3 were released from the pvm. Western blot analysis using the anti-20S proteasome antibody and ultrastructural analysis showed that immunoreactive proteasome was localized in the acrosomal region of the sperm. Inclusion of specific proteasome inhibitor MG132 in the incubation mixture, or depletion of extracellular ATP by the addition of apyrase, efficiently suppressed the sperm perforation of the pvm. These results demonstrate for the first time that the sperm proteasome is important for fertilization in birds and that the extracellular ubiquitination of ZP1 might occur during its transport via blood circulation.

담수순화 감성돔 Acanthopagrus schlegelii 동결보존 정자의 수정능력

Fertilization rates were over 90% when sperm from black porgy Acanthopagrus schlegelii acclimated and raised in freshwater and black porgy raised in seawater were fertilized with eggs from female black porgy raised in seawater, although cryopreserved sperm were significantly lower in fertilization rates than non-cryopreserved sperm. From the observations of embryos development at different salinities (0, 10, 20 and 32 psu) within 3 hours upon fertilization (16 cell stage), all were dead at 0 psu. However, the development process and speed at 10 and 20 psu were the same as at 32 psu. But, many developing embryos were egg envelope injury at low-salinities of 10 and 20 psu unlike at 32 psu. This is attributable to osmotic shock. Hatching rate of embryos at 32 psu was 60% or so, whereas low as 5% or less were successfully hatched at 10 and 20 psu, implying that osmotic shock could be responsible for the failure of embryo development.

Variations in the gene expression of zona pellucida proteins, zpb and zpc, in female European eel (Anguilla anguilla) during induced sexual maturation

Vertebrate eggs are surrounded by an extracellular glycoprotein coat termed zona pellucida (ZP). Integrity of ZP is critical for a correct embryo development. Two zona pellucida protein genes (zpb and zpc) from European eel were characterized, specific qPCR assays developed and their expression in immature males and females carried out.An experimental group of silver-stage eel females was maintained at 18°C and hormonally induced to sexual maturation by weekly injections of carp pituitary extract during 12weeks. Changes in zpb and zpc expression during sexual maturation were studied in liver and ovary by qPCR. In liver, no changes were recorded during hormonal treatment, while in ovary expression of both genes decreased during sexual development.These results are a first step in the characterization of ZP in European eel and in the understanding of the mechanism underlying egg envelope formation.

Food imprinting and visual generalization in embryos and newly hatched cuttlefish, Sepia officinalis

Juvenile cuttlefish spontaneously prefer shrimp to crabs. This preference can be changed by early visual learning during embryonic and postembryonic life and has been related to a form of food imprinting. Nevertheless, it is unknown whether generalization occurs in conjunction with this early learning process. We found that inexperienced hatchling cuttlefish preferred ‘black’ to ‘white crab’ for their first meal, the black ink envelope of cuttlefish eggs did not prevent embryos discriminating between black and white crabs and embryonic or postembryonic visual familiarization to ‘white crabs’ induced a subsequent visual preference for ‘white crabs’ over ‘black crabs’ in the hatchling's first meal. Finally, juvenile cuttlefish previously pre- or postnatally exposed to ‘white crabs’ preferred ‘black crabs’ to shrimp, indicating for the first time that prey generalization occurs as early as the embryonic stages in cuttlefish. Such cognitive abilities could confer important adaptive advantages in processing information about prey likely to be available in the egg-laying environment at hatching and in the course of juvenile dispersal.

Ultrastructural and cytochemical studies on oogenesis of the fern Pteridium aquilinum

Egg development in Pteridium aquilinum var. latiusculum was studied using ultrastructural and cytochemical methods to examine structural features influencing fertilization in leptosporangiate ferns. Ultrastructural observations indicate a separation cavity is first formed above the egg during oogenesis with a pore region persistently connecting the egg and the ventral canal cell. The egg envelope is formed by deposition of amorphous materials in the separation cavity on the outer surface of plasmalemma. The egg envelope was not formed across the pore region; instead, a fertilization pore was formed. During oogenesis, the egg nucleus produced extensive evaginations containing osmiophilic bodies. Cytochemical experiments revealed that the egg envelope displays strong periodic acid-Schiff reaction indicative of polysaccharides, with negligible Sudan black B staining for lipids, suggesting that the egg envelope is composed principally of polysaccharides, and not lipids. The present manuscript provides new insights into egg structure and development of Pteridium, including discovery and characterization of the fertilization pore and observations on the chemical nature of the egg envelope, thus contributing to the understanding of the cytological mechanism of the sexual reproduction of ferns.

Structure and Formation of the Unusual Sperm of Patelloida latistrigata (Mollusca : Patellogastropoda): Implications for Fertilization Biology

The structure of the spermatozoa and spermatogenesis of the lottiid limpet Patelloida latistrigata is described by transmission electron microscopy. Although the lengths of the spermatozoa (about 60 μm) and their head region (about 12 μm) are similar to those of other patellogastropods, the structure of the sperm head and midpiece are very different. The head consists of an unusually large acrosome (about 11-μm long) with a broad posterior invagination that houses the relatively small nucleus. The midpiece mitochondria, which are rather elongate with large folded tubular cristae, are housed in a cytoplasmic sheath posterior to the nucleus. The proximal centriole is unusually elongate (about 2-μm long). The axoneme that emerges from the distal centriole is surrounded anteriorly by the cytoplasmic sheath in which the cytoplasmic side of the plasma membrane has electron-dense material. The flagellum is enlarged at its terminal end. Spermatogenesis is similar to that described for other patellogastropods. Patelloida latistrigata, therefore, has spermatozoa that seem to meet the morphological criteria of ent-aquasperm, which raises the question of whether fertilization is truly external in this limpet. However, it is also possible that the modifications to the sperm are linked to unknown specializations of the egg or egg envelope.

Egg envelopes and cuticle renewal in Porcellio embryos and marsupial mancas

An important adaptation to land habitats in terrestrial isopod crustaceans is development of embryos in a fluid-filled female brood pouch, marsupium. The study brings insight into the structure and protective role of egg envelopes and cuticle renewal during ontogenetic development of Porcellio embryos and marsupial mancas. Egg envelopes cover embryos, the outer chorion until late-stage embryo and the inner vitelline membrane throughout the whole embryonic development. Egg envelopes of Porcellio have relatively simple ultrastuctural architecture compared to Drosophila egg envelopes. Exoskeletal cuticle is produced in late embryonic development by hypodermal cells of the embryo and is renewed in further development in relation to growth of developing embryos and mancas. Cuticle structure and renewal in prehatching late-stage embryos and marsupial mancas exhibit main features of cuticle in adults. Epicuticle is thin and homogenous. The characteristic arrangement of chitin-protein fibers and the dense distal layer in exocuticle are hardly discernible in prehatching embryo and distinct in marsupial mancas. Endocuticle consists of alternating electron dense and electron lucent sublayers and is perforated by pore canals in both stages. Differences from adult cuticle are evident in cuticle thickness, ultrastructure and mineralization. Signs of cuticle renewal in prehatching embryo and marsupial mancas such as detachment of cuticle from hypodermis, partial disintegration of endocuticle and assembly of new cuticle are described.

Caracterización electroforética de las proteínas del corion normal y del corion duro de Salmo salar

SUMMARY The chorion is an egg envelope that allows the early development of teleostean fishes. After reaching the alevin stage, hatching enzymes are secreted in order to digest the chorion and release the alevin. Massive mortality events have occurred in a number of salmon farms as a consequence of hatching problems, with alevins being unable to degrade the chorion. A previous study on the chorion structure of Salmo salar has shown that protein fibers forming the inner layer of non-degraded chorion are thicker than those observed in normal chorion, suggesting that polypeptides forming the choriogenin could exhibit an altered structure. It would be interesting to make a biochemical comparison between polypeptides forming protein fibers of the inner layer of normal and hard chorion in order to establish differences in the electrophoretic pattern of Salmo salar ova. According to our results, fibers forming the inner layer of normal chorion are thinner than those building the hard chorion. The electrophoretic pattern for normal chorion is described as four bands of molecular weight 107 kDa, 92 kDa, 38 kDa, and 31kDa in contrast to the 179 Kda, 157 Kda, 55 Kda and 54 Kda for non-hatched chorion. Consequently, protein fibers with higher molecular weight turned into thicker fibers with a different three dimensional structure, but also with different glycosylic radicals compared to normal fibers. These features make the inner layer of hard chorion different to normal chorion since it is very difficult for the hatching enzyme to dissolve it, leading the alevin to fail in the hatching process.

Ultra Structure Study of egg membrane in Osteobrama belangeri Val.

Osteobrama belangeri (Valenciennes) is a highly prized endemic medium carp available in Yunan province of China, Myanmar and Manipur (North Eastern part of India). The fish attains sexual maturity in 2+ years (200 - 25 g. body weight). Investigation of the fine structure of the egg envelope and micropyle of unfertilized spawned eggs of Osteobrama belangeri using Scanning Electron Microscope (SEM) was made. The surface of the egg membrane showed regularly arranged pores. The micropyle is a type II consisting of the flat pit with diameter of micropyle 11 µm to 12 µm and a long canal narrowing into a distinct canal. The surface of zona radiata was rough with a uniform distribution of round pores with little larger pores around the micropyle region.

Microarray gene expression profiles from mature gonad tissues of Atlantic bluefin tuna, Thunnus thynnus in the Gulf of Mexico

BackgroundBluefin tunas are highly prized pelagic fish species representing a significant economic resource to fisheries throughout the world. Atlantic bluefin tuna (Thunnus thynnus) populations have significantly declined due to overexploitation. As a consequence of their value and population decline, T. thynnus has been the focus of considerable research effort concerning many aspects of their life history. However, in-depth understanding of T. thynnus reproductive biology is still lacking. Knowledge of reproductive physiology is a very important tool for determining effective fisheries and aquaculture management. Transcriptome techniques are proving powerful and provide novel insights into physiological processes. Construction of a microarray from T. thynnus ESTs sourced from reproductive tissues has provided an ideal platform to study the reproductive physiology of bluefin tunas. The aim of this investigation was to compare transcription profiles from the ovaries and testes of mature T. thynnus to establish sex specific variations underlying their reproductive physiology.ResultsMale and females T. thynnus gonad tissues were collected from the wild and histologically staged. Sub-samples of sexually mature tissues were also measured for their mRNA differential expression among the sexes using the custom microarray design BFT 4X44K. A total of 7068 ESTs were assessed for differential expression of which 1273 ESTs were significantly different (p<0.05) with >2 fold change in expression according to sex. Differential expression for 13 of these ESTs was validated with quantitative PCR. These include genes involved in egg envelope formation, hydration, and lipid transport/accumulation more highly expressed in ovaries compared with testis, while genes involved in meiosis, sperm motility and lipid metabolism were more highly expressed in testis compared with ovaries.ConclusionsThis investigation has furthered our knowledge of bluefin tunas reproductive biology by using a contemporary transcriptome approach. Gene expression profiles in T. thynnus sexually mature testes and ovaries were characterized with reference to gametogenesis and potential alternative functions. This report is the first application of microarray technology for bluefin tunas and demonstrates the efficacy by which this technique may be used for further characterization of specific biological aspects for this valuable teleost fish.

Cytological features of oogenesis and their evolutionary significance in the fern Osmunda japonica

The development of the egg and canal cells in the fern Osmunda japonica Thunb. was studied during oogenesis by transmission electron microscopy. The mature egg possesses no fertilization pore and no typical egg envelope. In addition, an extra wall formed around the canal cells during oogenesis and apparently blocked protoplasmic connections between the egg and the canal cells. The periodic acid Schiff (PAS) reaction revealed that the extra wall was most likely composed of polysaccharides. Maturation of the egg was accompanied by the formation of a separation cavity above the egg and by some changes in the morphology of the nucleus and cytoplasmic organelles. The chromatin of the nucleus becomes condensed and the upper surface of the nucleus becomes closely associated with the plasmalemma. Amyloplasts in the egg cytoplasm were numerous and conspicuous, with most in close proximity to the nucleus. Finally, the cytoplasm on one side of the egg became vesiculated and the overlying plasmalemma was easily disrupted. These cytological features of the egg and the canal cells during oogenesis in O. japonica are markedly different from those of the leptosporangiate ferns and suggest a significant evolutionary divergence in reproductive cellular features between Osmundaceae and leptosporangiate ferns.