Haliotrema abaddon n. sp. (Monogenoidea: Dactylogyridae) from the gills of wild and maricultured West Australian dhufish Glaucosoma hebraicum (teleostei: Glaucosomatidae), in Australia

Haliotrema abaddon n. sp. (Dactylogyridae) is described from the gills of West Australian dhufish Glaucosoma hebraicum (Teleostei: Glaucosomatidae), from the Indian Ocean near Fremantle, Western Australia. The parasite is recorded from cultured dhufish and from a major portion of the known geographic distribution of its host. In cultured dhufish, H. abaddon causes branchitis and hyperplasia and metaplasia of the lamellar epithelial cells and may be a limiting factor in the development of an economically feasible mariculture industry. Comparable prevalences and densities of the parasite on wild and cultured dhufish were observed. In heavily infested captive fish, clusters of eggs (egg strands) appear to restrict blood flow to localized regions of the gills as a result of entanglement of egg filaments with secondary gill lamellae. Hatching of oncomiracidia occurs in 7-10 days at 20-25 C.     

Dionchus postoncomiracidia (Monogenea: Dionchidae) from the skin of blacktip sharks, Carcharhinus limbatus (Carcharhinidae)

Postoncomiracidia of Dionchus sp. are described from specimens collected from the skin of 2 blacktip sharks Carcharhinus limbatus, captured in the northern Gulf of Mexico. The parasites resemble nonciliated oncomiracidia hatched from eggs laid by Dionchus sp. on gills of a cobia Rachycentron canadum and adults of Dionchus remorae that were collected from gills of a common sharksucker Echeneis naucrates, captured in association with a third blacktip shark. The hamuli of the postoncomiracidia were morphologically similar to those of adult D. remorae. This is the first report of dionchids from an elasmobranch and from a location other than the gills. These findings support the idea that some dionchid oncomiracidia colonize the skin of sharks or other aquatic vertebrates that sponsor remoras, prior to transferring to other remoras and maturing.     

Morphology and distribution of blood fluke eggs and associated pathology in the gills of cultured Pacific bluefin tuna, Thunnus orientalis

Infestations of blood flukes of the genus Cardicola have been observed in juvenile Pacific bluefin tuna (PBT) cultured in Japan. Infected fish harbor large numbers of parasite eggs in their gills. Although the link between blood fluke infection and juvenile mortality is not clear, accumulation of parasite eggs appears to be pathogenic to the fish. We investigated the origins, general morphology/distribution, and histopathology of these eggs in artificially produced 0 yr old PBT. Dead and live fish were sampled on several occasions from two culture facilities in Wakayama prefecture, Japan. The number of eggs in each gill filament was enumerated under a microscope. In addition, we estimated the total number of eggs by dissolving the gills in a weak NaOH solution. We observed two morphologically distinct egg types in the gill filaments, smaller, oval shaped eggs in the gill lamellae and larger, crescent shaped eggs that occurred primarily in the filamentary arteries. Based on the ITS2 sequence, the ovoid and crescent shaped eggs were identified as C. orientalis and C. opisthorchis, respectively. Eggs of the former species were more abundant (maximum: 6400 per filament) than the latter (maximum: 1400), but the number was highly variable among filaments. The eggs of the latter species were relatively evenly distributed among the filaments. In a heavily infected individual, we estimated a total of >4.5 million eggs were present in the gills on one side of the fish. The number of eggs from the two species was positively correlated to each other and the dead fish tended to harbor more eggs than the live fish. Histological observation revealed host responses around the eggs, including encapsulation by fibroblasts and nodule formation, as seen in response to other aporocotylid eggs. In addition, we observed widespread fusion of gill lamellae and blockage of the filamentary arteries in some instances. Our results provide information that can be used for routine diagnosis of Cardicola blood flukes in cultured tuna and suggest they represent a risk to juvenile PBT.     

Environmental and developmental effects on external gill loss in the red-eyed tree frog, Agalychnis callidryas

I examined the effects of development, hatching, and oxygen availability on external gill loss in red-eyed tree frogs, Agalychnis callidryas. Under natural conditions, the arboreal embryos maintained large external gills until hatching, which occurred from 5-8 d after oviposition. At hatching, when tadpoles entered the water, external gills began to regress. In older hatchlings this process was extremely rapid. Gill circulation was lost on average within 16 min and sometimes within 5 min. Gills often regressed completely in under 2 h. Younger hatchlings reduced gill circulation, shortened and adducted their gills, then resumed normal circulation for some time after hatching; half had completely lost external gills within 24 h. Experimentally increasing the area of egg surface exposed to the air induced loss of external gills in unhatched embryos. Older hatchlings in hypoxic water without access to air maintained their external gills. This suggests that loss of external gills is a response to increased oxygen availability, rather than a response to hatching per se. Extended maintenance of external gills by large, late-hatching embryos may facilitate continued rapid development in closely packed eggs.     

Oxygen, gills, and embryo behavior: mechanisms of adaptive plasticity in hatching.

Many species alter the timing of hatching in response to egg or larval predators, pathogens, or physical risks. This plasticity depends on separation between the onset of hatching competence and physiological limits to embryonic development. I present a framework based on heterokairy to categorize developmental mechanisms and identify traits contributing to and limiting hatching plasticity, then apply it to a case of predator-induced hatching. Red-eyed treefrogs have arboreal eggs, and tadpoles fall into ponds upon hatching. Egg and tadpole predators select for earlier and later hatching, respectively. Embryos hatch up to 30% early in predator attacks, and later if undisturbed. They maintain large external gills throughout the plastic hatching period, delaying gill regression while development otherwise continues. Rapid gill regression occurs upon hatching. Prolonged embryonic development depends on external gills; inducing gill regression causes hatching. External hypoxia retards development, kills eggs, and induces hatching. Nonetheless, embryos develop synchronously and without hatching prematurely across a broad range of perivitelline PO2, from 0.5-12.5 kPa. Embryos exploit spatial variation of PO2 within eggs by positioning gills against patches of air-exposed surface. Respiratory plasticity and oxygen-sensitive behavior appear critical for the hatching plasticity that balances a predation risk trade-off across life stages.     

A possible evolutionary lag in the relationship between freshwater mussels and European bitterling

The coevolutionary dynamics between European bitterling Rhodeus amarus and freshwater unionid mussels, which the former parasitize by laying eggs on their gills, were tested. In a series of experiments fish preferences and mussel responses were compared in parasites and hosts of recent (Europe) and ancient (Asia) sympatry. Rhodeus amarus readily oviposited on the gills of all mussel species tested. Fish that laid their eggs on the gills of Asian Anodonta woodiana, however, suffered a dramatic reduction in reproductive success compared to fish that oviposited on the gills of European mussels: Unio pictorum , Unio tumidus , Anodonta anatina and Anodonta cygnea . This difference was the result of egg ejection behaviour by mussels rather than the unsuitability of the internal gill environment for European bitterling embryo development. The ejection response of mussels with a long sympatry with European bitterling was considerably more pronounced than that of mussels with a substantially shorter sympatry. The data support a coevolutionary arms race between bitterling and mussels and point to an evolutionary lag in the relationship between R. amarus and its European mussel hosts.     

Oxygen, gills, and embryo behavior: mechanisms of adaptive plasticity in hatching

Many species alter the timing of hatching in response to egg or larval predators, pathogens, or physical risks. This plasticity depends on separation between the onset of hatching competence and physiological limits to embryonic development. I present a framework based on heterokairy to categorize developmental mechanisms and identify traits contributing to and limiting hatching plasticity, then apply it to a case of predator-induced hatching. Red-eyed treefrogs have arboreal eggs, and tadpoles fall into ponds upon hatching. Egg and tadpole predators select for earlier and later hatching, respectively. Embryos hatch up to 30% early in predator attacks, and later if undisturbed. They maintain large external gills throughout the plastic hatching period, delaying gill regression while development otherwise continues. Rapid gill regression occurs upon hatching. Prolonged embryonic development depends on external gills; inducing gill regression causes hatching. External hypoxia retards development, kills eggs, and induces hatching. Nonetheless, embryos develop synchronously and without hatching prematurely across a broad range of perivitelline PO₂, from 0.5–12.5 kPa. Embryos exploit spatial variation of PO₂ within eggs by positioning gills against patches of air-exposed surface. Respiratory plasticity and oxygen-sensitive behavior appear critical for the hatching plasticity that balances a predation risk trade-off across life stages.     

Adaptive spatial utilization of host mussels by the Japanese rosy bitterling Rhodeus ocellatus kurumeus

The spatial pattern of resource utilization for oviposition in the Japanese rosy bitterling Rhodeus ocellatus kurumeus was investigated in two field experiments. The distribution of rosy bitterling eggs deposited in the four demibranchs of the gills of the test mussel species, Anodonta woodiana , differed with mussel reproductive state in pair spawnings, but not in group spawnings. In pair spawnings, female rosy bitterling may have had more time to select the site of oviposition in the gill in relation to the sex and reproductive state of the mussel, thereby maximizing embryo survival. Thus, the inner gill of female mussels may have been selected in preference to the outer gills to avoid mortalities of eggs due to the presence of the mussel's own embryos (glochidia) in the outer gill chambers. In male mussels, female rosy bitterling distributed their eggs equally among all parts of the mussel gill, thereby minimizing density-dependent mortality of embryos. During group spawnings, however, female rosy bitterling may have been more constrained in their decision making, ovipositing in the inner gills irrespective of mussel sex.     

Three new species of Huffmanela Moravec, 1987 (Nematoda: Trichosomoididae) from the gills of marine fish off New Caledonia

Three new species of Huffmanela, here described from eggs only, are reported from the gills of marine fish caught off Nouméa, New Caledonia. Eggs of Huffmanela branchialis n. sp., from Nemipterus furcosus (Nemipteridae), are 45-52 (mean 48) microm in length and 23-30 (mean 25) microm in width, with thin shells. Each egg is enclosed in a thin membrane forming a spindle-shaped envelope 53-85 (mean 63) microm in length. Eggs of H. filamentosa n. sp., from Gymnocranius grandoculis (Lethrinidae), are 48-53 (mean 50) microm in length and 25-30 (mean 27) microm in width, with thin shells. Each egg bears a few long (150 microm), thin filaments. Eggs of these two new species were compared to those of H. paronai Moravec & Garibaldi, 2000, which are redescribed. Eggs of H. ossicola n. sp. were found within the branchial arch bone of Bodianus loxozonus (Labridae) and also filled the spinal chord bone and other bones. This is the first species of Huffmanela reported from bone tissue. Eggs are large, 72-88 (mean 79) microm in length and 32-40 (mean 36) microm in width, with a very thick shell. Each egg is covered with numerous filaments enclosed in a thin envelope. Fresh eggs were unembryonated, but embryos were visible after incubation in seawater. The three new species can be distinguished from other species of Huffmanela by size and the nature of the egg covering. Egg morphology of and their location in the host suggest different life-cycles: those of the first two species (small eggs, thin shells, egg covering possibly favouring flotation) are released from the gill mucosa with the turnover of living tissues and immediately continue their life-cycle, but eggs of H. ossicola (large eggs, thick shell) are only available for the continuation of the life-cycle after the host's death.     

Divergence of ovipositor length and egg shape in a brood parasitic bitterling fish through the use of different mussel hosts

Bitterling fishes deposit their eggs on the gills of living mussels using a long ovipositor. We examined whether ovipositor length (OL) and egg shape correlated with differences in host mussel species in the family Unionidae among populations of the tabira bitterling (Acheilognathus tabira) in Japan. Bitterling populations that use mussels in the sub-family Anodontinae possessed longer ovipositors and more elongated eggs than those using mussels of Unioninae, as expected from the difference in host size between the sub-families (anodontine mussels are larger than unionine mussels). Based on a robust phylogeny of A. tabira populations, we demonstrated that the evolution of both OL and egg shape were correlated with host differences, but not with each other, suggesting that these traits have been selected for independently. Our study demonstrates how adaptive traits for brood parasitism may diverge with host shift due to different host availability and/or interspecific competition for hosts.     

版纳鱼螈胚胎和幼体鳃的退化观察

为了解版纳鱼螈(Ichthyophis bannanicus)胚胎和幼体鳃的退化特征,同窝卵中8枚在胚胎成熟阶段早期被随机取出剖产,随后余下的9枚卵在胚胎成熟阶段晚期时孵出或剖产,观察幼体或胚胎鳃的变化。成熟阶段早期的胚胎,初时其鳃色鲜红,鳃枝充盈,鳃丝与鳃轴近乎垂直;随后鳃色发白,鳃枝疲软,鳃丝卷曲,鳃丝与鳃轴夹角变小。成熟阶段晚期的胚胎和刚孵出的幼体,初时其鳃色纯白,鳃枝疲软,鳃丝卷曲,鳃丝与鳃轴夹角较小;随后鳃逐渐脱落。观察发现,版纳鱼螈胚胎或幼体鳃的退化模式不是重吸收,也不是重吸收加脱落,而仅为脱落。鳃退化过程经历外鳃供血减少-供血停止-鳃枝组织死亡和脱落3个阶段,每个阶段都有明显的外部形态特征。胚胎进入成熟阶段后,越早孵化,鳃枝留存越多,反之,鳃枝留存越少。发白后的鳃枝随机性脱落。     

Tissue damage and leukocytic infiltration following attachment of the mite Unionicola intermedia to the gills of the bivalve mollusc Anodonta anatina

Unionicola intermedia lives as a parasite in the gill region of Anodonta anatina. It attaches to the gills of its host by means of the pedipalps which cause displacement, rupture, and erosion of the gill epithelium. The pedipalps are sunk deeply into the underlying connective tissue of the gills and produce a leukocytic infiltration into the damaged area and a consequent edema of the gill filaments.     

Why do Red-winged Blackbrids accept eggs of Brown-headed Cowbirds?

Summary Avian brood parasites usually severely depress the reproductive success of their hosts, yet many host species, including those presumably capable of ejecting parasitic eggs, accept them. Female, brood-parasitic, Brown-headed Cowbirds typically remove a host egg when they lay their own and damage some host eggs in the process of ejecting a host egg. Data from a field study of Red-winged Blackbirds show that these costs, which cannot be avoided by ejecting the parasitic egg, account for some of the reproductive losses attributable to parasitism, but part is due to the presence of the cowbird egg in the nest. To assess whether ejection would be favoured under current circumstances, the probable damage a female Redwing could cause to her own eggs by attempting to eject a cowbird egg needs to be determined.     

Immunohistochemistry,ultrastructure and pathology of gills of Abramis brama from Lake Mondsee,Austria, infected with Ergasilus sieboldi (Copepoda)

Immunohistochemical, ultrastructural and pathological studies were carried out on the gills of bream Abramis brama (L.) from Lake Mondsee, Austria, that were naturally infected with Ergasilus sieboldi Nordmann, 1832. Of a total of 14 specimens of bream examined, the gills of 7 (50%) were parasitized with this copepod and the intensity of infection ranged from 1 to 23 crustaceans per host. Histopathological investigations of infected gill showed extensive tissue damage due to attachment and feeding of the crustacean. Parasites attached close to the base of filaments near the gill arch. Pressure exerted by the ectoparasite attached to the lateral margin of the gill filaments induced atrophy of the secondary lamellae. Tissue reactions included hyperplasia and mucous cell proliferation of the respiratory epithelium. Mucous cells displayed an intense immunohistochemical reactivity with the anti-nitric oxide synthase antibody. In parasitized primary and secondary lamellae, a high number of eosinophilic granular cells and rodlet cells were noticed. Rodlet cells represent an inflammatory cell type closely linked to other piscine inflammatory cells. Presence of a high number of inflammatory cells at the site of E. sieboldi attachment is related to intense host cellular reaction.     

Spatial distributions of two species of monogeneans on the gills of Siganus fuscescens (Houttuyn) and their seasonal dynamics in caged versus wild-caught hosts

Two monogeneans species, Polylabris mamaevi Ogawa & Egusa, 1980 and Tetrancistrum nebulosi Young, 1967, are sympatric on the gills of Siganus fuscescens (Houttugn, 1782) in the South China Sea. An investigation into their distribution on the host's gills based on monthly samples from both wild and caged populations revealed that these 2 species co-occurred on the same gill arches, but they were segregated. P. mamaevi attached to the distal half of the gill filaments, whereas T. nebulosi attached to the proximal half. This difference may partly be attributed to microhabitat specialization. Microhabitat distributions were intensity dependent for both species. As intensity increased, monogeneans were increasingly found on the second, third, and even fourth gill arches, and niche breadths increased. The changes in distribution and niche breadths at the host gill arch level in relation to differences in host size and sampling period were considered to represent a functional response to increased intensity. Differences in host resources, in either net-caged or wild populations, did not significantly influence the parasite distributions at the host gill arch level. Simultaneous infections of these 2 species were common, but there was no evidence of negative interspecific interactions.     

Egg removal by cuckoos forces hosts to accept parasite eggs

Many avian brood parasites remove one or more host eggs before laying their own eggs in the host nest. Various hypotheses have been proposed to explain the adaptive significance of this behaviour, but none of them provides an adequate explanation. Here we provide a new hypothesis for explaining why a parasite removes host eggs before laying its own. In this study, we attempted to answer this question by constructing a mathematical model that focused on the changes in host decision making according to reduced clutch size as a consequence of egg removal by parasites. We assume that a host selects one of the following two options to maximise the number of its own chicks: trying to eject a suspicious egg from the nest (trying‐to‐eject) or acceptance without trying to eject the egg (acceptance). The option selected depends on the number of eggs in the nest. Our model provides a new explanation for egg removal behaviour by showing that the host should select trying‐to‐eject if there is a large number of eggs in the nest but acceptance with a small number of eggs. This is because the relative payoff for a host that selects trying‐to‐eject decreases with the number of eggs in the nest. Therefore, parasites benefit by removing the host egg because this behaviour reduces the number of eggs in the nest, thereby increasing the probability of their own eggs being accepted. Thus, hosts have evolved egg ejection to combat brood parasites, but it may also have facilitated the evolution of egg removal by parasites. This hypothesis may also apply to brood parasitic species that do not eject host chicks. In addition, this hypothesis may explain other parasitic behaviours, such as egg damaging and egg puncturing, which lead to reductions in the host clutch size.     

Hatching timing,oxygen availability,and external gill regression in the tree frog,Agalychnis callidryas

The physiological role of the embryonic external gills in anurans is equivocal. In some species, diffusion alone is clearly sufficient to supply oxygen throughout the embryonic period. In others, morphological elaboration and environmental regulation of the external gills suggest functional importance. Since oxygen stress is a common trigger of hatching, I examined the relationships among hatching timing, oxygen stress, and external gill loss. I worked with the red-eyed tree frog, Agalychnis callidryas, a species with arboreal eggs and aquatic tadpoles in which gill regression is associated with hatching, and hatching timing affects posthatching survival with aquatic predators. Both exposure to a hypoxic gas mixture and submergence in water, a natural context in which hypoxic stress can occur, induced early hatching. Exposure to hyperoxic gas mixtures induced regression of external gills, and subsequent exposure to air induced early hatching. Prostaglandin-induced external gill regression also induced hatching, and this effect was partially ameliorated by exposure to hyperoxic gas. Together, these results suggest that external gills enhance the oxygen uptake of embryos and are necessary to extend embryonic development past the onset of hatching competence.     

Investigation of Paradiplozoon homoion (Monogenea, Diplozoidae) life cycle under experimental conditions

Diplozoids (Diplozoidae, Monogenea) are fish ectoparasites with a direct life cycle without intermediate hosts. Their free swimming larva, the oncomiracidium, hatches from eggs, invades a fish host and metamorphoses into a post-oncomiracidial larval stage, the diporpa. Later, two diporpae fuse and live as a pair in cross-copulation during their adult life. An experimental study was designed to investigate the life cycle of Paradiplozoon homoion (Monogenea, Diplozoidae) parasitizing their common fish hosts, gudgeon (Gobio gobio). A total of 35 gudgeon parasitized by diplozoids were collected from their natural environment of the Vlára River, Czech Republic, and kept together in tanks with 41 non-parasitized gudgeons reared in a laboratory environment. In total, 100 adult specimens of P. homoion were collected from the Vlára River gudgeon and a new parasite generation was expected to be observed on fish reared in the laboratory environment. Eight days after the first diplozoid eggs appeared on fish gills, the presence of diporpae with one or two pairs of clamps was noted. The appearance of the first juveniles was recorded at the same time as diporpae. Development of P. homoion from egg to sexually mature adult stage took 33 days at a constant temperature of 20 degrees C. The development of eggs in adults of the second generation was observed 2 days after the first observation of these adults. The behavior of oncomiracidia was also studied and this free swimming stage of diplozoids survived for 22 h in the absence of a host. When host fish were experimentally infected by oncomiracidia, diporpae were found attached to the fish gill apparatus within 2 h of infection.     

Egg mimicry by the Pacific koel: mimicry of one host facilitates exploitation of other hosts with similar egg types

When brood parasites exploit multiple host species, egg rejection by hosts may select for the evolution of host‐specific races, where each race mimics a particular host's egg type. However, some brood parasites that exploit multiple hosts with the ability to reject foreign eggs appear to have only a single egg type. In these cases, it is unclear how the parasite egg escapes detection by its hosts. Three possible explanations are: 1) host‐specific races are present, but differences in egg morphology are difficult for the human eye to detect; 2) the brood parasite evolves a single egg type that is intermediate in appearance between the eggs of its hosts; 3) or the parasite evolves mimicry of one of its hosts, which subsequently allows it to exploit other species with similar egg morphology. Here we test these possibilities by quantifying parameters of egg appearance of the brood‐parasitic Pacific koel Eudynamys orientalis and seven of its hosts. Koel eggs laid in the nests of different hosts did not show significant differences in colour or pattern, suggesting that koels have not evolved host‐specific races. Koel eggs were similar in colour, luminance and pattern to the majority of hosts, but were significantly more similar in colour and luminance to one of the major hosts than to two other major hosts, supporting hypothesis 3. Our findings suggest that mimicry of one host can allow a brood parasite to exploit new hosts with similar egg morphologies, which could inhibit the evolution of host defences in naïve hosts.     

Ultrastructure and development of the gills in<Emphasis Type="Italic"> Rana dalmatina</Emphasis> (Amphibia,Anura)

The appearance and the modification of the gill apparatus in Rana dalmatina tadpoles have been described in the different phases of larval development. The morphology and ultrastructure have been studied using light microscopy and both scanning and transmission electron microscopy. The organization of the gills during the initial phases of development (external gills or transient gills) brings to mind the characteristics of Urodela larvae in which the gills appear to consist of three tufts of filaments supported by the gill arches III, IV and V. The cellular composition of the transient gills appears to be extremely simple and the presence of specialized cells is not noted. Basal cells, pavement cells and ciliated cells form the thin mono- or bilayered epithelium. In the persistent gills (or internal gills) of the R. dalmatina tadpole (Ortons larval type 4) the gill arches carry four rows of gill tufts branching out to the ventral region. Meanwhile, from the dorsal portion of the arch the gill filters present an axial portion from which there is much branching out, which confers a characteristic appearance on this part of the gills. The cellular composition of the gill tufts and of the filters is different: in the gill tufts basal cells, pavement cells, ciliated cells, cubic cells and mitochondria-rich cells (MRCs) have been recognized, while in the gill filters the last cellular type does not appear. The MRC has highly variable forms and dimensions and is characterized by the presence of numerous mitochondria in the cytoplasm. Often the MRCs manifest themselves grouped together, in groups of three or more. The pavement cells and the cubic cells demonstrate identical ultrastructural characteristics and have an external surface area characterized by the presence of short superficial microridges and numerous vacuoles in the apical cytoplasm.