scholarly journals Circulation Pathways of Trematodes of Freshwater Gastropod Mollusks in Forest Biocenoses of the Ukrainian Polissia

2019 ◽  
Vol 53 (1) ◽  
pp. 13-22 ◽  
Author(s):  
E. P. Zhytova ◽  
L. D. Romanchuk ◽  
S. V. Guralska ◽  
O. Yu. Andreieva ◽  
M. V. Shvets
Keyword(s):  
Life Cycle ◽  
Life Cycles ◽  
Trematode Species ◽  
Intermediate Hosts ◽  
Alaria Alata ◽  
Gastropod Mollusks ◽  
Second Intermediate Host ◽  
Host Life ◽  
Taxonomic Groups ◽  
Diversity Of Life

Abstract This is the first review of life cycles of trematodes with parthenitae and larvae in freshwater gastropods from forest biocoenoses of Ukrainian Polissia. Altogether 26 trematode species from 14 families were found circulating in 13 ways in molluscs from reservoirs connected with forest ecosystems of the region. Three-host life cycle is typical of 18 trematode species, two-host life cycle has found in 7 species, and four-host cycles has found in one species. Alaria alata Goeze, 1782, has three-host (Shults, 1972) and four-host cycles. Opisthioglyphe ranae (Froehlich, 1791) can change three-host life cycle to two-host cycle replacing the second intermediate host (Niewiadomska et al., 2006) with the definitive host. Species with primary two-host life cycle belong to Notocotylidae Lühe, 1909, Paramphistomidae Fischoeder, 1901 and Fasciolidae Railliet, 1758 families. Trematodes with three-host cycle have variable second intermediate hosts, including invertebrates and aquatic or amphibious vertebrates. Definitive hosts of trematodes are always vertebrates from different taxonomic groups. The greatest diversity of life cycles is typical for trematodes of birds. Trematodes in the forest biocoenoses of Ukrainian Polissia infect birds in six ways, mammals in three, amphibians in four, and reptiles in one way. The following species have epizootic significance: Liorchis scotiae (Willmott, 1950); Parafasciolopsis fasciolaemorpha Ejsmont, 1932; Notocotylus seineti Fuhrmann, 1919; Catatropis verrucosa (Frölich, 1789) Odhner, 1905; Cotylurus cornutus (Rudolphi, 1808); Echinostoma revolutum (Fröhlich, 1802) Dietz, 1909; Echinoparyphium aconiatum Dietz, 1909; Echinoparyphium recurvatum (Linstow, 1873); Hypoderaeum conoideum (Bloch, 1782) Dietz, 1909; Paracoenogonimus ovatus Kasturada, 1914; Alaria alata Goeze, 1782.

Encystment site affects the reproductive strategy of a progenetic trematode in its fish intermediate host: is host spawning an exit for parasite eggs?

Parasitology ◽  
2011 ◽  
Vol 138 (9) ◽  
pp. 1183-1192 ◽  
Author(s):  
KRISTIN K. HERRMANN ◽  
ROBERT POULIN
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Body Cavity ◽  
Life Cycles ◽  
Temperature Changes ◽  
Fish Spawning ◽  
Second Intermediate Host ◽  
Host Life ◽  
Major Factors ◽  
Fish Hosts

SUMMARYEach transmission event in complex, multi-host life cycles create obstacles selecting for adaptations by trematodes. One such adaptation is life cycle abbreviation through progenesis, in which the trematode precociously matures and reproduces within the second intermediate host. Progenesis eliminates the need for the definitive host and increases the chance of life cycle completion. However, progenetic individuals face egg-dispersal challenges associated with reproducing within metacercarial cysts in the tissues or body cavity of the second intermediate host. Most progenetic species await host death for their eggs to be released into the environment. The present study investigated temporal variation of progenesis in Stegodexamene anguillae in one of its second intermediate fish hosts and the effect of the fish's reproductive cycle on progenesis. The study involved monthly sampling over 13 months at one locality. A greater proportion of individuals became progenetic in the gonads of female fish hosts. Additionally, progenesis of worms in the gonads was correlated with seasonal daylight and temperature changes, major factors controlling fish reproduction. Host spawning events are likely to be an avenue of egg dispersal for this progenetic species, with the adoption of progenesis being conditional on whether or not the parasite can benefit from fish spawning.

Progenesis in digenean trematodes: a taxonomic and synthetic overview of species reproducing in their second intermediate hosts

Parasitology ◽  
2005 ◽  
Vol 130 (6) ◽  
pp. 587-605 ◽  
Author(s):  
F. LEFEBVRE ◽  
R. POULIN
Keyword(s):  
Life Cycle ◽  
Cyst Wall ◽  
Egg Production ◽  
Biological Information ◽  
Trematode Species ◽  
Costs And Benefits ◽  
Intermediate Hosts ◽  
Digenean Trematode ◽  
Second Intermediate Host ◽  
The Subject

Precocious egg production, i.e. progenesis, has been documented for a number of species in scattered reports throughout the trematode literature. The last 2 extensive studies on the subject date from Buttner in the early 1950s (in French) and from Tang in the early 1980s (in Chinese). Overall, 43 species were then known for their ability to produce eggs at the metacercarial stage while still in the second intermediate host. Here, we update the list, and document the existence of progenesis in a total of 79 digenean trematode species, for which we provide information on the taxonomy of the hosts, the facultative or obligate character of progenesis, relevant references, as well as some other pertinent biological information. We then review the subject by asking 7 questions of fundamental evolutionary importance. These include: What favours progenetic development? What are the associated costs and benefits? How are progenetic eggs released from the host? While exposing the various opinions of previous authors, we attempt to give a synthetic overview and stress on the importance of the metacercarial cyst wall (whether it is present, and if so its thickness) in the evolution and the adoption of a progenetic life-cycle.

Metazoan parasites in an intermediate host population near its southern border: the common cockle (Cerastoderma edule) and its trematodes in a Moroccan coastal lagoon (Merja Zerga)

2008 ◽  
Vol 88 (2) ◽  
pp. 357-364 ◽  
Author(s):  
Mériame Gam ◽  
Hocein Bazaïri ◽  
K. Thomas Jensen ◽  
Xavier de Montaudouin
Keyword(s):  
Species Composition ◽  
Intermediate Host ◽  
Coastal Lagoon ◽  
Life Cycles ◽  
Geographical Range ◽  
Trematode Species ◽  
Intermediate Hosts ◽  
Metazoan Parasites ◽  
Cerastoderma Edule ◽  
Second Intermediate Host

The metazoan parasite community of Cerastoderma edule was studied in the southern geographical range of the host (the coastal lagoon Merja Zerga, Morocco). A total of 11 metazoan species was found in cockles. Nine of these were trematodes using cockles as either first intermediate host (three species) or second intermediate host (six species). In addition, two other endo-metazoan species (Pinnotheres pisum and Paravortex cardii) were recorded from cockles in the studied lagoon. All the observed metazoans in cockles from Merja Zerga have previously been recorded at sites north of Africa.Up to 10% of the cockles in the studied size-groups were first intermediate hosts to castrating parasites (Gymnophallus choledochus, Labratrema minimus and Monorchis parvus). Among trematodes having metacercariae in cockles (second intermediate host) Meiogymnophallus minutus was the most widespread as it was observed in all cockles from all the examined habitats in the lagoon and it occurred in record high intensities. Different sub-communities of the trematode fauna using cockles as second intermediate host could be identified (subtidal vs intertidal associations).The richness and species composition of the macroparasite community in cockles from Morocco are discussed in relation to patterns seen in cockles from other sites along their geographical range. Migratory fish and waterbirds (final hosts) are generally responsible for the large scale spread (latitudinal spread) of trematodes. However, the distributional patterns of involved intermediate hosts in the life-cycles of the different trematode species in cockles are determining the richness and species composition patterns seen in cockles at shallow water sites along the east Atlantic shoreline.

scholarly journals Diversity of echinostomes (Digenea: Echinostomatidae) in their snail hosts at high latitudes

Parasite ◽  
2021 ◽  
Vol 28 ◽  
pp. 59
Author(s):  
Camila Pantoja ◽  
Anna Faltýnková ◽  
Katie O’Dwyer ◽  
Damien Jouet ◽  
Karl Skírnisson ◽  
...  
Keyword(s):  
North America ◽  
Dna Sequences ◽  
Sequence Data ◽  
Molecular Data ◽  
Migratory Bird ◽  
Parasite Fauna ◽  
Life Cycles ◽  
Freshwater Ecosystems ◽  
Trematode Species ◽  
Host Life

The biodiversity of freshwater ecosystems globally still leaves much to be discovered, not least in the trematode parasite fauna they support. Echinostome trematode parasites have complex, multiple-host life-cycles, often involving migratory bird definitive hosts, thus leading to widespread distributions. Here, we examined the echinostome diversity in freshwater ecosystems at high latitude locations in Iceland, Finland, Ireland and Alaska (USA). We report 14 echinostome species identified morphologically and molecularly from analyses of nad1 and 28S rDNA sequence data. We found echinostomes parasitising snails of 11 species from the families Lymnaeidae, Planorbidae, Physidae and Valvatidae. The number of echinostome species in different hosts did not vary greatly and ranged from one to three species. Of these 14 trematode species, we discovered four species (Echinoparyphium sp. 1, Echinoparyphium sp. 2, Neopetasiger sp. 5, and Echinostomatidae gen. sp.) as novel in Europe; we provide descriptions for the newly recorded species and those not previously associated with DNA sequences. Two species from Iceland (Neopetasiger islandicus and Echinoparyphium sp. 2) were recorded in both Iceland and North America. All species found in Ireland are new records for this country. Via an integrative taxonomic approach taken, both morphological and molecular data are provided for comparison with future studies to elucidate many of the unknown parasite life cycles and transmission routes. Our reports of species distributions spanning Europe and North America highlight the need for parasite biodiversity assessments across large geographical areas.

Challenges for Diadromous Fishes in a Dynamic Global Environment

2009 ◽  
Keyword(s):  
Life Cycle ◽  
Life Histories ◽  
Life Cycles ◽  
Partial Migration ◽  
Environmental Stochasticity ◽  
Species Dynamics ◽  
Life Cycle Pattern ◽  
Aquatic Sciences ◽  
Diversity Of Life

<em>Abstract</em>.-In the study of species life histories and the structure of diadromous populations, an emerging trend is the prevalence of life cycle diversity-that is, individuals within populations that do not conform to a single life cycle pattern. A rapid rise in publications documenting within-population variability in life cycles has resulted in the use of numerous terms and phrases. We argue that myriad terms specific to taxa, ecosystem types, and applications are in fact describing the same phenomenon-life cycle diversity. This phenomenon has been obscured by the use of multiple terms across applications, but also by the overuse of typologies (i.e., anadromy, catadromy) that fail to convey the extent of life cycle variations that underlay population, metapopulation, and species dynamics. To illustrate this, we review migration and habitat-use terms that have been used to describe life cycles and life cycle variation. Using a citation index (Cambridge Scientific Abstracts © Aquatic Sciences and Fisheries Abstracts), terms were tallied across taxonomic family, ecosystem, type of application, analytical approach, and country of study. Studies on life cycle diversity have increased threefold during the past 15 years, with a total of 336 papers identified in this review. Most of the 40 terms we identified described either sedentary or migratory lifetime behaviors. The sedentary-migratory dichotomy fits well with the phenomenon of partial migration, which has been commonly reported for birds and Salmonidae and is postulated to be the result of early life thresholds (switch-points). On the other hand, the lexicon supports alternate modes of migration, beyond the simple sedentary-migratory dichotomy. Here more elaborate causal mechanisms such as the entrainment hypothesis may have application. Diversity of life cycles in fish populations, whether due to partial migration, entrainment, or other mechanisms, is increasingly recognized as having the effect of offsetting environmental stochasticity and contributing to long-term persistence.

Life cycles of species of Proteocephalus, parasites of fishes in the Palearctic Region: a review

1999 ◽  
Vol 73 (1) ◽  
pp. 1-19 ◽  
Author(s):  
T. Scholz
Keyword(s):  
Intermediate Host ◽  
Body Cavity ◽  
Life Cycles ◽  
The Body ◽  
Individual Species ◽  
Intermediate Hosts ◽  
Palearctic Region ◽  
Second Intermediate Host ◽  
Planktonic Crustaceans ◽  
Fish Hosts

The life cycles of species of Proteocephalus Weinland, 1858 (Cestoda: Proteocephalidea) parasitizing fishes in the Palearctic Region are reviewed on the basis of literary data and personal experimental observations, with special attention being paid to the development within the intermediate and definitive hosts. Planktonic crustaceans, diaptomid or cyclopid copepods (Copepoda), serve as the only intermediate hosts of all Proteocephalus species considered. A metacestode, or procercoid, develops in the body cavity of these planktonic crustaceans and the definitive host, a fish, becomes infected directly after consuming them. No previous reports of the parenteral location of metacestodes within the second intermediate host as it is in the Nearctic species P. ambloplitis have been recorded. Thus, the life cycles of Proteocephalus tapeworms resemble in their general patterns those of some pseudophyllidean cestodes such as Eubothrium or Bothriocephalus, differing from the latter in the presence of a floating eggs instead of possessing an operculate egg from which a ciliated, freely swimming larva, a coracidium, is liberated. The scolex of Proteocephalus is already formed at the stage of the procercoid within the copepod intermediate host; in this feature, proteocephalideans resemble caryophyllidean rather than pseudophyllidean cestodes. The morphology of procercoids of individual species is described with respect to the possibility of their differentiation and data on the spectrum of intermediate hosts are summarized. Procercoids of most taxa have a cercomer, which does not contain embryonic hooks in contrast to most pseudophyllidean cestodes. The role of invertebrates (alder-fly larvae — Megaloptera) and small prey fishes feeding upon plankton in the transmission of Proteocephalus tapeworms still remains unclear but these hosts are likely to occur in the life cycle. Data on the establishment of procercoids in definitive hosts, morphogenesis of tapeworms within fish hosts, and the length of the prepatent period are still scarce and new observations are needed. Whereas extensive information exists on the development of P. longicollis (syns. P. exiguus and P. neglectus), almost no data are available on the ontogeny of other taxa, in particular those occurring in brackish waters (P. gobiorum, P. tetrastomus). The morphology of P. cernuae and P. osculatus procercoids from experimentally infected intermediate hosts is described for the first time.

Coevolutionary interactions between host life histories and parasite life cycles

Parasitology ◽  
1998 ◽  
Vol 116 (S1) ◽  
pp. S47-S55 ◽  
Author(s):  
J. C. Koella ◽  
P. Agnew ◽  
Y. Michalakis
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Life Cycles ◽  
Microsporidian Parasite ◽  
History Of ◽  
Host Life ◽  
Host Parasite

SummarySeveral recent studies have discussed the interaction of host life-history traits and parasite life cycles. It has been observed that the life-history of a host often changes after infection by a parasite. In some cases, changes of host life-history traits reduce the costs of parasitism and can be interpreted as a form of resistance against the parasite. In other cases, changes of host life-history traits increase the parasite's transmission and can be interpreted as manipulation by the parasite. Alternatively, changes of host's life-history traits can also induce responses in the parasite's life cycle traits. After a brief review of recent studies, we treat in more detail the interaction between the microsporidian parasite Edhazardia aedis and its host, the mosquito Aedes aegypti. We consider the interactions between the host's life-history and parasite's life cycle that help shape the evolutionary ecology of their relationship. In particular, these interactions determine whether the parasite is benign and transmits vertically or is virulent and transmits horizontally.Key words: host-parasite interaction, life-history, life cycle, coevolution.

scholarly journals The helminth infracommunities of the wood mouse (Apodemus sylvaticus) two years after the fire in Mediterranean forests

2013 ◽  
Vol 50 (1) ◽  
pp. 27-38 ◽  
Author(s):  
I. Torre ◽  
A. Arrizabalaga ◽  
C. Feliu ◽  
A. Ribas
Keyword(s):  
Species Richness ◽  
Life Cycle ◽  
Wood Mouse ◽  
Final Host ◽  
Life Cycles ◽  
Helminth Species ◽  
Mediterranean Forests ◽  
Intermediate Hosts ◽  
Wood Mice ◽  
Short Period

AbstractParasites have been recognized as indicators for natural or man-induced environmental stress and perturbation. In this article, we investigated the role of two non-exclusive hypotheses on the response of helminths of wood mice to fire perturbation: 1) a reduction of the helminth infracommunity (species richness) in post-fire areas due to the temporal lack of worms with indirect (complex) life cycles linked to intermediate hosts that are more specialized than the final host, and 2) an increase of the abundance of helminths with direct (simple) life cycles as a response of increasing abundances of the final host, may be in stressful conditions linked to the post-fire recolonization process.We studied the helminth infracommunities of 97 wood mice in two recently burned plots (two years after the fire) and two control plots in Mediterranean forests of NE Spain. Species richness of helminths found in control plots (n = 14) was twice large than in burned ones (n = 7). Six helminth species were negatively affected by fire perturbation and were mainly or only found in unburned plots. Fire increased the homogeneity of helminth infracommunities, and burned plots were characterised by higher dominance, and higher parasitation intensity. We found a gradient of frequency of occurrence of helminth species according to life cycle complexity in burned areas, being more frequent monoxenous (66.6 %), than diheteroxenous (33.3 %) and triheteroxenous (0 %), confirming the utility of helminths as bioindicators for ecosystem perturbations. Despite the short period studied, our results pointed out an increase in the abundance and prevalence of some direct life cycle helminths in early postfire stages, whereas indirect life cycle helminths were almost absent. A mismatch between the final host (that showed a fast recovery shortly after the fire), and the intermediate hosts (that showed slow recoveries shortly after the fire), was responsible for the loss of half of the helminth species.

Experimental life-cycle studies of Raillietiella gehyrae Bovien, 1927 and Raillietiella frenatus Ali, Riley and Self, 1981: pentastomid parasites of geckos utilizing insects as intermediate hosts

Parasitology ◽  
1983 ◽  
Vol 86 (1) ◽  
pp. 147-160 ◽  
Author(s):  
J. H. Ali ◽  
J. Riley
Keyword(s):  
Life Cycle ◽  
Early Development ◽  
Post Infection ◽  
Egg Production ◽  
Fat Body ◽  
Life Cycles ◽  
Stage Larva ◽  
Intermediate Hosts ◽  
Selective Filter ◽  
Complete Development

SUMMARYThe life-cycles of two closely related cephalobaenid pentastomids, Raillietiella gehyrae and Raillietiella frenatus, which utilize geckos as definitive hosts and cockroaches as intermediate hosts, have been investigated in detail. Early development in the fat-body of cockroaches involves 2 moults to an infective, 3rd-stage larva which appears from 42–44 days post-infection. Complete development in geckos involves a further 5 moults in the case of males and 6 for females. Males mature precociously and copulation is a once-in-a-lifetime event which occurs around day 80 post-infection when both sexes are the same size but the uterus of the female is undeveloped. Sperm, stored in the spermathecae, is used to fertilize oocytes which slowly accumulate in the developing saccate uterus. Patency commences when the uterus carries approximately 4000–5500 eggs but only 25–36 % of these contain fully developed primary larvae. Since only mature eggs are deposited, we postulate that the vagina (?) of the female must be equipped with a selective filter that allows through large eggs but retains smaller, immature eggs. Thus the only limit on fecundity is the total number of sperms in the spermathecae and this is precisely the same factor that constrains egg production in the advanced order Porocephalida.

scholarly journals Integrating natural and sexual selection across the biphasic life cycle

2021 ◽  
Author(s):  
Craig Purchase ◽  
Jonathan Evans ◽  
Julissa Roncal
Keyword(s):  
Sexual Selection ◽  
Life Cycle ◽  
Natural Selection ◽  
Conceptual Framework ◽  
Life Cycles ◽  
Parental Effect ◽  
Biphasic Life Cycle ◽  
Evolutionary Trajectories ◽  
Taxonomic Groups ◽  
Natural And Sexual Selection

An alternation between diploid and haploid phases is universal among sexual eukaryotes. Across this biphasic cycle, natural selection and sexual selection occur in both phases. Together, these four stages of selection act on the phenotypes of individuals and influence the evolutionary trajectories of populations, but are rarely studied holistically. Here, we provide a conceptual framework that transcends taxonomic groups, and unifies the entire selection landscape within and across the diploid and haploid phases. Our synthesis produces six direct links among four selection stages, and from this we define four types of parental effect. We argue that knowledge of the complex and intertwined opportunities for selection within biphasic life cycles will offer clearer insights into key ecological and evolutionary processes, with benefits to applied science.

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