Pyxidiophora: life histories and arthropod associations of two species

1989 ◽  
Vol 67 (9) ◽  
pp. 2552-2562 ◽  
Author(s):  
Meredith Blackwell ◽  
David Malloch
Keyword(s):  
Life Cycle ◽  
New Brunswick ◽  
Life Histories ◽  
Field Studies ◽  
Life Cycles ◽  
Frequent Occurrence ◽  
Evolutionary Significance ◽  
Complex Life Cycles ◽  
Phoretic Mite

Based on field studies in New Brunswick and Ontario, two species of the genus Pyxidiophora are demonstrated to be of frequent occurrence. Pyxidiophora sp. and Pyxidiophora spinuliformis have complex life cycles involving anamorph formation and sporulation on a phoretic mite host. Pyxidiophora sp., the more common of the two species, appears to be parasitic on the apothecia of coprophilous Pezizales where it forms clusters of synnemata within a week of dung deposition. Later, perithecia develop among the synnemata and produce ascospores. Ascospores attach to mites that are, in turn, carried by beetles and flies to a new substrate. On the new substrate while attached to the mite, ascospores of Pyxidiophora sp. differentiate into linearly arranged or complex and often muriform Thaxteriola thalli, which produce phialoconidia. The phialoconidia appear to be the propagules that inoculate the new substrate. Pyxidiophora spinuliformis has a life cycle similar to that of Pyxidiophora sp. but differs in having a conidial anamorph with a different development and ascospores that never form muriform thalli on the phoretic mite host. The taxonomic, ecological, and evolutionary significance of these findings is discussed.

Autonomy and integration in complex parasite life cycles

Parasitology ◽  
2016 ◽  
Vol 143 (14) ◽  
pp. 1824-1846 ◽  
Author(s):  
DANIEL P. BENESH
Keyword(s):  
Life Cycle ◽  
Holistic Approach ◽  
Life Cycles ◽  
Complex Life Cycle ◽  
Functional Specialization ◽  
Life Stages ◽  
Free Living ◽  
New Host ◽  
Complex Life Cycles ◽  
Life Cycle Stages

SUMMARYComplex life cycles are common in free-living and parasitic organisms alike. The adaptive decoupling hypothesis postulates that separate life cycle stages have a degree of developmental and genetic autonomy, allowing them to be independently optimized for dissimilar, competing tasks. That is, complex life cycles evolved to facilitate functional specialization. Here, I review the connections between the different stages in parasite life cycles. I first examine evolutionary connections between life stages, such as the genetic coupling of parasite performance in consecutive hosts, the interspecific correlations between traits expressed in different hosts, and the developmental and functional obstacles to stage loss. Then, I evaluate how environmental factors link life stages through carryover effects, where stressful larval conditions impact parasites even after transmission to a new host. There is evidence for both autonomy and integration across stages, so the relevant question becomes how integrated are parasite life cycles and through what mechanisms? By highlighting how genetics, development, selection and the environment can lead to interdependencies among successive life stages, I wish to promote a holistic approach to studying complex life cycle parasites and emphasize that what happens in one stage is potentially highly relevant for later stages.

Life Cycles

2001 ◽  
Author(s):  
Jan A. Pechenik
Keyword(s):  
Life Cycle ◽  
Genetic Material ◽  
Life Cycles ◽  
Offspring Size ◽  
Free Living ◽  
Complex Life Cycles ◽  
Volume Number ◽  
Larval Stages ◽  
Underlying Mechanisms ◽  
Life Cycle Evolution

I have a Hardin cartoon on my office door. It shows a series of animals thinking about the meaning of life. In sequence, we see a lobe-finned fish, a salamander, a lizard, and a monkey, all thinking, “Eat, survive, reproduce; eat, survive, reproduce.” Then comes man: “What's it all about?” he wonders. Organisms live to reproduce. The ultimate selective pressure on any organism is to survive long enough and well enough to pass genetic material to a next generation that will also be successful in reproducing. In this sense, then, every morphological, physiological, biochemical, or behavioral adaptation contributes to reproductive success, making the field of life cycle evolution a very broad one indeed. Key components include mode of sexuality, age and size at first reproduction (Roff, this volume), number of reproductive episodes in a lifetime, offspring size (Messina and Fox, this volume), fecundity, the extent to which parents protect their offspring and how that protection is achieved, source of nutrition during development, survival to maturity, the consequences of shifts in any of these components, and the underlying mechanisms responsible for such shifts. Many of these issues are dealt with in other chapters. Here I focus exclusively on animals, and on a particularly widespread sort of life cycle that includes at least two ecologically distinct free-living stages. Such “complex life cycles” (Istock 1967) are especially common among amphibians and fishes (Hall and Wake 1999), and within most invertebrate groups, including insects (Gilbert and Frieden 1981), crustaceans, bivalves, gastropods, polychaete worms, echinoderms, bryozoans, and corals and other cnidarians (Thorson 1950). In such life cycles, the juvenile or adult stage is reached by metamorphosing from a preceding, free-living larval stage. In many species, metamorphosis involves a veritable revolution in morphology, ecology, behavior, and physiology, sometimes taking place in as little as a few minutes or a few hours. In addition to the issues already mentioned, key components of such complex life cycles include the timing of metamorphosis (i.e., when it occurs), the size at which larvae metamorphose, and the consequences of metamorphosing at particular times or at particular sizes. The potential advantages of including larval stages in the life history have been much discussed.

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.

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.

Detection of a new Clytia species (Cnidaria: Hydrozoa: Campanulariidae) with DNA barcoding and life cycle analyses

2013 ◽  
Vol 93 (8) ◽  
pp. 2075-2088 ◽  
Author(s):  
Konglin Zhou ◽  
Lianming Zheng ◽  
Jinru He ◽  
Yuanshao Lin ◽  
Wenqing Cao ◽  
...  
Keyword(s):  
Life Cycle ◽  
Dna Barcoding ◽  
Ribosomal Rna ◽  
Coastal Waters ◽  
Large Subunit ◽  
Life Cycles ◽  
Complex Life Cycles ◽  
Distinct Lineage ◽  
Whole Life Cycle ◽  
Medusa Stage

The genus Clytia is distributed worldwide, but most accepted species in this genus have been examined either only at the hydroid or medusa stage. The challenge in identifying Clytia species reflects their complex life cycles and phenotypic plasticity. In this study, molecular and morphological investigations of Clytia specimens from the coastal waters of China revealed an as yet unreported species, designated C. xiamenensis sp. nov., that was considered as conspecific to two nearly cosmopolitan species, C. hemisphaerica and C. gracilis. DNA barcoding based on partial mitochondrial cytochrome c oxidase subunit I (COI) and large subunit ribosomal RNA gene (16S) confirmed the highly distinct lineage of C. xiamenensis sp. nov. These results were corroborated by the detailed observations of its mature medusae and its colonies, which showed that C. xiamenensis sp. nov. was morphologically distinct from other species of Clytia. Thus, based on our findings, the nearly cosmopolitan distribution attributed to some species of Clytia might rather be due to the misidentification, and it is necessary to elucidate their whole life cycle in order to establish the systematic validity of all species within the genus Clytia.

The diversity and natural history of parasites

2021 ◽  
pp. 19-50
Author(s):  
Paul Schmid-Hempel
Keyword(s):  
Life Cycle ◽  
Natural History ◽  
Food Chain ◽  
Life Cycles ◽  
Growth Phases ◽  
New Host ◽  
Complex Life Cycles ◽  
Parasitic Species ◽  
Parasitic Lifestyle ◽  
History Of

Parasites are more numerous than non-parasitic species and have evolved in virtually all groups of organisms, such as viruses, prokaryotes (bacteria), protozoa, fungi, nematodes, flatworms, acantocephalans, annelids, crustaceans, and arthropods (crustacea, mites, ticks, insects). These groups have adapted to the parasitic lifestyle in very many ways. Evolution towards parasitism has also followed different routes. Initial steps such as phoresy, followed by later consumption of the transport host, are plausible evolutionary routes. Alternatively, formerly free-living forms have become commensals before evolving parasitism. Complex life cycles with several hosts evolved by scenarios such as upward (adding a new host upwards in the food chain), downward, or lateral incorporation, driven by the advantage of extending growth phases within hosts and increasing fecundity. Examples are digenea; other parasites have added vectors to their life cycle.

Life History Studies on Trematodes of the Subfamily Reniferinae

Parasitology ◽  
1933 ◽  
Vol 25 (4) ◽  
pp. 518-545 ◽  
Author(s):  
S. Benton Talbot
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Life Histories ◽  
Life Cycles ◽  
Small Fish ◽  
Intermediate Hosts ◽  
Natural Group ◽  
Remarkable Similarity ◽  
Physella Gyrina ◽  
Mother Sporocyst

1. The life histories of Lechriorchis primus Stafford, L. tygarti n.sp. and Caudorchis eurinus n.gen. et sp. have been experimentally completed in three hosts, the first complete life histories to be worked out for species of the subfamily Reniferinae.2. The definitive hosts of the three forms were found to be two species of garter snakes, Thamnophis sauritus and T. sirtalis.3. Three species of snails, Physella gyrina, P. parkeri, and P. ancillaria, have been found to serve as the first intermediate host in the life cycles of Lechriorchis primus and Caudorchis eurinus n.gen. et sp., and two species of snails, Physella gyrina and P. heterostropha, in the life cycle of Lechriorchis tygarti n.sp.4. The tadpoles of two species of frogs, Rana clamitans and R. pipiens, were found to serve as the second intermediate hosts in the life cycles of all three trematodes. The cercariae penetrate larvae of Triturus and small fish, but live only a short time in these animals.5. Every stage in the life history of Lechriorchis primus, including egg, miracidium, mother sporocyst, daughter sporocyst, cercaria, metacercaria, and developmental stages in the definitive host, has been described in detail.6. The mother sporocyst of forms having a stylet cercaria is described for the first time.7. The flame cell pattern of the cercariae of L. primus, L. tygarti n.sp., and Caudorchis eurinus n.gen. et sp. has been determined to be of the “2 × 6 × 3’ type. Also the adult stage of C. eurinus was determined to have the same type.8. It has been pointed out that the life histories of the members of the subfamily are uniform in that their life history stages display a remarkable similarity.9. It has been suggested that this uniform type of life cycle and remarkable similarity of larval stages offer the most logical basis for establishing the subfamily Reniferinae as a natural group.

Identification of life cycle stages of the nematode Echinocephalus overstreeti by allozyme electrophoresis

1988 ◽  
Vol 62 (2) ◽  
pp. 153-157 ◽  
Author(s):  
R. H. Andrews ◽  
I. Beveridge ◽  
M. Adams ◽  
P. R. Baverstock
Keyword(s):  
Life Cycle ◽  
Electrophoretic Analysis ◽  
Life Cycles ◽  
Allozyme Electrophoresis ◽  
Larval Form ◽  
Complex Life Cycles ◽  
Life Cycle Stages ◽  
Allelic Differences ◽  
Mollusc Species ◽  
Shared Alleles

ABSTRACTData presented in this study highlight the potential of allozyme electrophoresis in providing unequivocal genetic evidence for the identification of life cycle stages, particularly where species have complex life cycles. Adults of the nematode Echinocephalus overstreeti parasitize the elasmobranch Heterodontus portusjacksoni. The putative larval form which is morphologically dissimilar is found in two species of marine molluscs, Chlamys bifrons and Pecten albus. Electrophoretic analysis indicated that the adult and larval forms shared alleles at all of the 34 enzyme loci established. Furthermore, there were no fixed allelic differences between larval forms from different mollusc species.

Euphausiid life cycles and distribution around South Georgia

1990 ◽  
Vol 2 (1) ◽  
pp. 43-52 ◽  
Author(s):  
Peter Ward ◽  
Angus Atkinson ◽  
Julie M. Peck ◽  
Andrew G. Wood
Keyword(s):  
Life Cycle ◽  
Life Histories ◽  
Life Cycles ◽  
Seasonal Migration ◽  
Frequency Data ◽  
Oceanic Water ◽  
Limited Evidence ◽  
South Georgia ◽  
The North ◽  
One Year

Euphausiid life histories and distribution in the vicinity of South Georgia were studied from a series of samples taken in April 1980, November–December 1981, and July–August 1983. Size frequency data indicated a two-year life cycle for Euphausia frigida and the possibility of a three-year cycle for E. triacantha. The genus Thysanoessa was represented by a mixture of T. macrura and the dominant T. vicina. A one-year life cycle is proposed for the latter but that of the former is unknown. Spawning in E. frigida and to a lesser extent Thysanoessa spp. commenced as early as July and euphausiid calyptopes were a feature of the plankton for much of the year. E. superba eggs were found in low abundance over the shelf to the north of the island, but no hatched larvae were found. Behaviour patterns such as diurnal and seasonal migration partially confounded attempts to relate euphausiid distribution to environmental features. However calyptopes of most species, were generally more abundant in oceanic water deeper than 500 m and there was limited evidence that in August, E. frigida had commenced spawning in the colder part of the survey area.

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