The diversity and natural history of parasites

2021 ◽  
pp. 19-50
Author(s):  
Paul Schmid-Hempel

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.

Parasitology ◽  
2016 ◽  
Vol 143 (14) ◽  
pp. 1824-1846 ◽  
Author(s):  
DANIEL P. BENESH

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.


Author(s):  
Jan A. Pechenik

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.


2000 ◽  
Vol 60 (3) ◽  
pp. 503-509 ◽  
Author(s):  
C. E. ALMEIDA ◽  
E. F. RAMOS ◽  
E. GOUVÊA ◽  
M. do CARMO-SILVA ◽  
J. COSTA

Ctenus medius Keyserling, 1891 is a common species in several spots of Mata Atlântica, however there is a great lack of studies in all aspects of its natural history. This work aims to elucidate aspects of ecotope preference compared to large spiders, and to provide data on the development of chromatic patterns during its life cycle. The observations on the behavior of C. medius were done in the campus of Centro Universitário de Barra Mansa (UBM) by means of observations and nocturnal collections using cap lamps. For observations on the development of chromatic patterns, spiderlings raised in laboratory, hatched from an oviposition of a female from campus of UBM, and others spiderlings collected in field were used. The field observations indicate that: C. medius seems to prefer ecotopes characterized by dense shrub vegetation or herbal undergrowth; Lycosa erythrognatha and L. nordeskioldii seems to prefer open sites; Phoneutria nigriventer seems to prefer shrub vegetation and anthropogenic ecotopes as rubbish hills; Ancylometes sp. seems to prefer ecotopes near streams. Concerning chromatic patterns, it was observed that males and females show well distinct patterns during the last two instars, allowing distinction by sex without the use of a microscope. Through chromatic patterns it was also possible to draw a distinction between C. medius and C. ornatus longer that 3 mm cephalothorax width. 69 specimens of C. medius (males and females) collected in the campus of UBM did not show a striking polymorphism in chromatic pattern, but one among 7 adult females collected in National Park of Itatiaia, showed a distinct chromatic pattern.


2021 ◽  
Author(s):  
Dustin T. Dial ◽  
Kathryn M. Weglarz ◽  
Akintunde O. Aremu ◽  
Nathan P. Havill ◽  
Taylor A. Pearson ◽  
...  

AbstractMany plant-sap-feeding insects have maintained a single, obligate, nutritional symbiont over the long history of their lineage. This senior symbiont may be joined by one or more junior symbionts that compensate for gaps in function incurred through genome-degradative forces. Adelgids are sap-sucking insects that feed solely on conifer trees and follow complex life cycles in which the diet fluctuates in nutrient levels. Adelgids are unusual in that both senior and junior symbionts appear to have been replaced repeatedly over their evolutionary history. Genomes can provide clues to understanding symbiont replacements, but only the dual symbionts of hemlock adelgids have been examined thus far. Here, we sequence and compare genomes of four additional dual-symbiont pairs in adelgids. We show that these symbionts are nutritional partners originating from diverse bacterial lineages and exhibiting wide variation in general genome characteristics. Although dual symbionts cooperate to produce nutrients, the balance of contributions varies widely across pairs, and total genome contents reflect a range of ages and degrees of degradation. Most symbionts appear to be in transitional states of genome reduction. Our findings support a hypothesis of periodic symbiont turnover driven by fluctuating selection for nutritional provisioning related to gains and losses of complex life cycles in their hosts.


Zootaxa ◽  
2017 ◽  
Vol 4319 (2) ◽  
pp. 386 ◽  
Author(s):  
IVAN N. BOLOTOV ◽  
ILYA V. VIKHREV ◽  
OLGA V. AKSENOVA ◽  
YULIA V. BESPALAYA ◽  
MIKHAIL Y. GOFAROV ◽  
...  

The mussel leech Batracobdella kasmiana (Oka, 1910) (Hirudinida: Glossiphoniidae) inhabits the mantle cavity of large freshwater mussels (Sawyer 1986; Lai & Chen 2010). This specific lifestyle is unusual in leeches although a few additional parasitic species from mussels have been reported (Grizzle & Brunner 2009). The known localities of B. kasmiana are situated in Japan (Honshu), continental China and Taiwan (Oka 1910, 1917; Gee 1919; Yang 1996; Yamauchi et al. 2008; Lai & Chen 2010). The majority of records were reported from continental China, in which this species is widely distributed across the eastern half of the country from Yunnan to Beijing (Yang 1996). It has never been mentioned as a member of the Russian fauna (Lukin 1976). A few naiad species in the family Unionidae are known hosts of B. kasmiana, including Sinanodonta spp., Cristaria plicata (Leach, 1815), and Nodularia douglasiae (Griffith and Pidgeon, 1833) (Oka 1917; Yang 1996; Yamauchi et al. 2008). The biology and ecological preferences of this leech species are poorly known (Yang 1996; Yamauchi et al. 2008; Lai & Chen 2010). 


1972 ◽  
Vol 79 (4) ◽  
pp. 284-294 ◽  
Author(s):  
Allen M. Young

A knowledge of life cycle and natural history are often important prerequisites to studies of population biology in butterflies. Although studies on the systematics and broad distribution patterns of that familiar New World Tropical group, the Ithomiinae, have been conducted (Seitz, 194; Fox, 1956; Fox, 1968), a lot remains to be known about the biology of many species in Central America. This is surprising in light of the considerable interest in these butterflies as members of mimicry complexes. In this spirit, this paper summarizes life cycle and natural history data on a clear wing ithoreiine Hymenitis nero (Hewitson) (Nymphalidae: Ithomiinae) in Costa Rica. Similar studies of several other sympatric ithomiines have either been completed (Young, in prep.) or begun, as a preliminary step towards understanding the local patterns of diversity of this family in selected tropical plant communities.


1972 ◽  
Vol 79 (3) ◽  
pp. 165-178 ◽  
Author(s):  
Allen M. Young

This paper summarizes the life cycle and some aspects of natural history of the tropical pierid, Dismorphia virgo (Dismorphiinae) in Costa Rica. The precise taxonomic status of the butterfly in Central America has not been established, and it may represent a variable northern isolate of the common South American D. critomedia. Therefore, independent of whether the Central American form discussed in this paper has achieved full species status as the more northern virgo or is a subspecies or variety of critomedia evolving towards species status, this paper provides new information on the biology of the butterfly in Costa Rica. The establishment of precise taxonomic position awaits further study, and for the present purpose, I refer to the butterfly as D. virgo.


Parasitology ◽  
1998 ◽  
Vol 116 (S1) ◽  
pp. S47-S55 ◽  
Author(s):  
J. C. Koella ◽  
P. Agnew ◽  
Y. Michalakis

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.


2013 ◽  
Vol 93 (8) ◽  
pp. 2075-2088 ◽  
Author(s):  
Konglin Zhou ◽  
Lianming Zheng ◽  
Jinru He ◽  
Yuanshao Lin ◽  
Wenqing Cao ◽  
...  

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.


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