scholarly journals A Review of the Biology of Cerataphidini (Hemiptera, Aphididae, Hormaphidinae), Focusing Mainly on Their Life Cycles, Gall Formation, and Soldiers

2010 ◽  
Vol 2010 ◽  
pp. 1-34 ◽  
Author(s):  
Shigeyuki Aoki ◽  
Utako Kurosu

Species of the aphid tribe Cerataphidini (Hormaphidinae) form galls of various shapes onStyraxtrees, their primary host, throughout East and Southeast Asia including tropical rainforests. All known species of the tribe produce second-instar sterile soldiers on the primary host and some also produce first-instar sterile soldiers on the secondary host. Here, we review their complicated life cycles with or without host alternation, the formation process of their remarkable galls (flower-like multiple-cavity galls in particular), and all morphs including soldiers. The life cycles of cerataphidines are basically the same as those of the subfamily Eriosomatinae, but in tropical and subtropical regions their life cycles are not very rigidly tuned to seasonal changes in the climate if any. In addition, cerataphidine galls in these regions last at least several months, or at times even for over one year; thus it often takes longer than one year to complete their life cycles.

2018 ◽  
Author(s):  
Peter Thorpe ◽  
Carmen M. Escudero-Martinez ◽  
Sebastian Eves-van den Akker ◽  
Jorunn I.B. Bos

AbstractAphids are phloem-feeding insects that cause yield losses to crops globally. These insects feature complex life cycles, which in the case of many agriculturally important species involves the use of primary and secondary host plant species. Whilst host alternation between primary and secondary host can occur in the field depending on host availability and the environment, aphid populations maintained as laboratory stocks generally are kept under conditions that allow asexual reproduction by parthenogenesis on secondary hosts. Here, we used Myzus cerasi (black cherry aphid) to assess aphid transcriptional differences between populations collected from primary hosts in the field and those adapted to secondary hosts under controlled environment conditions. Adaptation experiments of M. cerasi collected from local cherry tress to reported secondary host species resulted in low survival rates. Moreover, aphids were unable to survive on secondary host Land cress, unless first adapted to another secondary host, cleavers. Transcriptome analyses of populations collected from primary host cherry in the field and the two secondary host plant species in a controlled environment showed extensive transcriptional plasticity to a change in host environment, with predominantly genes involved in redox reactions differentially regulated. Most of the differentially expressed genes across the M. cerasi populations from the different host environments were duplicated and we found evidence for differential exon usage. In contrast, we observed only limited transcriptional to a change in secondary host plant species.


2020 ◽  
Vol 20 (5) ◽  
Author(s):  
Tetsuya Yamamoto ◽  
Mitsuru Hattori ◽  
Takao Itino

Abstract About 10% of aphid species show host alternation. These aphids migrate between primary and secondary host plant species in spring and autumn. Host alternation has not been observed in subfamily Lachninae, although it has been suggested on the basis of circumstantial evidence that Stomaphis japonica (Takahashi) may alternate its host between Quercus serrata (Murray) and Quercus acutissima (Carruth). However, a molecular phylogenetic study has indicated that the Stomaphis individuals feeding on these two plant species belong to two different lineages and aphids feeding on Q. acutissima and Pinus densiflora (Sieb. & Zucc.) belong to the same lineage. Here, we examined host alternation in Stomaphis species by comparing molecular phylogenetic identities, morphological features, and life cycles. The molecular analysis and morphological examination showed that aphids feeding on Q. acutissima were the same as those feeding on P. densiflora, whereas aphids feeding on Q. serrata were different from those feeding on Q. acutissima or on P. densiflora. Furthermore, winged aphids were observed on both Q. acutissima and P. densiflora in autumn, but we did not observe winged aphids on Q. serrata. These results indicate that Stomaphis (Walker) individuals feeding on Q. serrata and Q. acutissima belong to two species, one that feeds year-round on Q. serrata, and another, heteroecious species that feeds on P. densiflora as a primary host and on Q. acutissima as a secondary host. This study documents host alternation in subfamily Lachninae for the first time and discusses the acquisition of host alternation by Stomaphis from evolutionary and ecological perspectives.


2005 ◽  
Vol 37 (5) ◽  
pp. 373-382 ◽  
Author(s):  
William B. SANDERS

The utility of plastic cover slips as a substratum for in situ study of lichen developmental stages is further explored in a neotropical foliicolous lichen community and in a European temperate corticolous community. Twenty-one months after placement in the tropical forest, the cover slips bore foliicolous lichen thalli with several species producing characteristic ascocarps and ascospores, indicating the suitability of the substratum for completion of the life cycle of these lichens. On cover slips placed within the temperate corticolous community, lichen propagules anchored to the substratum with relatively short attachment hyphae but did not develop further within the one year observation period. Intimately intermixed microbial communities of short-celled, mainly pigmented fungi and chlorophyte algae developed upon the transparent substratum. Among the algae, Trebouxia cells, often in groups showing cell division and without associated lichenizing hyphae, were commonly observed. The potential significance of the free-living populations in the life cycle of Trebouxia and in those of Trebouxia-associated lichen fungi is discussed.


Author(s):  
Alan D. Ansell

Seasonal changes in the gonads of both sexes of Venus striatula were followed by macroscopic and microscopic examination, in over 700 animals from a population consisting mainly of one year-group. The sex ratio was approximately equal, and no hermaphrodite adults were found.


1979 ◽  
Vol 11 (4) ◽  
pp. 411-424
Author(s):  
H. Mary Fellowes ◽  
Catherine A. Hytten ◽  
W.Z. Billewicz ◽  
A.M. Thomson

SummaryOne hunderd and forty 'normal' children aged 0—5 years, selected from three large general medical practices to represent a wide socioeconomic range, were seen monthly for periods of at least one year. Average growth patterns, previously shown to be related to the energy value of diets, conformed to British standards. Height and weight were not significantly related to socioeconomic status, maternal 'efficiency', number of sibs nor place in family. About half the children aged 0.5 years or less changed growht 'channels', falling to 0.4% in children aged 2 years or more. Respiratory illnesses showed seasonal changes, but growth rates did not, and there was no evidence that illness of any kind or severity had more than a transient effect on growth rates. Developmental test scores were not found to be related to growth rates. Girls tended to have higher scores than boys. Children from non-manual families and those with sїbs at least 5 years older scored more highly in tests of language than those in other types of family.


1991 ◽  
Vol 81 (3) ◽  
pp. 283-289 ◽  
Author(s):  
J. N. Matthiessen

AbstractIn undisturbed annual pasture in a Mediterranean-climate region of Australia adults of the whitefringed weevil, Graphognathus leucoloma (Boheman), were present from summer to early winter (December–June), with upsurge in numbers of first instar larvae only occurring after the rains began in April. The G. leucoloma population was predominantly first instar larvae in high abundance throughout the winter period (May–August). Larval growth, with high mortality, occurred in the spring period (September–January). The survival of eggs during the dry summer when adults were most abundant, although only at times of unseasonal rainfall, indicated that low larval recruitment at that time resulted primarily from the absence of high-quality legume food essential for oogenesis. It was inferred that most larvae arose from heavy oviposition by the few adults present in autumn when rainfall germinated annual legumes. A steady year-round abundance of late-instar larvae indicated that not all individuals completed their development in the one year.


The supertanker Amoco Cadiz wrecked on the coast of northern Brittany in April 1978. The resulting spill of 223000 t of crude oil polluted some 360 km of rocky or sandy shores, salt marshes and estuaries. An immediate mortality impact was observed. Populations of bivalves, periwinkles, limpets, peracarid crustaceans, heart urchins and sea birds were the most severely affected. Populations of polychaete worms, large crustaceans and coastal fishes were less affected. Three to six generations (5—10 years for bivalves but up to 60 years for birds) may be necessary before populations retrieve their stable age distribution. Delayed effects on mortality, growth and recruitment were still observed up to 3 years after the spill. Estuarine flat fishes and mullets had reduced growth, fecundity and recruitment; they were affected by fin rot disease. Populations of clams and nematodes in the meiofauna declined one year after the spill. Weathered oil is still present in low-energy areas. Species with short life cycles tend to replace long-lived species. A fauna of cirratulid and capitellid polychaete worms now prevails in sandy to m uddy areas. For several clam populations, recruitment remains unstable. Three years after the spill it is still premature to decide how long it will take before populations and ecosystems reach their former or new equilibria.


2007 ◽  
Vol 139 (4) ◽  
pp. 443-471 ◽  
Author(s):  
H. V. Danks

AbstractIn cold climates most aquatic habitats are frozen for many months. Nevertheless, even in such regions the conditions in different types of habitat, in different parts of one habitat, and from one year to the next can vary considerably; some water bodies even allow winter growth. Winter cold and ice provide challenges for aquatic insects, but so do high spring flows, short, cool summers, and unpredictable conditions. General adaptations to cope with these constraints, depending on species and habitat, include the use of widely available foods, increased food range, prolonged development (including development lasting more than one year per generation), programmed life cycles with diapause and other responses to environmental cues (often enforcing strict univoltinism), and staggered development. Winter conditions may be anticipated not only by diapause and related responses but also by movement for the winter to terrestrial habitats, to less severe aquatic habitats, or to different parts of the same habitat, and by construction of shelters. Winter itself is met by various types of cold hardiness, including tolerance of freezing in at least some species, especially chironomid midges, and supercooling even when surrounded by ice in others. Special cocoons provide protection in some species. A few species move during winter or resist anoxia beneath ice. Spring challenges of high flows and ice scour may be withstood or avoided by wintering in less severe habitats, penetrating the substrate, or delaying activity until after peak flow. However, where possible species emerge early in the spring to compensate for the shortness of the summer season, a trait enhanced (at least in some lentic habitats) by choosing overwintering sites that warm up first in spring. Relatively low summer temperatures are offset by development at low temperatures, by selection of warm habitats and microhabitats, and in adults by thermoregulation and modified mating activity. Notwithstanding the many abiotic constraints in cold climates, aquatic communities are relatively diverse, though dominated by taxa that combine traits such as cold adaptation with use of the habitats and foods that are most widely available and most favourable. Consequently, except in the most severe habitats, food chains and community structure are complex even at high latitudes and elevations, including many links between aquatic and terrestrial habitats. Despite the complex involvement of aquatic insects in these cold-climate ecosystems, we know relatively little about the physiological and biochemical basis of their cold hardiness and its relationship to habitat conditions, especially compared with information about terrestrial species from the same regions.


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