Life cycle of Simulium jenningsi (Diptera: Simuliidae) in southern West Virginia.

The life cycle of Simulium jenningsi Malloch was compared at two study sites representing the largest and smallest streams (New River and Indian Creek, respectively) where this species is known to breed in southern West Virginia. Larvae first appeared in March, and the first generation emerged in April, followed by two to four more generations by September. A few larvae and adults persisted in autumn, then the population overwintered in the egg stage. There were considerable differences in life cycle at the two study sites. In the New River, emergence of the first generation was 2-3 wk earlier, there were five generations rather than three, and the last larvae of the season persisted 1 mo later as compared with Indian Creek. Warmer temperature and higher quality food in the New River are probable explanations for differences in life cycle. Effective pest management of this species will require larviciding at frequent intervals (1-2 wk) from April through September in many streams over a broad geographic area because of the species' nonsynchronous life cycle, occurrence in different size streams, and strong dispersal ability.     

The cytotaxonomy of Simulium sanctipauli and Simulium soubrense (Diptera: Simuliidae)

It is noted that the chromosomal inversion 2L-7, which has been used in the past to separate S. Sanetipauli from S. soubrense, occurs as an intraspecific polymorphism and hence cannot be considered diagnostic, although in some populations 2L-7 can still strogly indicate the presence of two species. However, two newly recognised inversions, 1L-A and 2L-A, can be used in combination to identify S. sanctipauli, S. soubrense and a new species S. soubrense B. The absence of the relevant heterozygotes for these two new inversion confirms the separate specific status of S. sanctipauli from S. soubrense from S. soubrense B as well as providing a reliable means of larval identification. The misuse of 2L-7 as a species diagnostic inversion has undoubtedly led to past misidentifications of S. sanctipauli and S. soubrense, and it is possible, for example, that only S. sanctipauli is resistant to organophosphate insecticides in Ivory Coast and not S. soubrense. Beffa form appears to be a distinctive geographic race of S. soubrense, but forme konkouré remains as yet unassigned. A cytotaxonomic key for the identification of members of the S. sanctipauli sub-complex is presented.     

Polytene chromosomes of Simulium craigi (Diptera: Simuliidae)

Simulium craigi Adler and Currie is a polymorphic species based on polytene chromosome banding patterns in the long arm of chromosome III (IIIL). Three cytotypes are described based on the predominant IIIL sequences. These correspond to three broad geographic areas: cytotype CC from Pennsylvania; cytotype AF from Ontario and Manitoba; and cytotype ACF/BCF from New Hampshire. In the absence of sympatric populations, these cytotype differences are best explained by clinal variation within a single species. The relationship of S. craigi to other described members of the S. vernum group is discussed.     

Patterns of polytene-chromosome replication in Simulium ornatipes (Diptera: Simuliidae)

Double labelling of Simulium ornatipes polytene chromosomes with H³- and C¹⁴-thymidine shows that chromosome synthesis follows three distinct phases viz. a short phase of initiation in puffs and interbands spreading to more condensed regions; a long continuous labelling phase, then a discontinuously labelled end phase as bands complete their replication in temporal sequence. Analysis of H³ labelling patterns indicates that while heterochromatic bands replicate there is no clear correlation between heterochromatic or C-banding regions and band replication time. The major characteristic governing band replication time appears to be band size and density. However, in some bands this relationship is modified, perhaps it is suggested, by DNA organisation influencing the efficiency of replicons. The existence of great variability in homologous band replication times, even within a chromosome pair, indicates that the control of band replication is highly autonomous. It is suggested that polymorphisms at the molecular level determine this variation. Replication time of active nucleolar organisers is very long in contrast to the short replication of condensed inactive organisers. This may reflect differential polytenisation of ribosomal DNA as a result of a developmental polymorphism, or the amplification of ribosomal DNA by active nucleolar organisers.     

Two new black fly species of Simulium (Simulium) (Diptera: Simuliidae) from South India

Two new black fly species, Simulium (Simulium) pothigaiense sp. n. and Simulium (Simulium) valparaiense sp. n., are described based on females, males, pupae and larvae. Simulium (Simulium) pothigaiense sp. n. is characterized by a claw simple without subbasal tooth and the base of radial vein with hair tuft in the females, maxillary palp with small sensory vesicle in the males, pupal gill with 10 short slender filaments and very short common basal stalk in the pupae and 5 hypostomal bristles per side lying parallel to lateral margin in the larvae. Simulium (Simulium) valparaiense sp. n. is characterized by hind basitarsus 6.6 times as long as its greatest width and claw with small distinct subbasal tooth in the females, gonostyle in medial view 2.3 times longer than coxite in the males, common basal stalk of pupal gill 0.31 times as long as interspiracular trunk, and larval thoracic and abdominal cuticle with pair of dorsolateral protuberances. Taxonomic notes are given to distinguish these two new species from closely related species. www.zoobank.org/urn:lsid:zoobank.org:pub:7285F6BC-607D-4F76-B6EE-9CAC67CDE651     

The Identity of Simulium murmanum Enderlein, 1935 (Diptera: Simuliidae)

The identity of Simulium murmanum is re-established by designation of lectotype and paralectotype. The species is common and widespread in the northern Holarctic Region and has up to now been reported from the Nearctic Region as S. corbis and from the Palaearctic Region as S. relictum (and S. rostratum, auct., nec Lundstrüm).     

Oviposition response of Simulium reptans (Diptera: Simuliidae) to the presence of conspecific eggs

Abstract.

• 1 The oviposition behaviour of Simulium reptans L. is described from two sites on the River Spey, Scotland. Female aggregations were observed immediately downstream of oviposition sites and were composed mainly of gravid flies (range 60–80%0) together with smaller numbers that were either freshly bloodfed (range 2–17%) or infected with mermithid nematodes (range 0–30%).
• 2 The time from landing on the oviposition sites to the onset of oviposition was recorded. The time in the presence of greater than 1-day-old eggs did not significantly differ from sites with no eggs present. However, the presence of freshly laid or I-day-old eggs significantly shortened the time to onset of oviposition. The cues that elicit oviposition are unknown but it is speculated that they may involve a pheromone.

     

Simulium berneri Freeman (Diptera: Simuliidae) and its mayfly host (Ephemeroptera: Oligoneuridae)

An analysis is given of collections of Elassoneuria nymphs bearing immature Simulium berneri from the forest zone of West Cameroon near Kumba. The size and sex of the mayfly nymphs, the size and attachment sites of S. berneri and the infestation rates are recorded. The method of dispersion is discussed.     

Cytogenetical analysis of the Simulium damnosum complex (Diptera: Simuliidae) in Guinea Bissau

Abstract. In a 3-year study during 1990–92, larval collections of the Simulium damnosum complex from the River Corubal system in Guinea Bissau revealed that the only sibling species present were S. sirbanum and the Konkouré form of S. konkourense , but not S. damnosum s.s. which had been found at some of the localities (Saltinho and Cusselinta) in a previous survey by Quillévéré et at. (1981). Their differential distributions were seasonally consistent between years. S. sirbanum was concentrated in the upper reaches of the Corubal, moving downstream at the end of the dry season to exploit new breeding grounds, whereas S. konkourense seemed to be concentrated in the lower reaches and moved upstream in the middle of the dry season.
Since the previous survey, it appears that S. konkourense has largely replaced S. sirbanum and S. damnosum s.s. in the lower reaches of the Corubal. S. sirbanum was consistently associated with man-biting behaviour and, although infection studies were not performed, it is likely that S. sirbanum is the main vector of onchocerciasis in Guinea Bissau as S. konkourense does not seen to be anthropophilic.
Among five polymorphic inversions in S. sirbanum , the frequency of inversion IL-B increased during the dry season; IL-2 and IIL-7 showed homozygous disadvantage whereas IIL-3 and IIIL-6 did not; IS-2 tended to be fixed in all populations. Simulium konkourense populations in the River Corubal differ from those found upstream in its tributary the River Koumba, in the Fouta Djallon of Guinea, by their sex chromosomes (having no sex-linked inversions) and biting preferences, indicating that the populations are not freely interbreeding. Inversion IIIL-X was found for the first time in populations of S. konkourense outside the Fouta Djallon area and a new inversion IIL-Y was identified in samples from the Rivers Corubal and Féfiné.     

Cytotaxonomy of Simulium cauchense Floch & Abonnenc and Simulium quadrifidum Lutz (Diptera: Simuliidae) in Brazilian Amazonia

Simulium cauchense Floch & Abonnenc and Simulium quadrifidum Lutz are widely distributed in the Amazon region and are morphologically similar at the larval and pupal stages. Chromosomally, these species are readily distinguished by the position of the nucleolar organizer, which is in the short arm of chromosome I in S. cauchense and in the long arm of chromosomes III in S. quadrifidum. They also differ by three fixed inversions. Sex chromosomes are undifferentiated in both species. Chromosomal resolution of the two species allowed us to evaluate four structural features previously used as diagnostic aids at the larval stage. Characters that distinguish larvae of the two species are the number of branches and branching patterns of the dorsal abdominal setae and the dark band on each primary fan. Branching patterns of the gill histoblasts were often diagnostic, with S. quadrifidum exhibiting more proximal branching and S. cauchense more distal branching. Sites where both species occurred sometimes had larvae with one petiole branching proximally and the other distally; in these cases examination of the chromosomes permitted assignment of the specimen to species. Pigmentation patterns of larvae, on the other hand, are highly variable. Color typically is sex linked in both species.     

Novel aquatic silk genes from Simulium (Psilozia) vittatum (Zett) Diptera: Simuliidae

The silks of arthropods have an elementary role in the natural history of the organisms that spin them, yet they are coded by rapidly evolving genes leading some authors to speculate that silk proteins are non-homologous proteins co-opted multiple times independently for similar functions. However, some general structural patterns are emerging. In this work we identified three major silk gland proteins using a combined biochemical, proteomic, next-generation sequencing and bioinformatic approach. Biochemical characterization determined that they were phosphorylated with multiple isoforms and potentially differential phosphorylation. Structural characterization showed that their structure was more similar to silk proteins from distantly related aquatic Trichopteran species than more closely related terrestrial or aquatic Diptera. Overall, our approach is easily transferable to any non-model species and if used across a larger number of aquatic species, we will be able to better understand the processes involved in linking the secondary structure of silk proteins with their function between in an organisms and its habitat.     

C banding in polytene chromosomes of Simulium ornatipes and S. melatum (Diptera: Simuliidae)

Polytene and mitotic chromosomes of Simulium ornatipes and S. melatum were subjected to C banding procedures. In both species polytene chromosomes consistently show C banding of centromere regions, telomeres, nucleolar organiser and, unexpectedly, numerous interstitial sites. The interstitial C banding sites correspond to morphologically single polytene bands. Their response is graded and independent of band size. Interstitial C bands in S. ornatipes are scattered throughout the complement, whereas in S. melatum they are clustered. Supernumerary heterochromatic segments in S. ornatipes also exhibit strong C banding and inverted segments can differ from standard in C banding pattern. — Mitotic chromosomes of both species show a single centric C band with indications of two weak interstitial bands in S. ornatipes, suggesting that many C band regions, detectable in polytene chromosomes, are not resolved by present techniques in mitotic chromosomes. — Contrary to current opinion that C banding is diagnostic for constitutive heterochromatin, the interstitial C band sites of polytene chromosomes are regarded as euchromatic. Conversely, the heterochromatic pericentric regions of S. ornatipes are not C banded. — It appears that polytene chromosomes offer a promising system for the elucidation of C banding mechanisms.     

The annual cycle of Simulium erythrocephalum (Diptera: Simuliidae) at a site in Norfolk

SUMMARY. Size frequency distributions of larvae of Simulium erythrocephalum sampled regularly throughout 1978 from the River Tiffey at Carlton Forehoe, Norfolk, revealed five generations per year. The number of larval instars could be determined for the second and fifth generations, being six and seven respectively. Individuals of the overwintering generation were of larger ultimate size, had more ovarioles and apparently laid larger eggs than those of the summer generations. Females were larger than males throughout the year.