Cytogenetics and evolution of Simulium ornatipes skuse (Diptera:Simuliidae) I. Sibling speciation

Larval populations of the morphologically distinct species Simulium ornatipes and S. neornatipes and a subspecies of the former, S. ornatipes norfolkense, were analysed using polytene chromosome cytology. Fixed inversion differences, distinct differentiated sex chromosomes and unique arrays of chromosomal polymorphisms reveal two sibling species, S. ornatipes A and B, within S. ornatipes, and two, S. neornatipes 1 and 2, within S. neornatipes. Chromosomally S. ornatipes norfolkense is similar to S. ornatipes A. An unprecedented level of shared inversion polymorphism is shown by S. ornatipes A and B indicating a very close relationship between them. While it may be postulated that such a situation has arisen by independent origin of the shared inversions within each species, or by introgression of these rearrangements between the two species, it is concluded that the shared polymorphisms in fact originate from a common ancestor. Within the four chromosomally defined species, differentiated sex chromosome systems occur which may involve any of the three chromosome pairs. Simulium ornatipes A is particularly interesting because there are indications that it may be polymorphic for differentiated sex chromosomes on two different elements and that it may also share a sex chromosome marker with S. ornatipes B, a unique situation in the Simuliidae. The evolution of sex chromosome systems in the four species is compared with that of other Simulids and its intimate connection with speciation emphasised. Finally the data on fixed inversions, differentiated sex chromosomes and shared polymorphisms is used to construct a phylogeny of the four species outlining their patterns of speciation.     

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 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.     

Cladistic analysis of Simulium (Trichodagmia) and Simulium (Thyrsopelma) (Diptera: Simuliidae)

A cladistic analysis of Simulium ( Trichodagmia ) sensu Crosskey and Howard, using 34 morphological characters of larvae (6 characters), pupa (5) and adults (23), yields nine most parsimonious trees under equal weights (length 101 steps CI 0.49 RI 0.73). Successive weighting based on the maximal rescaled consistency index preferred one of the nine (31.37 steps CI 0.62 RI 0.87 total fit_con3= 235.8), which was also one of two trees found under implicit weights with concavity values of 3–6. The cladogram justifies the recognition of two subgenera. Simulium ( Trichodagmia ) sensu stricto (containing S. muiscorum, sumapazense, S. wygodzinskyorum, S. nigrimanum, S. chalcocoma, S. huairayacu and S. lahillei ) is supported by the branchial tip sclerotization and the presence of cibarial teeth, larval body tegument covered with lanceolate hairs, female with simple claw, and gonapophysis size. Simulium ( Thyrsopelma ) (containing S. scutistriatum, S. hirtipupa, S. orbitale, S. guianense, S. perplexum and S. itaunense ) is supported by the hypostomial teeth.     

The water velocity preferences of Austrosimulium furiosum and Simulium ornatipes (Diptera: Simuliidae) larvae,and the implications for micro-habitat partitioning

The aquatic larvae of two simuliid species, Austrosimulium furiosum (Skuse) and Simulium ornatipes Skuse, which often occur together in Victorian streams, were shown in laboratory experiments to have preferences for different water velocities: larvae of A. furiosum preferred water velocities of 0.2–0.3 m s^–1, and S. ornatipes preferred water velocities of 0.9–1.3 m s ^–1 . Final instar larvae of both species selected slow water speeds of less than 0.25 m s ^–1 prior to pupation. Flow patterns around a cylinder in a laboratory stream were mapped, and the distribution of A. furiosum larvae within the wake, paired vortices and horseshoe vortex was recorded. Larvae selected areas with suitable water velocities and aligned with the flow, providing flow visualization of micro-current speed and direction. The potential for micro-habitat partitioning is discussed in relation to benthic sampling strategies.     

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     

Cytosystematics of the Simulium tuberosum group (Diptera: Simuliidae) in Thailand

The polytene chromosomes of 3347 larvae of the Simulium tuberosum group in Asia were analysed, representing the largest ever cytogenetic study of black flies in the Oriental Region. Band‐by‐band comparisons, relative to the established standard chromosome map for the subgenus Simulium, revealed 17 cytogenetically distinct taxa in Thailand, plus an 18th in China. Six of these taxa correspond to morphologically described species (S. doipuiense, S. rufibasis, S. setsukoae, S. tani, S. yuphae and S. weji). Recognition of the 18 taxa is based largely on unique inversions, either fixed or sex linked, primarily in the long arm of chromosome III. The greatest cytological diversity was discovered in the S. tani lineage, with ten cytoforms. This marked chromosomal diversification within S. tani is based largely on two inversions that have assumed different roles over evolutionary time, variously functioning in different combinations as fixed inversions, sex‐linked inversions and autosomal polymorphisms. Shared unique chromosomal features, relative to the subgeneric standard chromosome map, allowed evolutionary relationships among the cytotaxa to be inferred. Fluctuations in climate during the Pleistocene might have promoted differentiation of the Southeast Asian S. tuberosum group in isolated refugia such as mountains. © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 155 , 289–315.     

贵州蚋属一新种 (双翅目：蚋科)

 记述采自贵州雷公山的蚋属一新种, 显著蚋Simulium (Simulium) prominentum, 新种 。根据其蛹和幼虫的特征显著而命名, 对其幼期形态进行描述并与其近缘种作分类讨论。     

贵州蚋属一新种(双翅目：蚋科)

记述采自贵州雷公山的蚋属一新种, 显著蚋Simulium (Simulium) prominentum, 新种。根据其蛹和幼虫的特征显著而命名, 对其幼期形态进行描述并与其近缘种作分类讨论。     

兴义维蚋多线染色体研究（英文）

首次在国内对兴义维蚋Simulium (Wilhelmia) xingyiense的多线染色体进行研究, 并提供其多线染色体标准图。选取兴义维蚋的成熟幼虫, 用改良苯酚品红染色法进行唾腺多线染色体制备, 并进行测量、 描述及分析。结果表明： 兴义维蚋多线染色体数目为3对（2n=6）。Ⅰ号染色体具中央着丝粒, Ⅱ和Ⅲ号染色体均为亚中央着丝粒染色体。核仁组织者区位于Ⅰ号染色体短臂近着丝粒端。巴尔比尼氏环和双泡位于Ⅱ号染色体短臂近中央位置。3对染色体的着丝粒区可形成明显的染色中心。兴义维蚋多线染色体具有多态性的倒位, 倒位频率为0.64。兴义维蚋多线染色体的着丝粒、 核仁组织区、 巴氏环、 双泡等主要特征性结构的位置及形态恒定一致,可作为该种的重要鉴别特征。其多态性的倒位可为该蚋种在细胞水平上进行蚋类分类鉴别和系统发育等研究提供基础资料。     

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).     

Phylogeography of Simulium siamense Takaoka and Suzuki complex (Diptera: Simuliidae) in Thailand

The phylogeography of Simulium siamense complex was inferred from mitochondrial DNA sequences. A 586‐bp fragment of the cytochrome oxidase I was sequenced for 92 individuals from 13 populations throughout Thailand, representing five cytoforms (A, B, C, F and G). The cytoforms are not genetically different at the molecular level except for cytoform B, which is genetically distinct from the others. This might indicate that cytoform B is a distinct species. Further morphological and molecular work using other genes is needed to clarify this. Our results also argue for the need of integrated approach, both cytological and molecular studies to understanding biodiversity of black flies. The star‐like shape of the mtDNA genealogy is consistent with the sudden population expansion of the mismatch distribution analysis and large negative values of Fu's F_s and Tajima's D‐tests, indicating a population demographic expansion. The expansion time is estimated to be in the late Pleistocene (about 120 000 years ago). Therefore, the overall low level of genetic structure could be due to sharing a recent history. The ancestral haplotype was found in the mountainous area in northeastern Thailand, suggesting that this area could have been the refugium of the species complex during the Pleistocene glaciations. Our results are consistent with previous findings about population expansion in response to the Pleistocene climatic change, thus revealing the importance of this historical event in shaping the genetic structure and diversity of Southeast Asian mainland species.     

陕西省蚋属一新种记述(双翅目:蚋科)

Simulium (Simulium) liubaense, sp. nov. is described based on the female specimens collected from Liuba, Shaanxi Province, China. This species is assigned to the variegotum-group of the subgenus Simulium, and is closely related to S. (S.) jingfui Cai and An, 2008, S. (S.) taiwanicum Takaoka, 1979, S. (S.) hackeri Edwards 1928, S. (S.) chamlongi Takaoka and Suzuki, 1984. However it is clearly differentiated from them by the structure of cibarium, genital fork, genital plate, paraproct and cercus of the female. All the specimens are kept in the Medical Entomology Collection Gallery, Academy of Military Medical Sciences, Beijing.     

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.