A pair of closely linked genes controlling high scutellar chaeta number in Drosophila

Summary 1. A line selected for high scutellar chaeta number reached a mean of about 16 chaetae in females and 13.5 in males at the 69th generation of selection following an accelerated response to selection which commenced at generation 65 and added five chaetae. 2. The accelerated response can probably be explained in terms of two recessive high chaeta number genes 1.05 cM apart, and which are located between po and vg on chromosome II. The gene closest to vg was found to be scabrous, sca, which causes rough eyes when homozygous and has a pleiotropic effect on scutellar chaeta number. The gene was found in one of the strains used in setting up the selection lines. 3. The results are discussed in relation to other theories of control of the scutellar chaeta system.     

Selection for six scutellar chaetae in Drosophila melanogaster

Summary 1. From a base population showing some flies with more than the normal 4 scutellar chaeta phenotype directional selection was carried out and lead to a line with many flies having 6 chaetae. 2. Selection was then practised for 6 chaetae such that the extra 2 chaetae were in the anterior left and anterior right positions on the scutellum. This lead to a line with most flies having this chaeta number and pattern, therefore showing some canalization. 3. Additive genetic activity controlling the increased chaeta number was found on all the 3 major chromosomes.     

Directional selection in lines founded from different parts of the phenotypic distribution of sternopleural chaetae number in Drosophila melanogaster

Summary Divergent directional selection lines were initiated from base populations founded from parents taken from different parts of the sternopleural chaetae distribution in a cage population of Drosophila melanogaster. Lines founded from parents taken from the central part of the distribution showed greater response and higher realised heritability than lines derived from parents with extreme high or extreme low chaetae number. The results suggest that centrally derived phenotypes have higher heterozygosity for chaetae factors than extreme phenotypes and that these factors have a large effect on the character.     

Association of allozyme heterozygosity and sternopleural chaetae number inDrosophila melanogaster

Variation at two polymorphic allozyme loci (Adh and Gpdh) has been assayed in relation to sternopleural chaetae number in flies derived from a cage population ofD. melanogaster known to be under stabilising selection with respect to chaetae number. Central phenotypes were significantly more heterozygous at these loci than more extreme phenotypes. Analysis of the base popylation and of divergent directional selection lines derived from it suggested that alleles atAdh and Gpdh have a pleiotropic effect on chaetae number or are in strong linkage disequilibrium with chaetae factors. In addition, homozygotes atAdh and Gpdh were observed to have a higher variance in chaetae number than heterozygotes. It is concluded that additive and homeostatic models of gene action might both partly explain the higher heterozygosity of central phenotypes.     

Genetic heterogeneity among the founders of laboratory populations of Drosophila IV. Scutellar chaetae in different environments

The incidence of flies with more than four seutellar chaetae (additional chaetae) has been followed for up to 3 years in 4 lines at 15°C, 20°C, 25°C and 27.5°C derived from each of 3 strains, initially set up from single inseminated females of Drosophila melanogaster, collected in the wild single the same locality at the same time. Within each set of temperature lines, the incidence of additional chaetae was highest in one strain, intermediate in another strain, and lowest in the third. This shows that the differences between lines can be at least partly attributed to differences between the founder females of the three strains, although some divergence occurred between lines within strains in some cases. With respect to quantitative traits, the results indicate that in situations where new habitats are occupied by a small number of colonists, the nature of the founder female is possibly of greater importance than the different environments of the new habitats.Some of this work was supported by the Australian Research Grants Committee.     

Genetic heterogeneity among the founders of laboratory populations ofDrosophila. I. Scutlllar chaetae

The incidence of flies with mor than four scutellar chaetae (additional chaetae) has been followed for 45 generations in three strains set up from single inseminated females ofDrosophila melanogaster collected in the wild from the same locality at the same time. Each strain differed in the incidence of additional chaetae over this time, and the differences between strains were found to be controlled largely by additive genes.Fifteen further such strains were followed for 9 generations and each maintained consistent incidences of additional chaetae.Thus there may be genetic differences between populations derived from single inseminated females present in a given wild population, so lending support to a role for genetic drift (as a founder effect) in these situations. These differences may be maintained for many generations.Some possibilities for obtaining rapid responses in directional selection experiments based on the initial selection of favourable strains derived from single individuals are discussed briefly.     

Egg lengths inDrosophila melanogaster and correlated responses to selection

Egg lengths were studied inDrosophila using three lines, namely a high line, where selection for increased egg length was carried out, a low line where selection for decreased egg length was carried out, and a control line. Selection was more effective in the low than the high line. Adult fly weight assayed in the 18th and 19th generations of selection responded similarly to egg length. Sternopleural chaetae number, however, responded more in the high than in the low line. In the high line the response occurred earlier than for egg length. This rather surprising result can probably be explained by assuming that the genetic architectures controlling chaetae number and egg length differ.     

SELECTION, PREDICTION AND RESPONSE

1. The biometric approach to selection experiments has been outlined, and found to be rather deficient because it is based on excessively restrictive models which cannot take into account the complex architectures of quantitative traits as are being revealed today. 2. The nature of polygenes is discussed in detail from the theoretical point of view. In out breeding species, some form of the balanced polygenic complex is likely, showing polymorphism for the constituent genes. Although polymorphism is implicit in the argument, definitive evidence for poiymorphisms has only just appeared. 3. There is no evidence that polygenes differ from any other gene. 4. Several artificial selection experiments are described, in particular in Drosophila. By means of appropriate breeding techniques after obtaining responses to selection, genetic activity controlling quantitative traits can be located to chromosomes, and even specific loci found. Such few studies as have been carried out reveal, in general, the types of genetic architecture predicted on theoretical grounds. 5. Selection for behavioural traits is considered briefly and it appears that no new principles are needed, except that careful environmental control and objective measurement present problems. 6. The results of selection for quantitative traits in micro-organisms reveal similarities to results in higher organisms in the few cases where definitive work has been carried out. 7. Work on the simulation of models by computers has not greatly advanced selection experiment theory, mainly because, with few exceptions, linkage has been ignored. 8. The existing theory on which selection experiments are based is inadequate for several reasons. It cannot predict the rate of response to selection nor the ultimate limits to selection, the nature of correlated responses to selection, nor the nature of gene segregation underlying the observed variability. 9. Strains set up from single inseminated founder females from the same population of Drosophila have been shown to differ genetically for several quantitative traits. Therefore the base population is polymorphic for genes controlling these traits. This was exploited by carrying out directional selection on lines derived from those strains showing a high incidence of scutellar chaetae. This led to far more rapid responses to selection than lines derived from strains where the incidence of scutellar chaetae was lower. 10. Ultimately, one can envisage the selection experiment as it is known today being partly replaced by the manipulation of located genes controlling quantitative traits into certain combinations.     

Polygenes and polymorphism

Summary Single inseminated founder females in D. melanogaster derived from the same population have led to genetically discrete strains for three quantitative traits, namely scutellar chaeta number, mating speed and duration of copulation. The base population from which the females were derived can therefore be argued to be polymorphic for these traits. Although polymorphisms for genes (or polygenes) for quantitative traits are expected to be ubiquitous in outbreeding species on theoretical grounds, this has not previously been generally demonstrated.     

Chaetal arrangement and chaetogenesis of hooded hooks in Lumbrineris (Scoletoma) fragilis and Lumbrineris tetraura (Eunicida,Annelida)

As the structure and arrangement of chaetae are highly specific for annelid species and higher taxonomic entities, we assume that rather conservative information guarantees formation of specific chaetae. Each chaeta of an annelid is formed within an ectodermal invagination, and the modulation of the apical microvilli pattern of the basalmost cell of this invagination determines the structure of the chaeta. Any hypothesis of the homology of chaetae could thus be tested by examining the process of chaetal formation. Investigations into the ultrastructure and formation of hooded hooks in different capitellids and spionids revealed that these chaetae can be homologized. The hood of each of their hooded hooks is formed by elongation of two rings of microvilli peripheral to the chaetal anlage, which give rise to the inner and outer layers of the hood. The hood layers are well separated and surround an empty space. Superficially similar hooded hooks are described for certain Eunicida. Presently available cladistic analyses suggest that the hooded hooks of eunicidans evolved independently of those in Capitellidae and Spionidae. Compared with the latter two families, we therefore expected to find differences in chaetogenesis of the hooded hooks in the eunicids Lumbrineris (Scoletoma) fragilis and Lumbrineris tetraura (Lumbrineridae). This was the case. In these eunicidans, the hood was formed by the bisected apical wall of the chaetoblast right after the mid‐apical section of the chaeta had been sunk deeply into the chaetoblast during its formation. The apical wall generated a brush of microvilli that preformed the hood. Because the microvilli of the hood showed some accelerated differentiation, they soon merged with those of the slowly growing setal shaft to form the broad manubrium of the hooded hook in lumbrinerids. Our study confirms the predicted differences in chaetogenesis of the superficially similar hooded hooks of capitellids and spionids compared with those of eunicids.     

Effects of different base populations on selection response in Drosophila

Of two laboratory strains of Drosophila melanogaster used in this study, the +3 strain had slightly higher mean abdominal bristle number and estimated heritability of this character than the Oregon‐R. Their F₁ hybrid exhibited 5 % heterosis. Fourteen generations of the two original strains and the F₃ of the hybrid were selected for high and low numbers of abdominal bristles on the 4th and 5th sternites, at a selection intensity of 20%. A mass‐mated unselected control was maintained for each population. The +3 population responded considerably more to selection for low numbers of bristles than high, and the Oregon‐R population showed a similar, though less marked, tendency; the Crossbred population responded more strongly to selection for high numbers. Except for the Crossbred high selection line, all lines declined in response rate, phenotypic variance, and realised heritability. The average realised heritability of the Oregon‐R and +3 high and low selection lines over 14 selection generations fell short of their predicted base population heritabilities. The deviation from the predicted was particularly pronounced with selection for high bristle number in the +3 line.     

Effects of extreme temperatures on phenotypic variation and developmental stability in Drosophila melanogaster and Drosophila buzzatii

The effect of stressful and nonstressful rearing temperatures on phenotypic variation of four quantitative characters (thorax length, wing length, number of sternopleural chaetae, number of arista branches) and on developmental stability (fluctuating asymmetry) of the three latter characters was estimated in two Drosophila species: Drosophila melanogaster and Drosophila buzzatii . In both species, a general trend for increasing of phenotypic variation and fluctuating asymmetry at stress temperatures was observed; in fluctuating asymmetry, this effect was more pronounced. An increase of phenotypic variation under stress was shown for all characters examined except sternopleural chaeta number in D. buzzatii . Comparison of species responses suggests that the increase of variation in D. melanogaster was somewhat higher than in D. buzzatii .     

Developmental Stability of DROSOPHILA MELANOGASTER under Artificial and Natural Selection in Constant and Fluctuating Environments

Populations of Drosophila melanogaster in constant 25° and fluctuating 20/29° environments showed increases in developmental stability, indicated by decreases in bilateral asymmetry of sterno-pleural chaeta number. In both environments, rates of decrease in asymmetry were greater under natural selection (control lines) than under artificial stabilizing selection. Overall mean asymmetry was greater in the fluctuating environment.—There was no evidence that decreased asymmetry was due to heterozygosity, and the decline in asymmetry was not explained by the decline in chaeta number in the lines under only natural selection. However, the decline was consistent with changes in total phenotypic variance and environmental variance.—The divergence between lines after 39 generations of selection was seen in differences in asymmetry and also in the genotype-environment interaction expressed in cross-culturing experiments.     

Homology and Evolution of the Chaetae in Echiura (Annelida)

Echiura is traditionally regarded as a small phylum of unsegmented spiralian worms. Molecular analyses, however, provide unquestionable evidence that Echiura are derived annelids that lost segmentation. Like annelids, echiurans possess chaetae, a single ventral pair in all species and one or two additional caudal hemi-circles of chaetae in two subgroups, but their evolutionary origin and affiliation to annelid chaetae are unresolved. Since annelids possess segmental pairs of dorsal (notopodial) and ventral (neuropodial) chaetae that are arranged in a row, the ventral chaetae in Echiura either represent a single or a paired neuropodial group of chaetae, while the caudal circle may represent fused rows of chaetae. In annelids, chaetogenesis is generally restricted to the ventral part of the notopodial chaetal sac and to the dorsal part of the neuropodial chaetal sac. We used the exact position of the chaetal formation site in the echiuran species, Thalassema thalassemum (Pallas, 1766) and Echiurus echiurus (Pallas, 1767), to test different hypotheses of the evolution of echiurid chaetae. As in annelids, a single chaetoblast is responsible for chaetogenesis in both species. Each chaeta of the ventral pair arises from its own chaetal sac and possesses a lateral formation site, evidencing that the pair of ventral chaetae in Echiura is homologous to a pair of neuropodia that fused on the ventral side, while the notopodia were reduced. Both caudal hemi-circles of chaetae in Echiurus echiurus are composed of several individual chaetal sacs, each with its own formative site. This finding argues against a homology of these hemi-circles of chaetae and annelids’ rows of chaetae and leads to the hypothesis that the caudal chaetal rings evolved once within the Echiura by multiplication of ventral chaetae.     

Getting to the root of fireworms' stinging chaetae—chaetal arrangement and ultrastructure of Eurythoe complanata (Pallas, 1766) (Amphinomida)

Amphinomid species are since long known to cause urtication upon contact with the human skin. Since it has been reported that amphinomid chaetae are hollow, it has repeatedly been suggested that poison is injected upon epidermal contact. To test predictions for the structural correlate of such a stinging device we studied the structure and formation of chaetae in the fireworm Eurythoe complanata (Amphinomida). Neither the structure of the chaetae nor their formation and their position within the parapodium provide evidence for their function as hollow needles to inject poison. The chaetae even turned out to be not hollow, but containing calcareous depositions. The latter most likely cause artificial ruptures of delicate chitin lamellae in the inner of the chaeta when treated with acidic fixatives. Inorganic calcium compounds harden the chaetae and make them brittle so that they break easily. Additional information on the structure of the chaetal sac, the site of formation and the acicula do not contradict the position of the Amphinomida within Annelida as revealed by phylogenomic studies.     

Endonura Cassagnau in Iran,with a key to species of the genus (Collembola,Neanuridae, Neanurinae)

Three new species of Endonura are described from Iran. Endonura dichaeta sp. n. can be recognized by an ogival labrum, head without chaetae O and E, chaeta D connected with tubercle Cl, tubercle Dl with five chaetae on head, absence of tubercles Di on thorax I and tubercle (Di+Di) of thorax V with 2+2 chaetae. Endonura ceratolabralis sp. n. is characterized by large body size, reduction of labral chaetotaxy, ogival labrum, head without chaeta O and fusion of tubercles Di and De on first thoracic segment. Endonura persica sp. n. is distinguished from its congeners by a nonogival labrum, absence of chaeta O, tubercles Dl and (L+So) with five and eight chaetae respectively and claw with inner tooth. The key to all species of the genus is given.     

Fridericia larix sp. nov. (Enchytraeidae, Oligochaeta) from Irish soils

A new species of Fridericia (Enchytraeidae, Oligochaeta) is described from soils in Ireland. It was found during sampling campaigns in the framework of a comprehensive taxonomic revision of the genus (Schmelz, 2003. Taxonomy of Fridericia (Oligochaeta, Enchytraeidae). Revision of species with morphological and biochemical methods. Abh. Naturw. Ver. Hamburg, N.F. 38, 1–415, figs. 1–73), but it was not included in that study. Fridericia larix sp. nov., named in reference to the type locality, belongs to the large and taxonomically difficult group of species with two diverticula per spermatheca. It is distinguished from all known congeners by the following combination of characters: (1) a maximum of four chaetae in ventral preclitellar bundles; (2) oesophageal appendages poorly branched; (3) no pharyngeal glands in segment VII; (4) coelomocytes without refractile vesicles; (5) clitellum girdle-shaped, cell distribution alike on all sides; (6) bursal slit of male copulatory organ mainly transverse; (7) no subneural glands; (8) spermathecal diverticula not stalked. Further distinguishing characters are: (9) an asymmetrical arrangement of chaetae in the first lateral postclitellar bundles, with one large chaeta and one small chaeta per bundle (Fig. 1b, “lc XVI”); (10) the length ratio of spermatozoa to spermatozoal nuclei (6:1–7:1); and (11) a wavy inner surface in parts of the epithelium of the spermathecal ampulla (Fig. 1i, arrow).See also Electronic Supplement at: http://www.senckenberg.de/odes/05-05.htm     

Review of Chinese Oligaphorurini (Collembola, Onychiuridae) with descriptions of two new Palaearctic species

A checklist of Chinese Oligaphorurini is given. Two new Chinese species, Micraphorura changbaiensissp. n. and Oligaphorura pseudomontanasp. n., are described from Changbai Mountain Range. Micraphorura changbaiensis sp. n. has the same dorsal pseudocelli formula and number of papillae in Ant. III sensory organ as Micraphorura uralica, but they can be easily distinguished by number of chaetae in Ant. III sensory organ, ventral pseudocelli formula, ventral parapseudocelli formula, number of pseudocelli on subcoxa 1 of legs I-III, dorsal axial chaeta on Abd. V and number of chaetae on tibiotarsi. Oligaphorura pseudomontana sp. n. is very similar to the species Oligaphorura montana having an increased number of pseudocelli on body dorsally, well marked base of antenna with 1 pseudocellus and 3 pseudocelli outside, subcoxa 1 of legs I-III with 1 pseudocellus each, dorsally S-chaetae formula as 11/011/22211 from head to Abd. V, S-microchaeta present on Th. II-III, claw without inner teeth and with 1+1 lateral teeth, and unguiculus with basal lamella; but they can be separated easily by the number of pseudocelli on Abd. V and VI terga, parapseudocelli on the body, number of chaetae on Th. I tergum, and number of chaetae on tibiotarsi. A key to Chinese species of Oligaphorurini is provided in the present paper.     

Morphological variation and preadult viability at one-generation inbreeding in Drosophila melanogaster: A family selection hypothesis

Wing length, thorax length, sterno-pleural and sternal chaetae numbers were determined in offspring of sib crosses in a Drosophila melanogaster population, in relation to egg-to-adult viability. It appears that high between- and within-family variabilities for wing and thorax length together with lack of developmental homeostasis are associated with a high rate of embryonic and larvo-pupal mortality. Effects on chaetae numbers are more controversial. Results suggest that families which are homozygous for particular gene combinations may be eliminated by natural selection. Maintenance of high levels of heterozygosity might result in populations where circumstances foster substantial inbreeding.     

Locomotion and fine structure of parapodia in <Emphasis Type="Italic">Myzostoma cirriferum</Emphasis> (Myzostomida)

Most myzostomids are ectocommensals of crinoids on which they move freely. Their locomotion is ensured by five pairs of parapodia located laterally below their trunk. Each parapodium in Myzostoma cirriferum is a conical structure that includes a hook-like chaeta, replacement chaetae and an aciculum. Structure and ultrastructure of the myzostomid chaetae are similar to those of polychaetes: they are formed by a chaetoblast, which gives rise to microvilli where chaetal material is assembled on the outer surface. Myzostoma cirriferum walks on its host. It moves the anterior part, the posterior part or the lateral parts forwards but is able to rotate of 180° on itself. Its locomotion entirely depends on parapodial motions and not on trunk movements. Three pairs of muscles are involved in parapodial motions: parapodium flexor and parapodium extensor, aciculum protractor and aciculum retractor, and hook protractor with conjunctor. A functional model is proposed for explaining the global motion of a parapodium in M. cirriferum that may be extended to all ectocommensal myzostomids.