SECRETION AND DEPLOYMENT OF BRISTLES IN MALLOMONAS SPLENDENS (SYNUROPHYCEAE)1

Mallomonas splendens (G. S. West) Playfair has a cell covering of siliceous scales and bristles. Interphase cells bear four anterior and four posterior bristles that each articulate, at their flexed basal ends via a complex of labile fibers (the fibrillar complex), on a specialized body scale (a base-plate scale). Body scales, base-plate scales and bristles are formed independently of each other and at different times in silica deposition vesicles (SDVs) that are associated with one of the two chloroplasts. The fine structure of scale and bristle morphogenesis in M. splendens agrees with that previously described for Synura and Mallomonas. Four new posterior bristles are formed at late interphase with their basal ends towards the cell posterior. The fibrillar complex is formed in situ on the bristle in the SDV. Mature bristles are secreted one by one onto the surface of the protoplast, beneath the layer of body scales, where the basal ends of the bristles adhere to the plasma membrane via the fibrillar complex. The extrusion of posterior bristles and their deployment onto the cell surface was monitored with video. A fine cellular protuberance accompanies the bristles as they are extruded from beneath the scale layer with their basal ends leading. When distant from the cell, the basal ends of the bristles appear attached to the protuberance, possibly by way of their fibrillar complexes. Once bristles are fully extruded, and their tips free in the surrounding environment, the bristle bases are drawn back to the posterior apex of the cell, apparently by the now shortening protuberance. Thus a 180° reorientation of the posterior bristles has been effected outside the cell. Thin-sections of cells that are extruding bristles show a threadlike, cytoplasmic extension of the cell posterior which may be analogous to the protuberance seen in live cells. Four new posterior base-plate scales are secreted after the bristles have reoriented. Scanning electron microscopy indicates that the fibrillar complex is involved in positioning the bristles onto their respective base-plate scales. Anterior bristles are formed in new daughter cells in the same orientation as the posterior bristles; thus they are extruded tip first and no reorientation is required.     

Arrangement of bristles as a function of bristle number on a leg segment inDrosophila melanogaster

Summary The arrangement of bristles on a leg segment of the fruitflyDrosophila melanogaster was studied in various mutants that have abnormal numbers of bristles on this segment. Eighteen mutations at six different genetic loci were analyzed, plus five double or triple mutant combinations. Recessive mutations at theachaete-scute locus were found to affect distinct groups of bristles:achaete mutations remove mechanosensory bristles, whereasscute mutations remove mainly chemosensory bristles. Mechanosensory bristles remain uniformly spaced along the longitudinal axis unless their number decreases below a certain threshold, suggesting that spacing is controlled by cell interactions that cannot function when bristle cells are too far apart. Above a certain threshold, bristle spacing and alignment both become irregular, perhaps due to excessive force from these same interactions. Chemosensory bristles occupy definite positions that are virtually unaffected by removal of individual bristles from the array. Extra chemosensory bristles develop only near the six normal sites. At two of the six sites the multiple bristles tend to exhibit uniform longitudinal spacing — a property confined to mechanosensory bristles in wild-type flies. To explain the various mutant phenotypes the following scheme is proposed, with different mutations directly or indirectly affecting each step: (1) spots and stripes are demarcated within the pattern area, (2) one bristle cell normally arises within each spot, multiple bristle cells within each stripe, (3) incipient bristle cells inhibit neighboring cells from becoming bristle cells, and (4) the bristle cells within each stripe become aligned to form rows and then repel one another to generate uniform spacing.     

Selection for canalization at extra dorsocentral and scutellar bristles in Drosophila melanogaster.

Direct artificial selection for a specific pattern, in the number and position of extra bristles, was carried out in a wild-type population of Drosophila melanogaster to canalize (estimated by probit width) the selected phenotypes. From the same population, independent lines were selected for extra dorsocentral bristles (lines D3 and D4) and for extra scutellar bristles (lines E2, E3, and E4). Differences at canalization between both dorsocentral and scutellar systems were detected. Results fit an independent control hypothesis for canalization, at two symmetrical extra bristles, in the main regions in which extra bristles appear.     

Variations in the arrangement of sensory bristles along butterfly wing margins

The surfaces of insect wings exhibit numerous sensilla, which have been suggested to have a behavioral function. Some evidence suggests that the sensory bristles along the wing margin of lepidopteran insects (butterflies and moths) are involved in the regulation of wing movement. We investigated the arrangement of sensory bristles along the wing margins of 62 species of papilionoid butterflies, using light-microscopic examination of mounts of whole wings after removing the scales surrounding the bristles. In the majority of the wings examined, bristles were located on the ventral wing surfaces and were continuously distributed along the wing margins, except in the vicinity of the wing bases. In some wings, bristles were also located on the dorsal wing surfaces, and were continuously or discontinuously distributed along the wing margins of different species. In a minority of the species studied, we observed bristle distribution in the vicinity of the wing base, discontinuous bristle distribution on both the dorsal and ventral wing surfaces, or an absence of bristles along the wing margins. This variation in the arrangement of bristles along the wing margins is discussed in relation to the reception and transmission of sensory information in the wings.     

On the nature of bristles in Scenedesmus

Summary The existence of bristles, the hair-like appendages in several species of the genus Scenedesmus has been confirmed.The ultrastructure of bristles in Scenedesmus helveticus Arlet, Sc. acutus Meyen and Sc. acuminatus/Lagerh./Chodat has been studied by negative staining. While bristles of Sc. helveticus are composed of several microstrands with a regular pattern of cross-striation, the bristles of spineless species Sc. aculus and Sc. acuminatus seem to be composed only of individual microstrands.These investigations of bristles suggest their protein composition.     

Facial bristle feather histology and morphology in New Zealand birds: Implications for function

Knowledge of structure in biology may help inform hypotheses about function. Little is known about the histological structure or the function of avian facial bristle feathers. Here we provide information on morphology and histology, with inferences for function, of bristles in five predominantly insectivorous birds from New Zealand. We chose species with differing ecologies, including: brown kiwi (Apteryx mantelli), morepork (Ninox novaezealandae), hihi (Notiomystis cincta), New Zealand robin (Petroica australis), and New Zealand fantail (Rhipidura fuliginosa). Average bristle length corrected for body size was similar across species. Bristles occurred in distinct groups on different parts of the head and upper rictal bristles were generally longest. The lower rictal bristles of the fantail were the longest possessed by that species and were long compared to bristles of other species. Kiwi were the only species with forehead bristles, similar in length to the upper rictal bristles of other species, and the lower rictal bristles of fantails. Herbst corpuscles (vibration and pressure sensitive mechanoreceptors) were found in association with bristle follicles in all species. Nocturnal and hole‐nesting birds had more heavily encapsulated corpuscles than diurnal open‐nesting species. Our results suggest that avian facial bristles generally have a tactile function in both nocturnal and diurnal species, perhaps playing a role in prey handling, gathering information during flight, navigating in nest cavities and on the ground at night and possibly in prey‐detection. These differing roles may help explain the observed differences in capsule thickness of the corpuscles. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.     

Shaggy (zeste-white 3) and the formation of supernumerary bristle precursors in the developing wing blade of Drosophila.

The development of supernumerary bristle precursors induced by the mutation shaggy (sgg; also known as zeste-white 3) was examined in the developing wing blade of imaginal and pupal Drosophila. sgg clones were induced by mitotic recombination; clones were marked using enhancer-trap flies which express beta-galactosidase ubiquitously in imaginal tissues, while bristle precursors were identified using sensillum and bristle-specific enhancer-trap lines. It was shown that the precursors of supernumerary sgg bristles in the wing blade mimicked the development of morphologically similar margin bristles, developing in a manner similar to that of anterior sensory bristles in anterior clones and posterior noninnervated bristles in posterior clones. Interestingly, supernumerary anterior sensory bristles appeared outside the normal regions of "proneural" gene activity as identified using anti-achaete. Moreover, sgg could induce the ectopic expression of achaete in anterior clones. Thus, in the anterior wing blade the sgg mutation leads to the formation of ectopic proneural regions.     

STRUCTURE AND FUNCTION OF THE BRISTLES OF PEDIASTRUM BORYANUM (CHLOROPHYTA)1

Tufts of long delicate bristles were detected on mature colonies of Pediastrum boryanum (Turp.) Meneghini. The bristles are not uniform in length and can exceed 100 μm. Bristle number per tuft can exceed eighty. Ultrastructure studies revealed that tufts are an aggregate of hexagonal tubules arranged in staggered rows. Each hexagonal tubule has an inner diameter of 6 nm and is made up of six interconnected subunits 4 nm in diameter that are shared by adjoining tubules. The bristles can be easily removed from mature colonies with a vortex stirrer. Removal of bristles from mature colonies in culture results in the loss of buoyancy and subsequent settling to the bottom of the flask.     

Pattern as a function of cell number and cell size on the second-leg basitarsus ofDrosophila

Summary The bristle pattern of the second-leg basitarsus inDrosophila melanogaster was studied as a function of the number and size of the cells on this segment in well-fed and starved wild-type flies, in triploid flies, and in two mutants (dachs andfour-jointed) that have abnormally short basitarsi. The second-leg basitarsi of well-fed, wild-type flies from 22 otherDrosophila species were studied in a similar manner. There are typically 8 longitudinal rows of evenly-spaced bristles on the second-leg basitarsus, and in each row the number of bristles was consistently found to vary in proportion to the estimated number of cells along the segment, and the interval between bristles was found to vary in proportion to the average cell diameter on the segment. These correlations are interpreted to mean that the spacing of the bristles within each row is controlled developmentally, whereas the number of bristles is not. The interval between bristles is evidently measured either as a fixed number of cells or as a distance which indirectly depends upon cell diameter.     

Is There a Gene Regulating the Scute Locus on the Third Chromosome of D. MELANOGASTER?

A section of the third chromosome of D. melanogaster some 25 to 40 centimorgans long including sr was transferred from a wild-type stock selected by Latter for high scutellar bristle number into a scute stock with a large number of scutellar bristles. This segment is shown to have a large effect on the bristle numbers of wild-type flies, to reduce the strength of canalization of the scute phenotype at 4 bristles, to have little, if any, effect on bristle numbers of scute flies with less than 4 bristles but to increase the number of flies with 5 and 6 scutellar bristles in scute stocks that normally have a large number of flies with 4 bristles. It is suggested that this segment in unselected chromosomes contains a gene that regulates bristle number by repressing the scute locus and that Latter has selected a mutant of the regulator which fails to repress the action of the scute locus.     

A new genus and a new species of tachinids (Diptera,Tachinidae) from the south of middle Asia

Ventoplagia gen. n. is described, with the type species Ventoplagia brevirostris sp. n. The frontal bristles extending only to the base of the pedicel, 2+3 dorsocentral bristles, 0+2 intraalar bristles, the absence of prealar bristle, the short and fine anepimeral (pteropleural) bristle, the scutellum without lateral bristles, and the welldeveloped posteroventral bristle of the hind tibia indicate that the new genus belongs to tribe Minthoini. Ventoplagia gen. n. is closely related to the genus Palmonia Kugler. The characters distinguishing these genera are given.     

Convergent evolution between Echidnophora and Termitoxeniinae (Diptera: Phoridae)

Echidnophora dondroi sp.nov. is described from females collected in the fungus gardens of a nest of the termite Odontotermes takensis in North Sumatra. Resemblances between Echidnophora and Termitoxeniinae are discussed and interpreted as examples of convergence. The peculiarly modified basal sockets of some major abdominal bristles in many Termitoxeniinae are illustrated and discussed. The hypothesis is advanced that these modified sockets are the sites from which exudates attractive to termite workers are discharged. It is further postulated that these exudates are primarily lipid material. Furthermore, the abdominal bristles of the Termitoxeniinae examined are smooth, in contrast to the fluted bristles characteristic of Echidnophora , other Phoridae, and those of workers of termite hosts of the Termitoxeniinae. This is probably an adaptation that renders the bristles more pliant, and thus less liable to being broken off when stroked by a termite worker. Enlarged collars, arising from the basal sockets and embracing the bases of the bristles, probably serve as an additional protection.     

Selection for canalization at two extra dorsocentral bristles in Drosophila melanogaster.

From 10 isofemale lines of D. melanogaster, the D2 line was established with the aim of obtaining an invariant phenotype at two extra dorsocentral bristles. Line D2 was also subdivided into two other lines, SA and ASD, based on their different bristle patterns. The SA line was selected for two symmetrical anterior extra bristles, and the ASD line was selected for two asymmetrical extra bristles, one anterior and one posterior. Only the SA line showed any canalizing response (estimated by the width of the probit transformation) at the two-extra-bristle class. Nevertheless, the results from the different lines were more consistent with the independent ones of both the anterior and posterior regions of the extra dorsocentral bristles. This analysis showed some independent genetic systems for each region, developmental canalization being at two extra symmetrical bristles per region in all the selected lines (D2, ASD, and SA). Therefore, this canalization did not depend directly on the extra-bristle positional pattern used in the selection. The wild-type canalizing system is suggested to explain the fast canalizing response in a phenotype that had not been previously canalized by natural selection.     

Taxonomic significance of asymmetrical helmet and lance bristles in the genus Mallomonas (Synurophyceae) and their discovery in Eocene lake sediments

Complex bristle types formed by species in the genus Mallomonas include those with helmet or lance-shaped apices. The ornamentation on each side of the helmet has been thought to be equivalent or symmetrical, whereas on a lance-shaped bristle an expanded portion folds over one side of the shaft to form an asymmetrical structure. We describe, for the first time, helmet bristles with a distinctly asymmetrical design, also formed by the folding of a siliceous membrane over one side of the helmet. We postulate that the asymmetrical helmet represents a structure that combines the formation of a symmetrical helmet and a lance-shaped design on the same bristle. Further, we report structurally similar asymmetrical helmet bristles, lance-shaped bristles and scales that are unambiguously assigned to Mallomonas asmundiae in Middle Eocene sediments from a maar lake in northern Canada, supporting the hypothesis that scale and bristle morphology in the Synurophyceae has undergone extensive prolonged evolutionary stasis. Given differences in scale morphology and the presence of asymmetrical helmet bristles, we transfer the North American endemic Mallomonas acaroides var. muskokana to the rank of species. Further, we formally describe Mallomonas dispar and M. lancea, fossil species with asymmetrical helmet bristles and lance-shaped bristles, respectively. The taxonomic and biogeographic significance of asymmetrical and lance-bearing bristles is discussed.     

SCENEDESMUS MORPHOLOGY AND FLOTATION1

Various flotation studies were conducted on several strains of Scenedesmus. Inverted microscope flotation experiments run on culture 614 with bristles, culture 614 centrifuged to remove bristles, and bristle-less strain 76 revealed that bristles aid in flotation. Cultures grown in NH₄NO₃-Bristol's compared to cultures grown in Bristol's medium exhibited a positive buoyancy as do cells transferred, to fresh media. Differential centrifugation procedures demonstrate that colonies with bristles and spines exhibit a greater buoyancy than spineless and bristle less colonies, and furthermore that unicells and newly released colonies exhibit greater buoyancy than older cultures and large, granular, dividing cells.     

Obervations on the occurrence of scales and bristles of mallomonas spp. (Chrysophyceae) in the micro-laminated sediments of a small lake in finnish North Karelia

Scales and bristles ofMallomonas crassisquama (Asmund) Fott andM. elongata Reverdin are reported from the laminated sediments of Laukunlampi, a small kettlehole lake in N. Karelia, Finland. The white summer laminae in the deeper sediment are composed almost entirely ofM. crassisquama scales and bristles. The taxonomy, ecology and distribution ofM. crassisquama andM. elongata are briefly discussed and factors influencing the preservation of scales and bristles in sediments are considered. It is suggested that analysis of sedimentary associations of scales, bristles and cysts could be used to improve cyst taxonomy inMallomonas.     

Mutational analysis of Stubble-stubbloid gene structure and function in Drosophila leg and bristle morphogenesis

The Stubble-stubbloid (Sb-sbd) gene is required for ecdysone-regulated epithelial morphogenesis of imaginal tissues during Drosophila metamorphosis. Mutations in Sb-sbd are associated with defects in apical cell shape changes critical for the evagination of the leg imaginal disc and with defects in assembly and extension of parallel actin bundles in growing mechanosensory bristles. The Sb-sbd gene encodes a type II transmembrane serine protease (TTSP). Here we use a Sb-sbd transgenic construct to rescue both bristle and leg morphogenesis defects in Sb-sbd mutations. Molecular characterization of Sb-sbd mutations and rescue experiments with wild-type and modified Sb-sbd transgenic constructs show that the protease domain is required for both leg and bristle functions. Truncated proteins that express the noncatalytic domains without the protease have dominant effects in bristles but not in legs. Leg morphogenesis, but not bristle growth, is sensitive to Sb-sbd overexpression. Antibody localization of the Sb-sbd protein shows apical expression in elongating legs. Sb-sbd protein is found in the base and shaft in budding bristles and then concentrates at the growing tip when bristles are elongating rapidly. We propose a model whereby Sb-sbd helps coordinate proteolytic modification of extracellular matrix attachments with cytoskeletal changes in both legs and bristles.