SOME ERYTHRONEURA (GRAPE LEAF HOPPERS) OF THE MACULATA GROUP. (HOMOPTERA, CICADELLIDAE)

1932 ◽  
Vol 64 (6) ◽  
pp. 134-144
Author(s):  
R. H. Beamer

The foliowing is the original description: “Markings of head, thorax and scutellum as usual inthe maculata type, yellow; tegmen with a streak along claval suture auteriorly, an oblique dash at base of corium and another at anterior end of costal plaque, yellow; dot at posterior end of plaque, and in base of fourth apical cell black; and the following markings red, broad vitta based on costal plaque, extending inwardly and crossing clavus as oblique broad band, and a straight narrow stripe, connected narrowly behind to a spot which spreads so as to fill spaces betuween sectors anterior to third and fourth apical cells, also ramose marking on cross veins ; costal plaque dusky bluish hyaline, apical cells fumose. Color below pale yellow. Length: 2.75 mm.

1868 ◽  
Vol 1 (5) ◽  
pp. 33-38
Author(s):  
E. T. Cresson

1. Banchus Flavescens.— ♂ . Pale yellow ; a bilobed mark behind antennæ, extending between them downward upon middle of face, band across vertex from eye to eye, covering ocelli, posterior margin of occiput, maxillary palpi, two apical joints of labial palpi, antennæ above, stripe on middle of mesothorax. dilated anteriorly, a stripe on each side over the wings, basal suture of scutellum, base of metathorax, broader laterally, spot on each side of pleura posteriorly, posterior coxæ within, their femora beneath, apex of their tibiæ and a broad band at base of four basal segments of abdomen, black; antennæ longer than body, slender at tips ; scutellum with an acute dusky spine ; wings hyaline, faintly yellowish, nervures brown, stigma and costa pale honey-yellow; posterior coxæ and femora stained with ferruginous; abdomen shining, short, apex broad, truncate and compressed. Length five lines.


1906 ◽  
Vol 38 (3) ◽  
pp. 81-82 ◽  
Author(s):  
A. Arsene Girault

In the original description of this insect, * Dr.Riley says that on account of its uniform pale yellow colour it is easily distinguished from Trichogramma minutum, Riley, which is black. Unfortunately, this does not hold.† Out of the hundreds of specimens of pretiosa reared during the enire season of 1904, at Paris, Texas, from the eggs of Heliothis obsoleta, Fabricius, there appeared from a lot of host eggs on Sept. 20th a number of dark individuals, which could easily have been mistaken for a distinct species.


1890 ◽  
Vol 22 (2) ◽  
pp. 21-23
Author(s):  
W. H. Edwards

Melitæa Augusta.Male.—Expands from 1.6 to 1.75 inch; belongs to Chalcedon group, but is an conspicuously red as the species Chalcedon is black; upper side black, the surface nearly covered with light red and pale yellow spots, disposed as in the group; the basal areas dusted with yellow scales which, on primaries, extend along both margins; costa of same wing edged red; both hind margins bordered by small red spots, varying in shape, sometimes narrow and as of a broken stripe, sometimes more or lesss rounded to ovate; the spots of second row ar small, lunular, largest of secondaries, edged with red, the interior being yellow, or they are nearly all red with a small yellow patch in middle; sometimes this yellow is thinly washed red; the third row on primaries is either wholly yellow, or yellow with red edges, particularly on the outer side; on secondaries wholly red, and often very deep, so as to make a conspicuous broad band; the fourth row on primaries is red, sometimes with the spots next the two margins either yellow or in put yellow; around the end of cell yellow spots four or five in number; in the cell spots of red and yellow alternately, four in all, the yellow one at base more or less stained red; two yellow spots below cell with black ground between, and nearer base a small duplex red one; the fourth row on secondaries is yellow, either of small spots or pretty large ones, and the three or four from costal margin are red on their outer side; a red stripe outside the cell from the end to costal margin; two small yellow spots inside cell, with a red one between them and a yellow spot below; fringes yellow, black at the tips of the nervules.


1879 ◽  
Vol 168 ◽  
pp. 166-166

The species collected are four in number, three of which were previously known to occur on the shore of the Island, viz. :— Harpagifer bispinis, Choenichthys rhinoceratus , and Notothenia coriiceps . The fourth is a Ray, apparently undescribed, which may he characterised thus :— Raja eatonii. Allied to B. smithii . Snout of moderate length, the anterior margins meeting at a right angle; the width of the inter-orbital space is two-sevenths of the distance of the eye from the end of the snout. The anterior profile, from the snout to the angle of the pectoral fin, is slightly emarginate, the outer pectoral angle being rounded. The greater part of the upper surface of the body is smooth, minute spines are distributed between the eyes, and in a narrow stripe along the margins of the body; a broad band of minute spines along the median line of the back and the upper surface of the tail ; a single larger recurved spine in the middle of the back ; a series of nine or ten rather small spines placed at a considerable distance from each other along the median line of the tail; no spines on the side of the tail. Lower parts smooth. Upper lip fringed on the side; teeth pointed, conical, in about 30 series in the upper jaw. Male with a patch of claw-like spines on each pectoral fin. Brownish black above, with indistinct round whitish spots ; whitish below, with some irregular brownish-black spots; lower part of the tail brownish-black.


2014 ◽  
Vol 2 (18) ◽  
pp. 1 ◽  
Author(s):  
Thiago Xisto ◽  
Maria Cleide de Mendonça

Dicranocentrus heloisae Arlé & Mendonça 1982 is redescribed based on specimens collected from its type locality, “Parque Nacional da Tijuca”, Rio de Janeiro municipality, State of Rio de Janeiro. The presence of 6+6 macrochaetae S, 1+1 macrochaeta P, and absence of macrochaetae A1 and Ps dorsally on head, puts Dicranocentrus heloisae in the gracilis-group sensu Mari-Mutt (1979). This species is easily indentified mainly due to general color pattern of pale yellow on body with bluish to blackish pigmentation on head. Taxonomic characteristics not illustrated in the original description are given (dorsal cephalic chaetotaxy, sensory organ of the third antennal segment, eyes, labrum, maxillary palp, outer labial papilla, labial triangle, trochanteral organ, femur, tibiotarsus, unguis, ventral tube and tenaculum). New records from other localities in Brazil are provided. A neotype for Dicranocentrus heloisae is designated.


2006 ◽  
Vol 6 (2) ◽  
pp. 253-261 ◽  
Author(s):  
Allen Wang ◽  
Shelley Lane ◽  
Zhen Tian ◽  
Amir Sharon ◽  
Idit Hazan ◽  
...  

ABSTRACT The human fungal pathogen Candida albicans can undergo a morphological transition from a unicellular yeast growth form to a multicellular hyphal growth form. During hyphal growth, cell division is asymmetric. Only the apical cell divides, whereas subapical cells remain in G1, and cell surface growth is highly restricted to the tip of the apical cell. Hgc1, a hypha-specific, G1 cyclin-like protein, is essential for hyphal development. Here, we report, using indirect immunofluorescence, that Hgc1 is preferentially localized to the dividing apical cells of hyphae. Hgc1 protein is rapidly degraded in a cell cycle-independent manner, and the protein turnover likely occurs in both the apical and the subapical cells of hyphae. In addition to rapid protein turnover, the HGC1 transcript is also dynamically regulated during cell cycle progression in hyphal growth. It is induced upon germ tube formation in early G1; the transcript level is reduced during the G1/S transition and peaks again around the G2/M phase in the subsequent cell cycles. Transcription from the HGC1 promoter is essential for its apical cell localization, as Hgc1 no longer exhibits preferential apical localization when expressed under the MAL2 promoter. Using fluorescence in situ hybridization, the HGC1 transcript is detected only in the apical cells of hyphae, suggesting that HGC1 is transcribed in the apical cell. Therefore, the preferential localization of Hgc1 to the apical cells of hyphae results from the dynamic temporal and spatial control of HGC1 expression.


Plant Disease ◽  
2012 ◽  
Vol 96 (6) ◽  
pp. 913-913 ◽  
Author(s):  
M. Zhang ◽  
Y. Wang ◽  
C. Y. Wen ◽  
H. Y. Wu

Winter jujube, Zizyphus jujuba Mill., is a Chinese crop with fruit that has an extremely high nutritional value (4). In early November 2010, a severe fruit rot affecting ~20% of 1,000 kg of winter jujube fruit was observed in a storehouse in Zhengzhou, Henan province, China. The same fruit rot symptoms were found in two supermarkets in Zhengzhou in late November 2010 in ~10% of 100 kg of fruit in one supermarket and 25% of 50 kg of fruit in the other. Symptoms first appeared as small, round, pale yellow brown lesions on the fruits, 1 to 3 mm in diameter, then developed into 5- to 10-mm, sunken, brown spots, each with a pale brown margin. Three Fusarium isolates (DZF001 to DZF003) showing similar morphological characteristics were isolated from three specimens (collected from one storehouse and two supermarkets) by surface sterilizing small pieces of necrotic fruit tissue for 1 min in 2% NaOCl, washing the tissue pieces three times with sterile distilled water, and plating the pieces on potato dextrose agar (PDA). Fungal colonies for each isolate were white to light pink, and the adaxial side of each culture was pale yellow. Macroconidia were produced in pale orange sporodochia and were slender, relatively straight, three to five septa, 29.0 to 55.2 × 2.5 to 4.0 μm, with a curved apical cell and a poorly developed basal cell. Microconidia were produced in chains or false heads on synthetic nutrient-poor agar, clavate with a planar base, aseptate, and 4.5 to 8.0 × 2.5 to 3.5 μm. Conidiophores terminated in verticils of two to three phialides or monophialides. Chlamydospores were absent. The cultural and morphological characteristics were similar to those of Fusarium proliferatum (1,2). The identity of the three fungal isolates was confirmed to be F. proliferatum by DNA sequencing of the internal transcribed spacer (ITS) rDNA region (GenBank Accession Nos. JN889713 to JN889715), which were 99 to 100% homologous to those of other F. proliferatum isolates (GU066714, HQ113948, and GU363955); and the elongation factor 1-alpha (EF-1a) gene (JN889713 to JN889715), which was 99% homologous to those of other F. proliferatum isolates (FJ538244, FJ895277, and GQ848536) (3). Pathogenicity tests were conducted on 20 winter jujube fruits using a mycelial plug harvested from the periphery of a 7-day-old colony of strain DZF001, and placed on the surface of the fruit after the inoculated area of the fruit had been surface sterilized with 75% ethanol for 2 min; an equal number of fresh winter jujube fruits treated with non-colonized plugs of PDA served as the control treatment. Each jujube fruit was pricked three times with an insect needle to create three holes close together before inoculation with an agar plug. Each fruit was then enclosed in a clear plastic box with a cup of sterile distilled water to maintain high relative humidity, and held at 25°C. Symptoms similar to those originally observed on the naturally infected fruit were observed 3 days after inoculation, and the same fungus was reisolated from each of the symptomatic fruits; control fruits remained asymptomatic and no fungus was isolated from the control fruit. Koch's postulates were repeated three times with the same results. To our knowledge, this is the first report of F. proliferatum causing rot of winter jujube fruit in China. References: (1) K. Chehri et al. Saudi J. Biol. Sci. 18:341, 2011. (2) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual, Blackwell Publishing, 2006. (3) H. T. Phan. Studies Mycol. 50:261, 2004. (4) J. Sheng et al. Acta Hort. 620:203, 2003.


Development ◽  
2002 ◽  
Vol 129 (14) ◽  
pp. 3403-3410 ◽  
Author(s):  
Alexandria Saulsberry ◽  
Paula R. Martin ◽  
Tim O’Brien ◽  
Leslie E. Sieburth ◽  
F. Bryan Pickett

Creation of an embryonic fate map may provide insight into the patterns of cell division and specification contributing to the apical region of the early Arabidopsis embryo. A fate map has been constructed by inducing genetic chimerism during the two-apical-cell stage of embryogenesis to determine if the orientation of the first anticlinal cell division correlates with later developmental axes. Chimeras were also used to map the relative locations of precursors of the cotyledon and leaf primordia. Genetic chimeras were induced in embryos doubly heterozygous for a heat shock regulated Cre recombinase and a constitutively expressed β-glucuronidase (GUS) gene flanked by the loxP binding sites for Cre. Individual cells in the two-apical-cell stage embryo responding to heat shock produce GUS-negative daughter cells. Mature plants grown from seed derived from treated embryos were scored for GUS-negative sector extent in the cotyledons and leaves. The GUS-negative daughters of apical cells had a strong tendency to contribute primarily to one cotyledon or the other and to physically adjacent true leaf margins. This result indicated that patterns of early cell division correlate with later axes of symmetry in the embryo and that these patterns partially limit the fates available for adoption by daughter cells. However, GUS-negative sectors were shared between all regions of the mature plant, suggesting that there is no strict fate restriction imposed on the daughters of the first apical cells.


2010 ◽  
Vol 191 (5) ◽  
pp. 943-952 ◽  
Author(s):  
Tiffiney R. Hartman ◽  
Daniel Zinshteyn ◽  
Heather K. Schofield ◽  
Emmanuelle Nicolas ◽  
Ami Okada ◽  
...  

Stem cells depend on signals from cells within their microenvironment, or niche, as well as factors secreted by distant cells to regulate their maintenance and function. Here we show that Boi, a Hedgehog (Hh)-binding protein, is a novel suppressor of proliferation of follicle stem cells (FSCs) in the Drosophila ovary. Hh is expressed in apical cells, distant from the FSC niche, and diffuses to reach FSCs, where it promotes FSC proliferation. We show that Boi is expressed in apical cells and exerts its suppressive effect on FSC proliferation by binding to and sequestering Hh on the apical cell surface, thereby inhibiting Hh diffusion. Our studies demonstrate that cells distant from the local niche can regulate stem cell function through ligand sequestration, a mechanism that likely is conserved in other epithelial tissues.


2014 ◽  
Vol 66 (4) ◽  
pp. 25-34 ◽  
Author(s):  
Aneta Sulborska

Micromorphology and distribution of glandular and non-glandular trichomes on the above-ground organs of <em>Inula helenium </em>L. were investigated using light and scanning electron microscopy (SEM). Two types of biseriate glandular trichomes, i.e. sessile and stalk hairs, and non-glandular trichomes were recorded. Sessile glandular trichomes were found on all examined <em>I. helenium </em>organs (with their highest density on the abaxial surface of leaves and disk florets, and on stems), whereas stalk glandular trichomes were found on leaves and stems. Sessile trichomes were characterised by a slightly lower height (58–103 μm) and width (32–35 μm) than the stalk trichomes (62–111 μm x 31–36 μm). Glandular hairs were composed of 5–7 (sessile trichomes) or 6–9 (stalk trichomes) cell tiers. Apical trichome cell tiers exhibited features of secretory cells. Secretion was accumulated in subcuticular space, which expanded and ruptured at the top, and released its content. Histochemical assays showed the presence of lipids and polyphenols, whereas no starch was detected. Non-glandular trichomes were seen on involucral bracts, leaves and stems (more frequently on involucral bracts). Their structure comprised 2–9 cells; basal cells (1–6) were smaller and linearly arranged, while apical cells had a prozenchymatous shape. The apical cell was the longest and sharply pointed. Applied histochemical tests revealed orange-red (presence of lipids) and brow colour (presence of polyphenols) in the apical cells of the trichomes. This may suggest that beside their protective role, the trichomes may participate in secretion of secondary metabolites.


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