A COMPARATIVE MORPHOLOGY OF THE VENOM APPARATUS OF FEMALE BRACONIDS (HYMENOPTERA: BRACONIDAE)

1979 ◽  
Vol 111 (9) ◽  
pp. 1013-1024 ◽  
Author(s):  
Kathryn M. Edson ◽  
S. Bradleigh Vinson
Keyword(s):  
Comparative Morphology ◽  
Thin Walled ◽  
Ancestral Character States

AbstractThe venom apparatus was examined in 160 species of female Braconidae. The venom apparatus is illustrated for females of 26 representative genera and those of the remaining females are described.Our findings indicate that there are two types of venom apparatus present in Braconidae. Type 1 is found in females of subfamilies having more ancestral character states: Doryctinae, Spathiinae, Braconinae, Opiinae, Rogadinae, Alysiinae, and Ichneutinae. Typically, type 1 venom apparatus consists of a cone-shaped reservoir which is surrounded by many longitudinal and circular muscles and lined with a relatively thick cuticular intima, gland filaments, and a venom duct. Type 2 is found in females of subfamilies having more derived character states: Cheloninae, Microgasterinae, Agathidinae, Macrocentrinae, Helconinae, Neoneurinae, Centistinae, Paxylommatinae, and Euphorinae. Typically, type 2 consists of a thin-walled reservoir surrounded by relatively few muscles, two gland filaments, and a venom duct.The Aphidiinae is the only subfamily in which the females examined have both types of venom apparatus represented. Of those genera examined, only females of Praon have type 2, while females of the remaining genera have type 1 venom apparatus.Braconid females with type 1 venom apparatus are either ectoparasitoids or endoparasitoids which pupate within the host remains, while those females with type 2 are endoparasitoids which pupate outside the host remains.

Permineralized fruits and seeds from the Princeton chert (Middle Eocene) of British Columbia: Vitaceae

1990 ◽  
Vol 68 (2) ◽  
pp. 288-295 ◽  
Author(s):  
Sergio R. S. Cevallos-Ferriz ◽  
Ruth A. Stockey
Keyword(s):  
British Columbia ◽  
Middle Eocene ◽  
Outer Zone ◽  
Structural Features ◽  
Anatomical Structure ◽  
Thin Walled ◽  
Polyhedral Cells ◽  
A New Species

Four permineralized vitaceous seeds are described from the Middle Eocene Princeton chert, Allenby Formation, British Columbia. Three distinct types of ruminate perchalazal seeds are recognized, one is described as a new species Ampelocissus similkameenensis Cevallos-Ferriz et Stockey sp.nov., while the remaining seeds are referred to as type 1 and type 2 seeds. Five integumentary zones are recognized in each seed: zone 1 is an outer zone of thin-walled rectangular to polyhedral cells; zone 2 is a zone of thick-walled sclereids; zone 3 is a zone of cells with spiral thickenings; zone 4 is a zone of rectangular thin-walled cells (when preserved); and zone 5 is a zone of tangentially elongated thin-walled cells with dark contents. The chalaza in seeds of A. similkameenensis and the type 1 seed has three distinct zones, while in the type 2 seed it contains cells similar to integumentary zone 2. These Princeton seeds illustrate that structural features of Eocene Vitaceae include characters unlike those of extant taxa. This information contributes to our knowledge of anatomical structure within the group as a whole and underscores the need for review of both fossil and extant Vitaceae. Paucity of vitaceous seeds in the Princeton chert compared to the large number of preserved aquatic and semiaquatic remains suggests that they represent plants that grew in a nearby environment. Abrasion of the integument suggests that like extant seeds, they may have been dropped after passing through the gut of a bird.

Type 2 Diabetes Overtakes Type 1 in Hispanic Girls

2008 ◽  
Vol 38 (15) ◽  
pp. 18
Author(s):  
SHERRY BOSCHERT
Keyword(s):  
Type 2 Diabetes

Molecular analysis of FVIII gene in severe HA patients of Costa Rica

2010 ◽  
Vol 30 (S 01) ◽  
pp. S150-S152
Author(s):  
G. Jiménez-Cruz ◽  
M. Mendez ◽  
P. Chaverri ◽  
P. Alvarado ◽  
W. Schröder ◽  
...  
Keyword(s):  
Factor Viii ◽  
Coagulation Factor ◽  
Costa Rican ◽  
Factor Viii Gene ◽  
Intron 22 Inversion ◽  
Intron 1 ◽  
Polymerase Chain ◽  
Inversion Analysis

SummaryHaemophilia A (HA) is X-chromosome linked bleeding disorders caused by deficiency of the coagulation factor VIII (FVIII). It is caused by FVIII gene intron 22 inversion (Inv22) in approximately 45% and by intron 1 inversion (Inv1) in 5% of the patients. Both inversions occur as a result of intrachromosomal recombination between homologous regions, in intron 1 or 22 and their extragenic copy located telomeric to the FVIII gene. The aim of this study was to analyze the presence of these mutations in 25 HA Costa Rican families. Patients, methods: We studied 34 HA patients and 110 unrelated obligate members and possible carriers for the presence of Inv22or Inv1. Standard analyses of the factor VIII gene were used incl. Southern blot and long-range polymerase chain reaction for inversion analysis. Results: We found altered Inv22 restriction profiles in 21 patients and 37 carriers. It was found type 1 and type 2 of the inversion of Inv22. During the screening for Inv1 among the HA patient, who were Inv22 negative, we did not found this mutation. Discussion: Our data highlight the importance of the analysis of Inv22 for their association with development of inhibitors in the HA patients and we are continuous searching of Inv1 mutation. This knowledge represents a step for genetic counseling and prevention of the inhibitor development.

Polymorphisms of the Plasminogen Activator Inhibitor- 1 Gene in Type 1 and Type 2 Diabetes, and in Patients with Diabetic Retinopathy

1994 ◽  
Vol 71 (06) ◽  
pp. 731-736 ◽  
Author(s):  
M W Mansfield ◽  
M H Stickland ◽  
A M Carter ◽  
P J Grant
Keyword(s):  
Diabetic Retinopathy ◽  
Plasminogen Activator Inhibitor ◽  
Allelic Frequency ◽  
Repeat Sequence ◽  
Dinucleotide Repeat ◽  
Plasminogen Activator Inhibitor 1 ◽  
The Difference ◽  
Pai 1

SummaryTo identify whether genotype contributes to the difference in PAI-1 levels in type 1 and type 2 diabetic subjects and whether genotype relates to the development of retinopathy, a Hind III restriction fragment length polymorphism and two dinucleotide repeat polymorphisms were studied. In 519 Caucasian diabetic subjects (192 type 1, 327 type 2) and 123 Caucasian control subjects there were no differences in the frequency of the Hind III restriction alleles (type 1 vs type 2 vs control: allele 1 0.397 vs 0.420 vs 0.448; allele 2 0.603 vs 0.580 vs 0.552) nor in the allelic frequency at either dinucleotide repeat sequence. In 86 subjects with no retinopathy at 15 years or more from diagnosis of diabetes and 190 subjects with diabetic retinopathy there was no difference in the frequency of Hind III restriction alleles (retinopathy present vs retinopathy absent: allele 1 0.400 vs 0.467; allele 2 0.600 vs 0.533) nor in the allelic frequencies at either dinucleotide repeat sequence. The results indicate that there is no or minimal influence of the PAI-1 gene on either PAI-1 levels or the development of diabetic retinopathy in patients with diabetes mellitus.

Causes of diabetic ketoacidosis: type 1 diabetes versus type 2 diabetes

2017 ◽  
Author(s):  
Marwa Omri ◽  
Rayene Ben Mohamed ◽  
Imen Rezgani ◽  
Sana Mhidhi ◽  
Aroua Temessek ◽  
...  
Keyword(s):  
Type 2 Diabetes ◽  
Type 1 Diabetes ◽  
Diabetic Ketoacidosis
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