1,378 research outputs found
Total Lipid and Fatty Acid Composition in Male and Female Larvae of Indian-Meal Moth and Almond Moth (Lepidoptera: Pyralidae)
The total body lipid and fatty acid composition of last instar larvae of the Indian-meal moth, Plodia interpunctella, and almond moth, Cadra cautella, reared on a turkey mash diet was determined. Male P. interpunctella larvae contained significantly higher (lA-fold) total body lipid than females, while no differences between the sexes of C. cautella larvae were observed. The relative abundance of the fatty acids palmitate, palmitoleate, stearate, oleate, lineoleate, and linolenate was similar in both sexes of P. interpunctella and C. cautella. The accumulation of individual fatty acids in larvae of both the moth species did not correspond to levels of fatty acids in the diet. The accumulation of palmitate, palmitoleate, and oleate in moth larvae of both the species was greater than linoleate and linolenate, suggesting a sparing effect by the former on the latter, more unsaturated fatty acids
Malathion Resistance in Larvae of Some Southern Minnesota Populations of the Indianmeal Moth,\u3ci\u3e Plodia Interpunctella\u3c/i\u3e (Lepidoptera: Pyralidae), Infesting Bulk-Stored Shelled Corn
Larvae of 21 field collected populations of the Indianmeal moth, Plodia interpunctella, infesting stored shelled corn in southern Minnesota were tested for their susceptibility to malathion in the laboratory. A population that was a composite of the 21 populations and a malathion susceptible population were also tested for their susceptibility to malathion, pirimiphos-methyl and chlorpyrifos-methyl. Comparison of the LDso values of the field populations with the malathion susceptible population indicated that the field populations were ca. 33- to 625-fold resistant to malathion. The composite field population was ca. 243-fold resistant to malathion, and this population was 3.2-fold cross-resistant to pirimiphos-methyl, but was highly susceptible to chlorpyrifos-methyl
New Convertible Authenticated Encryption Scheme with Message Linkages
The digital signature provides the signing message with functions like authentication, integration and non-repudiation. However, in some of the applications, the signature has to be verified only by specific recipients of the message and it should be hidden from the public. For achieving this, authenticated encryption systems are used. Authenticated Encryption schemes are highly helpful to send a confidential message over an insecure network path. In order to protect the recipients benefit and for ensuring non-repudiation, we help the receiver to change the signature from encrypted one to an ordinary one. With this we avoid any sort of later disputes. Few years back, Araki et al. has proposed a convertible authenticated scheme for giving a solution to the problem. His scheme enables the recipient to convert the senders signature into an ordinary one. However, the conversion requires the cooperation of the signer. In this thesis, we present a convertible authenticated encryption scheme that can produce the ordinary signature without the cooperation of the signer with a greater ease. Here, we display a validated encryption plan using message linkages used to convey a message. For the collector's advantage, the beneficiary can surely change the encrypted signature into an ordinary signature that which anyone can check. A few attainable assaults shall be examined, and the security investigation will demonstrate that none of the them can effectively break the proposed plan
New or rare Hedyotis Linn. (Rubiaceae) from South India
Three taxa of Hedyotis Linn. (Rubiaceae), viz., H. gamblei Henry & Subr. sp. nov., H. eualata var. agastyamalayana Henry & Subr. var. nov. and H. barberi (Gamble) Henry & Subr. comb. nov., collected from Agastyamalai Hills and surrounding regions in Tirunelveli District, Tamil Nadu, South India, are described in this paper
A contribution to the floral anatomy of Nepenthes khasiana Hook F.
Two kinds of multicellular trichomes, glandular and non-glandular, occur on the abaxial side of the perianth lobes, androphore and ovary wall; sunken multicellular glands are generally present on the adaxial surface of the perianth lobes. The development of these trichomes and glands shows that they are epidermal in origin. The flowers are uni-sexual. The perianth is tetramerous and each perianth lobe is traversed by three bundles. The origin and distribution of the staminal traces recall the condition in fasciculate androecium. The ovary is tetralocular below and unilocular above. The placentae which lie along the septal radii receive the half ventrals of adjacent carpels but do not fuse to form common ventral bundles. Thus the placentation may be described as tending towards the parietal condition. The stigma is commissural
A new species of Marsdenia R. Br. (Asclepiadaceae) from South India
Marsdenia raziana which represents a new species of Asclepiadaceae, collected around Yelnir ghats forests (W. ghats), Samse, Chikmagalur District, has been described and illustrated
Dichotomous venation and anastomosis in the corolla of an orchid-Habenaria dentata (SW.) Schltr
The lip of the corolla in habenaria dentata (Sw.) Schltr. is tripartite. The lateral lobes show dichotomously branched veins. While the majority of the vein-endings are related to crenulation in the corolla and terminate at the tip, others end blindly. Usually each crenulation receives one vein. In exceptional cases two veins enter a crenulation. Cases of veins ending beneath an incision (sinus) separating two crenulations have been observed. Sinus vein dichotomies are present. Nine types of anastomoses are described. In Type I, two branches of a single vein-dichotomy remain united. Type II is characterized by the union of adjacent branches of two vein dichotomies and their separation. Type III is similar to Type II but the branches do not separate after confluence. In Type IV an arcuate vein unites with the branch of contiguous vein dichotomy and then separates. Type V is similar to Type IV but the fused branches do not separate. Type VI is formed by the union of the outer branch of a second order vein-dichotomy and the outer branch of a first order vein-dichotomy. In Type VII one outer branch each of two adjacent second order vein-dichotomies unite and separate. Type VIII is similar to Type VII but the branches do not separate after confluence. In Type IX the outer branch of a third order vein-dichotomy and the outer branch of a second order vein-dichotomy unite and separate after a short area of confluence. Cases of vein-approximations also have been observed
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