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1.
J Econ Entomol ; 104(5): 1514-24, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22066180

RESUMO

The light brown apple moth, Epiphyas postvittana (Walker) (Lepidoptera: Tortricidae), is a highly successful biological invader. It was accidentally introduced to several countries including New Zealand, Hawaii, England, and California. Light brown apple moth attacks a wide range of crop plants and other woody and herbaceous plants, but a more comprehensive analysis of its host range is needed for risk assessments, to evaluate the likely economic and environmental impacts, and to enable targeting of particular plant species for detection surveys and treatments. We reviewed and synthesized the host range and host selection behavior of light brown apple moth by using information from Australia and invaded countries. The host range of light brown apple moth is determined by the behavior of both adult females and larvae. Females use visual, chemical and physical cues to choose host plants. Larvae are capable of limited active dispersal by walking and longer range dispersal by ballooning on silken strands; therefore, larvae also may need to select host plants. We review larval performance indicators across a range of plants. Based on our review, there are at least 545 plant species in 363 genera from 121 families that have been reported as hosts of light brown apple moth. Some plants were reported only once and need verification. Nevertheless, many host plant species and their wide phylogenetic range (from ferns to higher dicotyledons) indicates that light brown apple moth is one of the most polyphagous insects known. This information and our categorization of frequency of host use are valuable for incursion response and pest management activities.


Assuntos
Dieta/veterinária , Mariposas/fisiologia , Plantas/classificação , Animais , Dieta/classificação , Feminino , Larva/fisiologia , Masculino , Mariposas/crescimento & desenvolvimento , Filogenia
2.
Mol Phylogenet Evol ; 16(1): 96-112, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10877943

RESUMO

A phylogenetic study of Asteridae sensu lato was conducted based on chloroplast ndhF gene sequences for 116 ingroup and 13 outgroup species. Prior molecular studies based on rbcL sequences identified terminal groups corresponding to families, but were unable to resolve relationships among them. These results are largely consistent with earlier rbcL studies, but provide much greater resolution and stronger bootstrap support throughout the tree. The parsimony analysis found eight equally parsimonious trees, all of which recognize four major clades with the following relationship: (Cornales (Ericales (Euasterids I, Euasterids II))). Euasterids I includes (Garryales ((Solanales, Boraginaceae) (Gentianales, Lamiales))), although with weak support for relationships among the named clades. Euasterids II includes (Aquifoliales (Asterales (Apiales, Dipsacales))) with strong support for these relationships. Relationships within Ericales are weakly supported and merit further attention.


Assuntos
DNA de Cloroplastos/genética , Genes de Plantas , Magnoliopsida/classificação , Magnoliopsida/genética , NADH Desidrogenase/genética , Filogenia , Ribulose-Bifosfato Carboxilase , Magnoliopsida/enzimologia , Dados de Sequência Molecular , Proteínas de Plantas/genética
3.
Am J Bot ; 86(9): 1346-56, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10487821

RESUMO

Analysis of ITS sequences provides support for a clade that includes Carmichaelia, Clianthus, Montigena, and Swainsona. We provide a node-based definition and recommend that this clade be called Carmichaelinae. Results suggest that Carmichaelinae are derived from northern hemisphere Astragalinae. The clade has extensively radiated in Australia, and two independent lineages have diversified in New Zealand. The New Zealand lineages differ in species richness. One lineage consists of 24 species placed in Carmichaelia and Clianthus, while the other corresponds to the monotypic genus Montigena. The pattern of relationships inferred from ITS sequences suggests that the New Zealand radiation was recent and possibly accompanied episodes of mountain-building and glaciation.

4.
Regul Pept ; 71(2): 67-71, 1997 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-9416988

RESUMO

The effects of pituitary adenylate cyclase activating peptide (PACAP) 38, PACAP 27 and vasoactive intestinal peptide (VIP) on plasma extravasation were investigated in vivo in rat skin. PACAP 38, PACAP 27 and VIP, caused concentration-dependent extravasation in rat skin. The order of potency was PACAP 38 > PACAP 27 = VIP, whereas the order of maximal induced extravasation was PACAP 38 = PACAP 27 > VIP, suggesting that PACAP 38 might be the most powerful inducer of plasma extravasation of the three tested members of the secretin-glucagon-VIP family. Substance P (SP) was about 5 times more potent than PACAP 38 and 15 times more potent than PACAP 27. These data indicate that PACAP 38 induced plasma extravasation in concentrations roughly equimolar to SP. Pyrilamine (H1 receptor antagonist) reduced the PACAP 38-induced plasma extravasation more than 50%; cimetidine (H2 receptor antagonist) was without effect. To investigate whether a cAMP-mediated process is involved in the induction of plasma extravasation, the synthetic adenosine 3',5'-cyclic monophosphate (cAMP), dibutyryl adenosine cyclic monophosphate (DBcAMP) and the cAMP-inducing drug, salbutamol, were each injected in the skin; neither of these drugs caused extravasation. We conclude that PACAP 38 and PACAP 27 cause potent plasma extravasation which, at least in part, involves histamine release.


Assuntos
Permeabilidade Capilar/efeitos dos fármacos , Neuropeptídeos/farmacologia , Pele/irrigação sanguínea , Peptídeo Intestinal Vasoativo/farmacologia , Vasodilatadores/farmacologia , Albuterol/farmacologia , Animais , Bucladesina/farmacologia , Cimetidina/farmacologia , Relação Dose-Resposta a Droga , Antagonistas dos Receptores Histamínicos/farmacologia , Polipeptídeo Hipofisário Ativador de Adenilato Ciclase , Pirilamina/farmacologia , Ratos , Ratos Endogâmicos F344 , Organismos Livres de Patógenos Específicos , Substância P/farmacologia
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