Academic literature on the topic 'Rutaceae Victoria'

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Journal articles on the topic "Rutaceae Victoria"

1

Giles, Robyn L., Andrew N. Drinnan, and Neville G. Walsh. "Variation in Phebalium glandulosum subsp. glandulosum: morphometric and anatomical evidence (Rutaceae)." Australian Systematic Botany 21, no. 4 (2008): 271. http://dx.doi.org/10.1071/sb07023.

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Specimens of Phebalium glandulosum Hook. subsp. glandulosum representing the entire geographic range of the subspecies were examined for morphological and anatomical variation. Phenetic patterns were identified with the pattern analysis package PATN, and three distinct groups were identified. One group consists of plants from inland areas of New South Wales, north-western Victoria, and the Yorke and Eyre Peninsulas of South Australia; a second group consists of plants collected from alongside the Snowy River in eastern Victoria and south-eastern New South Wales; and a third group consists of plants from Queensland and northern New South Wales. The climate analysis program BIOCLIM was used to compare climate variables across the geographic range, and showed clear climatic separation in support of the phenetic analysis. The three groups are formally recognised here as distinct subspecies. Plants from Queensland and the Bourke region of northern New South Wales belong to the typical subspecies; plants from north-western Victoria, central New South Wales, and the Yorke and Eyre Peninsulas of South Australia form a cohesive assemblage and are recognised as a new subspecies P. glandulosum subsp. macrocalyx; and plants from the Snowy River in far eastern Victoria and the Southern Tablelands of New South Wales form a distinct and isolated group recognised as a new subspecies P. glandulosum subsp. riparium. These new subspecies are formally described, and an identification key and summaries distinguishing all six subspecies of P. glandulosum are presented.
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2

Wright, Wendy, Xuan Zhu, and Mateusz Okurowski. "Identification of key environmental variables associated with the presence of Toothed Leionema (Leionema bilobum serrulatum) in the Strzelecki Ranges, Victoria, Australia." Australian Journal of Botany 59, no. 3 (2011): 207. http://dx.doi.org/10.1071/bt10197.

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Toothed Leionema is one of four subspecies of Leionema bilobum from the Rutaceae family. A dense shrub or small tree, growing to ~4 m high, it is a poorly investigated species which is considered rare in Victoria, Australia. This paper presents the results of a study using Geographical Information Systems and Weights-of-Evidence predictive modelling to assess the importance of seven environmental factors in determining habitat suitability for this species in the Strzelecki Ranges, Victoria. This method is particularly useful in understanding the distribution of rare species, especially where the ecology of the species of interest is not well understood. Of the seven environmental factors considered here, four were found to be important: elevation, aspect, distance to water and distance to plantation (disturbed) areas. The modelling results indicate that areas with elevations between 350 and 550 m and a dominant south-western aspect that are close to plantation areas (within 700 m), and to water (within 1100–1200 m), provide potentially suitable habitat for Toothed Leionema in the region.
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3

BHASKAR, HASEENA, S. MELVIN MOHAN, and M. SREESHA. "Establishment and spread of the invasive mite, Tetranychus gloveri Banks (Prostigmata: Tetranychidae) in Kerala, India." Zoosymposia 22 (November 30, 2022): 164. http://dx.doi.org/10.11646/zoosymposia.22.1.107.

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Tetranychus gloveri Banks was first recorded as Tetranychus okinawanus Ehara in India on an ornamental plant, Adenium obesum from Thrissur district, Kerala state, during 2016 (Zeity et al. 2016). Recently, Sharkey et al. (2022) synonymized T. okinawanus with T. gloveri based on morphological and molecular data. In Kerala, T. gloveri has emerged as a predominant species of mite infesting major agricultural and horticultural crops in the district (Arunima et al. 2018). In order to investigate the distribution and host range of the mite species in Kerala, periodical surveys were conducted in different agricultural ecosystems across the state during March 2020 to June 2022. Spider mite infested samples were collected from fruit crops, vegetables, ornamental plants, medicinal plants and other non-crop plants from different localities, kept in polythene bags. The GPS data of the locality and host plants were recorded. In the laboratory, a single gravid female from each sample was used to establish isoline culture providing unique accession number. Male and female specimens from each isoline culture were slide mounted on Hoyer’s medium and morphological characterization of the slide mounted mite specimens were carried to establish the species identity. Characters such as chaetotaxy of hysterosoma and legs, structure of empodium and pattern of dorsal striae between e1 and f1 of female were used for genus level identification, while the shape of male genitalia, aedeagus, was used for species level identification. In this study, T. gloveri was recorded from a wide host range of 35 host plants in 24 plant families viz., Malvaceae, Cucurbitaceae, Fabaceae, Amaranthaceae, Rutaceae, Solanaceae, Musaceae, Moraceae, Anacardiaceae, Caricaceae, Adoxaceae, Rosaceae, Compositae, Gentianaceae, Convolvulaceae, Balsaminaceae, Orchidaceae, Asparagaceae, Goodeniaceae, Apocyanaceae, Euphorbiaceae, Oxalidaceae, Lamiaceae and Pontederiaceae. The mite species was distributed in seven districts covering northern, central and southern regions viz., Wayanad, Malappuram, Thrissur, Palakkad, Ernakulam, Alappuzha and Thiruvananthapuram districts of Kerala. Curry leaf, country kreat (Exacum bicolor), sunflower, Victoria corn plant (Dracaena sp.), Calotropis gigantea, little tree plant (Biophytum sensitivum), holy basil (Ocimum sanctum) and the aquatic pickerel weed (Monochoria vaginalis) are new host records for T. gloveri. The study confirms that the mite species has established and spread across Kerala by widening its host range and expanding its geographical area of distribution, within a short span after its introduction into the state.
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4

Martin, J. H. "A new Toxoptera species from Rutaceae in Hong Kong (Homoptera: Aphididae)." Bulletin of Entomological Research 81, no. 3 (September 1991): 277–81. http://dx.doi.org/10.1017/s000748530003354x.

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AbstractToxoptera victoriae sp. n. is described from Hong Kong. The economic importance of the genus Toxoptera is discussed. Separate keys are provided to adult and first instar larvae of the species of Toxoptera.
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5

"Phyllocnistis citrella. [Distribution map]." Distribution Maps of Plant Pests, no. 4) (August 1, 2003). http://dx.doi.org/10.1079/dmpp/20066600274.

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Abstract A new distribution map is provided for Phyllocnistis citrella Stainton Lepidoptera: Gracillariidae Hosts: Citrus spp. and other Rutaceae. Information is given on the geographical distribution in EUROPE, Croatia, Cyprus, Franca, Greece, Italy, Malta, Portugal, Madeira, Mainland Portugal, Spain, Yugoslavia (Fed. Rep.), ASIA, Afghanistan, Bangladesh, Brunei Darussalam, Cambodia, China, Fujian, Guangdong, Guangxl, Hong Kong, Hunan, Jlangsu, Macau, Sichuan, Zhejiang, Republic of Georgia, India, Andaman and Nicobar Islands, Andhra Pradesh, Arunachal Pradesh, Assam, Bihar, Gujarat, Himachal Pradesh, Karnataka, Madhya Pradesh, Maharashtra, Meghalaya, Punjab, Rajasthan, Tamil Nadu, Uttar Pradesh, West Bengal, Indonesia, Irian Jaya, Java, Kalimantan, Sulawesi, Sumatra, Iran, Iraq, Israel, Japan, Honshu, Kyushu, Ryukyu Archipelago, Shikoku, Jordan, Korea Republic, Laos, Lebanon, Malaysia, Peninsular Malaysia, Sabah, Sarawak, Myanmar, Nepal, Pakistan, Philippines, Saudi Arabia, Singapore, Sri Lanka, Syria, Taiwan, Thailand, Turkey, Turkmenistan, Vietnam, Yemen, AFRICA, Algeria, Cote d'Ivoire, Egypt, Eritrea, Ethiopia, Libya, Mauritius, Morocco, Nigeria, Reunion, South Africa, Sudan, Tanzania, Tunisia, NORTH AMERICA, Mexico, USA, Alabama, Florida, Louisiana, Texas, CENTRAL AMERICA & CARIBBEAN, Antigua and Barbuda, Bahamas, Barbados, Belize, Bermuda, British Virgin Islands, Cayman Islands, Costa Rica, Cuba, Dominica, Dominican Republic, Granada, Honduras, Jamaica, Martinique, Netherlands, Antilles, Nicaragua, Panama, Panama, St kitts-Nevis, St Lucia, Trinidad and Tobago, SOUTH AMERICA, Argentina, Brazil, Espirito Santo, Minas Gerais, Parana, Piaui, Rio de Janeiro, Rio Grande do Sul, Santa Catarina, Sao Paulo, Chile, Colombia, French Guiana, Guyana, Peru, Venezuela, OCEANIA, Australia, New South Wales, Northern Territory, Queensland, South Australia, Victoria, Fed States of Micronesia, Guam, Northern Mariana Islands, Palau, Papua New Guinea, Samoa, Solomon Islands.
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