Didymosphaeria oblitescens. [Descriptions of Fungi and Bacteria].

Author(s):  
V. P. Hayova

Abstract A description is provided for Didymosphaeria oblitescens. Some information on its dispersal and transmission and conservation status is given, along with details of its geographical distribution (Kenya, Canada (British Columbia, Ontario), USA (Alabama, Arizona, Connecticut, Georgia, Hawaii, Minnesota, New Jersey, Utah), Argentina, Venezuela, Brunei Darussalam, China, Republic of Georgia, India (Bihar, Rajasthan, West Bengal), Maldives, Pakistan, Taiwan, Austria, Belgium, Bosnia-Hercegovina, Czech Republic, Denmark, France, Germany, Hungary, Iceland, Irish Republic, Italy, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Spain, Sweden, Switzerland, Ukraine and UK) and hosts (Microdiplodia rosarum, Alnus sp., Arbutus menziesii, Arbutus unedo, Arundo donax, Poaceae, Barleria prionotis, Berberis sp., Bryophyllum sp., Cadaba farinosa, Camellia japonica, Carya sp., Casuarina equisetifolia, Cercidium microphyllum, Cornus sanguinea, Cornus sericea subsp. sericea, Cornus sp., Coronilla emerus, Dodonaea viscosa, Dryas octopetala, Fraxinus excelsior, Gaultheria shallon, Gossypium sp., Cortaderia selloana, Humulus lupulus, Hydrangea sp., Indigofera sp., Jasminum frutescens, Lantana camara, Leycesteria sp., Livistona sp., Lonicera caprifolium, Lupinus sp., Malus sp., Margyricarpus setosus, Mesembryanthemum sp., Pinus sylvestris, Prunus persica, Quercus garryana, Rhododendron ponticum, Rosa canina, Rosa villosa, Rosa sempervirens, Rosa sp., Rubus caucasicus, Rubus caesius, Rubus fruticosus, Rubus idaeus, Rubus inermis, Rubus sp., Saccharum munja, Saccharum officinarum, Salix caprea, Salix glauca, Smilax sp., Solidago canadensis, Strelitzia reginae, Platycladus orientalis, Tilia sp., Trachycarpus fortunei and Viburnum opulus).

Author(s):  
V. P. Hayova

Abstract A description is given for Gloniopsis praelonga. Some information on its dispersal and transmission and conservation status is given, along with details of its geographical distribution (Kenya, Morocco, South Africa, Zambia, Canada (British Columbia), Mexico, USA (Alabama, California, Florida, Illinois, Louisiana, Maryland, Massachusetts, Michigan, Nebraska, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, Texas, Virginia), Argentina, Chile, Ecuador, China (Hubei), India (Karnataka, Tamil Nadu), Pakistan, Taiwan, Azores, Australia (Australian Capital Territory, Queensland), New Zealand, Papua New Guinea, Austria, Belgium, Denmark, France, Gibraltar, Germany, Greece, Irish Republic, Italy, Lithuania, Netherlands, Norway, Portugal, Russia (Leningradskaya oblast), Spain and UK), hosts (Acacia filiculoides, Acacia mearnsii, Acacia sp., Acer campestre, Acer pseudoplatanus, Acer sp., Alnus sp., Andromeda sp., Arbutus menziesii, Arbutus unedo, Arctostaphylos tracyi, Arctostaphylos sp., Aronia sp., Arundo donax, Atalantia sp., Azalia sp., Bambusa sp., Poaceae, Berchemia scandens, Berchemia sp., Betula pendula, Betula sp., Buddleja sp., Buxus sempervirens, Calicotome spinosa, Calluna vulgaris, Carya tomentosa, Carya sp., Castanea sativa, Castanea sp., Catalpa bignonioides, Catalpa sp., Ceanothus sp., Chamaerops sp., Cistus salviifolius, Cistus sp., Cladium jamaicense, Coccoloba ewifera, Combretum zeyheri, Combretum sp., Cornus sp., Corylus avellana, Corylus colurna, Corylus sp., Crataegus laevigata, Crataegus monogyna, Crataegus sp., Duvaua longifolia, Erica arborea, Ericaceae indet., Eucalyptus coccifera, E. globulus, Eucalyptus sp., Fagus sylvatica, Fagus sp., Francoa sonchifolia, Rhamnus frangula, Fraxinus excelsior, Fraxinus ornus, Fraxinus sp., Poaceae indet., Hedera helix, Hedera sp., Hippophae rhamnoides, Ilex aquifolium, Ilex sp., Jasminum sp., Juglans cinerea, Juniperus sp., Lavandula stoechas, Leucothoe axillaris, Ligustrum japonicum, Ligustrum vulgare, Ligustrum sp., Lithocarpus sp., Lonicera periclymenum, Lonicera sp., Malus sylvestris, Malus sp., Melia azedarach, Metrosideros robusta, Myrica gale, Myrtus communis, Ostrya sp., Prunus persica var. persica, Phormium tenax, Phragmites australis, Pinus halepensis, Pinus pinaster, Pinus sylvestris, Pinus sp., Pittosporum sp., Plantae indet., Populus alba, Populus sp., Prunus spinosa, Prunus sp., Malus domestica, Malus fusca, Quercus agrifolia, Q. alba, Q. ilex, Q. petraea, Q. robur, Quercus sp., Rhamnus sp., Rhododendron ponticum, Rhododendron sp., Robinia pseudoacacia, Robinia sp., Rosa arvensis, Rosa canina, Rosa sp., Rosaceae indet., Rubus fruticosus, Rubus idaeus, Rubus inermis, Rubus sp., Sabal palmetto, Salix caprea, Salix fragilis, Salix sp., Sambucus nigra, Sambucus sp., Sequoia sp., Serenoa repens, Smilax aspera, Sorbus sp., Spiraea canescens, Spiraea sp., Symphoricarpos albus, Trachycarpus fortunei, Ulex europaeus, Ulex sp., Ulmus procera, Ulmus sp., Vaccinium glabrum, Vaccinium vitis-idaea, Vaccinium sp., Verbascum sp., Viburnum lantana, Viburnum opulus, Viburnum sp., Vitis vinifera subsp. sylvestris, Vitis sp., Xanthorrhoea sp. and Xolisma ferruginea) and associated fungi (Actinocladium rhodosporum, Ascochyta deformis, Circinotrichum olivaceum, Clypeosphaeria mamillana, Dasyscypha cerina, Farlowiella carmichaeliana, Glonium lineare, Herpotrichiella sp., Hysterium angustatum, Keissleriella caudata, Lophiostoma ulicis, Metasphaeria longispora, Orbilia alnea, Phaeostalagmus cyclosporus, Lophiostoma compressum, Pleospora sp., Pseudospiropes obclavatus, Strossmayeria atriseda, Strossmayeria bakeriana, Sporothrix ghanensis, Taeniolina scripta, Valsa ceratophora and Zygosporium gibbum).


Author(s):  

Abstract A new distribution map is provided for Chilo sacchariphagus (Böjer). Lepidoptera: Crambidae. Hosts: rice (Oryza sativa), sugarcane (Saccharum officinarum), sorghum (Sorghum bicolor) and maize (Zea mays). Information is given on the geographical distribution in Asia (Bangladesh, Brunei Darussalam, Cambodia, China (Guangdong, Hebei, Hong Kong, Hunan, Jiangsu), India (Andhra Pradesh, Delhi, Gujarat, Karnataka, Tamil Nadu, Uttar Pradesh, West Bengal), Indonesia (Java, Sumatra), Iran, Japan, Laos, Malaysia, Pakistan, Philippines, Singapore, Sri Lanka, Taiwan, Thailand, Vietnam), Africa (Comoros, Madagascar, Mauritius, Mozambique, Reunion, Tanzania).


Author(s):  
D. W. Minter

Abstract A description is provided for Hilberina breviseta, which is apparently saprobic and able to colonize a diverse range of plants, with records from old dead and decaying wood. Some information on its associated organisms and substrata, habitats, dispersal and transmission, and conservation status is given, along with details of its geographical distribution (Central America (Costa Rica), North America (USA (New York and North Carolina)), Asia (Brunei Darussalam, China (Yunnan), Taiwan and Thailand), Europe (Austria, Finland, France, Germany, Lithuania, Spain, Sweden and UK)) and hosts (including Padus sp.).


Author(s):  
T. I. Krivomaz

Abstract A description is provided for Lepidoderma carestianum, a nivicolous myxomycete. Some information on its dispersal and transmission and conservation status is given, along with details of its geographical distribution (Canada (Ontario), USA (Arizona, California, Colorado, Iowa, Kansas, Massachusetts, Michigan, New Hampshire, New Mexico, Washington), Japan, Russia (Chukotskyi Avtonomnyi okrug), Australia (New South Wales), New Zealand, Austria, Denmark, France, Italy, Norway, Poland, Russia (Leningradskaya oblast), Slovenia, Spain, Sweden, Switzerland, UK, and Ukraine), hosts (Deschampsia cespitosa, Empetrum nigrum subsp. hermaphroditum, Graminae indet., Juncus trifidus, Nardus stricta, Plantae indet., Rubus idaeus, Sasa kurilensis, Taxus sp.,Vaccinium myrtillus), other substrata (soil), interactions and habitats.


Author(s):  

Abstract A new distribution map is provided for Scutellonema brachyurus (Steiner) Andrássy. Nematoda: Hoplolaimidae. Hosts: Cotton (Gossypium hirsutum), grapevine (Vitis vinifera), maize (Zea mays), mandarin (Citrus reticulata), pummelo (Citrus maxima), rice (Oryza sativa), soyabean (Glycine max) and sugarcane (Saccharum officinarum). Information is given on the geographical distribution in Europe (Germany, Italy, Netherlands, Poland, Sweden, UK), Asia (Brunei Darussalam, China, Sichuan, India, Gujarat, Karnataka, Madhya Pradesh, Sikkim, West Bengal, Japan, Honshu, Kyushu, Korea Republic, Malaysia, Nepal, Pakistan, Singapore, Sri Lanka, Thailand), Africa (Congo Democratic Republic, Egypt, Kenya, Madagascar, Malawi, Mauritius, Mozambique, Nigeria, Reunion, South Africa, Swaziland, Tanzania, Uganda, Zambia, Zimbabwe), North America (Canada, USA, Arkansas, California, Florida, North Carolina, South Carolina), Central America and Caribbean (Barbados, Costa Rica, Cuba, Jamaica), South America (Brazil, Bahia, Minas Gerais, Sao Paulo, Colombia, Falkland Islands, Peru, Venezuela), Oceania (Australia, New South Wales, Northern Territory, Queensland, South Australia, Fiji, New Zealand, Samoa, Tonga).


Author(s):  
D. W. Minter

Abstract A description is provided for Ganoderma applanatum. Sporophores of this fungus are found on both living and dead trees, where the fungus causes a decay of heartwood resulting in a white soft spongy heart and butt rot. Some information on its associated organisms and substrata, dispersal and transmission, habitats and conservation status is given, along with details of its geographical distribution (Africa (Angola, Benin, Congo, Democratic Republic of the Congo, Equatorial Guinea, Ivory Coast, Kenya, Madagascar, Morocco, Mozambique, São Tomé and Principe, Sierra Leone, South Africa, Sudan, Tanzania, Togo), Asia (Azerbaijan, Brunei Darussalam, China (Anhui, Fujian, Gansu, Guangdong, Guangxi, Guizhou, Hainan, Hebei, Heilongjiang, Henan, Hong Kong, Hunan, Jiangsu, Jiangxi, Jilin, Nei Mongol Autonomous Region, Qinghai, Shaanxi, Shanxi, Sichuan, Xinjiang, Yunnan, Zhejiang), Christmas Island, Cyprus, Georgia, India (Assam, Chhattisgarh, Gujarat, Himachal Pradesh, Jammu & Kashmir, Karnataka, Kerala, Madhya Pradesh, Maharashtra, Meghalaya, Orissa, Punjab, Rajasthan, Uttarakhand, Uttar Pradesh, West Bengal), Indonesia, Iran, Israel, Japan, Kazakhstan (Almaty, East Kazakhstan, Kostanay, South Kazakhstan), Laos, Malaysia, Nepal, North Korea, Oman, Pakistan, Papua New Guinea, Philippines, Russia (Altai Krai, Altai Republic, Irkutsk Oblast, Kamchatka Krai, Kemerovo Oblast, Khanty-Mansi Autonomous Okrug, Krasnoyarsk Krai, Novosibirsk Oblast, Omsk Oblast, Primorsky Krai, Sakha Republic, Sverdlovsk Oblast, Tomsk Oblast, Tyumen Oblast, YamaloNenets Autonomous Okrug), Singapore, South Korea, Sri Lanka, Taiwan, Tajikistan, Thailand, Turkey, Uzbekistan, Vietnam), Australasia (Australia (Australian Capital Territory, New South Wales, Northern Territory, Queensland, South Australia, Tasmania, Victoria, Western Australia), New Zealand), Caribbean (American Virgin Islands, British Virgin Islands, Cuba, Dominican Republic, Guadeloupe, Haiti, Jamaica, Puerto Rico, Trinidad and Tobago), Central America (Belize, Costa Rica, El Salvador, Guatemala, Honduras, Nicaragua, Panama. Europe: Austria, Belarus, Belgium, Bulgaria, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Ireland, Isle of Man, Italy, Latvia, Lithuania, Luxembourg, Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Russia (Arkhangelsk Oblast, Belgorod Oblast, Bryansk Oblast, Chuvash Republic, Ivanovo Oblast, Kaliningrad Oblast, Kaluga Oblast, Kirov Oblast, Kostroma Oblast, Krasnodar Krai, Kursk Oblast, Leningrad Oblast, Mari El Republic, Moscow Oblast, Nizhny Novgorod Oblast, Orenburg Oblast, Oryol Oblast, Penza Oblast, Perm Krai, Pskov Oblast, Republic of Bashkortostan, Republic of Tatarstan, Samara Oblast, Smolensk Oblast, Tula Oblast, Tver Oblast, Udmurt Republic, Vladimir Oblast, Vologda Oblast, Voronezh Oblast, Yaroslavl Oblast), Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Ukraine, UK), Indian Ocean (Seychelles. North America: Canada (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundland and Labrador, Northwest Territories, Nova Scotia, Ontario, Prince Edward Island, Quebec, Saskatchewan), Mexico, USA (Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming)), Pacific Ocean (American Samoa, Cook Islands, Federated States of Micronesia, Fiji, French Polynesia, Guam, Marshall Islands, Samoa, Tuvalu, USA (Hawaii)), South America (Argentina, Bolivia, Brazil (Acre, Alagoas, Amapá, Amazonas, Bahia, Espírito Santo, Minas Gerais, Pará, Paraíba, Paraná, Pernambuco, Rio de Janeiro, Rio Grande do Sul, Rondônia, Roraima, Santa Catarina, São Paulo), Chile, Colombia, Ecuador, French Guiana, Peru, Suriname, Uruguay, Venezuela)).


2013 ◽  
Vol 664 ◽  
pp. 23-26
Author(s):  
Min Hui ◽  
Yu Ding ◽  
Xin Ying Wang ◽  
Yang Zhuang ◽  
Ji Fei Xu

Selecting rhizosphere soil as the object of study which from 5 different kinds of plants in the Inner Mongolia University campus, we use fumigation extraction method and liquid chlorine fumigation extraction-water bath method to determine the microbial biomass carbon in the rhizosphere soil of different plants, in order to compare that whether or not liquid chlorine fumigation extraction-water bath method applicable to this type of soil sample. The results show that, there are significant differences in the rhizosphere soil microbial biomass carbon of 5 different kinds of plants, determination results is that Pyrus sorotina (LS) > Platycladus orientalis (CB) > Prunus persica (TS)> Syringa vulgaris (DX) > Pinus tabuliformis (YS), the content of P. sorotina is highest, 260.53 mg/kg, and P. tabulaeformis is lowest, 121.11 mg/kg, the differ is 139.42 mg/kg. There is a big gap between the measure values of the two methods, so that liquid chlorine fumigation extraction-water bath method doesn’t apply to the determination of this type microbial biomass carbon.


2016 ◽  
Vol 15 ◽  
Author(s):  
Huwaida Hj Masmin ◽  
Kahtleen Collier ◽  
Pallavi Sirajuddin ◽  
Ulmar Grafe

The forests of Brunei Darussalam harbour rich bat assemblages. In this study we update current knowledge of the abundance and distribution of bats in Brunei by comparing bat diversity between two lowland forest sites: Temburong and Tasek Merimbun. We recorded 27 bat species with three new locality records for each of the two sites surveyed. Temburong had higher bat diversity than Merimbun, suggesting that it has more diverse habitat types. This study highlights the need for further bat surveys as full inventories of bat communities have not yet been reached and little is known about the ecology and conservation status of bat populations.


REINWARDTIA ◽  
2014 ◽  
Vol 14 (1) ◽  
pp. 137
Author(s):  
Suzana Sabran ◽  
Reuben Nilus ◽  
Joan T. Pereira ◽  
Joan Baptist Sugau ◽  
Frederick Kugan

The Heart of Borneo (HoB) declaration is a conservation agreement initiated by WWF and signed by three countries, i.e., Brunei Darussalam, Indonesia and Malaysia in Bali, Indonesia on 12th February 2007 to protect more than 23 million hectares of forested region on Borneo Island. These forested areas could be well protected when conservation management plan is in place. One of the crucial activities to facilitate the planning and formulation of conservation plan is to conduct scientific expeditions that include botanical exploration. The primary objective of the expedition is to identify the key conservation targets within the forest reserves. For the past five years, several expeditions have been conducted by the Sabah Forestry Department under the auspices of the HoB project to explore various forest reserves with conservation issues within the Heart of Borneo area. This paper will present the findings which include plant richness, endemism and plant conservation status in each forest reserves that has been explored.


2021 ◽  
Vol 50 (8) ◽  
pp. 2283-2292
Author(s):  
Mokhtar Mohamedalamin Mokhtar ◽  
Jianfeng Li ◽  
Zhiping Du ◽  
Fangqin Cheng

Application of botanical pesticides is a new trend in pest control nowadays as an environmentally safe alternative measures for synthetic chemicals. Hence, this study was aimed to analyze the phytochemical constituents of four medicinal Chinese plants, namely Lonicera maackii, Platycladus orientalis, Viburnum opulus, and Crataegus pinnatifida, and to investigate the insecticidal potentialities of leaves extracts of these plants against Tribolium castaneum. The research was carried out under laboratory conditions, at the Institute of Resources and Environmental Engineering, Shanxi University, China. Ethyl acetate, methanol and water extracts of the plant leaves were tested at different concentrations (5, 2.5, and 1.25% w/v). Yields of extracting materials, mortality and repellent effects were the important parameters evaluated. The phytochemical screening showed the presence of alkaloids, saponins, tannins, flavonoid, and terpenoids in C. pinnatifida, but the other plants contain some of these compounds. The highest ethyl acetate extract concentration (5%) of V. opulus and C. pinnatifida obtained the best mortality means (5.00±0.41 and 4.75±0.25a, respectively), compared to the other treatments, but without significant differences from the middle concentration (2.5%) of both extracts. In repellency test, L. maackii methanol achieved the highest repellency percentage (91.38%). The findings proved that ethyl acetate extract of V. opulus and C. pinnatifida are the best insecticidal treatment, whereas methanol extract of L. maackii is the best repellent effect, against T. castaneum. These three plants require additional studies to be assessed as a component in pest management of store pests.


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