scholarly journals New record of Duttaphrynus stomaticus (Lutken, 1864) (Anura: Bufonidae) from Aligarh, Uttar Pradesh, with systematic account, conservation status and differences from D. melanostictus (Schneider, 1799)

2020 ◽  
Vol 7 (2) ◽  
Author(s):  
Akhlaq Husain ◽  
Ashwani Kumar Dubey ◽  
Hishmi Jamil Husain
Keyword(s):  
New Record ◽  
Conservation Status ◽  
Uttar Pradesh ◽  
Systematic Account

scholarly journals New record of Common Owlet Moth Spirama helicina (Hubner, 1831) (Lepidoptera: Erebidae: Catocalinae) from Aligarh (Uttar Pradesh) with systematic account, distribution, host plants and biological control

2020 ◽  
Vol 1 (1) ◽  
pp. 37-41
Author(s):  
Akhlaq Husain ◽  
◽  
Wajid Hasan ◽  
Keyword(s):  
Biological Control ◽  
Life Cycle ◽  
New Record ◽  
Host Plants ◽  
Uttar Pradesh ◽  
Present Communication ◽  
Systematic Account ◽  
The Common

The present communication deals with the new record of Spirama helicina (Hubner, 1831), the Common Owlet Moth from Aligarh (Uttar Pradesh) and its systematic account, distribution, life cycle, host plants and biological control.

Fomes fomentarius. [Descriptions of Fungi and Bacteria].

2021 ◽  
Author(s):  
D. W. Minter
Keyword(s):  
New York ◽  
Rhode Island ◽  
Tamil Nadu ◽  
Conservation Status ◽  
Uttar Pradesh ◽  
Voronezh Oblast ◽  
Moscow Oblast ◽  
Novosibirsk Oblast ◽  
Novgorod Oblast ◽  
Fomes Fomentarius

Abstract A description is provided for Fomes fomentarius. Sporophores of this fungus are found on both living and dead trees, where the fungus causes a decay of heartwood. 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 (São Tomé and Principe, Somalia, Tunisia), Asia (Azerbaijan, China (Hong Kong), Cyprus, Georgia, India (Himachal Pradesh, Jammu & Kashmir, Karnataka, Meghalaya, Sikkim, Tamil Nadu, Uttarakhand, Uttar Pradesh, West Bengal), Iran, Japan, Kazakhstan (Akmola, Aktobe, Almaty, East Kazakhstan, Kostanay, North Kazakhstan, Pavlodar, South Kazakhstan, West Kazakhstan), Kyrgyzstan, Mongolia, Nepal, North Korea, Pakistan, Russia (Altai Krai, Altai Republic, Buryatia, Chelyabinsk Oblast, Irkutsk Oblast, Khabarovsk Krai, Novosibirsk Oblast, Primorsky Krai, Sakha Republic, Sakhalin Oblast, Tyumen Oblast, Zabaykalsky Krai), South Korea, Tajikistan, Turkey, Uzbekistan), Central America (Panama), Atlantic Ocean (Portugal (Madeira)), Europe (Andorra, Austria, Belarus, Belgium, Bosnia and Herzegovina, Bulgaria, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Ireland, Italy, Kosovo, Latvia, Luxembourg, Moldova, Netherlands, Norway, Poland, Portugal, Romania, Russia (Komi Republic, Krasnodar Krai, Moscow Oblast, Nizhny Novgorod Oblast, Orenburg Oblast, Republic of Karelia, Saratov Oblast, Voronezh Oblast), Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Ukraine, UK), North America (Canada (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundland and Labrador, Ontario, Quebec, Saskatchewan), USA (Alabama, Alaska, California, Connecticut, District of Columbia, Florida, Idaho, Iowa, Kentucky, Maine, Massachusetts, Michigan, Minnesota, Montana, Nebraska, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Vermont, Virginia, Washington, West Virginia, Wisconsin)), South America (Brazil (Minas Gerais, Santa Catarina), Chile)).

Diplodia rosarum. [Descriptions of Fungi and Bacteria].

2011 ◽  
Author(s):  
V. P. Hayova
Keyword(s):  
New York ◽  
South Carolina ◽  
Czech Republic ◽  
Geographical Distribution ◽  
West Bengal ◽  
Conservation Status ◽  
Uttar Pradesh ◽  
Republic Of Georgia ◽  
Irish Republic ◽  
Botryotinia Fuckeliana

Abstract A description is provided for Diplodia rosarum, which has been implicated in canker or dieback of cultivated roses. Some information on its dispersal and transmission and conservation status is given, along with details of its geographical distribution (USA (California, Massachusetts, New York, Ohio, South Carolina, Texas), Brazil, Azerbaijan, Republic of Georgia, India, (Delhi, Uttar Pradesh, West Bengal), Kyrgyzstan, Pakistan, Cuba, Belgium, Bosnia-Hercegovina, Bulgaria, Czech Republic, Denmark, Estonia, France, Germany, Greece, Irish Republic, Italy, Moldova, Netherlands, Poland, Portugal, Romania, Russia, Slovakia, Sweden, Ukraine and UK), hosts (Rosa arvensis, R. banksiana, R. canina, R. centifolia, R. corymbifera, R. hybrida, R. multiflora, R. spinosissima, R. tomentosa, R. willmottiae and Rosa sp.) and associated fungi (Botryotinia fuckeliana, Hendersonula sp., Macrophoma camarana, Microdiplodia rosarum, Coniothyrium olivaceum, Pleospora herbarum f. microspora and Valsa ambiens).

Clonostachys candelabrum. [Descriptions of Fungi and Bacteria].

2018 ◽  
Author(s):  
D. W. Minter
Keyword(s):  
Tamil Nadu ◽  
Andhra Pradesh ◽  
Conservation Status ◽  
District Of Columbia ◽  
Uttar Pradesh ◽  
Arunachal Pradesh ◽  
Australian Capital Territory ◽  
Leningrad Oblast ◽  
Tver Oblast ◽  
Samara Oblast

Abstract A description is provided for Clonostachys candelabrum, usually found on pine debris (typically dead, wet and blackened needles, twigs and cones attached to trash). Some information on its morphology, habitat, dispersal and transmission and conservation status is given, along with details of its geographical distribution (Cote d'Ivoire, Kenya, South Africa, USA (District of Columbia, Louisiana, Maryland, New Jersey, Washington), Brazil (Pernambuco), Chile, Venezuela, India (Andhra Pradesh, Arunachal Pradesh, Bihar, Karnataka, Kerala, Maharashtra, Rajasthan, Madhya Pradesh, Tamil Nadu, Uttar Pradesh), Japan, Korea Republic, Syria, Thailand, Uzbekistan, Spain (Canary Islands), Australia (Australian Capital Territory), New Zealand, Cuba, Puerto Rico, Belarus, Belgium, Germany, Italy, France, Netherlands, Portugal, Russia (Leningrad Oblast, Samara Oblast, Tver Oblast), Spain, Switzerland, Ukraine and UK) and host (Pinus sylvestris).

scholarly journals New record of Allamanda blanchetti Kunth (Apocynaceae) for the Brazilian Atlantic Forest

2021 ◽  
Vol 5 (3) ◽  
pp. 112
Author(s):  
Diego Santos ◽  
Swami Leitão Costa ◽  
Francisco Carlos Pinheiro Costa
Keyword(s):  
Atlantic Forest ◽  
New Record ◽  
Conservation Status ◽  
First Record ◽  
Brazilian Atlantic Forest ◽  
Information Distribution ◽  
Upland Forest ◽  
Distribution Maps ◽  
New Information ◽  
Status Assessment

This study report the first record of Allamanda blanchetii Kunth in the Atlantic Forest, Brazil. This species was collected from an upland forest in Semi-deciduous Seasonal Forest. This occurrence adds new information about the distribution of this species and expands its range to Brazil, which is important for its conservation. We provide taxonomic information, distribution maps, conservation status assessment, photograps, and an identification key for the Allamanda L. species in the Atlantic Forest.

scholarly journals The Gustavia clade (Lecythidaceae) in Central America: a new record of Gustavia sessilis and a key to its species

2020 ◽  
Author(s):  
Juvenal Enrique Batista Guerra ◽  
Orlando O. Ortiz
Keyword(s):  
Endangered Species ◽  
Central America ◽  
New Record ◽  
Conservation Status ◽  
Central American ◽  
Type Specimens ◽  
Neotropical Tree ◽  
Natural Range ◽  
First Time ◽  
Conservation Of Biodiversity

Background and Aims: Gustavia sessilis is a neotropical tree, belonging to the Lecythidaceae family, until now known from the Colombian Chocó region only. In this paper, we report G. sessilis for the first time for Central America. Methods: Central American specimens of G. sessilis were collected in 2019 from the Darién Province (eastern Panama). Plant identifications were confirmed by comparing collected specimens with those identified earlier and housed in the MO, PMA, SCZ and UCH herbaria. Type specimens were examined by consulting the JSTOR Global Plants database. The estimations of the conservation status were made based on the criteria of the IUCN.Key results: The record of G. sessilis for Central America is presented, based on a collection made from eastern Panama (Darién Province). Photographs, taxonomic comments, and conservation notes are provided. Additionally, a key for the Central American Gustavia species is included.Conclusions: The distribution of G. sessilis now ranges from Bahía Piñas, Darién Province, Panama to the Condoto river, Chocó region, Colombia, highlighting the importance of the Chocó Panama-Colombia region for the conservation of biodiversity, since it could act as a natural corridor for species. Taking into account the small number of records and the restricted natural range of this species, we recommend considering G. sessilis as an endangered species.

Hymenoscyphus albidus. [Descriptions of Fungi and Bacteria].

2013 ◽  
Author(s):  
P. F. Cannon
Keyword(s):  
Czech Republic ◽  
Geographical Distribution ◽  
Conservation Status ◽  
Uttar Pradesh ◽  
Himachal Pradesh ◽  
Jammu And Kashmir

Abstract A description is provided for Hymenoscyphus albidus, an endosymbiont presumed but not yet confirmed to be non-pathogenic; later becoming saprobic and fruiting on dead petioles of Fraxinus species which have fallen. Some information on its dispersal and transmission and conservation status is given, along with details of its geographical distribution (Asia (Georgia, India (Himachal Pradesh, Jammu and Kashmir, Uttar Pradesh, Uttarakhand), Japan, Nepal), Europe (Austria, Belgium, Czech Republic, Denmark, Estonia, France, Germany, Ireland, Luxembourg, Netherlands, Norway, Poland, Slovenia, Spain, Sweden, Switzerland, Ukraine, UK)).

Typification of the name Opuntia soederstromiana (Cactaceae), a new record for the Flora of Colombia

Phytotaxa ◽  
2020 ◽  
Vol 452 (2) ◽  
pp. 116-123 ◽  
Author(s):  
DANIELA PORRAS-FLÓREZ ◽  
SOFÍA ALBESIANO ◽  
LEOPOLDO ARRIETA-VIOLET
Keyword(s):  
New Record ◽  
Conservation Status ◽  
Habitat Conservation ◽  
Distribution Area ◽  
Morphological Description ◽  
Opuntia Species ◽  
Flora Of Colombia ◽  
First Time

Opuntia soederstromiana is recorded in Colombia for the first time. Botanical explorations were carried out in eastern Colombia sub-xerophytic enclaves, as well as examination of specimens deposited at the herbaria AZUAY, COL, GH, NY, QCA, QCNE, UPTC, and US was made. Lectotypes for the names O. dobbieana (here treated as heterotypic synonym of O. soederstromiana) and O. soederstromiana are designated on specimens preserved at US and NY. A detailed and expanded morphological description of O. soederstromiana, as well as data about type, habitat, conservation status, selected iconographies, and distribution area were given. The number of Opuntia species recorded in Colombia has increased to 10. A key for identification of Opuntia species occurring in the departments of Boyacá and Santander (Colombia) was also provided.

scholarly journals Ophiodes intermedius Boulenger, 1894 (Squamata: Anguidae): Uruguay distribution extension with conservation comments

Check List ◽  
2012 ◽  
Vol 8 (5) ◽  
pp. 896 ◽  
Author(s):  
Marcelo Colina ◽  
Diego Arrieta ◽  
Santiago Carreira
Keyword(s):  
New Record ◽  
Conservation Status ◽  
The South ◽  
Frequent Assessment ◽  
Regional Conservation

A new locality for Ophiodes intermedius is reported for Uruguay. The new record at Punta Gorda, Departamento Colonia, is the first departmental record, and extends the known distribution in Uruguay approximately 150 km to the south. This taxon is restricted to the fast developing western littoral of Uruguay, and a frequent assessment of its regional conservation status is recommended.

Notes on the genus Gypsophila (Caryophyllaceae) in Turkey, with a description of G. guvengorkii sp. nov.

Phytotaxa ◽  
2017 ◽  
Vol 295 (3) ◽  
pp. 271
Author(s):  
METİN ARMAĞAN ◽  
FEVZİ ÖZGÖKÇE ◽  
ALİ ÇELİK
Keyword(s):  
New Species ◽  
New Record ◽  
Conservation Status ◽  
Similar Species ◽  
Flora Of Turkey ◽  
Emended Description ◽  
A New Species

Gypsophila guvengorkii (Caryophyllaceae) is described as a new species from Karabük province, Turkey. Morphology, distribution in Turkey, notes on ecology, and the conservation status are provided, as well as a comparison with the similar species G. brachypetala, G. briquetiana, and G. davisii. Additionally, an emended description of G. brachypetala is given. G. patrinii is excluded from the Flora of Turkey since the specimens collected from Doğubayazıt, which were previously identified as G. patrinii, actually refer to G. transcaucasica, which represents a new record for Turkey.

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