New material of Psychrolutes sio (Scorpaeniformes, Psychrolutidae) from the eastern Pacific of South America and comments on the taxonomy of Psychrolutes inermis and Psychrolutes macrocephalus from the eastern Atlantic of Africa

1985 ◽  
Vol 63 (2) ◽  
pp. 444-451 ◽  
Author(s):  
Joseph S. Nelson ◽  
Norma Chirichigno ◽  
Fernando Balbontsín

Psychrolutes sio Nelson, previously known only from the holotype and one small paratype, is redefined from six new specimens. The species is now known to range from northernmost Peru to near Valparaíso, Chile, and to occur at depths of 700–1200 m. Psychrolutes macrocephalus (Gilchrist) is recognized as a separate species from Psychrolutes inermis (Vaillant) and as the more common species in South Africa.

Zootaxa ◽  
2007 ◽  
Vol 1613 (1) ◽  
pp. 23-44 ◽  
Author(s):  
ROBERT J. BLAKEMORE ◽  
CSABA CSUZDI ◽  
MASAMICHI T. ITO ◽  
NOBUHIRO KANEKO ◽  
TATSUYA KAWAGUCHI ◽  
...  

The synonymy of Perichaeta darnleiensis Fletcher, 1886, first described from Australian Darnley Island in the Torres Straits, was confused since Beddard (1900) and Michaelsen (1900) wrongly applied the names Perichaeta cingulata Schmarda, 1861 (= Megascolex cingulatus) and Megascolex indicus Horst, 1883 [= Amynthas corticis (Kinberg, 1828)], respectively. Taxonomic revision of this species now merges several parthenogenetic morphs, including Pheretima decipiens Beddard, 1912 syn. nov. from Luzon, Philippines. Final resolution depends on location of missing types or, alternatively, on neotypification, nevertheless new material from Mt. Kinabalu, north Sabah (Borneo) allows augmentation of the description of Pheretima darnleiensis from that given by Sims & Easton (1972) who, for its lobate/serrate intestinal caeca, remarked that these “cannot be regarded as taxonomic characters as they are more fully formed in the larger specimens”. Body size range is now 45–700 mm, although this suggests either high plasticity or too wide synonymy. Its distribution in the tropical Indo-Australasian Archipelago and islands of Malaysia, Indonesia and Fiji is attributed to human-mediated introductions in recent and pre-historic times that mask its true provenance; reports from Hawaii, Sri Lanka, South Africa and South America are disputed. Sympatric Amynthas omeimontis kinabalu Sims & Easton, 1972 was elevated to species level by Blakemore (2005). Descriptions of Pheretima (Parapheretima) saba Sims & Easton, 1972 and Polypheretima everetti (Beddard & Fedarb, 1895: 69) – somewhat similar to Polypheretima kinabaluensis (Beddard & Fedarb, 1895: 71) – are augmented and specimens are figured on newly collected material. A new Mt Kinabalu earthworm, Metaphire paka Blakemore sp. nov. is proposed that compares with Metaphire cai (Michaelsen, 1916) from Java [originally “Pheretima inflata (Horst) var. cai”], bringing the total known earthworms from Mt Kinabalu to six species. Ecological associations are briefly discussed.


Crustaceana ◽  
2014 ◽  
Vol 87 (3) ◽  
pp. 328-339 ◽  
Author(s):  
Hui Ming Li ◽  
Bo Ping Han ◽  
Fei Fei Guo ◽  
Henri J. Dumont

In 1964 and 1965, Shen & Tai described two species of calanoids, which they classified in the South American genus Argyrodiaptomus. We examined new material from the terra typica, South China, and show that both species belong in the Asian genus Sinodiaptomus. A biogeographic anomaly is thus corrected. Moreover, the two appear to be sister species and males are morphologically well separable. No intermediate morphotypes have so far been detected. S. cavernicolax (Shen & Tai, 1965), known only from the type locality, was claimed to be cavernicolous, but shows no stygobitic adaptations, and has eyes. It may have been pushed back into the cave environment by its congener S. ferus (Shen & Tai, 1964) with which it coexists in the same lake system. So far, four species of Sinodiaptomus have been found in China: the two mentioned above, i.e., S. cavernicolax only in Longyan Cave of Zhaoqing City, and S. ferus at about five locations, but its range is limited to a small part of Guangdong Province. All five other species of Sinodiaptomus, among which the other two that occur (also) in China, also occupy small to very small ranges, with the type species (S. chaffanjoni Richard, 1897) only living in North China, and S. indicus Kiefer, 1936 and S. mahanandiensis Reddy & Radhakrishna, 1980 confined to South India (Reddy & Radhakrishna, 1980). S. valkanovi Kiefer, 1938 from Japan is invasive (Ueda & Ohtsuka, 1998; Makino et al., 2010). S. sarsi Rylov, 1923, distributed in Japan, China, and most of Mongolia, is separated by a wide disjunction from a group of populations in Iran, the Caucasus, and East Anatolia. This western group of populations might be a separate species and deserves more study.


Plant Disease ◽  
2003 ◽  
Vol 87 (11) ◽  
pp. 1329-1332 ◽  
Author(s):  
J. Roux ◽  
H. Myburg ◽  
B. D. Wingfield ◽  
M. J. Wingfield

Cryphonectria cubensis is an economically important pathogen of commercial Eucalyptus spp. Differences have been reported for disease symptoms associated with Cryphonectria canker in South Africa and other parts of the world, and recent DNA-based comparisons have confirmed that the fungus in South Africa is different from that in South America and Australasia. During a disease survey in the Republic of Congo, Cryphonectria canker was identified as an important disease on Eucalyptus grandis and E. urophylla. In this study, we compared Congolese and South African isolates of C. cubensis using DNA sequence data and pathogenicity under greenhouse conditions. The β-tubulin and internal transcribed spacer (ITS) region sequences show that C. cubensis in Congo is different from the fungus in South Africa and that Congolese isolates group most closely with South American isolates. Furthermore, pathogenicity tests showed that a South African isolate was more aggressive than two Congolese isolates. We conclude that two distinct Cryphonectria spp. occur in Africa and hypothesize that the fungus in the Congo probably was introduced into Africa from South America. Both fungi are important pathogens causing disease and death of economically important plantation trees. However, they apparently have different origins and must be treated separately in terms of disease management and quarantine considerations.


Author(s):  

Abstract A new distribution map is provided for Claviceps purpurea (Fr.). Tul. Hosts: Rye (Seale cereale), other cereals and Gramineae. Information is given on the geographical distribution in AFRICA, Algeria, Canary Islands, Ethiopia, Guinea, Kenya, Malawi, Mauritius, Morocco, Rhodesia, South Africa, Sudan, Tanzania, ASIA, China, India (Punjab, Uttar Pradesh, Madras, Mysore), Iran, Israel, Japan, Korea, Nepal, Philippines, Turkey, USSR (Siberia), AUSTRALASIA & OCEANIA, Australia, New Zealand, EUROPE, Austria, Belgium, Britain and Northern Ireland, Bulgaria, Czechoslovakia, Denmark, Faroes, Finland, France, Germany, Greece, Hungary, Iceland, Irish Republic, Italy, Netherlands, Norway, Poland, Portugal, Romania, Spain, Sweden, Switzerland, USSR (general), Yugoslavia, NORTH AMERICA, Canada (general), Mexico, USA, SOUTH AMERICA, Argentina, Brazil (Rio Grande do Sul), Chile, Colombia, Peru, Tristan da Cunha, Uruguay.


Author(s):  

Abstract A new distribution map is provided for Peronospora farinosa Kiessl. Hosts: Beet (Beta vulgaris) and other B. spp., Spinach (Spinacia oleracea), Chenopodium spp. Information is given on the geographical distribution in AFRICA, Ethiopia, Kenya, Libya, Morocco, South Africa, Tanzania, Zimbabwe, ASIA, Afghanistan, Burma, China, Hong Kong, India (Northern States) (Uttar Pradesh) (Madhya Pradesh), Iran, Iraq, Israel, Japan, Korea, Lebanon, Mongolia, Nepal, Pakistan, Taiwan, Thailand, Turkey, USSR, AUSTRALASIA & OCEANIA, Australia, New Zealand, EUROPE, Austria, Belgium, Britain, Bulgaria, Cyprus, Czechoslovakia, Denmark, France, Germany, Greece, Hungary, Iceland, Irish Republic, Italy (Sardina), Malta, Netherlands, Norway, Poland, Portugal, Romania, Spain, Sweden, Switzerland, USSR, Yugoslavia, NORTH AMERICA, Canada, Mexico, USA, CENTRAL AMERICA & WEST INDIES, Guatemala, SOUTH AMERICA, Argentina, Bolivia, Brazil (Sao Paulo), Chile, Ecuador, Peru, Uruguay.


Author(s):  

Abstract A new distribution map is provided for Corynebacterium michiganense pv. michiganense (E.F. Smith) Jensen. Hosts: Tomato (Lycopersicon esculentun). Information is given on the geographical distribution in AFRICA, Kenya, Madagascar, Morocco, South Africa, Tunisia, Uganda, Zambia, Zimbabwe, ASIA, China, India (Nagpur), Israel, Japan, Lebanon, Turkey, AUSTRALASIA & OCEANIA, Australia, Hawaii, New Zealand, EUROPE, Austria, Britain, Channel Islands (Jersey), Bulgaria, Germany, Greece, Hungary, Ireland, Italy (incl. Sicily), Norway, Portugal, Romania, Sardinia, Switzerland, USSR (general, Lithuania, W. Siberia and Crimea), Yugoslavia, NORTH AMERICA, Canada, Nova Scotia, Mexico, USA (general), CENTRAL AMERICA & WEST INDIES, Costa Rica, Cuba, Dominica, Dominican Republic, Panama, SOUTH AMERICA, Argentina (Buenos Aires), (Goldenberg), (Mendoza), (Misiones & Rio Negro), Brazil (Sao Paulo), Chile (Santiago), Colombia, Peru.


Author(s):  

Abstract A new distribution map is provided for Plum bark necrosis stem pitting-associated virus (Closteroviridae: Ampelovirus). Hosts: Prunus spp. Information is given on the geographical distribution in Africa (Egypt, Morocco, South Africa, Tunisia), Asia (China, Hainan, Hubei, Shandong, Japan, Honshu, Jordan, Pakistan, Korea Republic, Turkey), Europe (Bulgaria, France, Italy, Serbia, Spain), North America (USA, California, District of Columbia), Oceania (Australia) and South America (Chile).


Author(s):  
J. N. Kapoor

Abstract A description is provided for Podosphaera leucotricha. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Malus spp., chiefly on M. pumila (apple), peach (Prunus persica), quince (Cydonia ualgaris) and Photinia spp. also attacked (Hirata, 1966). Also reported on almond fruit (43, 2544). DISEASE: Powdery mildew of apple. GEOGRAPHICAL DISTRIBUTION: Africa (? Kenya, Rhodaia, South Africa, Tanzania); Asia (China, India, Israel, Japan, U.S.S.R.); Australia and New Zealand, Europe (widely distributed) North America (Canada and U.S.A.); South America (Argentina, Brazil, Chile, Colombia, Peru). (CMI map 118). TRANSMISSION: Overwinters on host as dormant mycdium in blossom buds. The role of deistothecia in overwintering is doubtful. Spread by wind-borne conidia (Anderson, 1956).


Author(s):  

Abstract A new distribution map is provided for Pseudomonas andropogonis[Burkholderia andropogonis] (E.F. Smith) Stapp Sorghum, Maize (Zea mays), Velvet bean. Hosts: (Stizolobium deeringianum), Clover (Trifolium), Vicia & other hosts. Information is given on the geographical distribution in AFRICA, Ethiopia, Kenya, Nigeria, Rhodesia, South Africa, Sudan, Uganda, Zambia, ASIA, China (E.), Japan, Taiwan (Formosa), USSR (Soviet Far East), AUSTRALASIA & OCEANIA, Australasia (New South Wales), Hawaii, EUROPE, Hungary, NORTH AMERICA, USA, SOUTH AMERICA, Argentina, Brazil (Minas Gerais).


Author(s):  

Abstract A new distribution map is provided for Xanthomonas campestris pv. vasculorum (Cobb) Dye. Hosts: Sugarcane (Saccharum officinarum). Information is given on the geographical distribution in AFRICA, Ghana, Madagascar, Madeira, Malawi, Mauritius, Mozambique, Reunion, South Africa (Natal), Swaziland, Zimbabwe, ASIA, AUSTRALASIA & OCEANIA, New Guinea, NORTH AMERICA, Mexico, CENTRAL AMERICA & WEST INDIES, Belize, Dominica, Dominican Republic, Panama, Puerto Rico, St. Kitts and Nevis, SOUTH AMERICA, Argentina (Tucuman), Brazil, Colombia, French Guiana.


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