Occurrence and properties of lepidocrocite in some soils of New Zealand, South Africa and Australia

Soil Research ◽  
1985 ◽  
Vol 23 (4) ◽  
pp. 543 ◽  
Author(s):  
RW Fitzpatrick ◽  
RM Taylor ◽  
U Schwertmann ◽  
CW Childs

Fifty-one samples, collected from 26 sites in New Zealand, South Africa and Australia, were tested for the presence of lepidocrocite (�-FeOOH) and goethite (�-FeOOH). The samples were predominantly orange-coloured mottles, bands, crusts and pipestems from hydromorphic soils, but also included a placic horizon, iron-rich precipitates from water courses, altered pyrite cubes, and geode-like features in weathered saprolites. The iron oxides were identified and characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Lepidocrocite was identified in 49 of the samples, and in 44 was present in concentrations exceeding I%, with the highest being approximately 70%. Crystallinities of the lepidocrocite were assessed from the widths and positions of XRD peaks, and, in some cases, from TEM. Goethite was also present in most samples, and predominated over lepidocrocite in some. In all three countries, the most common occurrence of lepidocrocite was associated with the gleyed soil materials commonly found in wet, poorly drained pseudogley soils (mostly 'humic slope gley') of humid temperate climate. Under these climatic conditions the high degree of water supply, relatively lower soil temperatures, lower evaporation and slower water movement caused reductomorphic conditions. At these sites soil iron oxides are reduced and, on reoxidation, lepidocrocite and goethite are generally formed. The colour generally associated with lepidocrocite in iron-rich segregations in hydromorphic soils is 7.5YR6-7/4-8 Lepidocrocite was also identified in all of the other samples mentioned above. A study of the relative proportions of lepidocrocite and goethite, and the crystallinity of these associated minerals in the various morphological concentrations (profile trends), suggests that their formation is strongly governed by soil microenvironmental factors (pH, Eh, and ionic environment). However, climatic and pedogenic factors such as podzolization and high organic matter contents may modify these mineral phases or induce further transformation. These findings indicate that lepidocrocite occurs in a remarkably wide range of materials and weathering environments. Moreover, the morphology, crystallinity, differential XRD line broadening and line shift of the lepidocrocite, and the commonly associated goethite also vary markedly in the respective materials. This suggests that other factors associated with particular weathering environments, such as those involved in pseudomorphous alteration of pyrite and the influence of chloride ions, may be more important in the formation of lepidocrocite than the conditons associated with hydromorphy. The morphology and characteristics of lepidocrocite and goethite, together with field associations, appear to be useful indicators of soil genesis.

Author(s):  
E. Punithalingam

Abstract A description is provided for Phomopsis juniperivora. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a wide range of conifers, including Juniperus ashei, J. horizontalis var. douglasii, J. japonica, J. scopulorum, J. chinensis, J. virginiana, J. communis, J. sabina var. tamariscifolia, Chamaecyparis lawsoniana, C. thyoides, Cupressus macrocarpa, C. arizonica, C. lusitanica, C. sempervirens, C. torulosa, Cryptomeriajaponica, Thuja orientalis, Larix decidua, Pinus banksiana, Pseudotsuga taxifolia, Cephalotaxus drupacea, Abies spp., Taxus baccata. GEOGRAPHICAL DISTRIBUTION: N. America (USA, Canada), Europe (UK, France, Denmark), Africa (Kenya, South Africa, Mozambique), Australasia and Oceania (New Zealand). TRANSMISSION: By airborne conidia produced in pycnidia on diseased tissues, liberated by a splash take-off mechanism.


Author(s):  
C. Booth

Abstract A description is provided for Nectria flammea. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: The fungus occurs on a variety of scale insects, Aspidiotus nerii, Hemiberlesia rapax (53, 1-694), Pseudaulacaspis pentagona (55, 2093) etc. on a wide range of hosts, Acacia, Brachyglottis, Camellia, Citrus, Coffea, Morus, Ribes, Salix, Thea, Weinmannia, etc. GEOGRAPHICAL DISTRIBUTION: Australia, Belize, Fiji, India, Japan, New Zealand, Papua and New Guinea, Tanzania, Tonga, Uganda, South Africa, Sarawak, Zambia. TRANSMISSION: Airborne by ascospores or by moisture droplets as conidia.


Author(s):  

Abstract A new distribution map is provided for Brevipalpus obovatus Donn. (Acarina, Tenuipalpidae) Hosts: Citrus, wide range of ornamentals and weeds. Information is given on the geographical distribution in EUROPE (excl.USSR), Austria, France, Germany, Netherlands, Spain, ASIA (excl.USSR), Ceylon, Cyprus, Israel, Japan, Persia, USSR, AFRICA, Canary Islands, Congo, Egypt, Kenya, Libya, Mauritius, Republic of South Africa, Tanganyika, AUSTRALASIA and PACIFIC ISLANDS, Australia, Hawaii, New Zealand, NORTH AMERICA, Canada, U.S.A., CENTRAL AMERICA and WEST INDIES, Porto Rico, SOUTH AMERICA, Argentina, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Phytomyza atricornis[Chromatomyia horticola] Mg. (Dipt., Agromyzidae) (Chrysanthemum leaf-miner). Hosts: Wide range of herbaceous plants, notably bean, pea, brassicas, Chrysanthemum. Information is given on the geographical distribution in EUROPE, Austria, Belgium, Britain, Bulgaria, Czechoslovakia, Denmark, Faeroe Islands, Finland, France, Germany, Hungary, Iceland, Ireland, Italy, Netherlands, Norway, Poland, Spain, Sweden, Switzerland, Yugoslavia, ASIA, Afghanistan, China, Cyprus, Formosa, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Japan, Korea, Pakistan, Thailand, Turkey, USSR, AFRICA, Azores, Cameroun, Canary Islands, Cape Verde Islands, Congo, Egypt, Eritrea, Kenya, Libya, Madeira, Morocco, Republic of South Africa, Rhodesia, Senegal, AUSTRALASIA and PACIFIC ISLANDS, Australia, New Zealand, NORTH AMERICA, Canada, U.S.A.


2021 ◽  
Author(s):  
Julissa Rojas-Sandoval

Abstract F. convolvulus is a weedy species of gardens, cultivated fields, open habitats, orchards, non-crop areas, waste areas, and disturbed sites. It is well-adapted to a wide range of climatic conditions and soils. This species is a prolific seed producer and has the potential to produce up to 30,000 seeds/plant. Seeds can be dispersed by farm machinery, and water. It is also a common contaminant of wheat and other cereal crops. F. convolvulus is often a serious weed in cereals, vegetables and horticultural crops (FAO, 2015). Currently, it is listed as invasive in the Dominican Republic, Cuba, Australia, New Caledonia, and New Zealand (Webb et al., 1988; MacKee, 1994; Wilson, 2008; Acevedo-Rodriguez and Strong, 2012), but it is also ranked as a serious weed in 20 crops in more than 41 countries around the world (Holm et al., 1991). Distribution.


2008 ◽  
Vol 61 ◽  
pp. 392-392 ◽  
Author(s):  
J. Baskarathevan ◽  
M.V. Jaspers ◽  
E.E. Jones ◽  
H.J. Ridgway

Worldwide 11 species of Botryosphaeria have been isolated from grapevines in association with a wide range of decline and dieback symptoms Currently there is little knowledge on what species are present in New Zealand A comprehensive survey was carried out during June to December 2007 to collect Botryosphaeria species from New Zealand vineyards More than 450 isolates including B parva B lutea B australis B stevensii B obtusa and B iberica were isolated from symptomatic material No correlation was observed between the species of Botryosphaeria and grapevine variety or age The highest incidence of Botryosphaeria species (977 ) was from Blenheim and lowest (164 ) was from Otago The most commonly isolated species was B parva followed by B stevensii Fusicoccum type Botryosphaeria species such as B parva and B lutea were more prevalent in the North Island and Diplodia type species including B stevensii and B obtusa dominated in the South Island It is likely that the Botryosphaeria species distribution in New Zealand is influenced by climatic conditions This information has implications for development of control strategies


Author(s):  

Abstract A new distribution map is provided for Listroderes costirostris Schönh. (obliquus Klug) (Col., Curculionidae) (Vegetable Weevil). Hosts: Wide range of vegetables and weeds. Information is given on the geographical distribution in ASIA, Japan, AFRICA, Republic of South Africa, AUSTRALASIA and PACIFIC ISLANDS, Australia, Hawaii, New Caledonia, New Zealand, Norfolk Island, NORTH AMERICA, U.S.A., SOUTH AMERICA, Argentina, Bolivia, Brazil, Chile, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Graphognathus leucoloma (Boh.) (Col., Curculionidae) (A White-fringed Beetle). Hosts: Wide range of vegetables and other crops and weeds. Information is given on the geographical distribution in AFRICA, Republic of South Africa, AUSTRALASIA, and PACIFIC ISLANDS, Australia, New Zealand, NORTH AMERICA, U.S.A., SOUTH AMERICA, Argentina, Brazil, Chile, Peru, Uruguay.


Author(s):  
M. A. Spencer

Abstract A description is provided for Pythium spinosum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASES: Seedling damping-off. HOSTS: Wide range of plant hosts. GEOGRAPHICAL DISTRIBUTION: AFRICA: South Africa. NORTH AMERICA: Canada, USA (Florida, Hawaii, Iowa). SOUTH AMERICA: Argentina. ASIA: China (Zhejiang), India, Japan, Korea, Taiwan. AUSTRALASIA: Australia (Queensland), New Zealand. EUROPE: France, Germany, Great Britain, Italy, Netherlands. TRANSMISSION: Contaminated soil, organic matter (oospores) and water (sporangia).


2011 ◽  
Vol 63 (4) ◽  
pp. 1069-1075 ◽  
Author(s):  
Jasmina Bacic ◽  
L. Barsi ◽  
P. Strbac

The life cycle of a population of the quarantine nematode Globodera rostochiensis on the root of susceptible potato variety, Desiree, originating from an infected field (CC Ljubovija no. 413) on the mountain of Jagodnja in the district of Macva, was studied under experimental conditions in Belgrade in 2002-2003. The golden cyst nematode completed one generation per year in the temperate climate of this region. In 2002, the life cycle lasted 29 days after the penetration of the second stage juveniles into the roots. An adverse effect of high soil temperatures above 25 ?C was observed in 2003, influencing the development of the nematode and making the life cycle last two months longer.


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