A Decade of Biological Control of Parthenium hysterophorus L. (Asteraceae) in South Africa Reviewed: Introduction of Insect Agents and Their Status

2021 ◽  
Vol 29 (3) ◽  
Author(s):  
L.W. Strathie ◽  
B.W. Cowie ◽  
A.J. McConnachie ◽  
F. Chidawanyika ◽  
J.N. Musedeli ◽  
...  
Plant Disease ◽  
2002 ◽  
Vol 86 (3) ◽  
pp. 327-327 ◽  
Author(s):  
A. R. Wood ◽  
M. Scholler

Parthenium weed (Parthenium hysterophorus L., family Asteraceae), an annual herb of neotropic origin, is an invasive noxious weed with a pantropical distribution (1). It is particularly undesirable because of the serious health risks it poses to people living close to infestations (1). In January 1995, S. Neser (ARC-Plant Protection Research Institute, Pretoria, South Africa) collected a rust fungus on this plant near Brits, Northwest Province, South Africa (25°35′S, 27°46′E). Only uredinia were present. The same rust fungus was collected in the same area in January, March, and June of 2001, and again only uredinia were observed. In its native range, P. hysterophorus is infected by two rust fungus species, Puccinia abrupta Diet. & Holw. var. partheniicola (Jackson) Parmelee and Puccinia melampodii Diet. & Holw., but the latter species is microcyclic with telia only. The morphology of the urediniospores in the South African collections corresponds to Puccinia abrupta var. partheniicola (3): obovoid to almost triangular, 22 to 27 × 18 to 25 µm, echinulate, two subequatorial and one apical germ pores, spines absent around germ pores, wall 1 to 2.5 µm thick. The native range of Puccinia abrupta var. partheniicola is Mexico and northern South America (3). In addition, it has been recorded from Mauritius (3), Kenya, and India (H. C. Evans and C. A. Ellison, International Institute of Biological Control, CAB, 1987, unpublished data). It was intentionally introduced into Australia for the biological control of P. hysterophorus (2). Thirteen specimens in the Arthur Herbarium were examined, and only two had telia in addition to uredinia. The other 11 had only uredinia, indicating that nonformation of telia is common. Telia and uredinia are produced in high altitude, semiarid areas of Mexico, whereas in low altitude, more humid areas only uredinia are produced (1). The production of telia appears to depend on environmental conditions, and their absence is not unexpected at the Brits site, which is a high altitude (1,120 m) area with high summer rainfall (400 to 600 mm per year from November to February) and dry winters. Voucher specimens were deposited at the National Collection of Fungi, Plant Protection Research Institute, Pretoria (PREM 57298) and the Arthur Herbarium, West Lafayette, IN (PUR N1117). To our knowledge, this is the second report of this rust fungus in Africa and the first in southern Africa. References: (1) H. C. Evans. Trans. Br. Mycol. Soc. 88:105, 1987. (2) A. Parker et. al. Plant Pathol. 43:1, 1994. (3) J. A. Parmelee. Can. J. Bot. 45:2267, 1967.


1952 ◽  
Vol 43 (1) ◽  
pp. 43-50 ◽  
Author(s):  
Wendell F. Sellers

Collections of Cactophagus spinolae (Gylh.) were made in Mexico in 1946, 1947, and 1948 to supplement the biological control of prickly pear (Opuntia spp.) in South Africa. During these three years, 862, 1,396, and 15,584 adults, respectively, were dispatched to South Africa. The weevils were sent by air express in specially designed containers, and arrived in excellent condition.This paper includes information on the distribution, life history and food preferences of C. spinolae. The need is stressed for anticipating the effects of transit conditions upon living insect material transported by aircraft.


2011 ◽  
Vol 19 (2) ◽  
pp. 434-442 ◽  
Author(s):  
L.G. Madire ◽  
A.R. Wood ◽  
H.E. Williams ◽  
S. Neser

2021 ◽  
Author(s):  
Sarah E. Thomas ◽  
Julissa Rojas-Sandoval ◽  
Pedro Acevedo-Rodríguez

Abstract L. camara is a highly variable ornamental shrub, native of the neotropics. It has been introduced to most of the tropics and subtropics as a hedge plant and has since been reported as extremely weedy and invasive in many countries. It is generally deleterious to biodiversity and has been reported as an agricultural weed resulting in large economic losses in a number of countries. In addition to this, it increases the risk of fire, is poisonous to livestock and is a host for numerous pests and diseases. L. camara is difficult to control. In Australia, India and South Africa aggressive measures to eradicate L. camara over the last two centuries have been largely unsuccessful, and the invasion trajectory has continued upwards despite control measures. This species has been the target of biological control programmes for over a century, with successful control only being reported in a few instances.


2021 ◽  
Vol 29 (3) ◽  
Author(s):  
C.A. Kleinjan ◽  
J.H. Hoffmann ◽  
F. Heystek ◽  
P. Ivey ◽  
Y. Kistensamy

Sign in / Sign up

Export Citation Format

Share Document