The Spider Genus Theridula in North and Central America and the West Indies (Araneae: Theridiidae)

1954 ◽  
Vol 73 (4) ◽  
pp. 331 ◽  
Author(s):  
Herbert W. Levi
Keyword(s):  

1917 ◽  
Vol 8 (2) ◽  
pp. 135-154 ◽  
Author(s):  
A. Ingram ◽  
J. W. S. Macfie

Howard, Dyar and Knab in their monograph “ The Mosquitoes of North and Central America and the West Indies,” in discussing the rearing of mosquitos, emphasise the importance of larvae in specific determination. They write (Vol. I, p. 181) “ Many species of Culex are of uncertain determination without the associated larvae, while some Aëdes have identical adults, yet dissimilar larvae. The characters of the larvae reside in the modifications of the chitinous appendages of the skin and the arrangement of the hairs. As these are fully retained by the cast skins, it is possible to preserve both the larva and the adult of the same identical specimen, thus assuring absolutely correct associations.”



1968 ◽  
Vol 75 (4) ◽  
pp. 351-359 ◽  
Author(s):  
Arthur M Chickering
Keyword(s):  


Nature ◽  
1913 ◽  
Vol 91 (2278) ◽  
pp. 420-421 ◽  
Keyword(s):  


1933 ◽  
Vol 24 (3) ◽  
pp. 345-348 ◽  
Author(s):  
Hubert W. Simmonds

The plant Clidemia hirta belongs to the natural order Melostomaceae. It is of shrubby growth, with a hard tough stem and produces quantities of dark purple berries, filled with minute seeds. These berries are much relished by certain birds, which feed upon them and distribute the seeds. The leaves are covered with fine hairs and the plant is not eaten by stock.The plant is a native of the West Indies, Central America and the Northern portion of South America. It is supposed to have been introduced into Fiji from British Guiana at some time prior to 1890. That this was the origin of the plant is supported by slight differences observed by the writer in the foliage of the Trinidad, Panama and British Guiana forms of the plant, the Fijian one closely resembling those of the last named country.In Fiji the plant was first observed along the fences of paddocks in the Waimanu Valley, whence it spread with great rapidity, quickly becoming a weed of major importance. By 1919, when the writer arrived in the country, thousands of acres were covered with it to the exclusion of almost all other growth. On good soil it formed a stand five or six feet high, through which the cattle were only able to keep open narrow paths. Not only did it rapidly occupy the open grass lands, particularly the rich dairying and fattening country, but it thrived almost equally well under the shade of coconut and rubber plantations, leading to loss of many fallen nuts and entailing greatly increased weeding costs.



1972 ◽  
Vol 50 (7) ◽  
pp. 1441-1452 ◽  
Author(s):  
Gerrit Davidse ◽  
Richard W. Pohl

Chromosome numbers and meiotic behavior are reported for 99 collections of grasses representing 47 genera and 88 species. First chromosome counts are reported for the following 20 species: Aristida laxa, n = 22; Chloris ekmanii, n = 20; Chusquea scandens, n = 20; Danthonia domingensis, n = 18; Eragrostis hypnoides, n = 10; E. prolifera, n = 20; Festuca mirabilis, n = 14; Leptochloa scabra, n = 30; Manisuris ramosa, n = 18; Paspalum carinatnm, n = 40; P. distortum, n = 10; Pharus glaber, n = 12; Raddia sympodica, 2n = 22; Raddiella nana, n = 10; Schizachyrium gracile, n = 20; Setaria crus-ardeae, n = 18; Thrasya paspaloides, n = 20; Trachypogon ligularis, n = 10; Trichachne laxa, n = 18; Tristachya avenacea, n = 24. The count for Raddiella nana represents a first generic report. Counts that differ from previous counts for the same taxon are reported for these 11 species: Andropogon gerardii, n = 40; Aristida orizabensis, n = 22; Eragrostis trichocolea, n = 30; Ichnanthus nemoralis, n = 10; Microchloa kunthii, n = 22; Olyra latifolia, n = 22; Panicum cyanescens, n = 27; Paspalum caespitosum, n = 10; P. millegrana, n = 20, 30; Schizachyrium hirtiflorum, n = 20; Trachypogon montufari, n = 30.



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