COUNTY RECORDS AND MAJOR RANGE EXTENSIONS FOR VASCULAR PLANTS FROM THE WEST CROSS TIMBERS IN ERATH COUNTY, TEXAS

2018 ◽  
Vol 70 (1) ◽  
Author(s):  
T. Cotton ◽  
A. D. Nelson

Abstract Floristic data for Erath County, Texas, is unknown or limited. In this investigation plants were collected from 35 sites in Erath County from September 2003 to April 2008. Plants were identified and categorized based on the following status: introduced, endemic, threatened, and endangered species, as well as county records and major range extensions. One hundred and nineteen new county records were recorded for Erath County. Sixty five species were major range extensions, occurring greater than one county away from the border of Erath County. Twenty-six species were introduced while 93 species were native. Six of the native species were endemic to Texas, with Penstemon guadalupensis classified as endemic to north-central Texas and the Edwards Plateau. There were no rare, threatened, or endangered plants found. Convolvulus arvensis was the only noxious weed found, being state-listed as a noxious species.

2021 ◽  
Vol 15 (2) ◽  
pp. 715-737
Author(s):  
Allan D. Nelson ◽  
Turner Cotton ◽  
Sarah Brown ◽  
Paige Cowley ◽  
Sara Harsley

Knowledge of county floras in Texas is crucial for determining species composition, management, preservation, and restoration across the state. Like most Texas counties, floristic data for Erath County, Texas, is poorly known. The objectives of this investigation were to compile a flora for Erath County, determine the intro-duced, endemic, threatened, and endangered species, as well as make comparisons to the county’s original flora and that of the North Central Texas region. Field work was conducted from September 2003 to December 2009 at 35 sites in Erath County. In addition herbaria were searched to locate specimens from Erath County. A total of 870 species (888 taxa) were identified in 103 families. One hundred forty-four taxa were introduced while 744 taxa were native. Eighteen of the species are Texas endemics. There were two rare plants, Dalea reverchonii and Penstemon guadalupensis, but no threatened or endangered plants were found during the inves-tigation. Four state-listed noxious species were collected during the investigation—Arundo donax (giant reed), Convolvulus arvensis (field bindweed), Tamarix chinensis, and T. gallica (salt-cedars).


Plant Disease ◽  
1999 ◽  
Vol 83 (6) ◽  
pp. 587-587 ◽  
Author(s):  
S. C. Bost ◽  
F. L. Mitchell ◽  
U. Melcher ◽  
S. D. Pair ◽  
J. Fletcher ◽  
...  

Yellow vine (YV) is a recently recognized decline of cucurbits expressed as plant yellowing, phloem discoloration, and death of vines as fruit approach maturity. In severely affected fields, YV incidence can range from 50 to 100% with similar yield loss. The disease has been associated with a phloem-limited, walled bacterium belonging to the gamma-3-proteobacteria (1), for which specific polymerase chain reaction (PCR) primers have been developed and used in diagnosis (2). First observed in 1988 in Oklahoma and Texas squash and pumpkin, YV was not detected in watermelon and cantaloupe until 1991. The disease has never been detected in cucumber. Efforts to date have been unsuccessful in transmitting the disease with dodder, grafting, or selected insects. Initially, the geographic range of the disease appeared to be generally confined to central and northeastern Oklahoma and north central Texas, an area known as the Cross Timbers Region. In 1997 to 1998, YV was diagnosed in commercial fields of watermelon and muskmelon from east Texas (Post Oak Savannah) and all cucurbit-growing areas of Oklahoma. In late summer 1998, symptoms similar to those of YV were observed in one watermelon (Hardeman County) and three pumpkin (Rhea and Morgan counties) fields in Tennessee where the leaves turned yellow and chlorotic and affected plants exhibited phloem discoloration. Estimated incidence of YV ranged from less than 1 to 20% of the plants in affected fields. PCR, with the YV-specific primers (2), amplified a band of the expected size (409 bp) from all watermelon and pumpkin plants exhibiting phloem discoloration. In contrast, no bands were amplified from asymptomatic (no phloem discoloration) watermelon or pumpkin. The nucleotide sequence of the DNA fragment amplified from a Tennessee watermelon and pumpkin plant was identical to that of the YV bacterium. The occurrence of YV outside of the Cross Timbers Region, and in a location as distant as Tennessee, suggests that the disease may be much more widespread than previously recognized. Diagnosis and monitoring of YV in all cucurbit-growing areas is critical for determining the geographic distribution and losses caused by this emerging disease. References: (1) F. J. Avila et al. Phytopathology 88:428, 1998. (2) U. Melcher et al. (Abstr.) Phytopathology. 89(suppl.):S95, 1999.


1980 ◽  
Vol 33 (2) ◽  
pp. 95
Author(s):  
Dee A. Quinton ◽  
Alan Kent Montei ◽  
Jerran T. Flinders

1975 ◽  
Vol 53 (23) ◽  
pp. 2776-2795 ◽  
Author(s):  
D. H. Vitt ◽  
P. Achuff ◽  
R. E. Andrus

Three patterned fens in north central Alberta were analyzed to elucidate vegetation patterns in vascular plants and bryophytes. Two flark associations dominated by Menyanthes trifoliata and Carex limosa, both of which had Sphagnum jensenii and Drepanocladus exannulatus phases, were recognized. The strings consist of two associations; one is dominated by Betula glandulosa, Tomenthypnum falcifolium, and Aulacomnium palustre; the second is dominated by Picea mariana, Sphagnum magellanicum, and Ledum groenlandicum. An intensive analysis of one fen reveals that these mires are ‘poor fens’ with a mean pH of 5.2 and Ca2+concentration of 2.3 ppm. The fens occur on low drainage divides and Ca2+ is depleted as water flows through the fens. An ecological series of bryophytes is described in the transitions between flarks and strings.


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