scholarly journals Doğal Olarak Yayılış Gösteren Lepidium draba L. Türünün Fitoremediasyon Yönteminde Kullanılabilirliğinin Araştırılması

Author(s):  
Burak SÜRMEN ◽  
Dudu Duygu Kılıç ◽  
Hamdi Güray Kutbay ◽  
Emine Ebru Tuna
Keyword(s):  
2018 ◽  
Vol 8 (4) ◽  
pp. 265-271
Author(s):  
Bensaid Sara Ouissem ◽  
Bicha Sabrina ◽  
Benmekhebi Lotfi ◽  
Rebbas Khellaf ◽  
Bensouici Chawki ◽  
...  

Plant Disease ◽  
2009 ◽  
Vol 93 (8) ◽  
pp. 846-846 ◽  
Author(s):  
A. J. Caesar ◽  
R. T. Lartey

The exotic, rangeland weed Lepidium draba L., a brassicaceous perennial, is widely distributed in the United States. For example, Oregon contains 100,000 ha of land infested with L. draba (2). Because it is capable of aggressive spread and has the potential to reduce the value of wheat-growing land (4), it is the target of biological control research. The application of multiple pathogens has been advocated for control of other brassicaceous weeds, including the simultaneous application of biotrophic and necrotrophic pathogens (3). In pursuit of this approach, in 2007, we discovered the occurrence of leaf spots on approximately 90% of L. draba plants near Shepherd, MT, which were distinct from leaf lesions caused by Cercospora bizzozeriana (1). The lesions were initially tiny, black spots enlarging over time to become circular to irregular and cream-colored around the initial black spots and sometimes with dark brown borders or chlorotic halos. Conidia from the lesions were light brown, elongate and obclavate, produced singly from short conidia, with 8 to 12 transverse septa, and 2 to 6 longitudinal septa. The spore body measured 25 to 35 × 200 to 250 μm with a beak cell 42 to 100 μm long. On the basis of conidial and cultural characteristics, the fungus was identified as Alternaria brassicae (Berk.) Sacc. Leaf tissues bordering lesions were plated on acidified potato dextrose agar. Colonies on V8 and alfalfa seed agar were black with concentric rings, eventually appearing uniformly black after 10 to 14 days. The internal transcribed spacer region of rDNA was amplified using primers ITS1 and ITS4 and sequenced. BLAST analysis of the 575-bp fragment showed a 100% homology with a sequence of A. brassicae Strain B from mustard (GenBank Accession No. DQ156344). The nucleotide sequence has been assigned GenBank Accession No. FJ869872. For pathogenicity tests, aqueous spore suspensions approximately 105/ml were prepared from cultures grown at 20 to 25°C for 10 to 14 days on V8 agar and sprayed on leaves of three L. draba plants. Inoculated plants were enclosed in plastic bags and incubated at 20 to 22°C for 72 to 80 h. In addition, three plants of the following reported hosts of A. brassicae were inoculated: broccoli, canola, Chinese cabbage, collards, broccoli raab, kale, mustard greens, radish, rape kale, and turnip. Within 10 days, leaf spots similar to those described above developed on plants of radish, canola, Chinese cabbage, and turnip and A. brassicae was reisolated and identified. Control plants sprayed with distilled water remained symptomless. These inoculations were repeated and results were the same. To our knowledge, this is the first report of a leaf spot disease caused by A. brassicae on L. draba in North America. A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI No. 878750A). References: (1) A. J. Caesar et al. Plant Dis. 93:108, 2009. (2) G. L. Kiemnec and M. L. McInnis. Weed Technol. 16:231, 2002. (3) A. Maxwell and J. K. Scott. Adv. Bot. Res. 43:143, 2005. (4) G. A. Mulligan and J. N. Findlay. Can. J. Plant Sci. 54:149, 1974.


2021 ◽  
Author(s):  
Philip Weyl

Abstract Lepidium draba is found in a wide range of habitats ranging from roadsides (highly disturbed sites) to rangelands, meadows and pastures, cultivated fields, home gardens, national parks and wasteland. It exists at high and low latitudes, above and below sea level. It is found under irrigation and in soils of high moisture content and also exists in arid regions. It invades all soil types, although it prefers alkaline conditions and can germinate in saline soils. All of these characteristics and adaptations provide exceptional advantages for this noxious weed and reflect its high potential to invade different agricultural systems. The absence of L. draba plants from plantations or sites where it has not been reported may not be due to the species' ability to invade, survive, grow or develop in these sites but rather to the absence of initial infestation. The weed can invade both agricultural and natural ecosystems (Larson et al., 2000). In summary, L. draba is a serious threat to agriculture and the environment. It is of a high ecological tolerance and is potentially harmful to human and animal health. Its ability to invade and reproduce by different means and to host plant pathogenic agents make this weed invasive with significant problems to man and natural resources.


Weed Science ◽  
2019 ◽  
Vol 67 (05) ◽  
pp. 560-571 ◽  
Author(s):  
Said Mohammed ◽  
Veronika Turečková ◽  
Danuše Tarkowská ◽  
Miroslav Strnad ◽  
Klaus Mummenhoff ◽  
...  

AbstractThis study provides a comparative analysis of the dormancy and germination mechanisms of the indehiscent fruits of hoary cress (Lepidium draba L.) and hairy whitetop (Lepidium appelianum Al-Shehbaz), two invasive weeds of the Brassicaceae. Germination assays comparing isolated seeds (manually removed from the fruits) and intact indehiscent fruits showed that the isolated seeds are nondormant and provided full germination for both species. In contrast to this, the species differed in the germination properties of their indehiscent fruits, in that L. appelianum fruits were nondormant, while the L. draba fruit coat (pericarp) conferred a coat-imposed dormancy. The pericarp of L. draba fresh fruit was water permeable, and neither mechanical scarification nor surface sterilization affected germination, supporting the concept that pericarp-mediated dormancy was not due to water impermeability or mechanical constraint. Washing of L. draba fruits with water, afterripening (dry storage), and treatment with gibberellin (GA) stimulated the germination of this species, all of which are indicative of physiological dormancy. Analyses of endogenous abscisic acid (ABA) and GA levels combined with treatment experiments with wash water from fresh and afterripened L. draba pericarps and with ABA dose–response quantification of germination revealed that ABA is a key component of a pericarp-mediated chemical dormancy in this species. Consistent with this, pericarp ABA levels decreased during afterripening and upon fruit washing, and isolated fresh or afterripened seeds did not differ in their ABA sensitivities. The possible roles of the ABA-mediated pericarp dormancy for the germination ecophysiology and weed management of these species are discussed.


2007 ◽  
Vol 97 (4) ◽  
pp. 387-397 ◽  
Author(s):  
H. Baur ◽  
F.J. Muller ◽  
G.A.P. Gibson ◽  
P.G. Mason ◽  
U. Kuhlmann

AbstractFour species of Mesopolobus Westwood were reared as parasitoids of Ceutorhynchinae hosts in Europe during surveys in 2000–2004. An illustrated key is given to differentiate the four species, M. gemellus Baur & Muller sp. n., M. incultus (Walker), M. morys (Walker) and M. trasullus (Walker), plus M. moryoides Gibson, a parasitoid of the cabbage seedpod weevil, Ceutorhynchus obstrictus (Marsham), in North America. Pteromalus clavicornis Walker is recognized as a junior synonym of M. incultussyn. n., and Pteromalus berecynthos Walker (also a junior synonym of M. incultus) is considered a correct original spelling. For Disema pallipes Förster (a junior synonym of Mesopolobus morys), a lectotype is designated. Mesopolobus morys is for the first time accurately associated with the seed weevil Ceutorhynchus turbatus (Schultze), a potential agent for classical biological control, of hoary cress, Lepidium draba L. (Brassicaceae), in North America. Mesopolobus gemellus is associated with another seed weevil, Ceutorhynchus typhae (=C. floralis) (Herbst), in pods of shepherd's purse, Capsella bursa-pastoris (L.) Medik. (Brassicaceae). Implications of the host–parasitoid associations are discussed relative to the introduction of species to North America for classical biological control of the cabbage seedpod weevil.


2017 ◽  
Vol 70 ◽  
pp. 21-30 ◽  
Author(s):  
Yaser Fattahian ◽  
Ali Riahi-Madvar ◽  
Reza Mirzaee ◽  
Gholamreza Asadikaram ◽  
Mohammad Reza Rahbar
Keyword(s):  

2013 ◽  
Vol 31 (3) ◽  
pp. 247-254 ◽  
Author(s):  
Yusuf Kaya ◽  
Ozkan Aksakal ◽  
Serap Sunar ◽  
Filiz Aygun Erturk ◽  
Sedat Bozari ◽  
...  

Author(s):  
Q Ali ◽  
R Khalil ◽  
M Nadeem ◽  
MM Azhar ◽  
MM Hafeez ◽  
...  

The Lepidium draba or white tope also known as hoary cress belongs to family Brassicaceae, has been known as one of the perennial herbs which grow normally from seeds and also produced horizontal long creeping roots. It normally grows as a weed plant in farm fields. The present study was conducted to find out the antibacterial and antioxidant activities along with the plant traits of Lepidium draba. The shoot, root and inflorescence extracts were taken through using ethanol, water and n-hexan as extraction solvents. It was found from our studies that the plant extracts were heaving alkaloids, saponins, flavonoids, coumarins, anthocyans, quinons, steroids, sterols and terpenoids as potential phenolic compounds. The bacterial strains including Escherichia coli, Klebsiella pneumonia and Staphylococcus aureus were cultured to access the antibacterial activities of plant extracts. The higher antibacterial activity was reported from n-hexan extract which indicate that the n-hexan extract may be used for extracting phytochemicals to be used as potential antibacterial biomedicines. The water extract showed higher antioxidant activities as compared with ethanol and n-hexan extracts which indicated that the use of water extract may be as a useful antioxidant under stress conditions, may also have anticancer activities. The lower coefficient of variation was recorded for all of the studied traits which indicated the consistency of results and reliability of selecting plants from various locations. There was significant and positive correlation among plant height with inflorescence weight, leaf area and leaf length, the inflorescence weight showed positive correlation with plant height, lea length and leaf area. There was higher contribution of plant height while leaf area contributed lower and negatively towards fresh plant weight. We have concluded from our study that the Lepidium draba plant extract showed antibacterial and antioxidant activities through using ethanol, water and n-hexan as extraction solvents. The significant correlation and regression associations indicated that the plants can tolerate harsh environmental conditions.


Plant Disease ◽  
2009 ◽  
Vol 93 (1) ◽  
pp. 108-108 ◽  
Author(s):  
A. J. Caesar ◽  
R. T. Lartey ◽  
D. K. Berner ◽  
T. Souissi

The herbaceous perennial Lepidium draba L. is an invasive weed of rangelands and riparian areas in North America and Australia. As of 2002, it had infested 40,500 ha of rangeland in Oregon and large areas in Wyoming and Utah. Little is known of plant pathogens occurring on L. draba, especially in the United States, that could be useful for biological control of the weed. Leaf spots were first noted on a stand of L. draba near Shepherd, MT in 1997. The spots were mostly circular but sometimes irregularly shaped and whitish to pale yellow. The pathogen was erroneously assumed to be Cercospora beticola since its morphological traits closely resembled that species and the area had large fields of sugar beet with heavy Cercospora leaf spot incidence. Diseased leaves of L. draba were collected in 1997 and 2007. Conidia, borne singly on dark gray, unbranched conidiophores produced on dark stromata late in the season, were elongate, hyaline, multiseptate, 38 to 120 × 2 to 6 μm (mostly 38 to 50 × 2 to 5 μm) and had bluntly rounded tips and wider, truncate bases. These characteristics were consistent with the description of C. bizzozeriana Saccardo & Berlese (2). To isolate the fungus, spores were picked from fascicles of conidiophores with a fine-tipped glass rod, suspended in sterile water, and spread on plates of water agar. Germinated spores were transferred to potato dextrose agar (PDA). The ITS1, 5.8S, and ITS2 sequences of this fungus (GenBank Accession No. EU887131) were identical to sequences of an isolate of C. bizzozeriana from Tunisia (GenBank Accession No. DQ370428). However, these sequences were also identical to those of a number of Cercospora spp. in GenBank, including C. beticola. We also compared the actin gene sequences of the Montana isolate of C. bizzozeriana (GenBank Accession No. FJ205397) and an isolate of C. beticola from Montana (GenBank Accession No. AF443281); the sequences were 94.6% similar, an appreciable difference. For pathogenicity tests, cultures were grown on carrot leaf decoction agar. Aqueous suspensions of 104 spores per ml from cultures were sprayed on 6-week-old L. draba plants. Plants were covered with plastic bags and placed on the greenhouse bench at 20 to 25°C for 96 h. Koch's postulates were completed by reisolating the fungus from the circular leaf spots that appeared within 10 days, usually on lower leaves. Spores of C. bizzozeriana were also sprayed on seedlings of sugar beet, collard, mustard, radish, cabbage, and kale under conditions identical to those above. No symptoms occurred. After the discovery of the disease in 1997, plants of L. draba in eastern Montana, Wyoming, and Utah were surveyed from 1998 to 2003 for similar symptoms and signs, but none were found. This, to our knowledge, is the first report of C. bizzozeriana in the United States. The initial report of the fungus in North America was from Manitoba in 1938 (1). It has recently been reported as occurring on L. draba in Tunisia (4) and Russia (3) and is reported as common in Europe (2). A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI No. 878750A). References: (1) G. R. Bisby. The Fungi of Manitoba and Saskatchewan. Natl. Res. Council of Canada, Ottawa, 1938. (2) C. Chupp. A Monograph of the Fungus Genus Cercospora. C. Chupp, Ithaca, NY, 1953. (3) Z. Mukhina et al. Plant Dis. 92:316, 2008. (4) T. Souissi et al. Plant Dis. 89:206, 2005.


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