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2,989 results on '"Myriophyllum"'

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201. Co-occurrence of the charophyte Lychnothamnus barbatus with higher trophy submerged macrophyte indicators

202. Phytoextraction and biodegradation of atrazine by Myriophyllum spicatum and evaluation of bacterial communities involved in atrazine degradation in lake sediment

203. Growth and oxidative stress response of aquatic macrophyte Myriophyllum spicatum to sediment anoxia

204. High phenolic content fails to deter mesograzer consumption of Myriophyllum spicatum (Eurasian watermilfoil) in New England

205. Zebra mussels and Eurasian watermilfoil reporting patterns in Minnesota

206. Weather conditions and chlorophyll concentrations determine long-term macrophyte community dynamics of Lake Bohinj (Slovenia)

207. Effect of submerged plant species on CH4 flux and methanogenic community dynamics in a full-scale constructed wetland

208. Transfer kinetics of phosphorus (P) in macrophyte rhizosphere and phytoremoval performance for lake sediments using DGT technique

209. Compound-specific δD and its hydrological and environmental implication in the lakes on the Tibetan Plateau

210. Hydrological alteration exacerbates the negative impacts of invasive Eurasian milfoil Myriophyllum spicatum by creating hypoxic conditions in a northern Gulf of Mexico estuary

211. The existence of cyanobactericidal bacteria and growth-inhibiting bacteria on water plants in Lake Ohnuma, Japan

212. The water clarity of Polish lakes with charophyte vegetation in the years 1953-1968

213. Nutrient bioextraction and microalgae growth inhibition using submerged macrophyte Myriophyllum spicatum in a low salinity area of East China Sea

214. Impact of Flood Cycle on Phytoplankton and Macroinvertebrates Associated with Myriophyllum spicatum in Lake Nasser Khors (Egypt)

215. Correspondence : Brandegee (Townsend) and Engelmann (George), 1873-1882.

216. Seasonal changes in the concentration of some trace elements in macrophyte shoots

217. Correspondence : Brandegee (Townsend) and Engelmann (George), 1873-1882.

218. Enhanced nitrogen removal and quantitative molecular mechanisms in a pilot-scale multistage constructed wetlands planted with Myriophyllum aquaticum treating lagoon swine wastewater

219. Cutting-edge spectroscopy techniques highlight toxicity mechanisms of copper oxide nanoparticles in the aquatic plant Myriophyllum spicatum

220. Efficient treatment of digested piggery wastewater via an improved anoxic/aerobic process with Myriophyllum spicatum and bionic aquatic weed

221. Abiotic and Biotic Factors That Influence the Bioavailability of Gold Nanoparticles to Aquatic Macrophytes.

222. Laboratory crosses and genetic analysis of natural populations demonstrate sexual viability of invasive hybrid watermilfoils (Myriophyllum spicatum × M. sibiricum).

223. Comparative leaf development of aerial and aquatic growth forms of Myriophyllum aquaticum.

224. THE ECONOMIC AND ECOLOGICAL POTENTIAL OF MACROPHYTIC VEGETATION IN URBAN LAKES.

225. Chara can outcompete Myriophyllum under low phosphorus supply.

226. Myriophyllum heterophyllum Michaux [Haloragaceae] en Haute-Vienne (Limousin, France), et situation de cette plante invasive en France et en Europe.

227. Statistical classification of vegetation and water depths in montane wetlands.

228. The relative sensitivity of macrophyte and algal species to herbicides and fungicides: An analysis using species sensitivity distributions.

229. Dynamic reconfiguration of aquatic plants and its interrelations with upstream turbulence and drag forces.

230. Effects of substrate and shading on the growth of two submerged macrophytes.

231. Efficient distinction of invasive aquatic plant species from non-invasive related species using DNA barcoding.

232. A model for the effect of submerged aquatic vegetation on turbulence induced by an oscillating grid

233. Hybridization, cryptic diversity, and invasiveness in introduced variable-leaf watermilfoil.

234. Higher nitrate-reducer diversity in macrophyte-colonized compared to unvegetated freshwater sediment.

235. Does light heterogeneity affect structure and biomass of submerged macrophyte communities?

236. Effects of turion size and water depth on germination and growth of an aquatic plant (Myriophyllum oguraense Miki subsp, yangtzense).

237. Loopholes in the regulation of invasive species: genetic identifications identify mislabeling of prohibited aquarium plants.

238. Interactions of gold nanoparticles with freshwater aquatic macrophytes are size and species dependent.

239. Does nature and persistence of substrate at a mesohabitat scale matter for Chironomidae assemblages? A study of two perennial mountain streams in Patagonia, Argentina.

240. Evidence against early nineteenth century major European induced environmental impacts by illegal settlers in the New England Tablelands, south eastern Australia

241. Can time-weighted average concentrations be used to assess the risks of metsulfuron-methyl to Myriophyllum spicatum under different time–variable exposure regimes?

242. Allelopathic effects of Cyperus alternifolius and Myriophyllum aquaticum on phytoplankton.

243. Physiological, anatomical and phenotypical effects of a cadmium stress in different-aged chlorophyllian organs of Myriophyllum alterniflorum DC (Haloragaceae)

244. Herbivory in omnivorous fishes: effect of plant secondary metabolites and prey stoichiometry.

245. On correct identification, range expansion and management implications of Myriophyllum aquaticum in Kashmir Himalaya, India.

246. Resprouting Response of Aquatic Clonal Plants to Cutting May Explain Their Resistance to Spate Flooding.

247. Influences of water column nutrient loading on growth characteristics of the invasive aquatic macrophyte Myriophyllum aquaticum (Vell.) Verdc.

248. Differential responses of Myriophyllum alterniflorum DC (Haloragaceae) organs to copper: physiological and developmental approaches.

249. Lobe-generating centres in the simple leaves of Myriophyllum aquaticum: evidence for KN1-like activity.

250. The aquatic leaf beetle species Macroplea mutica and M. appendiculata (Coleoptera, Chrysomelidae, Donaciinae) differ in their use of Myriophyllum spicatum as a host plant.

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