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1 regulation, effectively reducing the spring algal bloom.
2 es but appeared to be absent during the post algal bloom.
3 from episodic disturbances, such as harmful algal blooms.
4 some additional mechanisms of regulation of algal blooms.
5 f available nutrients and the termination of algal blooms.
6 take up to 0.3 micromol.m(-2).s(-1) in dense algal blooms.
7 s or one with potentially disruptive harmful algal blooms.
8 yanotoxin microcystin-LR produced by harmful algal blooms.
9 es, (2) microbial community structure during algal blooms.
10 n degradation, a prominent polysaccharide in algal blooms.
11 anobacteria and Chlorophyta mainly dominated algal blooms.
12 ing as a key biological indicator of harmful algal blooms.
13 articularly as major contributors of harmful algal blooms.
14 king management decisions related to harmful algal blooms.
15 ystems, including the development of harmful algal blooms.
16 eases the frequency and intensity of harmful algal blooms.
17 fe nature-based solution for combating toxic algal blooms.
18 induce respiratory syndromes during harmful algal blooms.
19 d lead to harmful ecological events, such as algal blooms.
20 enters the marine food chain during harmful algal blooms.
21 pounds in contaminated water such as harmful algal blooms.
22 ions in regulating the occurrence of harmful algal blooms.
23 smarter bio-hydrochar materials by utilizing algal blooms.
24 -eutrophication and it is plagued by harmful algal blooms.
25 nd can accelerate eutrophication and harmful algal blooms.
26 itating the formation of large scale harmful algal blooms.
27 cluding the potential development of harmful algal blooms.
28 e waters impaired by wastewater effluents or algal blooms.
31 ypoxia)(1) and increases in the incidence of algal blooms.Although recent work has suggested that ind
32 ion, with peak N(SSA) during the first mixed algal bloom and a decline during the G. huxleyi bloom an
33 Biomagnification occurred during the pre algal bloom and algal bloom phases but appeared to be ab
34 ater samples were collected during a harmful algal bloom and analyzed by LC-MS with simultaneous HRMS
36 aquatic ecosystems with nutrients leading to algal blooms and anoxic events) is a persistent conditio
37 can be released to the water during harmful algal blooms and are a serious threat to animals and hum
38 monly encountered macroalgal species forming algal blooms and are responsible for many Green Tide eve
40 cated in key ecological phenomena (including algal blooms and diel vertical migration) that shape the
41 rimary producers in the oceans, the cause of algal blooms and endosymbionts of marine invertebrates.
43 Erie has experienced a resurgence of harmful algal blooms and hypoxia driven by increased nutrient lo
47 ication or decline, particularly in areas of algal blooms and near coral reefs, as well as in areas a
48 rope and North America show that controlling algal blooms and other symptoms of eutrophication depend
49 e environment has focused primarily on toxic algal blooms and pathogenic bacteria that multiply in nu
51 iogeochemical environmental perturbations on algal blooms and their influence on biospheric environme
52 e fluids is important to many natural (e.g., algal blooms) and industrial (e.g., biofuel, vaccine pro
54 and treated waters include chemical spills, algal blooms, and increased salinization, organoleptic e
55 ater, cyanobacterial cultures, extracts, and algal blooms, and may be useful in detecting metabolites
57 of the most toxic compounds produced by the algal blooms, and reveal that the degradation efficiency
58 minant sources of TONO and their precursors, algal blooms, and to a lesser degree agricultural or sto
60 poxia, disease outbreaks and toxin-producing algal blooms are all possible causes of mass mortality e
65 s, for example, the increased persistence of algal blooms as observed in our mesocosm experiment.
68 cteria may play a role in regulating harmful algal blooms, but little is known about the biochemical
69 physiological traits associated with harmful algal blooms, but the genetic basis for this variation i
70 esponse to a Karenia brevis red tide harmful algal bloom by examining sound spectrum levels recorded
71 for modelling outcome of grazing control of algal blooms by zooplankton in nutrient-rich ecosystems.
73 Pond slime is a problem in garden pools, algal blooms can produce toxins that incapacitate or kil
79 ce the development of cyanobacterial harmful algal blooms (cHABs), but those biotic factors are poorl
80 obal proliferation of cyanobacterial harmful algal blooms (CHABs), yet we have limited understanding
81 lgal biodiversity and species distributions, algal bloom control, dimethyl sulphide formation and gen
82 tified in a Lake Erie cyanobacterial harmful algal bloom (cyanoHAB), using high-resolution UHPLC-MS a
83 the proliferation of cyanobacterial harmful algal blooms (cyanoHABs) and production of the hepatotox
88 synthetic prokaryotes, but some form harmful algal blooms (cyanoHABs) that disrupt ecosystems and pro
89 produced during some cyanobacterial harmful algal blooms (cyanoHABs), can harm ecosystems and requir
90 acteria and eukaryotes in urban lakes during algal bloom development stage (i.e., April, May, and Jun
95 tion of karlotoxin 2 (KmTx2; 1), the harmful algal bloom dinoflagellate Karlodinium sp. was collected
96 s lowest in the central basin with recurrent algal blooms due to their shading effect and is highest
97 ngs underscore the complex interplay between algal bloom dynamics and SSA production, with implicatio
98 plore the effects of an Ecosystem Disruptive Algal Bloom (EDAB) on the microbial community separated
100 change pressures likely to influence harmful algal blooms, exposure to microcystin, a known hepatotox
101 dilution (MeHg burden per cell decreases in algal blooms), extending patterns of contaminant accumul
102 ons of DMS, HOBr, and CHBr(3) during typical algal bloom fluxes of DMS and HOBr (10(-13) to 10(-9) M
103 experiment revealed two main blooms: a mixed algal bloom followed by an extensive bloom of the coccol
104 an alleviate environmental issues, including algal bloom formation and greenhouse gas emissions from
106 tative morphological analysis of the harmful-algal-bloom-forming raphidophyte Heterosigma akashiwo to
108 in-producing microalga, which causes harmful algal blooms globally, frequently leading to massive fis
109 nto waterbodies, initiating numerous harmful algal bloom (HAB) events, especially in fragile ecosyste
112 sphorus (P) loads from the MRW drive harmful algal bloom (HAB) severity in Lake Erie; hence changes i
113 brevetoxins (PbTxs), produced by the harmful algal bloom (HAB) species Karenia brevis, are essential
124 aerosolization of toxins from marine harmful algal blooms (HABs) has been well documented, the aeroso
133 s is critical for early detection of harmful algal blooms (HABs) to enable efficient response by wate
134 With the increase in frequency of harmful algal blooms (HABs) worldwide, a better understanding of
135 can play a central role in promoting harmful algal blooms (HABs), and therefore many HAB studies to d
136 ies, mostly dinoflagellates, causing Harmful Algal Blooms (HABs), produce toxins which may affect the
142 Lake Erie, whereas a record-setting harmful algal bloom in 2011 was likely associated with only mild
143 1, Lake Erie experienced the largest harmful algal bloom in its recorded history, with a peak intensi
144 ake, Seattle during a cyanobacterial harmful algal bloom in the summer of 2014 were studied using a n
146 atersheds suggests greater potential to fuel algal blooms in coastal areas, especially given the like
148 and comprehensive assessment of the roles of algal blooms in generating fixed carbon for the food cha
150 The recent resurgence of hypoxia and harmful algal blooms in Lake Erie, driven substantially by phosp
151 encounter complex unsteady flows, including algal blooms in marine settings, microbial infections in
154 erial-algal interactions, control of massive algal blooms in the ocean, and the maintenance and degra
157 redictive biomarkers for forecasting harmful algal bloom initiation, potentially mitigating detriment
159 rence of multiple types of extremes, notably algal blooms, lake heatwaves, and low lake levels, have
161 ude an example of how compounds from harmful algal blooms may yield both tools for measuring environm
165 amplicon sequencing as a supporting tool in algal bloom monitoring or water-resource management.
166 nce data set collected during the spring ice-algal bloom near Utqiagvik, Alaska in 2021 to study sea-
168 ase whereas snowmelt duration, that controls algal blooms' occurrences, is less sensitive to global t
169 d in proximity to the sea concomitantly with algal blooms of Ostreopsis spp. in the Mediterranean are
171 presence, diversity and bioalbedo effects of algal blooms on Antarctic ice cap systems based on field
172 as attributed to a persistent Karenia brevis algal bloom or 'red tide' centered in Southwest Florida.
176 ecrease in snow albedo by red pigmented snow algal blooms over the course of one melt season can be 1
179 tion occurred during the pre algal bloom and algal bloom phases but appeared to be absent during the
182 se changes are predicted to increase harmful algal bloom prevalence and toxicity, as rising temperatu
184 80% relative abundance), coincided with the algal bloom raising questions about hydrocarbon exposure
185 vailability of Fe(EPS) in AS inoculums-after algal bloom-selects cyanobacteria, and the limitation of
186 mmediately after the death of massive annual algal blooms showed that no selenomethionine or selenome
187 th the global proliferation of toxic harmful algal bloom species, there is a need to identify the env
188 sults indicate that postfire ash loading and algal bloom stage may significantly affect DBP formation
189 Much of the evolutionary ecology of toxic algal blooms (TABs) remains unclear, including the role
190 eriences annual red tides, a type of harmful algal bloom that results from high concentrations of Kar
191 collected directly from Lake Erie during the algal blooms that affected 500000 residents in Toledo in
193 presents the first iRF application to marine algal blooms that helps to identify ocean, microbial, an
194 sota, USA suffers from recurring late summer algal blooms that often contain toxin-producing cyanobac
197 ritical research is needed regarding harmful algal blooms threatening ecosystem and human health, esp
198 om cultural eutrophication including harmful algal blooms, threatening both ecosystem and public heal
199 ion history, and six species causing harmful algal blooms, to determine the ecoregions most likely to
200 ation between exposure to the common harmful algal bloom toxin microcystin and the altered host gut m
201 Here, we address this challenge and quantify algal blooms' turnover using a combination of satellite
205 on local fisheries, proliferation of harmful algal blooms, water clarity, and submerged aquatic veget
206 roach to samples collected during an induced algal bloom, which enabled pairing active giant viruses
207 rophic, selenium-impacted river with massive algal blooms, which consisted of filamentous green algae
208 enic inputs of nutrients have fueled massive algal blooms, which deplete bottom waters of oxygen (O(2
209 ising temperatures increase the frequency of algal blooms, which often have negative effects such as
210 o linked to eutrophication and the spread of algal blooms with an increasing economic and environment
211 ning a critical nursery habitat into harmful algal blooms with catastrophic impacts on coastal ecosys
212 number concentration (N(SSA)) during induced algal blooms within three airtight mesocosm enclosures.