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Journal articles on the topic 'Cyclops3D'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Muellner, T., R. Kdolsky, K. Großschmidt, R. Schabus, O. Kwasny, and H. Plenk Jr. "Cyclops and cyclopoid formation after anterior cruciate ligament reconstruction: clinical and histomorphological differences." Knee Surgery, Sports Traumatology, Arthroscopy 7, no. 5 (September 27, 1999): 284–89. http://dx.doi.org/10.1007/s001670050165.

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2

Weisse, Thomas, Dunja Lukić, and Xiaoteng Lu. "Container volume may affect growth rates of ciliates and clearance rates of their microcrustacean predators in microcosm experiments." Journal of Plankton Research 43, no. 2 (March 2021): 288–99. http://dx.doi.org/10.1093/plankt/fbab017.

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Abstract We studied the effect of volume in small containers (microcosms) on five common planktonic freshwater ciliates and three zooplankton species, namely Daphnia sp., the calanoid copepod Eudiaptomus sp., and the cyclopoid copepod Cyclops sp. We measured ciliate specific growth rates and their loss rates due to microcrustacean predation in short-term experiments. We hypothesized that container volume ranging from 10 to 200 mL would not affect the activity of our prey and predator species. We found that the response to volume was species-specific; growth rates of three ciliate species were sensitive to volume. However, the volume effect was not unequivocal because different timing of the microcosm experiments (block effects) may have caused random bias due to varying morphological and/or physiological conditions of the ciliates and their predators. For predator clearance rate, the volume effect was insignificant in the filter-feeding Daphnia and Eudiaptomus but was significant for the predatory copepod Cyclops, which was hampered in the smallest experimental containers. Total crustacean clearance rates averaged over all treatments appeared unaffected by predator species, while ciliate species significantly affected the results. Our growth and clearance rates are close to previous findings with the same or similar planktonic prey and predator species.

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3

Burghard, Wiebke, and Gerhard Maier. "THE EFFECT OF TEMPERATURE ON MATING DURATION IN THE FRESHWATER CYCLOPOID COPEPOD CYCLOPS VICINUS (ULJANIN, 1875)." Crustaceana 73, no. 10 (2000): 1259–62. http://dx.doi.org/10.1163/156854000505236.

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4

Kobari, Toru, and Syuhei Ban. "Life cycles of two limnetic cyclopoid copepods, Cyclops vicinus and Thermocyclops crassus, in two different habitats." Journal of Plankton Research 20, no. 6 (1998): 1073–86. http://dx.doi.org/10.1093/plankt/20.6.1073.

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5

Orfeo, Michela, Marc Ventura, Barbara Tartarotti, and Ruben Sommaruga. "Body distribution and source of mycosporine-like amino acids in the cyclopoid copepod Cyclops abyssorum tatricus." Journal of Plankton Research 33, no. 9 (May 9, 2011): 1430–44. http://dx.doi.org/10.1093/plankt/fbr037.

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6

Salvo, Flora, Dounia Hamoutene, and Suzanne C. Dufour. "Trophic analyses of opportunistic polychaetes (Ophryotrocha cyclops) at salmonid aquaculture sites." Journal of the Marine Biological Association of the United Kingdom 95, no. 4 (February 11, 2015): 713–22. http://dx.doi.org/10.1017/s0025315414002070.

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A new species of dorvilleid polychaete,Ophryotrocha cyclops, has been observed on the rocky seafloor underneath deep salmonid aquaculture sites on the south coast of Newfoundland, Canada. The distribution of these opportunistic worms is likely related to organic matter accumulation on the seafloor, and this species may have a role in remediation processes. To better understand the functional role ofO. cyclopsat aquaculture sites, it is important to know what they feed upon. Here, stable isotope analyses (δ13C, δ15N and δ34S) and trace element analyses were performed on dorvilleids and their potential food sources at three aquaculture sites. Stable isotope analyses revealed spatial and temporal variation in the isotopic carbon signature ofO. cyclops, highlighting possible differences in the food sources of individual dorvilleids within and between sites. The isotopic composition of dorvilleids was closest to that of fish pellets; the presence of abundant lipid droplets in gut epithelial cells ofO. cyclopssuggests the assimilation of fish pellet-derived lipids. Trace element analysis indicated thatO. cyclopsdoes not concentrate the aquaculture tracers Zn or Cu to a large extent. However, concentrations of sulphur were high inO. cyclopscompared with other sources. Taken together, results show thatO. cyclopsmost likely consume both fish pellets and flocculent matter-associated bacteria. As such, they are involved in sulphur cycling and fish pellet degradation at aquaculture sites.

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7

Kettle, W. D., M. F. Moffett, and F. deNoyelles Jr. "Vertical Distribution of Zooplankton in an Experimentally Acidified Lake Containing a Metalimnetic Phytoplankton Peak." Canadian Journal of Fisheries and Aquatic Sciences 44, S1 (December 18, 1987): s91—s95. http://dx.doi.org/10.1139/f87-284.

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A large biomass of phytoplankton occurred as a narrow band in the metalimnion of a small Canadian Shield lake which had been undergoing experimental acidification. This community represented the maximum concentration of algal biomass in the lake and was composed of small phytoplankton species. The diurnal distribution of crustacean zooplankton was determined in relation to this potential food source. Cyclopoid nauplii, Cyclops bicuspidatus thomasi, and Daphnia catawba remained diurnally associated with the peak while other species were uniformly distributed throughout the water column. Those species which remained diurnally associated with the peak were exposed to the greatest food concentration in the lake and were also exposed to lower acid conditions than those in the upper waters. A deep-dwelling phytoplankton community may offer a refuge for some zooplankton species in acid lakes by providing a large food supply under less acidic conditions. The importance of sampling acid lakes through the entire water column is supported by these observations.

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8

Schaffner, William R. "Effects of Neutralization and Addition of Brook Trout (Salvelinus fontinalis) on the Limnetic Zooplankton Communities of Two Acidic." Canadian Journal of Fisheries and Aquatic Sciences 46, no. 2 (February 1, 1989): 295–305. http://dx.doi.org/10.1139/f89-040.

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The zooplankton communities in two acidified lakes in the Adirondack region of New York changed considerably following liming and the reintroduction of brook trout (Salvelinus fontinalis). Most rotifer taxa were greatly reduced in numbers within a week following base addition. Keratella taurocephala declined by orders of magnitude in both lakes. Rotifer species that replaced K. taurocephala were far less abundant. The crustacean communities were also affected by liming. Diaptomus minutus, the dominant in both lakes, declined following base addition. Longer-term population responses appeared to be related to the dynamics of the individual populations, and changes in predation pressure. Four additional crustacean species became prominent in the lakes after liming: the caldocerans Bosmina longirostris and Daphnia catawba in Cranberry Pond, and D. catawba and the cyclopoid copepod Cyclops scutifer in Woods Lake. Over the longer-term liming and the introduction of brook trout tended to have an overall positive effect on the zooplankton communities in the two lakes.

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9

Marten, Gerald G., and Janet W. Reid. "CYCLOPOID COPEPODS." Journal of the American Mosquito Control Association 23, sp2 (July 2007): 65–92. http://dx.doi.org/10.2987/8756-971x(2007)23[65:cc]2.0.co;2.

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10

Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 42, no. 2 (April 2007): 199. http://dx.doi.org/10.3129/can.j.ophthalmol.i07-037.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 42, no. 3 (June 2007): 375. http://dx.doi.org/10.3129/i07-069.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 45, no. 4 (August 2010): 327. http://dx.doi.org/10.1016/s0008-4182(10)80130-9.

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Chi, Ying-Ju, Ricardo Oliveira, and Lixia Zhang. "Cyclops." ACM SIGCOMM Computer Communication Review 38, no. 5 (September 30, 2008): 5–16. http://dx.doi.org/10.1145/1452335.1452337.

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Steinbach, Martin J. "CYCLOPS." Canadian Journal of Ophthalmology 43, no. 3 (2008): 284. http://dx.doi.org/10.1139/i08-054.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 46, no. 6 (December 2011): 469. http://dx.doi.org/10.1016/j.jcjo.2011.09.003.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 47, no. 1 (February 2012): 3. http://dx.doi.org/10.1016/j.jcjo.2011.12.014.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 47, no. 2 (April 2012): 105. http://dx.doi.org/10.1016/j.jcjo.2012.03.001.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 49, no. 5 (October 2014): 406. http://dx.doi.org/10.1016/j.jcjo.2014.08.001.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 50, no. 4 (August 2015): 256. http://dx.doi.org/10.1016/j.jcjo.2015.06.002.

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Steinbach, Martin J. "Cyclops." Canadian Journal of Ophthalmology 50, no. 5 (October 2015): 337. http://dx.doi.org/10.1016/j.jcjo.2015.08.006.

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21

Hansen, Anne-Mette, and Barbara Santer. "The influence of food resources on the development, survival and reproduction of the two cyclopoid copepods: Cyclops vicinus and Mesocyclops leuckarti." Journal of Plankton Research 17, no. 3 (1995): 631–46. http://dx.doi.org/10.1093/plankt/17.3.631.

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22

Kambhampati, Srinivas B. S., Srikanth Gollamudi, Saseendar Shanmugasundaram, and Vidyasagar V. S. Josyula. "Cyclops Lesions of the Knee: A Narrative Review of the Literature." Orthopaedic Journal of Sports Medicine 8, no. 8 (August 1, 2020): 232596712094567. http://dx.doi.org/10.1177/2325967120945671.

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Cyclops lesion is a known complication of anterior cruciate ligament reconstruction (ACLR). Although the incidence of cyclops lesion appears to be decreasing, it remains an important cause of restriction of extension after ACLR. We reviewed the available literature regarding the cyclops lesion and syndrome and cyclops-like lesions to analyze available evidence on cyclops lesions and variants of cyclops lesions. A keyword search in PubMed, Scopus, Web of Science, and EMBASE, Ovid Medline, and Ovid journals provided 47 relevant articles in the English literature, which were used to create this review. We classified cyclops lesions based on clinical presentation, pathology, and location. Risk factors, management options, tips to reduce the condition, and controversies related to the condition have been discussed. Female sex, greater graft volume, bony avulsion injuries, excessively anterior tibial tunnel, double-bundle ACLR, and bicruciate-retaining arthroplasty appear to predispose patients to cyclops lesions. Cyclops syndrome is a cyclops lesion that causes a loss of terminal extension. Arthroscopic debridement is an effective treatment for cyclops syndrome, whereas cyclops lesions are usually managed conservatively. It is important to distinguish between cyclops lesion and cyclops syndrome, as management differs based on symptoms. Cyclops lesion is diagnosed using magnetic resonance imaging. The management of choice for symptomatic lesions is surgical excision. Outcomes after excision are very good, and recurrence is rare.

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23

Choi, Jong-Yun, and Seong-Ki Kim. "The Use of Winter Water Temperature and Food Composition by the Copepod Cyclops vicinus (Uljanin, 1875) to Provide a Temporal Refuge from Fish Predation." Biology 10, no. 5 (May 1, 2021): 393. http://dx.doi.org/10.3390/biology10050393.

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Frequent predation induces various defense strategies in prey, including morphological changes or migration patterns in zooplankton. We hypothesized that the winter dominance of Cyclops vicinus in the Upo Wetlands, South Korea, is an evolved temporal defense mechanism to avoid fish predation. Long-term data (2014–2019) showed that fish consumed the most cyclopoid copepods from spring to autumn. Lepomis macrochirus preferentially consumed C. vicinus; thus, C. vicinus density was lower from spring to autumn. However, C. vicinus was abundant in winter when fish consumed fewer copepods. Nauplii density began to increase in late autumn (October–November), and their population growth was fueled through consumption of Cyclotella sp. and Rhodomonas sp. Culture experiments showed that Cyclotella sp. contributed more to the growth stage (copepodite or subadult) after nauplii than Rhodomonas sp. C. vicinus density was lower in the winters of 2013 and 2016 when the densities of these phytoplankton prey species were lower. In summary, although winter conditions were suitable for copepod survival and population growth, C. vicinus relied heavily on the diversity and species composition of its food sources. The winter dominance of C. vicinus could increase regional biodiversity and contribute significantly to the stability of the freshwater food web.

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24

Kadhar, Abdul, Arun Kumar, Jawahar Ali, and Akbar John. "Studies on the Survival and Growth of Fry ofCatla catla(Hamilton, 1922) Using Live Feed." Journal of Marine Biology 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/842381.

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Effect of live feed on the survival and growth of fry ofCatla catlausing three different live feeds namely, Cyclopoid (Thermocyclops decipiens), Cladoceran (Moina micrura), and mixed diet (Cyclopoid and Cladoceran) were studied. Commercial feed (Sunder’s feed) was used as control. Feeding experiments were carried out in 100 L tanks for 40 days. Fish fry fed with the mixed diet showed significantly better survival rate (54.80 ± 2.43%) than those fed with other food types(P<0.001). Fish fry fed with Cyclopoid had significantly(P<0.001)better growth (26.03 ± 1.88 mm, weight 61.07 ± 3.53 mg) than those fed with other food types. Biochemical studies showed higher level of protein, carbohydrate, and lipid content inCatlafry fed with Cyclopoid diet. The results are discussed in the light of the literature available. It could be suggested that the Cyclopoid diet can be used as live feed for effective production ofCatlafry.

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25

Dumas, Pascal, and Françoise Lescher-Moutoué. "Cyclopoid distribution in an agriculturally impacted alluvial aquifer." Fundamental and Applied Limnology 150, no. 3 (January 20, 2001): 511–28. http://dx.doi.org/10.1127/archiv-hydrobiol/150/2001/511.

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26

Dörücü, Mustafa. "DIFFERENCES IN OXYGEN CONSUMPTION, REPRODUCTION, FEEDING, AND GROWTH OF THE FRESHWATER CYCLOPOID COPEPOD CYCLOPS VICINUS (ULJANIN, 1875), INFECTED WITH A CESTODA PROCERCOID." Crustaceana 75, no. 5 (2002): 711–15. http://dx.doi.org/10.1163/156854002760202697.

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27

Maier, Gerhard. "The effect of temperature on the development, reproduction, and longevity of two common cyclopoid copepods ? Eucyclops serrulatus (Fischer) and Cyclops strenuus (Fischer)." Hydrobiologia 203, no. 3 (September 1990): 165–75. http://dx.doi.org/10.1007/bf00005685.

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28

Einsle, Ulrich K. "Cyclops canadensis n.sp. and Cyclops scutifer Sars, 1863 (Crustacea: Copepoda) from northern Canada." Canadian Journal of Zoology 66, no. 10 (October 1, 1988): 2146–49. http://dx.doi.org/10.1139/z88-319.

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The occurrence and distribution of Cyclops s.str. species (strenuus subgroup) in Canada and the United States has not yet been reliably studied. In this first attempt, Cyclops scutifer Sars, 1863 is characterized, and a new species, Cyclops canadensis, is established. As no cytological investigations were possible, the species are described on the basis of morphological and morphometrical data. Most probably, the new species, Cyclops canadensis, formerly was identified as Cyclops strenuus.

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29

Michelini, Ann, and Richard Seaford. "Euripides: Cyclops." Classical World 80, no. 6 (1987): 448. http://dx.doi.org/10.2307/4350100.

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30

Isaakyan, Irina L. "Cyclops Cave." Symbolic Interaction 32, no. 3 (August 2009): 207–35. http://dx.doi.org/10.1525/si.2009.32.3.207.

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31

Almási, George, Cǎlin Caşcaval, José G. Castaños, Monty Denneau, Derek Lieber, José E. Moreira, and Henry S. Warren. "Dissecting Cyclops." ACM SIGARCH Computer Architecture News 31, no. 1 (March 2003): 26–38. http://dx.doi.org/10.1145/773365.773369.

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32

Decher, Jan, and Jakob Fahr. "Hipposideros cyclops." Mammalian Species 763 (July 2005): 1–7. http://dx.doi.org/10.1644/1545-1410(2005)763[0001:hc]2.0.co;2.

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33

Rasch, Ellen M., and Grace A. Wyngaard. "Endopolyploidy in Cyclopoid Copepods." Journal of Crustacean Biology 28, no. 2 (May 2008): 412–16. http://dx.doi.org/10.1651/0278-0372(2008)028[0412:eicc]2.0.co;2.

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34

Rasch, Ellen M., and Grace A. Wyngaard. "Endopolyploidy in Cyclopoid Copepods." Journal of Crustacean Biology 28, no. 2 (January 1, 2008): 412–16. http://dx.doi.org/10.1163/20021975-99990385.

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35

Guerra-Pinto, Francisco, Mathieu Thaunat, Matt Daggett, Charles Kajetanek, Tiago Marques, Tales Guimaraes, Bénédicte Quelard, and Bertrand Sonnery-Cottet. "Hamstring Contracture After ACL Reconstruction Is Associated With an Increased Risk of Cyclops Syndrome." Orthopaedic Journal of Sports Medicine 5, no. 1 (January 1, 2017): 232596711668412. http://dx.doi.org/10.1177/2325967116684121.

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Background: Cyclops syndrome is characterized by loss of terminal knee extension due to proliferative fibrous nodule formation in the intercondylar notch. This complication occurs in the early postoperative period after anterior cruciate ligament reconstruction (ACLR). The pathogenesis of Cyclops syndrome is not well understood. Hypothesis: Persistent hamstring contracture after ACLR is associated with an increased risk of subsequent Cyclops syndrome. Study Design: Case-control study; Level of evidence, 3. Methods: The files of 45 patients who underwent arthroscopic debridement of a Cyclops lesion after ACLR were analyzed. Recorded data included demographic information and technical details of surgery. Preoperative magnetic resonance images were also analyzed, and patients with femoral bone bruising were identified. Passive and active range of motion were recorded in all patients preoperatively and at 3 and 6 weeks after surgery to address the Cyclops lesion. Passive extension deficit was evaluated in comparison with the contralateral limb and classified as secondary to hamstring contracture when contracture was observed and palpated in the prone position and when the extension deficit was reversed after exercises performed to fatigue the hamstrings. A control group was selected using a random numbers table among our entire ACLR cohort. Statistical analysis was performed to analyze differences between the 2 groups. Results: There was no significant difference between the groups with regard to age at ACLR, sex distribution, time from injury to surgery ( P > .05), proportion of professional athletes, presence of femoral bone bruise, or technical aspects of surgery. The overall extension deficit incidence was significantly higher in the Cyclops group at 3 weeks (Cyclops, 71%; control, 22%) ( P < .001) and at 6 weeks (Cyclops, 60%; control, 7%) ( P < .001). The extension deficit related to hamstring contracture was significantly higher in the Cyclops group at 3 weeks (Cyclops, 58%; control, 22%) ( P < .001) and at 6 weeks (Cyclops, 29%; control, 2%) ( P < .001). Conclusion: The Cyclops lesion is associated with a persistent hamstring contracture at 3 and 6 weeks after ACLR.

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36

Gaponova, L. P. "The Seasonal Population Dynamics of the Cyclopoid Copepods (Cyclopoida, Cyclopidae) in Ponds of Kyiv Region (Ukraine)." Vestnik Zoologii 48, no. 4 (August 1, 2014): 377–81. http://dx.doi.org/10.2478/vzoo-2014-0046.

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Abstract The seasonal variation of faunistic complexes of cyclopids has been monitored over 2007-2010 in ponds of tributary of the Vita River. The results of our investigation showed that eurythermal complex of cyclopid species dominated in all seasons except for summer period. In contrast to the previous studies, in summer period warm-water stenothermal complex of cyclopid species were the most abundant and reached the highest cyclopid nu`mbers

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37

"Cyclops." Canadian Journal of Ophthalmology 42, no. 1 (February 2007): 17. http://dx.doi.org/10.3129/can.j.ophthalmol.06-125.

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"Cyclops." Canadian Journal of Ophthalmology 41, no. 6 (December 2006): 673. http://dx.doi.org/10.3129/i06-084.

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"Cyclops." Canadian Journal of Ophthalmology 42, no. 4 (August 2007): 523. http://dx.doi.org/10.3129/i07-128.

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"Cyclops." Canadian Journal of Ophthalmology 42, no. 5 (October 2007): 664. http://dx.doi.org/10.3129/i07-148.

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"Cyclops." Canadian Journal of Ophthalmology 42, no. 6 (December 2007): 793. http://dx.doi.org/10.3129/i07-191.

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"Cyclops." Canadian Journal of Ophthalmology 43, no. 1 (February 2008): 19. http://dx.doi.org/10.3129/i07-216.

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"Cyclops." Canadian Journal of Ophthalmology 43, no. 2 (April 2008): 159. http://dx.doi.org/10.3129/i08-031.

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"Cyclops." Canadian Journal of Ophthalmology 43, no. 3 (June 2008): 284. http://dx.doi.org/10.3129/i08-054.

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"Cyclops." Canadian Journal of Ophthalmology 43, no. 4 (August 2008): 401. http://dx.doi.org/10.3129/i08-101.

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"Cyclops." Canadian Journal of Ophthalmology 43, no. 6 (December 2008): 637. http://dx.doi.org/10.3129/i08-125.

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"Cyclops." Canadian Journal of Ophthalmology 44, no. 1 (February 2009): 15. http://dx.doi.org/10.3129/i08-173.

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"Cyclops." Canadian Journal of Ophthalmology 44, no. 2 (April 2009): 141. http://dx.doi.org/10.3129/i09-032.

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"Cyclops." Canadian Journal of Ophthalmology 44, no. 5 (October 2009): 511. http://dx.doi.org/10.3129/i09-174.

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"Cyclops." Canadian Journal of Ophthalmology 44, no. 6 (2009): 649. http://dx.doi.org/10.3129/i09-226.

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