• Korean journal of applied entomology
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• v.48 no.3
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• pp.347-354
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• 2009

This study was conducted on the biological control effects of the natural enemy, Amblyseius cucumeris, against Polyphagotarsonemus latus. The broad mite moved to a new habitat after the carrying capacity of the preferred habitat on the upper leaf has been reached. Population dynamics between predator, Amblyseius cucumeris, and prey, P. latus, were quite well synchronized since the predator followed the movement of the prey. In predation test by Amblyseius cucumeris on P. latus, A. cucumeris fed on 8.8, 15.2, 27.0 and 30.3 individuals/day under the temperatures of 15, 20, 25, and $30^{\circ}C$, respectively. The A. cucumeris larva, protonymph, deutonymph, adult male, and adult female fed on 0.5, 1.6, 5.2, 3.8, and 27 individuals of adult P. latus per day, respectively, under $25^{\circ}C$ condition. The functional response curve of adult P. latus to the densities of A. cucumeris showed Holling's Type II curve. The consumption of prey by A. cucumeris increased with the prey density increase, but the consumption rate decreased. The critical ratio of predator vs. prey effectively to suppress (98% over) the population of P. latus by releasing A. cucumeris was 1:40 on red pepper.

• ALGAE
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• v.34 no.2
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• pp.127-140
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• 2019

The species in the dinoflagellate order Suessiales have 5-24 latitudinal paraplate series and include many fossil and extant species. There have been a few studies on the ecophysiology of the phototrophic species Biecheleriopsis adriatica, and no study on its predators. Thus, we explored the feeding occurrence by common heterotrophic protists on B. adriatica and the growth and ingestion rates of the heterotrophic dinoflagellate Oxyrrhis marina on B. adriatica BATY06 as a function of prey concentration. The common heterotrophic dinoflagellates Aduncodinium glandula, O. marina, Gyrodinium dominans, Gyrodinium moestrupii, Luciella masanensis, Pfiesteria piscicida, and Oblea rotunda and two naked ciliates Strombidinopsis sp. and Pelagostrobilidium sp. were able to feed on B. adriatica, but the heterotrophic dinoflagellate Polykrikos kofoidii was not. However, B. adriatica supported the positive growth of O. marina, but did not support that of G. dominans and O. rotunda. With increasing prey concentrations, the growth and ingestion rates of O. marina on B. adriatica increased and became saturated. The maximum growth rate of O. marina on B. adriatica was $0.162d^{-1}$. Furthermore, the maximum ingestion rate of O. marina on B. adriatica was $0.2ng\;C\;predator^{-1}\;d^{-1}$ ($2.0cells\;predator^{-1}\;d^{-1}$). In the order Suessiales, the feeding occurrence by common heterotrophic protists on B. adriatica is similar to that on Effrenium voratum and Biecheleria cincta, but different from that on Yihiella yeosuensis. However, the growth and ingestion rates of O. marina on B. adriatica are considerably lower than those on E. voratum and B. cincta, but higher than those on Y. yeosuensis. Therefore, B. adriatica may be less preferred prey for O. marina than E. voratum and B. cincta, but more preferred prey than Y. yeosuensis.

• ALGAE
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• v.37 no.1
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• pp.49-62
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• 2022

Water temperature affects plankton survival and growth. The dinoflagellate Shimiella gracilenta survives using the plastids of ingested prey, indicating kleptoplastidy. However, studies on the effects of water temperature on kleptoplastidic dinoflagellates are lacking. We explored the growth and ingestion rates of S. gracilenta as a function of water temperature. Furthermore, using data on its spatiotemporal distribution in Korean coastal waters during 2015-2018, we predicted its distribution under elevated temperature conditions of +2, +4, and +6℃. Growth rates of S. gracilenta with and without Teleaulax amphioxeia prey as well as ingestion rates were significantly affected by water temperature. Growth rates of S. gracilenta with and without prey were positive or zero at 5-25℃ but were negative at ≥30℃. The maximum growth rate of S. gracilenta with T. amphioxeia was 0.85 d^-1, achieved at 25℃, and 0.21 d^-1 at 20℃ without prey. The ingestion rate of S. gracilenta on T. amphioxeia at 25℃ (0.05 ng C predator^-1 d^-1) was greater than that at 20℃ (0.04 ng C predator^-1 d^-1). Thus, feeding may shift the optimal temperature for the maximum growth rate of S. gracilenta from 20 to 25℃. In spring and winter, the distributions of S. gracilenta under elevated temperature conditions were predicted not to differ from those during 2015-2018. However, S. gracilenta was predicted not to survive at some additional stations under elevated temperature conditions of +2, +4, and +6℃ in summer or under elevated temperature conditions of +6℃ in autumn. Therefore, global warming may affect the distribution of S. gracilenta.

• Journal of applied mathematics & informatics
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• v.17 no.1_2_3
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• pp.195-215
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• 2005

In this paper, we investigate the dynamics of the mathematical model of two non-interacting preys in presence of their common natural enemy (predator) based on the non-autonomous differential equations. We establish sufficient conditions for the permanence, extinction and global stability in the general non-autonomous case. In the periodic case, by means of the continuation theorem in coincidence degree theory, we establish a set of sufficient conditions for the existence of a positive periodic solutions with strictly positive components. Also, we give some sufficient conditions for the global asymptotic stability of the positive periodic solution.

• ALGAE
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• v.31 no.1
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• pp.17-31
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• 2016

To explore the feeding ecology of the newly described heterotrophic dinoflagellate Aduncodinium glandula in the family Pfiesteriaceae, its feeding behavior and prey species were investigated. Additionally, the growth and ingestion rates of A. glandula on the mixotrophic dinoflagellates Heterocapsa triquetra and Akashiwo sanguinea, its optimal and suboptimal prey, respectively were measured. A. glandula fed on prey through a peduncle after anchoring to the prey using a tow filament. A. glandula ate all algal prey and perch blood cells tested and had the most diverse prey species in the family Pfiesteriaceae. Unlike for other pfiesteriacean species, H. triquetra and A. sanguinea support the positive growth of A. glandula. However, the cryptophytes Rhodomonas salina and Teleaulax sp. and the phototrophic dinoflagellate Amphidinium carterae did not support the positive growth of A. glandula. Thus, A. glandula may have a unique kind of prey and its optimal prey differs from that of the other pfiesteriacean dinoflagellates. With increasing mean prey concentration, the growth rates of A. glandula on H. triquetra and A. sanguinea increased rapidly and then slowed or became saturated. The maximum growth rates when feeding on H. triquetra and A. sanguinea were 1.004 and 0.567 d⁻¹, respectively. Further, the maximum ingestion rates of A. glandula on H. triquetra and A. sanguinea were 0.75 and 1.38 ng C predator⁻¹ d⁻¹, respectively. There is no other pfiesteriacean species having H. triquetra and A. sanguinea as optimal and suboptimal prey. Thus, A. glandula may be abundant during blooms dominated by these species not preferred by the other pfiesteriacean dinoflagellates.

• Honam Mathematical Journal
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• v.30 no.2
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• pp.259-272
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• 2008

We are concerned with the robust control problem for the chemotaxis equations with predator-prey dynamics. That is, we present the existence and uniqueness of the solution. We also show the existence of the robust control and deduce the corresponding optimality conditions.

• Journal of the Chungcheong Mathematical Society
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• v.10 no.1
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• pp.87-95
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• 1997

In general, the positive solution to biological reaction-diffusion equations is not unique. In this paper, we state the sufficient and necessary conditions of the existence of positive solutions, and give and the proof for the uniqueness of positive solutions for a certain elliptic interacting system.

• Korean journal of applied entomology
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• v.48 no.2
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• pp.123-158
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• 2009

An attempt was made to stimulate future research by providing exemplary information, which would integrate published knowledge to solve specific pest problem caused by resistance. This review was directed to find a way for delaying resistance development with consideration of chemical(s) nature, of mixture, rotation, or mosaics, and of insecticide(s) compatible with the biological agents in integrated pest management (IPM). The application frequency, related to the resistance development, was influenced by insecticide activity from potentiation, residual period, and the vulnerability to resistance development of chemical, with secondary pest. Chemical affected feeding, locomotion, flight, mating, and predator avoidance. Insecticides with negative cross-resistance by the difference of target sites and mode of action would be adapted to mixture, rotation and mosaic. Mixtures for delaying resistance depend on each component killing very high percentage of the insects, considering allele dominance, cross-resistance, and immigration and fitness disadvantage. Potential disadvantages associated with mixtures include disruption of biological control, resistance in secondary pests, selecting very resistant population, and extending cross-resistance range. The rotation would use insecticides in high and low doses, or with different metabolic mechanisms. Mosaic apply insecticides to the different sectors of a grid for highly mobile insects, spray unrelated insecticides to sedentary aphids in different areas, or mix plots of insecticide-treated and untreated rows. On the evolution of pest resistance, selectivity and resistance of parasitoids and predator decreased the number of generations in which pesticide treatment is required and they could be complementary to refuges from pesticides To enhance the viability of parasitoids, the terms on the insecticides selectivity and factors affecting to the selectivity in field were examined. For establishment of resistant parasitoid, migration, survivorship, refuge, alternative pesticides were considered. To use parasitoids under the pressure of pesticides, resistant or tolerant parasitoids were tested, collected, and/or selected. A parasitoid parasitized more successfully in the susceptible host than the resistant. Factors affecting to selective toxicity of predator are mixing mineral oil, application method, insecticide contaminated prey, trait of individual insecticide, sub-lethal doses, and the developmental stage of predators. To improve the predator/prey ratio in field, application time, method, and formulation of pesticide, reducing dose rate, using mulches and weeds, multicropping and managing of surroundings are suggested. Plant resistance, predator activity, selective insect growth regulator, and alternative prey positively contributed to the increase of the ratio. Using selective insecticides or insecticide resistant predator controlled its phytophagous prey mites, kept them below an economic level, increased yield, and reduced the spray number and fruits damaged.

• 제어로봇시스템학회:학술대회논문집
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• 2001.10a
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• pp.164.1-164
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• 2001

Q-learning is a recent reinforcement learning algorithm that does not need a modeling of environment and it is a suitable approach to learn behaviors for autonomous agents. But when it is applied to multi-agent learning with many I/O states, it is usually too complex and slow. To overcome this problem in the multi-agent learning system, we propose the successive Q-learning algorithm. Successive Q-learning algorithm divides state-action pairs, which agents can have, into several Q-functions, so it can reduce complexity and calculation amounts. This algorithm is suitable for multi-agent learning in a dynamically changing environment. The proposed successive Q-learning algorithm is applied to the prey-predator problem with the one-prey and two-predators, and its effectiveness is verified from the efficient avoidance ability of the prey agent.

• The Pure and Applied Mathematics
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• v.25 no.4
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• pp.345-355
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• 2018

This paper looks into phase plane behavior of the solution near the positive steady-state for the system with prey density dependent response functions. The positive invariance and boundedness property of the solution to the objective model are proved. The existence result of a positive steady-state and asymptotic analysis near the positive constant equilibrium for the objective system are of interest. The results of phase plane analysis for the system are proved by observing the asymptotic properties of the solutions. Also some numerical analysis results for the behaviors of the solutions in time are provided.