The Spatial Dynamics of Host--Parasitoid Systems
1. We consider models for host--parasitoid interactions in spatially patchy environments, where in each generation specified fractions of the host and parasitoid subpopulations in each patch move to adjacent patches. In most previous work of this general kind, the movement is not localized in this w...
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Veröffentlicht in: | The Journal of animal ecology 1992-01, Vol.61 (3), p.735-748 |
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description | 1. We consider models for host--parasitoid interactions in spatially patchy environments, where in each generation specified fractions of the host and parasitoid subpopulations in each patch move to adjacent patches. In most previous work of this general kind, the movement is not localized in this way, but involves `global' mixing of the populations prior to dispersal. 2. A remarkable range of dynamical behaviour is exhibited by a mathematically explicit model with constant host reproductive rate, deterministically unstable local dynamics and dispersing hosts and parasitoids that only move to nearest-neighbour patches in a density-independent way. The density of the host and parasitoid subpopulations in a two-dimensional array of patches may exhibit complex patterns of spiral waves, spatial chaos, a so-called static `crystal lattice' pattern, or they may become extinct. The probability of extinction rises rapidly when the number of patches present decreases below some characteristic arena size which varies with the scale of the spatial dynamics. 3. The different types of spatial dynamics that are observed depends critically on the fractions of hosts and adult parasitoids that disperse in each generation from the patches in which they emerged. Low rates of host dispersal tend to lead to chaotic patterns unless this rate is very low and parasitoid dispersal rates very high, in which case `crystal lattice' patterns may occur. Intermediate to high rates of host dispersal tend to result in spiral patterns. The effect of varying host rates of increase, within-patch parasitism that is inherently stabilizing and random patch-to-patch variation are also discussed. 4. The results are relatively insensitive to the details of the interaction. Thus, a similar range of behaviour (spirals, chaos and crystal lattices) is discernible from a very general `cellular automaton' model in which only qualitative categories of patch densities are specified together with a very simple set of `transition rules'. The diffusive dispersal of the explicit model is parallelled by making the new state in each generation depend, not only on the current state of the given `cell', but also on the states of a specified set of neighbouring cells. |
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We consider models for host--parasitoid interactions in spatially patchy environments, where in each generation specified fractions of the host and parasitoid subpopulations in each patch move to adjacent patches. In most previous work of this general kind, the movement is not localized in this way, but involves `global' mixing of the populations prior to dispersal. 2. A remarkable range of dynamical behaviour is exhibited by a mathematically explicit model with constant host reproductive rate, deterministically unstable local dynamics and dispersing hosts and parasitoids that only move to nearest-neighbour patches in a density-independent way. The density of the host and parasitoid subpopulations in a two-dimensional array of patches may exhibit complex patterns of spiral waves, spatial chaos, a so-called static `crystal lattice' pattern, or they may become extinct. The probability of extinction rises rapidly when the number of patches present decreases below some characteristic arena size which varies with the scale of the spatial dynamics. 3. The different types of spatial dynamics that are observed depends critically on the fractions of hosts and adult parasitoids that disperse in each generation from the patches in which they emerged. Low rates of host dispersal tend to lead to chaotic patterns unless this rate is very low and parasitoid dispersal rates very high, in which case `crystal lattice' patterns may occur. Intermediate to high rates of host dispersal tend to result in spiral patterns. The effect of varying host rates of increase, within-patch parasitism that is inherently stabilizing and random patch-to-patch variation are also discussed. 4. The results are relatively insensitive to the details of the interaction. Thus, a similar range of behaviour (spirals, chaos and crystal lattices) is discernible from a very general `cellular automaton' model in which only qualitative categories of patch densities are specified together with a very simple set of `transition rules'. The diffusive dispersal of the explicit model is parallelled by making the new state in each generation depend, not only on the current state of the given `cell', but also on the states of a specified set of neighbouring cells.</description><identifier>ISSN: 0021-8790</identifier><identifier>EISSN: 1365-2656</identifier><identifier>DOI: 10.2307/5627</identifier><identifier>CODEN: JAECAP</identifier><language>eng</language><publisher>Oxford: British Ecological Society</publisher><subject>Animal and plant ecology ; Animal ecology ; Animal, plant and microbial ecology ; Biological and medical sciences ; Cellular automata ; Chaos theory ; Crystal lattices ; Demecology ; Fundamental and applied biological sciences. Psychology ; General aspects ; Parasite hosts ; Parasitism ; Parasitoids ; Population density ; Population dynamics ; Spatial models</subject><ispartof>The Journal of animal ecology, 1992-01, Vol.61 (3), p.735-748</ispartof><rights>Copyright 1992 British Ecological Society</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c331t-f3d7dc9fa5e6a50271e343fc510992b724c261fd2954dbd3775058bdafaeefb53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/5627$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/5627$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27869,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4395072$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Comins, H.N.</creatorcontrib><creatorcontrib>Hassell, M.P.</creatorcontrib><creatorcontrib>May, R.M.</creatorcontrib><title>The Spatial Dynamics of Host--Parasitoid Systems</title><title>The Journal of animal ecology</title><description>1. We consider models for host--parasitoid interactions in spatially patchy environments, where in each generation specified fractions of the host and parasitoid subpopulations in each patch move to adjacent patches. In most previous work of this general kind, the movement is not localized in this way, but involves `global' mixing of the populations prior to dispersal. 2. A remarkable range of dynamical behaviour is exhibited by a mathematically explicit model with constant host reproductive rate, deterministically unstable local dynamics and dispersing hosts and parasitoids that only move to nearest-neighbour patches in a density-independent way. The density of the host and parasitoid subpopulations in a two-dimensional array of patches may exhibit complex patterns of spiral waves, spatial chaos, a so-called static `crystal lattice' pattern, or they may become extinct. The probability of extinction rises rapidly when the number of patches present decreases below some characteristic arena size which varies with the scale of the spatial dynamics. 3. The different types of spatial dynamics that are observed depends critically on the fractions of hosts and adult parasitoids that disperse in each generation from the patches in which they emerged. Low rates of host dispersal tend to lead to chaotic patterns unless this rate is very low and parasitoid dispersal rates very high, in which case `crystal lattice' patterns may occur. Intermediate to high rates of host dispersal tend to result in spiral patterns. The effect of varying host rates of increase, within-patch parasitism that is inherently stabilizing and random patch-to-patch variation are also discussed. 4. The results are relatively insensitive to the details of the interaction. Thus, a similar range of behaviour (spirals, chaos and crystal lattices) is discernible from a very general `cellular automaton' model in which only qualitative categories of patch densities are specified together with a very simple set of `transition rules'. The diffusive dispersal of the explicit model is parallelled by making the new state in each generation depend, not only on the current state of the given `cell', but also on the states of a specified set of neighbouring cells.</description><subject>Animal and plant ecology</subject><subject>Animal ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Biological and medical sciences</subject><subject>Cellular automata</subject><subject>Chaos theory</subject><subject>Crystal lattices</subject><subject>Demecology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Parasite hosts</subject><subject>Parasitism</subject><subject>Parasitoids</subject><subject>Population density</subject><subject>Population dynamics</subject><subject>Spatial models</subject><issn>0021-8790</issn><issn>1365-2656</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>K30</sourceid><recordid>eNpt0F9LwzAUBfAgCs7N71BRfKve5DbN-ij-mzBQ2HwuaZpgR9vU3Oxh396OiYL4dB_uj8PhMDbjcCMQ1K3MhTpiE465TEUu82M2ARA8nasCTtkZ0QYAlACcMFh_2GQ16NjoNnnY9bprDCXeJQtPMU3fdNDURN_UyWpH0XY0YydOt2TPv--UvT89ru8X6fL1-eX-bpkaRB5Th7WqTeG0tLmWIBS3mKEzkkNRiEqJzIicu1oUMqurGpWSIOdVrZ221lUSp-z6kDsE_7m1FMuuIWPbVvfWb6nkOSqOkI3w8g_c-G3ox27l-AeBCBJHdXVQJniiYF05hKbTYVdyKPejlfvRftmgyejWBd2bhn5shoUchxvZxYFtKPrwf9QXFWdy3A</recordid><startdate>19920101</startdate><enddate>19920101</enddate><creator>Comins, H.N.</creator><creator>Hassell, M.P.</creator><creator>May, R.M.</creator><general>British Ecological Society</general><general>Blackwell</general><general>Blackwell Scientific Publications</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>HFIND</scope><scope>HZAIM</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope><scope>7SN</scope><scope>7SS</scope><scope>C1K</scope></search><sort><creationdate>19920101</creationdate><title>The Spatial Dynamics of Host--Parasitoid Systems</title><author>Comins, H.N. ; Hassell, M.P. ; May, R.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c331t-f3d7dc9fa5e6a50271e343fc510992b724c261fd2954dbd3775058bdafaeefb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animal and plant ecology</topic><topic>Animal ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Biological and medical sciences</topic><topic>Cellular automata</topic><topic>Chaos theory</topic><topic>Crystal lattices</topic><topic>Demecology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Parasite hosts</topic><topic>Parasitism</topic><topic>Parasitoids</topic><topic>Population density</topic><topic>Population dynamics</topic><topic>Spatial models</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Comins, H.N.</creatorcontrib><creatorcontrib>Hassell, M.P.</creatorcontrib><creatorcontrib>May, R.M.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 16</collection><collection>Periodicals Index Online Segment 26</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>The Journal of animal ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Comins, H.N.</au><au>Hassell, M.P.</au><au>May, R.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Spatial Dynamics of Host--Parasitoid Systems</atitle><jtitle>The Journal of animal ecology</jtitle><date>1992-01-01</date><risdate>1992</risdate><volume>61</volume><issue>3</issue><spage>735</spage><epage>748</epage><pages>735-748</pages><issn>0021-8790</issn><eissn>1365-2656</eissn><coden>JAECAP</coden><abstract>1. We consider models for host--parasitoid interactions in spatially patchy environments, where in each generation specified fractions of the host and parasitoid subpopulations in each patch move to adjacent patches. In most previous work of this general kind, the movement is not localized in this way, but involves `global' mixing of the populations prior to dispersal. 2. A remarkable range of dynamical behaviour is exhibited by a mathematically explicit model with constant host reproductive rate, deterministically unstable local dynamics and dispersing hosts and parasitoids that only move to nearest-neighbour patches in a density-independent way. The density of the host and parasitoid subpopulations in a two-dimensional array of patches may exhibit complex patterns of spiral waves, spatial chaos, a so-called static `crystal lattice' pattern, or they may become extinct. The probability of extinction rises rapidly when the number of patches present decreases below some characteristic arena size which varies with the scale of the spatial dynamics. 3. The different types of spatial dynamics that are observed depends critically on the fractions of hosts and adult parasitoids that disperse in each generation from the patches in which they emerged. Low rates of host dispersal tend to lead to chaotic patterns unless this rate is very low and parasitoid dispersal rates very high, in which case `crystal lattice' patterns may occur. Intermediate to high rates of host dispersal tend to result in spiral patterns. The effect of varying host rates of increase, within-patch parasitism that is inherently stabilizing and random patch-to-patch variation are also discussed. 4. The results are relatively insensitive to the details of the interaction. Thus, a similar range of behaviour (spirals, chaos and crystal lattices) is discernible from a very general `cellular automaton' model in which only qualitative categories of patch densities are specified together with a very simple set of `transition rules'. The diffusive dispersal of the explicit model is parallelled by making the new state in each generation depend, not only on the current state of the given `cell', but also on the states of a specified set of neighbouring cells.</abstract><cop>Oxford</cop><pub>British Ecological Society</pub><doi>10.2307/5627</doi><tpages>14</tpages></addata></record> |
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subjects | Animal and plant ecology Animal ecology Animal, plant and microbial ecology Biological and medical sciences Cellular automata Chaos theory Crystal lattices Demecology Fundamental and applied biological sciences. Psychology General aspects Parasite hosts Parasitism Parasitoids Population density Population dynamics Spatial models |
title | The Spatial Dynamics of Host--Parasitoid Systems |
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