Studies that have evaluated potential determinants of network structure
Interaction type | Explanatory variable | Predicted network attribute | No. of networks | Result | Reference |
---|---|---|---|---|---|
Plant–pollinator | Abundance | Nestedness | 1 | Abundance partly predicts nestedness | Ollerton et al. (2003) |
Plant–pollinator | Abundance | Nestedness | 1 | Abundance partly predicts degree | Dupont et al. (2003) |
Plant–seed disperser | Abundance | Pairwise interactions | 1 | Abundance explains 83 % of variation of interactions | Burns (2006) |
Plant–ant, plant–pollinator | Abundance | Strength asymmetry | 1 | Abundance partly predicts strength asymmetry | Vázquez et al. (2007) |
Plant–pollinator | Abundance and trait matching (complementarity and barriers) | Connectance–richness and nested–richness correlations | 40 | Abundance and complementarity (but not barriers) separately partly predict these correlations | Santamaría and Rodríguez-Gironés (2007) |
Plant–pollinator | Abundance and trait matching (complementarity and barriers) | Size-specific interaction patterns | 1 | Abundance, complementarity and barriers predict interactions among size classes of plants and flower visitors | Stang et al. (2009) |
Plant–pollinator | Abundance and trait matching (exploitation barriers) | Interaction asymmetry, nestedness | 1 | Abundance and exploitation barriers predict number of interaction partners and degree asymmetry | Stang et al. (2007) |
Theoretical | Abundance and trait matching (complementarity) | Nestedness | 2 | Abundance explains most variation in nestedness, but trait complementarity also contributes | Krishna et al. (2008) |
Plant–pollinator | Abundance and trait matching (exploitation barriers) | Plant degree | 1 | Abundance and exploitation barriers explain 71 % of variation in plant degree | Stang et al. (2006) |
Plant–pollinator | Abundance and spatio-temporal distribution | Connectance, nestedness, interaction evenness, strength asymmetry, overall network structure | 1 | Abundance and spatio-temporal distribution predict aggregate properties, but only partially overall structure | Vázquez et al. (2009) |
Plant–seed disperser | Abundance, geographic range, phenological spread and phylogenetic structure | Degree | 2 | Abundance, geographic range, phenological spread and phylogenetic structure partly predict degree | Jordano and Bascompte unpubl. (cited in Bascompte and Jordano, 2007) |
Plant–ant | Body size | Degree | 8 | Body size partly predicts degree (R2 = [0·05, 0·20]) | Chamberlain and Holland (2009) |
Simulation | Evenness of species observation records | Connectance, nestedness, degree distribution, strength asymmetry, interaction evenness, generality, standardized diversity (H2′) | 0 | Evenness in species observation records influences network statistics | Blüthgen et al. (2008) |
Anemone–anemonefish | Geographic range | Nestedness | 1 | Geographic range partly predicts nestedness | Ollerton et al. (2007) |
Plant–pollinator, plant–seed disperser | Interaction frequency | Shape of degree distribution | 12 (p–p), 5 (p–sd) | Interaction frequency predicts degree distribution | Vázquez (2005) |
Plant–ant | Interaction intimacy | Nestedness and compartmentalization | 19 | Interaction intimacy explains both nestedness and compartmentalization | Guimarães et al. (2007) |
Plant–hemiptera–ant | Interaction type | Network specialization (H2′) | 1 | H2′ higher for plant–hemiptera than ant–hemiptera and ant–plant associations | Blüthgen et al. (2006a) |
Plant–ant, plant–pollinator, plant–seed disperser | Interaction type, species richness, total frequency, network asymmetry | Network specialization (H2'), species-level specialization (d') | 51 | Interaction type influences specialization after correcting for the effect of total frequency | Blüthgen et al. (2007) |
Plant–pollinator | Latitude, sampling effort | Degree | Sampling effort partly predicts degree | Ollerton and Cramer (2002) | |
Simulation | Trait matching and phylogenetic relatedness | Nestedness | 1 | Trait complementarity and phylogenetic relationships can result in observed network patterns | Rezende et al. (2007a) |
Plant–seed disperser | Phylogenetic structure | Degree, species strength and ecological–phylogenetic distance correlation | 36 (p–p), 37 (p–sd) | There is a detectable phylogenetic signal in some of the networks analysed | Rezende et al. (2007b) |
Plant–pollinator | Sampling effort | Degree–frequency correlation | 1 | Sampling effort does not drive this correlation | Vázquez and Aizen (2006) |
Plant–pollinator | Sampling effort, species richness and number of links | Nestedness | 4 | Nestedness is more influenced by sampling than by species richness and number of links | Nielsen and Bascompte (2007) |
Plant–pollinator | Sampling effort, species richness, richness ratio, precipitation | Connectance, number of links | 8 | Sampling effort, species richness and richness ratio influence connectance and number of links | Devoto et al. (2005) |
Simulation | Spatial aggregation and scale of animal movement | Connectance, nestedness, strength asymmetry, interaction evenness, CV of rare interactions | 0 | Spatial aggregation and animal movement influence network properties | Morales and Vázquez (2008) |
Plant–seed disperser | Spatial distribution and trait matching | Occurrence of pairwise interactions | 1 | Spatio-temporal segregation and trait matching partly explain absence of interactions | Jordano et al. (2006) |
Plant–pollinator | Species richness | Connectance | 24 | Connectance decreases with increasing richness | Thébault and Fontaine (2008) |
Plant–pollinator | Species richness | Connectance and other metrics | Species richness predicts network attributes | Olesen et al. (2006) | |
Plant–pollinator, plant–seed disperser | Species richness | Connectance, number of links | 33 (p–p), 19 (p–sd) | Connectance decreases and number of links increases with increasing richness | Jordano (1987) |
Plant–pollinator | Species richness | Degree asymmetry | 18 | Asymmetric specialization increasing with increasing richness | Vázquez and Aizen (2004) |
Theoretical, plant–pollinator | Species richness | Degree distribution, nestedness | 5 | Truncation of degree distribution and nestedness depend on network size | Medan et al. (2007) |
Plant–pollinator | Species richness | Modularity, nestedness | 51 | Networks >150 plants always modular, <50 never; most networks nested | Olesen et al. (2007) |
Plant–ant | Species richness | Nestedness | 4 | Nestedness increases with increasing richness | Guimarães et al. (2006) |
Plant–pollinator, plant–seed disperser | Species richness | Nestedness | 25 (p–p), 27 (p–sd) | Nestedness increases with increasing richness | Bascompte et al. (2003) |
Plant–pollinator | Species richness | Proportion of species with only one link (extreme specialists) | 23 | Proportion of species with one link increases with network size | Vázquez and Stevens (2004) |
Simulation | Species richness of network core | Shape of degree distribution | 0 | Truncation increases with increasing network core | Guimarães et al. (2005) |
Plant–pollinator | Species richness, latitude | Connectance | 29 | Connectance decreases with increasing richness | Olesen and Jordano (2002) |
Plant–pollinator, plant–seed disperser | Species richness, richness ratio | Shape of degree distribution | 29 (p–p), 24 (p–sd) | Species richness and richness ratio may determine truncation of degree distribution | Guimarães et al. (2007) |
Plant–pollinator | Temporal variation (between years) | Between-year similarity, matrix size, connectance, degree centralization, clustering, nestedness, average distance, network diameter | 1 | Aggregate network properties temporally invariant, but identity of interactions highly variable | Petanidou et al. (2008) |
Plant–pollinator | Temporal variation (between years) | Between-year similarity, matrix size, connectance, degree distribution, nestedness | 1 | Aggregate network properties temporally invariant, but identity of interactions highly variable | Chacoff and Vázquez (unpubl.) |
Plant–pollinator | Temporal variation (between years) | Number of unique links, comparison of entire matrix composition, nestedness, centrality scores | 1 | Invariant nestedness, high variation in identity of generalized core and composition of reciprocally specialized groups | Alarcón et al. (2008) |
Plant–pollinator | Temporal variation (within and between years) | Similarity, matrix size, connectance, linkage level, shape of degree distribution | 1 | Aggregate properties temporally invariant, but identity of interactions highly variable | Olesen et al. (2008) |
Plant–pollinator | Temporal variation (within year) | Matrix size, connectance, assemblage similarity, shape of degree distribution | 1 | Month-to-month fluctuation in partners' identity, matrix size and connectance | Basilio et al. (2006) |