“…We touch on several such directions here. - Well‐designed comparative approaches comparing ecological patterns across ecological gradients and boundaries produce new and more general insights (see Chatelain, Elias, Guilbert, & Soulier‐Perkins, ; Mottl, Fayle, Yombai, Novotný, & Klimeš, ; Rabl, Gottsberger, Brehm, Hofhansl, & Fiedler, ; Raine, Slade, & Lewis, , all available in this issue).
- Expanding attention into a wider spread of invertebrate taxa adds insights as a wider range of ecosystem functions is encompassed (see Chatelain et al, , Drinkwater, Williamson, Clare, & Rossiter, , Luke, and Phillips, Chung, Edgecombe, & Ellwood, , all available in this issue).
- Using the rapid response times of invertebrates in terrestrial ecosystems allows us to evaluate impacts of and recovery from environmental transformations due to natural and human actions (see Franca et al , Luke et al, , Stone, Shoo, Stork, Sheldon, & Catterall, , Torppa, Wirta, & Hanski, , all available in this issue).
- The availability of effectively limitless computing power potentially allows the enormous complexity of tropical food webs and distribution maps (see Scriven et al, , this issue) to be modeled realistically: Interpreting very complex model systems of course may be as challenging as contemplating the real thing (McLane, Semeniuk, Mcdermid, & Marceau, ).
- Aligning pattern and process: Does tropical biodiversity matter beyond its intrinsic value? Can ecosystem processes and service survive a massive decline in invertebrate species and density?
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