Average proportional abundances of Pm I, Pm II and Pm III adults and juveniles on different structures of Fucus spiralis (in order: receptacula, thalli and non-fertile tips; n = 6, except for the first sampling in November, where n = 4) and Fucus vesiculosus (in order: receptacula, thalli and bladders; n = 6) for the two sampling moments (n = 6) in (a) November and (b) April.</p
distribution, redundancy hypothesis The influence of soil matric potential on nematode community com...
In this study the importance of spatial scales on nematode species distribution and patterns of biod...
<div><p>The discovery of morphologically very similar but genetically distinct species complicates a...
Average proportional abundances of Pm I, Pm II and Pm III adults and juveniles at two sampling times...
Coexistence of highly similar species is at odds with ecological theory of competition; coexistence,...
Coexistence of highly similar species is at odds with ecological theory of competition; coexistence,...
Behind the morphological similarity of many species, a substantial hidden genetic diversity can be f...
The role of habitat complexity has been widely neglected in the study of meiofaunal community patter...
Resource partitioning is a mechanism for niche differentiation which can facilitate coexistence of s...
The use of fine-grained maintenance dredged material for habitat enhancement has increased in recent...
This study has determined the ways in which the density, number of species, species composition and ...
The coexistence of four cryptic species of Rhabditis (Pellioditis) marina (Nematoda: Rhabditidae) at...
<p>Dissimilarity (%) of nematode assemblages within and between areas (averaged over replicates and ...
Vernal pools are ephemeral wetlands, typically with a diverse and highly adapted flora and fauna. We...
Cryptic species are morphologically identical but genetically distinct, and are prominent across num...
distribution, redundancy hypothesis The influence of soil matric potential on nematode community com...
In this study the importance of spatial scales on nematode species distribution and patterns of biod...
<div><p>The discovery of morphologically very similar but genetically distinct species complicates a...
Average proportional abundances of Pm I, Pm II and Pm III adults and juveniles at two sampling times...
Coexistence of highly similar species is at odds with ecological theory of competition; coexistence,...
Coexistence of highly similar species is at odds with ecological theory of competition; coexistence,...
Behind the morphological similarity of many species, a substantial hidden genetic diversity can be f...
The role of habitat complexity has been widely neglected in the study of meiofaunal community patter...
Resource partitioning is a mechanism for niche differentiation which can facilitate coexistence of s...
The use of fine-grained maintenance dredged material for habitat enhancement has increased in recent...
This study has determined the ways in which the density, number of species, species composition and ...
The coexistence of four cryptic species of Rhabditis (Pellioditis) marina (Nematoda: Rhabditidae) at...
<p>Dissimilarity (%) of nematode assemblages within and between areas (averaged over replicates and ...
Vernal pools are ephemeral wetlands, typically with a diverse and highly adapted flora and fauna. We...
Cryptic species are morphologically identical but genetically distinct, and are prominent across num...
distribution, redundancy hypothesis The influence of soil matric potential on nematode community com...
In this study the importance of spatial scales on nematode species distribution and patterns of biod...
<div><p>The discovery of morphologically very similar but genetically distinct species complicates a...