9780521861724htl 1..2

(Jacob Rumans) #1
adult body-size distributions, and within the size range of adult pelagic animals
(Fig.11.9). In these ‘enrichment communities’ of opportunistic species the
meiofauna/macrofauna traits dichotomy (Table11.2) breaks down; all the
species have direct benthic development and are non-selective deposit feeders
with approximately the same lifespan. This may also be the reason why the
bimodal body-size distribution also breaks down.

Discussion and conclusion
The mechanisms usually invoked to explain species size distributions, as with
most other attributes of multispecies assemblages, have generally involved local
ecological processes; species interactions (resource partitioning, predation, etc.)
or environmental constraints (habitat architecture, disturbance, etc.). This chap-
ter advocates the alternative, or additional, view that it is evolutionary processes
acting over geological time that shape the structure of the regional species pool,

1 10 100 1000
Species rank

0

20

40

60

80

100

Mesh size (μm)
63
125
250
500
1000
Cumulative % dominance

Figure 11.8k-dominance curves
averaged over all replicates for each
mesh size in the same samples as
Figure11.7 (after Warwicket al.,
2006).

Number of species
0

10

20

30

0

5

benthic

pelagic

Pollution indicators
0102030
X2 geometric weight class

Figure 11.9Species body-size
distribution of the metazoan
pelagos (solid histogram)
compared with the metazoan
benthos (upper curve) at a
station in the Celtic Sea. Also
shown (dotted histogram) is
the size distribution of the
‘pollution indicator’ species
listed in Table11.3 (after
Warwicket al.,1986).

220 R.M. WARWICK

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