As described in Sect. 2 we determine the mass
ellipsoid for each of the cluster sized halos. The distribution of the
intrinsic shapes of clusters in our sample is illustrated in
Fig. 2. There we plot the ratios between the lengths of
the three principal axes
:
the upper panel shows the
ratios a/b versus a/c, whereas the lower panel shows b/c versus
a/c. For prolate rotational ellipsoids (a>b, b = c) all points
would coincide with the dashed diagonal on the upper panel. In the
case of oblate rotational ellipsoids (a=b, a>c) all data points
would coincide with the dashed diagonal plotted in the lower panel.
Clearly the majority of the data points tend to be concentrated rather
along the upper panels' diagonal than along the lower panels'
diagonal. Therefore, the clusters in our simulations typically have
prolate shape, in good agreement with observations (e.g. Basilakos et al. 2000;
Cooray 2000) and other CDM simulations, cp. (Cole & Lacey 1996).
In the following we will use the direction of the major axis of the
mass ellipsoid (the "a-axis'') as a vector mark
.
Figure 3 shows the mark
correlation functions
and
.
The increased
towards smaller scales indicates that pairs of
clusters with a distance smaller than 30 h-1 Mpc prefer a parallel
orientation of their orientation axes
and
.
This
deviation of
from the signal of a purely random orientation
is clearly outside the random fluctuations shown by the shaded region.
We determine these random fluctuations by repeatedly and randomly
redistributing the orientation axes among the clusters. The positions
of the clusters remain fixed.
The filamentary alignment of the orientation of the clusters
and
towards the connecting vector
as quantified by
is significantly stronger (up to 20% deviation from the
signal of purely random orientation on small scales). Remarkably this
signal extends out to 100 h-1 Mpc.
In a qualitative picture this may be explained by a large number of
clusters elongated in the direction of the filaments of the large
scale structures. Filaments are prominent features found in
the observed galaxy distribution (Huchra et al. 1990) as well as in
N-body simulations (Melott & Shandarin 1990), often with an extent
up to 100 h-1 Mpc. The inspection of the density field of the simulation
utilized here confirms this view (see Fig. 5).
Up to now we used the orientation of the mass ellipsoid in three
dimensional space. Most observations, however, only provide the
projected galaxy number density or X-ray intensity. In the following
we will investigate whether the clear signal found in
Fig. 3 will be reduced by projection.
In close analogy to our three dimensional analysis we determine the
orientation of the mass-ellipse of a halo from the mass-density orthogonally
projected onto a side of the simulation box. We repeat our analysis
with the major axis of the mass ellipse in two-dimensions as a
two-dimensional vector mark. Also the normalized direction
is given in the plane. However, for the radial distance r we use the
three dimensional separation of the clusters. With this setting, we
mimic the observational constraints, e.g. in the REFLEX
cluster survey.
In this projected sample the signal in
is only visible on
scales smaller than 10 h-1 Mpc (Fig. 4). The amplitude of the
deviation from random orientation (in two dimension
)
is
reduced, as well. But still, the filamentary alignment quantified with
indicates a strong alignment of the orientation of the
clusters with the connecting vector
(Fig. 4). Although the amplitude is
slightly reduced, this alignment is still visible out to scales of
100 h-1 Mpc, as in the three dimensional analysis.
The question arises, why do we find two different regimes of the
vector correlations, using either
or
.
The direct
alignment, quantified with
extends out to 30 h-1 Mpc, whereas
the filamentary alignment (
)
is visible out to 100 h-1 Mpc. A
glimpse on the real density distribution in
Fig. 5 sheds light on this topic. Clearly one can
see filamentary structures with sizes extending up to 100 h-1 Mpc, for
example the two pronounced filaments which end up in the knot at
h-1 Mpc and
h-1 Mpc.
Generically, such filaments are not straight but crinkled and show a
lot of small branches. This implies that the coherence of the angles
between the major axes of clusters harbored in these filamentary
structures is lost soon. Consequently the positive correlation seen
with
is confined to comparatively small scales
30 h-1 Mpc (in the case of projected data even to
10 h-1 Mpc). On the other hand, the signal exploring the
angle between orientation and connecting vector is not affected by the
small scale disorder. Thus
is tracing the filamentary
alignment out to scales of 100 h-1 Mpc.
Copyright ESO 2002