A&A 385, 986-994 (2002)
DOI: 10.1051/0004-6361:20020186
Y. Frémat 1 - J. Zorec 2 - A.-M. Hubert 1 - L. S. Cidale 3 - R. D. Rohrmann 4 - J.-M. Désert 2 - R. Ferlet 2 - - A. Vidal-Madjar 2
1 - Observatoire de Paris, Section d'Astrophysique de Meudon,
GEPI, FRE K2459,
5 place Jules Janssen, 92195 Meudon
Cedex, France
2 -
Institut d'Astrophysique de Paris, CNRS, 98bis boulevard Arago,
75014 Paris, France
3 -
Facultad de Ciencias Astronómicas y Geofisicas, Universidad
Nacional de La Plata, Paseo del Bosque S/N, 1900 La Plata,
Argentina
4 -
Observatorio Astronómico, Universidad Nacional de Córdoba, Laprida 854, 5000 Córdoba,
Argentina
Received 26 October, 2001 / Accepted 29 January 2002
Abstract
New spectra have been obtained for the pole-on Be star HR 5223
(HD 120991) using the Far Ultraviolet Satellite Explorer (FUSE).
We give a complete description of the far-UV spectral range (920
to 1180 Å). The spectra are affected by strong blends with
interstellar lines and molecular bands that also significantly
lower the energy distribution of the star. We produce a synthetic
spectrum of the interstellar medium (ISM) to determine the column
densities of several elements (H2, H I, N I, O
I ...) seen towards HR 5223 and to disentangle the
components due to the ISM, the photosphere and/or to the
circumstellar envelope. The line identification list is available
at the CDS. Using the obtained column densities, we determine the
reddening of the star due to the ISM only and locate the star
relative to the nearby IS clouds. The fit of the dereddened UV
flux distribution with models that account for the gravitational
darkening due to the stellar fast rotation allowed us to estimate
the stellar fundamental parameters (
= 22000 K;
= 3.7) and its distance (
pc). The
distance obtained, which has to be considered as the most
accurate available at the moment, is in agreement with the
characteristics of the ISM matter distribution that affects the
observed spectrum of the star and with the detecting limits of
the HIPPARCOS satellite.
Key words: stars: emission-line, Be - stars: fundamental parameters - stars: individual: HR 5223 - stars: rotation - ISM: abundances - stars: distances
It is commonly accepted that Be stars are non-supergiant stars showing - or having shown - one or more Balmer lines in emission (Jaschek et al. 1981). They represent 17% of the whole galactic B type stars population and are subject to fast rotation. Rotation not only affects stellar evolution, but it deforms also the photosphere and produces non-uniform surface gravity and temperature distributions. Consequently, all observable stellar parameters are dependent on the viewing angle i between the star's rotation axis and the line of sight. If we combine these effects with electron scattering, bound-free and free-free emission arising from the surrounding envelope, the interstellar extinction and the stellar fundamental parameters are very difficult to determine. This difficulty is furthermore increased by the fact that Be stars are generally far-away objects with very low angular diameters, so that the shape of the circumstellar envelope (CE, disk or ellipsoid) is still an actively debated subject. Remoteness implies also that their parallaxes, if known, are often inaccurate even when they are measured with the HIPPARCOS satellite. The distance knowledge is, however, very useful to determine the absolute radiation fluxes observed at the stellar surface in order to test the theoretically predicted fluxes.
In the present work, we are mainly dealing with the difficulties related to the fundamental parameter determination and the distance knowledge of the pole-on Be star HR 5223 recently observed by FUSE (Far Ultraviolet Satellite Explorer). The studied star is briefly described in Sect. 2. Interstellar lines appearing in the FUSE spectra (see Sect. 3) are first studied in order to evaluate their effect on the energy distribution and the stellar line profiles. The methods used to compute the synthetic spectra are fully explained in Sect. 4, while the derived column densities, the identification line lists and interstellar reddening for the star are given and discussed in Sect. 5. Using FUSE fluxes combined with IUE spectra, we determine in Sect. 6 the distance to HR 5223 and compare our value and its location relative to the local interstellar clouds. Conclusions are finally given in Sect. 7.
The star (HR 5223
HD 120991
V767 Cen) was
classified B2IIIe by Hiltner et al. (1969). All along its
recorded lifetime, it showed strong and variable emission
features. Fleming (1890) was the first to notice
emission in the H
hydrogen line while
Campbell (1895) observed a strong H
emission
line. Following Hanuschik (1996) and
Hanuschik et al. (1996) the Fe II class 2 emission
line profiles are well defined, asymmetrical and double peaked.
They also show a weak V/R variability
(Hanuschik et al. 1995), while hydrogen emission lines
exhibit strong line profile variations
(Dachs et al. 1992). Modeling the winebottle structure
observed in 1987 for the H
emission line,
Hummel (1994) deduced an inclination angle for
HR 5223 of the order of 15 degrees. However, his model could not fit
the broad wings of the line, which are probably due to
non-coherent electron scattering. In this case, electron
scattering should be an important opacity source in the star's
circumstellar environment.
The IUE spectra, which are typically those of an early type-star have been studied by Dachs & Hanuschik (1984) for the first time. Most of the observed resonance lines are dominated by features arising from the interstellar medium and showing heliocentric radial velocities close to zero. The profiles of N V, C IV and Si IV UV resonance lines are slightly asymmetric but there is no clear evidence that these lines are formed in a high velocity expanding envelope (Hubeny et al. 1986). Following Hubeny et al. (1986), the studied ultraviolet spectra seem to correspond to the stellar photospheric spectrum. The fact that the UV energy distribution observed by IUE at different dates does not vary significantly tends to confirm this assertion.
| Dataset Name | Date |
| Q1140101001 | June 30, 2000 |
| Q1140101002 | June 30, 2000 |
| Q1140101003 | July 01, 2000 |
| Q1140101004 | July 01, 2000 |
The FUSE (Far Ultraviolet Spectroscopic Explorer) satellite and the on board spectrograph have been described by Moos et al. (2000) and Sahnow et al. (2000). The total exposure time for the observations, described in Table 1, was 518 s. They were performed with the large aperture (LWRS) in TTAG mode (photon mode). Data were extracted using the CALFUSE (Version 1.8.7) standard reduction pipeline which provided us with flux and wavelength calibrated spectra for the complete set of individual exposures. In order to increase the S/N ratio, the exposures from segments "a" and "b" of each channel (SiC1, SiC2, LiF1, LiF2) were co-added with the IAP XIPLOT IDL package.
Due to observational and satellite guiding errors, the wavelength scale was redshifted. This shift has been corrected using the line centers of several narrow molecular hydrogen lines. The absolute wavelength calibration was obtained by aligning the FUSE ISM absorption lines with those observed in the IUE spectra analyzed and discussed by Dachs & Hanuschik (1984). The final spectra were finally rebinned over 3 pixels. In this way, the mean spectral resolution we obtained is about 0.07 Å.
The computed theoretical spectrum contains both photospheric and interstellar medium effects. In our approach, the interstellar (Sect. 4.3) and photospheric contribution (Sects. 4.1 and 4.2) are computed in two different, fairly independent, but consecutive steps of an iterative procedure, which allows us to determine both the ISM characteristics and the stellar fundamental parameters. In the first step, only the far-UV interstellar line profiles and bands are fitted. In the second step, we reproduce the FUSE and IUE spectral ranges of the observed star by multiplying the theoretical photospheric contribution by the normalized synthetic spectrum of the interstellar component calculated in the first step. The result thus obtained is then used to fit the observed energy distribution. It is the goodness of this fit that determines the final choice of the stellar fundamental parameters. In the next sections we deepen somewhat into details of each iteration step.
As stated in Sect. 2, the far-UV spectrum of HR 5223
observed by IUE reveals no variations while the star changes in
the visible spectral range. Thus its fundamental parameters have
been determined using the ultraviolet energy distribution between
920 and 3300 Å, which yields:
= 22000 K and
.
As this determination is closely related to the
distance determination, we postpone the discussion of the method
used to Sect. 6.1.
Differential Doppler broadening of line shapes due to stellar
rotation has be accounted for with a projected rotational
velocity
= 70 kms-1 (Slettebak 1982).
The line list we used is the one of Kurucz updated by Hubeny and
also available at the CCP7 ftp server.
In order to account for the effects of rapid rotation on the continuum, we used the Roche approximation and the von Zeipel law which enabled us to compute, respectively, the local gravity and effective temperature distributions on the stellar surface. Each local atmospheric structure has been described with Kurucz's LTE model atmospheres (1994).
As stated above, the spectral range covered by FUSE is dominated by blends with strong interstellar molecular bands (H2, CO) and interstellar lines (H I, O I etc.). Identification of these blends have been carried out according to a line list updated from Morton (2001) and provided with the OWENS computer code developed by Lemoine et al. (1999).
![]() |
Figure 1: Fit of the interstellar spectrum. The extracted interstellar spectrum (solid line) is compared to the fit results (dotted line). |
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The OWENS code was further used to fit the interstellar
lines by a
minimization procedure allowing to adjust
parameters such as the kinetic temperature, radial velocity,
turbulence speed, column density (CD), background level and
continuum shape. In order to avoid numerical instabilities, due
to the complexity of the continuum fitting in the FUSE spectra
and to the strong ISM line and bands blending, we divided the
observed spectrum by a model photospheric spectrum; both spectra
are normalized previously. The theoretical spectrum is only to
give an approximate representation of the background radiation,
which helps to draw the pseudo continuum underlying the
observed ISM lines and bands. We note that the fit of the ISM
lines and blends actually does not depend strongly on the precise
choice of the fundamental parameters for the model continuum
spectrum. In the end, the representation of the continuum is done
using second order polynomials and the fit of the ISM lines and
bands is sought so as to account simultaneously for the whole
spectral range studied. In this fit we excluded the regions
polluted by airglow emission (Feldman et al. 2001) and
those exhibiting saturated absorption lines. This procedure (see
Fig. 1 for an example of the results obtained) gave
us a coherent set of CDs for all elements detected in the
interstellar medium towards HR 5223.
As we fitted a large spectral range including gradually all the studied molecules and atoms, we think that the major uncertainty source affecting the column densities is related to the continuum fitting. The continuum is, indeed, not only perturbed by noise but also by the remaining effects due to the stellar spectrum. In order to estimate the error bars on the CDs given by our best fit, we used several intermediary results provided by the procedure we adopted. This allowed us to explore a set of column density values computed for a smaller spectral range but assuming polynomials of different orders (first, second and third order) to fit the continuum. The column density error bars were directly deduced from the variance of these intermediary results while the accuracy of the b factor adopted in Table 3 was derived from the largest deviation that occurred relative to its best value.
The theoretical spectrum in the FUSE spectral range is compared to the observed one. Figure 2 shows the results obtained. In this figure the observed spectrum is represented by a solid line, the computed spectrum without IS lines is shown in dashed lines and the spectrum with IS lines is in a dotted line. For clarity purposes all these spectra were shifted.
The line identification list is given in Table 2 which is available at the CDS. In this table are given the observed wavelengths (Col. 1); the laboratory wavelengths (Col. 2) and the line identification (Col. 3).
![]() |
Figure 2: Comparison between theoretical and observed spectra (full line). Theoretical spectra computed with (dotted line) and without (dashed lines) IS lines have been shifted vertically. Interstellar H2 lines are identified by up (Werner Series) and down (Lyman Series) black triangles. Identified instrumental artifacts are cross marked while some stellar lines are identified. Solar chemical composition is assumed for the theoretical stellar spectrum. |
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| Element | |
b |
| [cm-2] | [km s-1] | |
| H2 (J=0) |
|
|
| H2 (J=1) |
|
3.5 |
| H2 (J=2) |
|
3.5 |
| H2 (J=3) |
|
3.5 |
| H2 (J=4) |
|
3.5 |
| H2 (J=5) | 3.5 | |
| H I | 20.49 |
|
| C I |
|
6.0 |
| N I |
|
6.0 |
| O I |
|
6.0 |
| Al II | 6.0 | |
| Si II |
|
6.0 |
| P II |
|
6.0 |
| Cl I | 6.0 | |
| Ar I |
|
6.0 |
| Fe II |
|
6.0 |
231 transitions arising from the interstellar medium have been
identified. Our best fit shows two ISM regions: a cold component
where H2 lines are formed with a total Doppler line width b =
3.5 kms-1, and a second component where arise neutral and
singly ionized lines (H I, Fe II etc.) with a
Doppler line width of about 6 km s-1. Heliocentric radial
velocities of both components are close to 0 km s-1, if we
refer to the IUE spectra as the absolute wavelength calibration
(Dachs & Hanuschik 1984). The column densities
(cm
)
and Doppler widths (km s
)
obtained
in both regions are given for each ion or molecule in Col. 2
and 3 of Table 3, respectively. It is worth
noting that our results do not depend very
much on the background
radiation (Sect. 4) considered during the fit.
Neutral hydrogen was the most affected IS element with a maximum
relative variation on its CD of about 8%. The expected
uncertainty on the column densities given in Table
3 accounts for this effect.
The column density of neutral hydrogen has been deduced from the
red wing of the interstellar L
line. In this way, the
derived hydrogen CD gives a good agreement between observations
and theory for the complete series of the hydrogen lines observed
by FUSE (see Fig. 2), in particular for the
L
line detected by IUE (Fig. 3). Following
the N(H I)/E(B-V) relation derived by
Shull & van Steenberg (1985), this CD corresponds to an ISM colour
excess:
![]() |
(1) |
![]() |
Figure 3:
Comparison between the observed (solid line) and
theoretical (vertically shifted dotted line) L |
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![]() |
Figure 4: Solar reference ion abundances normalized to hydrogen (Grevesse & Sauval 1998) are shown by filled circles while open circles are for the chemical composition of the ISM towards HR 5223. |
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| = | |||
| = | (2) |
This value is in good agreement with the results that can be obtained from H2 indirectly using the statistical relations of Welty & Hobbs (2001, cf. Table 5).
C II, N I and O I are the dominant ionization stages for CNO elements in the cold ISM. Concerning carbon, from 920 to 1180 Å no reliable C II line profile was available and the detected C I lines were very weak and blended. Consequently, it was only possible to set up an upper limit for the C I column density.
The nitrogen CD determination has been made using mostly the
1134 N I multiplet lines and provides us the
result N/H = (78.7
13)
10-6 which is very
close to the mean value, N/H = (75
4)
10-6,
proposed by Meyer et al. (1997), but which is not
significantly lower than the solar abundance, N/H = 83.2
10-6 reported by Grevesse & Sauval (1998). As expected the
N depletion is about negligible.
Our determination of the interstellar oxygen abundance is mainly
based on the study of the
989 and 1039 O I
line profiles. Following Cardelli et al. (1996) a depletion
up to 180.
10-6 relative to the Sun can be explained by dust
formation. The O/H ratio, (516.
155.)
10-6,
that we derived is 4/5 of the solar value proposed by
Grevesse & Sauval (1998), which means a depletion of 160.
10-6 and the observed ratio is 1.7 times greater
than the average value, O/H = 319.
10-6, derived by
Meyer et al. (1998) using GHRS data. The same authors
found no significant dependence with the mean hydrogen density
=
)/d*), where d* is the distance to
the observed star. However the STIS observations analyzed by
Howk et al. (2000, see Fig. 2) show that at
< 0.30 the O/H ratio is more scattered than at
larger values. It is also worth noting that in a recent review
paper Holweger (2001) determined, accounting for
departures from LTE and solar granulation, an O/H = (545
42)
10-6 which is not significantly different from
our result. If these results are confirmed, it implies that the
ISM towards our star is not depleted in oxygen relative to the
Sun.
We produce CDs for other elements such as Al, Si, P, Cl, Ar and Fe. If we except Cl I, which also exists in a single ionized form, all these ions represent the dominant ionization stage in the ISM (Savage & Sembach 1996).
The available and most visible Al II and Cl I lines
(Al II
935.28 Å and Cl I
1004.68, 1031.51 Å) are strongly blended with molecular
hydrogen lines and the respective ion abundances have to be taken
carefully. At worse, they could be considered as an upper limit.
Si, P and Ar are found to be underabundant relative to the Solar
abundance by -0.24, -0.09 and -0.29 dex respectively. Using
observations from the Copernicus satellite,
Jenkins et al. (1986) already found that phosphorus could
be depleted by -0.17 dex while high resolution GHRS observations
(Sembach & Savage 1996) and Interstellar Medium Absoption
Profile Satellite observations (Sofia & Jenkins 1998) showed
that the silicon and argon depletion may vary respectively from
-0.35 to -0.51 and from -0.18 to -0.61. As expected for
refractory species, Iron was also found to be depleted and
follows the trend outlined by the recent GHRS observations
(Wakker & Mathis 2000).
![]() |
Figure 5: Fits of observed spectra with theoretically predicted fluxes. In both panels the theoretical spectra (dotted lines) are computed assuming 0.7 dex lower carbon abundance than in the Sun. Observations are represented with a solid line, while the possible location of the O VI doublet is showed by plain triangles. |
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221 transitions belonging to the photosphere were identified in
the FUSE spectrum of HR 5223. Most elements are present in a
single or doubly ionized form and the highest ionization level is
reached by phosphorus (
1030.5 P IV) and sulphur
(
1073 S IV). No emission has been detected and
generally there is a good agreement between theory and
observations, if we exclude the spectral regions containing carbon
lines, those perturbed by instrumental line features or those
exhibiting airglow emission lines (mainly in the core of the
hydrogen lines). Discrepancies due to carbon can be explained by
an abundance 0.7 dex lower than in the Sun (Fig.
5). If we except this peculiar case, element
abundances are close to the solar pattern.
In some active early B type stars, lines belonging to
superionized atoms that should be produced by Auger ionization in
the stellar wind (Owocki et al. 1988; Cassinelli & Olson 1979), and such as the
1032 and
1037 O VI doublet for the far-UV, have been detected
(Lamers & Rogerson 1978). As our calculations do not account
for this possible ionization process, the presence of the O VI
doublet in the spectra of HR 5223 could be nevertheless identified
if a disagreement between the observations and the computed
spectrum appeared at 1032 Å and 1037 Å. Consequently, in
order to test the possible presence of the O VI lines, and only
once the peculiar carbon abundance in our star has been accounted
for, we analyzed in detail the spectral range between 1030 and
1040 Å. As seen in Fig. 5, where observations
are represented with a solid line and theory with a dotted line,
at 1032 Å there is a clear disagreement between observations
and theory. This disagreement could be attributed to the
existence of an asymmetric line profile such as the one we could
expect from the O VI lines. The same type of signature, though
smaller, could also be expected in the second component of the
doublet, but we find no visible trace of it at 1037 Å. This
would imply that there is no O VI line at all in the spectrum.
However, it is worth noting that the carbon abundance we
estimated in order to reproduce the studied region can still be
too high. In this case, the strong blends that we identified at
these wavelengths might be possibly hiding an underlying
1037 O VI small component. So, as the presence of
the O VI doublet in the stellar spectrum of HR 5223 should
not be excluded, a further more detailed analysis of this
spectral region is needed to assert its presence.
![]() |
Figure 6:
a)
Comparison at low resolution (50 Å) between observations
(filled dots) and computed spectra with (solid line and cross)
and without IS lines (dotted line). b) |
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We determined the fundamental parameters of the star by fitting the energy distribution between 920 and 3300 Å. Observations are from FUSE (920-1180 Å), IUE (1180-2200 Å) and ANS (2200-3300 Å), which were dereddened using the mean extinction curves proposed by Cardelli et al. (1989) and O'Donnell (1994). The theoretical fluxes take into account the effects of gravitational darkening due to the stellar fast rotation.
Four slightly different procedures were
adopted to carry out the fits. In the first one (marked as n=1 in
Table 4) we studied the observed
flux in the
1700- 3300 Å wavelength interval,
normalized at 5555 Å. The normalization of the observed fluxes
was done adopting the V magnitude corresponding to a phase of
minimum line and continuum emission (V = 6.25 mag, Moujtahid et al. 1999), when the CE has no visible effect on
the Balmer discontinuity. The same procedure was also used for
the attempt n = 2, where the spectral range studied was
920-3300 Å, which includes the FUSE far-UV
spectral region. In n = 3 we used the same spectral range as in n
= 1, but normalized at 3300 Å. Finally, in a fourth attempt (n
= 4) we simply calculated monochromatic flux ratios
=
in the
920-3300 Å spectral region and
sought for the (
parameters which produced
the smallest dispersion of
values.
The
synthetic spectra were computed accounting for the effects of fast
rotation, effective temperatures ranging from 16000 K to 27000 K
by steps of 500 K and for
varying from 3.0 dex to 4.5
dex by steps of 0.1 dex. The angular velocity,
,
of
HR 5223 was taken to be
= 0.8
(Chauville et al. 2001), where
is the breakup
velocity. The inclination angle i was determined using
70 km s-1 and the step by step (
)-dependent mass, luminosity and radius of the star at rest
taken from the evolutionary tracks calculated by
Schaller et al. (1992). We finally selected the best fit by
using the
test (e.g. Fig. 6b). The
final (
and inclination angle i adopted in
each procedure are given in Table 4.
| n | Range |
|
i | |
| Å | K | [g] = cgs | deg. | |
| 1 | 1700 - 3300 | 20500 | 3.7 | 14 |
| 2 | 920 - 3300 | 22000 | 3.7 | 15 |
| 3 | 920 - 3300 | 23500 | 3.9 | 14 |
| 4 | 920 - 3300 | 23000 | 3.9 | 14 |
The fit carried out in n = 1 showed no clear dependence with
.
We
used in this case the wings of the Balmer hydrogen lines to
determine the parameter
.
Differences in the (
determinations can be partially due to the fitting
failures in the monochromatic fluxes used for normalizations,
which determine the minimum
value. However, we also see
that including the far-UV spectrum, which is generally formed in
the upper layers of the photosphere, leads to a higher effective
temperature. This suggests that the temperature in the outermost
layers may perhaps be somewhat hotter than predicted in Kurucz'
radiative equilibrium model atmospheres. It should not also be
excluded that energy release due to hydrodynamic instabilities
produced by the fast rotation and/or back radiation from the CE
(Hoeflich 1988) could be the cause of this heating
that increases the uncertainty on the fundamental parameters of
HR 5223. We finally adopted the (
estimate
which not only produced the lowest value of
,
but also
better represented the flux in the V magnitude at the stellar
minimum emission phase. Thus, the parameters we have obtained for
a HR 5223 homologous rotationless star, are:
![]() |
(3) |
HR 5223 has been observed with the HIPPARCOS satellite, but the
telescope could not resolve its parallax (
0.00
0.84 mas). If we define the horizon of the HIPPARCOS
satellite as the distance above which each star observed has a
relative parallax error greater or equal to 100%, then HR 5223
is probably located close or beyond this limit. To estimate the
stellar distance, we used then the theoretical fluxes in the
920-3300 Å wavelength interval for the
adopted fundamental parameters. We calculated the average angular
diameter:
| (5) |
We also point out that the distance obtained is much greater than the value
given by the statistical relation proposed by
Shull & van Steenberg (1985):
![]() |
Figure 7: Colour excess versus distance for a sample of stars within 5 degrees around HR 5223 (triangle). Galactic reddening in the same direction is represented by a dashed-dotted line (Schlegel et al. 1998). E(B-V) gradients proposed by Lucke (1978) for the studied region are labeled on the same figure. Dotted lines represent the confidence level on the polynomial fit (solid line). |
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Far-UV data obtained by FUSE for the pole-on Be star HR 5223 allowed us to determine the column densities of several elements which appear in the ISM. Most of the studied elements are depleted relative to the solar abundance in the same way that they are in other lines of sight.
The presence of the interstellar lines sensitively lowers the global energy distribution in the far-UV (Fig. 6). Once accounting for this effect, neither continuum emission nor line emission, even in the first hydrogen lines of the Lyman series were observed in the FUSE spectra. In particular, in the FUSE wavelength range we found no trace of any spectral characteristic that could be attributed to the circumstellar envelope. As shown by the good agreement we found between observations and theory, the total hydrogen column density enabled us to determine a reliable value of the E(B-V)colour excess towards HR 5223 due only to the ISM.
The column densities of the IS elements observed towards the star clearly show that HR 5223 is located between 250 pc and 900 pc. The distance of the star was determined from a direct comparison of the UV observations to theoretical spectra that accounted for effects of fast rotation.
The characteristics of the O VI resonance lines in the FUSE spectral region and the circumstances of its appearance, together with those of C IV and Si IV resonance lines seen in the IUE spectra, will be discussed in a separate contribution.
Acknowledgements
We would like to thank Drs M. Lemoine, I. Hubeny and T. Lanz for allowing us to use their computer codes. We thank Dr A. Lecavelier des Etangs for his comments and help in using the OWENS computer code. We also wish to thank Dr B.D. Savage, our referee, for useful comments that improved the final version of our paper.
This research has been partially supported by a Marie Curie Fellowship of the European Community programme FP5 under contract number HPMF-CT-2000-00497.
Our work is based on INES data from the IUE and FUSE satellites while bibliographic researches were perform using the SIMBAD and ADS databases.
|
|
|
Id. |
| 922.22 | 922.18 | Cr III * |
| 922.22 | 922.31 | H2 J=4 |
| 923.14 | 923.15 | H I * |
| 923.14 | 923.15 | H I |
| 923.98 | 923.99 | H2 J=0 |
| 924.66 | 924.65 | H2 J=1 |
| 924.98 | 925.02 | O I * |
| 924.98 | 925.02 | O I |
| 925.18 | 925.24 | Fe III * |
| 926.03 | 926.14 | H2 J=2 |
| 926.23 | 926.23 | H I * |
| 926.23 | 926.23 | H I |
| 926.23 | 926.21 | Fe II |
| 926.83 | 926.90 | Fe II |
| 927.03 | 927.03 | H2 J=2 |
| 928.03 | 928.01 | Fe III * |
| 928.47 | 928.44 | H2 J=3 |
| 929.15 | 929.16 | Fe III * |
| 929.63 | 929.54 | H2 J=0 |
| 929.63 | 929.70 | H2 J=1 |
| 929.63 | 929.70 | H2 J=3 |
| 929.63 | 929.60 | O I |
| 930.23 | 930.26 | O I |
| 930.51 | 930.46 | H2 J=2 |
| 930.67 | 930.75 | H I * |
| 930.67 | 930.75 | H I |
| 930.67 | 930.59 | H2 J=1 |
| 931.11 | 931.07 | H2 J=0 |
| 931.80 | 931.74 | H2 J=1 |
| 931.80 | 931.79 | H2 J=2 |
| 931.80 | 931.82 | H2 J=3 |
| 932.28 | 932.27 | H2 J=1 |
| 932.64 | 932.61 | H2 J=2 |
| 933.24 | 933.24 | H2 J=2 |
| 933.60 | 933.59 | H2 J=3 |
| 933.84 | 933.80 | H2 J=4 |
| 934.16 | 934.15 | H2 J=2 |
| 934.80 | 934.71 | Fe III * |
| 934.80 | 934.80 | H2 J=3 |
| 935.29 | 935.28 | Al II |
| 935.60 | 935.58 | H2 J=3 |
| 935.60 | 935.52 | Fe II |
| 936.00 | 935.97 | H2 J=4 |
| 936.64 | 936.63 | O I |
| 936.64 | 936.76 | O I |
| 937.33 | 937.43 | S II * |
| 937.53 | 937.70 | S II * |
| 937.77 | 937.80 | H I |
| 937.77 | 937.80 | H I |
| 938.49 | 938.47 | H2 J=0 |
| 939.13 | 939.13 | H2 J=1 |
| 939.73 | 939.71 | H2 J=1 |
| 940.66 | 940.63 | H2 J=2 |
| 941.62 | 941.64 | Fe III * |
| 941.62 | 941.61 | H2 J=2 |
| 942.42 | 942.63 | Fe III * |
| 942.74 | 942.68 | Fe III * |
| 942.98 | 942.97 | H2 J=3 |
| 943.90 | 943.94 | Fe III * |
|
|
|
Id. |
| 944.38 | 944.34 | H2 J=3 |
| 944.82 | 944.77 | Co III * |
| 944.82 | 944.90 | Mn III * |
| 944.98 | 945.03 | Fe III * |
| 945.18 | 945.12 | Fe III * |
| 945.18 | 945.19 | C I * |
| 945.18 | 945.19 | C I |
| 946.15 | 946.05 | Fe III * |
| 946.15 | 946.20 | C II * |
| 946.39 | 946.43 | H2 J=0 |
| 946.39 | 946.39 | H2 J=1 |
| 947.03 | 947.01 | Fe III * |
| 947.03 | 946.98 | H2 J=1 |
| 947.03 | 947.12 | H2 J=2 |
| 947.47 | 947.43 | H2 J=1 |
| 947.87 | 947.88 | Fe III * |
| 948.47 | 948.48 | H2 J=2 |
| 948.47 | 948.43 | H2 J=3 |
| 948.67 | 948.69 | O I * |
| 948.67 | 948.62 | H2 J=2 |
| 948.67 | 948.69 | O I |
| 949.39 | 949.36 | H2 J=2 |
| 949.63 | 949.62 | H2 J=2 |
| 949.87 | 949.74 | H I * |
| 949.87 | 949.74 | H I |
| 950.39 | 950.41 | H2 J=3 |
| 950.87 | 950.88 | O I |
| 950.87 | 950.82 | H2 J=3 |
| 950.87 | 950.88 | O I |
| 951.07 | 951.08 | N I |
| 951.68 | 951.68 | H2 J=3 |
| 952.36 | 952.30 | N I |
| 952.36 | 952.28 | H2 J=3 |
| 952.76 | 952.73 | Fe III * |
| 953.40 | 953.38 | Fe III * |
| 953.40 | 953.42 | N I |
| 953.68 | 953.66 | N I * |
| 953.68 | 953.66 | N I |
| 954.04 | 953.97 | N I * |
| 954.04 | 954.02 | Fe III * |
| 954.04 | 954.10 | N I |
| 954.44 | 954.42 | H2 J=0 |
| 955.08 | 955.07 | H2 J=1 |
| 955.52 | 955.57 | Fe III * |
| 955.72 | 955.72 | H2 J=1 |
| 956.40 | 956.36 | Fe III * |
| 956.60 | 956.59 | H2 J=2 |
| 956.85 | 956.93 | Fe III * |
| 957.65 | 957.50 | S II * |
| 957.65 | 957.66 | H2 J=2 |
| 958.21 | 958.25 | S II * |
| 958.97 | 958.95 | H2 J=3 |
| 959.49 | 959.49 | N I |
| 960.45 | 960.46 | H2 J=3 |
| 961.00 | 961.04 | P II |
| 961.22 | 961.21 | Mn III * |
| 961.82 | 961.70 | Fe III * |
| 961.98 | 961.90 | Fe III * |
| 962.70 | 961.66 | Fe III * |
| 962.98 | 962.98 | H2 J=0 |
|
|
|
Id. |
| 963.58 | 963.62 | H2 J=1 |
| 964.62 | 964.63 | N I |
| 963.78 | 963.80 | P II |
| 963.98 | 963.99 | N I * |
| 963.98 | 963.99 | N I |
| 964.34 | 964.32 | H2 J=1 |
| 964.62 | 964.63 | N I * |
| 965.02 | 965.04 | N I |
| 965.02 | 964.99 | H2 J=0 |
| 965.02 | 965.07 | H2 J=1 |
| 965.02 | 965.05 | H2 J=2 |
| 965.82 | 965.79 | H2 J=2 |
| 966.15 | 966.10 | H2 J=1 |
| 966.15 | 966.28 | H2 J=2 |
| 966.79 | 966.79 | H2 J=3 |
| 967.27 | 967.19 | Fe III * |
| 967.27 | 967.28 | H2 J=2 |
| 967.71 | 967.68 | H2 J=3 |
| 967.99 | 967.81 | S III * |
| 968.31 | 968.30 | H2 J=2 |
| 969.03 | 969.05 | H2 J=3 |
| 970.55 | 970.56 | H2 J=3 |
| 970.83 | 970.84 | H2 J=4 |
| 971.44 | 971.39 | H2 J=4 |
| 971.76 | 971.74 | O I * |
| 971.76 | 971.74 | O I |
| 972.00 | 972.14 | O I |
| 972.00 | 971.99 | H2 J=0 |
| 972.76 | 972.54 | H I * |
| 972.76 | 972.78 | P II |
| 972.76 | 972.64 | H2 J=1 |
| 973.36 | 973.35 | H2 J=1 |
| 974.16 | 974.16 | H2 J=2 |
| 975.36 | 975.35 | H2 J=2 |
| 976.52 | 976.49 | O I |
| 976.52 | 976.56 | H2 J=3 |
| 977.09 | 977.02 | C III * |
| 977.81 | 979.90 | N III * |
| 980.37 | 980.42 | Fe III * |
| 981.42 | 981.37 | Fe III * |
| 981.42 | 981.44 | H2 J=0 |
| 982.06 | 982.08 | H2 J=1 |
| 982.86 | 982.84 | H2 J=1 |
| 983.58 | 983.59 | H2 J=2 |
| 983.82 | 983.86 | Fe III * |
| 984.86 | 984.87 | H2 J=2 |
| 985.62 | 985.64 | H2 J=0 |
| 985.62 | 985.65 | H2 J=1 |
| 985.95 | 985.83 | Fe III * |
| 985.95 | 985.97 | H2 J=3 |
| 986.27 | 986.25 | H2 J=2 |
| 986.79 | 986.80 | H2 J=1 |
| 987.47 | 987.45 | H2 J=3 |
| 987.99 | 987.98 | H2 J=2 |
| 988.63 | 988.65 | O I |
| 989.11 | 989.09 | H2 J=2 |
| 989.79 | 989.80 | N III * |
| 989.79 | 989.73 | H2 J=3 |
| 990.75 | 990.76 | S II * |
|
|
|
Id. |
| 991.35 | 991.58 | N III * |
| 991.35 | 991.38 | H2 J=0 |
| 991.35 | 991.38 | H2 J=3 |
| 992.00 | 992.02 | H2 J=1 |
| 992.80 | 992.81 | H2 J=1 |
| 993.56 | 993.55 | H2 J=2 |
| 994.20 | 994.23 | H2 J=4 |
| 994.88 | 994.72 | Fe III * |
| 994.88 | 994.79 | Si III * |
| 994.88 | 994.88 | H2 J=2 |
| 995.96 | 995.97 | H2 J=3 |
| 997.13 | 997.08 | Fe III * |
| 997.41 | 997.39 | Si III * |
| 997.81 | 997.83 | H2 J=3 |
| 999.33 | 999.38 | Fe III * |
| 999.33 | 999.27 | H2 J=4 |
| 1000.41 | 1000.49 | S II * |
| 1000.99 | 1000.88 | Cr III * |
| 1000.99 | 1001.00 | Fe III * |
| 1001.86 | 1001.83 | H2 J=0 |
| 1002.46 | 1002.46 | H2 J=1 |
| 1003.30 | 1003.30 | H2 J=1 |
| 1003.98 | 1003.99 | H2 J=2 |
| 1004.65 | 1004.68 | Cl I |
| 1005.10 | 1005.28 | Cl III * |
| 1005.34 | 1005.40 | H2 J=2 |
| 1006.43 | 1006.42 | H2 J=3 |
| 1008.51 | 1008.78 | Cl III * |
| 1008.51 | 1008.56 | H2 J=0 |
| 1008.51 | 1008.50 | H2 J=1 |
| 1009.03 | 1009.03 | H2 J=2 |
| 1009.79 | 1009.86 | C II * |
| 1009.79 | 1009.78 | H2 J=1 |
| 1009.79 | 1009.72 | H2 J=4 |
| 1010.15 | 1010.08 | C II * |
| 1010.15 | 1010.37 | C II * |
| 1010.15 | 1010.14 | H2 J=3 |
| 1010.95 | 1010.95 | H2 J=2 |
| 1011.84 | 1011.82 | H2 J=4 |
| 1012.20 | 1012.18 | H2 J=2 |
| 1012.20 | 1012.27 | H2 J=4 |
| 1012.48 | 1012.50 | S III * |
| 1012.76 | 1012.82 | H2 J=0 |
| 1012.76 | 1012.69 | H2 J=3 |
| 1013.40 | 1013.44 | H2 J=1 |
| 1014.32 | 1014.33 | H2 J=1 |
| 1014.48 | 1014.51 | H2 J=3 |
| 1015.00 | 1015.02 | Cl III * |
| 1015.00 | 1014.98 | H2 J=2 |
| 1015.00 | 1014.99 | H2 J=4 |
| 1015.64 | 1015.51 | S III * |
| 1016.32 | 1016.17 | Fe III * |
| 1016.48 | 1016.47 | H2 J=2 |
| 1017.13 | 1017.15 | Cr III * |
| 1017.13 | 1017.25 | Fe III * |
| 1017.41 | 1017.43 | H2 J=3 |
| 1017.41 | 1017.39 | H2 J=4 |
| 1017.61 | 1017.75 | Fe III * |
| 1018.33 | 1018.29 | Fe III * |
|
|
|
Id. |
| 1019.49 | 1019.51 | H2 J=3 |
| 1019.81 | 1019.79 | Fe III * |
| 1020.73 | 1020.77 | H2 J=4 |
| 1020.73 | 1020.70 | Si II |
| 1021.22 | 1021.34 | S III * |
| 1022.86 | 1022.87 | Fe III * |
| 1024.42 | 1024.38 | H2 J=0 |
| 1025.22 | 1025.72 | H I |
| 1025.62 | 1025.76 | O I |
| 1026.10 | 1025.94 | H2 J=1 |
| 1028.11 | 1028.11 | H2 J=2 |
| 1028.99 | 1028.99 | H2 J=3 |
| 1029.51 | 1029.55 | Fe III * |
| 1029.95 | 1029.92 | Fe III * |
| 1030.55 | 1030.52 | P IV * |
| 1030.91 | 1030.92 | Fe III * |
| 1031.19 | 1031.20 | H2 J=3 |
| 1031.50 | 1031.51 | Cl I |
| 1032.20 | 1032.12 | Fe III * |
| 1032.32 | 1032.12 | Fe III * |
| 1033.20 | 1033.30 | Fe III * |
| 1033.84 | 1033.82 | Fe III * |
| 1034.44 | 1034.44 | Cr III * |
| 1034.80 | 1034.86 | Cr III * |
| 1035.28 | 1035.19 | H2 J=4 |
| 1035.68 | 1035.57 | Cr III * |
| 1035.68 | 1035.77 | Fe III * |
| 1035.92 | 1035.77 | Fe III * |
| 1036.48 | 1036.34 | C II * |
| 1036.48 | 1036.55 | H2 J=0 |
| 1037.09 | 1037.02 | C II * |
| 1037.09 | 1037.16 | H2 J=1 |
| 1038.17 | 1038.16 | H2 J=1 |
| 1038.60 | 1038.69 | H2 J=2 |
| 1039.21 | 1039.23 | O I |
| 1039.93 | 1040.05 | Cr III * |
| 1040.37 | 1040.37 | H2 J=2 |
| 1041.18 | 1041.16 | H2 J=3 |
| 1041.70 | 1041.74 | Fe III * |
| 1042.82 | 1042.76 | Mn III * |
| 1043.54 | 1043.51 | H2 J=3 |
| 1044.54 | 1044.55 | H2 J=4 |
| 1045.14 | 1045.06 | Cr III * |
| 1045.14 | 1045.11 | Fe III * |
| 1046.02 | 1045.96 | Fe III * |
| 1047.59 | 1047.56 | H2 J=4 |
| 1048.23 | 1048.22 | Ar I |
| 1048.63 | 1048.56 | Fe III * |
| 1049.35 | 1049.37 | H2 J=0 |
| 1049.95 | 1049.97 | H2 J=1 |
| 1051.03 | 1051.04 | H2 J=1 |
| 1051.51 | 1051.51 | H2 J=2 |
| 1052.60 | 1052.57 | Fe III * |
| 1053.28 | 1053.29 | H2 J=2 |
| 1054.00 | 1053.95 | H2 J=3 |
| 1054.28 | 1054.25 | Fe III * |
| 1054.68 | 1054.68 | Mn III * |
| 1054.68 | 1054.74 | Fe III * |
| 1055.08 | 1055.07 | Fe III * |
|
|
|
Id. |
| 1055.24 | 1055.26 | Fe II |
| 1055.96 | 1055.88 | Cr III * |
| 1055.96 | 1056.05 | Fe III * |
| 1056.52 | 1056.48 | H2 J=3 |
| 1056.80 | 1056.76 | Fe III * |
| 1057.41 | 1057.39 | H2 J=4 |
| 1057.93 | 1057.85 | Cr III * |
| 1058.65 | 1058.58 | Fe III * |
| 1059.13 | 1059.12 | Cr III * |
| 1059.49 | 1059.48 | Fe III * |
| 1060.17 | 1060.15 | Cr III * |
| 1060.17 | 1060.26 | Fe III * |
| 1060.61 | 1060.59 | H2 J=4 |
| 1061.14 | 1061.24 | Fe III * |
| 1061.74 | 1061.71 | Fe III * |
| 1062.18 | 1062.27 | FE III * |
| 1062.90 | 1062.89 | H2 J=0 |
| 1063.22 | 1063.18 | Fe II |
| 1063.50 | 1063.47 | H2 J=1 |
| 1063.90 | 1063.87 | Fe III * |
| 1064.30 | 1064.33 | Cr III * |
| 1064.58 | 1064.61 | H2 J=1 |
| 1065.02 | 1065.00 | H2 J=2 |
| 1065.94 | 1065.89 | C II * |
| 1066.67 | 1066.66 | Ar I |
| 1066.91 | 1066.91 | H2 J=2 |
| 1067.47 | 1067.49 | H2 J=3 |
| 1068.23 | 1068.29 | Fe III * |
| 1069.07 | 1069.02 | Fe III * |
| 1069.63 | 1069.69 | C III * |
| 1070.15 | 1070.15 | H2 J=3 |
| 1070.39 | 1070.33 | C III * |
| 1070.95 | 1070.91 | H2 J=4 |
| 1071.72 | 1071.75 | Fe III * |
| 1072.96 | 1072.99 | S IV * |
| 1073.64 | 1073.73 | Cr III * |
| 1074.08 | 1074.07 | Fe III * |
| 1074.32 | 1074.32 | H2 J=4 |
| 1074.96 | 1074.96 | O II * |
| 1074.96 | 1075.02 | Fe III * |
| 1076.24 | 1076.15 | Cr III * |
| 1076.60 | 1076.51 | Fe III * |
| 1077.17 | 1077.14 | H2 J=0 |
| 1077.69 | 1077.70 | H2 J=1 |
| 1078.93 | 1078.93 | H2 J=1 |
| 1079.25 | 1079.23 | H2 J=2 |
| 1079.49 | 1079.42 | Cr III * |
| 1080.17 | 1080.15 | Fe III * |
| 1081.02 | 1080.92 | Mn III * |
| 1081.30 | 1081.27 | H2 J=1 |
| 1081.74 | 1081.71 | H2 J=2 |
| 1081.90 | 1081.90 | Fe II |
| 1082.42 | 1082.30 | Mn III * |
| 1083.22 | 1083.22 | Si III * |
| 1083.98 | 1083.99 | N II * |
| 1084.58 | 1084.60 | N II * |
| 1084.58 | 1084.56 | H2 J=3 |
| 1085.62 | 1085.60 | N II * |
| 1086.59 | 1086.52 | Fe III * |
|
|
|
Id. |
| 1088.07 | 1088.00 | Fe III * |
| 1088.07 | 1088.04 | Fe III * |
| 1089.07 | 1089.06 | Fe III * |
| 1089.71 | 1089.67 | Fe III * |
| 1089.71 | 1089.83 | Fe III * |
| 1089.71 | 1089.90 | Fe III * |
| 1091.11 | 1091.08 | Fe III * |
| 1091.31 | 1091.34 | Fe III * |
| 1092.24 | 1092.20 | H2 J=0 |
| 1092.72 | 1092.74 | H2 J=1 |
| 1094.08 | 1094.06 | H2 J=1 |
| 1094.28 | 1094.25 | H2 J=2 |
| 1094.72 | 1094.75 | S II * |
| 1095.48 | 1095.48 | Fe III * |
| 1096.44 | 1096.45 | H2 J=2 |
| 1096.88 | 1096.88 | Fe II |
| 1096.88 | 1096.73 | H2 J=3 |
| 1098.21 | 1098.21 | Fe III * |
| 1098.21 | 1098.25 | Fe III * |
| 1098.97 | 1098.89 | Cr III * |
| 1098.97 | 1099.06 | Fe III * |
| 1099.49 | 1099.46 | Cr III * |
| 1099.81 | 1099.80 | H2 J=3 |
| 1100.61 | 1100.58 | Cr III * |
| 1101.34 | 1101.24 | Cr III * |
| 1101.34 | 1101.42 | Cr III * |
| 1101.94 | 1101.98 | S II * |
| 1102.22 | 1102.36 | S II * |
| 1102.22 | 1102.21 | Fe III * |
| 1102.90 | 1102.87 | Cr III * |
| 1103.74 | 1103.62 | Cr III * |
| 1104.14 | 1104.17 | Fe III * |
| 1106.06 | 1105.98 | Fe III * |
| 1106.92 | 1106.95 | Fe III * |
| 1107.75 | 1107.65 | Fe III * |
| 1108.15 | 1108.36 | Si III * |
| 1108.15 | 1108.14 | H2 J=0 |
| 1108.63 | 1108.64 | H2 J=1 |
| 1109.03 | 1109.02 | Fe III * |
| 1110.07 | 1109.90 | Si III * |
| 1110.07 | 1110.07 | H2 J=1 |
| 1112.08 | 1112.05 | Fe II |
| 1112.56 | 1112.51 | H2 J=2 |
| 1112.56 | 1112.59 | H2 J=3 |
| 1113.20 | 1113.20 | Si III * |
| 1114.56 | 1114.55 | Mn III * |
| 1115.92 | 1115.91 | H2 J=3 |
| 1117.89 | 1117.89 | Fe III * |
| 1118.53 | 1118.55 | Cr III * |
| 1119.37 | 1119.45 | Fe III * |
| 1120.29 | 1120.25 | Fe III * |
| 1121.26 | 1121.24 | Fe III * |
| 1121.98 | 1121.97 | Fe II |
| 1122.50 | 1122.53 | Fe III * |
| 1123.74 | 1123.79 | Cl IV * |
| 1123.74 | 1123.83 | Fe III * |
| 1124.90 | 1124.88 | Fe III * |
| 1125.42 | 1025.45 | Fe II |
| 1125.66 | 1125.62 | Fe III * |
|
|
|
Id. |
| 1126.71 | 1126.73 | Fe III * |
| 1128.31 | 1128.10 | Fe III * |
| 1129.15 | 1129.19 | Fe III * |
| 1130.31 | 1130.40 | Fe III * |
| 1131.15 | 1131.20 | Fe III * |
| 1131.84 | 1131.92 | Fe III * |
| 1132.80 | 1132.75 | Cr III * |
| 1133.68 | 1133.67 | Fe II |
| 1134.16 | 1134.17 | N I |
| 1134.44 | 1134.41 | N I |
| 1135.00 | 1134.98 | N I |
| 1136.60 | 1136.67 | Cr III * |
| 1137.13 | 1137.09 | Cr III * |
| 1137.13 | 1137.09 | Ni II * |
| 1138.85 | 1138.85 | Fe III * |
| 1138.85 | 1138.94 | C II * |
| 1139.33 | 1139.33 | C II * |
| 1140.53 | 1140.55 | Si III * |
| 1141.30 | 1141.27 | Fe III * |
| 1141.62 | 1141.58 | Si III * |
| 1142.38 | 1142.37 | Fe II |
| 1142.98 | 1142.96 | Fe III * |
| 1143.22 | 1143.23 | Fe II |
| 1143.62 | 1143.58 | S III * |
| 1143.62 | 1143.55 | Fe III * |
| 1144.30 | 1144.31 | Si III * |
| 1144.30 | 1144.31 | Fe III * |
| 1144.94 | 1144.94 | Fe II |
| 1145.66 | 1145.67 | Si III * |
| 1146.27 | 1146.14 | Fe III * |
| 1147.99 | 1147.97 | Fe III * |
| 1149.59 | 1149.60 | O III * |
| 1149.95 | 1149.95 | V III * |
| 1149.95 | 1149.95 | P II * |
| 1150.91 | 1150.88 | O III * |
| 1150.91 | 1150.91 | Fe III * |
| 1152.16 | 1152.15 | O I * |
| 1152.16 | 1152.17 | V III * |
| 1152.80 | 1152.82 | P II |
| 1153.92 | 1153.91 | Fe III * |
| 1155.44 | 1155.38 | Cr III * |
| 1156.00 | 1156.05 | Fe III * |
| 1158.09 | 1157.91 | C I |
| 1159.09 | 1159.02 | Fe III * |
| 1159.09 | 1159.08 | P II * |
| 1159.61 | 1159.59 | Fe III * |