The Arecibo Arp 220 Spectral Census I: Discovery of the
Pre-Biotic Molecule Methanimine and New Cm-wavelength
Transitions of Other Molecules
arXiv:0805.1205v1 [astro-ph] 8 May 2008
C. J. Salter, T. Ghosh, B. Catinella1 , M. Lebron2 , M. S. Lerner, R. Minchin and
E. Momjian3
Arecibo Observatory, HC 03 Box 53995, Arecibo, PR 00612
csalter@naic.edu
ABSTRACT
An on-going Arecibo line search between 1.1 and 10 GHz of the prototypical
starburst/megamaser galaxy, Arp 220, has revealed a spectrum rich in molecular
transitions. These include the “pre-biotic” molecules: methanimine (CH2 NH) in
emission, three v2 = 1 direct l-type absorption lines of HCN, and an absorption
feature likely to be from either 18 OH or formic acid (HCOOH). In addition, we
report the detection of two, possibly three, transitions of λ4-cm excited OH not
previously detected in Arp 220 which are seen in absorption, and a possible
absorption feature from the 6.668-GHz line of methanol. This marks the first
distant extragalactic detection of methanimine, a pre-biotic molecule. Also, if
confirmed, the possible methanol absorption line presented here would represent
the first extragalactic detection of methanol at a distance further than 10 Mpc.
In addition, the strong, previously undetected, cm-wave HCN v2 = 1 direct l-type
lines will aid the study of dense molecular gas and active star-forming regions in
this starburst galaxy.
Subject headings: Radio lines: galaxies, galaxies: starburst, galaxies: individual
(Arp 220), galaxies: ISM
1
also, MPIfA, Karl-Schwarzschild-Straße 1, Postfach 1317, D-85741, Garching, Germany
2
also, Department of Physical Sciences, University of Puerto Rico, P.O. Box 23323, San Juan, PR 009313323
3
also, NRAO, Array Operations Center, P.O. Box O, 1003 Lopezville Road, Socorro, NM 87801-0387
–2–
1.
Introduction
Star formation in galaxies occurs in two modes – “quiescent”, in which stars form at a
relatively modest rate over a long period of time across the entire galaxy disk, and “starburst”, in which gas is turned into stars extremely rapidly, confined to compact regions of
the galaxy, often its circumnuclear volume (Kennicutt 1998). Starbursts are often triggered
by external dynamical disturbances such as galaxy mergers. The dust heating associated
with these intense bursts of star formation within giant molecular clouds can produce hugely
increased IR luminosity and conditions favorable for maser emission. The strong 18-cm
OH megamaser emission in some of these galaxies is many orders of magnitude more luminous than its counterparts in our Galaxy (Baan et al. 1982; Baan 1989; Martin et al.
1989; Lonsdale et al. 1998; Darling & Giovanelli 2002). Ultra Luminous Infrared Galaxies
(ULIRGs) are thought to be systems where all of these processes are occurring simultaneously (Elston et al. 1985; Lawrence et al. 1986; Sanders & Mirabel 1996). The existence of
obscured AGNs in these objects are also considered as an alternative (or additional) energy
source where these are fueled by molecular gas falling into the central regions of the merging
systems (Surace & Sanders 1999; Scoville et al. 2000; Sanders & Mirabel 1996; Genzel et al.
1998; Lutz et al. 1999; Veilleux et al. 2002, 2006; Armus et al. 2007; Imanishi et al. 2007a).
Molecular gas is thus one of the most important constituents of the ISM and plays a critical
role in the evolution of galaxies.
To date, over 140 molecules have been identified in space, mostly in the ISM of our
Milky Way Galaxy. Some of these are rather complex, containing as many as 8 to 13 atoms.
Interstellar organic molecules are thought to form mostly on the surface of dust grains.
Heating events, such as the formation of a protostar, release the icy grain mantles into the
gas phase (Nomura & Millar 2004; Caselli et al. 1993). Once released, these molecules may
form amino acids by the combination of organic species known as “pre-biotic” molecules
(Blagojevic et al. 2003). (We note that non-gas phase reaction pathways for the formation of extraterrestrial amino acids have been described in Elsila et al. 2007). Methanimine is one such molecule (CH2 NH; Kirchoff et al. 1973) which can form the simplest
amino acid, glycine (NH2 CH2 COOH), either by (i) first combining with hydrogen cyanide
(HCN) to form aminoacetonitrile (NH2 CH2 CN), with subsequent hydrolysis (Strecker Synthesis; Dickerson 1978), or (ii) directly combining with formic acid (HCOOH) (Godfrey et al.
1973). Methanimine has been previously detected in the interstellar medium of our own
Galaxy (Godfrey et al. 1973; Dickens et al. 1997) and tentatively in the nearby galaxy,
NGC 253 (Martı́n et al. 2006), but never beyond the neighborhood of our Galaxy (i.e. beyond ∼5 Mpc).
The majority of interstellar molecules (both galactic and extragalactic) have been dis-
–3–
covered at millimetric wavelengths, as molecules with small moments of inertia are the most
abundant cosmically, with their rotational lines occurring at mm or shorter wavelengths.
However, although less abundant, many complex molecules have spectral lines in the radio
regime for λ > 3 cm, where “line confusion” does not set a limit to their detectability. Many
transitions of small polycyclic aromatic hydrocarbons (PAHs), pre-biotic molecules, and even
a number of transitions of the simplest amino acid, glycine, fall within the relatively unexplored spectral range between 1 and 10 GHz. In addition, observations in this frequency
range are complementary to mm spectral-line surveys which probe colder, lower density gas.
At Arecibo, we are conducting a spectral line census of Arp 220 between 1.1 and 10 GHz,
for which the initial observations took place between 31 March and 22 April, 2007. It is
planned that the remaining observations will be made in 2008. Here we report the discovery
of methanimine emission in this galaxy, plus the detection of three v2 = 1 direct l-type
absorption lines of HCN (Thorwirth et al. 2003) from the J=4, 5 and 6 vibrational levels.
Also reported is the possible detection of another pre-biotic molecule, formic acid, albeit
not unambiguously due to the presence of a nearby 18 OH line. In addition, we present the
first detections of two, possibly three, λ4-cm transitions of the OH radical in absorption,
high signal-to-noise ratio detections of the λ6- and 5-cm transitions of OH, and the possible
detection of the 6.7-GHz methanol (CH3 OH) transition in absorption.
2.
Arp 220
At a distance of ∼77 Mpc (redshift, z=0.018126), Arp 220 is the nearest Ultra-Luminous
Infra-Red Galaxy. Much of its IR luminosity arises from a powerful, dust-enshrouded starburst, triggered by the merger of two gas-rich galaxies (Sakamoto et al. 1999; Mundell et al.
2001; Sanders & Mirabel 1996). Evidence for this is provided by high resolution optical
and radio images revealing a double nucleus with tidal tails and dust lanes. A high supernova rate has been found from recent high resolution VLBI studies (Lonsdale et al. 2006).
Molecules such as the OH radical (Baan et al. 1982; Ghosh et al. 2003), CO (Scoville et al.
1986), formaldehyde (Araya et al. 2004), ammonia (Takano et al. 2005), and mm-transitions
of HCN (Solomon et al. 1992; Evans et al. 2006; Imanishi et al. 2007b) have been detected
in Arp 220. In fact, Downes & Eckart (2007) have recently used high resolution imaging of
the CO(2–1) line and the λ1.3 mm dust radiation to provide strong evidence for the existence of a “buried” AGN in the western nucleus of the galaxy, a conclusion heavily affecting
interpretation of the situation within Arp 220.
Arp 220 is also known as the prototype OH megamaser galaxy. Its OH λ18-cm maser
emission was first reported by Baan et al. (1982). High-resolution maps of the OH maser re-
–4–
vealed complex structures which could be interpreted either as a dual-component distribution
(Diamond et al. 1989; Lonsdale et al. 1998; Rovilos et al. 2003) or, by clumpy unsaturated
masers within a single-component medium (Parra et al. 2005; Momjian et al. 2006).
3.
Observations
Using several of the complement of receivers on the Arecibo 305-m telescope, we are in
the process of making an almost-complete spectral scan of Arp 220 between 1.1 and 10 GHz.
To do this, we have employed the WAPP (Wideband Arecibo Pulsar Processor) spectrometer
in its recently-commissioned “dual-board” mode. In this mode, eight independent boards,
each of 100-MHz bandwidth with 3-level quantization, can be used to cover a spectral band
of up to 800 MHz at a single time. Compared to the earlier WAPP capacity, this doubles the
total bandwidth covered. The present project serves both for the scientific commissioning of
this new option, and as a demonstration of its capabilities.
In practice, we have overlapped the eight boards for each observation such that their
centers are separated by 85 MHz. As the final 5-or-so MHz are affected by filter roll-off,
this allows high quality data to be acquired for an instantaneous bandwidth of 680 MHz,
meaning that those Arecibo receivers which have total bandwidths of 2 GHz can be fully
covered via three separate frequency settings. The basic spectral resolution is 24.4 kHz, and
both orthogonal polarizations of the celestial signal are recorded.
The observations are being made via a modified version of the Double Position Switching
(DPS) technique (Ghosh & Salter 2002). An ON/OFF position-switched observation with
5-min component phases is made on Arp 220, followed by an ON/OFF with 1-min phases
on the strong, angularly-nearby, continuum source, J1531+2402, which is used as a bandpass calibrator. In the presence of band-pass ripples or trapped-modes in the orthomode
transducer of the feed, this strategy is necessary at all frequencies to produce acceptable
spectral baselines. In addition, apparent features observed in the data can often be recognized
as astronomical, and not due to the presence of radio frequency interference (RFI), via a
comparison of the spectra for Arp 220 and J1531+2402. Data for a total ON-source observing
time of about 60 min for Arp 220 will eventually be acquired for each frequency setting.
Data reduction has been performed using the Arecibo IDL analysis package written
by Phil Perillat. The individual ON/OFF scans on Arp 220 were processed to yield (ONOFF)/OFF spectra, and these were “bandpass corrected” using similar spectra for J1531+2402.
Each individual Arp 220 and J1531+2402 scan was inspected for quality, and all RFI present
was noted. A number of scans were rejected either due to technical problems or because of
–5–
excessive RFI. All acceptable scans for a particular frequency setting were then co-added
to produce the final spectra. These spectra were smoothed in frequency to a number of
resolutions, and the resultant spectra inspected visually to identify the presence of possible emission or absorption lines. Considerable cross-checking was performed to ensure that
candidate lines were real, and not the effect of RFI or equipment problems.
4.
Results & Discussion
A complete cm-wavelength line census for Arp 220, and its full implications for the
physical and chemical properties of the interstellar medium of this galaxy, are deferred until
completion of the observations. Here we present the detection of methanimine in emission,
and of the v2 = 1 direct l-type transitions of HCN, excited-OH transitions, a line that could
be either 18 OH or HCOOH, and possibly methanol in absorption for this prototypical nearby
ULIRG. The spectra are presented in Figs. 1–10, and the parameters derived from them are
given in Tables 1 & 2.
Table 1 presents the results for the emission line of methanimine. The table is ordered
as follows: Columns (1–3) present the name of the molecule, the relevant transition and its
rest frequency in MHz. Col. (4) is the peak flux density of the line in mJy. Col. (5) is the
rms noise on the spectrum in mJy at a velocity resolution of ∼30 km s−1 . Col. (6) is the
radial velocity in km s−1 at the peak of the measured line, derived from the rest frequency
of the strongest of the six lines in the multiplet (i.e. that at 5289.813 MHz). Col. (7) is the
full-velocity width in km s−1 of the entire emission feature at half of the peak intensity.
Table 2 presents the results for lines seen in absorption. The table is ordered as follows:
Columns (1–3) are as for Table 1. Col. (4) is the maximum optical depth of the absorption
line. Col. (5) is the rms noise on the optical-depth spectrum at a velocity resolution of
∼30 km s−1 . Col. (6) is the radial velocity in km s−1 at the maximum optical depth. Col. (7)
R
is the full width in km s−1 of the line at half of the peak optical depth. Col. (8) is τ dV ,
the integrated area in km s−1 under the absorption feature.
In the following sections, we discuss the spectra of each molecule separately.
4.1.
Methanimine (CH2 NH)
The broad emission feature covering all six 110 – 111 transitions of the C-band multiplet
of methanimine is presented in Fig. 1. In Fig. 1a, the rest frequencies of the transitions in the
frame of Arp 220 were derived using a recessional velocity of 5373 km s−1 , as found for the
–6–
western component of the OH megamaser emission of Arp 220, while the heliocentric velocity
axis of Fig. 1b is for the transition expected to be the strongest in the methanimine multiplet,
that at a rest frequency of 5289.813 MHz (Godfrey et al. 1973). The total velocity width
(FWHM) of this emission line is 270 km s−1 ; we note that a large velocity width is observed
for almost all molecular spectra in Arp 220 (e.g. Takano et al. 2005). Using the angular
size of 0.27′′ × 0.21′′ measured for the strongest component of the formaldehyde (H2 CO)
emission (Baan & Haschick 1995) as an upper limit for the angular size of the methanimine
emission region, we derive a lower limit to the brightness temperature of ∼2800 K. Taking
into account the six lines in the multiplet and their relative intensities, we calculate a reduced
value of this lower limit to be ∼1000 K for the strongest component. This is similar to the
methanimine decomposition temperature of 1300 K (Nguyen et al. 1996). If the solid angle
of the emission is smaller than the above, for instance if the emission comes from a number
of very compact components, then the brightness temperature could be much higher. We
conclude that, as for formaldehyde (Araya et al. 2004), methanimine in Arp 220 is likely
to be showing weak maser emission for this transition. We have been awarded time with
the MERLIN array to observe this source at higher spatial resolution in order to determine
the brightness temperature more accurately and to discover where exactly in the galaxy the
emission is located.
4.2.
Hydrogen Cyanide (HCN)
Fig. 2 shows the energy diagram for the v2 =1 direct l-type transitions of hydrogen
cyanide (HCN) in the J=1 to J=6 vibrational levels. Our spectra of the J=2, 4, 5 and
6 HCN transitions are presented in Fig. 3. The J=4, 5 and 6 transitions are detected in
absorption against the continuum emission of Arp 220, and we place an upper limit at the
3-σ level of 0.0025 for the optical depth of the J=2 line. The first detailed study of this type
of HCN transition was carried out for the Galactic proto-planetary nebula, CRL 618, by
Thorwirth et al. (2003). These observers detected a number of the higher vibrational levels
in this HCN ladder (J=8–14). However we note that the lower energy transitions presented
here seem not to have been previously detected in any celestial source. We also note that
these lines represent a high excitation energy above the HCN ground state, (e.g. 1067 K for
the J=4 line.)
HCN is a well known indicator of high gas density. Gao & Solomon (2004) demonstrated
that a very strong linear correlation exists between the luminosities LIR and LHCN for mmwave transitions of HCN, extending over a wide range of LIR from normal galaxies to ULIRGs.
They found the similar LIR – LCO correlation to have a less linear form, marking out LHCN as
–7–
the best tracer of dense molecular gas mass in galaxies, and hence of active star-formation.
However, Graciá-Carpio et al. (2008) present evidence that LIR /LHCN is systematically higher
in (U)LIRGs than in normal star forming galaxies. The relative line integrals from the J=4
and 6 lines suggest an approximate excitation temperature of ∼ 150 K. These transitions
represent high excitation, and given the complicated scenarios now emerging for the central
region of Arp 220, it would be of great interest to ascertain the precise circumstances in
which these absorptions arise.
Unlike the relatively “smooth” line profiles seen for the excited-OH lines (e.g. Fig. 5), the
HCN lines each show evidence for the presence of a number of discrete components. In fact,
the central, strongest HCN component becomes increasingly dominant from J=4 to 6. The
absence of the J=2 line requires explanation, as the predicted absorption line is expected to
be an order of magnitude stronger than the 3-σ limit we place above. It is highly improbable
that the fraction of the continuum emission “covered” by the clouds producing the HCN
absorption could have decreased by such a large amount between 4488 and 1347 MHz that
the J=2 line is rendered unobservable. Much more likely is that free-free absorption in the
foreground ionized screen of this starburst galaxy is greatly attenuating the J=2 line. For
this to be the case, an opacity of & 2.25 at 1347 MHz (in the rest frame of Arp 220) would be
required. This would imply an optical depth of & 1.5 at 1630 MHz in the galaxy, as found
for the spectra of a number of the SNRs near the twin nuclei of Arp 220 by Parra et al.
(2007). These authors attributed this high opacity to the combined presence of “a patchy
FFA [free-free absorption] ISM with a median opacity of less than 1”, plus absorption in the
regions of ionized circumstellar mass-loss envelopes surrounding the SN progenitors. The
HCN lines we see are expected to arise from star-forming regions of high gas density, and a
detailed study of all possible lines in the v2 = 1 direct l-type transitions of the HCN ladder
would provide useful evidence concerning the properties of the foreground gas screen to these
regions. Clearly, the spectrum of the HCN J=3 line (with a rest frequency of 2693.3 MHz)
will be crucial to such a study, and we will be observing this line during our 2008 campaign
to complete the present observations. It should be noted that for the implied optical depths
at 1347 MHz, even the J=4 line will be reduced through FFA by & 20%, which would reduce
the above derived excitation temperature to ∼120 K.
4.3.
Excited Hydroxyl (OH)
The energy levels for the various OH transitions are shown in Fig. 4. In Figs. 5–8
we present the λ6-, 5- and 4-cm Λ-doublet transitions of the OH radical seen in absorption
against the continuum emission of Arp 220. The relevant quantum numbers, rest frequencies
–8–
and other measured line parameters are presented in Table 2. The λ6- and 5-cm lines have
been previously detected by Henkel et al. (1987) and Henkel et al. (1986) respectively.
Contrary to the findings of Henkel et al. (1987), we find that the 4660-, 4751- & 4766MHz lines have intensity ratios closely in agreement with their expected local thermodynamic
equilibrium (LTE) values of 1:2:1.
The λ5-cm main lines presented here have considerably higher signal-to-noise ratio than
the measurements of Henkel et al. (1986) but show similar form. The expected LTE intensity
ratios for the 6017-, 6031-, 6035- & 6049-MHz lines are 1:14:20:1. However, we measure
ratios of 1:13:13:<0.4. The two main lines of the λ5-cm transition (6031 and 6035 MHz)
are blended due to their large velocity widths and give the appearance of being “saturated”,
as suggested by their similar optical depths. This may be due to their having high optical
depths, resulting in saturation of the lines against a continuum component containing of
order 10% of the total flux density of Arp 220. However, we note that there is a low-velocity
component to (presumably) the 6031-MHz absorption line, seen in Fig. 6 at 6026 MHz, which
if also present for the 6035-MHz line would contribute significantly at the frequency of the
6031-MHz line. The satellite lines are seen at much lower signal-to-noise level. However, the
greater strength of the 6017-MHz line relative to that at 6049 MHz is interesting. A similar
effect was also found by Gardner & Martı́n-Pintado (1983) for four compact HII regions in
our own Galaxy. While they saw the 6017-MHz lines enhanced above the LTE ratio to the
main lines, the 6049-MHz line was weaker than predicted, and may even sometimes have
appeared in weak emission.
The two λ4-cm OH lines at 7761 and 7820 MHz (Fig. 7) are detected for the first
time in Arp 220, and show similar velocity widths to most other molecular species in the
galaxy. The expected ratio for these 2Π1/2 , J = 3/2 main lines (7761:7820 MHz) is 1:1.8 in
thermal equilibrium, very close to the derived ratio of the peak and integrated brightnesses
for the lines of 1:1.89 (see Table 2). The satellite lines in this multiplet are expected to be
present only at the 1-σ level, and indeed are not detected. Considering the absorption lines
in the 2Π1/2 ladder of Fig. 4 at 4750 and 7820 MHz, in thermal equilibrium the ratio of
their integrated optical depths would imply an excitation temperature of about 88 K. In a
detailed Large Velocity Gradient (LVG) study of their CO observations, Greve et al. (2006)
find that in Arp 220, the spectra of low density tracers such as CO (and OH) can only be
fitted with a two-phase molecular ISM with the kinetic temperature of one being > 30 K,
while their mm-wave spectra for the high-density tracer molecules, HCN and CS, indicate
kinetic temperatures of ∼50-70 K.
A very tentative detection of the 2Π1/2 , J = 5/2, F = 2–2 line of OH at 8135 MHz is
shown in Fig. 8. If confirmed by the addition of the remaining data to be acquired in this
–9–
project, this would be at least twice as strong as expected for an excitation temperature of
88 K. Further, this line is expected to be only 0.7 times as strong as for the other 2Π1/2 , J =
5/2 main line at 8189 MHz. While the 8189 MHz line is also possibly detected, contrary
to expectations this would be at an even lower signal-to-noise level than for the 8135 MHz
transition.
4.4.
Formic Acid (HCOOH) or “Heavy” Hydroxyl ( 18 OH)
In Fig. 9, we present a high signal-to-noise detection of an absorption line from our
L-band spectrum. Despite the presence of nearby RFI caused by Glonass emissions (at
∼1605 MHz), the reality of this absorption line has been verified by its presence with similar
optical depth in each of 13 individual spectra of Arp 220, but in none of the spectra of the
bandpass calibrator. As demonstrated by the horizontal lines in Fig. 9, there is an ambiguity
as to the species responsible for this absorption, which could be either the 1639.5-MHz main
line of 18 OH or the 1638.8-MHz line of formic acid (HCOOH). Given the prevalence of
OH in Arp 220, it would perhaps not be unreasonable to detect the presence of 18 OH as
well. However, since formic acid is relevant to the chemical origin of life, it would be most
interesting to resolve this ambiguity.
As is seen in Fig. 9, as well as the strong absorption line detected near 1611 MHz, an
apparently weaker absorption is also seen near 1609 MHz, close to where the second, 1637.6MHz, main line of 18 OH should be found. If this feature were indeed to be real, the ratio of
the peak intensity of the higher frequency absorption to this would be 3.1:1. This is higher
than the expected ratio of 1.8:1 were the pair to be the main lines of 18 OH (Barrett & Rogers
1964) and in local thermal equilibrium. The frequencies of the peak depths of the two features
are separated by an amount that would correspond to a rest frequency separation of about
2.05 MHz were they both to be due to absorption in Arp 220. The laboratory separation of
the 18 OH main lines is 1.939 ± 0.003 MHz (Lovas 1986), and hence given the weakness of
the feature near 1609 MHz, the agreement is considered to be satisfactory.
If the absorption near 1611 MHz is indeed the higher frequency component of the 18 OH
main lines, then its radial velocity is closer to that of the peak velocity found for other
molecules in Arp 220 than would be the case were the detection to be of formic acid (see
Table 2 and the horizontal bars displayed in Fig. 9.) However, even for 18 OH, this velocity
of ∼5265 km s−1 is significantly lower than that of the normal molecular peak velocity in
Arp 220. In addition, its width of about 190 km s−1 is narrower than for any other species
that we detect. Were this absorbing gas to represent 18 OH, we note that a velocity of
5265 km s−1 is “allowed” in Arp 220 from the HI absorption study of Mundell et al. (2001).
– 10 –
However, a peak velocity of 5135 km s−1 , appropriate for the formic acid transition, has
little associated HI absorption. Nevertheless, if the absorption were to be due to 18 OH at
5265 km s−1 this would imply a remarkably high isotopic ratio of 18 OH:16 OH for a cloud
at this velocity, especially so as this is well away from the peak velocity range of the OH
megamaser line as seen at low angular resolution (Baan et al. 1982).
Given the proximity of the Glonass RFI, it is difficult to establish the origins of this
absorption feature. However, 18 OH would seem a more likely identification than formic acid.
Confirmation of the reality of the second, weaker, absorption component near 1609 MHz
would effectively establish this identification. The possibility that the feature represents
absorption in our galaxy from the 1612.231 MHz satellite OH line has to be very small given
the high galactic latitude of the line-of-sight (b = 53◦ .0), the implied large radial velocity
(∼+185 km s−1 ), and large line width (∼190 km s−1 ).
4.5.
Methanol (CH3 OH)
In Fig. 10, we present a possible detection of the 51 –60 A+ methanol line in absorption.
Although this line is apparently detected with a signal-to-noise ratio of almost 6:1, and the
entire 100-MHz band in which it is observed is basically RFI-free, the quality of the baseline
in this case is rather poor. We await our remaining observations for confirming the reality
of this line. We note that while the excited-OH absorption line at 7761.7 MHz (Fig. 7:
upper) has a somewhat lower signal-to-noise ratio than this possible methanol detection, the
combination of a better overall baseline, and the 10.5-σ level detection of the associated line
at 7820.1 MHz (Fig. 7: lower) yielding the expected LTE intensity ratio (see Section 4.3),
makes for a more solid detection in that case. We can certainly conclude that at the 1 mJy
level (5σ) no methanol maser emission, such as is commonly detected for this transition from
regions of massive-star formation in our own Galaxy, is seen in Arp 220.
Assuming the reality of the methanol absorption line, an excitation temperature for the
transition of Tex = 20 K, and an Einstein coefficient of A = 0.1532 × 10−8 s−1 (Cragg et al.
1993), and a covering factor of unity, in LTE the column density of the lower energy level,
N6,0 is;
N6,0 = 1.34 × 10
where the integral
R
15
Z
τ δv cm−2
(1)
τ δv is expressed in units of km s−1 .
An approximation for the total column density of methanol can be obtained assuming a
– 11 –
Boltzmann distribution for the methanol energy-level population. If the relative abundances
of the A and E species of this molecule is taken to be 1:1 based on their having a relatively
small ground state energy difference, then the total column density of methanol molecules
is;
E6,0
N = N6,0 2/13 Q(Tex ) e kTex
(2)
where Q(Tex ) is the partition function, taken to be 39.8 (Cragg, D., quoted in Houghton &
Whiteoak 1995), and E6,0 is the energy above the ground state of the 60 A+ level. Thus, the
presence of a 6668-MHz methanol absorption line in Arp 220 would imply a total column
density for this molecule of NCH3 OH ∼ 2.5 × 1017 cm−2 .
5.
Concluding Remarks
The Arecibo Arp 220 Spectral Census is an on-going project and a detailed analysis will
be presented in a separate paper, as will the final spectra from the completed project. We
have presented here the discovery of methanimine in this galaxy and the detection of three
previously unseen cm-wavelength transitions of HCN. We have also observed, for the first
time in Arp 220, an absorption line that may be either formic acid or 18 OH, two (possibly
three) λ4-cm transitions of excited OH, and what may be the first extragalactic detection of
methanol.
The discovery of high abundances of “pre-biotic” molecules, such as methanimine, HCN
and possibly formic acid in Arp 220 raises the possibility that other ULIRGs might contain
similarly high abundances of such molecules, which could be detectable with the Arecibo
305-m telescope.
We thank Paul Goldsmith (JPL), Sven Thorwirth and Karl Menten (MPIfR) for fruitful
discussions, and an anonymous referee for a number of useful suggestions which considerably
improved the paper. The Arecibo Observatory is a part of the National Astronomy and
Ionosphere Center (NAIC) operated by Cornell University under a cooperative agreement
with the National Science Foundation (NSF).
Facilities: Arecibo (L-wide, S-high, C, C-high, X)
– 12 –
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This preprint was prepared with the AAS LATEX macros v5.2.
– 15 –
0.004
Methanimine 111110
multiplets
Flux Density (Jy)
0.003
0.002
0.001
-0.000
-0.001
5280
5285
5290
5295
Rest Frequency (MHz) for Vhel = 5373 km/s
5300
0.004
Flux Density (Jy)
0.003
0.002
0.001
-0.000
-0.001
4800
5000
5200
5400
5600
Heliocentric Velocity (km/s)
5800
6000
Fig. 1.— The blended emission line from the six 110 – 111 multiplet transitions of methanimine in Arp 220. The rest frequencies of the individual transitions are shown by vertical
lines in the upper panel for an assumed heliocentric velocity of 5373 km s−1 (corresponding to the western nucleus of the galaxy). The lower panel shows the same spectrum as
a function of the heliocentric velocity appropriate for the strongest line (rest frequency =
5289.813 MHz) in the multiplet. The velocity resolution is ∼30 km s−1 .
– 16 –
1125
HCN, v2 = 1
1067.10
f
6
1067.05
1105
5
E/k (K)
4488.4718 MHz
1085
1065
4
1067.00
1066.95
3
1045
1066.90
2
1
1025
J
e
1066.85
Fig. 2.— Term value diagram for HCN in its v2 =1 vibrational state from J = 1 to J = 6.
Only the direct l-type transitions with ∆J = 0 are shown. The diagram on the right-hand
side shows the J = 4 direct l-type transition at 4488.4718 MHz in detail. We have presently
observed the J = 2, 4, 5 and 6 transitions at 1346, 4488, 6731 and 9423 MHz respectively
(see Fig. 3). This diagram was drawn using the energy level values obtained from the CDMS
database (Müller et al. 2005, 2001)
.
– 17 –
0.005
0.003
HCN v2 =1, ∆ J=0
J=2
J=4
0.000
Fractional Absorption
Fractional Absorption
0.002
0.001
0.000
-0.001
-0.005
-0.010
-0.002
-0.015
-0.003
4500
5000
5500
Heliocentric Velocity (km/s)
6000
4500
5000
5500
Heliocentric Velocity (km/s)
6000
0.010
0.005
J=5
J=6
0.000
Fractional Absorption
Fractional Absorption
0.000
-0.005
-0.010
-0.015
-0.010
-0.020
-0.020
4500
5000
5500
Heliocentric Velocity (km/s)
6000
-0.030
4500
5000
5500
Heliocentric Velocity (km/s)
6000
Fig. 3.— The first astronomical detections of the v2 = 1 direct l-type absorption lines of
HCN with vibrational levels J=4, 5 and 6 (at 4488, 6731 and 9423 MHz respectively). The
spectra are plotted with heliocentric velocity as abscissa. The non-detection of the J=2
vibrational level (at 1346 MHz) is also included in the figure. The velocity resolution is
∼30 km s−1 .
– 18 –
OH
2
2Π
Π3/2
F
1/2
3
J=5/2
300
2
E (cm 1 )
3
2
F
(Fig 8)
4
3
J=7/2
(Fig 7)
2
200
4
1
J=3/2
3
2
1
1
J=1/2
0
1
3
100
J=5/2
2
0
(Fig 5)
3
2
(Fig 6)
2
J=3/2
0
1
2
1
Fig. 4.— The energy diagram (not to scale) for various Λ-doublet transitions of the OH
radical. The transitions that we have detected (all in absorption) are shown by upward
directed arrows, with the relevant figure numbers also marked. We note that 2Π1/2 , J=1/2,
F=0-0 and 1-1 have identical transition energies.
– 19 –
0.010
OH: 2Π 1/2 J = 1/2,
F = 0 _1
Fractional Absorption
0.000
-0.010
-0.020
-0.030
4500
5000
0.010
OH: 2Π 1/2 J = 1/2,
5500
Heliocentric Velocity (km/s)
6000
F = 1_1
0.000
Fractional Absorption
-0.010
-0.020
-0.030
-0.040
-0.050
-0.060
4500
5000
OH: 2Π 1/2 J = 1/2,
5500
Heliocentric Velocity (km/s)
6000
F = 1_ 0
Fractional Absorption
0.000
-0.010
-0.020
-0.030
4500
5000
5500
Heliocentric Velocity (km/s)
6000
Fig. 5.— The three λ6-cm excited OH transitions from 2Π1/2 , J=1/2, F=0-1, 1-1/0-0 and
1-0 (at 4660, 4750 and 4765 MHz respectively). The spectra are plotted with heliocentric
velocity as abscissa. The F=1-1/0-0 line is about twice as strong as the other two lines. The
velocity resolution is ∼30 km s−1 .
– 20 –
OH: 2Π 3/2 J = 5/2, F=2-3, 2-2, 3-3, 3-2
0.020
0.000
Fractional Absorption
-0.020
-0.040
-0.060
-0.080
-0.100
-0.120
6010
6020
6030
6040
Rest Frequency (MHz) for Vhel = 5325
5425 km/s
6050
6060
Fig. 6.— The four λ5-cm excited OH transitions as a function of rest frequency for an
assumed heliocentric velocity of 5425 km s−1 (as appropriate for the λ6-cm OH lines). The
frequencies of the four transitions 2Π3/2 , J=5/2, F=2-3, 2-2, 3-3 and 3-2 are indicated by
vertical lines. The two main lines form a blended absorption line profile. The velocity
resolution is ∼30 km s−1 .
– 21 –
OH: 2Π1/2 J = 3/2, F = 1-1
Fractional Absorption
0.005
0.000
-0.005
-0.010
4500
0.005
5000
5500
Heliocentric Velocity (km/s)
6000
OH: 2Π1/2 J = 3/2, F = 2-2
Fractional Absorption
0.000
-0.005
-0.010
-0.015
-0.020
4500
5000
5500
Heliocentric Velocity (km/s)
6000
Fig. 7.— First detections of the two λ4-cm excited OH main-line transitions, 2Π1/2 , J=3/2,
F=1-1 and 2-2 (at 7761 and 7820 MHz respectively). The spectra are plotted with heliocentric velocity as abscissa. The velocity resolution is ∼30 km s−1 .
– 22 –
0.010
OH: 2Π 1/2 J = 5/2, F = 2-2
Fractional Absorption
0.005
0.000
-0.005
-0.010
-0.015
4500
5000
5500
Heliocentric Velocity (km/s)
6000
Fig. 8.— A possible detection of the λ4-cm excited OH transition 2Π1/2 , J=5/2, F=2-2 (at
8135 MHz). The spectrum is plotted with heliocentric velocity as abscissa. The velocity
resolution is ∼30 km s−1 .
– 23 –
0.010
0.005
Fractional Absorption
-0.000
-0.005
-0.010
} 18OH main lines
-0.015
Formic acid
-0.020
-0.025
1606
1608
1610
1612
1614
Observed Frequency (MHz)
1616
1618
Fig. 9.— This plot shows one (or possibly two) absorption line(s) that could be either formic
acid or 18 OH. The expected location of the formic acid line and of the two main 18 OH lines are
indicated with horizontal bars. The band is affected by interference from the Glonass system
at about 1605 MHz, but the authenticity of the deep absorption feature has been verified
by its non-appearance in the spectra of the bandpass calibrator. The velocity resolution is
∼30 km s−1 .
– 24 –
CH 3 OH: 51 − 6 0 A+
Fractional Absorption
0.005
0.000
-0.005
-0.010
4500
5000
5500
Heliocentric Velocity (km/s)
6000
Fig. 10.— A possible detection of the 51 –60 A+ methanol line (at 6668 MHz) in absorption.
However, more data is needed to confirm the detection. The spectrum is plotted with
heliocentric velocity as abscissa. The velocity resolution is ∼30 km s−1 .
– 25 –
Table 1. Derived parameters for the emission multiplet of methanimine (CH2 NH).
1
Molecule
Transition
Rest frequency
(MHz)
Sp
(mJy)
σ
(mJy)
vp
(km s−1 )
FWHM
(km s−1 )
Methanimine (CH2 NH)
110 –111 , ∆F = 0, ±1
5289.8131
3.5
0.22
5362
270
The subscript p stands for “peak”.
The strongest of the six lines of this multiplet has this frequency in laboratory measurements.
Table 2. Derived parameters from the molecular absorption lines.
Transition
Rest frequency
(MHz)
τp
στ
vp
(km s−1 )
FWHM
(km s−1 )
τ dV
(km s−1 )
Hydrogen cyanide (HCN)
v2 = 1, ∆J = 0, J = 2
J=4
J=5
J=6
2Π1/2 , J = 1/2, F = 0–1
F = 1–1
F = 1–0
2Π3/2 , J = 5/2, F = 2–3
F = 2–2
F = 3–3
F = 3–2
2Π1/2 , J = 3/2, F = 1–1
F = 2–2
2Π1/2 , J = 5/2, F = 2–2
2Π3/2 , J = 3/2, F = 2–2
1(1,0)–1(1,1)
51 –60 A+
1346.7650
4488.4718
6731.9098
9423.3338
4660.242
4750.656
4765.562
6016.7462
6030.7471
6035.0921
6049.084
7761.747
7820.125
8135.8702
1639.503
or 1638.805
6668.5192
< 0.0025
0.016
0.0205
0.0268
0.0254
0.0549
0.0295
0.0086
0.11
0.00085
0.0009
0.001
0.002
0.00082
0.00080
0.00080
0.0016
0.0016
···
5407
5404
5398
5425
5429
5447
5313
5425
···
363
330
202
300
287
281
···
480
···
5.22
5.02
6.14
7.99
15.91
8.41
···
56.20
< 0.0033
0.0087
0.0162
< 0.01
0.019
···
0.0018
0.00153
0.0021
0.00137
···
5359
5432
···
5265
5135
5384
···
296
321
···
∼192
···
2.62
5.04
···
—3
360
2.53
Hydroxyl radical (OH)
18 OH
or
Formic acid (HCOOH)
Methanol (CH3 OH)
1
2
3
R
Molecule
0.0077
0.0013
The subscript p stands for “peak”.
Since the two main lines F = 2-2 and 3-3 are blended, values presented here are for the two lines combined together.
For these low signal-to-noise detections some of the parameters were not estimated.
Since the identification of this absorption feature is ambiguous, an optical-depth integral was not estimated for it.