Using field plots, three species (Mercurialis
perennis L., Rubus fruticosus L., and
Trientalis europaea L.) were tested
for their potential to emit gaseous ammonia to the
atmosphere. Canopies were misted with 5 mM methionine
sulphoximine (MSO) to inhibit glutamine synthetase (GS),
the enzyme of ammonium assimilation. Leaf tissue
NH4+
concentration of control plants was
0·03–0·1 μmol g−1 f. wt.
Although NH4+
accumulated in the leaf tissue
of MSO-treated plants of all three species to similar
concentrations (6-10 μmol g−1 f. wt
after 4 d), emissions were
only detected from the leaves of M. perennis,
with potential rates of 2·5 nmol m−2
leaf s−1. Experiments carried out
in a controlled environment confirmed this rate of emission
over 9 d, during which time leaf tissue ammonium
increased to 66 μmol g−1 f. wt.
Comparisons with Hordeum vulgare grown under the
same conditions showed that tissue NH4+
concentration reached a plateau of about 40 μmol g
−1f. wt after 2 d. Emissions of NH3
during the 5 d of treatment reached a maximum rate of
10 nmol m−2 s−1
by the third day.
Apoplastic pH of the plants was determined, and it is
suggested that this is an important factor explaining the
differences in NH3 emission between species.
The higher the apoplastic pH, the greater the likelihood of
loss of NH3 from sub-stomatal spaces to the
atmosphere. T. europaea (non-emitter) had an apoplastic
pH of 5, R. fruticosus (non-emitter) a pH of
c. 5·6, whereas that of M. perennis
(emitter) was c. pH 6·3. The apoplastic pH
is thought to be dictated in part by the N nutrition of
a species, nitrophilous species tending to have high pH.
Without NO3− fertilization,
H. vulgare had an apoplastic pH of 6·8 but
this increased to 7·3, 3 d after feeding with
NO3−.
Short-term fumigation (2 h) of shoots of H.
vulgare with 60 μg (≈32 mg NH3
m−3) of labelled gaseous
15N-NH3 (in the absence of MSO) showed
that a substantial proportion (60%) of the applied label
was found in the leaves,
as well as in stems and roots (3%). There was also a change
in amino acid pools, with an increase in shoot amino
acids and a decrease in those in the root, while tissue
NH4+ was very low in both shoots and
roots. This provided indirect evidence that some of the
applied label had been incorporated into an organic form.
Following the fumigation treatment, emissions of NH3
were collected for 3 h, then c. 6·5 μg
of N was recovered, of which c. 17% was
15N-labelled. Some of this label could have
resulted from desorption of NH3 from leaf
surfaces, but it was more likely that the remaining
14N isotope was from sub-stomatal emissions
of NH3.
It is argued that non-nitrophilous plants tend to rely
on mixed sources of N (NO3−,
NH4+ or organic-N) and
are more likely to favour root rather than shoot
assimilation. Under these circumstances, their apoplastic pH is
relatively low (compared with that of nitrophiles, which
tend to assimilate NO3−
mainly in their shoots), and at
atmospheric concentrations most wild species are likely to
be net assimilators, rather than emitters, of atmospheric
ammonia.