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Bol. Soc. Argent. Bot. 55 (4) 2020
would preclude it from being placed in Hantzschia.
According to Round et al. (1990, p. 610), “All
Hantzschia spp., however, seem to have a type of
division in which cells of hantzschioid symmetry
always give rise to two daughter cells both of which
have hantzschioid symmetry; this contrasts with the
situation in Nitzschia.” We tentatively include the
species within Nitzschia, even though the genus, as
currently construed, is non-monophyletic (Kim et
al., 2019). If one envisions a narrow circumscription
of the genus Nitzschia, as typied by N. sigmoidea
(Nitzsch) W. Smith, it would contain those species
that have sigmoid valves and a conopeum, features
not found in Nitzschia araucana.
diScuSSion
The exemplars that we observed showed some
remarkable differences in morphological and
morphometric data as compared to the description
offered by Frenguelli. In observations on hundreds
of valves in Frenguelli’s samples, we never
encountered valves that were both dorsiventral
in shape and possessed a wide spacing of bulae
in the centre of the valves (Fig. 1). Differences,
for example, exist in the size ranges between
our observations and the description offered by
Frenguelli (see Table 1). This mis-match between
the reported sizes by Frenguelli and subsequent
measurements is unfortunately a characteristic
common to Frenguelli’s work and has been
previously documented in studies of type materials
of Frenguelli’s taxa (Gorriti et al., 2000; Sala &
Maidana, 2003; Sunesen et al., 2017; Wetzel et
al., 2017; García et al., 2018; Vouilloud et al.,
2018, among others). There does not seem to be
some consistent factor that is common to these
reports (e.g. that all of Frenguelli’s measurements
are 2X the size measured subsequently). It is a
good reminder of the value of looking directly
at specimens in collections, rather than relying
on even primary (let alone secondary or tertiary)
reports of features that might be incorporated into
a table for species comparisons.
We note here that neither of the taxa considered
here have been recorded since Frenguelli (1942)
described Hantzschia subandina. This is a reminder
that there have been few taxonomic studies in the
region. In addition, due to lack of information in
the original publication, we actually know very
little about the ecology of these species. It is hoped
that studies like the present report will stimulate a
review of Frenguelli’s taxa, and the diatom ora of
Neuquén Province.
Nitzschia, with nearly 3,000 named species and
subspecic taxa (Kociolek et al., 2020), might
be considered ‘the next Navicula’, given both the
morphological diversity that has been forced into
this genus (e.g. Krammer & Lange-Bertalot, 1988).
Results of phylogenetic studies which suggest
that the genus is not only non-monophyletic,
but that several other genera are nested within it
(Hantzschia among them) (Witkowski et al., 2015;
Kim et al., 2019) seem to argue for a a more narrow
circumscription of Nitzschia.
The symmetry of Nitzschia araucana sp. nov.
and the structure of its bulae argue for a closer
relationship with Hantzschia, while variable
products of division (hantzschioid + hantzschioid
and hantzschioid + nitzschioid symmetry of
the sibling cells) suggest this species differs
from Hantzschia. Similarities between Nitzschia
araucana sp. nov. and Hantzschia in terms of
asymmetry might suggest this species occupies
a more basal position in the tree of life for the
Bacillariales, within the context of the formal
analysis presented by Witkowski et al. (2015). If
so, the possibility exists that Nitzschia araucana
sp. nov., along with N. alba J.C. Lewin & R.A.
Lewin (Lauritis et al., 1967), N. hierosolymitana
D.G. Mann (formerly H. fenestrata) and N.
sigmoidea (Mann, 1980), are transition taxa
between the primitive condition of true-breeding
Hantzschia taxa and the more derived condition
of true-breeding Nitzschia taxa (Mann’s 1980,
groups 2 and 3) (Witkowski et al., 2015; Kim et al.,
2019). Mann & Trobajo (2014) described species
of Nitzschia that have conopea and hantzschioid
symmetry. The species that are able to produce
frustules with both types of symmetry may not
necessarily represent a natural group, however,
since the morphological features observed in N.
sigmoidea (Mann, 1986; Knattrup et al., 2007), N.
hierosolymitana (Mann, 1980) and N. araucana
reect a broad diversity of valve features in terms
of raphe, fibulae, cingulum organization and
structure, presence or absence of a conopeum,
among others. Further research is required to detail
the phylogenetic relationships of the Bacillariales