(Figs. 1, 3-6)
Material. Holotype ♂, Chile, Region Metropolitana, Estero La Leonera, Santuario Nacional Yerba Loca, altitude 1812 m; 33 ° 18’ 40.5’’ S; 70 ° 19’ 15.24’’ W, Oct. 2003, Simon Elliott (MNHNC); 1 paratype mature female larva, Chile, Region Metropolitana, Estero La Leonera, altitude 1812 m; 33 ° 18’ 40.5’’ S; 70 ° 19’ 15.24’’ W, Oct. 2003, Simon Elliott (BENTHOS); 4 paratype female larvae, Chile, Region Metropolitana, Estero La Leonera, Santuario Nacional Yerba Loca, altitude 2297 m; 33 ° 18’ 54.72’’ S; 70 ° 18’ 22.92’’ W, Oct. 2003, Simon Elliott (MNHNC); 1 paratype male larva, 2 paratype female larvae, Chile, Region Metropolitana, Estero La Leonera, Santuario Nacional Yerba Loca, altitude 2297 m; 33 ° 18’ 54.72’’ S; 70 ° 18’ 22.92’’ W, Oct. 2003, Simon Elliott (NZAC).
Other Material Examined. 51 larvae, Chile, Region Metropolitana, Santuario Nacional Yerba Loca, 17 – 20 Sept. 2003, A. Vera (MNHNC).
Male. Body length 19.5 mm; antenna 13.5 mm; cercus 8.5 mm. A teneral wingless specimen with pale legs and pronotum; remainder of body light brown with darker bars on antennae. Dorsal surface of body glabrous. Ventral surface of abdomen with last 3 sternites and ventral plate densely covered with short bristles, those in the center of ventral plate with circular bases. Head with large black eyes and 3 prominent ocelli; distal segment of maxillary palp not expanded at tip; Antennae clothed in minute dark hairs, pedicel with prominent Johnston’s organ (Fig. 3). Pronotum subrectangular, wider posteriorly and with all angles well rounded. Mesonotum and metanotum without wings, with small flaps in their place. All legs with a pair of tibial spurs. Forelegs with a sharply pointed triangular procoxal production (Fig. 1), this production not as pronounced on the remaining legs.
Male genitalia. Tergite 10 with medial sclerite sclerotized but almost transparent with white papillate setae scattered over its surface; membranous cone about as long as medial sclerite with minute dark spines over its surface; posterior sclerite lightly sclerotized, about half as long as cone and with a rounded tip. Epiproct with smooth, unadorned basal half; distal half abruptly curved upwards, each margin tapered and with a row of triangular teeth, apex rounded and ventral hook
large. Paraprocts broad, not tapered, short (terminating before ventral hook) and with rounded tip. Penis membranous with 4 lobes (a pair of large lateral lobes, a large ventral lobe and a small dorsal lobe). Cerci clothed in short dark hairs.
Female. Unknown.
Larva. Fringe of hairs mediodorsally on the body, and also dorsally on cerci and legs. Procoxal projections on the front legs are pointed and triangular. Distinct dark marks across abdominal tergites 1-9 and 4 dark marks on the mid base of tergite 10. Hind margin of abdominal tergite of mature male larva not greatly produced and much rounded.
Etymology. This species is dedicated Dr. R. M. McDowall (NIWA, Christchurch, New Zealand) for his extensive work on the freshwater fishes of the Southern Hemisphere.
Comparison with other species. The adults of N. macdowalli are apterous but those of N. fuegiana, the type species of the genus and N. archiplatae and N. tunelina, are winged although wing length may vary from full length to brachypterous. In the male genitalia the epiproct of N. macdowalli is much shorter and thicker than that of N. fuegiana, N. archiplatae and N. tunelina, but the posterior sclerite and membranous cone of N. fuegiana, N. macdowalli and N. archiplatae are similar in length. However in the holotype of the latter species it looks shorter because the shrivelled condition of the specimen has caused a depression at the tip of the membranous cone and the posterior sclerite is sunk in it. The membranous cone of N. tunelina is much longer than that of the other species. The paraprocts of all species are similar.
The larvae of N. fuegiana, N. archiplatae and N. tunelina havewingpadsbut N. macdowalli larvae have none. N. macdowalli and N. tunelina larvae possess pointed and triangular procoxal projections but those of N. fuegiana and, N. archiplatae are rounded. There is a hairy fringe along the dorsal midline of thorax and abdomen of N. macdowalli, N. archiplatae and N. tunelina but not on N. fuegiana. The larva of the new species is more robust than the more slender larva of N. archiplatae. The abdominal markings are darker and more pronounced than in N. archiplatae where they are fainter on tergites 1-9 and absent on tergite 10. Also tergite 10 in the larva of N. macdowalli, is not
Illiesia, 1(5):33-39. Available online: http://www2.pms-lj.si/ illiesia / Illiesia 01-05.pdf
produced much and is very rounded, even in male larvae, but in N. archiplatae it is produced to a sharp point in both male and female larvae.
Remarks. Tibial spurs are present only in the last instar larvae of all Notoperla species. Their absence on earlier instars has caused some confusion in attempts to construct keys for South American gripopterygids. A lobed penis used for producing and inserting a spermatophore is common to all members of the Antarctoperlaria (McLellan 1993). This organ is invaginated under the subgenital plate and evaginated just prior to copulation. There is some variability in the number of lobes. In Austroperlidae for example in the Klapopteryx of South America K. armillata has 3 lobes and K. kuscheli has 7 (McLellan 2001). In New Zealand the monotypic austroperlid genus Austroperla has 5 (McLellan 1997), in Zelandobius (Antarctoperlinae) there are between 3 and 5 (McLellan 1993), yet all Stenoperla (Eustheniidae) have 4 lobes (McLellan 1996) and all species of Zelandoperla have 3 lobes (McLellan 1999). In some genera, but not others, the number of lobes and their shape could be useful characters in distinguishing species, however specimens with evaginated penes are not common.
There are quite a number of apterous species in Gripopterygidae of South America and New Zealand. They are usually alpine species or species at higher latitudes where they are subject to cold temperatures and high winds. In some cases a species may have wing variation in populations ranging from apterous through to full wing populations.
Locality and environment description. Estero La Leonera (see Figure 7) is located in the Yerba Loca Natural Sanctuary in the Andean piedmont of the Metropolitan Region of Chile. It is a permanent first order stream, main tributary of Estero Yerba Loca and ultimately part of the larger Maipo basin.
As with most Andean watercourses at this latitude, La Leonera has a nivo-glacial regime with violent late spring runoffs in December and minimal flow in late fall (autumn).
The environment is semiarid piedmont with sparse vegetation of Andean sclerophytes that form low forests along the watercourses and deep creeks. Such woods are seldom more than 10 m wide but can be quite dense and in some stretches even cast a canopy over the watercourse. The dominating arboreal species at La Leonera are Escallonia revoluta (Lun o Ñipa) aprox.70%, and Kageneckia angustifolia (Olivillo), aprox. 30%. Both are native and they provide ample allochthonous matter although the wood and leaves are hard and slow to decay.
Physico-chemical conditions in La Leonera, as sampled in September 2004, showed cold oligotrophic waters (pH: 7.65, Conductivity: 95.9 µS/cm, TDS: 76.6 mg /L, BOD5: <2.0 mg/L, PO4-P: 3.2 µg /L, P: 11.2 µg /L, T°: 4.6°C). The accompanying macrozoobenthic fauna (Table 1) is consistent with good water quality. Other Plecoptera were found such as Antarctoperla michaelseni and Neonemura barrosi, as well as abundant mayflies such as Massartellopsis irarrazavali and Metamonius anceps, the latter is known to be very demanding in environmental quality, inhabiting only rhithronic waters undisturbed by human activity.
In contrast, there is no macrozoobenthos in Estero Yerba Loca, nor is there any aquatic vegetation, apparently because of the high sulphate, arsenic, copper and iron content of the water plus high acidity (pH 3.45). These characteristics are entirely natural, because Estero Yerba Loca issues from La Paloma Glacier where it is poisoned by minerals which the glacier pours into it as it grinds over the rocks containing those elements. Therefore Yerba Loca may be considered a barrier for the dispersal of freshwater fauna from and into La Leonera.