6b. Chironomus 'paracastaneum' n. sp.

This species is recognized as close to C. 'castaneum' on the basis of the cytology and mtCOI sequences, and also close to C. sp.NZ9.

In Bold Bin: BOLD AAL7010.
Along with C. 'castaneum' and C. sp. NZ9.  (see under C. sp.NZ9 for further detail)

Adult:

Two males, one a somewhat incomplete reared male were available for study.  The name C. 'paracastaneum' is suggested for this species and the adult male from Lake Hawea, Otago, South Island, NZ.48.1 male 1 (7.I.1974) has been chosen as the potential holotype since there is also DNA barcode data for this specimen.  Colouration not recorded before DNA extraction and slide mounting.

AR about 3.8;  Wing length 5.37 mm, width 0.86 mm.; VR 1.08; LR 1.33: anterior tarsi without a beard, BR 1.7).
Frontal tubercles present, length about 40-69 µm long and 16-18 µm wide.Palpal proportions (micron): 78 : 56 : 280, 278 : 420.  About 26 clypeal setae.
Thoracic setae: at least 10 acrostichals; 22 dorsolaterals; 6-7 prealars; 1 supra-alar; 27 scutellar in two rows (10 in anterior row, 17 in posterior row).
Leg lengths (micron) and proportions:
 
Fe
Ti
Ta1
Ta2
Ta3
Ta4
Ta5
LR
F/T
BR
PI
1700
1680
2240
1320
1000
820
340
1.33
1.01
0.15
PII
1820
1810
1030
630
440
290
230
0.57
1.01
0.22 
PIII
2120
2260
1540
940
680
420
250
0.68
0.94
0.11 

Abdomen with somewhat triangular (Don Forsyth referred to them as 'bell shaped') brown markings on the tergites, narrowing towards the posterior margin on segments II-IV, then covering most of the tergites.  TIX with 9 setae in a single pale area.


Hypopygium of the proposed type male.

Anal point narrow at base and widening a little at the distal end.  Superior volsella closest to the E(h) type of Strenzke (1959); Inferior volsella reaching about to the end of the anal point or a quarter to a third along the gonostylus, with simple setae.  Gonostyle moderately swollen and narrows markedly from about the distal third to half; about 6+1, 7+1 setae at tip.

Additional data from the other male: AR about 3.7.  Wings damaged LR about 1.33-1.52, anterior tarsi without a beard (BR about 1.7).
Frontal tubercles present, length about 69 µm; for palp only P2 (50 µm) and P3 ( 241 µm) could be measured. about 22 clypeal setae.
Thoracic setae: acrostichals - at least 10; dorsocentrals - about 22; supra-alars 1; scutellar in two rows - 10 anterior, 17 posterior.Leg lengths (micron) and proportions:

 
Fe
Ti
Ta1
Ta2
Ta3
Ta4
Ta5
LR
F/T
BR
PI
1392
1316
2000
1139
810
633
304
1.52
1.06
1.67
PII
1544
2146
873
557
380
266
203
0.59
1.05
 
PIII
1797
1835
1342
835
557
354
228
0.73
0.98
 
Fore Ta5/Ti about 0.23.  Sensilla chaetica difficult to see, perhaps 4 mTa1, 7 hTa1.

.

Female: There is data for a female collected at the same time and from the same site as the proposed type male. It is included here although there is no proof that it belongs to this species (C. forsythi was also present at the location, but the leg ratios are more similar to those of the type male than to those of C. forsythi females).

Wing length 5.37 mm;  wing width: 1.14 mm; VR 1.09.
AR: 0.35; flagella length (micron): 225 : 130 : 155 : 140 : 230, A5/A1 1.02.
Palpal segments (micron): - : - : 105 : 275 : 301; P5/P4 1.35; P5/P3 2.86.   Clypeal width 1.8 times antennal pedicel; 37 setae.
Thoracic setae: About 16 acrostichal; 4-5 humeral; 25-29 dorsolateral (30-33 dl+humls); 8 prealars; scutellars in two approximate rows - anterior row about 15, posterior row about 19 (34 total) setae.
Leg lengths (micron) and proportions:
 
Fe
Ti
Ta1
Ta2
Ta3
Ta4
Ta5
LR
F/T
Ta4/Ti
PI
1620
1560
2100
1080
780
680
340
1.35
1.04
0.45
PII
1620
1700
930
500
360
260
200
0.55
0.95
 
PIII
1900
2140
1400
820
610
360
220
0.65
0.89
 
Sensilla chaetica: about 14 on mTa1, at least 16 on hTa1.

.

Colour of abdominal tergites undetermined but apparently over most of the segment. GcIX with 3 setae; segment X appressed to cercus, crescent shaped, about 280 µm long and 5.9 times longer than its greatest width, with 16 setae.  Cercus (below) with rounded outline; ventral margin longer.


Cercus with closely applied segment X (at left).

Pupa:  Length about 9.4 mm.  Pedes spurii B developed on segment II, and about 55 hooks on posterior margin.  Pedes spurii A well developed on segment IV.
Caudolateral spur of segment VIII with about 3-6 appressed spines.
Anal lobe with a hair fringe of about 132 taeniae on each side.

Fourth instar larva::  A salinarius-type larva, length 12.7-17.2 mm (female); 12.3-14.8 mm (male).  A larva from Winton showed a small bump for the posterior VT (about 0.06mm).  Anal tubules short (200-400 µm) and rounded, only about 2-3x (1.8-3.2) longer than wide.
Frontoclypeus and posterior half to two thirds of gula, dark to very dark, sometimes with some slight darkening at posterior of head capsule.
Mentum (Fig. c) of type II, c1 tooth of mentum broad (broad IIA), 6th laterals turned out.
Ventromentum (Fig. d) about 223.5 (190-248) µm wide and 3.26-3.7 times wider than deep; with about 37.4 (35-40) striae, which reach almost to the anterior margin, particularly at the lateral edges; VMR 0.36 (0.30-0.39).
Pecten epipharyngis (Fig. a) with about 10-14 teeth narrowing towards the edges.  Premandible (Fig. b) with broad teeth, inner tooth about 3-5x the width of the outer tooth and coming to a broad point.
Distance between antennal bases, 164.9 (157-184.5) µm, less than the distance between the S4 setae, 181.3 (164-195) µm.
Antennae (Fig. c) with basal segment about 40% of the VHL and 2.81 (2.38-3.38) times longer than wide, AR 1.84 (1.59-2.07); Ring organ about one third (0.29-0.36) up from base of segment; proportions (µm) 125 : 35 ; 10 : 15 : 7 ; A3 shorter than A4, but longer than A5.
Mandible (Fig. f) about 297.75 (245-328) µm long; generally type IIB, but sometimes 3rd inner tooth darker and more distinct (IIC), and with about 22.5 (18-26) furrows on outer surface near base;12.4 (11-14) taeniae in Pecten mandibularis; Mdt-Mat 22.5-40.5, MTR 0.26-0.36.

Cytology: 4 polytene chromosomes, with the pseudothummi group arm combination (BF, CD, EA, G).
There may be a smaller nucleolus in arm G, but otherwise basic sequences as in C. 'castaneum', with a nucleolus in both arms B and F. Polymorphic in all arms, some unique to this species.Arm A with a sequence differing from A4 of the Australian C. oppositus by a simple inversion which is also found in C. forsythi; arm E commonly differs from E1 of Australian species by a large inversion.  Arm F1 appears identical to that of oppositus F3 and australisF1.    Arm G often partly unpaired.

camA1:    1a-e, 2e - 3, 1f - 2c, 10 - 11, 2d, 8 - 9, 3f-i, 12c-a, 4 - 7, 13 - 19                                                                            as zeaA1 & casA1
camA2:    1a-e, 2e - 3, 1f - 2c, 10 - 11, 2d, 8 - 9, 3f-i, 12c-a, 4 - 7, 13-19                                                                                        i.e. as casA2
camA3:    1a-e, 12a-c, 3i-f, 9 - 8, 2d, 11 - 10, 2c - 1f, 3 - 2e, 4 - 7, 13 - 19                                                                                       from camA1
               (Winton, & also Poutu as casA3)
camB1:    Nucleolus just distal to 4 characteristic bands (grps 24-26), and puff with distal dark bands (grps 8-7) near distal end. i.e. as casB1
camB2:    Inversion of distal third of arm, as nzlB3, bringing puff and proximal dark bands (groups 7-8) close to nucleolus.        i.e. as casB2
camB3:    Inversion of region of the nucleolus,                                   from camB2 (different breakpoints to the difference of camB1 to forB2)
camC1:    groups 4-3 about 1/3 from distal end, with groups 6-5 distal to it.                                                                                    i.e. as casC1
camC2:   simple inversion of distal third from camC1.  (in NZ.67.1 Em#1)
camD1:    as casD1
camD2:    as casD2
camE1:    1 - 3e, 10b - 3f, 10c - 13                                                                                                                                  i.e. as oppE1, etc., casE1
camE2:    1a-e, 3f - 10b, 3e - 2a, 10c - 13                                                                                                                                           i.e. as casE2
camF1:    1 - 2a, 10 - 2c, 15c - 11a, 2b, 15d - 23                                                                                                          i.e. as casF1, oppF3, forF1
camF2:    (approx.) 1 - 2a, 10 - 9c, 4 - 9b, 3 - 2c, 15c - 11, 2b, 15d - 23                                                                                                   as forF2
camG1:    with small subterminal nucleolus
camG2:    from camG1 by a smaller inversion around the median BR than that differentiating camG1 from forG1.   (in NZ.67.1 Em#1)

Click here to see chromosome BF heterozygous for the inversion in each arm.

Known Localities
North Island:
      Lake Rotoaira (37.94°S, 175.56°E), South Auckland (NZ.70.2) (Sofia Ibarrarán) 27-viii-2007
      Lake Okaro (38.30°S, 176.40°E), South Auckland (NZ.10.9) (Sofia Ibarrarán) 14-ii-2007
      Karapiro (39.056°S, 175.705°E), South Auckland (NZ.77.1) (Sofia Ibarrarán) 14-ii-2007

South Island
      abt.1 m in Lake Te Anau (45.17°S, 167.50°E), Te Anau, Southland (NZ.46.2) (Jon Martin) 7-i-1974
      Lake Hawea (44.50°S, 169,17°E), Otago (NZ.48.1) (Jon & C.J. Martin) 7-i-1974
      Owaka River (44.50°S, 169,17°E), South Otago (NZ.56.1) (T.Dodgshun & J.S.Pillai) 14-iii-1974
      Creek at Winton (46.10°S, 168.20°E), Westland (NZ-43-1) (Jon Martin) 5-i-1974

The evidence for this species comes from the cytology and the MtCOI sequence.  The cytology and the MtCOI sequence suggests that there may also be hybridization between C. 'paracastaneum' and C. analis, since at least one specimen has been found with the C. 'campanello' cytology, but the C. analis CO1 sequence.

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Modified: 22 September 2023
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