Categories
Australia Entomology Pterophoridae

Australian Tetraschalis species

Australian occurrences of moths in the genus Tetraschalis (Lepidoptera: Pterophoridae) are distributed down the east coast from around Cairns to the north-eastern corner of Victoria.

At present (July 2026), the Australian Faunal Directory and Atlas of Living Australia include these records under the species Tetraschalis arachnodes Meyrick, 1887, with Trichoptilus inclitus Lucas, 1892 as a synonym. The closely related Tetraschalis lemurodes Meyrick, 1907 is found across the Torres Strait in New Guinea. The species currently known as Oxyptilus causodes Meyrick, 1905 has been found interspersed with Tetraschalis specimens in Australian collections and (based on female genitalia, general habitus, abdominal pattern and overall colouration) may be related to Tetraschalis.

Based on specimen review in ANIC and using iNaturalist observations, it seems clear that lemurodes occurs at least in Far North Queensland. Occurrences from Brisbane and to the south (as far as north-eastern Victoria) seem to be arachnodes (== inclitus). The few Australian occurrences of causodes are from Far North Queensland and the Top End of the Northern Territory.

The original descriptions for all taxa are included at the end of this post.

Separating the species

The available records show that there is significant variation in the markings and colouration of arachnodes and lemurodes, although the two species can readily be separated in well-marked individuals. Structural aspects are also sometimes difficult to assess. As with many other plume moths, the shape of the forewing can be obscured by angle, rolling of the segments and the breadth of the fringes.

More review is required to confirm whether the species overlap in south Queensland, but the specimens in ANIC (for which structural aspects are easier to assess) seem to divide cleanly between with arachnodes from the Sunshine Coast south through New South Wales, and with lemurodes from regions north of Mackay. The iNaturalist observations show the same geographic break in distribution between northern and southern records and, to the extent that this can be judged, the images are compatible with the same assigment (arachnodes to the south and lemurodes to the north).

Tetraschalis arachnodes Meyrick, 1887

© Ken Harris, some rights reserved CC BY-NC, November 9, 2016, near Mallacoota, VIC

Currently the most southerly record in iNaturalist is this individual from Mallacoota in Victoria. It shows the following characters:

  • The wings and abdomen appear disproportionately long.
  • The four black-scale teeth (two on each hind-wing) show clearly.
  • The ground colour is greyish brown.
  • The pale forewing markings matching those in Meyrick’s description for arachnodes (“a cloudy narrow white band on base of first segment, a broader one at its middle, and a narrow one at three-fourths”).
  • The antennae are not dark
  • The scale-tufts on the forelegs are very bushy.
  • The first forewing segment dilates a little after the cleft and has a visible termen with a clear tornus (angle).
  • The second forewing segment is also moderately broad (relative to lemurodes).
CC0 by Barb, December 15, 2022, Brisbane, QLD

This record from Brisbane in south Queensland shows a reddish individual, and in particular the bushy tufts on the legs are reddish-brown and contrast with the colour of the tibiae. This seems to be a good character for arachnodes. This insect also shows the whiteness of the antennae. However, although the shape of the first lobe remains clear, the second lobe appears narrow, perhaps as a result of angle or rolling.

© Nicholas John Fisher, some rights reserved CC BY-NC, September 20, 2024, Lismore, NSW

This insect from Lismore in northern New South Wales is much more fuscous. Although the shape of the first forewing lobe is again clear, the colouration on the lobe resembles that of typical lemurodes.

Tetraschalis lemurodes Meyrick, 1907

© domf, some rights reserved CC BY-NC, July 2026, Lockhart River, QLD

One of the most northerly Australian records for the genus is this individual from the Lockhart River in Far North Queensland. It

Original descriptions

Tetraschalis Meyrick, 1887

Meyrick, E. (1887) On Pyralidina from Australia and the South Pacific. Transactions of the Entomological Society of London 1887: 267:

TETRASCHALIS, n. g.

Forehead without tuft. Antennae minutely ciliated (1⁄4). Palpi moderately long, ascending, with appressed scales, terminal joint long, filiform. Tibiae tufted with scales on origin of spurs. Fore wings bifid, cleft from middle; veins 2 and 4 stalked, 3 absent, 5 and 6 very short, 7 from below angle of cell, long, 9, 10, and 11 out of 8. Hind wings trifid, third segment with tuft of black scales in dorsal cilia; vein 2 from middle of cell, 3 absent, 5 and 6 very short, 7 to apex.

Allied to Oxyptilus, but distinguished by having vein 11 of the fore wings rising out of the stalk of 8, 9, and 10.

Tetraschalis arachnodes Meyrick, 1887

Meyrick, E. (1887) On Pyralidina from Australia and the South Pacific. Transactions of the Entomological Society of London 1887: 267-268:

Tetraschalis arachnodes, n. s.

♂, 21—24 mm. Head, palpi, thorax, and abdomen light brownish-ochreous, mixed with whitish, reddish, and dark fuscous scales. Antennae whitish. Legs very slender, whitish, irrorated with reddish-fuscous, anterior and middle pair tending to be longitudinally striped. Fore wings with segments linear, first slightly, second posteriorly moderately dilated, pointed; reddish-fuscous, sprinkled with whitish and irrorated with dark fuscous; a cloudy narrow white band on base of first segment, a broader one at its middle, and a narrow one at three-fourths, two latter also indicated on second segment; cilia grey, irregularly mixed throughout with black scales. Hind wings cleft firstly from one-fourth, secondly from near base, segments linear; fuscous, third segment dark reddish-fuscous; cilia grey, third segment with a few black scales on upper margin, on lower margin with a tolerably continuous row of close black scales from near base to apex and a fringe of white hair-scales, a large triangular tooth of black scales beyond middle and another at apex.

Newcastle, New South Wales; two specimens, in indifferent condition (Australian Museum).

Trichoptilus inclitus Lucas, 1892

Lucas, T.P. (1892) On 34 new species of Australian Lepidoptea, with additional localities, &c. Proceedings of the Royal Society of Queensland 8: 94:

TRICHOPTILUS (?) INCLITUS, sp.nov.

♂ ♀. 23-26 mm. Head fuscous, closely irrorated with ochreous. Palpi dark fuscous. Antennae ochreous fuscous. Thorax fuscous grey, irrorated with ferruginous fuscous. Abdomen ochreous fuscous, longitudinally streaked with grey, black and fuscous. Tibiae alternately banded light ochreous, fuscous and dark fuscous, anterior pair specially thickened with scales on origin of spurs. Forewings cleft from before middle, segments linear, ferruginous ochreous with dark fuscous, darker toward hindmargin; an ochreous white spot on costa at ⅚. Cilia smoky-grey, on costa narrowly based with fuscous ochreous, darker toward apex; 2nd segment with cilia of darker shade toward base. Hindwings cleft first from before ⅓, secondly from base, segments linear, ferruginous fuscous. Cilia of 1st and 2nd segments smoky grey; 3rd segment darker ferruginous with black cilia.

This appears much the largest species of the genus taken in
Australia. Mr. Boyd of Toowoomba found the first specimen
and Dr. T. L. Bancroft found a second near Brisbane which unfortunately got damaged by ants.

Tetraschalis lemurodes Meyrick, 1907

Meyrick, E. (1908) Notes and descriptions of Pterophoridae and Orneodidae. Transactions of the Entomological Society of London 1907: 476:

Tetraschalis lemurodes, n. sp.
♂ ♀. 23-24 mm. Head, palpi, and thorax dark reddish-fuscous sprinkled with blackish and whitish. Antennae grey, above dotted with black and white scales. Abdomen very long and slender, dark reddish-fuscous sprinkled with whitish. Legs dark reddish-fuscous lined with white. Fore-wings very narrow, cleft from ⅓, segments almost linear, second segment with tornus slight but distinct, its apex extremely slender and elongate ; dark reddish-fuscous sprinkled with whitish ; first segment with a broad band of whitish suffusion beyond its middle, and a narrow fascia towards apex, sometimes also much suffused with whitish anteriorly : cilia dark fuscous, on costa whitish with several dark fuscous patches, on lower margin of first segment with some scattered white and black scales, on both margins of second segment irregularly mixed with black scales. Hind-wings cleft firstly from ⅕, secondly from near base, segments linear ; dark fuscous ; cilia dark fuscous, on upper margin of third segment with scattered black scales, on dorsum much mixed with black and white scales from base to apex, forming a rather longer and more conspicuous accumulation beyond middle.

KEI ISLANDS, in April and May; two specimens.

Oxyptilus causodes Meyrick, 1905

Meyrick, E. (1905) Descriptions of Indian Microlepidoptera. Journal of the Bombay Natural History Society 16: 582:

Oxyptilus causodes n. sp.

♂ ♀. 20 — 22mm. Head, thorax, and abdomen dark reddish-fuscous, face without tuft. Palpi long, slender. Forewings with segments narrow ; dark reddish-fuscous, slightly sprinkled with whitish-grey, especially on first segment ; an ochreous-whitish costal dot or small spot at middle of first segment, and a slender ochreous-whitish bar near its apex ; cilia fuscous, with numerous scattered blackish scales, forming a bar at lower angle of tip of first segment, rounded dark fuscous black-edged spots at tip of second and tornus, and two undefined projections on its dorsum. Hindwings with segments linear ; dark fuscous; cilia fuscous, on third segment mixed with black scales at base on both margins, with a large triangular black scale-tooth on lower margin at 3⁄4, and a small one beneath apex.

Nine specimens, Peradeniya, Ceylon, in August and October (Green). Larva feeds in fleshy fruits of Dillenia retusa, in August ; when about to pupate, it leaves the fruit and attaches itself to any neighbouring support (Green).

Categories
Alucitidae Australia Biodiversity

Australian Alucita species

Australia currently has six named species in the genus Alucita (Lepidoptera: Alucitidae). This post is to bring together the original descriptions for these species and link these to images for each species.

Alucita acascaea (Turner, 1913)

Turner, A.J. (1913) Studies in Australian Lepidoptera, Pyralidae. Proceedings of the Royal Society of Queensland 24: 161:

ORNEODES ACASCAEA, n. sp.

ἀκασκαιος, delicate.

♀ 9 mm. Head, thorax, palpi, and antennae white. Palpi moderate, ascending ; terminal joint about ½ second. Abdomen whitish with several median reddish-fuscous dots Legs white. Forewings white ; markings very pale reddish-fuscous : first segment with a broad fascia beyond middle and a second before apex; other segments with similar markings but much less pronounced ; cilia white. Hind-wings white; segments barred at intervals by fuscous irroration ; cilia white.

In size and fragility this agrees with O. pygmaea.

Type in Coll., Turner.

N.Q. Cardwell, in August; one specimen.

Alucita agapeta (Turner, 1913)

Turner, A.J. (1913) Studies in Australian Lepidoptera, Pyralidae. Proceedings of the Royal Society of Queensland 24: 161-162:

ORNEODES AGAPETA, n. sp.

ἀγαπητος, lovely.

♂ 17 mm. Head white: face grey with some white scales. Palpi short, ascending ; terminal joint ¼, whitish. Antennae grey-whitish ; in ♂ finely serrate and minutely ciliated. Thorax and abdomen white. Legs white ; anterior pair suffused with fuscous anteriorly. Forewings white ; costa interruptedly fuscous ; first segment with four or five pale-fuscous bars in posterior half; bars formed by dark-fuscous irroration on second, third, fourth, and fifth segments before middle; broad pale-fuscous fasciae edged by dark-fuscous scales on second and third segments at ⅚, on fourth and fifth segments at ¾, and on sixth segment at ⅔ ; pale-fuscous sub-terminal bars and dark-fuscous terminal dots on all segments; cilia white, on apices of segments pale-fuscous. Hindwings as forewings but ante-median bars nearer to base, and with a faintly-marked series of median bars.

Near O. xanthodes though very different in coloration.

Type in Coll., Turner.

N.A. Port Darwin, in April; one specimen received from Mr. F. P. Dodd.

Alucita phricodes Meyrick 1886

Meyrick, E. (1886) On the classification of the Pterophoridae. Transactions of the Entomological Society of London 1886: 20–21:

Alucita phricodes, n.s.
♂, ♀, 14—17 mm. Head, thorax, and abdomen dark fuscous, sprinkled with whitish, and tuft whitish ; abdomen with a narrow white ring at one-third from base. Palpi dark fuscous, internally whitish, 2nd joint obscurely banded with whitish at three-fourths and apex, terminal joint banded with whitish at one-fourth and three-fourths; 2nd joint long, porrected, beneath with dense projecting scales on apical half, forming a very short broad truncate tuft, terminal joint about three-fourths of 2nd, anteriorly roughened with scales, somewhat thickened in middle, pointed. Antennae dark fuscous. Legs whitish, suffused with dark fuscous
above, except on posterior tibiae, of which the basal half is clothed with short rough whitish hairs above. Wings formed as in A. hexadactyla. Fore wings with segments blackish, 1st segment with six ochreous white-margined spots, last two largest, remaining five segments with small white and ochreous spots, and an ochreous subapical band; cilia pale greyish, with dark grey obscurely whitish-margined markings, forming three irregular transverse
fasciae ; first narrow, about one-fourth ; second moderate, angulated outwards above middle, and sinuate inwards below middle; third broader, obsolete near inner margin, towards costa obscurely dilated so as to appear connected with last three anteapical dark costal spots. Hind wings with segments blackish, with small white and ochreous spots; cilia pale greyish; markings obscurely whitish-margined; a rather narrow dark grey fascia before middle, extending from vein 1 to 4; on posterior half of wing three indistinct grey regularly dentate narrow fasciae, second becoming double on first two segments, and much darker towards inner margin and on posterior costal branch.

Duaringa, Queensland; Sydney, New South Wales ; locally common, especially at rest on fences, in August, September, November, and January.

Alucita pygmaea Meyrick 1890

Meyrick, E. (1890) Descriptions of additional Australian Pyralidina. Proceedings of the Linnean Society of New South Wales 4: 1112–1113:

Aluc. pygmaea, n.sp.
♂, ♀, 8—9 mm. Head and thorax white, speckled with dark fuscous. Palpi white. Antennae whitish. Abdomen ochreous-white, sides speckled or suffused with dark fuscous, second segment white with a dark fuscous blotch on each side. Legs white, anterior tibiae dark fuscous. Forewings and hindwings white, clearly and finely striated transversely throughout with ochreous-brown ; six irregular clear snow-white transverse bars, finely margined on both sides with black : cilia wholly whitish.

Duaringa and Brisbane, Queensland, in February ; five specimens received from Mr. G. Barnard and Dr. T. P. Lucas. Mr. Barnard states that they sometimes swarm by thousands in the scrubs. It is a curious and interesting little insect, much the smallest species of the genus.

Alucita xanthodes Meyrick, 1890

Meyrick, E. (1890) Descriptions of additional Australian Pyralidina. Proceedings of the Linnean Society of New South Wales 4: 1112:

Aluc. xanthodes, n.sp.

♂, 15 mm. Head white, crown light ochreous-yellow. Palpi white. Antennae ochreous-whitish. Thorax yellow-ochreous, spotted with white. Legs white, anterior pair banded with dark fuscous. Forewings and hindwings bright yellow-ochreous, crossed by six irregular white lines ; fifth and part of third lines finely margined anteriorly with black, fourth and sixth (subterminal) finely margined posteriorly with black : cilia alternately ochreous and white.

Duaringa, Queensland, in February ; one specimen received from Mr. G. Barnard. A very pretty and distinct species.

Alucita xanthosticta (Turner, 1923)

Turner, A.J. (1923) Art. VI. New Australian Micro-Lepidoptera. Proceedings of the Royal Society of Victoria n.s. 36(1): 58:

ORNEODES XANTHOSTICTA, n.sp.
♂ 13 mm. Head yellow; face white. Palpi whitish; a slight fuscous suffusion on outer surface of second joint. Antennae white. Thorax and abdomen yellow. Legs whitish ; anterior tibiae suffused with fuscous. Forewings and hindwings yellow; wing segments very obscurely barred with whitish; a series of fuscous dots on segments at ⅓, and another double series at ⅔ ; a series of subapical fuscous dots.

Very similar to O. xanthodes, Meyr., but much smaller, with white face and antennae, no fuscous costal spots, but with subapical dots; xanthodes expands 20 mm.

Queensland: Rosewood in April; one specimen taken at light.

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Miscellaneous

Digital cameras for wildlife observations

What I photograph

These are notes from my personal history on experiences with capturing images as a tool for recording wildlife. My perspective is limited. I don’t take time to produce really stunning artistic photographs. I use my camera to record what I see as faithfully and as crisply as I can. My targets are usually insects and other invertebrates, birds, mammals, reptiles and smaller numbers of flowering plants and fungi.

My primary goals are to provide reference shots for myself and others to improve identification for less well-recorded species and to provide evidence for mapping and monitoring species distributions and populations.

Over the years, these basic goals have led me to try many different cameras to find one best suited to my needs and to maximising simplicity. Most of this post is a cursory examination of what has driven my choices at each stage and where I find myself today.

TL;DR - My needs seem to be well met by a combination including the Sony RX10 IV camera, the Marumi DHG Achromat 330 (+3) macro lens, and a GODOX MF12 macro flash set.

I share my photographs in a few key places on the web, always under a Creative Commons Attribution (CC BY) licence so that I can maximise the potential value others can gain from my images and so that there’s a way I can be contacted in cases of misidentifications:

  • Flickr – my primary destination for all my photos that are not of irretrievably low-quality.
  • iNaturalist – my primary channel for making these images useful for biodiversity research and monitoring (and to get identifications for organisms outside my expertise).
  • Global Biodiversity Information Facility (GBIF) and Atlas of Living Australia (ALA) – secondary channels, in that I rely on iNaturalist to pass them on, but these are in fact the main reason I take time to photograph wildlife.
  • Wikimedia Commons – secondary channel for long-term reuse, mainly from other Wikipedians taking the time to add my photos from Flickr.
  • Mastodon – cherry-picked photos I feel like talking about on a given day.

I also take a lot of photos under a microscope (mainly again insects and other invertebrates), but this piece is about field photography.

Before digital cameras

In the distant pre-digital past, I tried to photrograph birds with various largely unsuitable film cameras. Probably the only useful legacy from those efforts (aside from a few slides) is this photo of the only Little Auk I’ve ever seen, in Southwick (Sussex, UK) in 1995.

Photograph of choppy water in a marina with a tiny black and white bird occupying perhaps 0.25 percent of the image area.
Alle alle, Little Auk or Dovekie, Southwick, UK, 29 November 1995 (some long-forgotten film camera)

Around a year after that photo was taken, I began getting seriously interested in the UK’s moths, mostly with help from the only good guide readily available at the time, Bernard Skinner’s The Colour Identification Guide to Moths of the British Isles (1st edition). The only cameras I had lacked any macro capability, so I started my journey into entomology with a pack of coloured pencils and my appallingly limited artistic skills. The following drawings are sadly representative.

In 1999, we moved to New Zealand and purchased a video camera that wrote to magnetic tape (no idea what brand or model). With some care, it could capture and export still images, so my first insect photos are of relatively large moths attracted to our garden in Auckland, like this ghost moth, Aenetus virescens. These images were only 768 x 576 pixels in size.

Aenetus virescens, Mairangi Bay, Auckland, New Zealand, to MV light, 8/9 November 1999 (some video camera)

Coolpix 4500 and other bridge cameras

Canon PowerShot SX60 HS camera with Raynox DCR-250 macro lens and a collapsible flash diffuser
Canon PowerShot SX60 HS camera with Raynox DCR-250 macro lens and a collapsible flash diffuser

In 2002, as we returned to Europe (Denmark, during my first stint with GBIF), we bought a real digital camera. Internet discussion groups had identified the Nikon Coolpix 4500 as the camera of choice for reasonably inexpensive macro photography, boasting a 4 megapixel resolution (2272 x 1704 pixels) and the ability to focus as close as 2 cm without serious distortion, so that is what we got. The first insect I photographed with it was a many-plume moth, Alucita hexadactyla in August that year.

Alucita hexadactyla, to MV light, Hellerup, Denmark, 2 August 2002 (Nikon Coolpix 4500)

I went on to use it for thousands of images, mainly of moths I attracted to light but also other wildlife. It always took excellent photos, although it was completely unsuited to photographing birds or any animals at a distance.

Pogona barbata (Cuvier, 1829), Eastern Bearded Dragon, Aranda, ACT, 18 September 2009 (Nikon Coolpix 4500)

Somewhere around 2009, I was feeling constrained by the lack of zoom capability and tempted by the increasingly large sensors of newer cameras. Although though I continued to use the Coolpix 4500 for moths, I invested in a series of different bridge cameras to give more flexibility in the field. These included a Nikon Coolpix P6000, a Canon PowerShot SX40 HS, then a Canon PowerShot SX50 HS and finally a Canon PowerShot SX60 HS.

Macropus giganteus Shaw, 1790, Eastern Grey Kangaroo, female with joey, Aranda, ACT, 21 October 2009 (Nikon P6000)
Emmelina monodactyla (Linnaeus, 1758), to Robinson trap, Søborg, Denmark, 1/2 June 2014 (Canon PowerShot SX40 HS)
Notodryas vallata Meyrick, 1897, to actinic light, Blackheath, NSW, 8/9 November 2014 (Canon PowerShot SX50 HS)

I usually carried a Raynox DCR-150 or DCR-250 macro lens that I clipped in front of the camera lens when I needed true macro. With the PowerShot cameras, these lenses gave me the same versatility as the Coolpix 4500 but with larger image sizes and the ability to use the same camera for telephoto shots of birds.

This combination was very effective, but although it brought some improvements on the telephoto side, the PowerShot SX60 was less satisfactory than earlier models for macro use since images were heavily vignetted by the Raynox lens except at the very highest zoom levels. I was able to zoom in and take great pictures of the smallest insects, but I had to remove the lens, change camera settings and rely on non-macro zoom if the insect was larger than around 25 mm. Constantly switching backwards and forwards between Raynox macro and non-Raynox telephoto disrupted the experience of photographing moths at a light sheet (probably my most significant use for a camera).

Canon DSLRs

Canon EOS 7D camera with Canon EF 100 mm f/2.8L Macro IS USM lens and Canon MT-24EX twin macro flash
Canon EOS 7D camera with Canon EF 100 mm f/2.8L Macro IS USM lens and Canon MT-24EX twin macro flash

Eventually, because of my focus on macro imagery, I took the plunge and invested in a Canon EOS 7D DSLR with EF 100mm f/2.8L Macro IS USM lens and (ultimately) the MT-24EX twin macro flash unit. This is a fantastic and very flexible combination. The autofocus is great, and it’s easy to get good images. The flash unit is perfect for illuminating the area in front of the lens, although it can need to rest briefly to recycle. This delay has rarely been a problem for me, except when charge is very low.

So, for several years my standard field equipment has been a Canon DSLR for moths/macro and a bridge camera for other wildlife. The disparity between image quality for moths and birds caused me also to test a telephoto lens (Sigma 150-600 mm f/5-6.3 DG) and even to go into the field with two DSLR bodies (EOS 7D and EOS 6D) so I could switch more quickly between lenses.

Habrosyne pyritoides (Hufnagel, 1766), Buff Arches, to LepiLED and actinic light, Utterslev Mose, Søborg, Denmark, 15 June 2018 (Canon EOS 6D, Canon EF 100 mm)
Chrysopilus cristatus (Fabricius 1775), female, Rude Skov, Denmark, 30 June 2018 (Canon EOS 6D, Canon EF 100 mm)
Nucifraga columbiana (Wilson, 1811), Clark’s Nutcracker, Rocky Mountain National Park, Colorado, USA, 21 September 2016 (Canon EOS 7D, Sigma 150-600 mm)
Ochotona princeps (Richardson, 1828), American Pika, Rocky Mountain National Park, Colorado, USA, 21 September 2016 (Canon EOS 7D, Sigma 150-600 mm)

I was always exceptionally happy with the results from Canon DSLRs, but the bulk and weight is troublesome when carrying or traveling with multiple lenses and bodies. Taking so much equipment was particularly problematic when camping.

So, in recent years, I’ve found myself rarely carrying anything bulkier than the PowerShot SX60 except when I am photographing moths at light. Because of the hassle of doing everything properly, I’ve found myself taking many fewer pictures than formerly.

Sony RX10 IV

Sony RX10 IV camera with Marumi DHG Achromat 330 (+3) macro lens and GODOX MF12 macro flash set
Sony RX10 IV camera with Marumi DHG Achromat 330 (+3) macro lens and GODOX MF12 macro flash set

I recently decided to do something about this. I’ve been testing a simpler solution and have been immensely pleased with the results.

The Sony RX10 IV is a bridge camera with a Zeiss 24-600 mm equivalent zoom lens. It covers my desire to photograph birds and mammals much better than my past equipment, including the Sigma lens.

Macropus giganteus Shaw, 1790, Eastern Grey Kangaroo (with cloud of flies), Black Mountain, Canberra, ACT, 22 February 2024 (Sony RX10 IV)

The native macro capability of the camera is good for quick images of flowers, etc., but a couple of additions makes it an astoundingly good camera for macro.

First, the Marumi DHG Achromat 330 (+3) macro lens (in the 72 mm size) plays the same role the Raynox DCR-150/DCR-250 lenses did with my older PowerShot cameras, but with virtually no vignetting throughout the zoom range. This means I can go from a field of view around 20 cm wide down to little more than 20 mm simply by zooming. Focusing the camera of course relies on moving backwards and forwards to find the correct distance. This is less optimal than the autofocus offered by the EF 100 mm lens, but the camera does manage to adjust focus within a narrow relevant range.

Secondly, a pair of GODOX MF12 macro flash units and a GODOX XPro II Trigger replace the Canon MT-24EX flash unit but with greater flexibility and an unbelievably short refresh interval. The ring that holds the twin (or up to six) flashes can be attached to the camera itself or to the Marumi lens using a 72 mm screw adaptor.

So far, I’ve attached the flash outside the Marumi lens. The flash ring does very slightly vignette the frame when the zoom is below around 34 mm. I suspect that with some extra step-up/step-down rings I could mount the ring further back or even behind the Marumi lens and avoid all obstruction.

The camera is now giving me macro images that are every bit as good as those I was taking with the Canon setup. The complete Sony combination weighs 1.70 kg compared to 2.25 kg for the Canon. Another advantage is the relatively low profile of the GODOX trigger compared with the very upright trigger component of the MT-24EX. In the past, if I wanted to add light to help locate an insect, I held a torch below the EF 100 mm lens. Now I can use a head torch directed at a slight downward angle. This is much easier. The GODOX flash units also have LED focusing lights that seem very good for this but that clearly place some drain on the flash batteries. It should be noted that the MF12 batteries are not removable. When drained, the flash unit itself must be recharged. With the MT-24EX flash unit, all power comes from AA batteries. Hence the longer recycle times, but that does allow the batteries easily to be switched in the field.

Strepsinoma foveata, to light, Aranda, ACT, Australia, 2/3 March 2024 (Sony RX10 IV)
Stangeia xerodes, to light, Aranda, ACT, Australia, 2/3 March 2024 (Sony RX10 IV)
Christinus marmoratus, to light, Aranda, ACT, Australia, 2/3 March 2024 (Sony RX10 IV)

Conclusion

For now, it seems the Sony RX10 IV serves my needs exceptionally well. I am much more ready just to go out with the camera to see what wildlife I can find and photograph.

As a final comparison, here are two images of an ichneumon wasp taken with the Canon 7D and the Sony RX10 IV. I believe I could have done more to optimise each camera for these shots, so this should not be treated as a realistic comparative test, but these photos again show how well the Sony does in this macro configuration.

Lissonota macqueeni, sample from SLAM trap, Aranda, ACT, Australia, 17-24 February 2023, photographed 2 March 2024 (Canon EOS 7D, Canon EF 100 mm, Canon MT-24EX)
Lissonota macqueeni, sample from SLAM trap, Aranda, ACT, Australia, 17-24 February 2023, photographed 2 March 2024 (Sony RX10 IV, Marumi DHG Achromat 330, twin GODOX MF12)