Saturday, November 7, 2020

Outing Report October 2020: "Highwoods" East Jimbour

 Over several years now I have had the privilege of visiting a property owned by my good friends Martin and Karen Ambrose from Dalby. It is a great spot for the natural historian and is situated off Loves Road, East Jimbour in the southern section of the Brigalow Belt Bioregion. This bioregion holds a good number of Queensland’s rare and threated species of flora and fauna and has been greatly impacted since white colonis-ation, as it also contains extensive areas of deep, black cracking clay soils ideal for crop growing and the pastoral industry. As one local farmer once put it to me, “the soil here (on the Darling Downs) is so rich you could eat it with a spoon”. The Ambrose property is about 10 minutes’ drive from the small township of Jimbour and Jimbour House from whence the Prussian explorer Ludwig Leichhardt commenced his ill-fated journey to the Gulf in 1848.

Martin and Karen purchased the property towards the end of 2012 and named it “Highwoods” after a farm once owned by Karen’s parents in East Sussex in England. The area of the Ambrose property, part of a larger subdiv-ided block, is 77 hectares (188 acres). The main attraction that clinched the deal was the extent of remaining dry bottle tree scrub and the number of magnificent specimens of Queensland Bottle Tree Brachychiton rupes-tris remaining on the property. The Ambrose family are keen conservations and environmentalists and, as well, Martin was keen to try his hand at raising a few head of beef cattle to carry him into his retirement post QPWS. To these ends they have carried out extensive improvements to the property’s infrastructure including the fencing off of areas of remnant scrub and dams to exclude cattle and for the preservation of the local fauna and flora. At any one time, depending on the vagaries of the cattle market and climate, Martin runs about 20-35 Angus steers purchased at about 180kgs and marketed around 330kgs. They are run for about eight months on mainly couch and Rhodes Grass, also Green Panic and Buffel Grass waxing and waning depending on season. Bottle tree scrub occupies about 25% of “Highwoods”. African Boxthorn and feral Pigs are the major pest species on the property.

Fellow TFN member Mark Weaver and I met the main contingent of Field Nats in Jimbour on the morning of the outing around 9.15am after which we took the short drive to “Highwoods” to commence what proved to be very enjoyable day in good company. Martin has been assiduous in maintaining a list of the fauna on his property since moving there and now, after Trish and Lisa’s efforts, has an embryonic flora list to grow. The list now stands at 174 vertebrate species with the main taxon being birds (129 species), 151 invertebrate species with moths and butterflies being their main representatives at 119 species due to Wesley Jenkinson’s efforts. Aside to a few weeds and a couple of ferns the flora list stands at 50 thanks to Trish and Lisa. A list of the birds, plants and most of the invertebrates seen on this day will be appended to this report as composed by Ben, Trish and Glenda, respectively.

Male Red and Blue Damsel (Xanthagrion erythroneurum) (Photo: Robert Ashdown)

 

A few of the highlights of our day worth a mention include our flushing of an Eastern Barn Owl during our morning walk that. Unfortunately it disappeared into a hollow bough before we could indulge ourselves with a good look. The other bird of the day was a single Diamond Dove seen on the shore of one of the property’s dams. Martin had seen this bird in the same location a few days before and it was a new species for the property list. Fortunately, everyone got a good look, and some took photographs of this bird. This same dam is one that Martin has excluded his stock from and is a haven for wildlife. The water is clear, and you can easily see the Curly Pondweed in its depths with its surface presently covered in the pretty flowering Swamp Lily (Water Poppy) and the yellow-flowered Water Primrose. I’m particularly attracted to this dam, as it’s the haunt for a few favourites of mine, the Red-bellied Black Snake and Plum-headed Fiches although, sadly, none were seen on this day. We did, however, record a good number of odonates here, which is another mob I’m enamoured to. We recorded 10 species comprising the damselflies Red and Blue Damsel, Wandering Ringtail, Aurora Bluetail, Common Bluetail and Eastern Billabongfly plus the dragonflies Australian Emperor, Blue Skimmer, Scarlet Percher, Wandering Percher and Common Glider. The Wandering Ringtail and Eastern Billabongfly were new for the property list as was the Eastern Sedgefrog recorded by Robert Ashdown at this dam. Another “new” invertebrate found on the day was the exotic dung beetle, the Grey Dungball Roller Sisyphus spinipes, native to Central and Eastern Africa that was imported during CSIRO’s extraordinarily successful dung beetle programme. Whilst Australia’s dung beetles generally bury their breeding boluses, that can be of various configurations, the Grey Dungball Roller follows in the tradition of the Sacred Scarab Scarabaeus sacer associated in Egyptian mythology with the divine manifestation of the Sun God, Khepri. These ancients saw in this beetle’s trundling of its round dungball a direct association with Khepri’s rolling of the sun across the sky. The Grey Dungball Roller’s beautifully spherical dungballs are quite common on “Highwoods” stashed on the surface under grass tussocks, along edges of logs etc.

One of the many Bottle Trees on the farm
Photo by Robert Ashdown

After our morning’s walk we retired to the Warden’s cottage for lunch. The resurrection and restoration of this cottage has been one of Martin’s main innovations. It was originally constructed in Edward Street in Dalby by the Red Cross where cooked meals were prepared for the homeless and disadvantaged. Later it was moved to Jimbour in a failed attempt to establish a bed and breakfast behind the local store and where it gradually fell into disrepair. Martin purchased it for $1000 and moved it to “Highwoods” and has restored it to its former glory. The outhouse arrived by a similar circuitous route rescued from oblivion on an abandoned homestead site near Moonie. It, too, has been restored to its former glory – if an outback dunnie can be considered in any way glorious? After lunch some of us headed off on another walk whilst others remained at the cottage, as it was now getting quite hot. The afternoon was mainly passed in botanising and Trish would be far more qualified in commenting on the highlights of this aspect of our outing. If I can be so bold, I do remember her getting quite enthused about a tree that she eventually confirmed as the Rose (Crow’s) Apple

Owenia venosa. More than that is beyond my very limited botanical knowledge to relate. I do like plants though, despite what might appear my cavalier attitude here. After we returned from this walk the shadows were lengthening but everyone seemed to have enjoyed the day and there are plans in the offing for a return in the late summer/autumn of the New Year with the option of a campout. Looking forward to that already.
Welcome Swallows and Tree Martins at farm dam
Photo by Robert Ashdown



(Report by Rod Hobson)


Plant list, “Highwoods”, East Jimbour

Property of Martin and Karen Ambrose, 04 October 2020, Trish Gardner and Lisa Churchward, with help from Rod Hobson and Martin Ambrose. Arranged in the order that we found them.

Brachychiton rupestris COMMON BOTTLE TREE

Brachychiton populneus KURRAJONG

Capparis anomala (syn Apophyllum anomalum) WARRIOR BUSH

Carissa ovata KUNKERBERRY

Geijera salicifolia SCRUB WILGA Narrow-leafed form.

Clerodendron tomentosum HAIRY LOLLY BUSH

Cassinia laevis COUGH BUSH

Casuarina cristata BELAH

Erythroxylum sp. Splityard Creek REDWOOD BUSH

Callitris glauca WHITE CYPRESS

Eucalyptus crebra NARROW LEAFED IRONBARK

Alphitonia excelsa SOAP ASH

Acacia tenuinervis SCRUB WATTLE

Cymbidium canaliculatum BLACK ORCHID

Acacia maidenii MAIDEN’S WATTLE

Acacia salicina SALLY WATTLE

Bursaria incana FROSTY BURSARIA

Aristida caput-medusae MANY HEADED WIREGRASS

Ehretia membranifolia THIN-LEAFED KODA

Cheilanthes sieberi var. sieberi MULGA FERN

Teucrium junceum (syn Spartothamnella juncea) SQUARE-STEMMED BROOM

Alstonia constricta BITTERBARK

Pandorea pandorana WONGA VINE

Psydrax sp. CANTHIUM

Denhamia pittosporoides VEINY DENHAMIA

Cayratia clematidea SLENDER GRAPE

Notelaea idymiume SMALL-FRUITED MOCK OLIVE

Capparis sp. NATIVE CAPER

Ficus rubiginosa SCRUB FIG

Muellerina idymium CYPRESS MISTLETOE

Ottelia ovalifolia (syn. Hydrocleys nymphoides) WATER POPPY (flowering)

Ludwigia peploides subsp. Montevidensis WATER PRIMROSE

Potamogeton crispus CURLY PONDWEED

Dendrophthoe glabrescens ORANGE MISTLETOE (flowering)

Alectryon diversifolium SCRUB BOONAREE

Melia azedarach WHITE CEDAR (flowering)

Acacia idymiume DONKEYS EARS WATTLE

Pittosporum angustifolium GUMBY GUMBY

Backhousia angustifolia CURRY MYRTLE

Parsonsia lanceolata ROUGH SILKPOD

Jasminum idymium subsp. Racemosum TRIPLE-LEAF

JASMINE

Pittosporum viscidum BIRDS NEST BUSH (flowering)

Flindersia australis CROWS ASH

Eucalyptus melanophloia SILVER LEAFED IRONBARK

Owenia venosa ROSE APPLE

Croton phebalioides NARROW LEAFED CROTON (SASSAFRAS)

Invertebrates at Jimbour (by Glenda Walter)

Due to the dry weather, not many invertebrates were found on “Highwoods”, the property of Martin and Karen Ambrose at Jimbour. However, I’m sure this will change as soon as rain falls in the area. I photographed three species of ants, two of which were identified by users of the iNaturalist website. A small nest of a species in the genus Meranoplus were found under a dead log. Their common name is “Cautious ants”, appropriate as they moved slowly about, quietly shifting their pupae when disturbed. This was in contrast to the ants in the genus Campon-otus, also identified by an iNaturalist user, which tripped over each other, dashing madly in all directions when I invaded their rock shelter.

Three leaf beetles were found, family Chrysomelidae. Calomela pubiceps is an attractive green beetle which was found on an Acacia tree and for which there are few records; it was identified by Martin Lagerwey, Leaf Beetle expert. A second leaf beetle was identified only to tribe level, Luperini, in the Galerucinae subfamily, also by an iNaturalist user. Many leaf beetles feed only on specific plants, but I was unable to recognise the vegetation on which this one was seen.

Mantids have recently hatched, and the three I saw were tiny nymphs. The burying Mantis, Sphodropoda tristis, when very young curls the abdomen up over its back. It is so named for the female’s habit of burying her eggs in soil or leaf litter. Diana Ball spotted a large and colourful paper wasp, Polistes stigma townsvillensis which was untypically crawling on the ground near our feet while we lunched.

Fourteen spider species were photographed, but many were tiny juveniles. Diane Pagel found several nests of tiny black-spotted pink spiders, recently hatched but too small to identify. Anastasia saw a very small spider egg sac hanging from a fence. This was identified from a Field Guide as belonging to a small orb weaver, Argyrodes alannae. A female of this species was found in the bushes nearby. Anastasia also found a large female spider, Trichonephila plumipes, suspended in her golden web between trees. 

Invertebrate Species list, “Highwoods” East Jimbour SEQ - Oct 2020

Arachnida (spiders, scorpions etc.)

an orb-weaver Araneus albotriangulus (Araneidae)

an orb-weaver Trichonephila plumipes (Araneidae)

a lynx spider Oxyopes variabilis (Oxyopidae)

a comb-footed spider Argyrodes alannae (Theridiidae)

a comb-footed spider Theridion pyramidale (Theridiidae)

Jewel Spider Austracantha minax (Araneidae)

a sac spider Clubiona robusta (Clubionidae)

a crab spider Tmarus cinerasceus (Thomisidae)

Mantoidea (praying mantids)

Stick Mantis Archimantis latistyla (Mantidae)

Burying Mantis Sphodropoda tristis (Mantidae)

Green Mantis Orthodera ministralis (Mantidae)

Orthoptera (grasshoppers, locusts and katydids)

a grasshopper Callitala major (Morabidae)

Coleoptera (Beetles)

a leaf beetle Calomela pubiceps (Chrysomelidae)

a leaf beetle Paropsisterna nigerrima (Chrysomelidae)

a longicorn beetle Phoracantha semipunctata (Cerambycidae)

a lycid beetle Porrostoma rhipidium (Lycidae)

Hymenoptera (wasps, bees and ants)

a paper wasp, Polistes stigma townsvillensis (Vespidae)

Black-headed Strobe Ant Opisthopsis rufithorax (Formicidae



(All photos by Glenda Walter)
Leaf Beetle, tribe Luperini

Leaf Beetle (Calomela pubiceps)


Burying Mantid Nymph (Sphodropoda tristis)


Egg sac of spider (Argyrodes alannae)



                                                Orb weaver spider (Trichonephila plumipes)


Species of ant - genus Meranoplus








 

Bird list: “Highwoods”, East Jimbour, Sunday 04 October

Despite our early start, about 20 attendees assembled at Jimbour, where Rod Hobson and Mark Weaver met us, to lead us to Martin and Karen Ambrose’s property 10 kilometers to the north-east. Here, Martin and Robert Ashdown were waiting. [These four had spent the previous day on the property, and, bird-wise, they achieved a tally of mid-50s of sightings. So, we had a target for our fine weather, if somewhat breezy, day ahead.]

As we turned into Love Rd (the property’s access road), a Sulphur-crested Cockatoo head, crest excitedly displayed, popped out of a hollow in a roadside tree, as if registering disapproval of this early morning intrusion by our procession of eleven vehicles, thereby interrupting its Sunday morning sleep-in. Once past our much-put-out cockatoo, our day produced a further 34 species on the property (a little short of our aspirational target set the previous day).

Welcome Swallow, Tree Martin, Rainbow Bee-eater, Noisy Miner, Apostlebird, Noisy Friarbird, Striped Honeyeater, Spiny-cheeked Honeyeater, Brown Honeyeater, Yellow-faced Honeyeater, Striated Pardalote, Olive-backed Oriole,

Crested Pigeon, Diamond Dove, Yellow-rumped Thornbill, Little Yellow Thornbill, Superb Fairy Wren, Variegated Fairy Wren, Willy Wagtail, Magpie Lark, Double-barred Finch, Red-tailed Black Cockatoo, Galah, Pale-headed Rosella, Little Corella, Black-shouldered Kite, Grey Butcherbird, Pied Butcherbird, Barn Owl, Wedge-tailed Eagle, Channel-billed Cuckoo, Australian Raven, Crow (unknown species), Australasian Grebe (nest & well-grown baby).

Thursday, November 5, 2020

October Speaker Report: USQ Associate Professor John Dearnaley on the topic “Mycorrhizal Associations of Australian Plants”

 Fungi are referred to as the Fifth Kingdom and are more closely related to animals than plants even though many of them grow in soil. They have thread-like cells called “hyphae” which are composed not of cellulose but of chitin. It is estimated that worldwide there are more than 1 million species, about 100,000 of which have been described – many habitats have not been explored, and paid mycologists are rare.

The economic importance of fungi includes their value as high protein food, medicinal use, and as bio-controls. The downside is that they can cause disease, are poisonous in some cases, and can negatively affect our food. They are decomposers and recyclers. Fungal spores are invisible to the naked eye and can be found on every surface in our world.

The word mycorrhiza is derived from Greek words meaning “fungus root”. Symbiotic association between fungi and plants is present in about 80% of plants – fungal mycorrhiza live in or on plant roots, bringing with them nutrients such as water, phosphate, zinc and copper in return for sugar – some plants are highly depen-dent. Most mycorrhizal fungi don’t produce fruiting bodies, so are currently identified by the sequencing of their DNA and comparison to a large data base.

The four types of mycorrhizal association are:

·         Arbuscular mycorrhizas (AM) where mycorrhiza are found on the outside and inside of the plant roots. They are found in association with native plants such as ferns and allies, cycads, Araucaria spp., and Angiosperm families such as Asteraceae, Fabaceae, Mimosaceae, Rutaceae, Solanaceae and Poaceae. Fossilised remains dating back to 400 million years ago have been found – plants and fungi evolved side by side.

·         Ectomycorrhizal (ECM) association – the mycorrhiza form a sheath around plant cells rather than invading them. Examples include all Eucalypts, and species of Casuarina. Eucalypts are not fussy about their fungal partners, and may associate with fungi such as Amanita, Boletellus, Cortinarius, Russula, Pisolithus and others. Fruiting bodies of these fungi may be sometimes seen under trees or projecting from the trunks or roots.

·         Ericoid mycorrhizas (EM) form a loose mantle on plant roots, with coils inside the cells. Examples are plant families Ericaceae and Epacridaceae, heaths and heathers.

·         Orchid mycorrhizas (OM) form coils inside the plant cells. Orchidaceae is the largest plant family, and members are very specific and fussy about their fungal associations - the presence of a suitable fungus controls the distribution of the plant. In addition, the seeds of some orchids such as Dipodium spp. (hyacinth orchids) require certain fungi to germinate. Some orchids even have a three-way association with a Eucalypt and an ectomycorrhizal fungus, making the orchid parasitic on the Eucalypt! Orchids such as Gastrodia sesamoides and the Bootlace Orchid Erythrorchis cassythoides cannot produce their own food, but are dependent on wood-rotting fungi, Campanella spp. and Gymnopus spp. respectively. These are often seen on dead Eucalyptus trees.

Some plants don’t require the services of fungi to live and grow. These include Brassicas, saltbush, sundews, Banksias and Grevilleas. Appropriate mycorrhizal fungi added to agricultural crops can improve nutrient uptake, drought tolerance, and pathogen defence. They play important roles in both natural and agricultural/ horticultural systems. Our thanks to Associate Professor Dearnaley for his informative and interesting presentation, which included many more examples than have been listed here.
(Report by Glenda Walter)

Thursday, October 1, 2020

September 2020 Speaker Report: Plant and Animal Responses to Fire - by Craig Welden

 

Our September speaker’s address on “Fire in the Landscape” couldn’t be more timely or relevant to the past 16 months. But rather than speak about the raging wildfires of last summer, Craig Welden explained the numerous elements involved in successful controlled burns, and the plant and animal responses to them when carried out with due consideration.

As a Senior Scientist at Healthy Land and Water and coordinator of the Queensland Fire and Biodiversity Consortium, Craig has developed extensive skills and knowledge in fire management, weed and pest control, and flora and fauna surveying. 

He spoke of quite a few critical considerations and questions to be answered for successful “burns” and results.

Different areas require site specific planning for their vegetation and fauna, for example, dry vine thicket; brigalow, riparian and rainforest areas do not tolerate fire well at all. Are there exotic weeds in the mix that need intense concentration; how much heat will the native plants tolerate to regenerate; when was it last burnt; what are the expected flora and fauna results if there is no fire and will a plant or animal species become overly dominant, stifling diversity? Other factors to consider include seasonal and weekly weather predictions, the need to vary the months for burning, and nearby areas needing to be left unburnt to offer food and habitat while the burnt areas recover; so much to consider!

Craig also explained some of the unique interactions between Australian native plants and animals with fire: i.e. certain fungi will sprout on black burnt logs; hakeas and banksias release their seeds due to fire heat and smoke; some insects lay their eggs in (sometimes warm!) ashes; frogs and others escape by burrowing into the soil or under logs;  birds feed on insects escaping from ground flames.

The plants that regrow after fire are generally divided into “seeders” and/or “resprouters”, and the latter can be from lignotubers, rhizomes, or epicormic shoots under tree bark. Most eucalypt shoots emanate from deep under the bark and can therefore withstand more radiant heat and flame than other species. Some species require (are obliged to have) fire to sprout and so are called “obligate seeders”. Most of these adult species are killed by fire and their new seedlings are vulnerable to a second fire occurring too soon.

The takeaway message was that wisely controlled fire is integral to the Australian landscape, has been practised for centuries, and affords the recovery and continuation of a vast number of flora and fauna species.

Craig brought copies of two issues of excellent fire information booklets entitled “Living With Fire: Fire Ecol-ogy”, and “Fire Regimes”, which feature many photos taken by Craig himself, and from which I will include here a few major points and observations.

“Fire Regimes” describes 10 broad vegetation types in southeast Queensland, and outlines the recommended frequency, area, season, and intensity of controlled burns for each one. 80°C is a temperature which enables hard coated seeds to crack open, while 120°C kills most seeds and species. Post fire regrowth can be quite positive, especially following rain, with seed germination, seedling growth, and some prolific plant flowerings. 

“Fire Ecology” covers the effect fires have on the burnt flora, fauna (including insects) and soil biota. One major negative side effect on native animals is that open clear burnt understory terrain allows easier feral animal predation. On the other hand, some native fauna prefers the resultant new vegetation after cool fires. But it seems reptiles are more abundant in areas of fewer fires. With frogs, some prefer burnt sites (Litoria frycineti), others (Litoria olongburensis) do not. Ants of 16 taxa showed up strongly in areas burnt annually which was shown by research north of Gympie, along with long-horned beetles at those frequently burnt sites.

Fire also affects, alters, and changes the soil. It burns away surface organic matter, alters nutrient availability and the pH, depletes soil nitrogen, and moisture retention, so rain run-off erosion is more likely. However, indications are that many fungi, soil fauna, and bacteria do recover fairly quickly after a low intensity fire, although that can be quite variable depending on remaining leaf litter.     

(Report by Lauren Marlatt)


Friday, August 28, 2020

MOTH COCOON CLUSTER

 (Article and photos submitted by Michael Rooke)

This cocoon cluster was found on a property at the foot of the Toowoomba Range. It was lying beneath a eucalypt tree from which it had obviously fallen. John Moss, of the Butterfly and Other Invertebrates Club, has identified it as the cocoon cluster of the Mistletoe Emperor Moth (pictured). This moth has recently been assigned to the genus Austrocaligula. The eucalypt tree from which the cocoon cluster had fallen has many clumps of mistletoe, which is the host plant of this moth.

Coccoon cluster

                                Opodiphthera-loranthi


Report on Outing: Sunday 9 August 2020

 

Leopard Ash Park (Dougal Johnston)

Sunday the 09 August was a cool windy morning. A good group collected in Charmaine Court and assembled behind the "vine scrub" out of the wind for an introduction to the remnant dry rainforest park. We then walked through the small walking track in the middle of the forest from south to north.

There is a large variety of vines, creepers, epiphytic orchids, fungus and lichen intertwined with the trees.
There are many Flindersia collina (Leopard Ash) and Geijera salicifolia var latifolia (Broad leaf Scrub Wilga).
Of note was a large Flindersia xanthoxyla (Long Jack). The birds and insects were mostly trying to hide from the wind. Morning tea at Hampton, was a bit windy. The visit to the Motleys spring and waterfall on the head-waters of Gomaren Creek followed.

Bird List (compiled by Tricia Allen)

Despite a very cold, windy and mostly cloudy morning at Leopard Ash Park, members noted a reasonable number of bird species. The following list is as they were reported.

Currawong, Double barred finch, Brown honeyeater, Crested pigeon, Lewin's honeyeater, Yellow faced honeyeater, Rainbow lorikeet, Torresian crow, Superb fairy wren, Magpie-lark, Australian magpie, Brown thornbill, Yellow thornbill, Grey shrike-thrush, Golden whistler, Spotted turtle-dove. 

Jan Veacock noted several Fork-tailed kites on route to the site. 


Praying Mantis at Leopard Ash Park  (photo: Michael McGoldrick) 

The group then travelled to Motley's property east of Haden, where, despite sunnier weather, there were few birds. However we were delighted to see a Wood Duck escorting six to eight newly hatched ducklings on their first outing. A small flock of Wood ducks flew off as we arrived, but otherwise the only birds sighted were Welcome Swallow and Masked Lapwings. (Tricia Allen). 

Headwaters of Gomaren Creek on Motleys' property (photo: Linda Mangubhai)

Plant List for Leopard Ash Park:

Exotic species

Vines

Common Name

Scientific Name

Common Name

Scientific Name

Maderia Vine

Corky Passionfruit Vine

Moth vine

Asparagus (climbing)

Basket Asparagus

 

Chinese elm

Broad leafed privet

Lantana

Tree pear

Box thorn

Green Panic grass

African Love Grass

Anredera cordifolia

Passiflora suberosa

Araujia sericifera

Asparagus africanus

Asparagus aethiopicus cv. Sprengeri

Celtis sinensis

Ligustrum lucidum

Lantana camara

Opuntia tomentosa

Lycium ferocissimum

Megathyrsus maximus

Eragrastis curvula

Slender Grape vine

Scrambling Lily

Native Jasmine

Monkey Rope vine

Bower vine

Wonga vine

Barbed wire vine

Wombat berry vine

Cayratia clematidea

Geitonoplesium cymosum

Jasminium simplicifolium

Parsonia straminea

Pandora jasminoides

Pandorea pandoreana

Smilax australis

Eustrephus latifolius

Epiphytes

Ground cover

Rock felt fern

Mistletoe

 

Bamboo Grass

Aneilema acuminatum

Stinging nettle

Einadia hastata (red-berry saltbush)

Coffee bush

Red ash

Chainfruit

Python tree

Currant bush

Bush caper berry

Scrambling bumble-bush

Silver croton

Native holly

Square stemmed broom

Diamond-leaf pittosporum

Hickory wattle

Leopard ash

Scrub whitewood

Orange boxwood

Sweet Susie

Yellow wood

Blunt-leaved coondoo

Breynia oblongifolia

Alphitonia excelsa

Alyxia ruscifolia

Gossia bidwillii

Carissa ovata

Capparis arborea

Capparis sarmentosa

Croton insularis

Alchornea ilicifolia

Teucrum junceum

Pittosporum rhombifolium

Acacia implexa

Flindersia collina

Atalaya salicifolia

Denhamia sp.

Psydrax odorata

Flindersia xanthoxyla

Planchonella sp.

Narrow-leaf Red Olive-plum

 

Narrow-leaf orange thorn

Box-leaf Canthium

Black plum

Bitterbark

Hard Quandong

Blind your eye tree

Sandalwood

Small-leaved canthium

Blueberry ash

Hairy Birdseye

Scrub Boonaree

Narrow-leaved orange bark

Whalebone tree

Eastern Cottonbush

Broad-leaf Scrub Wilga

Elaeodendron australis var. integrifolium

Pittosporum viscidum

Psydrax buxifolium

Diospyros sp.

Alstonia constricta

Elaeocarpus obovatus

Excoecaria dallachyana

Santalum lanceolatum

Everistia vacciniifolia

Elaeocarpus reticulatus

Alectryon tomentosus

Alectryon diversifolius

Denhamia silvestris

Streblus brunonianus

Maireana microphylla

Geijera salicifolia var. latifolia


Report on Speaker at August 2020 Meeting: Glenda Walter

 

Small creatures of Hartmann Bushland Reserve 

I have been photographing and studying the invertebrates in Hartmann Reserve on the corner of Alderley and Rowbotham Streets over the past five years. This park is particularly interesting, as the insect life there seems to be more prolific than in other nearby parks.

Hartmann Bushland Reserve and homestead were gifted by the Hartmann family to Queensland Parks and Wildlife Service in the 1980s, having first been used as a nursery by the family who had owned it since the 1860s, and later as a rest home. Conditions were attached, such as the preservation of the trees and original vegetation and maintenance in perpetuity as a natural area. QPWS and the Friends of Escarpment Parks regularly remove weeds and care for the Reserve.

The variety and amount of original vegetation (Remnant Ecosystem 12.5.6), and the size of the block have played a part in the very prolific and varied invertebrate life found there. In the five years of the study, 718 species of invertebrates plus a number of birds, reptiles and mammals have been photographed, identified and recorded. Many were seen but escaped before an image was captured, and who knows what other creatures live above head height and in the tops of the mature trees?

I’m grateful to experts such as Martin Lagerwey (Leaf beetles), Ron Atkinson, Robert Raven and Rob Whyte (spiders), Ken Walker (bees), Bob Mesibov (Millipedes), Justin Bartlett (Clerid beetles), Geoff Monteith, Rod Hobson, Christine Lambkin and other Qld Museum staff members, for help with identifications (my apologies for not using titles). I also used websites and Field Guides.

Some examples of the invertebrates found in the five-year period 2015 to 2020 were 11 species of ants; eight species of bees; 122 species of beetles in 22 families; 67 species of bugs in 23 families; 28 species of moths in 13 families; 34 species of flies in 12 families; 26 species of wasps in 10 families; and lastly, 119 spiders in 19 families plus eight which were unidentified to family level. A new millipede was collected under permit and described and named by Bob Mesibov as Cladethosoma toowoomba.

Many images were shown during the talk, and brief mention was made of the habits of some of the subjects, such as spider camouflage (bird dropping spider Arkys curtulus, wrap-around spider Dolophones species, flower spider Thomisus spectabilis); insect mimicry (several Lycid beetle mimics, and spiders and bugs which mimic ants); insect and spider hunting techniques; insect mating habits (the wasp Catocheilus apterus); para-sitism of insects by wasps and flies.

I have now moved house and live some distance from Hartmann Reserve, but was still finding new species every time I visited, so I am sure that there are more to be discovered. It would be an interesting exercise to go back in 10- or 20-years’ time and conduct a similar survey to see how the invertebrate population had changed.

Please contact me on 0429185445 if you’d like a copy of the spreadsheet containing the list of names and other details of these creatures.

(Written by Glenda Walter)

Wednesday, August 5, 2020

OUTING REPORT Dingo Mountain Park, Crows Nest, Sunday 19 July 2020

Dingo Mountain Park, Crows Nest, Sunday 19 July 2020 (Deb Ford)

Twenty-three members and twenty-three visitors met in Chasely Park, Crows Nest, at 9.00am on a beautiful sunny morning, eager to enjoy the Club’s first outing since the beginning of March. Our guide for the morning was Steve Plant from Crows Nest Community Solutions. A long time Crows Nest resident with extensive knowledge of the local flora and fauna, Steve has been working on conserving this large area that represents a unique ecosystem type occurring only on sandstone near Crows Nest. 

Our morning commenced with Steve providing an overview of the extent of the park and neighboring Hart-mann Park and the Bungaree section of the Crows Nest National Park. He gave us a brief history of how the land was acquired and future plans for the park. Before European settlement this area was traversed by Abor-igines travelling from the east to the Bunya Mountains to take part in the triennial Bunya Feasts. Post European settlement (c.1848) the land was used variously for timber getting, grazing, cropping, and pig and chicken farming and as we walked through the park remnants of some of these activities were visible. 

We followed a path down to Crows Nest Creek, passing beside tall Grey Gums (Eucalyptus biturbinata) where Koalas (Phascolarctus cinereus) are often seen, but not on our visit. Spotlighting along this section at night will frequently reveal Greater Gliders (Petauroides Volans), Sugar Gliders (Petaurus breviceps), and Feathertail Gliders (Acrobates pygmaeus). Crossing the Crows Nest Creek, remnants of the old weir are visible, built in the 1930s to augment the town water supply. A permanent water hole is flanked on one side by an attractive sand-stone cliff. 

Leaving the creek, we walked up into Dingo Mountain Park following a track to an ephemeral waterhole, admiring a very large Forest Grasstree (Xanthorrhoea johnsonii) along the way. This first part of the walk was over land previously grazed and, sadly, African Lovegrass (Eragrostis curvula) and Blue Heliotrope (Helio-tropium amplexicaule), both environmental weeds, are well established. Stopping at several places, Steve described the historical use of each place, pointing out items of interest. Leaving the waterhole, we followed a track up the side of a long ridge that rises above the surrounding area. We meandered our way through attractive woodland to the ridge top, skirting sandstone boulders and admiring the many grasstrees. 


Queensland Silver Wattld (Photo: Mike Ford)

With such a large group, and so many questions and explanations, progress was slow but once we reached the ridge top, we were rewarded with 360o views of the surrounding countryside.  Retracing our steps, we returned to the shelter at Chasely Park around midday for a late morning tea/early lunch. With only the morning at our disposal we were unable to visit other areas of Dingo Mountain Park, which we hope to do at a later stage.

Here is a selection of some of the flora encountered along the way:

Acacia granitica GRANITE WATTLE, Acacia podalyriifolia QUEENS-LAND SILVER WATTLE, Angophora leiocarpa RUSTY APPLEGUM, Angophora subvelutina BROAD LEAVED APPLEGUM, Angophora woodsiana SMUDGEE APPLEGUM, Baeckia diosmifolia FRINGED BAECKIA, Banksia oblongifolia DWARF BANKSIA, Banksia spinulosa HAIRPIN BANKSIA, Breynia oblongifolia BREYNIA, Caustis flexuosa CURLY WIG, Chloanthes parviflora, Grevillea floribunda RUSTY FLOWERED GREVILLEA, Kunzea flavescens YELLOW KUNZEA, Leptospermum polygalifolium WILD MAY/ TANTOON, Leptospermum brachyandrum, HARLEQUIN BARK TEA TREE, Petrophile canescens CONESTICKS, Pimelia linifolia SLENDER RICE FLOWER, Pomax umellata, Stylidium laricifolium TREE TRIGGER PLANT, Persoonia sericea GEEBUNG, Xanthorrhoea johnsonii FOREST GRASS TREE.

(Report by Deb Ford)

Bird List compiled by Francis Mangubhai

Kookaburra, Noisy Miner, Striated Pardalote, Spotted Pardalote, White-throated Gerygone, Yellow-faced Honeyeater, Lewin’s Honeyeater, Currawong, Noisy Friarbird, Magpie, Pied Butcherbird, Little Lorikeet, Rainbow Lorikeet, Bar-shouldered Dove, Grey Shrike-thrush, Superb Fairy-wren, Red-backed Fairy-wren, Rufous Whistler, Whipbird, Galah, Torresian Crow, Rose Robin, King Parrot, Brown Treecreeper, Grey Fantail, Brown Thornbill, Yellow Thornbill, Fan-tailed Cuckoo, Black-faced Cuckoo-shrike.


During Dingo Mountain walk (Photo: Francis Mangubhai)