BDInsight – September 2023

Welcome to the September 2023 edition of the BDInsight. We have plenty of news to share and plenty of exciting events coming up. Read on to find out more…..

Biodiversity Observations

The graph shows that there were 2978 downloads of papers in Biodiversity Observations during August 2023. That is a new record! In 2023, we are working on Volume 13, and there have been 28 papers published this year so far, with a total of 232 pages.

Downloads from Biodiversity Observations
Histogram shows number of papers downloaded each month from Biodiversity Observation during the past six years

Of the papers published in 2023, the one with the most downloads is A Guide to the Common Garden Birds of Cape Town, South Africa which had been downloaded 1172 times by 31 August. You can find the the paper here: https://journals.uct.ac.za/index.php/BO/article/view/1316. This link does not download the paper itself; it takes you to the page where you click on the PDF to get the paper. The image below is the Common Waxbill page in the garden birds guide.

The Common Waxbill text in the Guide to the Garden Birds of Cape Town
This is the description for Common Waxbill in the Guide to the Common Garden Birds of Cape Town. If you make yourself a printed version, you can point your cell phone at the QR code on the right, and you get taken directly to the text for the Common Waxbill on the BDI website (see the next article in this BDInsight).

12 out of the 28 papers in Biodiversity Observations so far in 2023 deal with observations on birds in South Africa. This means that the journal is getting increasing support from other taxa and from other countries (and continents). For example there is an excellent paper by Mike Fraser on the reptiles and amphibians of the Cape of Good Hope section of the Table Mountain National Park (here), two papers on ducks in Algeria (here and here), one on a bullfinch on an island in the Caribbean (here), one on a snail in Turkey (here), etc. Here is a list of the 28 papers in 2023 volume to date: https://journals.uct.ac.za/index.php/BO/index

A key measure of the success of a journal is when other authors cite papers in it. One of the most fascinating papers in the 2022 volume last year described the havoc caused by an invasive snail in India. The Giant African Snail Lissachatina fulica is classified as one of 100 worst invasive alien species and has been introduced to more than 50 countries. These are huge snails and they are indigenous to Africa (believe it or not this snail gets kept as a pet). The Biodiversity Observations paper has been cited in a paper about this snail into Italy. The link to the original paper is here; the paper from Italy that cites it is here (and the new paper is in an Open Access journal).

File:Snail in Ubud, Bali, 2010 (1).jpg
Giant African Land Snail – photo by Alexander R. Jenner.

The first paper in the volume 13 of Biodiversity Observations provides a summary of the first 12 volumes! It is available here.

BDI Bird Species Identification Texts

Species identification consists mostly of moving backwards and forwards between an illustration, and text describing the key identification features. We have simplified that, and put the text onto the illustration. The image here is for the Karoo Lark:

The ID image for Karoo Lark
This is the identification photo for the Karoo Lark. You don’t need to learn the names of all the different parts of a bird before you can identify birds!

There are now 75 “BDI-style” species texts for birds on our website. Each of the texts starts with an annotated photograph like the one above. The next sections cover Habitat (with photos), Distribution (with bird atlas map), and Behaviour (with words and photos).

The website links for the 75 species which we have done to date can be found here: http://thebdi.org/bird-species/. Click on the name of any species on this page, and you get the BDI text for it. This is what the website looks like:

This is what the BDI website looks like for find bird species
This is only an image of the bird list, just to show what it looks like! You need to go to the bird list website itself to be able to click on a species and reach its text.

If you do a google search for any of these 75 species, the BDI text is usually on the first page of the search. Here is what to look out for in a google search for a species.

What the Hartlaub's Gull looks like in a Google Search
At the time when the google search was done for Hartlaub’s Gull, the BDI text for the species was in 6th position!

These species texts are available from the Virtual Museum. The Virtual Museum record for a species which has been done, has the word “Text” on the second line. Click on it, and you get the BDI species text. For example, this is a recent record of Cape Sugarbird:

Cape Sugarbird record in the Virtual Museum
This is also an image from the website. The links don’t work from here! To see this record in real life, go to
https://vmus.adu.org.za/?vm=BirdPix-258842

We are not doing the species at random. Our first target group of 32 species consisted of garden birds of Cape Town, and they were used to produce “A Guide to the Common Garden Birds of Cape Town”. As described above, this is the most downloaded paper in Biodiversity Observations so far this year. The species texts currently being produced “BDI-style” are for other similar themes. Watch this space.

With each BDInsight we will list the species with new texts.

Bird Ringing

We have learnt a huge amount about birds through bird ringing. Watch Mark Brown’s outstanding contribution called “Why ring birds?” to Conservation Conversations  

There is also a blog on this topic on the BDI website. It is called “The value of bird ringing to conservation and research.” It is recommended reading!

Among other initiatives, the BDI is focusing lots of attention on bird ringing and training bird ringers this past year. The bottom line is that there is still a vast amount to learn about our birds which can most readily be done through bird ringing. There are two quantities that are crucial for understanding species, and for designing management plans for them. One is survival and the other is movement. For both of these, we know very little for almost every South African species.

The way to find out these quantities is to focus ringing effort for a long time on a small number of sites. This is what we plan to do.

The blog on the BDI website contains links to past ringing events and courses, going back to 2019: http://thebdi.org/2023/07/14/bdi-bird-ringing-courses-and-events/ It is a fascinating account of how our thinking has grown and matured over the past five years (and how we have persevered with this vision in spite of all the hassles).

You can find out when the next ringing courses and events are taking place here: http://thebdi.org/upcoming-bdi-events/. You are warmly invited to participate.

Virtual Museum

Up-to-date distribution maps for species are critical for taking conservation decisions about species. Spring is springing, and the butterflies and moths, dragonflies and damselflies, will soon be out and about. Now is the time to dust off your cameras and get out into the field and start refreshing records in the Virtual Museum.

Records made long ago in a grid cell are slowly losing their value as evidence that the species is still present there, and need to be refreshed.

If your access to the Virtual Museum is not working (eg password issues) please contact Megan Loftie-Eaton for help (megan@thebdi.org).

RAVE 2023!

RAVE = RINGING, ATLASING AND VIRTUAL MUSEUMING EXPEDITION

What are the dates, places and costs?

  • 27 November–03 December at Botuin, Vanrhynsdorp
  • 4–10 December at Vondeling Wine Farm, Paardeberg, Wellington
  • 11–15 December at Ouberg Private Nature Reserve, Montagu
  • 16–18 December at Botuin, Vanrhynsdorp

We invite you to attend this citizen science event for as many days as are feasible for you. The cost for food and accommodation (sharing) is R750 per person per day. At Botuin, single accommodation is available at a facility close by. There is one single room at Vondeling. The cost of a single room is R900 per person per day. These dates are confirmed and the accommodation booked, but they can be extended, either by operating at more than one place at the same time, or by starting earlier

What will you gain and what will you give?

As a participant, the most important ingredient towards the success of the RAVE is enthusiasm!

This RAVE is the initial major event for setting up the BioObservatory. Our specific goals during the RAVE focus on ringing, atlasing and the Virtual Museum (VM). Through bird ringing, atlasing, and BirdPixing (for the Virtual Museum), we aim to:

  1. obtain annual survival estimates of key species via recaptures of ringed birds.
  2. build information on local movements of birds by systematically ringing at nearby sites.
  3. strengthen our understanding of moult.
  4. improve our knowledge of annual breeding success and the timing of breeding through a monitoring programme that estimates the percentage of juveniles in the populations at each site.
  5. develop guides that will help ringers and trainee ringers to age and sex birds.

These goals will not be attained through a single expedition, but with each event we are laying the foundations for a BioObservatory. RAVE goals contribute towards the wider goals of the BioObservatory:

  1. We aim to increase the numbers of ringed birds at the three sites (here is a summary of BDI ringing events, with many having been held at the three RAVE sites). We are aiming to increase the size of the existing database. Ultimately, the purpose is to improve the conservation outlook for as many of the species at these sites as possible. We aim to achieve this using the information and understanding gained from bird ringing.
  2. We want to build on the existing bird atlas data for the three sites, with a view to moving in the direction of systematic atlasing, as has been shown to be dramatically effective in monitoring bird population sizes in the Hessequa Region, centred on Stilbaai. For waterbirds, we will supplement the atlasing by undertaking counts of waterbirds at nearby wetlands.
  3. We plan to do as comprehensive surveys as we can for the other taxa represented in the Virtual Museum, but especially butterflies and moths, dragonflies and damselflies, and dung beetles. We will try to make substantive contributions to all sections of the Virtual Museum (digitally curated photographs of various taxa). We need to work out monitoring strategies for these taxa which are appropriate for the three sites.
  4. We would like to engage with local communities. We want to share our enthusiasm for biodiversity with the people who live in the areas close to our sites. We need to brainstorm how to achieve this. It could be through an Open Day, when anyone can join us in ringing or any other activity. Alternatively, we could invite the teachers at a local school or members of the farming community to join us.

Where will we stay?

At Botuin there are three cottages that each sleep two people. There is unlimited accommodation close by. We have all our meals at Botuin. Botuin lies on the southeastern edge of Vanrhynsdorp, 300 km north of Cape Town (three hours’ drive) along the N7 towards Namibia. It is on the edge of Namaqualand.

Gifberg, Vanrhynsdorp
Ringing at Botuin, Vanrhynsdorp

At Vondeling there are two comfortable cottages in the werf. One sleeps six people in two bedrooms for three people each. The other, which we also use as our main gathering place, sleeps five: two bedrooms each with a double bed, and one with a single bed. A couple of tents and caravans are feasible. Vondeling Wine Farm is 75 km northeast of Cape Town (one hour), on the eastern edge of the Paardeberg.

Vondeling Wine Farm
Vondeling Wine Farm

At Ouberg there is accommodation for 11 people. There is no alternative accommodation in easy striking distance, but a handful of tents and caravans are eminently feasible. Ouberg is 205 km east of Cape Town (2.5 hours), in the mountains on the edge of the Little Karoo. It is 20 km north of Montagu.

This is the house where we stay while bird ringing at Ouberg
Ouberg Private Nature Reserve

Who is in charge?

The expedition will be led by Les Underhill (overall coordination), Dieter Oschadleus (bird ringing), Salome Willemse (administration) and Jean Ramsay (finances). We are supported in multiple areas by other citizen scientists.

How do I apply to join the RAVE?

Send an email to Salome Willemse (ring@thebdi.org), and tell her the dates you would like to attend. We will do our best to accommodate you.

When will the next RAVE take place?

We don’t know. It all depends on the success of this one! But our biggest fear is that we won’t have the capacity to meet the demand.

We hope that you will join us, either now or in the future!

Gurney’s Sugarbird (Promerops gurneyi)

Cover image. Gurney’s Sugarbird by Colin Summergill – Carter’s Hill, KwaZulu-Natal – BirdPix No. 252816 

Identification

The Gurney’s Sugarbird is an interesting and attractive species, resembling an overgrown sunbird. The sexes are alike in colouration and plumage but males are larger and longer tailed.

Gurney’s Sugarbird (Promerops gurneyi) 
Paardeplaats Farm, Mpumalanga
Photo by Greg Goosen

The head and face are distinctively marked. The forehead and forecrown are russet-brown and the hind crown, neck, lores and ear coverts are greyish-brown. The chin, throat and supercilium are buffy white, and malar stripes are very indistinct or absent. The upper breast is warm, rufous-brown and the lower breast and belly is white, with long, blackish streaks, especially towards the flanks. The vent is bright yellow and conspicuous. The rump is greenish-yellow and best seen in flight. The dark brown tail is long and graduated with a wedge-shaped tip. The bill is black, long and slightly decurved.

Juveniles resemble females but have a plain brown breast (not warm rufous) and the vent is dull yellow.

Promerops gurneyi
Gurney’s Sugarbird (Promerops gurneyi) 
Sani Road, KwaZulu-Natal
Photo by Pamela Kleiman

The Gurney’s Sugarbird is distinctive and unlikely to be mistaken for any other species, with the exception perhaps of the Cape Sugarbird (Promerops cafer). Gurney’s Sugarbird is smaller, shorter tailed and more richly coloured than its Cape relative. The two species have almost exclusive distributions which overlap marginally in the Eastern Cape.

Gurney's Sugarbird
Gurney’s Sugarbird (Promerops gurneyi) 
Sani Road, KwaZulu-Natal
Photo by Pamela Kleiman

Status and Distribution

Gurney’s Sugarbird is uncommon to locally common and is endemic to Southern Africa. Its distribution is closely linked to that of the Silver Protea (Protea roupelliae). The core of its range lies along the eastern Drakensberg escarpment from the Eastern Cape to KwaZulu-Natal, extending into the high mountains of the eastern Free State. Scattered populations occur on the mountains between north-central Limpopo Province and north-western Eswatini (Swaziland), including the Waterberg and Soutpansberg ranges. There is an isolated population in the eastern highlands of Zimbabwe and adjacent Mozambique. Historically, its range overlapped with the Cape Sugarbird in the Amatole Mountains, Eastern Cape.

SABAP2 distribution maps Gurney's Sugarbird
SABAP2 distribution map for Gurney’s Sugarbird (Promerops gurneyi) – August 2023.
Details for map interpretation can be found here.

The Gurney’s Sugarbird is not currently threatened, but its Protea-savanna habitat is at risk from afforestation. Commercial protea farming in KwaZulu-Natal Midlands provides additional habitat, but the damage caused by birds to flowers could lead to control measures being taken.

Promerops gurneyi
Gurney’s Sugarbird (Promerops gurneyi)
Sani Road, KwaZulu-Natal
Photo by Pamela Kleiman

Habitat

The Gurney’s Sugarbird inhabits montane grassland and scrub in with Protea, Aloe and Strelitzia spp, including areas adjoining Afromontane forest. Distribution in South Africa largely coincides with that of Silver Protea (Protea roupelliae). Often found in gardens and stands of proteas on flower farms in the KwaZulu-Natal Midlands.

Habitat Gurney's Sugarbird
Typical habitat
Gurney’s Sugarbird (Promerops gurneyi)
Carter’s Hill, KwaZulu-Natal
Photo by Colin Summersgill

Behaviour

Usually encountered solitarily or in pairs, but sometimes in loose groups at a rich food source. Gurney’s Sugarbird is largely sedentary, but moves locally during the non-breeding season. This is either in response to food availability and the flowering phenology of proteas, or moving to lower altitudes in winter.

Gurney's Sugarbird
Gurney’s Sugarbird (Promerops gurneyi) 
Giant’s Castle, KwaZulu-Natal
Photo by Alan Manson

Gurney’s Sugarbird feeds mainly on the nectar of Protea species but also from a wide range of tubular-shaped flowers such as Aloes, coral-trees (Erythrina spp), bottlebrushes (Greyia spp), Tree-fuchsia (Halleria lucida), torch lilies (Kniphofia sp), wild daggas (Leonotis spp.) etc. Also takes invertebrates like beetles, bees, ants and spiders and sometimes also consumes pollen.

Promerops gurneyi
Gurney’s Sugarbird (Promerops gurneyi)
Goldengate Highlands National Park, Free State
Photo by Ilse Hulme

This species is monogamous and strongly territorial during the breeding season which normally coincides with the peak flowering time of Protea species. The breeding season runs from June to February in KwaZulu-Natal, from November to February in Limpopo and Mpumalanga, and from July to April in Zimbabwe. Males actively chase off rivals and any other nectar-feeding species during this time.

Gurney's Sugarbird
Gurney’s Sugarbird (Promerops gurneyi)
Sani Pass, KwaZulu-Natal
Photo by Gregg Darling

The nest is constructed by the female only with the male staying nearby to protect the territory and nest site. The nest is a loose bowl of twigs, rootlets, grass and bark fibres and is lined with soft grass and the fluffy heads of Protea seeds. The nest is most often situated 1 to 3 m above the ground amongst the branches of Silver Protea (Protea roupelliae) or Common Protea (Protea caffra) trees.

One or two sandy-brown eggs are laid per clutch and incubation begins once the second egg has been laid. The female is responsible for all the incubation duties and the incubation period lasts from 16 to 28 days. The nestlings are fed and cared for by both parents.

Gurney's Sugarbird
Gurney’s Sugarbird (Promerops gurneyi) 
Lydenburg district, Mpumalanga
Photo by Dawie De Swardt

Further Resources

Species text adapted from the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by Alan Manson, Colin Summersgill, Dawie De Swardt, Greg Goosen, Gregg Darling, Ilse Hulme and Pamela Kleiman is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Kaapse suikervoël (Afrikaans); Promérops du Cap (French); Kaapse Suikervogel (Dutch), Kap-Honigfresser (German), Papa-açúcar do Cabo (Portuguese)

Recommended citation format: Tippett RM 2023. Gurney’s Sugarbird Promerops gurneyi. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/08/30/gurneys-sugarbird-promerops-gurneyi/

Bird identificationbirding

Promerops gurneyi
Gurney’s Sugarbird (Promerops gurneyi)
Goldengate Highlands National Park, Free State
Photo by Ilse Hulme

Cape Sugarbird (Promerops cafer)

Cover image by Marna Buys – Kirstenbosch, Western Cape – BirdPix No. 61050 Cape Sugarbird

Identification

The Cape Sugarbird is a very distinctive species, resembling an overgrown and long-tailed sunbird.

The sexes are alike in plumage colouration but males are larger and have much longer tails. The tail length in adult males varies considerably and can be up to 3 times the length of the body.

Cape Sugarbird (Promerops cafer) Male
Van Stadens Wild Flower Reserve, Eastern Cape
Photo by Philip Nieuwoudt

The upperparts are brown with indistinct darker blotches or streaks, especially on the mantle. There is a prominent malar stripe on the lower face with a white stripe above it. The chin and throat are off-white and the upper breast is brown with feint paler mottling. The lower breast and belly are greyish-white with distinct brownish-black streaking. The vent is bright yellow and conspicuous. In flight they show a greenish-yellow rump. The dark brown tail is long (very long in males), graduated and ribbon-like.

Cape Sugarbird (Promerops cafer) Female
Near Stilbaai, Western Cape
Photo by Johan and Estelle van Rooyen

Juveniles resemble females in having shorter tails but they are duller with browner underparts and lack the yellow vent of the adults.

The Cape Sugarbird is easily recognisable and not easily mistaken for any other species. The closely related Gurney’s Sugarbird (Promerops gurneyi) is smaller with bolder patterning, richer colouration, and a shorter tail. The ranges of the two species overlap very marginally in the Eastern Cape.

A male Cape Sugarbird (Promerops cafer) showing the greenish-yellow rump.
Mpofu Dam, Eastern Cape
Photo by Gregg Darling

Status and Distribution

The Cape Sugarbird is a common resident or local-nomad and is endemic to South Africa and the Fynbos Biome. It is restricted to the Western and Eastern Cape provinces. It ranges from near Calvinia and Nieuwoudtville at the north-western edge of its distribution, across to near East London and the Amatola Mountains at the eastern edge of its range.

SABAP2 distribution map for Cape Sugarbird (Promerops cafer) – August 2023.
Details for map interpretation can be found here.

Habitat

The Cape Sugarbird is virtually restricted to the Fynbos Biome and is the quintessential fynbos bird.

Typical habitat
Cape Sugarbird (Promerops cafer)
Kleinmond, Western Cape
Photo by Les Underhill

It is sometimes attracted to suburban gardens or patches of alien vegetation, however, its occurrence in other vegetation types is usually due to that habitat being close to Fynbos, or of transient birds moving from one fynbos patch to another. Generally reluctant to leave fynbos, except in response to fire.

Within its chosen habitat, the Cape Sugarbird occurs almost exclusively in places with an abundance of Proteas (Family Proteaceae), often in hilly or mountainous areas.

Cape Sugarbird (Promerops cafer) Male
Rooi-Els, Western Cape
Photo by Gerald Wingate

Behaviour

The Cape Sugarbird is largely sedentary, but becomes nomadic during the non-breeding season, moving locally in response to food availability. The flight is fast and direct with the tail streaming out behind.

During the breeding season the Cape Sugarbird is most often encountered solitarily or in pairs. However, they may be found in groups of up to 12 at a rich food supply during the non-breeding season.

Cape Sugarbird (Promerops cafer)
Cederberg, Western Cape
Photo by Tino Herselman

Forages arboreally in shrubs and bushes, probing Protea flowers and those of other plant species for nectar and insects. Most probing is done while perched but may hover on occasion.

Cape Sugarbirds are strongly dependent on protea nectar and may visit up to 300 flowers per day to meet its energy requirements. It is by far the most important pollinator of many Protea species, even more so than sunbirds. Aside from proteas, sugarbirds will consume nectar from many other plant species including exotic and alien plants.

Note the yellow pollen-stained forehead of this male bird.
Cape Sugarbird (Promerops cafer) – Betty’s Bay, Western Cape
Photo by Les Underhill

Cape Sugarbirds supplement their diet with a range of insects and other invertebrates. These are captured by probing vegetation or hawking insects in flight. Large insect prey is killed by slapping them against a branch with quick, sideways head movements. Recorded invertebrate prey includes beetles, bees, flies, ants, wasps, aphids, moths, termite alates and spiders.

The nectar diet is supplemented by a range of insects. This female has captured a Cape Honeybee.
Cape Sugarbird (Promerops cafer) – Cederberg, Western Cape
Photo by David Kennedy

Highly territorial during the breeding season. At this time males become aggressive towards conspecifics as well as sunbirds, actively chasing them away from food sources. Females often assist in territorial defence. Potential predators like Southern Boubou (Laniarius ferrugineus), Bokmakierie (Telophorus zeylonus) and Southern Fiscal (Lanius collaris) are also chased off aggresively.

Males are aggresive towards rivals in the breeding season. These males are engaged in a territorial dispute.
Cape Sugarbird (Promerops cafer) – Near Greyton, Western Cape
Photo by Stuart Shearer

The Cape Sugarbird is monogamous and prior to egg laying the male becomes very protective towards the female and seldom strays far from her side.

The nest is built entirely by the female and is normally placed around 1m above the ground in dense foliage where the nest is well hidden. The nest is a shallow, loose bowl made from twigs, plant stems, rootlets and grass. The bowl is lined with brown protea fluff and bound in place with fine plant fibres.

1 or 2 eggs are laid per clutch, mainly between March and August (peak March-June). This winter breeding peak is closely linked to the main flowering time of proteas. The eggs are Cream to pale buff or pinkish white, marked with grey, brown, purple-black or glossy black blotches, streaks or spots.

Cape Sugarbird (Promerops cafer)
Kogelberg Nature Reserve, Western Cape
Photo by John Todd

Incubation starts after the second egg has been laid and all incubation is done by the female. The incubation period lasts for around 17 days. During this time the male remains nearby to protect the nest, either by noisily mobbing potential predators or by performing a distraction display to lure threats away from the nest site.

The nestlings are fed and cared for by both parents and are provided with food for around 15 days after fledging. The female chases fully fledged offspring from the territory after 21 days or so.

Cape Sugarbirds are multi-brooded meaning they will attempt to breed more than once in a single breeding season. In fact the female may start a new clutch while still with dependent offspring.

Cape Sugarbird (Promerops cafer) Male
Cedarberg, Western Cape
Photo by John Todd

Further Resources

Species text adapted from the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by David Kennedy, Gerald Wingate, Gregg Darling, Itxaso Quintana, Johan and Estelle van Rooyen, John Todd, Les Underhill, Marna Buys, Philip Nieuwoudt, Stuart Shearer and Tino Herselman is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Kaapse suikervoël (Afrikaans); Promérops du Cap (French); Kaapse Suikervogel (Dutch), Kap-Honigfresser (German), Papa-açúcar do Cabo (Portuguese)

Recommended citation format: Tippett RM 2023. Cape Sugarbird Promerops cafer. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/08/26/cape-sugarbird-promerops-cafer/

Bird identificationbirding

Cape Sugarbird (Promerops cafer) Male
Wolvengat, Western Cape
Photo by Itxaso Quintana

Common Bulbul (Pycnonotus tricolor)

Cover image of Common Bulbul by Lia Steen – Shellybeach, KwaZulu-Natal

Identification

The Common or Dark-capped Bulbul is a distinctive and easily recognisable species. The head is black and contrasts with the grey neck and breast. The rest of the upperparts are dusky grey-brown. The underparts are a paler greyish-white and the vent is bright-yellow. The eye is dark brown with a narrow black eye ring.

Common Bulbul (Pycnonotus tricolor)
Fairland, Gauteng
Photo by Lance Robinson

The sexes are alike and juveniles look similar but with duller plumage.

The Common Bulbul can only be mistaken for the African Red-eyed Bulbul (Pycnonotus nigricans) and the Cape Bulbul (Pycnonotus capensis). The Common Bulbul is easily separated by its black, not red or white eye ring.

Status and Distribution

SABAP2 distribution map for Common (Pycnonotus tricolor) – August 2023.
Details for map interpretation can be found here.

The Common Bulbul is a common to locally abundant resident. It is widespread across Africa, avoiding only the arid regions. In Southern Africa it is found in the moister eastern parts from the Eastern Cape, throughout KwaZulu-Natal, Mpumalanga, Gauteng and Limpopo. It is also found throughout southern Mozambique and Zimbabwe and the northern and eastern parts of Botswana and Namibia’s Caprivi Strip.

The Common Bulbul is not a conservation priority because it is common and widespread, and has benefited from its association with humans.

Habitat

Habitat – Ithala Game Reserve, KwaZulu-Natal
Photo by Ryan Tippett

The Common Bulbul occupies a wide range of habitats. These include moister woodland and savanna, riverine bush, forest edge and regenerating forest (but not normally the forest interior), dense montane scrub, alien tree plantations, orchards, gardens, and parks. The Common Bulbul flourishes in suburban habitats where it is usually one of the most abundant bird species.

Common Bulbul (Pycnonotus tricolor)
Wartburg district, KwaZulu-Natal
Photo by Malcolm Robinson

Behaviour

The Common Bulbul is usually encountered in pairs or loose groups particularly at good food sources like fruiting trees. They are highly vocal and conspicuous and become tame around human habitation. The Common Bulbul is a regular and noisy participant in mixed-species mobbing parties and is quick to spot snakes and other predators. Common Bulbuls are known to practise ‘anting’ by crouching among ants with the tail and wings spread. They drink and bathe regularly.

Common Bulbul (Pycnonotus tricolor)
Kruger National Park, Mpumalanga
Photo by Andre Harmse

The diet consists mostly of fruit, nectar and a range of insects and other invertebrates. Gleans insects and picks fruits from trees and shrubs and occasionally takes fallen food from the ground. Also feeds at bird tables and regularly forages around picnic sites and camping grounds.

Common Bulbuls are monogamous and become strongly territorial during the breeding season, which takes place during Spring and Summer.

The nest is a neat, strong, thin-walled cup of dry grass, rootlets and small twigs, bound on the outer edge with a thin layer of spider web. The interior is lined with fine plant fibres, animal hair, and other similar materials. The nest is built entirely by the female but the male remains close by, often singing from nearby trees or bushes. The nest is placed on a branch, or slung between twigs in a fork, and attached with spider web. It is generally situated in a tree canopy away from the trunk and is usually hidden by vegetation.

Common Bulbul (Pycnonotus tricolor)
Chilo Lodge, Zimbabwe
Photo by Doug Harebottle

2 to 3 eggs are laid per clutch. The eggs are either brown, pink or white with brown, red or purplish spotting or streaks. Markings vary in size, density and distribution. Incubation begins after clutch completion and lasts for 12 to 15 days. Incubation duties are performed almost exclusively by the female. The Male feeds the female on the nest and generally remains nearby, calling frequently. Later, both adults feed the chicks. The pair maintain contact when foraging, and return together to the nest. The nestling period lasts for 11 to 16 days. Chicks can barely fly when they leave the nest, remaining bunched together in nearby foliage for a few days before starting to follow their parents. Common Bulbuls are probably single-brooded. Broods are frequently parasitised by Jacobin Cuckoos, and occasionally by the African Emerald, Klaas’s, Diderick, and Red-chested Cuckoos.

Common Bulbul (Pycnonotus tricolor)
Fairland, Gauteng
Photo by Lance Robinson

Further Resources

Species text in the first Southern African Bird Atlas Project (SABAP1), 1997. At this time the scientific name was Pycnonotus barbatus.

The use of photographs by Ansie Dee Reis, Carel van der Merwe, Jon Blanco, Lappies Labuschagne, Sybrand Venter, Tino Herselman and Tony Archer is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Dark-capped Bulbul, Black-eyed Bulbul (Alternative English); Swartoogtiptol (Afrikaans); iPhothwe (Zulu); Ikhwebula (Xhosa); Bokota (Tswana); Bulbul aux yeux noirs, Bulbul tricolore (French); Grauwe Buulbuul (Dutch); Gelbsteißbülbül, Graubülbül (German); Tuta-negra (Portuguese)

Recommended citation format: Tippett RM 2023. Common Bulbul Pycnonotus tricolor. Biodiversity and Development Institute. Available online at https://thebdi.org/2023/08/23/common-bulbul-pycnonotus-tricolor/

List of bird species in this format is available here.

Bird identificationbirding

Common Bulbul (Pycnonotus tricolor)
St. Lucia, KwaZulu-Natal
Photo by Pieter Cronje

Bird ringing at Vondeling, 17 to 20 August 2023


Two weeks after our previous bird ringing visit, we were again at Vondeling Wine Farm. This time we focused on species diversity. We caught 26 species in four days, although the first day was rainy. A pair of Cape Batis showed the different eye colours of male and female.

Looking at the table at the bottom of this blog, our top captured species was 33 Cape Weavers, followed by 16 Southern Masked Weavers, and 10 Fiscal Flycatchers.

A patch of flowering Leonotus provided four Malachite Sunbirds, eight Streaky-headed Seedeaters and other species.

Malachite Sunbird – female and male



On the last morning, Sally led ringing in an almond grove which added numbers and the following species: Cape Turtle Dove, Cape Wagtail, Cape Canary and Southern Grey-headed Sparrow.

One of the most exciting catches was a female Greater Honeyguide, a species we had not seen or heard calling at Vondeling. The hosts of this brood parasite include several species that are at Vondeling: African Hoopoe (one ringed!), kingfishers and starlings (one Common Starling ringed!).

Female Greater Honeyguide, showing faint yellow shoulder patch

Numbers of birds of each species caught at Vondeling, 17 to 20 August 2023

Sp noEnglishCount
316Ring-necked Dove (Cape Turtle Dove)1
392Red-faced Mousebird1
418African Hoopoe 1
440Greater Honeyguide1
543Cape Bulbul2
581Cape Robin-chat4
621Long-billed Crombec2
622Bar-throated Apalis1
665Fiscal Flycatcher10
672Cape Batis2
686Cape Wagtail 1
707Southern Fiscal2
733Common Starling1
751Malachite Sunbird4
784House Sparrow2
786Cape Sparrow6
799Cape Weaver33
803Southern Masked Weaver16
810Yellow Bishop6
825Swee Waxbill1
857Cape Canary 1
863Brimstone Canary2
867Streaky-headed Seedeater8
1172Cape White-eye7
4139Karoo Prinia1
4142Southern Grey-headed Sparrow 1
TOTAL117

Links to the descriptions of previous ringing trips to Vondeling (and also elsewhere) are summarized in this blog. To join a future ringing event, see Events!

We have comfortable accommodation on the farm, in two cottages.

African Red-eyed Bulbul (Pycnonotus nigricans)

Cover image of African Red-eyed Bulbul by Jon Blanco – Karoo Gariep Nature Reserve, Northern Cape

Identification

The African Red-eyed Bulbul is an easily recognisable species. Its most distinguishing feature is the red eye wattle, which is diagnostic. The head is black and contrasts with the grey neck and breast. The rest of the upperparts are dusky grey-brown. The underparts are paler greyish-white and the vent is bright-yellow.

African Red-eyed Bulbul (Pycnonotus nigricans)
Thabazimbi district, Limpopo
Photo by Ansie Dee Reis

The sexes are alike and juveniles look similar but have duller plumage.

The African Red-eyed Bulbul can only be mistaken for the Common Bulbul Pycnonotus tricolor and the Cape Bulbul Pycnonotus capensis. The Dark-capped Bulbul, has a black, not red eye ring, and less contrast between the dark breast and white belly. The Cape Bulbul has a broader, white eye ring, and plain sooty brown underparts. The African Red-eyed Bulbul is known to hybridise with the Common Bulbul and Cape Bulbul in areas of overlap.

African Red-eyed Bulbul
African Red-eyed Bulbul (Pycnonotus nigricans)
Klerksdorp district, North West Province
Photo by Tony Archer

Status and Distribution

The African Red-eyed Bulbul is a common to abundant resident and is near-endemic to Southern Africa. Its range extends beyond the sub-region into south-western Angola and extreme southern Zambia. It is widespread in the central and western regions of Southern Africa, occurring virtually throughout Namibia and Botswana. In Zimbabwe it is found only in the far west of the country. It occurs in the central and western parts of South Africa where it is widespread.

SABAP2 distribution map of African Red-eyed Bulbul
SABAP2 distribution map for African Red-eyed Bulbul (Pycnonotus nigricans) – February 2023.
Details for map interpretation can be found here.

Habitat

Habitat
Habitat in Karoo scrub – Carnarvon district, Northern Cape
Photo by Ryan Tippett

The African Red-eyed Bulbul occurs in dry woodland, arid savanna, thickets, Karoo scrub, riverine bush, orchards, gardens and farmyards. It is generally found in drier habitats than other bulbuls, but regularly gathers near water during the dry season.

Replaces Dark-capped and Cape Bulbuls in arid and semi-arid regions and across a wide range of habitats.

African Red-eyed Bulbul (Pycnonotus nigricans)
Carnarvon district, Northern Cape
Photo by Sybrand Venter

Behaviour

The African Red-eyed Bulbul is usually encountered in pairs or small, loose groups. They are noisy and conspicuous, with continuous, excited contact calling from large groups gathered at fruiting trees. Flicks its wings and tail when alarmed or excited. They are prominent in mixed-species bird parties where they mob predators such as snakes and small owls. Becomes tame in gardens and camp sites, regularly visiting feeders and bird baths. Drinks regularly and is never far from water in arid country.

It forages in pairs or large, noisy groups with other fruit-eating species in trees and shrubs, but occasionally takes food from the ground. The African Red-eyed Bulbul feeds on a wide variety of wild and cultivated fruits. They are also known to eat flower petals and will probe aloe flowers and those of other plants for nectar. It also consumes a variety of arthropods, flying up to hawk insects above trees or shrubs and darts after insects flushed from foliage.

Pycnonotus nigricans
African Red-eyed Bulbul (Pycnonotus nigricans)
Noupoort, Northern Cape
Photo by Tino Herselman

The African Red-eyed Bulbul is a monogamous species. Pair members often perch in close contact, frequently allopreening around head area. The nest is usually built only by the female and is a flimsy-looking cup of dry grass, thin twigs, rootlets and other fine plant fibres. The nest is bound together with spider web and is lined with grass fibres. The nest is placed in the fork of a bush or tree and is usually well hidden.

Two or three eggs are laid per clutch and the eggs are pinkish white with red-brown speckles. Incubation begins with the first laid egg and the incubation period lasts from 12 to 13 days. All incubation duties are performed by the female. Hatchlings are fed and cared for by both parents. The nestling period lasts around 12 days and young birds can already fly competently after 18 days or so. Broods are regularly parasitised by the Jacobin Cuckoo.

Pycnonotus nigricans
African Red-eyed Bulbul (Pycnonotus nigricans)
Waterberg National Park, Namibia
Photo by Carel van der Merwe

Further Resources

Species text in the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by Ansie Dee Reis, Carel van der Merwe, Jon Blanco, Lappies Labuschagne, Sybrand Venter, Tino Herselman and Tony Archer is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Rooioogtiptol (Afrikaans); Rramorutiakolê (Tswana); Bulbul brunoir (French); Maskerbuulbuul (Dutch); Maskenbülbül (German); Tuta-de-olhos-vermelhos (Portuguese).

Recommended citation format: Tippett RM 2023. African Red-eyed Bulbul Pycnonotus nigricans. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/08/16/african-red-eyed-bulbul-pycnonotus-nigricans/

List of bird species in this format is available here.

Bird identificationbirding

Pycnonotus nigricans
African Red-eyed Bulbul (Pycnonotus nigricans)
Swakopmund district, Namibia
Photo by Lappies Labuschagne

Bokmakierie (Telophorus zeylonus)

Cover image of Bokmakierie by Ryan Tippett – Carnarvon District, Northern Cape – BirdPix No. 114349

Identification

The Bokmakierie should be familiar to many due to its bright colours, loud, ringing vocalisations and its willingness to adapt to suburban parks and gardens.

Adults are brightly coloured with an eye-catching black gorget (throat/neck band) that contrasts with the bright yellow throat and supercilium.

The crown, nape and ear coverts are grey. Upperparts, including the mantle, back and rump are olive green. The lower breast and belly are bright yellow with grey flanks.

The tail pattern is striking. The tail feathers are black with broad yellow tips forming a broad yellow terminal band at the tip of the tail. The central tail feathers, from base to tip are olive-green. This tail pattern is most obvious when in flight.

The bill is strong with a hooked tip and the legs are dark grey. The sexes are alike in plumage colouration.

Bokmakierie (Telophorus zeylonus) 
Near Jeffreys Bay, Eastern Cape
Photo by Gregg Darling

Juveniles are dull olive green above. The breast is greyish-green while the flanks and belly are dull yellowish green with grey barring. They have a greyish face and lack the adults yellow supercilium, black gorget and yellow throat. Juveniles share the same tail markings as the adults.

A juvenile Bokmakierie (Telophorus zeylonus) 
Klerksdorp Dam, North West Province
Photo by A.M. Archer

The Bokmakierie superficially resembles the Yellow-throated Longclaw (Macronyx croceus) and both have a black gorget (throat/neck band) and yellow underparts. However, the Bokmakierie has a uniform green back (not scaled brown as in the longclaw) and a stout hooked bill.

Status and Distribution

Generally common where it occurs. The Bokmakierie is near-endemic to Southern Africa, extending a short distance into south-western Angola. It is widespread in South Africa, and occurs in all provinces, although it is marginal in Limpopo. There is an isolated population of Bokmakieries in the Chimanimani Mountains of Zimbabwe and neighbouring Mozambique.

It is unlikely that the distribution of the Bokmakierie has changed in the historical past. It is not considered threatened and its preferred habitats, for the most part, do not coincide with prime agricultural land. This species has benefitted from the establishment of parks and gardens in suburbia.

SABAP2 distribution map for Bokmakierie (Telophorus zeylonus) – July 2023.
Details for map interpretation can be found here.

Habitat

Habitat – Carnarvon district, Northern Cape
Photo by Ryan Tippett

The Bokmakierie is most prevalent in scrubby habitats and is most abundant in the Karoo, Fynbos and Grassland biomes. It favours habitats with scattered shrubs or trees in open areas, including dune scrub, renosterveld, Nama and Succulent Karoo, Protea scrub, grasslands with bush clumps, bushy, boulder-strewn hillsides, alien tree plantations and orchards and vineyards. In the Karoo, the Bokmakierie favours wooded drainage lines, but also occurs commonly in open shrublands and around farmyards. The Bokmakierie readily enters parks and gardens in built-up areas.

It largely avoids woodlands with the exception of Valley Bushveld in the Eastern Cape in which it is common. However, around the edges of its range in KwaZulu-Natal, Mpumalanga, eSwatini and North West Province, it occurs at low densities in light mixed woodlands and savanna.

The Bokmakierie has been recorded from the coast to around 3000 m above sea level.

Bokmakierie (Telophorus zeylonus) 
Klipriviersberg Nature Reserve, Gauteng
Photo by Lance Robinson

Behaviour

The Bokmakierie calls frequently and has a loud ringing call that can be heard up to two kilometres away. They have a complex and diverse repertoire of vocalisations including duets and a mix of other harsh vocalisations.

Bokmakierie (Telophorus zeylonus
Near Klerksdorp, North West Province
Photo by A.M. Archer

Generally resident and sedentary throughout its range. There is, however, evidence of some altitudinal migration in the Lesotho highlands and the Drakensberg Mountains of KwaZulu-Natal. Here they may move seasonally away from high altitudes to find food and to avoid winter frost and snowfalls.

Bokmakierie (Telophorus zeylonus) 
Near Potchefstroom, North West Province
Photo by Alison Sharp

The Bokmakierie is usually encountered in pairs, or in family groups of 3. They are partly terrestrial and spend much of their time foraging on the ground. They run or hop quickly between cover or when capturing prey. They also glean food from twigs and foliage and occasionally hawk flying insects, especially termite alates.

Mainly feeds on invertebrates but some vertebrate prey is also captured. Consumes a wide range of insects including but not limited to grasshoppers, beetles, antlions, caterpillars, mantids, stick insects, termites, ants, plant bugs and flies. Other invertebrates taken include spiders, centipedes, millipedes, snails and earthworms. Vertebrate prey consists of lizards, geckos, chameleons, small snakes, frogs and small birds. The diet is also supplemented with small fruit and berries when available.

Large or awkward food items are wedged between forked branches to allow the bird to dismember its prey or to tear off pieces.

Bokmakierie (Telophorus zeylonus) 
Mountain Zebra National Park, Eastern Cape
Photo by Pamela Kleiman

Pairs are strongly territorial and can be very conspicuous in boundary disputes and involve pairs confronting each other with duetting, much posturing, exaggerated bobbing movements, wing-flicking and tail-fanning. They are often attracted to reflective surfaces such as windows and car rear-view mirrors where they ‘shadowbox’ their own image, often accompanied by guttural croaking sounds.

The Bokmakierie is monogamous and mate fidelity is strong due to well developed duets between the pair. These serve to strengthen and maintain partnership bonds. Males advertise their control of a territory by singing loudly from an elevated perch.

The nest is built by both sexes and is usually well hidden in dense foliage. The nest a neat, open cup, made from small twigs, leaves, grass and other fine plant material. Breeding can take place year-round, usually with a spring peak during August. They lay between two and six blueish eggs per clutch. Incubation starts upon completion of the clutch and incubation duties are shared by both sexes. The nestling period lasts for around 20 days Bokmakieries are usually double-brooded, meaning that they will attempt to breed more than once during the season. Some broods may, on occasion, be parasitised by the Jacobin Cuckoo (Clamator jacobinus).

They are frequently attracted to reflective surfaces where they ‘shadowbox’ their own reflections.
Bokmakierie (Telophorus zeylonus) 
Carnarvon district, Northern Cape
Photo by Ryan Tippett

Further Resources

Species text adapted from the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by Alison Sharp, A.M. Archer, Gregg Darling, Lance Robinson and Pamela Kleiman is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Bokmakierie (Afrikaans); iNkovu (Zulu); Ingqwangi (Xhosa); Pjempjete (South Sotho); Gladiateur bacbakiri (French); Bokmakierie-klauwier (Dutch); Bokmakiri (German); Boquemaquire (Portuguese).

Recommended citation format: Tippett RM 2023. Bokmakierie Telophorus zeylonus. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/08/07/bokmakierie-telophorus-zeylonus-2/

Bird identificationbirding

Bird ringing at Vondeling, 3 to 6 August 2023

We had an enjoyable long weekend of bird ringing at Vondeling Wines. Although we are still deep in winter, the first signs of spring were evident, green shoots on a single vine in one vineyard, and on a few leaves on one of the oak trees in the werf:

Looking at the table at the bottom of this blog, our top captured species was 77 Cape Weavers, followed by equal numbers of Cape Robin-chat, Fiscal Flycatcher and Cape White-eye (11 each). Interestingly, both a Karoo and an Olive Thrush were caught.

Both weaver species, Cape and Southern Masked, included males in full breeding plumage, but only Cape Weaver females had brood patches. The Cape Weaver was actively breeding at several different colonies. The dam below Bowwood farmhouse was full, with the reeds housing weaver nests standing in water, so we could not ring at this colony as we did in April 2023.

We also visited Schoon Farm and had a great ringing session in spite of the misty, freezing weather. Thanks to Loutjie for organising this!

Retrap of Brimstone Canary caught while bird ringing at  Vondeling, August 2023
Brimstone Canary

The most exciting catch was a recapture of a Brimstone Canary. When checking its ringing history, it was noted that it had been ringed on the other side of the Paardeberg Mountain in December 2019, three years and eight months ago, on an event described here!! The straight line distance between actual ringing and recapture sites was 6.0 km.

Map showing distance moved of Brimstone Canary while bird ringing at Vondeling
Movement of Brimstone Canary from Fynbos Estate (blue box) to Vondeling Wines (red box)

Numbers of birds of each species caught at Vondeling and Schoon, 3 to 6 August 2023

Sp noEnglishVondelingSchoon
390Speckled Mousebird1 
397Malachite Kingfisher1
543Cape Bulbul21
581Cape Robin-chat83
622Bar-throated Apalis3 
665Fiscal Flycatcher92
709Southern Boubou1
799Cape Weaver1562
803Southern Masked Weaver81
808Southern Red Bishop 6
810Yellow Bishop3
863Brimstone Canary3
867Streaky-headed Canary1
1104Karoo Thrush  1
1105Olive Thrush1
1172Cape White-eye83
4139Karoo Prinia31
 TOTALS6582

The grand total is 147 birds handled of 17 species. Unexpected highlight was the movement of a Brimstone Canary across the Paardeberg.

For the BirdPix section of the Virtual Museum, we uploaded photographic records for 38 species. Vondeling Wine Farm falls into the quarter degree grid cell called Paarl, with grid cell code 3318DB. The number of bird species record in this grid cell is 160. Together with the previous trips made here this year, the total number of 2023 records is 82. This means that more than half of the species recorded in this grid cell have been recorded this year. The BirdPix data for this grid cell can therefore be declared “up-to-date”. A map for the grid cell, together with a list of species and the last recorded dates for each of them is here. One species not seen for a surprisingly long time is the Little Stint, last recorded in March 2011. The waders that breed in the tundra in northern Siberia are known to be decreasing, so the long time period since it was last recorded here is not a surprise.

Links to the descriptions of previous bird ringing trips to Vondeling (and also elsewhere) are summarized in this blog. To join a future ringing event, see Events!

Greater Kestrel (Falco rupicoloides)

Cover image Greater Kestrel by Sybrand Venter – Carnarvon district, Northern Cape – BirdPix No. 246605

Identification

The Greater Kestrel is a smallish, attractively marked raptor. It is, however, the largest Kestrel species in Southern Africa.

The overall colouration of the head and body is light ginger-brown covered in black barring, blotches, bands and streaks. The head, throat and neck are finely streaked. The streaks become bolder and more prominent on the breast and belly while the flanks are densely barred. The back is strongly marked with thick black barring and the tail is grey with broad black bands.

The head appears fairly large and rounded. The legs and bare skin around the eyes and cere are yellow and the bill is horn-grey. Adults have striking pale coloured eyes.

Greater Kestrel (Falco rupicoloides)
Rietvlei Nature Reserve , Gauteng
Photo by Ansie Dee Reis

In flight the Greater Kestrel shows heavily barred upper wings and a grey and black banded tail. The under wings are white with indistinct, grey-barred flight feathers.

Greater Kestrel (Falco rupicoloides)
Near Middelburg, Eastern Cape
Photo by Gregg Darling

The sexes are alike in plumage but they differ in size, the females are slightly larger than males.

The juveniles resemble the adults but have dark-coloured (not pale grey) eyes. They are generally darker rufous in colour and have larger black markings than the adults.

The Greater Kestrel is most likely to be mistaken for females and juveniles of the Rock Kestrel (Falco rupicolis) and Lesser Kestrel (Falco naumanni). Both are smaller and slimmer than the Greater Kestrel and have smaller, less rounded looking heads.

Greater Kestrel (Falco rupicoloides)
Karoo-Gariep Nature Reserve, Northern Cape
Photo by Josu Meléndez

Distribution

The Greater Kestrel is locally common throughout its range. It has a disjunct distribution in the drier regions of Southern and East Africa. It occurs patchily in East Africa from northern Tanzania, up through Kenya to Ethiopia and Sudan. It is More widespread in Southern Africa, occurring over a large part of western and central South Africa and throughout Namibia and Botswana. It is sparsely distributed in Zimbabwe, western Zambia and eastern Angola.

In South Africa it has been recorded from all provinces but avoids the Lowveld and the higher rainfall, low-lying eastern and southern coastal regions.

The distribution of the Greater Kestrel is believed to have expanded due to the clearing of woodlands for cultivation. However the loss of natural grasslands to agriculture and bush encroachment could be a concern. The Greater Kestrel is not considered threatened.

SABAP2 distribution map for Greater Kestrel (Falco rupicoloides) – July 2023. Details for map interpretation can be found here.

Habitat

Habitat – Vanwyksvlei district, Northern Cape
Photo by Ryan Tippett

The Greater Kestrel is a bird of open, arid and semi-arid areas ranging from desert scrub to dry, open woodlands and grassland. It is most abundant in the Kalahari and Karoo vegetation types. It is also widespread in the grasslands of central South Africa but is less numerous. The Greater Kestrel prefers open veld with short vegetation and moderate to low rainfall. Also occurs in cultivated areas in north-eastern South Africa where it is expanding its distribution.

Greater Kestrel (Falco rupicoloides) in habitat.
Karoo-Gariep Nature Reserve, Northern Cape
Photo by Josu Meléndez Underhill

Behaviour

Greater Kestrels are normally found singly or in pairs and sometimes in loose groups of several birds. Perches conspicuously on whatever vantage points are available, such as termite mounds, trees, and telephone poles, pylons and fences. Advertises to conspecifics that a territory is occupied by perching conspicuously. The flight is bouyant, interspersed with flapping and gliding. Seldom soars but frequently hovers in windy conditions.

Most hunting is done from a perch but they also hunt aerially, usually by hovering into the wind. Prey is generally captured on the ground but may occasionally catch small birds, termite alates and locusts in flight. Males tend to perch-hunt more often than females, and females have better hunting success from hovering than males.

Greater Kestrel (Falco rupicoloides)
Near Middelburg, Eastern Cape
Photo by Tino Herselman

The majority of the Greater Kestrels diet consists of invertebrates especially locusts, grasshoppers, solifugids and termites. They also consume small reptiles like lizards, chameleons and snakes, as well as birds such as quails, doves and small passerines. Mammalian prey consists mostly of rodents. Greater Kestrels are not known to drink or bathe.

The Greater Kestrel breeds from August to December with a peak during September and October. Most egg laying takes place just before the Summer rains in order to maximise prey availability during the nestling period.

Pairs are monogamous and show strong mate fidelity. They do not construct their own nests and prefer to use old stick nests of other raptors or crows. They are dependant on these other species for nests which may limit the distribution of breeding birds. The pair actively defend the area around their nest against conspecifics, other raptor species and corvids (crows and ravens).

Greater Kestrel (Falco rupicoloides)
Kgalagadi Transfrontier Park, Northern Cape
Photo by David Kennedy

From 1 to 5 (usually 3 or 4) eggs are laid per clutch. The eggs are cream or buff coloured with variable reddish-brown speckling. Incubation starts with the first laid egg, as at some nests there is a distinct difference in the age and development of the young. The incubation period lasts for 32 to 33 days and is performed mostly by the female.

Both parents provision the chicks with food. Females tend to hunt close to the nest and mostly capture insects, while males hunt further afield and bring larger prey such as rodents back to the nest. The young are fully fledged after 32 to 35 days but remain dependant on their parents for at least 30 days after their first flight.

Greater Kestrel (Falco rupicoloides)
Garingboom Guest Farm, Free State
Photo by Phillip Nieuwoudt

Further Resources

This species text is adapted from the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by Ansie Dee Reis, David Kennedy, Gregg Darling, Josu Meléndez, Phillip Nieuwoudt, Sybrand Venter and Tino Herselman is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Grootrooivalk (Afrikaans); Phakalane (Tswana); Grote Torenvalk (Dutch); Crécerelle aux yeux blancs (French); Steppenfalke (German); Peneireiro-grande (Portuguese).

A list of bird species in this format is available here.

Recommended citation format: Tippett RM 2023. Greater Kestrel Falco rupicoloides. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/07/26/greater-kestrel-falco-rupicoloides/

Bird identificationbirding

Greater Kestrel (Falco rupicoloides)
Karoo Gariep Nature Reserve, Northern Cape
Photo by Ryan Tippett

Pale Chanting Goshawk (Melierax canorus)

Cover image of Pale Chanting Goshawk by Ryan Tippett – Carnarvon district, Northern Cape – BirdPix No. 60801

Identification

The Pale Chanting Goshawk is a fairly large and conspicuous all-grey raptor.

Pale Chanting Goshawk identification
Pale Chanting Goshawk (Melierax canorus) – Okomuparara, Namibia
Photo by Anthony Paton

The overall colouration is ash grey. The underparts, are whitish with fine grey barring while the upperparts are grey and unmarked. Bare skin, including the legs, cere and gape is bright pinkish-red to orange-red, and quite eye-catching. The legs are un-feathered and relatively long

In flight the Pale Chanting Goshawk shows black wing tips and a white rump. The underwings are light grey and the secondaries are pale and finely barred. There is a pale wing panel on the upper wing which is often visible when perched.

Pale Chanting Goshawk identification in flight
Pale Chanting Goshawk (Melierax canorus) 
Namaqualand National Park, Northern Cape
Photo by Vaughan Jessnitz

The sexes are alike in plumage but they differ in size, the females being noticeably larger than males.

The juveniles are brown above with paler buff-tipped feathers. The head is grey-brown with darker brown streaks. Under parts are blotched and barred in brown and buff. Like the adults, juveniles have a white rump which is most obvious in flight. The legs and bare skin are orangish becoming brighter and redder with age.

The Pale Chanting Goshawk is most likely to be mistaken for the Dark Chanting Goshawk Melierax metabates. They tend to prefer different habitats but their ranges do overlap in the northern parts of the Limpopo province, in eastern and northern Botswana and northern Namibia. The Pale Chanting Goshawk is slightly larger and has paler grey upperparts. The two are best told apart in flight. The Pale Chanting Goshawk has a white rump and a pale panel or window in the upper wing, whereas, the Dark Chanting Goshawk has a grey rump and dark wing panel. Juveniles are harder to tell apart but those of the Pale Chanting Goshawk are a little paler with a white rump and Dark Chanting Goshawk juveniles show a barred or mottled rump.

Young Pale Chanting Goshawk
Pale Chanting Goshawk (Melierax canorusJuvenile
Lamberts Bay, Western Cape
Photo by Kyle Finn

Distribution

The Pale Chanting Goshawk is a common species across its distribution. It is Near-endemic to Southern Africa, its range only reaching beyond Southern Africa into south-western Angola.

It is restricted to the western and central regions of Southern Africa, mainly Namibia, Botswana and western South Africa. Its range extends marginally to western Zimbabwe and north-eastern South Africa, especially along the Limpopo Valley.

SABAP2 distributiom map for Pale Chanting Goshawk
SABAP2 distribution map for Pale Chanting Goshawk (Melierax canorus) – July 2023. Details for map interpretation can be found here.

Habitat

Habitat for Melierax canorus
Habitat – Carnarvon district, Northern Cape
Photo by Ryan Tippett

Pale Chanting Goshawks occur in arid and semi-arid areas, especially the Karoo and Kalahari vegetation types. It is present in parts of the Namib Desert and also inhabits drier woodland and grasslands. It is typically a bird of open scrub and wooded drainage lines. They prefer flat terrain and require areas of open ground with places to perch.

Habitat for Pale Chanting
Habitat – Near Vanrhynsdorp, Western Cape
Photo by Les Underhill

Behaviour

Pale Chanting Goshawks are normally found singly or in pairs, and occasionally in family groups of five or more birds. They are not easily overlooked owing to their habit of perching prominently in the open on trees, bushes, telephone poles, fences and so on. Roadside telephone poles are favoured perches because they are often the tallest vantage points in their habitat and provide easy opportunities for scavenging at road-kills.

Melierax canorus on the ground
Pale Chanting Goshawk (Melierax canorus)
Addo Elephant National Park, Eastern Cape
Photo by Desire Darling

Pale Chanting Goshawks spend the vast majority of their time perched. Research has shown that they may spend as much as 75 to 89% of their time sitting. They frequently soar at midday.

Most hunting is done from a perch and they are known to change perch sites frequently. Sometimes forages on foot and may even run after insects and rodents. It has a broad diet and feeds on invertebrates (mainly insects and arachnids), reptiles including snakes, birds up to the size of korhaans and mammals up to the size of hares. They are fond of carrion and regularly feed on road kills. They can sometimes be observed following Honey Badgers and the Yellow Mongoose in the hope of snatching disturbed rodents and insects.

Drinks water only on very hot days.

Melierax canorus
Pale Chanting Goshawk (Melierax canorus
Kgalagadi Transfrontier Park, Northern Cape
Photo by Phillip Nieuwoudt

Breeding takes place mainly during spring and Summer (September to December) when food is most abundant. They may not breed at all during drought periods.

The nest is is a modest stick platform up to 40cm in diameter and is built by both sexes. The bowl of the nest is lined with an odd assortment of items that may include hair, dung, soil clods, bits of animal skin, ostrich feathers, grass, small bird nests and spider webs. They often use man-made items such as string, rope, old rags and bits of plastic when nesting close to roads or human habitation. Nests are most frequently placed in thorn trees but they may also nest on telephone poles in treeless regions.

Females lay one or two plain white to greenish-white eggs per clutch. Incubation duties are performed mostly by the female and the incubation period lasts for around 35 days. The young are fed mostly by the female although the male does most of the hunting at this time.

The pair are active in defence of the nest area and males in particular are quite focused on this during the breeding period. They defend the nest area from other raptors, crows, herons, mongooses and other mammalian predators. They will harass and dive at intruders and sometimes even make contact by striking with the feet.

Two Pale Chanting Goshawks
Pale Chanting Goshawk (Melierax canorus)
Near Bloemfontein, Free State
Photo by Dawie De Swardt

Young birds remain in the parental territory for up to two years but they are not tolerated at or near the nest during subsequent breeding efforts.

Further Resources

This species text is adapted from the first Southern African Bird Atlas Project (SABAP1), 1997.

The use of photographs by Andrew Keys, Anthony Paton, Dawie De Swardt, Desire Darling, Kyle Finn, Les Underhill, Phillip Nieuwoudt and Vaughan Jessnitz is acknowledged.

Virtual Museum (BirdPix > Search VM > By Scientific or Common Name).

Other common names: Bleeksingvalk (Afrikaans); Zanghavik (Dutch); Autour chanteur (French); Weißbürzel-Singhabicht, Heller Grauflügelhabicht (German); Açor-cantor-pálido (Portuguese).

Recommended citation format: Tippett RM 2023. Pale Chanting Goshawk Melierax canorus. Biodiversity and Development Institute. Available online at http://thebdi.org/2023/07/21/pale-chanting-goshawk-melierax-canorus/

List of bird species in this format is available here.

Bird identificationbirding

Melierax canorus in flight
Pale Chanting Goshawk (Melierax canorus)
Borakalalo National Park, North West
Photo by Andrew Keys