I love bacon and eggs, but there's a downside, and it's a common household dilemma: a frypan that's encrusted with fried egg.
First I plunged it in a sinkful of hot soapy water, and took to it with a green plastic scourer. It was pretty clear that was going to work, but only after a very long time and a lot of elbow grease. Then I remembered: egg white is protein, and kiwifruit is rich in proteases (enzymes are named something-ase where "something" is the substrate they act upon. Protease breaks down protein). That's why kiwifruit is a good meat tenderiser.
So I cut a disk of kiwifruit (and ate the rest), and sat it in the frypan for a couple of hours (2h 20m, to be more precise, seeing I'm being scientific here).
Then wiped it quickly with a sponge and cold water.
So kiwifruit protease is pretty powerful at digesting protein. But enzymes are proteins too, so why don't proteases self-destruct?
Disclaimer: this research was not funded by the Kiwifruit Marketing Board.
Friday, 27 July 2012
Tuesday, 24 July 2012
Wednesday wildflower: onion weed
I'm told a weed is a wildflower whose virtues have yet to be discovered. But onion weed or three-cornered garlic (Allium triquetrum) has virtues and is still a detested weed.
The plants spread rapidly, either sexually by seeds or vegetatively by bulbs, to infest large areas. The tiny black seeds germinate freely and get carried up on the tip of the first leaf as it grows. The Flora of New Zealand Vol. 3 (Healy & Edgar 1980) says the first wild collection in New Zealand was made in 1928, and it was probably first introduced as a garden plant.
![]() |
| Allium triquetrum, onion weed. |
![]() |
| Snowflake, Leucojum aestivum, a popular garden plant. |
Onion weed is a close relative of those marvellous vegetables onion (Allium cepa), leek (Allium ampeloprasum var. porrum or A. porrum), garlic (Allium sativum), and chives (Allium schoenoprasum). I understand it is edible, and at a pinch would be a substitute for garlic, but I haven't plucked up courage to try it yet. There's enough in our garden to keep us going for a while!
Reference.
Healy, A.J., Edgar, E. 1980. Flora of New Zealand Vol. 3. Government Printer, Wellington.
Reference.
Healy, A.J., Edgar, E. 1980. Flora of New Zealand Vol. 3. Government Printer, Wellington.
Saturday, 21 July 2012
Signs of Spring
Winter has just officially begun and I know there's a lot of wet and cold weather to come. Last year we had 3 days of snow in August, almost unheard of in Wellington. Yet in the Botanic Gardens this weekend I found unmistakeable signs of Spring:
![]() |
| This daffodiul, Narcissus, in the rock garden and others near the tree house were in flower. |
![]() |
| Corydalis in the rock garden. For a discussion on the shape of these flowers see my earlier blog. |
![]() |
| Snowflake, Leucojum aestivum. |
Tuesday, 17 July 2012
Wednesday wildflower: Tangier pea
Lathyrus tingitanus is a common legume throughout New Zealand. Its compound leaves are modified so that the first pair of leaflets are normal, but the others are adapted as tendrils, which help the plant climb on other plants. At the base of the leaf are a pair of stipules that clasp the stem. Sweet pea is another common species of Lathyrus: L. odoratus.
![]() |
| A leaf, buds, and flowers (seen from the front at left and the back at right) of Tangier pea, Lathyrus tingitanus. |
Lathyrus sativus is grown as a food crop in South and South-west Asia and East Africa, known as grass pea or Indian pea. Along with some other species of Lathyrus, it contains oxalyldiaminopropionic acid, which can lead to lathyrism if people are too reliant on these peas, or their flour, in their diet. Oxalyldiaminopropionic acid is a non-protein amino acid, which causes paralysis of the lower limbs and wasting of the buttocks, symptoms commonly seen in Africa during famines.
![]() |
| If this isn't Lathyrus tingitanus, it's a very similar species. Roca Grosso, Catalonia. |
Monday, 16 July 2012
Going through the motions: what did moa eat?
About 35 years ago, Michael Greenwood and Ian Atkinson (Greenwood & Atkinson 1977) proposed
that moa could have been a major influence on growth forms of New
Zealand plants. In particular,
they suggested the twiggy wiry tangled small-leaved growth forms that we call divaricating
shrubs could have evolved as a defense against moa browsing. That’s been a very popular and
appealing idea, but one that’s had its critics. While New Zealand botanists have been happy to attribute our
unusual flowers to pollination by our depauperate and unspecialised
pollinator fauna and our prevalence of small fleshy fruits to dispersal by
frugivorous birds, many have been wary of accepting the moa browse hypothesis.
Partly their objections have arisen from concern that
these ideas can’t directly be tested, because moa are no longer with us. Nevertheless, many other purely
historical ideas in biology can be tested, by indirect methods at least. Greenwood &
Atkinson’s seminal paper has spawned an industry in New Zealand ecology largely
driven by questions about the likely selection pressures of moa on New Zealand
plants. One recent test of moa browsing was a cafeteria experiment
(Bond et al. 2004), where two other large ratite birds—emus and ostriches—were
offered related pairs of divaricating and non-divaricating plants. The birds stripped the non-divaricating
plants in short order, but had trouble pulling the springy and wiry stems of
the divaricates and manipulating the twigs and small leaves in their beaks.
![]() |
| A divaricating shrub, Coprosma cuneata, Campbell Island. |
Another very successful research strategy is coproecology, the
gleaning of evidence from fossil droppings, coprolites. The most recent paper (Wood et al.
2012) by the moa coproecologists has received a lot
of press attention because it showed for the first time that moa fed on
flowers, as well as on fruits, leaves, and twigs.
The scientists found a pile of poo just inside the
entrance of a cave in the Garibaldi Range, South Island mountains. Dried in sunshine and breezes, but protected from rain, these
droppings had lain undisturbed for hundreds to thousands of years. Taking great pains to avoid contamination, the scientists
sampled 35 of the coprolites, collecting DNA to identify the species of moa as
well as plant species eaten, macrofossils (seeds, leaves, etc.), microfossils
(pollen grains), and measuring organic content of the dung. They also used radiocarbon dating to
estimate when the droppings were dropped.
The dung was all from one moa species, the upland moa
(Megalapteryx didinus), a stout bird that stood about 1m tall
at the rump. The oldest droppings
were dated from about 6,300 years ago, and the youngest from a bit less than 700
years ago, so they span a good proportion of the time from the last ice retreat
to the final extinction of moa.
Interestingly, several of the droppings had identical ages and plant contents and are thought to have been deposited in the same "defecation event".
The three methods of sampling plant remains (the
authors refer to these as proxies) in the droppings—pollen, macrofossils, and
DNA— were complimentary. Of these,
pollen could be contamination from outside, especially when it comes from
wind-pollinated trees that flower largely out of reach of moa, like Nothofagus (southern beech) or from plants that are highly poisonous, like wind-pollinated Coriaria. The plot below, from the paper, relates pollen abundance in the coprolites to abundance in the environment; plants above the null distribution line are the ones likely to have been part of the moas' diet.
A range of montane and subalpine plants were found, some (southern beech, buttercups, sedges, grasses and Fuchsia) in all three proxies. The results show moa were generalists, eating pretty much everything, and they ranged across all the available habitats, as the figure below demonstrates.
But only a few of the eaten plants might be divaricating shrubs. These include Myrsine and Coprosma, for which the DNA and pollen evidence can't distinguish if the plants eaten were divaricating or not, and Neomyrtus, which is divaricating.
A range of montane and subalpine plants were found, some (southern beech, buttercups, sedges, grasses and Fuchsia) in all three proxies. The results show moa were generalists, eating pretty much everything, and they ranged across all the available habitats, as the figure below demonstrates.
But only a few of the eaten plants might be divaricating shrubs. These include Myrsine and Coprosma, for which the DNA and pollen evidence can't distinguish if the plants eaten were divaricating or not, and Neomyrtus, which is divaricating.
![]() |
| A divaricating Myrsine, M. divaricata. |
![]() |
| A non-divaricating Coprosma, C. foetidissima. |
The finding of pollen from bird-pollinated flowers—Phormium and Fuchsia—is especially interesting.
These produce quite large amounts of sweet nectar and are pollinated by birds that are much smaller than moa, such as bellbirds and tūī. Yet their pollen is not likely to have got into coprolites other than by
passing through the gut of the moa. The authors aren't suggesting moa were
pollinating the flowers, rather that they were eating them. The large fleshy flower stalks of Phormium are probably quite nutritious
and the nectar from a single flower is a small but sweet treat for a
human. On the other hand, Fuchsia flowers are produced singly or in small clusters on the twigs or bare
trunks of the trees, and it must be quite finicky work to pick these one at a
time; they hardly look worth the effort for a large hungry bird. If moa had a taste for sweet nectar
such that they were a threat to flowers, could their grazing have driven the
evolution of tall scapes in Phormium
and the tree habit in Fuchsia excorticata? The controversy lives on.
![]() |
| Flowers of tree fuchsia, Fuchsia excorticata. |
![]() |
| Flowers and young fruits of mountain flax, Phormium cookianum. |
I was surprised to find in this paper evidence that
moa ate so many small alpine herbs and small fruits too. They might have been significant seed dispersers. This, like the Fuchsia flowers, suggests they might have been capable of choosing
tasty morsels.
A previous study by some of the same scientists (Wood et al. 2008) showed the
presence of a small buttercup, Ceratocephala
pungens, in moa coprolites from Otago. Ceratocephala is
tiny and seasonal. The plants are
ground-hugging rosettes at most a couple of centimetres across, and they grow in bare ground, yet their seeds
were found in coprolites from two species of moa. The genus is otherwise known only from Europe and W. Asia,
so when this new species was described from New Zealand, I entertained the
possibility that it might not be a native (Garnock-Jones 1984). Yet here it is, in coprolites produced
before humans arrived in New Zealand.
In the past, the deer-hunting lobby in New Zealand
has argued that introduced mammals were good for the environment because they replace these extinct
giant herbivorous birds. This
study suggests otherwise. Two very
palatable plants that were common in moa diet—Fuchsia and wineberry—are no longer found on the Garibaldi Range,
and many others are now confined to inaccessible cliffs and edges of sink-holes.
References.
Bond WJ, Lee WG, Craine JM (2004). Plant
structural defences against browsing birds: a legacy of New Zealand's extinct
moas. Oikos 104: 500–508.
Garnock-Jones PJ (1984). Ceratocephalus pungens (Ranunculaceae):
a new species from New Zealand. New Zealand Journal of Botany 22:
135–137 (Note the different spelling in this paper; the original spelling Ceratocephala is now preferred)
Greenwood RM, Atkinson IAE (1977). Evolution of divaricating plants in New Zealand
in relation to moa browsing. Proceedings of the New Zealand Ecological
Society 24: 21–33.
Wood JR, Rawlence NJ, Rogers GM, Austin JJ, Worthy TH, Cooper A (2008). Coprolite deposits reveal the diet and ecology of the extinct New Zealand megaherbivore moa (Aves, Dinornithiformes). Quaternary Science Reviews 27: 2593–2602.
Wood JR, Wilmshurst JM, Wagstaff SJ, Worthy TH, Rawlence NJ, & Cooper A (2012). High-Resolution Coproecology: Using Coprolites to Reconstruct the Habits and Habitats of New Zealand's Extinct Upland Moa (Megalapteryx didinus). PloS one, 7 (6) PMID: 22768206
Tuesday, 10 July 2012
Wednesday wildflower: ivy
The name ivy conjures up evocative images of established gentry in the northern hemisphere: old buildings covered in ivy, the Ivy-League colleges in the US, and the holly and the ivy at Christmas. In New Zealand, the reality is not so pretty. Ivy is an aggressive and unwelcome weed, partly because many people still plant it, or at least tolerate it until it's too late.
| Ivy flowers and mature leaves, Kelburn, Wellington. |
The flowers have an unpleasant smell, and are visited by flies, bees, and wasps, and also some moths and butterflies. Of these, Jacobs et al. (2009) concluded that wasps would likely be the most effective pollinators in England.
![]() |
| Ivy is an effective treatment for graffiti on this old wall in Kelburn, Wellingtom. |
References.
Jacobs, J.H.; Clark, S.J.; Denholm, I.; Goulson, D.; Stoate, C.; Osborne, J.L. 2009. Pollinator effectiveness and fruit set in common ivy, Hedera helix (Araliaceae). Arthropod-Plant Interactions DOI 10.1007/s11829-009-9080-9
Tuesday, 3 July 2012
Wednesday wildflower: red escallonia
Only about 10% of New Zealand's dicotyledon weeds come from Central and South America, and of those that do, many are cultivation escapes. Red escallonia, Escallonia rubra, is in that category. Plants from the Americas with red hanging flowers are often hummingbird pollinated (including E. rubra: Aizen & Rovere 2010).
![]() |
| Red escallonia, Escallonia rubra. The branch at left is shown from the underside. |
References
Aizen M.A.; Rovere, A.E. 2010. Reproductive interactions
mediated by flowering overlap in a temperate hummingbird–plant assemblage. Oikos 119: 696–706. doi: 10.1111/j.1600–0706.2009.17762.x
Webb, C.J., Sykes, W.R.; Garnock-Jones, P.J. 1988. Flora of New Zealand Vol. 4. DSIR, Christchurch.
Subscribe to:
Posts (Atom)

















.jpg)

.jpg)




