Chapter 3.11 Nut and fruit trees

Malcolm Ross

1. Introduction

Arboriculture apparently played a role in Bismarcks food production long before the arrival of Austronesian speakers and the latter quite possibly acquired some of their arboriculture practices from Papuan speaking neighbours (chapter 2, §4). With the introduction of agriculture, garden and forest tended to overlap. Sometimes the garden would include food-bearing trees that survived from the primary forest, and sometimes food-bearing species would be planted in a garden or orchard or near to the village. At the same time, forest trees continued to be tended in situ and came to be owned by particular families.

Kennedy & Clarke (2004) and others have emphasised the cline that ranges from trees which grow wild in the bush to trees that are cultivated in orchards, with various degrees of tree-tending between the two extremes. Continuous cultivation entails domestication, i.e. ongoing control of reproduction and selection of varieties through the planting of ripe fruits or germinated seeds or through the transplanting of vigorous seedlings (Yen 1991). The resulting cultivars often have separate local names, whereas forest varieties generally do not. Walter & Sam (2002: 73-74) suggest that the geographic distribution of domesticated tree species reflects human settlement in the Pacific. As domesticated species they list the following: canarium nuts, Canarium spp., the Tahitian chestnut, Inocarpus fagifer, cutnuts, Barringtonia edulis, Barringtonia novae-hiberniae and Barringtonia procera, the Polynesian plum, alias golden apple, Spondias cytherea, the island lychee, Pometia pinnata, and the Malay apple, Syzygium malaccense. To this list Mueller-Dombois & Fosberg (1998: 56-57) add the dragon plum, Dracontomelon vitiense and Yen (1991) adds Burckella obovata. Paijmans (1976: 123-124) notes that in the New Guinea region Terminalia catappa and Terminalia kaernbachii are also often planted.

All are actively cultivated close to villages and have been subject to continuous selection. Often they grow interspersed with coconut palms and breadfruit trees (themselves both domesticated species) on a piece of land close to the village, along with recently introduced citrus species. Actual tending is minimal; young seedlings are protected from the sun, weeds are removed, dead or damaged branches are cut off and the tree is sometimes pruned to reduce its height (Walter & Sam 2002: 74–76).

The remainder of this chapter is organised as follows. First, domesticated nut trees are treated (§2), then domesticated fruit trees (§3), and finally trees that are regularly exploited for their fruit but are generally not domesticated (§4). The boundary around this last category is somewhat arbitrary. It includes trees which are often mentioned in the literature as sources of edible fruit. It excludes trees that are more often mentioned as having other uses: these include Morinda citrifolia, and various species of Diospyros, Macaranga and Garcinia, the fruits of which are all mentioned by Paijmans (1976: 124) as occasionally consumed. It also excludes those species of Ficus which have edible figs, as these are treated in ch.10, §4.

The trees investigated by Kennedy & Clarke (2004) in their examination of arboriculture include three that are considered among the staple foods in chapter 9: the banana plant (ch.9, §3), the breadfuit tree (ch.9, §4), and the sago palm (ch.9, §5.1). Another cultivated tree is Gnetum gnemon, the leaves of which serve as a green vegetable, treated in chapter 10, §2.3. These trees and plants are not considered further here, nor is the coconut palm, which is discussed in some detail in chapter 12. Instead, the focus of this chapter is nut- and fruit-bearing species that loom large in Bismarcks arboriculture.

2. Domesticated nut trees

Ironically none of the genera considered in this section is a true nut, but agriculturalists writing about Pacific plants (Bourke 1996, Evans 1999) call them nuts and it is convenient to retain this usage. Botanically nuts are single-seed dry fruits in which the seed remains separate from its hard enveloping pericarp. Examples are the hazelnut, Corylus americana, and the chestnut, Castanea dentata. Many ‘nuts’ in popular parlance are botanically drupes rather than nuts. In a drupe the peri carp consists of an outer skin or exocarp, a middle layer or mesocarp and a very hard inner layer or endocarp surrounding the seed. ‘False nuts’ consist of the endocarp and seed of a drupe. They include the first five genera discussed here - canarium almonds, Canarium spp. (§2.1), the sea almond and the okari nut, Terminalia spp. (§2.4), cutnuts, Barringtonia spp. (§2.3), and the various species of Pandanus - as well as the coconut (see ch.12, figure 12.1), the candlenut, Aleurites moluccana (ch.13, §3.2), the macadamia, Macadamia integrifolia, and the almond proper, Prunus dulcis. Fleshy fruits like the peach, P. persica, the plum, P. domestica, the apricot, P. armeniaca, the ocean lychee, Pometia pinnata (§3 .5) and mangoes, Mangifera spp. (§3.4), are also drupes, but the fleshy mesocarp is eaten, not the endocarp and seed. Some ‘nuts’, like the Brazil nut, Bertholletia excelsa, and the canarium nut, Canarium indicum, are simply seeds.

2.1. Canarium spp. (Burseraceae)

Canarium is one of a suite of plants that were domesticated in the rain forests of northern New Guinea during the early Holocene. Other members of the suite were the breadfruit (Artocarpus altilis) and the two fruit trees Pometia pinnata and Burckella obovata (Yen 1996). Canarium is the most important nut-bearing genus in Papua New Guinea, cultivated by almost a third of the rural population (Bourke & Allen forthcoming).

Figure 11.1: Left Canarium indicum: A, tree; B, portion of leaf showing terminal four leaflets; C, portion of branch showing large stipules (leaflike appendages at base of leaf stalk); D, immature inflorescence; E, cluster of fruit.; F, opened pericarp (exocarp + mesocarp + endocarp); G, opened shell/endocarp; H, edible kernel. Right Parts of the Canarium indicum fruit

A number of Canarium species occur today in northwest island Melanesia (eight have been recorded in the Solomons) but only three cultivated species are common within their respective ranges: Canarium indicum (P ngali), Canarium salomonense (P andoa) and Canarium harveyi (Evans 1999: 3).1 Of these, only Canarium indicum occurs in New Guinea and the Bismarcks (Bourke 1996), and was presumably the only common species known to POc speakers before they reached the Solomons. Its range extends from Halmahera to Vanuatu. Canarium salomonense is found in Bougainville and the Solomons and in New Guinea, but not in the Bismarcks. Canarium harveyi apparently originated on Santa Cruz Island as the result of selection and has spread eastward to Tikopia, Anuta, Fiji, Samoa, Tonga and Niue (Leenhouts 1959,Yen 1996). 2

Canarium indicum grows to a height of 15-30 m and in the wild is one of the smaller trees of the rain forest canopy. The fruit is a drupe with an oily edible kernel. The skin (exocarp) of the fruit is green when unripe, black when ripe. The ripe flesh (mesocarp) is edible but astringent and deteriorates rapidly. Inside the flesh is the shell (endocarp) and inside the shell is the edible kernel consisting usually of two seeds, each enclosed in its own skin (testa), which is peeled off before the seeds are eaten (Evans 1999: 6; see Figure 11.1).

Particular tree species display considerable variation in their forms, and this variation reflects the time depth of cultivation and domestication. Thus round fruit predominate in Vanuatu, oval fruit in the Solomons. Nuts may contain one kernel or two, which may be white or yellow. The rhythm of flowering, which can be altered by vigorous pruning, varies so that trees can be harvested at different times. Canarium indicum trees are usually individually owned and in some areas are tended where they have grown naturally in the forest. In the Solomons most are planted near villages. Canarium salomonense is usually a cultivated tree. Solomon Islanders consider Canarium indicum to require more light than Canarium salomonense, and hence more attention has to be paid to clearing other trees around it (Evans 1999: 40). Walter & Sam (2002: 153) report that in Vanuatu spontaneously germinated seedlings or fully ripened fruits are sometimes planted in gardens or villages.

Canarium indicum and Canarium salomonense are especially valued for their oily nuts and there is evidence that this was already true in POc times (ch.2, §4). Canarium nuts are broken open with a stone. Along the northeast coast of New Guinea, in the Bismarcks, in Bougainville and in the Solomons, their kernels are eaten raw or smoked, or the smoked nuts are pounded with sago, bananas or a root crop3 to make an oily pudding (POc *puro-ŋ, ch.12, §4.2) (Paijmans 1976: 123-124, Peekel 1984:281, Bourke 1996, Kwa’ioloa&Burt2001: 102). A Takia speaker once described the pudding to me as ‘pork when there is no pig’: it is presented to honoured guests. Hviding (2005: 128, 133) says it is ‘a very important food, as much now as in the old days’ in Marovo, where traditionally the first puddings were presented to spirits. Similarly on Small Malaita and Ulawa there were ceremonies associated with the first nuts: on Small Malaita this occurred with the first harvest in early August, on Ulawa when the first smoked nuts are ready. In both cases a priest sacrificed nuts and pudding to the ancestors (Ivens 1927: 367-369). On Choiseul Canarium salomonense has been elevated to a high level of spiritual significance manifested in a variety of practices (McClatchey et al. 2006a ). The cultural importance of Canarium is seen in the Marovo term buruburuCanarium spp. (generic)’, which is also used for ‘year’, the interval between two ripenings of canarium nuts (Hviding 2005: 107).

Among the Kwara’ae Canarium wood is regarded as unsuitable for building, as it becomes worm-eaten (Kwa’ioloa & Burt 2001: 103), but Powell (1976) reports that the Bola use it for canoe hulls and building materials. The Kwara’ae use its resin for caulking cracks in canoes.

Canarium harveyi is almost identical in appearance to Canarium salomonense and was earlier thought to be a variety of the latter. Canarium salomonense is dioecious, whereas Canarium harveyi is polygamodioecious, presumably as a result of selection (Evans 1999: 59). Both are similar in appearance to Canarium indicum.4 The shell of a Canarium salomonense nut cracks into two halves when it is hammered, whereas the shell of Canarium indicum shatters. Both are processed and eaten in much the same ways (Record 1945; Kwa’ioloa & Burt 2001: 104).

Of the three terms reconstructed below, POc *[ka]ŋaRi was almost certainly the term for Canarium indicum as well as the generic term for Canarium species.5

Note that the initial syllable of *[ka]ŋaRi is reflected only in Admiralties, North New Guinea and Papuan Tip languages (and perhaps in Raga and Namakir), whereas Meso-Melanesian and Eastern Oceanic reflexes point to *ŋaRi. This distribution justifies the reconstruction of POc forms with and without initial *ka-, which may represent or have been reanalysed as the prefix *ka- ‘tree’ reflecting earlier *kayu ‘tree’ (ch.2, §7.1.2). Bola taŋari may reflect the addition of an otherwise unknown prefix ta- to *ŋaRi.

Marshallese kaŋalPisonia grandis’ looks as if it is a borrowing from a language retaining initial ka-, i.e. Admiralties or Western Oceanic, but on current knowledge of Oceanic settlement history it is difficult to see how this could have occurred.

PCEMP *ka(n,ŋ)aRi canarium almond, Canarium spp.
POc *[ka]ŋaRi canarium almond, Canarium indicum
Adm Lou kane canarium almond
Adm Titan aŋei almond
Adm Baluan kanai canarium almond’ (Nevermann 1934)
Adm Sori-Harengan kenai canarium almond’ (Nevermann 1934)
Adm Papitalai aŋei (glossed ‘almond’ by Nevermann 1934)
NNG Kove aŋahi canarium almond’ (A. Chowning, pers. comm.)
NNG Lukep kaŋar canarium almond
NNG Mengen kaŋali canarium almond
NNG Takia aŋar canarium almond
NNG Manam kaŋari canarium almond
PT Muyuw kinay canarium almond
MM Bola taŋari canarium almond, Canarium indicum’ (t- for expected †k-)
MM East Kara ŋai canarium almond, Canarium indicum
MM Patpatar ŋar canarium almond, Canarium indicum
MM Uruava nari canarium almond
MM Vangunu ŋari canarium almond
MM Kusaghe ŋari Canarium indicum’ (Evans 1999: 39)
PEOc *[qa]ŋaRi canarium almond, Canarium spp.
SES Bugotu ŋali canarium almond’ (W. McClatchey, pers. comm.)
SES Gela ŋali canarium almond
SES Kwara’ae ŋali canarium almond
SES Lau ŋali canarium almond
NCV Mwotlap na-ŋey canarium almond
NCV Mota ŋai canarium almond
NCV Ambae ŋai canarium almond
NCV Araki ŋa-ŋa canarium almond
NCV Raga aŋai native almond; kidney
NCV Naman n-eŋe canarium almond
NCV Nese n-eŋa canarium almond
NCV Port Sandwich ni-ŋai canarium almond
NCV Paamese iŋā canarium almond
NCV Lewo (pur)ŋi canarium almond
NCV Namakir ʔaŋa canarium almond
NCV Nguna na-ŋai canarium almond
NCV South Efate na-ŋe canarium almond
SV Sye na-ŋai canarium almond
SV Lenakel na-ŋe canarium almond
SV Anejom̃ na-ŋai canarium almond
SV Sye na-ŋai canarium almond
cf. also:
Mic Marshallese kaŋal Pisonia grandis

The denotatum of PWOc *pinuaq is not clear, as the one Papuan Tip witness is glossed ‘Terminalia catappa’, the Meso-Melanesian witnesses all ‘canarium almond’, presumably Canarium indicum. It is possible - but not probable - that lthe items listed below reflect POc *pinu(q)anMacaranga spp.’ (§2.5) with a change in denotatum.

PWOc *pinuaq a nut tree, perhaps Canarium sp. (?)
PT Lala viŋu Terminalia catappa
MM Patpatar hinuai canarium almond, Canarium indicum
MM Bilur inuai canarium almond
MM Kandas nui canarium almond
MM Tinputz winoa canarium almond
MM Kia finua Canarium salomonensis’ (W. McClatchey, pers. comm.)

The POc reconstructions *(q)alipa and *lalipa are problematic both semantically and formally. The nut described in the Drehet gloss is not readily recognisable; the Mangap reflex is glossed Terminalia catappa, the Kwara’ae Inocarpus fagifer, and the rest, all NNG or MM, ‘canarium almond’. The principal formal difficulty is the initial consonant. Drehet has accreted n-, reflecting the PAdm article *na, and points to POc initial *q- or the absence of an initial consonant (Ross 1988: 340-341), i.e. *(q)alip, as do the Tami and Numbami reflexes. The other North New Guinea forms and Kwara’ae (SES) reflect a variant *lalip. The Minigir and Tolai reflexes reflect a variant in g-, rather than expected †k- reflecting *q-. Finally, the Drehet, Mangap and Tolai forms point to the presence of a final vowel, and Tolai attests to -a,6 but Kwara’ae unexpectedly lacks the final syllable. If this term did indeed denote the canarium nut, then it may be that cultivars of this culturally significant item have been propagated from one location to another, and the term for them has been borrowed at the same time.

POc *(q)alipa, *lalipa nut sp., possibly canarium almond, Canarium sp.’ (?)
Adm Drehet n-elip k tree: nut, grows wild, very hard skin, oval, about one centimetre long, dark green’ (perhaps Canarium chinare; J. Kennedy, pers. comm.)
NNG Mangap lelivii Terminalia catappa
NNG Dami lali canarium almond
NNG Tami yalip canarium almond
NNG Numbami yalipa canarium almond
NNG Yabem lanip canarium almond
NNG Kaiwa lalip canarium almond
NNG Kairiru laliu big, red canarium almond
NNG Ulau-Suain liliu canarium almond
MM Minigir galip canarium almond
MM Tolai galipa canarium almond
SES Kwara’ae (ʔai)lali Tahitian chestnut, Inocarpus fagifer’ (lit. ‘kidney tree’)

Kwa’ioloa and Burt (2001: 119) note that Kwara’ae lali is also used for ‘kidney’. However, the semantic extension is from ‘nut’ to ‘kidney’, not vice versa, as the use of ‘nut’ words for kidneys is quite common, e.g. Arosi kora i mabʷe ‘kidneys’ (lit. ‘fruit of Tahitian chestnut’ ), Niuean fua-ifi ‘kidney’ (lit. ‘fruit of Tahitian chestnut’).

2.2. Inocarpus fagifer, Tahitian chestnut, Pacific chestnut, Polynesian chestnut, TP aila, B namambe (Fabaceae)

Figure 11.2: Inocarpus fagifer, Tahitian chestnut: A, tree; B, portion of branch bearing fruit; C, inflorescence.

Inocarpus fagifer is a common second storey tree of the foreshore or lowland forest, reaching 15-30 m in height in the Bismarcks but shorter on islands further east. Its trunk is straight and fluted (Figure 11.2). Its fruit is a pod about 8cm long which does not release its single white seed, which must be cooked to be palatable. The enormous variety of its forms reflects the fact that it has long been cultivated (Bourke & Allen (forthcoming) report that it is cultivated by a sixth of Papua New Guinea’s rural population). Leaves may be elongated and narrow or oblong and wide. The fruit may be rounded, crescent-shaped or elongated-oval and green, brown or yellow (Walter & Sam2002: 183-184). Right across Oceania it is either boiled or roasted like a chestnut (Paijmans 1976: 124, Evans 1999: 19-21, S. Foale 2001, Walter & Sam 2002: 183, Gardner & Pawley 2006). Hence the English term ‘Tahitian chestnut’. It is then either eaten without further treatment, or in the Solomons and Fiji grated on coral and made into bread or pudding (Capell 1941, Peekel 1984: 245, Evans 1999: 19, Walter & Sam 2002: 185). In parts of Vanuatu it is a major alternative food between the two yam seasons, and the nuts are stored in various ways (Walter & Sam 2002: 185).

The cooked seed varies in taste and villagers choose trees according to the taste of their seeds. The tree spreads naturally and prolifically and is then often carefully protected. Seedlings that grow around the base of the trunk are left in place if the tree is little used, but removed from others so that fallen fruit can be harvested more easily. In Vanuatu seedlings of trees bearing fruit preferred by villagers are transplanted close to the village, but this seems to occur less commonly in the Solomons (Walter & Sam 2002: 184–185).

On Lihir the leaves of Inocarpus fagifer are used to parcel up food for cooking in a stone oven (S. Foale 2001). The wood is brittle and susceptible to borers and in general little used, but in Fiji and Tonga tool handles are made from the flutes of its trunk (Walter & Sam 2002: 186, Gardner & Pawley 2006).

Blust (ACD) argues that Dempwolff (1938) confused reflexes of POc *qipil ‘ironwood, Intsia bijuga’ (ch.7, 4.9) with those of POc *ipi ‘Tahitian chestnut, Inocarpus fagifer’. The difference between the two denotata, he suggests, justifies separate reconstructions. He is certainly right, as Marovo has distinct reflexes of the two terms, respectively kivili and ivi.7

POc *ipi Tahitian chestnut, Inocarpus fagifer
Adm Mussau ii Tahitian chestnut
NNG Amara (e)ip Tahitian chestnut, Inocarpus fagifer
NNG Lukep ip nut-bearing tree
NNG Gitua ipi Tahitian chestnut
NNG Bing yip Tahitian chestnut
NNG Takia ip Tahitian chestnut
PT Bwaidoga ɣivi wild chestnut
MM Simbo ivi Tahitian chestnut
MM Nduke ivi Tahitian chestnut
MM Marovo ivi Tahitian chestnut
MM Gao na-efi Tahitian chestnut, Inocarpus fagifer’ (W. McClatchey, pers. comm.)
MM Maringe na-ifi Tahitian chestnut, Inocarpus fagifer’ (W. McClatchey, pers. comm.)
PEOc *ipi Tahitian chestnut, Inocarpus fagifer
Mic Kiribati ibi Tahitian chestnut
Fij Bauan ivi Tahitian chestnut
Fij Wayan ivi Tahitian chestnut
Fij Rotuman ʔifi Tahitian chestnut
Pn Tongan ifi Tahitian chestnut, Inocarpus fagifer
Pn Anutan ipi Tahitian chestnut
Pn Samoan ifi Tahitian chestnut, Inocarpus fagifer
Pn Rarotongan iʔi Tahitian chestnut

PEOc *mabʷe Tahitian chestnut, Inocarpus fagifer’ (Lynch 2004a; Chowning 2001: *m(ʷ)ap(ʷ)e)
SES Sa’a mapʷe Tahitian chestnut
SES Santa Ana mʷapʷe Tahitian chestnut
SES Kahua mabe Tahitian chestnut’ (Henderson and Hancock 1988)
NCV Mota mabʷe tree sp.
NCV Ambae magʷe Tahitian chestnut
NCV Nokuku mape Tahitian chestnut
NCV Kiai mape Tahitian chestnut
NCV Tamambo (vu)mabue Tahitian chestnut
NCV Araki uetᫀe Tahitian chestnut
NCV Raga mʷabʷe tree sp.
NCV Nese na-mab Tahitian chestnut
NCV Port Sandwich na-mbʷe Tahitian chestnut
NCV Namakir mʷamʷ Tahitian chestnut
NCV Nguna na-mʷapʷe Tahitian chestnut
SV Anejom̃ n-mapʷ Tahitian chestnut’ (Wheatley 1992: 143)
Pn Rapanui mape kidney
Pn Mangarevan mape local chestnut
Pn Pukapukan mape ovary
Pn Tahitian māpē kidney; Inocarpus fagifer

Ivens (1929) assumes that Sa’a (SES) mapʷeInocarpus fagifer’ is a borrowing from Mota, but this supposition seems unnecessary.

The Tahitian reflex above is glossed ‘kidney’ as well as ‘Inocarpus fagifer’, and the Rapanui reflex denotes only ‘kidney’. As noted in §2.1, there is a tendency for names of nuts also to be used as (or as part of) the term for the kidney.

2.3. Barringtonia spp. other than Barringtonia asiatica, cutnut, bush nut, TP pao, B navele (Lecythidaceae)

The genus Barringtonia has a number of species (see also ch.5, §5.2), but only three have edible nuts: Barringtonia novae-hiberniae (syn. Barringtonia oblongifolia, Barringtonia brosimos), Barringtonia procera (syn. Barringtonia magnifica, B. excelsa, Barringtonia schuchardtiana, Barringtonia guppyana) and Barringtonia edulis (syn. Barringtonia calyptrata, B. excelsa, Barringtonia samoensis, Barringtonia seaturae). They are small trees, growing to between 7 and 20m, which fruit 2-3 times a year, producing a fruit with a fleshy exocarp, a thin fibrous mesocarp and a thin, hard endocarp, within which is a large oily seed with a thin, minutely hairy skin (Figure 11.3).8 The seed is edible raw or cooked (Evans 1999: 12-17, 31, 44, Gardner & Pawley 2006). Barringtonia species with edible nuts grow today in villages on northeast mainland New Guinea and in the Bismarcks, the Solomons and in Vanuatu.

Peekel (1984: 397) says that the seeds of Barringtonia novae-hiberniae are superior to those of Barringtonia procera. Otherwise the three species are very similar and are sometimes confused in botanical reports. Jebb (1992) provides a careful and relatively recent study of the edible species, and the synonyms above are based on his listing. There are numerous cultivars, and this has led to the proliferation of synonyms as well as confusions about which species a given cultivar represents. Evans (1999: 38) comments that in indigenous Solomons taxonomies Barringtonia edulis is often classified with Barringtonia novae-hiberniae.

Figure 11.3: Barringtonia edulis, cut nut: A, tree; B, flowering shoot; C, flower; D, portion of string of fruit; E, longitudinal section of ripe fruit and edible kernel (from [Henderson & Hancock 1988](../sources/HendersonandHancock1988): 62), F, detailed longitudinal section of fruit; G, transverse section of fruit.

Of the three species, it seems probable that only Barringtonia novae-hiberniae was present in the Bismarcks in early Oceanic times, although, like Barringtonia edulis, it is only a minor food source in present-day Papua New Guinea. It is the only species of the three which grows wild in the forests of Papua New Guinea (Jebb 1992), and it is also the species which Peekel (1984: 397) reports as being tended or planted in gardens and around villages in New Ireland for its edible seeds.

All three species grow wild in the forests of the Solomon Islands, often in wet places. Barringtonia novae-hiberniae is more likely to grow wild (it is considered to be the most shade-tolerant of the three species), whilst Barringtonia procera and Barringtonia edulis are more likely to grow near villages where they are often transplanted to groves along with Canarium trees (Evans 1999:40-41, Hviding 2005: 146).

Nut and fruit trees 3 21

Jebb (1992) reports that wild specimens of Barringtonia procera have only been found in the Solomons. Cultivated varieties of Barringtonia procera abound in the Solomons and Vanuatu, suggesting that it has long been domesticated there (Walter & Sam 2002: 118). Indeed, local informants told Yen (1996) that Barringtonia procera originated on Santa Cruz Island in the extreme east of the Solomons, and he appears to entertain this possibility. Thus it seems to have been transported from the Solomons and Bougainville to New Ireland and thence to the Gazelle Peninsula of New Britain and the Admiralties (Bourke 1996), perhaps in the last thousand years. The fact that it had not spread to the rest of New Britain or to New Guinea by 1870 suggests that its spread occurred later rather than earlier.9 J. Kennedy’s (pers. comm.) informants in the Admiralties regard Barringtonia procera as old there, and Bourke (forthcoming) regards it as a pre-contact introduction. If this reconstruction of events is correct, then it may be that Barringtonia procera displaced earlier Barringtonia novae-hiberniae cultivation in the Bismarcks.10

Peekel apparently did not find Barringtonia edulis in New Ireland during his work, which predated the second World War. On the other hand, in Fiji it is the only edible Barringtonia species and grows wild in both open and dense forest (it is rarely cultivated there; Jebb 1992). It also grows in the wild and occurs in many varieties in the Solomons and Vanuatu, indicating a long cultivation history (Walter & Sam 2002: 112-113). These facts suggest that Barringtonia edulis may have been brought to the Bismarcks very recently.

These considerations influence the interpretation and glossing of the reconstructions below. Only one POc term, *pala(ŋ), can be convincingly reconstructed for edible Barringtonia, and it is a reasonable inference that it denoted Barringtonia novae-hiberniae. Peekel reports two varieties in New Ireland: the more desirable variety has fruit ‘blackish-purple to wine-red’, the other pale green. In Patpatar, the red variety is called paua kubar, the green paua pala.11 It is thus possible that POc *pala(ŋ) denoted the green variety.

The final *-(ŋ) is added on the basis of Kara falaŋ. However, the absence of a reflex in other Meso-Melanesian languages, where a final-consonant reflex is expected, makes its reconstruction doubtful.

POc *pala(ŋ) cut nut, bush nut, Barringtonia novae-hiberniae (green variety?)
MM East Kara faləŋ Barringtonia novae-hiberniae
MM Patpatar (paua) pala Barringtonia novae-hiberniae, variety with pale green fruit
MM Kokota fala cut nut
MM Gao fala Barringtonia edulis’ (W. McClatchey, pers. comm.)
MM Maringe fala Barringtonia procera, cut nut’ (Evans 1999: 39)
TM Tanibili no-volo cut nut
TM Tanema vara cut nut’ (-r- for †-l-)

PEOc *pala cut nut, bush nut, Barringtonia sp .
SES Talise vala cut nut
SES Kwara’ae fala Barringtonia procera, Barringtonia edulis, Barringtonia novae-hiberniae’ (W. McClatchey, pers. comm.)
SES Arosi hara Barringtonia edulis
SES Bauro hara cut nut
SES Kahua hara cut nut
NCal Nyelâyu pālac Barringtonia neocaledonica
Fij Wayan (kutu)vala Barringtonia edulis, with large seed edible raw or cooked

Also seemingly reconstructable on the basis of the cognate set below is POc *pele, but the fact that it differs from POc *pala(ŋ) only in its vowels suggests that some or all of the terms in the set reflect borrowings associated with the westward expansion of either Barringtonia procera or Barringtonia edulis. Additionally problematic are the fact that the two terms found in New Britain (Nakanai, Meramera uele) denote other nut trees and not a Barringtonia sp., and the fact that they reflect POc initial *w- rather than *p-.

MM Nakanai uele Canarium mehenbethene’(Floyd 1954)
MM Meramera uele Tahitian chestnut
MM Vaghua vele cut nut
MM Babatana vele Barringtonia procera, Barringtonia edulis, Barringtonia novae-hiberniae’ (W. McClatchey, pers. comm.)
NCV Mota vele Barringtonia edulis
NCV Tamambo (vu)vale Barringtonia edulis
NCV Raga vele Barringtonia edulis
NCV Apma vʷel Barringtonia edulis
NCV Lonwolwol woleh a common edible nut
NCV Namakir vil Barringtonia edulis
NCV Nguna na-vīla Barringtonia edulis
SV Sye vel(ŋah) Barringtonia edulis
SV Ura ni-ver(ŋi) Barringtonia edulis

Although *kinu ‘edible Barringtonia species’ has reflexes in both Meso-Melanesian and SE Solomonic languages, the members of the set are spread across the border between Western and Eastern Oceanic, so borrowing is more probable than shared inheritance from POc.

MM Roviana kinu Barringtonia sp., with edible nut
MM Nduke kino cut nut
MM Hoava kinu cut nut
MM Kusaghe kinu Barringtonia procera, cut nut’(Evans 1999: 39)
SES Gela kinu k shore tree with ed. fruit
SES Lau kinu cut nut, Barringtonia edulis
SES Kwaio kinu cut nut
SES Kwara’ae kiun-kinu cut nut, Barringtonia edulis’(Evans 1999: 39)

Figure 11.4: Terminalia catappa, sea almond: Left A, tree; B, shoot bearing fruit; C, flowering shoot; D, fruit with edible kernel (from [Henderson & Hancock 1988](../sources/HendersonandHancock1988): 71). Right Parts of fruit: E, longitudinal section.

2.4. Terminalia spp. (Combretaceae)

A number of Terminalia species have edible ‘nuts’, but only two are reported to be planted in NW Island Melanesia. They are Terminalia catappa (sea almond, Indian almond, Java almond, TP talis, P alite, B natavoa) and Terminalia kaernbachii (okari nut, B natalie).12 Terminalia catappa is distributed from southern India to Polynesia, but Terminalia kaernbachii occurs indigenously only in New Guinea and the Bismarck Archipelago (Bourke 1996, Walter & Sam 2002: 260). Several other species with edible nuts occur in NW Island Melanesia but are only harvested from the wild (Terminalia copelandii, Terminalia impediens; Paijmans 1976: 123-124), and yet other species have fruits with edible flesh (_Terminalia megalocarpa__, syn. T. solomonensis, T. lapalagon). Several Terminalia species found indigenously in the Solomons provide good timber: Terminalia brassii, T. calamansanai and Terminalia sepicana (Evans 1999: 10–11).

Terminalia catappa is a stout broad tree growing to 10-25 m, with a short, often twisted, easily climbed bole. It prefers moister environments, is a common foreshore tree in New Guinea and the Bismarcks, and grows along the coastal strip up to an altitude of 300 m. It also grows in the floodplain forests and streambanks of Bougainville (Peekel 1984:403, Mueller-Dombois & Fosberg 1998: 60, Bourke & Allen forthcoming). Its leaves turn red and fall about four times a year, providing a calendrical marker in lagoon environments in Fiji. The fruit of Terminalia catappa has a thin, fleshy exocarp covering a fibrous mesocarp fused with a thick, hard, irregular endocarp (the stone), within which is an edible seed with an almond-like taste enclosed in a red skin (testa) (Figure 11.4), eaten raw or roasted (Evans 1999: 12-13).

Terminalia kaernbachii is more slender and has thinner branches than Terminalia catappa. It is also taller, growing to 20-40 m (Peekel 1984:403, Evans 1999: 41). Its fruit is the largest known among the Combretaceae and contains a large edible seed which ranges in weight from 1.5 to 10 g. Its distribution is quite different from the coastal Terminalia catappa. It prefers instead inland environments up to an altitude of 1100 m with a greater diurnal temperature range. Until recently its distribution in the Bismarcks was limited to the extreme west of New Britain and to Manus Island in the Admiralties (Walter & Sam 2002:260, Bourke & Allen forthcoming, pers. comm.). Unfortunately, Terminalia kaernbachii has received relatively little attention in the literature, partly perhaps because of its restricted distribution and partly because it is overshadowed by the better known and far more widespread Terminalia catappa.

The literature also attributes little importance to Terminalia catappa, but this reflects a decline in its consumption since European contact. In the Solomons and Fiji the nuts tend to be eaten raw as snacks and collected by children, but they are not (or no longer?) used in cooking. Paijmans (1976: 123-124) and R.M. Bourke (pers. comm.) report that it is often planted and is a common village shade tree in New Guinea and the Bismarcks. Walter & Sam (2002: 255) say that Terminalia catappa nuts are sometimes preserved by smoking in New Britain and Bougainville. The situation in Vanuatu is ambiguous. Walter & Sam (2002: 255) report that Terminalia catappa is largely spread by birds and bats, and little cultivated, but the fact that there are many varieties there may point to past selection through planting.

In Vanuatu and on Waya (Fiji) the wood of Terminalia catappa was carved. In Vanuatu it is also used for canoes and for the frameworks of buildings (Walter & Sam 2002:255-256, Gardner & Pawley 2006). In Marovo juice squeezed from the leaves makes a medicine against various pains including toothache. Bark scrapings wrapped in leaves and heated over a fire are squeezed to produce a liquid given to children who have a sore throat, cough or diarrhoea, and it has similar uses in Vanuatu (Walter & Sam 2002:256, Hviding 2005: 145).

Comments in the agronomic literature about the relative insignificance of Terminalia catappa are belied by the fact that there is a term with very widespread reflexes, namely POc *talise. The denotatum of reflexes from New Guinea and the Bismarcks is usually noted simply as ‘Terminalia sp.’, but it is a reasonable inference that reflexes from coastal locations in New Guinea, from New Britain and New Ireland and from small islands all denote Terminalia catappa (R.M. Bourke, pers. comm.) and that this was the denotatum of POc *talise. If this interpretation is correct, then no term for Terminalia kaernbachii is reconstructable on the basis of the available data.

PMP *talisay Terminalia catappa’ (Dempwolff 1938)
POc *talise Terminalia catappa’ (Milke 1961)
Adm Seimat talil Terminalia sp.’ (Sorensen 1950)
Adm Lou telit Terminalia sp.
Adm Loniu tɛlus Terminalia sp.
Adm Titan drilis Terminalia sp.
NNG Mengen talisi Terminalia catappa
NNG Kove talize Terminalia sp.
NNG Tami talit Terminalia sp.
NNG Kela tarik Terminalia sp.
NNG Takia tali Terminalia sp.
NNG Kairiru talis Terminalia sp.
MM Vitu taðile Terminalia sp.’ (metathesis)
MM Bola tarile Terminalia sp.’ (metathesis)
MM Lavongai talisa Terminalia sp.
MM Madak ralis tree sp.
MM Sursurunga talis Indian chestnut
MM Tolai tali Terminalia sp.
MM Ramoaaina təliə Terminalia sp.
MM Babatana talike Terminalia catappa’ (-k- for †-∅-)
MM Nduke ta-talise Terminalia catappa
MM Roviana ta-talise Terminalia catappa
MM Marovo talise Terminalia catappa
MM Kia (na)klihe Terminalia catappa’ (W. McClatchey, pers. comm.)
MM Maringe (na)klise Terminalia catappa
PEOc *talise Terminalia catappa
SES Gela talihe Terminalia catappa
SES Lau alite Terminalia catappa
SES Kwara’ae alita Terminalia catappa
NCV Mwotlap t[ı]lıs Terminalia catappa
NCV Mota salite Terminalia catappa’ (metathesis)
NCV Tolomako na-talise Inocarpus fagifer
NCV Apma telis Terminalia catappa
NCV Nguna na-talie Terminalia catappa
NCV South Efate n-tali Terminalia catappa
PSV *nə-talis Terminalia catappa’ (Lynch 2001c)
SV Sye nteli Terminalia catappa
SV Lenakel telh k.o. tree with flattish oval brown fruit which is cracked open and eaten
SV Anejom̃ n-tejeθ Terminalia catappa
PCP *talise Terminalia catappa
Fij Bauan daliði Terminalia catappa
Pn Tongan telie Terminalia catappa
Pn Niuean telie Terminalia catappa
Pn East Futunan talie Terminalia catappa
Pn Samoan talie Terminalia catappa
Pn Luangiua talie tree sp. with big yellow berries
Pn Marquesan taʔie Terminalia catappa
Pn Rarotongan taria Terminalia catappa
Pn Rennellese tagie Terminalia catappa
Pn Tokelauan talie Terminalia catappa

Two other POc terms possibly denoted Terminalia species: *tapoRa and *qatV. The POc denotatum of *tapoRa is unclear. In PEOc it evidently denoted a species of Terminalia, possibly Terminalia catappa,13 but the glosses of the Takia and Nehan reflexes make it impossible to determine its POc denotation.

POc *tapoRa a nut-bearing tree sp.’ (Geraghty 1990)
NNG Takia tapal nut tree, like Canarium, but less oily14
MM Nehan tauol Inocarpus fagifer’ (Glennon and Glennon 2005)
PEOc *tapoRa Terminalia spp.’ (Geraghty 1990)
SES Kwara’ae dafo Terminalia brassii
NCV Mwotlap na-twoy Albizia saman
NCV Mota tawora Albizia saman
NCV Ambae tavoa Terminalia catappa
NCV Tamambo (vu)tavoa Terminalia catappa
NCV Maewo tavoa Terminalia catappa
NCV Raga tavoa Terminalia catappa
NCV Uripiv dawo Terminalia catappa
NCV Nese tavo Terminalia catappa
NCV Port Sandwich ravo Terminalia catappa
NCV Lonwolwol tavoro a fruit
NCV Paamese hoai Terminalia catappa
NCV Lewo (puru)tawo Terminalia catappa
NCV Baki (bur)tavu Terminalia catappa
NCV Namakir tauwo, tawo Terminalia catappa
Fij Bauan tāvola Terminalia catappa15

The set below appears to reflect a POc *qatV. Superficially Nehan kasasas appears cognate, but it is at best a borrowed reflex. The expected Nehan reflex would be *ata: Nehan k- and -s- reflect POc *k and *s respectively. Terminalia complanata and Terminalia sepicana are both uncultivated edible species, the nuts of which are occasionally consumed as snacks, and so the gloss ‘Terminalia sp. with edible nut’ is well enough supported.

POc *qatV Terminalia sp. with edible nut
MM Madak (var)ʔa Terminalia complanata
NCV South Efate n-at Terminalia sepicana (eaten only by fruit bat)
Mic Chuukese asas Terminalia catappa
Mic Carolinian asas Terminalia catappa
cf. also:
MM Nehan kasasas Terminalia samoensis

2.5. Pandanus spp., screw pines (Pandanaceae)

Pandanus trees are an easily recognised feature in the forests of NW Island Melanesia. All species have aerial roots and very large thick leaves. The leaves of some species serve on canoes as sails, awnings, deck-houses, bailers and in houses as roofing, mats and wall lining. Sewn leaves are used for rain capes. POc *qebal ‘pandanus mat’ is reconstructed in vol. 1, ch.4, §3.1. The fruits of all species are syncarps, compound fruits with many segments, each a drupe, arranged around a core, and the fruits and/or seeds of various species are a source of food. Recognition of the various species, however, is much more difficult, partly because of intra-species variability which is at least partly the result of cultivation. Barrau (1962: 161-163) remarks that there is much confusion in the Linnaean naming of Pandanus species, and Henderson & Hancock (1988: 80, 232-236) do not provide names for the Solomons species they describe. Our sources are also often vague in their glosses of terms for pandanus types. Consequently it is possible that there are inaccuracies here. The four species for which POc terms can be reconstructed with reasonable certainty are:16

  • Pandanus tectorius, the coastal pandanus: the most widespread and most exploited species throughout Oceania; its leaves are used for making mats;
  • Pandanus dubius: it is widely distributed and remarkable for the size and strength of its leaves.
  • Pandanus conoideus, with its long red or yellow fruit (Tok Pisin marita), a salient species in New Guinea but not common in the Bismarcks;
  • Pandanus lamekotensis: seemingly restricted to the Admiralties and to northern and central New Ireland, but a POc term for it is reconstructable.

All except Pandanus dubius are sources of food, and the third and fourth are cultivated. Although Pandanus dubius is not a food source, I have included it here in order to keep the genus together.

2.5.1. Pandanus tectorius (syn. Pandanus odoratissimus), coastal pandanus (Pandanaceae)

Pandanus tectorius usually grows just behind the shore line to a height of 5-10 m. Its leaves are 1-2 m long, flat sheets tapering to a point. The orange fruit is made up of ‘fingers’ 6–8 em long, 4–5cm wide, each consisting of 8–17 parallel nuts (Figure 11.5, left). The species shows considerable variability, consistent with having been cultivated over a long period of time, and is often found near villages and old village sites (Peekel 1984:38, Walter & Sam 2002: 216–217). In NW Island Melanesia its use is patchy: it is used in Manus, the south coast of New Britain, in New Ireland and in Bougainville (Bourke n.d.).17

Selection has resulted in cultivars with thick but pliable leaves with edges free from spines, which serve as rain hoods and are used for making mats and baskets. In Vanuatu baskets are made from leaves softened in the fire, cut into narrow strips, steeped in water, then bleached and dried in the sun (Walter & Sam 2002: 216-217).

The alimentary use of Pandanus tectorius is less significant than uses of its leaves, but it is reported from Papua New Guinea, Vanuatu, Tonga and Samoa. The ripe globular fruit are sucked to obtain a sweet juice, perhaps more by children than by adults. This practice may have been far more common in the past, before the arrival of sweetened soft drinks (Walter & Sam 2002:217, Bourke n.d.). On Waya (Fiji) the juice was famine food (Gardner & Pawley 2006). Barrau (1962: 88) reports that the ends of the aerial roots are baked and eaten in some Micronesian and Polynesian societies, especially in atoll communities, where its fruits are also an important food source.

On Waya the trunks are used for house rafters and leaves for thatching (Gardner & Pawley 2006).

POc *padran appears to have specifically denoted Pandanus tectorius, but was evidently also used as a generic for pandanus species. POc *kiRe and *poipoi probably denoted only Pandanus tectorius or perhaps certain cultivars of Pandanus tectorius.

PAn *paŋudaL pandanus’ (Blust 1982)
PMP *pandan pandanus’ (Dempwolff 1938)
POc *padran coastal pandanus, Pandanus tectorius; pandanus (generic)’ (Biggs 1965: *para)
Adm Mussau arana littoral pandanus the leaves of which are used in plaiting mats and baskets, Pandanus tectorius
Adm Leipon padr kind of pandanus with narrow light-green leaves, used in plaiting mats
Adm Lou par pandanus
Adm Titan par pandanus fruit’ (Bowern 1999)
NNG Amara (a)pada-pada pandanus sp. with succulent fruit
NNG Mangap pāⁿda pandanus tree
NNG Lukep pada pandanus sp.
NNG Malai padan pandanus
MM Lavongai aran pandanus
MM East Kara foran Pandanus tectorius
MM Kokota (i)fra pandanus variety, small, used for making mats
TM Tanema vadane pandanus
SES Lau fada-da pandanus
NCV Mota vana a pandanus, inedible variety of female Pandanus odoratissimus
NCV Lakon vac Pandanus tectorius’ (François 2004b)
NCV Vera’a vada Pandanus tectorius’ (François 2004b)
NCV Sakao ne-vor Pandanus cominsii
SV Kwamera nə-fara pandanus
NCal Jawe wan coastal pandanus
NCal Nyelâyu pān coastal pandanus
Mic Puluwatese fār pandanus, used for mats and thatch
Mic Carolinian fāṣa pandanus (generic)
Fij Wayan vadra Pandanus tectorius
Pn Tongan taxon of several Pandanus spp.’ (Whistler 1991b: 24)
Pn Hawaiian hala Pandanus tectorius

PMP *kiRay Pandanus sp.18
POc *kiRe coastal Pandanus sp., probably Pandanus tectorius’ (French-Wright 1983)
PT Gapapaiwa kire mat made of sewn pandanus leaves
PT Motu gere-gere Pandanus tectorius
SES Arosi gire Pandanus tectorius
NCV Mota gire Pandanus tectorius
NCV Mwotlap ne-gey Pandanus tectorius’ (François 2004b)
NCV Mwesen ger Pandanus tectorius’ (Walter and Sam 2002)
NCV Vurës (wö)gœr Pandanus tectorius’ (François 2004b)
NCV Raga gire native tree with fruit like pineapple; pandanus
NCV Tamambo hire-hire woven container from coconut leaf
NCV Big Nambas na-hei mat
NCV Nguna na-kie mat pandanus
Fij Bauan kie-kie Pandanus sp.
Pn Tongan kie a sterile variety of pandanus used for weaving mats’ (Whistler 1991b: 56)
Pn Pukapukan kie specially made mat sometimes used as sail
POc *poipoi Pandanus sp., perhaps Pandanus tectorius
MM Nakanai voivoi Pandanus sp.
SES West Guadalcanal voivoi pandanus
NCV Mwotlap wow Pandanus sp.
NCV Araki ðᫀeðᫀe Pandanus tectorius
NCV Apma wip Pandanus tectorius
NCV Uripiv waiw general word for pandanus
NCV Uripiv weiw(bur) shore pandanus, has big leaves, unusable
NCV Port Sandwich vaiv pandanus; skirt
NCV Paamese heiho Pandanus sp.
NCV Lewo (puru)vava pandanus
NCV Lewo vava pandanus
NCV Namakir vaiv smooth pandanus
SV Lenakel nu-vie pandanus sp.
Fij Bauan voivoi Pandanus thurstoni
Fij Wayan voivoi cultivars of Pandanus tectorius and possibly of Pandanus dubius or Pandanus whitmeeanus

Figure 11.5: Left Pandanus tectorius: A, tree at its tallest; B, young plant when leaves harvested; C, end portion of leaf (no thorns); D, portion of surface of syncarp; E, longitudinal section of fruit segment. Right Pandanus dubius: F, tree, height 3m; G, syncarp from above; H, longitudinal section of fruit segment with edible kernel; J, leaf tip showing curved spike.

Lynch (2004a) suggests that the following set may also reflect POc *poipoi.

PSOc *va(i,y)u Pandanus sp.
NCV Ambae ve-veo Pandanus sp.
NCV Tape na-viu Pandanus sp.
NCV Big Nambas ðᫀiu Pandanus sp.
NCV Nese na-ðᫀau Pandanus sp.
NCV Baki (buru)vewo Pandanus sp.
PSV *na-va(i,y)u Pandanus sp.’ (Lynch 2004a)
SV Sye na-(ri)vyu Pandanus tectorius
SV Sye n-(or)veyu bush pandanus
SV Lenakel nu-vie

2.5.2. Pandanus dubius (syn. Pandanus compressus) (Pandanaceae)

Nut and fruit trees 3 31

Pandanus dubius is a coastal species distributed from the Philippines southeastward as far as Vanuatu, where it is sometimes cultivated. It is the pandanus species with the broadest and stiffest leaves in the Bismarcks, 2 m or more in length and up to 16cm wide. The syncarps are made up of fingers 10-13cm long, 5-9cm wide, angular, but unlike other species not grooved (Figure 11.5, right)19 (Peekel 1984: 41, Walter & Sam 2002: 212-213).

The fruiting spike is edible but rarely eaten, Sorensen (1950) reports for the Ninigos and Walter & Sam (2002: 212) for Vanuatu. The leaves are used for thatching, and with the spiny parts removed dried leaves are sewn together as mats and large baskets (Sorensen 1950, Peekel 1984: 41).

The POc term for Pandanus dubius was *pakum.20

POc *pakum Pandanus dubius’ (Peekel 1984: 41)
Adm Mussau aum broad-leafed pandanus, Pandanus dubius
Adm Lou pɔk pandanus
Adm Titan pek pandanus
NNG Malai paum pandanus
NNG Takia wak pandanus
NNG Manam aku pandanus (big leaf); used to make grass skirt
NNG Bam wak pandanus
NNG Kairiru vʸak Pandanus dubius
MM East Kara faum Pandanus dubius
MM Patpatar hau pandanus
MM Tolai vaum Pandanus dubius
MM Sursurunga aum tree type similiar to pandanus
SES Kwara’ae faʔu pandanus (generic); mat
SES Kwaio faʔu pandanus
NCV Mota vau a pandanus
NCV Mwesen (wo)vag Pandanus dubius’ (Walter and Sam 2002: 295)
NCV Namakir na-vak Pandanus dubius’ (Walter and Sam 2002: 295)
NCV Nguna na-vaku pandanus sp.
NCV South Efate n-fak Pandanus dubius
Pn Tikopia fao broad-leaved Pandanus, Pandanus dubius’ (possibly a borrowing from a SES language)

2.5.3. Pandanus conoideus, red fruit pandanus, TP marita (Pandanaceae)

Pandanus conoideus is a small tree, 4-7 m high, found in New Guinea, from the coasts up to an altitude of 2000 m.It is less common in the Bismarcks. It grows in damp, shady places around villages and on old village sites, and displays the variability typical of cultivation. Its trunk is covered in short sharp spikes, and the long leaves have spiked edges. Its syncarps are typically 20-40cm long, and sometimes reach 1 m and weigh as much as 10 kg. The fruit are bright red or occasionally yellow, and get their colour from the oil in the pericarp (Figure 11.6) (French 1986:210, Walter & Sam 2002: 210–211.)

The fruit are prized as a foodstuff and widely consumed. They are typically split, wrapped in leaves and cooked in an earth oven or roasted over a fire. The pulp and seeds are removed from the core, mashed with water and strained to produce a thick, rich red sauce with which other foods are seasoned (Sorensen 1950, Barrau 1962: 163, May 1984, Bourke in preparation).

Figure 11.6: Pandanus conoideus, marita: A, syncarp.

POc *mʷafia apparently denoted Pandanus conoideus.21 This reconstruction is open to doubt, as there are no reflexes from New Ireland or New Britain, where the species is rare, and only one from mainland New Guinea. It is possible that Maisin moŋgiPandanus sp.’ and PMic *maŋu ‘pandanus leaf’ are also cognate. If so, they reflect a POc form in which *-ñ- has been replaced by *-ŋ-.

Another interpretation of the data is also possible, namely that the items listed below, other than Arosi mʷa-mʷana, reflect POc *moñak ‘fat, oil, coconut cream; tasty’ (ch.12, §4.2), since the fruit of Pandanus conoideus are both oily and tasty. If this were so, then Arosi mʷa-mʷana and the items listed under ‘cf. also’ would probably reflect a PEOc *mʷaŋV ’pandanus leaf.

POc *mʷaña Pandanus sp., perhaps Pandanus conoideus
PAdm *moña pandanus with long red or yellow fruit, probably Pandanus conoideus’ (Blust 1996b)
Adm Seimat maun Pandanus conoideus’ (*-o- > Seimat -au-) (Sorensen 1950)
Adm Lou mon Pandanus conoideus
Adm Wuvulu mona Pandanus conoideus
Adm Likum mon Pandanus conoideus
Adm Nali mon Pandanus conoideus
Adm Pak mon Pandanus conoideus
Adm Lou mon Pandanus conoideus
Adm Leipon moñ Pandanus conoideus
Adm Loniu moñ Pandanus conoideus
Adm Bipi moy Pandanus conoideus
Adm Kele moy Pandanus conoideus
Adm Lenkau moy Pandanus conoideus
Adm Nauna moy Pandanus conoideus
Adm Drehet muŋ Pandanus conoideus
NNG Mapos Buang mon Pandanus conoideus
SES Arosi mʷa-mʷana Pandanus sp., leaves plaited
cf. also:
PT Maisin moŋgi Pandanus sp.22
Mic Kosraean mᵚeŋ pandanus
Mic Marshallese māŋ pandanus leaves
Mic Chuukese mə̄ŋ pandanus leaf, especially when softened by a shell
Mic Woleaian māŋü pandanus leaf

2.5.4. Pandanus lamekotensis (Pandanaceae)

Peekel (1984: 41) remarks that Pandanus lamekotensis is readily distinguished from other species. However, I have otherwise found it mentioned only by Kennedy & Clarke (2004), who provide no additional information, and it is possible that its distribution is limited to New Ireland. Indeed, Peekel did not find it in the south of New Ireland or on the Gazelle Peninsula of New Britain. It grows only on swampy creek banks, 4–7 m high with from 5 to 8 leaves, and its fruit clusters are oval, not ‘fingers’. The ripe fruits, like those of Pandanus tectorius are sometimes sucked by New Ireland villagers.

POc *kaRi(q)ana Pandanus lamekotensis
Adm Baluan kayaŋ pandanus sp. similar to Pandanus lamekotensis
Adm Nyindrou kayaŋ Pandanus sp.
Adm Bipi kaihan Pandanus sp.
MM East Kara kaiat Pandanus lamekotensis’ (-t for †-n)
MM Nalik kariat Pandanus lamekotensis’ (-t for †-n) (Peekel 1984: 41)
MM Madak [va]keiŋ Pandanus lamekotensis
Mic Kiribati kaina Pandanus tectorius

2.5.5. Other names for Pandanus species

The four reconstructions below each denoted a species or a variety of Pandanus, but the glosses do not allow us to determine which.

PCEMP *ima Pandanus sp. with leaves useful for plaiting’ (ACD)
POc *ima Pandanus sp. with useful leaves
NNG Gedaged im Pandanus sp.; has aerial roots, and its leaves are used to make rain capes
NNG Kis im bush pandanus
PT Gapapaiwa imo(-kara) bush pandanus
MM Tangga im tall shrub with many stalks, the leaves of which provide wrapping material for a corpse prior to burial

POc *(p,pʷ)asa(r,R) large Pandanus sp.
Adm Drehet pʷāh large pandanus
PT Misima pala mat made: of pandanus
MM Babatana (poro) basa Pandanus sp.
MM Maringe vahara Pandanus conoideus’ (W. McClatchey, pers. comm.)
SES Bugotu vaha Pandanus aff. compressus martalli’ (W. McClatchey, pers. comm.)
Pn East Uvean faha Pandanus sp.
Pn Samoan fasa Pandanus tectorius
PWOc *(s,j)a(q,k)umu Pandanus sp.
NNG Sio samu pandanus
NNG Tami saŋ pandanus
NNG Misim seŋ pandanus
PT Saliba dam indigenous Pandanus sp.
MM Varisi saɣumu pandanus’ (Record 1945)
MM Babatana samu Pandanus dubius
PWOc *moke Pandanus sp.’ (Peekel 1984: 41–42)
NNG Kove moe Pandanus sp., used for sleeping mats, raincapes and sails’ (A. Chowning, pers. comm.)
NNG Gitua moge pandanus
MM Bulu moke Pandanus sp., inedible
MM Bola moke pandanus umbrella
MM Nakanai moe Pandanus sp.; sleeping mat and rain cape made of pandanus; used for house walls’ (Arentz 1989:93)
MM Sursurunga mo tree sp. similiar to pandanus with edible fruit; leaves used for making shelters
MM Patpatar moh pandanus shrub, Pandanus danckelmannianus

2.6. Sterculia vitiensis (syn. Sterculia tannaensis) (Sterculiaceae)

In a sense Sterculia vitiensis does not belong here, as it was not known to POc speakers. There are a number of small species of Sterculia in the Bismarcks and Solomons, but Sterculia vitiensis is a large canopy tree, up to 30m tall. It is found in the central and especially the southern islands of Vanuatu and in Fiji.

It is planted for its edible seeds (its wood is soft and not durable). The fruit is a large (9 x 7 cm) hollow capsule, light yellowish green when it is ripe, with a groove down one side which splits open to reveal a vermilion interior and a row of elongate (1-2 cm) glossy black seeds along the split edges. Sterculia vitiensis is not particularly abundant, and tends to be found in locations associated with human activity. The ripe seeds are grilled either in their shells or separately (Wheatley 1992: 230, 232, Walter & Sam 2002: 247-248).

Although the seeds of other species are sometimes eaten in the Bismarcks (Floyd 1954, Powell 1976), the only reconstructable name for a Sterculia species is, as one might expect, a PROc etymon, *wasi-wasiSterculia vitiensis’. There is a formally identical POc etymon, POc *wasi-wasiAbroma augusta’. Abroma augusta is a small shrub (ch.7, §6.1.1) and Sterculia vitiensis a large tree, so it is not clear whether the two terms were innovated independently or have a common origin.

PROc *wasi-wasi Sterculia vitiensis’ (from data in Wheatley 1992, Lynch 2004a)
NCV Ambae wah-wah
NCV Tangoa (vitu)vaha
NCV Raga wahi-wahi
NCV Apma wah-wah
NCV Tape (vən)woso-wos whitewood
SV Sye wo-wo
SV Lenakel nə-vha-vha 23
SV Anejom̃ n-woθ-waθ
Fij Buca Bay waði-waði (J. Parham 1972)

2.7. Pangium edule, pangi, ankle-rattle tree, TP sis, solomon, B navangge, nalake (Flacourtiaceae)

Pangium edule is included in this section because it is a cultivated tree (Peekel 1984: 384, Kennedy & Clarke 2004) and produces a fruit the flesh of which is eaten in some places. It is not a major food source.

The tree grows 25-30 m tall, with 3-5 triangular buttresses up to 1 m in height. Leaves are arranged in spirals at the ends of branches. The fruit of wild trees contains cyanogenetic glucosides and is poisonous, but the fruit of cultivated trees is edible (Peekel 1984: 384). The fruit, up to 15 cm long with a rough brown skin, is enclosed in a bright yellow mesocarp and green skin. It contains a number of red-brown seeds, each in its own very hard case, surrounded by a soft yellow strong-smelling pulp (French 1986: 193, Evans 1999: 19).

Figure 11.7: Pangium edule

The seed is buried for 2-3 weeks in beach sand or soaked in fresh or salt water to make it edible, then roasted and fermented (Peekel 1984: 384, Hviding 2005: 121, Bourke & Allen forthcoming). The Sengseng of New Britain trade it as a delicacy (A. Chowning, pers. comm.). The practice of eating the seeds extends eastward as far as Marovo (Evans 1999:21), but Hviding does not mention their consumption. The seeds are a famine food in Vanuatu (Walter & Sam 2002: 47).

A well known use of Pangium edule seed cases in the Bismarcks, the Solomons and Vanuatu is in the manufacture of bangles and rattles for traditional dances. In the Solomons the leaves are heated in the fire and used to kill headlice. The wood is generally not regarded as suitable for construction (Henderson & Hancock 1988:246, Hviding 2005: 121).

The only reconstructable term for Pangium edule is PEOc *paRage. Given that the tree is present in the Bismarcks, it seems odd that no POc or PWOc term can be reconstructed, but this may be due to the absence of relevant data from the sources.

PEOc *paRage Pangium edule
SES Tolo valage k.o. larger seed pod worn to make noise while dancing
SES Kwara’ae falake Pangium edule’ (Whitmore 1966)
SES Lau falake tree sp.; its seeds tied to legs in dancing
SES Kwaio falage rattle
SES Arosi harage sacred tree, has power to kill dogs
NCV Mwotlap (wo)pyak Pangium edule
NCV Mota varake tree sp .; its shells tied on the ankles as rattles in dancing
NCV Araki lahe Pangium edule
NCV Tamambo varaŋe Pangium edule
NCV Nduindui vaŋe Pangium edule
NCV Ambae vake Pangium edule
NCV Raga vaŋe Pangium edule
NCV Sakao ne-vaɣ Pangium edule
NCV Sa wak Pangium edule
NCV Nāti ne-vaŋk Pangium edule
NCV Port Sandwich (vi)vaŋg dance rattles

3. Domesticated fruit trees

3.1. Burckella obovata (syn. Bassia erskineana, Payena mentzelii, Illipe hollrungii), red silkwood, TP bukabuk, B naduldule, nandunde (Sapotaceae)

Burckella obovata tends to grow on smaller islands. It occurs on the small islands west of Manus in the Admiralties, in New Ireland, in the island groups north and east of New Ireland, on the Duke of York Islands between New Britain and New Ireland, and on Buka and nearby small islands in Bougainville Province. It is also found in the Solomons on Malaita and in the Temotu Islands (and Hviding 2005: 111 reports its presence at Marovo) and in Vanuatu (Paijmans 1976: 124, Bourke n.d.). It is a tree of medium size, about 20–30 m. tall, with a massive trunk 1-3m in diameter at the base and white flowers that have a strong, somewhat sickening scent. It has large edible fruit that has a rose-petal-like smell and is consumed uncooked. In Vanuatu there are two main types of fruit: a more common elongated type, reputed to be sweeter, and a round, sometimes very large type. The latter has two subtypes, wrinkled and smooth. The smooth subtype is apparently the outcome of selection, and is always cultivated. In the Solomons and Vanuatu the fruit is harvested before it is ripe in order to beat the fruit bats (Walter & Sam 2002: 125). Two varieties grow in Marovo, wild and planted. Coconut crabs eat the fruit of the wild variety (Hviding 2005: 111).

In the Solomons and Vanuatu the wood is used for crossbeams in houses, for outrigger booms and for canoe paddles (Record 1945, Henderson & Hancock 1988:55, Walter & Sam 2002: 125). In Marovo it was formerly used for the keels of war canoes and is still sometimes used for making dugouts (Hviding 2005: 111).

The POc form *ñatu was first reconstructed by Blust (1978b) as an unnamed but described tree type. Further reflexes indicate that this is Burckella obovata, to which Gowers (1976: 38) gives the English designation ‘red silkwood’. Evidence for POc *-q is provided by Sye yetu and Ura ni-yere (John Lynch, pers. comm.), where preservation of the final vowel reflects the earlier presence of *-q.

The gloss of PMP *ñatuq below, ‘a hardwood tree taxon, including at least Palaquium spp.’, is inferred from the glosses of Blust’s supporting data. Species of Burckella and Palaquium and perhaps other genera seem to have been included in a single taxon throughout Oceanic history (see the discussion associated with PCP *bau ‘hardwood taxon’ in ch.7, §4.10).

Figure 11.8: Burckella obovata: A, tree; B, flowering shoot; C, shoot bearing fruit; D, old seed.
PMP *ñatuq a hardwood tree taxon, including at least Palaquium spp.’ (Blust 1978b: 38-39)
POc *ñatuq Burckella obovata’ (Blust 1978b: 38-39: *ñatu; Ross 1996d)
Adm Mussau natu Burckella obovata
Adm Nauna ñot tall timber tree with large sweet green fruit
Adm Titan ñat tall timber tree with large sweet green fruit
Adm Nyindrou ñek tall timber tree with large sweet green fruit
Adm Bipi ñak tall timber tree with large sweet green fruit
Adm Loniu ñat tall timber tree with large sweet green fruit
Adm Baluan nout Burckella obovata
NNG Takia nat tree (with edible nuts or fruit, also used for timber)
NNG Gedaged nat tree, Sapotaceae
PT Kilivila natu sp. of fruit tree
PT Muyuw a-ntu-nat Palaquium sp.
PT Wedau natu Malay apple, Eugenia megacarpa
MM East Kara nətu Burckella obovata
MM Sursurunga nat tree sp. with avocado-type fruit
MM Ramoaaina natu tree sp. with a large pulpy fruit like an apple
MM Nehan not Palaquium sp.; Burckella obovata
MM Babatana natu Burckella obovata
MM Nduke natu tree sp.
MM Kubokota ñatu Burckella obovata
TM Äiwoo ñi-nou Burckella obovata
TM Natügu no-neu Burckella obovata
PEOc *ñatuq Burckella obovata
SES Sa’a nau a fruit tree, teak
SES Arosi nau tree sp., fruit is eaten
NCV Mwotlap net Burckella obovata
NCV Mota natu a fruit tree
NCV Araki (vi)naru Burckella obovata
NCV Uripiv nor Burckella obovata
NCV Paamese a-natu Burckella obovata
NCV Lewo nar Burckella obovata
NCV Nguna na-natu Burckella obovata
PSV *nə-yatuq Burckella obovata’ (Lynch 2001c)
SV Sye yetu Burckella obovata
SV Anejom̃ n-yat Burckella obovata
SV Ura ni-yere Burckella obovata
Pn Rennellese natu Burckella obovata
Pn Tikopia natu Burckella obovata
Pn Anutan natu Burckella obovata

3.2. Clymenia polyandra and Citrus spp. (Rutaceae)

Barrau (1955: 85) considers that all edible species of the genus Citrus were introduced to Melanesia by Europeans, and R. M. Bourke’s (pers. comm.) research confirms this. We would not therefore expect to find a reconstructable POc term meaning ‘citrus’. But the reconstruction of POc *molis ‘citrus fruit’ is well-supported (Lynch 1984), and its reflexes are today used in many languages for several citrus species.

How are we to explain this? There are two possible answers. One is that *molis referred not to Citrus species but to citrus-like fruit indigenous to western Melanesia. Aburu (1982) reports on two indigenous citrus-like genera, Clymenia and Microcitrus in Papua New Guinea. French (1986: 232) describes Clymenia polyandra as a ‘Citrus relative’ whose fruit is yellow, the size of a large lime, and in some cases ‘sweet and pleasant-tasting’. The tree is 5-8 m tall. It is cultivated in Manus and New Ireland (where it was also recorded by Peekel (1984: 272)) and does not occur outside Papua New Guinea.

The alternative answer is that there were inedible or barely edible Citrus species in Melanesia before European contact, which have been largely replaced by imported edible species. A bush lemon, Citrus hystrix, with almost no edible flesh (French 1986: 226) may be one of these. We can only infer that POc *molis designated either citrus-like genera or inedible species of Citrus, or both.24

POc *molis citrus fruit or citrus-like fruit, perhaps Clymenia polyandra’ (Lynch 1984)
Adm Mussau muli citrus fruit
Adm Drehet mʷili citrus fruit: pomelo
NNG Atui molis citrus fruit
NNG Mangseng mɔlis citrus fruit
MM Vitu moli citrus fruit
MM Patpatar mulis citrus fruit
MM Nehan molih Clymenia polyandra
MM Halia molihi citrus fruit
MM Kia mholi Citrus sp.
SES Bugotu moli Citrus sinensis’ (W. McClatchey, pers. comm.)
SES Lau moli introduced citrus fruit
SES Arosi mori wild orange
NCV Mwotlap nı-mʷıl Citrus medica
NCV Mota mʷol Citrus medica
NCV Tamambo moli orange
NCV Tape mʷələs citrus fruit
NCV Uripiv na-mul citrus fruit
NCV Port Sandwich vi-mor orange
NCV Lonwolwol wo-mul citrus fruit
NCV Paamese a-moli citrus fruit
NCV Lewo mʷolu citrus fruit
NCV Namakir mol citrus fruit
NCV Nguna na-mwoli citrus fruit
PSV *ne-molis citrus fruit’ (Lynch 2001c)
SV Sye ne-mli citrus fruit
SV Lenakel nə-məlh citrus fruit
SV Southwest Tanna (kʷa)n-məlh citrus fruit
SV Kwamera nə-mərhi citrus fruit
SV Anejom̃ ne-pceθ citrus fruit’ (p unexplained)
Fij Wayan moli citrus fruit (generic)

3.3. Corynocarpus cribbianus (syn. Corynocarpus australasicus, Corynocarpus cribbiana, Helicia cribbiana) (Cocynocarpaceae)

A small fruit tree which was apparently cultivated in the past, Corynocarpus cribbianus is reported from the Admiralties, from offshore islands around Madang (north coast of New Guinea), from Tangga Island (east of New Ireland) and in the Solomons from Guadalcanal and Malaita, but apparently not in New Britain or New Ireland.25 It grows to a height of 7-10 m on Tangga Island, but sometimes to 20m elsewhere in Papua New Guinea. The mango-shaped fruit, 10–12cm long and 8-10cm in diameter, grow in clusters at the ends of branches. They are sweet but not juicy, and eaten raw or boiled. Two varieties are reported from Tangga and Kwara’ae: one has red, pear-shaped fruit, the other white and more ovoid. Corynocarpus cribbianus continues to be grown from seed in some places but has become rare in the Solomons, where it was apparently more widely cultivated in the past. Today it is only a snack food for hunters in the forest (French 1986:234, O’ Collins & Lamothe 1989, Kwa’ioloa & Burt 2001: 168).

Yen (1974a) reports a previously domesticated species of Corynocarpus on Santa Cruz Island (Te Motu group, Solomon Islands). This may well have been Corynocarpus similis, which grows wild under the forest canopy in parts of Vanuatu and is cultivated there. Indeed, Walter and Sam’s (2002: 152-153) description could easily be a description of Corynocarpus cribbianus, right down to its two varieties. Today it is regularly eaten only on the Torres Islands, where it was formerly cultivated and the fruits eaten boiled just before they became ripe, and on Tanna. Elsewhere it is a famine food. The wood is used for digging sticks or utensil handles.

POc *i(u)buCorynocarpus cribbianus’ is tentatively reconstructed - ‘tentatively’ because the forms shown under ‘cf. also’ appear to be formally connected with the members of this set, suggesting a PEOc *tabʷV, but the history of these forms or their relationship to the apparent reflexes of *i(u)bu is unclear.

POc *i(u)bu Corynocarpus cribbianus
Adm Nyindrou ñ-iubu Corynocarpus sp.’ (O’Collins and Lamothe 1989)
MM Roviana ib-ibu Cleidion spiciflorum’ (Henderson and Hancock 1988)
TM Äiwoo (nua)dabu Corynocarpus cribbianus’ (Henderson and Hancock 1988)
SES Kwara’ae ibo Corynocarpus cribbianus’ (Henderson and Hancock 1988)
SES Kwaio ibo Corynocarpus cribbianus’ (Henderson and Hancock 1988)
cf. also:
SES Lengo tebu Corynocarpus cribbianus’(Henderson and Hancock 1988)
SES To’aba’ita tebu Corynocarpus cribbianus’(Henderson and Hancock 1988)
NCV Tamambo tabʷea Corynocarpus similis’(Walter and Sam 2002)
NCV Apma tabʷi Corynocarpus similis’(Walter and Sam 2002)

3.4. Mangifera spp., mango (Anacardiaceae)

We cannot be completely sure of the original referents of the five mango terms reconstructed below. When Austronesian speakers arrived in the Bismarcks, they encountered the fibrous and ill-tasting indigenous mangoes Mangifera minor and Mangifera foetida. The sweet-tasting Mangifera indica, the species widely consumed today, arrived with Europeans after about 1870 (Bourke forthcoming).

It is possible that PMP *pahuq referred to Mangifera indica and PMP *wai to other Mangifera species (ACD). I have found only two reflexes of PMP *pahuq in Oceanic languags, namely Vitu vau and Bola vao. Vitu (in the French Islands, north of New Britain) is among the most conservative of Oceanic languages, and has remained quite isolated at least since early in the spread of the Western Oceanic dialect network. Bola is close by on New Britain. One may infer that *pau(q) occurred in POc, but not with the gloss ‘Mangifera indica’. It was replaced at a very early stage by *wai, as this was the appropriate term for the indigenous (non-indica) species, with *wai-wai perhaps denoting wild varieties (§7.2). The species Mangifera minor was specifically designated by POc *koRa.

Mangifera minor, the traditional wild mango indigenous to the Bismarcks, is 10-25 m tall. The introduced Mangifera indica needs a drier period each year to bear, whereas Mangifera minor does not, and so the latter continues to be eaten mainly in locations where Mangifera indica does not bear regularly. It is occasionally cultivated from seed. Its leaves are narrower than those of M . indica (Peekel 1984: 326, French 1986:206–207, Bourke in preparation, n.d.).

PMP *pahuq mango, probably Mangifera indica’ (Dyen 1953)
POc *pau(q) mango, Mangifera sp. (not indica)’ (Ross 1996d)
MM Vitu vau mango
MM Bola vao mango’ (Arentz et al. 1989: 91)
PMP *wai mango spp.’ (Blust 1986)
POc *wai, *waiwai mango (generic)’ (Ross 1996d)
Adm Titan we-wey mango
Adm Baluan wie mango
NNG Gitua wo-wai mango
NNG Mangap we mango
NNG Tami woa-wai mango
NNG Gitua wo-wai mango
NNG Mangap we mango
PT Kilivila wei-wa mango
PT Hula wai-wai mango
SES Arosi wai-wai sp. of small tree
POc *koRa wild mango, Mangifera minor’ (Ross 1996d)
NNG Mengen kula mango; has strings in it, Mangifera minor(?)
PT Roro or-or mango
MM Tolai ko-kor Mangifera minor(?)
SES Gela kola mango

PWOc *kasuwai ‘mango’ seems to be a compound, with an unidentified element *kasu- and *wai ‘mango’. The SE Solomons terms below reflect PSES *ɣohai, which in turn reflects a putative POc †*koyai. However, PSES *ɣohai probably reflects the borrowing of a reflex of *kasuwai, perhaps before the dispersal of PSES, as the terms are regular reflexes of *ɣohai.

PWOc *kasuwai mango’ (Ross 1996d)
NNG Kove korae mango’ (A. Chowning, pers. comm.)
PT Dobu kasawe mango
PT Tawala kasawe mango
MM Patpatar kasaua mango, Mangifera indica
MM Bulu korae mango
MM Tolai koai mango
MM Siar kaswai mango
MM Banoni dasowe mango’ (for †_zasowe)
MM Blablanga kesu mango
cf. also:
SES West Guadalcanal ɣoai mango
SES Longgu ʔeðai mango
SES Arosi ʔāi mango
SES Fagani ɣāi mango
PWOc *basi mango’ (Ross 1996d)
PT Tawala basi(awa) mango
PT Sudest mbaði mango
MM Teop bai mango
MM Tinputz pᴂʔ mango

3.5. Pometia pinnata, ocean lychee, island lychee, TP ton, taun, P obit, inkori, B nandao (Sapindaceae)

Pometia pinnata, an ancient New Guinea domesticate (Yen 1996), is a tall canopy hardwood tree of 20–45 m (Figure 11.9, left). Peekel (1984: 335) writes that its fruit, green or red and 4–6cm in diameter, the sweet pulp of which similar in taste and texture to a lychee and is eaten raw, is the most valued in the Bismarck Archipelago after the Malay apple. The skin of the ripe fruit is peeled off like that of a mandarin. The pulp surrounds a seed, up to 3 cm in diameter, which is poisonous and requires extensive processing and cooking before it can be eaten. French (1986: 215) reports that there are also varieties of Pometia pinnata with inedible flesh.

Pometia pinnata displays considerable variety in form, especially in the New Guinea region, attesting to long cultivation. Walter & Sam (20102: 229-230) report that its better forms are often transplanted in the Bismarcks and in Vanuatu but apparently less so in the Solomons. There are also widespread reports that it makes good building timber (Floyd 1954, Gowers 1976: 118, French 1986: 215). The wood is also used for carving on Waya (Gardner & Pawley 2006), and its plank buttresses provide axe handles in Marovo (Hviding 2005: 129).

The POc term for Pometia pinnata was *tawan, reflected in all major Oceanic subgroups except Micronesian.

PEMP *tawan Pometia pinnata’ (Blust 1978a)
POc *tawan Pometia pinnata
Adm Mussau taon Pometia pinnata
Adm Lou ta Pometia pinnata
NNG Mengen taua Pometia pinnata
NNG Gedaged tau tree sp. with edible fruit; stem makes good timber.
NNG Matukar ta Pometia pinnata’ (Kasprus 1945)
NNG Megiar tau(ber) Pometia pinnata’ (Kasprus 1945)
PT Bwaidoga tawana tree sp.
MM Lavongai ton Pometia pinnata
MM East Kara tawən Pometia pinnata
MM Lihir ta Pometia pinnata
MM Sursurunga tawan Pometia pinnata
MM Patpatar tawan Pometia pinnata
MM Tolai ton Pometia pinnata
MM Tangga taun Pometia pinnata
MM Sursurunga taoana a hardwood tree
MM Petats tan Pometia pinnata
MM Teop tauana Pometia pinnata
TM Natügu no-dae Pometia pinnata
PEOc *tawan Pometia pinnata
SES Lengo tao Pometia pinnata’ (Henderson and Hancock 1988)
SES Arosi awa Pometia pinnata
SES Sa’a awa Nephelium pinnatum
SES Kwara’ae ako Pometia pinnata
SES Kwara’ae dawa Pometia pinnata’ (borrowed form)
NCV Mwotlap na-twen Pometia pinnata
NCV Mota tawan Pometia pinnata
NCV Ambae dao Pometia pinnata
NCV Araki (vi)ca Pometia pinnata
NCV Raga dao Pometia pinnata’ (Walsh 2004)
NCV Big Nambas da-dau Pometia pinnata
NCV Port Sandwich na-ⁿrao Pometia pinnata
NCV Namakir to Pometia pinnata
NCV Nguna na-dau Pometia pinnata
PSV *na-ntawa(n) Pometia pinnata’ (Lynch 2001c)
SV Sye ntau Pometia pinnata
SV Lenakel natəm Pometia pinnata’ (-m unexplained)
SV Kwamera nətumʷi Pometia pinnata’ (-mʷi unexplained)
SV Anejom̃ netva Pometia pinnata
PCP *tawa Pometia pinnata
Fij Wayan tawa Pometia pinnata
Fij Bauan dawa Pometia pinnata
Pn Tongan tava Pometia pinnata
Pn Niuean tava Pometia pinnata
Pn Samoan tava Pometia pinnata
Pn East Futunan tava Pometia pinnata
Pn Emae tava Pometia pinnata
Pn Tikopia tava Pometia pinnata
Pn Tuamotuan tava Pandanus sp.
Pn Māori tawa Beilschmiedia tawa

Figure 11.9: Left Pometia pinnata, island lychee: A, young tree; B, shoot and edible fruit; C, inflorescence. Right Spondias cytherea, golden apple: D, young tree; E, shoot with leaves, leaflets and a cluster of edible fruit.

3.6. Spondias cytherea (syn. Spondias dulcis, Spondias mangifera), golden apple, Polynesian plum, hog plum, Tahitian apple, Bnaos (Anacardiaceae)

Spondias cytherea is a lowland sub canopy tree of medium height, 10-25 m. tall, distributed from island SE Asia to western Polynesia, and occurring in several varieties, a probable result of domestication (Figure 11.9, right). Within the Bismarcks it occurs mainly in the Admiralties, on Mussau Island and in New Ireland (Bourke n.d.). The tree is widely cultivated near villages in the Bismarcks, the Solomons (mainly in the Reeflslands) and Vanuatu, but is also spread by fruit bats (Henderson & Hancock 1988:47, Walter & Sam 2002:243-244, French 1986: 219).

The mature tree has a long trunk of up to 20 m with large buttresses up to 3 m. Its small white flowers grow in clusters, and it has yellow or orange ellipsoid fruit, up to 7cm long. According to Henderson & Hancock (1988: 47) there are two varieties. The fruit of one are acidic and bitter, of the other slightly tart but pleasant to eat. The former are baked before eating, whilst the latter are eaten raw. Hviding (2005: 135) reports of the second variety that in Marovo the fruit are best eaten when unripe and rather sour. In Vanuatu the fruit are of better quality than in the Bismarcks and the Solomons. They are picked while still green, just before they ripen, and eaten a few days later after they have ripened inside the house.

The wood is too soft for use in buildings, but in Vanuatu it is used to make canoe outriggers. It has a variety of medicinal uses: a decoction from the leaves is used for coughs and other ailments (Henderson & Hancock 1988: 49).

There was a single widely reflected POc term, *quRis. I have assumed below that the PCP form was *wi, with irregular loss of *q- from expected †*qul. However, loss of *q- is regular in Fijian, and so Fijian is a regular reflex of either proto form. Geraghty (2004: 87) suggests that the PCP form was indeed *qui and that the Polynesian forms reflect borrowing from Fijian - but such a borrowing would have had to occur very early, to find its way to the extremes of Polynesia. It seems more likely that the PCP indeed had *wī.

POc *quRis Spondias cytherea’ (Grace 1969 (Wilhelm Milke, pers. comm.: *quRi); Ross 1996d)
Adm Loniu wi Spondias cytherea
NNG Mengen kuli Spondias cytherea
PT Motu uri Garuga sp.’ (Lane-Poole 1925) 26
MM Nakanai huri Spondias cytherea
MM East Kara us Spondias cytherea
MM Patpatar kulis Spondias cytherea
MM Tolai kuri Spondias cytherea
TM Natügu n-oli Spondias cytherea
SES Lau uli Spondias cytherea
SES Kwaio uli Spondias cytherea
NCV Mwotlap ıy Spondias cytherea
NCV Mota ur Spondias cytherea
NCV Vera’a n-ur Spondias cytherea
PSV *na-viris Spondias cytherea’ (Lynch 21004a)
SV Sye ne-viwi Spondias cytherea
SV Ura (u)vasele Spondias cytherea’ (metathesis)
SV Kwamera nə-kori Dracontomelon vitiensis
SV Anejom̃ n-huri Dracontomelon vitiensis
PCP *wī Spondias cytherea
Fij Bauan Spondias cytherea
Pn Tongan Spondias cytherea
Pn Niuean Spondias cytherea
Pn East Futunan Spondias cytherea
Pn Emae Spondias cytherea
Pn Rennellese Spondias cytherea
Pn Tikopia Spondias cytherea
Pn Samoan Spondias cytherea
Pn Tokelauan mango species found only in Samoa
Pn Rapanui bi Indian mango tree, Mangifera indica
Pn Marquesan Spondias cytherea
Pn Mangarevan Spondias cytherea
Pn Hawaiian Spondias cytherea
Pn Tahitian Spondias cytherea
Pn Rarotongan Spondias cytherea

In the Bismarcks an imported thorny shrub, Ximenia americana (syn. X. elliptica, X. aculeata),27 is evidently perceived as resembling Spondias cytherea, to judge from the names below. The resemblance is based on the fact that Ximenia americana also has edible yellow ellipsoid fruit, but no larger than a cherry (Peekel 1984: 160). E Kara combines the POc prefix *mala- ‘resembling’ (ch.2, §7.1.4) and ukisSpondias cytherea’. The base ukis is the reflex of POc *quRisSpondias cytherea’ that would be expected in Tigak, immediately to the north of Kara. Further south, in Patpatar, the term for Ximenia americana is ku-kuris, the reduplication implying that Ximenia americana is an inferior or wild version of Spondias cytherea (ch.2, §7 .2).

MM East Kara mala-ukis Ximenia americana’ (‘false Spondias cytherea)
MM Patpatar ku-kuris Ximenia americana’ (‘small Spondias cytherea)
MM Tolai kuri-val Ximenia americana’ (kuriSpondias cytherea)(Record 1945)

PNCV *usi below appears to be an irregular reflex of POc *quRis. Two possible explanations present themselves. First, *(q)usi is a metathesised reflex of *quRis (> †*uis > *usi). Second, although POc final consonants were regularly lost in PNCV, Clark (2009) points to a dozen or so words in which the expected CVCV form exists alongside an extended form CVCVCV, representing the full POc form with an added vowel, most often *-i. The extended forms, for which Clark offers no explanation, are found throughout North Vanuatu and north Malakula, but without much consistency in any one language. One of these, in the form he reconstructs, is *quRisi, which with regular deletion of POc *q- and *-R- gives *u(i)si.

Some of these reflexes are (also) used to denote the pawpaw/papaya, Carica papaya, a recent introduction; this reflects a perception in Vanuatu that Spondias cytherea and papaya are similar and somehow related.

PNCV *usi Spondias cytherea’ (from data in Wheatley 1992)
NCV Nduindui uhi Spondias cytherea
NCV Nduindui uhi(gai) (gai ‘tree’)
NCV Ambae uhi Carica papaya
NCV Tangoa (vi)usi Spondias cytherea
NCV Nokuku o-usi Spondias cytherea
NCV Tolomako na-us Spondias cytherea
NCV Kiai usi Spondias cytherea
NCV Raga uhi Spondias cytherea, Carica papaya
NCV Uripiv na-us Spondias cytherea, Carica papaya
NCV Nese na-us Spondias cytherea
NCV Southwest Bay ni-vus(-saruei) Spondias cytherea

There are two possible external cognates of the PNCV etymon below. The first is Mussau (Adm) malaiSpondias cytherea’ (Lepofsky 1992). However, Mussau -ai does not correspond regularly with Paamese, Nguna -i. The second is Wayan (Fij) māoliSpondias cytherea’, but Wayan -āo- does not correspond regularly with PNCV *-a-. In parts of northern Vanuatu the term has been reapplied to Dracontomelon vitiense (ch.7, §4.4).

PNCV *mali Spondias cytherea’ (Clark 1996)
NCV Nokuku mal Dracontomelon vitiense
NCV Araki (vi)nᫀali Dracontomelon
NCV Port Sandwich mar(kokoc) Spondias cytherea
NCV Lonwolwol mel a large tree with yellow edible fruit
NCV Southeast Ambrym mal Dracontomelon vitiense
NCV Paamese mali-mali Spondias cytherea
NCV Lewo (puru)mel-mel Spondias cytherea
NCV Baki (bur)mel-mel Spondias cytherea
NCV Namakir mali-mal Spondias cytherea
NCV Nguna na-mali Spondias cytherea
NCV South Efate n-mal Spondias cytherea, S. edulis

Also puzzling is the connection between PNCV *mali and the items for Garuga floribunda listed below. There is reason to think that this is not a chance resemblance, as the PROc term *mala-usi ‘Garuga sp.’ literally meant ‘like Spondias cytherea’ (ch.7, §4.8), i.e. there was/is a perceived resemblance between Garuga and Spondias species. We cannot simply include the items below in the cognate set for PNCV *mali above, however, as the Paamese, Lewo and S Efate reflexes of *mal-mali differ from their reflexes of *mali.

PNCV *mal-mali Garuga floribunda
NCV Mwotlap na-mal-mali (ey) Garuga floribunda
NCV Paamese e-imoumol Garuga floribunda
NCV Lewo (puru)mal-mal Garuga floribunda
NCV Baki (buru)mar-maro Garuga floribunda
NCV South Efate n(a)-mal-mil Garuga floribunda

3.7. Syzygium malaccense (syn. Eugenia malaccensis, Eugenia jambos, jambosa malaccensis), Malay apple, rose apple, TP laulau, P kabarae, B nakavika (Myrtaceae)

Many Syzygium species which occur in the Pacific have edible fruit. The most important is Syzygium malaccense, which is distributed from SE Asia to Polynesia, but Peekel (1984: 408-415) and Walter & Sam (2002: 251-252) list numerous species which occur in NW Island Melanesia.

Figure 11.10: Syzygium malaccense: A, tree; B, shoot; C, branch with opened and unopened flowers; D, edible fruit.

Syzygium malaccense is an erect tree of medium height, 5-25 m tall, with spectacular white or pink flowers that look like small powder puffs and ellipsoid two-seeded fruit 4–9cm long that are white, pink or red when they are mature. The fruit approach a European apple in texture, but are often more watery in flavour. They are widely and, to quote Sorensen, ‘avidly’ consumed throughout the Pacific (Sorensen 1950, Peekel 1984: 408, Walter & Sam 2002: 250, Bourke in preparation). They are eaten fresh, soon after picking. Syzygium malaccense is found around villages and in coconut groves, in gardens and old fallows, and in open forests, although it is not clear whether it is indigenous to Melanesia or whether cultivated varieties have simply propagated themselves into the wild. Transplantation of better forms to village and garden areas is widespread (Paijmans 1976: 123-124, Walter & Sam 2002: 250). The wood is used for buildings in Vanuatu and Fiji, and for canoes in Vanuatu. Juice extracted from the leaves is used for abdominal pains, sore throats, toothache and generally for pain and fever (Henderson & Hancock 1988: 43-44, Walter & Sam 2002: 250).

The POc term for Syzygium malaccense was *kapika, reflected in all major Oceanic subgroups except Micronesian. It may also have served as a generic for Syzygium species in general.

POc *kapika Malay apple, rose apple, Syzygium malaccense’ (Milke 1968)
Adm Mussau kaviu Syzygium samarangense’ (-u for †-a)
Adm Seimat ahi Syzygium sp.’ (Sorensen 1950)
Adm Lou keik large variety of Malay apple, Syzygium gomata28
PWOc *kapika Syzygium malaccense
NNG Mengen gaiva rose apple, Syzygium malaccense
NNG Tami kapig rose apple, Syzygium malaccense
NNG Yabem àiŋ rose apple
PT Motu ɣavika name of tree sp., leaves of which are used as cigarette wrappers
MM Nakanai gaiva Syzygium malaccense’ (Floyd 1954)
MM Bola kavika Syzygium malaccense
MM Bulu kavika Syzygium malaccense
MM Babatana kapika Syzygium malaccense
PEOc *kapika Syzygium malaccense
SES Gela ɣaviɣa Syzygium malaccense
SES Kwara’ae ʔafiʔo Syzygium malaccense
SES Lau afio Syzygium onesimum
NCV Mota gaviga Syzygium malaccense, wild inedible variety
NCV Araki haviha Syzygium malaccense
NCV Tamambo haviha Malay apple
NCV Raga ɣaviɣa Malay apple (Walsh 2004)
NCV Uripiv n-avi Malay apple
NCV Port Sandwich xavik Malay apple
NCV Paamese ahie Malay apple
NCV Lewo kavika Malay apple
NCV Namakir kavik Malay apple
NCV Nguna na-kavika Malay apple
NCV South Efate n-kafik Malay apple
PSV *na-ɣaviɣ Syzygium malaccense’ (Lynch 2001c)
SV Lenakel nə-kəvək Syzygium malaccense
SV Anejom̃ n-yeheɣ Syzygium malaccense
NCal Pije cāk Syzygium malaccense
NCal Iaai xəiə Syzygium malaccense
NCal Nyelâyu cāc Syzygium malaccense
NCal Xârâcùù kʌɨ Syzygium malaccense
PCP *kavika Syzygium malaccense
Fij Wayan kavika Syzygium malaccense
Fij Bauan kavika Syzygium malaccense
Pn Tongan fekika Syzygium malaccense’ (metathesis)
Pn Niuean kafika Syzygium sp.
Pn Anutan kapika Syzygium malaccense
Pn East Futunan kafika Syzygium malaccense
Pn East Uvean kafika Syzygium malaccense
Pn Tikopia kafika Syzygium malaccense
Pn Marquesan kehika Syzygium malaccense
Pn Mangarevan keʔika Syzygium malaccense
Pn Tahitian ʔahiʔa Syzygium malaccense
Pn Hawaiian ʔoohia(ʔai) Syzygium malaccense
Pn Hawaiian ʔoohia(lehua) Metrosideros spp.
Pn Rarotongan kaʔika Syzygium malaccense
Pn Māori kahika Metrosideros fulgens, Dacrycarpus dacrydioides’ (R. Gardner, pers. comm.)

The three more narrowly distributed cognate sets below reflect other terms for Syzygium species. Whether these denoted cultivars of Syzygium malaccense or other species, it is impossible to say.

POc *poka(q) variety of Malay apple
Adm Mussau small variety of Malay apple, Syzygium gomata
NNG Bariai poai Syzygium sp.’ (Goulden 1996)
NNG Kilenge pokai Syzygium sp.’ (Goulden 1996)
POc *mari(a)sapa Syzygium sp.
Adm Nyindrou marisah Syzygium sp.
MM Patpatar mariasa Syzygium acutangulum’ (for †_mariasaha)
cf. also:
MM Nehan mariah Alpinia sp.
PAdm *cay Syzygium sp. with large red fruit
Adm Baluan sai Syzygium malaccense
Adm Wuvulu tae Syzygium sp. with large red fruit
Adm Loniu cay Syzygium sp. with large red fruit
Adm Titan cay Syzygium sp. with large red fruit

4. Other nut and fruit trees

This section is devoted to nut- or fruit-bearing species that are popularly eaten in at least parts of NW Island Melanesia but for which there is no evidence of arboriculture.

In several cases, the literature on plant food production describes species for which we have been unable to reconstruct a term. These are:

  • Flacourtia rukam is a small tree with a twisted trunk and red spherical fruits of 2cm diameter, distributed from island SE Asia to the Solomons but found cultivated further east. The fruit is occasionally eaten (Walter & Sam 2002: 173-174, Bourke n.d.).
  • Pouteria maclayana is a common, self-sown, small, buttressed coastal tree with a bushy crown that grows in New Guinea, on offshore islands along its north coast and in the southeastern Solomon Islands. Its yellow-fleshed fruit, shaped like a flattened sphere, is occasionally eaten raw, in some places as a famine food (Henderson & Hancock 1988: 142-143, Walter & Sam 2002:233, Bourke n.d. ). Allen et al. (1994) list it among previously important foods on Karkar Island.
  • Castanopsis acuminatissima is a tall oak-like tree whose seeds are a traditional forest food, eaten after boiling in New Guinea, New Britain and perhaps parts of the Solomons (Henty 1982, Evans 1999: 19).
  • Omphalea gageana (syn. 0. papuana, 0. queenslandiae) is an uncommon large woody, high-climbing forest creeper, 20–30 m. long. Its fruit has three seeds enclosed in a thin fleshy mesocarp and a ridged undulating woody shell, which are eaten raw or cooked around the Huon Gulf and in SE Papua (Henty 1982, Peekell984: 317, Henderson & Hancock 1988: 76, Evans 1999: 19).
  • Gnetum latifolium is another large woody, high-climbing forest creeper, 5-20 m long, with yellow-red fruits, the seeds of which are eaten after roasting (Peekel 1984: 37, Henderson & Hancock 1988:78, Evans 1999: 20).

Nut and fruit trees 3 51

The distributions of some of the above are such that they may have been unknown to speakers of POc, but it is also possible that our sources are not detailed enough to provide us with the data needed to support a reconstruction.

The fruits of several species of Ficus are eaten. Bourke (n.d.) names Ficus copiosa, Ficus tinctoria and Ficus wassa. These are treated in ch.lO, §4.

4.1. Finschia chloroxantha (syn. Finschia waterhousiana, Finschia densiflora, Grevillea densiflora) (Proteaceae)

Finschia chloroxantha is a medium-sized lowland rain forest tree with a blackish trunk and stilt roots (Figure 11.11, right). When it blooms it makes a spectacular display of bright orange or light golden yellow pendulous flowers. Its seeds are edible, eaten raw as snacks in the Solomons and after cooking in New Guinea. Its red-brown wood is strong and is used for timber, furniture and drums in the Solomons. Its leaves were used to treat sores and ulcers on Santa Isabel (Henty 1982, Henderson & Hancock 1988:74–76, Evans 1999: 19, Kwa’ioloa & Burt 2001: 124).

The cognate set below allows only a PEOc reconstruction. The one Western Oceanic item, Maringe ɣlama, is probably a borrowing from a neighbouring SE Solomonic language, especially as Maringe ɣl- typically reflects POc *l-, not *g-. The species is not mentioned by Peekel (1984), a major source of botanical terms from New Ireland.

MM Maringe ɣlama Finschia chloroxantha’(Henderson and Hancock 1988: 74)
PEOc *gama Finschia chloroxantha
SES Kwara’ae (a)kama Finschia chloroxantha
SES Lau (a)kame Finschia densiflora
NCV Tamambo (vu)kame Finschia chloroxantha’ (Walter and Sam 2002: 293)
NCV Apma (wa)gam Finschia chloroxantha
PSV *na-(i)gam Finschia chloroxantha’ (Lynch 2001c)
SV Sye ne-iŋkom Finschia chloroxantha
SV Anejom̃ n-ikam Finschia chloroxantha

4.2. Parartocarpus venenosa (syn. Parartocarpus involucrata) (Moraceae)

Parartocarpus venenosa is a large lowland forest tree growing to about 35m, with girths of over 1.5 m, which resembles the breadfruit (Figure 11.11, left) (ch.9, §4). Its fruit is brown or yellow and highly aromatic; it forms an irregularly shaped syncarp about 18cm across, a compound fruit with many segments about 3cm long arranged around the core, and is eaten raw. It is especially popular in New Britain, but there is no record of cultivation. Elsewhere in lowland New Guinea, the Bismarcks and the Solomons it is generally less significant but is known and consumed (Barrau 1962: 177, Paijmans 1976: 124, Peekel 1984: 132, Bourke in preparation, French 1986: 259). Henderson & Hancock (1988) report that it is not very sweet and has a powdery texture: it is filling but not succulent. Its timber is generally not regarded as useful.

Figure 11.11: Left Parartocarpus venenosa: A, young tree; B, branch bearing shoot, male flower and edible fruit; C, seed. Right Finschia chloroxantha: D, tree with stilt roots; E, flowering shoot; F, fruit cluster.

Although reflexes of PWOc *lapuka mean ‘breadfruit’ in some languages, the fact that there were at least two other POc terms for breadfruit (ch.9, §4) suggests that the reflexes glossed ‘Parartocarpus venenosa’ retain the POc denotation. Kwara’ae rakʷa-na is irregular, with initial r- for expected †l- and suffixed -na (medial -kʷ- is a regular reflex of *-pʷ-). Araki levu is irregular with -e- for †-a-.

PWOc *lapuka k.o. tree with fruit similar to breadfruit, Parartocarpus venenosa’ (?)
NNG Takia lou k.o. breadfruit
NNG Kaiwa lavuk breadfruit, Artocarpus altilis
NNG Medebur lapu breadfruit, Artocarpus altilis
PT Are napo breadfruit
MM Notsi lipua breadfruit
MM Sursurunga lapu tree type whose fruit, similiar to a breadfruit, is yellow and sweet and is eaten raw (possibly Parartocarpus venenonus)
MM Patpatar lapuo Parartocarpus venenosa
MM Tolai lapua Parartocarpus venenosa
cf. also:
SES Kwara’ae rakʷa-na Parartocarpus venenosa
NCV Araki levu breadfruit, Artocarpus altilis

Notes