20Sheppard, 1976; Foster <strong>and</strong> Nicolson,1981).VAM fungi are important for building<strong>and</strong> maintaining the structure of s<strong>and</strong>dunes <strong>and</strong> for plant stabilization. Aconsiderable amount of hyphalconnections of fungal mycelium wasfound in the top 1-20 cm of mobile s<strong>and</strong>in Cooloola (Queensl<strong>and</strong>), Australia(Jehne <strong>and</strong> Thompson, 1981). VAMfungi bind loose s<strong>and</strong> grains into largeraggregates with their sticky hyphae <strong>and</strong>thus limit s<strong>and</strong> dune loss. Foster <strong>and</strong>Nicolson (1981) found that 1.5% of theaggregate s<strong>and</strong> grains reach a diameterof 2 mm in Scotl<strong>and</strong> dunes. The 2-mms<strong>and</strong> grain aggregations may be as highas 9% in Lake Huron dunes (Koske etal., 1975). Migration of s<strong>and</strong> grains bywind can be significantly reduced bys<strong>and</strong> grain aggregations. The aggregatesalso can improve soil structure bytrapping organic matter, limiting waterloss, <strong>and</strong> by becoming sites of microbialactivity.All major genera (Acaulospora,Entrophospora,Gigaspora,Scutellospora, Sclerocystis, <strong>and</strong> Glomus)of VAM fungi have been found in arid,semi-arid, <strong>and</strong> s<strong>and</strong> dune soils aroundthe globe (Khan, 1974; El-Giahmi et al.,1976; Redhead, 1977; Diem et al., 1981;Schwab <strong>and</strong> Reeves, 1981; Bloss, 1985;Halvorson <strong>and</strong> Koske, 1988; McGee,1989). <strong>Of</strong> the 148 species of VAMfungi, 31 species were first reportedfrom s<strong>and</strong> dunes (Schenck <strong>and</strong> Pérez,1990). The 31 species are in threegenera: Glomus (14 species),Scutellospora (12 species), <strong>and</strong>Acaulospora (5 species).VAM inoculum density varies from siteto site <strong>and</strong> decreases with soil depth(Sutton <strong>and</strong> Barron, 1972; Miller, 1979;Reeves et al., 1979; Buchholz <strong>and</strong>Motto, 1981; Schwab <strong>and</strong> Reeves, 1981;Allen et al., 1984; Zajicek et al., 1986;Koide <strong>and</strong> Mooney,1987). The distribution of VAM fungalspecies appears to be more closelyrelated to host plant, soil structure, <strong>and</strong>environmental conditions than to thecompetition by other VAM fungalspecies (Koske, 1981a).All these studies involved maritime s<strong>and</strong>dunes, <strong>and</strong> they were limited to the studyof the percentage colonization in s<strong>and</strong>
21dune plants, the development of externalmycelium, <strong>and</strong> propagule density. Thereare no comprehensive studies ofmycorrhizal relationship in inl<strong>and</strong> s<strong>and</strong>dunes.III. PLANT NUTRIENTS AND VAMFUNGAL DEPENDENCYVAM fungi offer significant benefits totheir host when compared tononmycorrhizal host plants grown innatural soil. Safir (1987) characterizedplants as independent (e.g., species ofthe Brassicaceae), facultativelydependent (e.g., seral species), orobligately dependent (e.g., tropical foresttrees) on VAM fungi for mineralnutrient uptake. VAM fungi provideplants with phosphorus that enablesmycorrhizal plants to grow better thannonmycorrhizal plants when thiselement is limiting (Mosse, 1972;Williams et al., 1974; Roncadori <strong>and</strong>Pokory, 1982; Pleachett et al., 1983;Koske <strong>and</strong> Polson, 1984; Backhaus etal., 1986). Yield or biomass often isincreased when plants form VAM fungalassociations (Bolgiano et al., 1983;Singh <strong>and</strong> Singh, 1986).VAM fungi improve growth in bothnitrogen-fixing <strong>and</strong> non-nitrogen fixingplants. Singh <strong>and</strong> Singh (1986)inoculated lentil plants with Glomusfasciculatum <strong>and</strong> found that lentilshowed mycorrhizal dependency forphosphorus uptake. Glomusfasciculatum increased Rhizobiumnodulation, nitrogen fixation, lentilgrowth, <strong>and</strong> lentil yield. Citrus alsoappears to have a high level ofmycorrhizal dependency, especiallywhen rock phosphate is used as thephosphorus source. Mycorrhizal citrusplants show much better growth thannonmycorrhizal citrus plants (Graham<strong>and</strong> Timmer, 1984).
- Page 1 and 2: Taxonomy and EcologyOf Inland Sand
- Page 3 and 4: AbstractAgropyron inerme root syste
- Page 5 and 6: IntroductionInland sand dunes in Co
- Page 7 and 8: 3Literature Review"Mycorrhiza" is a
- Page 9 and 10: 5nonsporocarpic, and produced spore
- Page 11 and 12: 7Spores of VAM fungi are multinucle
- Page 13 and 14: 9germination shield is formed, andg
- Page 15 and 16: 11wall thickening or spore inner wa
- Page 17 and 18: 13especially phosphate ions, some o
- Page 19 and 20: 15by the relative location of GOT a
- Page 21 and 22: 17D. DIFFICULTIES IN VAMFUNGAL TAXO
- Page 23: 19fungi are distributed over a wide
- Page 27 and 28: 23annually, a mean annual temperatu
- Page 29 and 30: 25C. EFFECTS OF SOIL DEPTH,MOISTURE
- Page 31 and 32: 27vegetated quadrats on each of the
- Page 33 and 34: 29Table 1 Occurrence of genera and
- Page 35 and 36: 31G. dominkii is the most abundant
- Page 37 and 38: 33abc d eFIG. 2 Glomus sp Light and
- Page 39 and 40: 35percent usually was strongly infl
- Page 41 and 42: 37FIG. 8 Regression of mycorrhizali
- Page 43 and 44: 39July transect data analyses (TABL
- Page 45 and 46: 41significantly with changes in the
- Page 47 and 48: 43FIG. 10 Regression of mycorrhizal
- Page 49 and 50: 45the July transect (FIG. 15). Howe
- Page 51 and 52: 47FIG. 17 Regression of mycorrhizal
- Page 53 and 54: 49C. COMPARISONS OF VAMCOLONIZATION
- Page 55 and 56: 51the survival strategies that adap
- Page 57 and 58: 53association with other species. T
- Page 59 and 60: 55believe the overriding factor is
- Page 61 and 62: 57my understanding of the ecology o
- Page 63 and 64: 59that soil characteristics and dis
- Page 65: 60AKNOWLEDGEMENTSI would like to ex
- Page 68 and 69: 61Allen, M. F., J. A. MacMahon, and
- Page 70 and 71: 63Bolgiano, N. C., G. R. Safir, and
- Page 72 and 73: 65mycorrhizal fungi: a determinant
- Page 74 and 75:
67Hayman, D. 1982. Influence of soi
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69Koske, R. E. 1985. Glomusaggregat
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71Morton, J. B. 1986. Three new spe
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73Powell, C. L., and D. J. Bagyaraj
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75Simon, L., M. Lalonde, and T. D.
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77Trappe, J. M. 1982. Synoptic keys
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79Wullstein, L. H., and S. A. Pratt