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1

Autumn leaves. New York: Scholastic Press, 1998.

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2

Hardin, James W. Foliar morphology of the common trees of North Carolina and adjacent states. Raleigh, N.C: North Carolina Agricultural Research Service, North Carolina State University, 1992.

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3

Leaf venation patterns. Berlin: Cramer, 1986.

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4

Rao, T. A. Compendium of foliar sclereids in Angiosperms: Morphology and taxonomy. New Delhi: Wiley Eastern, 1991.

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5

Yuexing, Jin, and Wu Zhujun, eds. He ben ke ye pian biao pi wei xing tai tu pu: Micromorphological atlas of leaf epidermis in Gramineae. [Nanjing]: Jiangsu ke xue ji shu chu ban she, 1993.

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6

Group, Leaf Architecture Working. Manual of leaf architecture: Morphological description and categorization of dicotyledonous and net-veined monocotyledonous angiosperms. Washington, DC: Leaf Architecture Working Group, 1999.

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7

Klucking, Edward P. Myrtaceae. Berlin: J. Cramer, 1988.

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8

Cheng-hong, Yu. Leaf architecture of the woody dicotyledons from tropical and subtropical China. Beijing, People's Republic of China: International Academic Publishers, 1991.

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9

J, Harr, and Guggenheim R, eds. The leaf surface of major crops. Basel: Friedrich Reinhardt Verlag, 1995.

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10

Beth, Ellis, ed. Manual of leaf architecture. Ithaca: Cornell University Press, 2009.

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11

Wolfe, Jack A. A method of obtaining climatic parameters from leaf assemblages. Washington, D.C: U.S. G.P.O., 1993.

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12

Mikhaĭlovich, Kozubov Gennadiĭ, ed. Struktura assimili͡a︡t͡s︡ionnogo apparata khvoĭnykh pri vozdeĭstvii ionizirui͡u︡shchego izluchenii͡a︡. Sankt-Peterburg: "Nauka", 1994.

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13

Lannoo, Michael J. Larval life in the leaves: arboreal tadpole types, with special attention to the morphology, ecology, and behavior of the Oophagous Osteopilus brunneus (Hylidae) larva. Chicago: Field Museum of Natural History, 1987.

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14

Autumn leaves. Scholastic, 1999.

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15

Robbins, Ken. Autumn Leaves. Scholastic Trade, 2003.

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16

Leaf Venation Patterns: Flacourtiaceae. Lubrecht & Cramer Ltd, 1992.

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17

Leaf Venation Patterns: Myrataceae (Leaf Venation Patterns, Vol 3). Lubrecht & Cramer Ltd, 1988.

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18

Leaf Venation Patterns: Combretaceae. Lubrecht & Cramer Ltd, 1991.

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19

Leaf Venation Patterns: Lauraceae. Lubrecht & Cramer Ltd, 1987.

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20

Georgiady, Michael Scot. Pattern formation in leaves: Dicot leaf venation. 1992.

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21

Fall Walk. Gibbs Smith, 2013.

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22

Fall Walk. Gibbs Smith, Publisher, 2019.

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23

Hickey, Leo J., Mitchell John D, Beth Ellis, Kirk R. Johnson, and Douglas C. Daly. Manual of Leaf Architecture. CABI, 2009.

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24

Manual of Leaf Architecture. CABI, 2009.

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25

Townsend, Daniel S., Michael J. Lannoo, and Richard J. Wassersug. Larval Life in the Leaves: Arboreal Tadpole Types, With Special Attention to the Morphology, Ecology, and Behavior of the Oophagous Osteopilus Brunn. Field Museum of Natural, 1987.

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26

Fleischmann, Andreas. Systematics and evolution of Lentibulariaceae: II. Genlisea. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198779841.003.0007.

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Systematics and evolution of Genlisea (corkscrew plants) (Lentibulariaceae) are treated. Vegetative and generative morphology of the plants, and anatomy of their rhizophylls (‘root-leaves’) that function as sophisticated eel traps are explained and illustrated. A simplified phylogenetic tree and a detailed distribution map are provided, and the evolutionary history, including genome and karyotype evolution, and phylobiogeography of the 30 currently known species of Genlisea are discussed.
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27

Brooker, Ian, and Dean Nicolle. Atlas of Leaf Venation and Oil Gland Patterns in the Eucalypts. CSIRO Publishing, 2013. http://dx.doi.org/10.1071/9780643109865.

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Atlas of Leaf Venation and Oil Gland Patterns in the Eucalypts is an aid to the identification of eucalypts in the field and a confirmation of the natural affinities between species and higher-level taxa on the basis of their comparative morphology. Its purpose is to standardise leaf venation and oil gland terminology and to demonstrate the taxonomic value of leaf venation and oil gland patterns within the eucalypts. The work discusses the visible features of the adult leaves of eucalypts as seen with reflected and transmitted light. Because venation and oil glands become obscure in dried specimens this work relies entirely on the comprehensive sampling and observation of fresh leaves. High quality, scaled, leaf venation images of vouchered specimens are used to compare all taxonomic groups in the eucalypts. All genera, sections, series and subseries are represented.
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28

Kaufman, Daniel. Lexical Category and Alignment in Austronesian. Edited by Jessica Coon, Diane Massam, and Lisa Demena Travis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780198739371.013.24.

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Philippine-type languages are often cited as exemplifying a cross-linguistically unique voice system, in which verb morphology can select not only an agent or patient, but also locative, instrumental and other adjunct type relations as the nominative argument. In this paper, we examine three approaches to this typologically remarkable system: the ergative analysis, the case agreement analysis and the nominalization analysis, arguing for the latter based on strong parallels between verbal and nominal predication from the root level to the clause level. The morphologically symmetric nature of Philippine-type languages is argued to stem from their nominal roots. The historical development of verbal roots leads to a more fixed argument structure in which canonical ergative languages develop. Mamuju, an Austronesian language of West Sulawesi, Indonesia, is offered as an example of a classically ergative language, in contrast to Philippine-type systems.
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29

Chamoreau, Claudine. Purepecha, a Polysynthetic but Predominantly Dependent-Marking Language. Edited by Michael Fortescue, Marianne Mithun, and Nicholas Evans. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199683208.013.38.

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Purepecha (language isolate, Mexico) has one relevant characteristic that leads to identifying it as a polysynthetic language: productive verbal morphology (in particular locative suffixes). Purepecha is a predominantly dependent-marking language, as its pronominal markers are enclitics, generally second position enclitics. But, in some contexts Purepecha shows head-marking characteristics. Today, pronominal enclitics exhibit variation, tending to move to the rightmost position in the clause; they may encliticize to the predicate itself, showing a head-attraction or polypersonalism strategy and making Purepecha more polysynthetic. But this language lacks noun incorporation. Purepecha has three types of non-finite clause: two subordinate clauses (non-finite complement clauses and purpose clauses) and a syntactically independent clause (the chain-medial clause). This seemingly inconsistent situation (characterized by a correlation of different properties, some of which have not been identified as polysynthetic) calls for addressing the typological classification of Purepecha among the polysynthetic languages.
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