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1

Yu, Xianxian, Yanlei Feng, and Jie Zhang. "Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids." Life 14, no. 2 (2024): 182. http://dx.doi.org/10.3390/life14020182.

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Mitochondrial genome sequencing is a valuable tool for investigating mitogenome evolution, species phylogeny, and population genetics. Chimonanthus praecox (L.) Link, also known as “La Mei” in Chinese, is a famous ornamental and medical shrub belonging to the order Laurales of the Calycanthaceae family. Although the nuclear genomes and chloroplast genomes of certain Laurales representatives, such as Lindera glauca, Laurus nobilis, and Piper nigrum, have been sequenced, the mitochondrial genome of Laurales members remains unknown. Here, we reported the first complete mitogenome of C. praecox. T
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HEO, KWEON, HENK VAN DER WERFF, and HIROSHI TOBE. "Embryology and relationships of Lauraceae (Laurales)." Botanical Journal of the Linnean Society 126, no. 4 (1998): 295–322. http://dx.doi.org/10.1111/j.1095-8339.1998.tb01383.x.

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ENDRESS, PETER K., and ANTON IGERSHEIM. "Gynoecium diversity and systematics of the Laurales." Botanical Journal of the Linnean Society 125, no. 2 (1997): 93–168. http://dx.doi.org/10.1111/j.1095-8339.1997.tb02250.x.

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Kimoto, Yukitoshi, and Hiroshi Tobe. "Embryology of Laurales: a Review and Perspectives." Journal of Plant Research 114, no. 3 (2001): 247–67. http://dx.doi.org/10.1007/pl00013988.

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ROMANOV, MIKHAIL S., PETER K. ENDRESS, ALEXEY V. F. CH BOBROV, ALEXANDER P. MELIKIAN, and ALEJANDRO PALMAROLA BEJERANO. "Fruit structure and systematics of Monimiaceae s.s. (Laurales)." Botanical Journal of the Linnean Society 153, no. 3 (2007): 265–85. http://dx.doi.org/10.1111/j.1095-8339.2007.00609.x.

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Staedler, Yannick M., Peter H. Weston, and Peter K. Endress. "Floral Phyllotaxis and Floral Architecture in Calycanthaceae (Laurales)." International Journal of Plant Sciences 168, no. 3 (2007): 285–306. http://dx.doi.org/10.1086/510417.

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Romanov, Mikhail S., Peter K. Endress, Alexey V. F. Ch Bobrov, Anton A. Yurmanov, and Ekaterina S. Romanova. "Fruit Structure of Calycanthaceae (Laurales): Histology and Development." International Journal of Plant Sciences 179, no. 8 (2018): 616–34. http://dx.doi.org/10.1086/699281.

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Pignal, Marc, Bernard Lugardon, Joe¨l Jérémie, and Annick Le Thomas. "Morphologie et ultrastructure du pollen des Siparunaceae (Laurales)." Grana 38, no. 4 (1999): 210–17. http://dx.doi.org/10.1080/001731300750044591.

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Kimoto, Yukitoshi, and Hiroshi Tobe. "Embryology of Siparunaceae (Laurales): characteristics and character evolution." Journal of Plant Research 116, no. 4 (2003): 281–94. http://dx.doi.org/10.1007/s10265-003-0091-9.

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Endress, Peter K., and David H. Lorence. "Inflorescence Structure in Laurales—Stable and Flexible Patterns." International Journal of Plant Sciences 181, no. 3 (2020): 267–83. http://dx.doi.org/10.1086/706449.

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Staedler, Yannick M., Peter H. Weston, and Peter K. Endress. "Comparative Gynoecium Structure and Development in Calycanthaceae (Laurales)." International Journal of Plant Sciences 170, no. 1 (2009): 21–41. http://dx.doi.org/10.1086/593045.

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Renner, Susanne S., and Hyosig Won. "Repeated Evolution of Dioecy from Monoecy in Siparunaceae (Laurales)." Systematic Biology 50, no. 5 (2001): 700–712. http://dx.doi.org/10.1080/106351501753328820.

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Renner, S. S., A. E. Schwarzbach, and L. Lohmann. "Phylogenetic Position and Floral Function of Siparuna (Siparunaceae: Laurales)." International Journal of Plant Sciences 158, S6 (1997): S89—S98. http://dx.doi.org/10.1086/297509.

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14

Peña, Jorge E., Scott W. Weihman, Stephen McLean, et al. "Predators and parasitoids associated with Scolytinae in Persea species (Laurales: Lauraceae) and other Lauraceae in Florida and Taiwan." Florida Entomologist 98, no. 3 (2015): 903–10. https://doi.org/10.1653/024.098.0314.

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Peña, Jorge E., Weihman, Scott W., McLean, Stephen, Cave, Ronald D., Carrillo, Daniel, Duncan, Rita E., Evans, Gregory, Krauth, Stephen, Thomas, M. C., Lu, S. S., Kendra, Paul E., Roda, Amy L. (2015): Predators and parasitoids associated with Scolytinae in Persea species (Laurales: Lauraceae) and other Lauraceae in Florida and Taiwan. Florida Entomologist 98 (3): 903-910, DOI: 10.1653/024.098.0314, URL: http://www.bioone.org/doi/10.1653/024.098.0314
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15

Stone, Donald E. "Developmental Evidence for the Convergence ofSassafras(Laurales) andHeliconia(Zingiberales) Pollen." Grana 26, no. 3 (1987): 179–91. http://dx.doi.org/10.1080/00173138709428914.

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Kimoto, Yukitoshi, and Hiroshi Tobe. "Embryology of Illigera and Sparattanthelium (Hernandiaceae, Laurales): Family Characteristics and Relationships." International Journal of Plant Sciences 169, no. 3 (2008): 391–408. http://dx.doi.org/10.1086/526465.

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17

Wang, Wenyue, Changyao Liu, Guiju Zhang, et al. "Green Synthesis of Decaglycerol Laurates by Lipase-Catalyzed Transesterification of Methyl Laurate with Decaglycerol." Journal of Chemistry 2019 (June 12, 2019): 1–7. http://dx.doi.org/10.1155/2019/6342475.

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Decaglycerol laurates have been widely used as emulsifiers in food, medicine, and cosmetic industries for many years. Currently, they are synthesized using alkaline catalysts under stringent conditions. Here, decaglycerol laurates were prepared through a green lipase-catalyzed process, employing the transesterification of methyl laurate with decaglycerol by the immobilized lipase (Novozym 435). Single-factor experiments and orthogonal test were used for reaction optimization. The optimum conditions were obtained as follows: reaction temperature of 65°C, a laurate/decaglycerol molar ratio of 2
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18

Paudel, Niroj, and Kweon Heo. "Comparative leaf morphology and anatomy on ten taxa of Calycanthaceae Lindl. (Laurales)." Our Nature 19, no. 1 (2021): 1–9. http://dx.doi.org/10.3126/on.v19i1.41212.

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The comparative leaf morphology and anatomy of ten species of family Calycanthaceae have been studied. Leaf anatomy is very comparable to each other in cell shape and their arrangement. Collected leaves were preserved in FAA and alcohol series were applied for LM and SEM. The layer of epidermis is two in Idiospermum and one in rest of other genera. The structure of vascular bundle is V-shape in Sinocalycanthus and Calycanthus whereas U-shape in Idiospermum and Chimonanthus. The density of trichome is higher in Calycanthus than other genera. The presence of trichome, stomata, epidermal layer, d
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19

KIMOTO, YUKITOSHI, and HIROSHI TOBE. "Embryology of Hortonioideae and Monimioideae (Monimiaceae, Laurales): characteristics of the ‘lower’ monimioids." Botanical Journal of the Linnean Society 158, no. 2 (2008): 228–41. http://dx.doi.org/10.1111/j.1095-8339.2008.00847.x.

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20

ter Welle, Ben J. H., and Charles Russell Metcalfe. "Anatomy of the Dicotyledons, Ed. 2 Vol. 3: Magnoliales, Illiciales, and Laurales." Kew Bulletin 44, no. 2 (1989): 377. http://dx.doi.org/10.2307/4110819.

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21

Friis, Else Marie, Peter R. Crane, and Kaj Raunsgaard Pedersen. "Saportanthus, an Extinct Genus of Laurales from the Early Cretaceous of Portugal." International Journal of Plant Sciences 178, no. 8 (2017): 650–72. http://dx.doi.org/10.1086/693108.

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Ren, Xiaolong, Chao Yang, Guiliang Xin, et al. "Complete chloroplast genome of Cinnamomum japonicum (Laurales: Lauraceae), an endangered tree species." Conservation Genetics Resources 11, no. 3 (2018): 267–69. http://dx.doi.org/10.1007/s12686-018-1004-5.

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23

Mankin, R. W., H. Burman, O. Menocal, and D. Carrillo. "Acoustic Detection ofMallodon dasystomus(Coleoptera: Cerambycidae) inPersea americana(Laurales: Lauraceae) Branch Stumps." Florida Entomologist 101, no. 2 (2018): 321–23. http://dx.doi.org/10.1653/024.101.0226.

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24

Renner, Susanne S. "Circumscription and phylogeny of the Laurales: evidence from molecular and morphological data." American Journal of Botany 86, no. 9 (1999): 1301–15. http://dx.doi.org/10.2307/2656778.

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25

Zavatin, Danilo Alvarenga, Renato Ramos, Mauricio Takashi Coutinho Watanabe, Luciano Gonçalves Pedrosa, and Elton John de Lírio. "A new species of Mollinedia (Monimiaceae, Laurales) from the Quadrilátero Ferrífero, Brazil." PhytoKeys 234 (October 23, 2023): 189–201. http://dx.doi.org/10.3897/phytokeys.234.109804.

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Monimiaceae comprises approximately 26 genera and 250 species, with a pantropical distribution, predominantly occurring in humid forests. In Brazil, it is represented by five genera and 47 species, most of which are found in the Atlantic Forest, particularly in dense ombrophilous forest. Nevertheless, studies on this family in other biomes and vegetation types in Brazil are still scarce. The Quadrilátero Ferrífero (QF), a region located in the state of Minas Gerais, exhibits high plant species richness and endemism. During collections and analysis of herbarium materials from this region, some
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Zavatin, Danilo Alvarenga, Renato Ramos, Mauricio Takashi Coutinho Watanabe, Luciano Gonçalves Pedrosa, and Lírio Elton John de. "A new species of Mollinedia (Monimiaceae, Laurales) from the Quadrilátero Ferrífero, Brazil." PhytoKeys 234 (October 23, 2023): 189–201. https://doi.org/10.3897/phytokeys.234.109804.

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Monimiaceae comprises approximately 26 genera and 250 species, with a pantropical distribution, predominantly occurring in humid forests. In Brazil, it is represented by five genera and 47 species, most of which are found in the Atlantic Forest, particularly in dense ombrophilous forest. Nevertheless, studies on this family in other biomes and vegetation types in Brazil are still scarce. The Quadrilátero Ferrífero (QF), a region located in the state of Minas Gerais, exhibits high plant species richness and endemism. During collections and analysis of herbarium materials from this region, some
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27

RASINGAM, LADAN, and KALIYAMURTHY KARTHIGEYAN. "Two new names in the family Lauraceae." Phytotaxa 491, no. 2 (2021): 191–92. http://dx.doi.org/10.11646/phytotaxa.491.2.9.

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The family Lauraceae Jussieu (1789: 80) is one of the economically important families in the Magnoliopsida-Laurales, distributed mostly in the tropical and subtropical forests of the New and the Old World, comprising 56 genera and 2700 species (Mabberley 2017). We came across two names viz., Litsea microphylla (Elmer 1908: 375) Merrill (1923: 196) and Persea microphylla (Mez 1889: 166) Mez (1892: 115), which are later homonyms to the fossil species Litsea microphylla Marion (1872: 346) and Persea microphylla Engelhardt (1891: 650), respectively. According to Art. 53.1. of the ICN (Turland et a
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28

Schmid, Rudolf, and C. R. Metcalfe. "Anatomy of the Dicotyledons, Vol. 3, Magnoliales, Illiciales, and Laurales (Sensu Armen Takhtajan)." Taxon 37, no. 4 (1988): 934. http://dx.doi.org/10.2307/1222107.

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Lorence, David H. "A Monograph of the Monimiaceae (Laurales) in the Malagasy Region (Southwest Indian Ocean)." Annals of the Missouri Botanical Garden 72, no. 1 (1985): 1. http://dx.doi.org/10.2307/2399135.

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Oginuma, Kazuo, and Hiroshi Tobe. "Chromosome evolution in the Laurales based on analyses of original and published data." Journal of Plant Research 119, no. 4 (2006): 309–20. http://dx.doi.org/10.1007/s10265-006-0273-3.

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Poinar, Jr., George O., Kenton L. Chambers, Urszula T. Iwaniec, and Fernando E. Vega. "Valviloculus pleristaminis gen. et sp. nov., a Lauralean fossil flower with valvate anthers from mid-Cretaceous Myanmar amber." Journal of the Botanical Research Institute of Texas 14, no. 2 (2020): 359–66. http://dx.doi.org/10.17348/jbrit.v14.i2.1014.

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The flower described here as Valviloculus pleristaminis, a new genus and species of fossil angiosperms, was obtained from Myanmar amber deposits dating to the mid-Cretaceous period. The flower is staminate, with an ovoid, hollow floral cup. The perianth consists of 6 tepals, one of which was lost prior to preservation. Numerous helically arranged stamens are borne at the summit of the flower. The anthers are bilocular, with pollen sacs that dehisce by laterally hinged valves. The tip of the connective bears a cup-shaped appendage. The gynoecium is represented only by a cluster of vestigial sty
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Renner, S. S., D. B. Foreman, and D. Murray. "Timing Transantarctic Disjunctions in the Atherospermataceae (Laurales): Evidence from Coding and Noncoding Chloroplast Sequences." Systematic Biology 49, no. 3 (2000): 579–91. http://dx.doi.org/10.1080/10635159950127402.

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Chen, Yang, Xiupeng Li, Minfen Yu, Bin Wei, Yan Huang, and Jianhong Zhang. "The complete chloroplast genome and phylogenetic analysis of Cinnamomum daphnoides (Laurales: Lauraceae)." Mitochondrial DNA Part B 10, no. 5 (2025): 387–91. https://doi.org/10.1080/23802359.2025.2492098.

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Williams, Roger N., Nuris M. Acosta, and Michele B. Price. "Nitidulidae (Coleoptera) Found in Flowers of Calycanthus floridus Linnaeus (Laurales: Calycanthaceae) in Northeastern Ohio, U.S.A." Entomological News 119, no. 4 (2008): 397–402. http://dx.doi.org/10.3157/0013-872x-119.4.397.

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Poinar, Jr., George O., and Kenton L. Chambers. "Dispariflora robertae gen. et sp. nov., a mid-Cretaceous flower of possible Lauralean affinity from Myanmar amber." Journal of the Botanical Research Institute of Texas 13, no. 1 (2019): 173–83. http://dx.doi.org/10.17348/jbrit.v13.i1.839.

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Three flowers of a fossil angiosperm preserved in amber from Myanmar (Burma) are described as the new genus and species Dispariflora robertae. Although joined in a single cymose inflorescence, the flowers are variable in size and, in addition, they possess an unusual perianth in which 1 sepal is much enlarged and leaf-like, while the remaining 4 are smaller and unequal. The flowers each have 1 superior pistil with a peculiarly plumose and bristly ovary. The number of stamens is uncertain because most were lost before floral preservation, but scars on the receptacle suggest that at least 15 wer
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Das, Mukesh Lal, Sarat Chandran, and Sreenath Subrahmanyam. "Impact of Climate Change on the Distribution of Cinnamomum malabatrum (Laurales—Lauraceae), a Culturally and Ecologically Important Species of Malabar, Western Ghats, India." Diversity 17, no. 7 (2025): 476. https://doi.org/10.3390/d17070476.

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The impact of climate change on the distribution of Cinnamomum malabatrum (Laurales—Lauraceae), a culturally and ecologically important species in the Malabar region of Western Ghats, India, was studied using a MaxEnt machine learning algorithm. The findings are rooted in extensive field data and advanced modeling techniques. The predicted range shifts and contraction of suitable habitats for the species indicate significant challenges ahead, especially in the Malabar midlands and coastal plains—areas of high endemicity. The proposed conservation strategies provide a comprehensive framework th
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SHEARER, ADRIENNE E. H., C. PATRICK DUNNE, ANTHONY SIKES, and DALLAS G. HOOVER. "Bacterial Spore Inhibition and Inactivation in Foods by Pressure, Chemical Preservatives, and Mild Heat." Journal of Food Protection 63, no. 11 (2000): 1503–10. http://dx.doi.org/10.4315/0362-028x-63.11.1503.

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Sucrose laurates, sucrose palmitate, sucrose stearates, and monolaurin (Lauricidin) were evaluated for inhibitory effects against spores of Bacillus sp., Clostridium sporogenes PA3679, and Alicyclobacillus sp. in a model agar system. The combined treatment of sucrose laurate, high hydrostatic pressure, and mild heat was evaluated on spores of Bacillus and Alicyclobacillus in foods. The minimum inhibitory concentrations of the sucrose esters were higher than that of Lauricidin for all spores tested in the model agar system, but Lauricidin was not the most readily suspended in the test media. Th
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Poinar, Jr., George O., and Kenton L. Chambers. "Setitheca lativalva gen. et sp. nov., a fossil flower of Laurales from mid-Cretaceous Myanmar amber." Journal of the Botanical Research Institute of Texas 12, no. 2 (2018): 643–53. http://dx.doi.org/10.17348/jbrit.v12.i2.964.

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A single staminate flower preserved in mid-Cretaceous Myanmar amber is described as Setitheca lativalva gen. et sp. nov. The fossil’s affinities appear to be with Monimiaceae and allied families of order Laurales. The perianth is composed of ca. 12 spirally arranged tepals of varying size and shape. A single whorl of 10 stamens is attached to the margin of a flat central disc. There is no gynoecium. In some of the stamens, the bilocular anthers are held upright, but in the others, the filaments are arched abaxially and the anthers are reflexed. Dehiscence is extrorse via 2 lateral, dorsally-hi
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Silva-Aguayo, Gonzalo, J. Concepción Rodríguez-Maciel, Angel Lagunes-Tejeda, et al. "Bioactivity of Boldo (Peumus boldusMolina) (Laurales: Monimiaceae) onSpodoptera frugiperda(J.E. Smith) andHelicoverpa zea(Boddie) (Lepidoptera: Noctuidae)." Southwestern Entomologist 35, no. 3 (2010): 215–31. http://dx.doi.org/10.3958/059.035.0301.

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Michalak, Ingo, Li-Bing Zhang, and Susanne S. Renner. "Trans-Atlantic, trans-Pacific and trans-Indian Ocean dispersal in the small Gondwanan Laurales family Hernandiaceae." Journal of Biogeography 37, no. 7 (2010): 1214–26. http://dx.doi.org/10.1111/j.1365-2699.2010.02306.x.

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Rohwer, J. G. "A Note on the Evolution of the Stamens in the Laurales, with Emphasis on the Lauraceae." Botanica Acta 107, no. 2 (1994): 103–10. http://dx.doi.org/10.1111/j.1438-8677.1994.tb00415.x.

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Peña, Jorge E., Scott W. Weihman, Stephen McLean, et al. "Predators and Parasitoids Associated with Scolytinae inPerseaSpecies (Laurales: Lauraceae) and Other Lauraceae in Florida and Taiwan." Florida Entomologist 98, no. 3 (2015): 903–10. http://dx.doi.org/10.1653/024.098.0314.

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Wu, Yi, Wei Wei, Li Liu, Gang Liu, Qi-Qiang Guo, and Zeng-Qiang Qian. "The complete chloroplast genomes of the evergreen tree species Cinnamomum camphora and Cinnamomum parthenoxylon (Laurales: Lauraceae)." Mitochondrial DNA Part B 4, no. 1 (2019): 813–14. http://dx.doi.org/10.1080/23802359.2019.1574677.

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Beurel, Simon, Julien B. Bachelier, Jérôme Munzinger, et al. "First flower inclusion and fossil evidence of Cryptocarya (Laurales, Lauraceae) from Miocene amber of Zhangpu (China)." Fossil Record 27, no. 1 (2024): 1–11. http://dx.doi.org/10.3897/fr.27.109621.

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Lauraceae have one of the oldest fossil records of angiosperms with the earliest known evidence from the mid-Cretaceous. However, most of these records are based on leaves, especially from the Cenozoic of Asia, which are often challenging to assign to extinct or extant genera or species. In contrast, fossils of reproductive organs are more informative, but remain scarce. We here described the first Cenozoic Lauraceae flower of Asia and confirmed the presence of Cryptocarya in the Miocene Zhangpu flora (Fujian Province, south-eastern China) based on an amber inclusion. We scanned the specimen u
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Golovneva, Lina, Eugenia Bugdaeva, Elena Volynets, Yuewu Sun, and Anastasia Zolina. "Angiosperm diversification in the Early Cretaceous of Primorye, Far East of Russia." Fossil Imprint 77, no. 2 (2021): 231–55. http://dx.doi.org/10.37520/fi.2021.017.

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The Partizansk and Razdolnaya coal basins of Primorye, Far East of Russia, contain diverse early angiosperm fossils (pollen, leaves, and fruits). In this paper, we revise the previous data on early angiosperms of this region and summarize the results of our latest research. Age of the plant-bearing deposits was clarified using isotopic U-Th-Pb LA-ICP-MS and U-Pb ID-TIMS methods. Age of the upper part of the Lipovtsy Formation is 118 ± 1.4 Ma, which corresponds to the late Aptian. The early Albian age (109 ± 1 Ma) is assigned to the upper part of the Frentsevka Formation. The diversification of
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Endress, Peter K. "The evolution of floral biology in basal angiosperms." Philosophical Transactions of the Royal Society B: Biological Sciences 365, no. 1539 (2010): 411–21. http://dx.doi.org/10.1098/rstb.2009.0228.

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In basal angiosperms (including ANITA grade, magnoliids, Choranthaceae, Ceratophyllaceae) almost all bisexual flowers are dichogamous (with male and female functions more or less separated in time), and nearly 100 per cent of those are protogynous (with female function before male function). Movements of floral parts and differential early abscission of stamens in the male phase are variously associated with protogyny. Evolution of synchronous dichogamy based on the day/night rhythm and anthesis lasting 2 days is common. In a few clades in Magnoliales and Laurales heterodichogamy has also evol
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Munzinger, Jérôme, and Gordon McPHERSON. "Novitates neocaledonicae XII: Two additional new species of Cryptocarya R.Br. from New Caledonia." Adansonia 43, no. 13 (2021): 151–61. https://doi.org/10.5252/adansonia2021v43a13.

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Munzinger, Jérôme, McPHERSON, Gordon (2021): Novitates neocaledonicae XII: Two additional new species of Cryptocarya R.Br. from New Caledonia. Adansonia (3) 43 (13): 151-161, DOI: 10.5252/adansonia2021v43a13
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Bobrov, Alexey V. F. CH, Mikhail S. Romanov, Nikita S. Zdravchev, and Peter K. Endress. "Fruit structure and development in Eupomatiaceae and comparison of fruit histology with other Magnoliales and with Laurales." Botanical Journal of the Linnean Society 185, no. 2 (2017): 129–46. http://dx.doi.org/10.1093/botlinnean/box047.

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Staedler, Yannick M., and Peter K. Endress. "Diversity and Lability of Floral Phyllotaxis in the Pluricarpellate Families of Core Laurales (Gomortegaceae, Atherospermataceae, Siparunaceae, Monimiaceae)." International Journal of Plant Sciences 170, no. 4 (2009): 522–50. http://dx.doi.org/10.1086/597272.

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Endress, Peter K. "Structural and temporal modes of heterodichogamy and similar patterns across angiosperms." Botanical Journal of the Linnean Society 193, no. 1 (2020): 5–18. http://dx.doi.org/10.1093/botlinnean/boaa001.

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Abstract Different kinds of synchronization of flowering, and of male and female function, have evolved in many angiosperms. The most complex patterns are heterodichogamy, pseudoheterodichogamy and duodichogamy. In this review, their occurrence across angiosperms is shown and the diversity in heterodichogamy and duodichogamy is outlined. Heterodichogamy is characterized by the occurrence of two temporally complementary genetic morphs, whereas in peudoheterodichogamy and duodichogamy only one morph occurs. In duodichogamy, the two phases result from alternating periods of several days of the sa
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