Millipedes! How to manage populations so they do not become damaging at vintage

Millipedes prefer high relative humidity and moderate temperatures (Baker 1980). They typically inhabit areas with mean annual rainfall of >300 mm, mean daily minimum temperatures in winter of 0-15°C and mean daily maximum temperatures in summer of 18-33°C (Baker et al. 2013). Several species of native millipede occur in southern Australia, but they are found infrequently in agricultural environments. The black Portuguese millipede is tolerant of much drier conditions than native species (Paoletti et al. 2007). Millipedes are generally considered to be important macro-detritivores due to their capacity to breakdown organic matter (Baker 1985, Paoletti et al. 2007).

[1]  M. Keller,et al.  Predatory arthropods associated with potential native insectary plants for Australian vineyards , 2019, Australian Journal of Grape and Wine Research.

[2]  M. Retallack The potential functional diversity offered by native insectary plants to support populations of predatory arthropods in Australian vineyards , 2019 .

[3]  S. Macfadyen,et al.  Broad spectrum pesticide application alters natural enemy communities and may facilitate secondary pest outbreaks , 2017, PeerJ.

[4]  L. Vujisić,et al.  Chemical Ecology of Cave-Dwelling Millipedes: Defensive Secretions of the Typhloiulini (Diplopoda, Julida, Julidae) , 2017, Journal of Chemical Ecology.

[5]  L. Vujisić,et al.  Chemical Defence in a Millipede: Evaluation and Characterization of Antimicrobial Activity of the Defensive Secretion from Pachyiulus hungaricus (Karsch, 1881) (Diplopoda, Julida, Julidae) , 2016, PloS one.

[6]  L. Thomson,et al.  Ophyiulus in Victoria: results of millipede surveys from south-eastern Australia , 2015 .

[7]  W. Shear The chemical defenses of millipedes (diplopoda): Biochemistry, physiology and ecology , 2015 .

[8]  F. Roets,et al.  Arthropods vector grapevine trunk disease pathogens. , 2014, Phytopathology.

[9]  V. Tešević,et al.  Chemical Defense in Millipedes (Myriapoda, Diplopoda): Do Representatives of the Family Blaniulidae Belong to the ‘Quinone’ Clade? , 2014, Chemistry & biodiversity.

[10]  B. Mandic,et al.  QUINONES AND NON-QUINONES FROM THE DEFENSIVE SECRETION OF UNCIGER TRANSSILVANICUS (VERHOEFF, 1899) (DIPLOPODA, JULIDA, JULIDAE), FROM SERBIA , 2014 .

[11]  G. Baker,et al.  Invasions of the Portuguese millipede, Ommatoiulus moreleti, in southern Australia , 2013 .

[12]  A. Hoffmann,et al.  Identifying signature of chemical applications on indigenous and invasive nontarget arthropod communities in vineyards. , 2010, Ecological applications : a publication of the Ecological Society of America.

[13]  G. Baker The water and temperature relationships of Ommatoiulus moreletii (Diplopoda: Iulidae) , 2009 .

[14]  M. Paoletti,et al.  Detritivores as indicators of landscape stress and soil degradation , 2007 .

[15]  M. Jaworska Entomopathogenic nematodes for the biological control of crustaceans (Porcellio scaber Latr.) and millipedes (Blaniulus guttulatus Bosc.) in greenhouse , 1994, Anzeiger für Schädlingskunde, Pflanzenschutz, Umweltschutz.

[16]  M. Sallam Classical Biological Control of Arthropods in Australia , 2002 .

[17]  T. Eisner,et al.  Rendering the inedible edible: circumvention of a millipede's chemical defense by a predaceous beetle larva. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[18]  S. McKillup,et al.  Assessment of a rhabditid nematode, Rhabditis necromena Sudhaus and Schulte, as a biological control agent against the millipede Spinotarsus caboverdus Pierrard in the Cape Verde Islands, West Africa , 1991 .

[19]  T. Mabry,et al.  Biochemical Systematics and Ecology , 1974 .