GMC collisions as triggers of star formation – VIII. The core mass function

4Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Compression in giant molecular cloud (GMC) collisions is a promising mechanism to trigger the formation of massive star clusters and OB associations. We simulate colliding and non-colliding magnetized GMCs and examine the properties of pre-stellar cores, selected from projected mass surface density maps, including after synthetic ALMA observations. We then examine core properties, including mass, size, density, velocity, velocity dispersion, temperature, and magnetic field strength. After 4 Myr, ∼1000 cores have formed in the GMC collision, and the high-mass end of the core mass function (CMF) can be fit by a power-law dN/dlogM ∝ M-α with α ≃ 0.7, i.e. relatively top heavy compared to a Salpeter mass function. Depending on how cores are identified, a break in the power law can appear around a few ×10 M☉. The non-colliding GMCs form fewer cores with a CMF with α ≃ 0.8–1.2, i.e. closer to the Salpeter index. We compare the properties of these CMFs to those of several observed samples of cores. Considering other properties, cores formed from colliding clouds are typically warmer, have more disturbed internal kinematics, and are more likely to be gravitational unbound, than cores formed from non-colliding GMCs. The dynamical state of the protocluster of cores formed in the GMC–GMC collision is intrinsically subvirial but can appear to be supervirial if the total mass measurement is affected by observations that miss mass on large scales or at low densities.

Cite

CITATION STYLE

APA

Hsu, C. J., Tan, J. C., Christie, D., Cheng, Y., & O’Neill, T. J. (2023). GMC collisions as triggers of star formation – VIII. The core mass function. Monthly Notices of the Royal Astronomical Society, 522(1), 700–720. https://doi.org/10.1093/mnras/stad777

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free